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Volumn 23, Issue 4, 2016, Pages 383-405

Natural endoperoxides as drug lead compounds

Author keywords

Anticanceragent; Antimalarial peroxides; Artemisinin; Endoperoxide; Natural peroxide; Steroids

Indexed keywords

1,2 DIOXANEPEROXIDE; DITERPENOID; ENDOPEROXIDE; MONOTERPENOID; SESQUITERPENE; SESQUITERPENOID; SESTERTERPENOID; TERPENE; TRITERPENE; TRITERPENOID; UNCLASSIFIED DRUG; BIOLOGICAL PRODUCT; PEROXIDE; STEROID;

EID: 84959455613     PISSN: 09298673     EISSN: 1875533X     Source Type: Journal    
DOI: 10.2174/0929867323666151127200949     Document Type: Review
Times cited : (54)

References (200)
  • 1
    • 0033083665 scopus 로고    scopus 로고
    • Peroxy natural products
    • Casteel, D.A. Peroxy natural products. J. Nat. Prod., 1999, 16(1), 55-73.
    • (1999) J. Nat. Prod. , vol.16 , Issue.1 , pp. 55-73
    • Casteel, D.A.1
  • 2
    • 26644456170 scopus 로고    scopus 로고
    • Natural peroxides. Chemistry and biological activity
    • Tolstikov, G.A.; Tolstikov, A.G.; Tolstikova, O.V. Natural peroxides. Chemistry and biological activity. Rus. Chem. Rev., 1996, 65(9), 769-783.
    • (1996) Rus. Chem. Rev. , vol.65 , Issue.9 , pp. 769-783
    • Tolstikov, G.A.1    Tolstikov, A.G.2    Tolstikova, O.V.3
  • 4
    • 38949159992 scopus 로고    scopus 로고
    • Bioactive natural peroxides as potential therapeutic agents
    • Dembitsky, V.M. Bioactive natural peroxides as potential therapeutic agents. Eur. J. Med. Chem., 2008, 43(2), 223-251.
    • (2008) Eur. J. Med. Chem. , vol.43 , Issue.2 , pp. 223-251
    • Dembitsky, V.M.1
  • 5
    • 0032862255 scopus 로고    scopus 로고
    • Steroids from sponges: Recent reports
    • Anna, A.; Ernesto, F.; Marialuisa, M. Steroids from sponges: Recent reports. Steroids, 1999, 64(10), 687-714.
    • (1999) Steroids , vol.64 , Issue.10 , pp. 687-714
    • Anna, A.1    Ernesto, F.2    Marialuisa, M.3
  • 6
    • 84944174789 scopus 로고    scopus 로고
    • Anti-parasite drugs sweep Nobel prize in medicine 2015
    • Callaway, E.; Cyranoski, D. Anti-parasite drugs sweep Nobel prize in medicine 2015. Nature, 2015, 526(7572), 174-175.
    • (2015) Nature , vol.526 , Issue.7572 , pp. 174-175
    • Callaway, E.1    Cyranoski, D.2
  • 7
    • 80052937334 scopus 로고    scopus 로고
    • Artemisinin: Discovery from the Chinese herbal garden
    • Miller, L.H.; Su, X.Z. Artemisinin: Discovery from the Chinese herbal garden. Cell, 2011, 146(6), 855-858.
    • (2011) Cell , vol.146 , Issue.6 , pp. 855-858
    • Miller, L.H.1    Su, X.Z.2
  • 8
    • 42349104331 scopus 로고    scopus 로고
    • Qinghaosu(Artemisinin): The price of success
    • White, N.J. Qinghaosu(Artemisinin): The price of success. Science, 2008, 320(5874), 330-334.
    • (2008) Science , vol.320 , Issue.5874 , pp. 330-334
    • White, N.J.1
  • 9
    • 84939784451 scopus 로고    scopus 로고
    • Main anti-tumor angiogenesis agents isolated from Chinese herbal medicines
    • Yang, X.; Wu, X.Z. Main anti-tumor angiogenesis agents isolated from Chinese herbal medicines. Mini. Rev. Med. Chem., 2015, 15(12), 1011-1023.
    • (2015) Mini. Rev. Med. Chem. , vol.15 , Issue.12 , pp. 1011-1023
    • Yang, X.1    Wu, X.Z.2
  • 10
    • 84928382772 scopus 로고    scopus 로고
    • Quantitative structure-activity relationship and molecular docking of artemisinin derivatives to vascular endothelial growth factor receptor 1
    • Saeed, M.E.; Kadioglu, O.; Seo, E.J.; Greten, H. J.; Brenk, R.; Efferth, T. Quantitative structure-activity relationship and molecular docking of artemisinin derivatives to vascular endothelial growth factor receptor 1. Anticancer Res., 2015, 35(4), 1929-1934.
    • (2015) Anticancer Res. , vol.35 , Issue.4 , pp. 1929-1934
    • Saeed, M.E.1    Kadioglu, O.2    Seo, E.J.3    Greten, H.J.4    Brenk, R.5    Efferth, T.6
  • 11
    • 84920807545 scopus 로고    scopus 로고
    • Dihydroartemisinin exhibits anti-glioma stem cell activity through inhibiting p-AKT and activating caspase-3
    • Cao, L.; Duanmu, W.S.; Yin, Y.; Zhou, Z.H.; Ge, H.F.; Chen, T.N.; Tan, L.; Yu, A.Y.; Hu, R.; Li, F. Dihydroartemisinin exhibits anti-glioma stem cell activity through inhibiting p-AKT and activating caspase-3. Pharmazie, 2014, 69(10), 752-758.
    • (2014) Pharmazie , vol.69 , Issue.10 , pp. 752-758
    • Cao, L.1    Duanmu, W.S.2    Yin, Y.3    Zhou, Z.H.4    Ge, H.F.5    Chen, T.N.6    Tan, L.7    Yu, A.Y.8    Hu, R.9    Li, F.10
  • 12
    • 84858078951 scopus 로고    scopus 로고
    • The endoperoxide ascaridol shows strong differential cytotoxicity in nucleotide excision repairdeficient cells
    • Abbasi, R.; Efferth, T.; Kuhmann, C.; Opatz, T.; Hao X.J. ; Popanda, O.; Schmezer, P. The endoperoxide ascaridol shows strong differential cytotoxicity in nucleotide excision repairdeficient cells. Appl. Pharm., 2012, 259(3), 302-310.
    • (2012) Appl. Pharm. , vol.259 , Issue.3 , pp. 302-310
    • Abbasi, R.1    Efferth, T.2    Kuhmann, C.3    Opatz, T.4    Hao, X.J.5    Popanda, O.6    Schmezer, P.7
  • 13
    • 33846237367 scopus 로고    scopus 로고
    • Synthesis of novel polar derivatives of the antimalarial endoperoxides ascaridole and dihydroascaridole
    • Hatzakis, E.; Opsenica, I.; Solaja, B.A.; Stratakis, M. Synthesis of novel polar derivatives of the antimalarial endoperoxides ascaridole and dihydroascaridole. ARKIVOC, 2006, 2007(8), 124-135.
    • (2006) ARKIVOC , vol.2007 , Issue.8 , pp. 124-135
    • Hatzakis, E.1    Opsenica, I.2    Solaja, B.A.3    Stratakis, M.4
  • 14
    • 57149112773 scopus 로고    scopus 로고
    • Dietary inclusion of dried Artemisiaannua leaves formanagement of coccidiosis and growth enhancement in chickens
    • Brisibe, E.A.; Umoren, U.E.; Owai, P.U.; Brisibe, F. Dietary inclusion of dried Artemisiaannua leaves formanagement of coccidiosis and growth enhancement in chickens. Afr. J. Biotechnol., 2010, 7(22), 4083-4092.
    • (2010) Afr. J. Biotechnol. , vol.7 , Issue.22 , pp. 4083-4092
    • Brisibe, E.A.1    Umoren, U.E.2    Owai, P.U.3    Brisibe, F.4
  • 16
    • 84991966525 scopus 로고    scopus 로고
    • Chemical composition and antimicrobial activity of essential oils of different organs of three Artemisiaspecies from Iran
    • Zanousi, M.B.P.; Aberoomand, A.P.; Raeesi, M. Chemical composition and antimicrobial activity of essential oils of different organs of three Artemisiaspecies from Iran. J. Med. Plants Res., 2012, 6(42), 5489-5494.
    • (2012) J. Med. Plants Res. , vol.6 , Issue.42 , pp. 5489-5494
    • Zanousi, M.B.P.1    Aberoomand, A.P.2    Raeesi, M.3
  • 17
    • 84902955993 scopus 로고    scopus 로고
    • Advances in the chemical synthesis of artemisinin
    • Wang, Z.L.; Yang, L.Y.; Yang, X.W.; Zhang, X.H. Advances in the chemical synthesis of artemisinin. Synthetic Commun., 2014, 44(14), 1987-2003.
    • (2014) Synthetic Commun. , vol.44 , Issue.14 , pp. 1987-2003
    • Wang, Z.L.1    Yang, L.Y.2    Yang, X.W.3    Zhang, X.H.4
  • 18
    • 84857752407 scopus 로고    scopus 로고
    • Antimalarial peroxides: Advances in drug discovery and design
    • Slack, R.D.; Jacobine, A.M.; Posner, G.H. Antimalarial peroxides: Advances in drug discovery and design. Med. Chem. Commun., 2012, 3(3), 281-297.
    • (2012) Med. Chem. Commun. , vol.3 , Issue.3 , pp. 281-297
    • Slack, R.D.1    Jacobine, A.M.2    Posner, G.H.3
  • 20
    • 80052337277 scopus 로고    scopus 로고
    • An artemisinin-derived dimer has highly potent anti-cytomegalovirus(CMV) and anti-cancer activities
    • He, R.; Mott, B.T.; Rosenthal, A.S.; Genna, D.T.; Posner, G.H.; Arav-Boger, R. An artemisinin-derived dimer has highly potent anti-cytomegalovirus(CMV) and anti-cancer activities. PLoS One, 2011, 6(8), e24334.
    • (2011) PLoS One , vol.6 , Issue.8 , pp. e24334
    • He, R.1    Mott, B.T.2    Rosenthal, A.S.3    Genna, D.T.4    Posner, G.H.5    Arav-Boger, R.6
  • 21
    • 84940375244 scopus 로고    scopus 로고
    • Novel spirobicyclic artemisinin analogues( artemalogues): Synthesis and antitumor activities
    • Liu, G.; Song, S.S.; Shu, S.Q.; Miao, Z.H.; Zhang, A.; Ding, C.Y. Novel spirobicyclic artemisinin analogues( artemalogues): Synthesis and antitumor activities. Eur. J. Med. Chem., 2015, 103, 17-28.
    • (2015) Eur. J. Med. Chem. , vol.103 , pp. 17-28
    • Liu, G.1    Song, S.S.2    Shu, S.Q.3    Miao, Z.H.4    Zhang, A.5    Ding, C.Y.6
  • 22
    • 84857752045 scopus 로고    scopus 로고
    • Synthetic peroxides as potent antimalarials. News and views
    • Charles, W.J. Synthetic peroxides as potent antimalarials. news and views. Curr. Top. Med. Chem., 2012, 12(5), 373-399.
    • (2012) Curr. Top. Med. Chem. , vol.12 , Issue.5 , pp. 373-399
    • Charles, W.J.1
  • 23
    • 78649484865 scopus 로고    scopus 로고
    • Effects of artemisinin and Artemisia extracts on Haemonchuscontortus in gerbils(Meriones unguiculatus)
    • Squires, J.M.; Ferreira, J.F.; Lindsay, D.S.; Zajac, A.M. Effects of artemisinin and Artemisia extracts on Haemonchuscontortus in gerbils(Meriones unguiculatus). Vet. Parasitol., 2011, 175(1), 103-108.
    • (2011) Vet. Parasitol. , vol.175 , Issue.1 , pp. 103-108
    • Squires, J.M.1    Ferreira, J.F.2    Lindsay, D.S.3    Zajac, A.M.4
  • 24
    • 78649251920 scopus 로고    scopus 로고
    • Heme as trigger and target for trioxane-containingantimalarial drugs
    • Meunier, B.; Robert, A. Heme as trigger and target for trioxane-containingantimalarial drugs. Acc. Chem. Res., 2010, 43(11), 1444-1451.
    • (2010) Acc. Chem. Res. , vol.43 , Issue.11 , pp. 1444-1451
    • Meunier, B.1    Robert, A.2
  • 25
    • 17744377209 scopus 로고    scopus 로고
    • Total syntheses of Yingzhaosu A and of its C(14)-epimer includingthe first evaluation of their antimalarial and cytotoxic activities
    • Szpilman, A.M.; Korshin, E.E.; Rozenberg, H; Bachi, M.D. Total syntheses of Yingzhaosu A and of its C(14)-epimer includingthe first evaluation of their antimalarial and cytotoxic activities. J. Org. Chem., 2005, 70(9), 3618-3632.
    • (2005) J. Org. Chem. , vol.70 , Issue.9 , pp. 3618-3632
    • Szpilman, A.M.1    Korshin, E.E.2    Rozenberg, H.3    Bachi, M.D.4
  • 26
    • 0037021402 scopus 로고    scopus 로고
    • Antimalarial chemotherapeutic peroxides: Artemisinin yingzhaosu A and related compounds
    • Borstnik, K.; Paik, I.H.; Shapiro, T.A.; Posner, G.H. Antimalarial chemotherapeutic peroxides: Artemisinin, yingzhaosu A and related compounds. Int. J. Parasitol., 2002, 32(13), 1661-1667.
    • (2002) Int. J. Parasitol. , vol.32 , Issue.13 , pp. 1661-1667
    • Borstnik, K.1    Paik, I.H.2    Shapiro, T.A.3    Posner, G.H.4
  • 27
    • 38549149302 scopus 로고    scopus 로고
    • Weak chemiluminescence emission during base induced rearrangement of Gfactors
    • Bernat, V.; Andre, C.; Ander-Barres, C. Weak chemiluminescence emission during base induced rearrangement of Gfactors. Org. Biomol. Chem., 2008, 6(3), 454-457.
    • (2008) Org. Biomol. Chem. , vol.6 , Issue.3 , pp. 454-457
    • Bernat, V.1    Andre, C.2    Ander-Barres, C.3
  • 28
    • 18844442917 scopus 로고    scopus 로고
    • Alkylation of natural endoperoxide G3-factor. Synthesis and antimalarial activity studies
    • Najjar, F.; Gorrichon, L.; Baltas, M.; Andre-Barres, C.; Vial, H. Alkylation of natural endoperoxide G3-factor. Synthesis and antimalarial activity studies. Org. Biomol. Chem., 2005, 3(9), 1612-1614.
    • (2005) Org. Biomol. Chem. , vol.3 , Issue.9 , pp. 1612-1614
    • Najjar, F.1    Gorrichon, L.2    Baltas, M.3    Andre-Barres, C.4    Vial, H.5
  • 29
    • 84911366424 scopus 로고    scopus 로고
    • Antimalarial bicyclic peroxides belonging to the G-factor family: Mechanistic aspects of their formation and iron(II) induced reduction
    • Ruiz, J.; Azema, J.; Payrastre, C.; Baltas, M.; Tuccio, B.; Vial, H.; Andre-Barres, C. Antimalarial bicyclic peroxides belonging to the G-factor family: Mechanistic aspects of their formation and iron(II) induced reduction. Curr. Top. Med. Chem., 2014, 14(14), 1668-1683.
    • (2014) Curr. Top. Med. Chem. , vol.14 , Issue.14 , pp. 1668-1683
    • Ruiz, J.1    Azema, J.2    Payrastre, C.3    Baltas, M.4    Tuccio, B.5    Vial, H.6    Andre-Barres, C.7
  • 30
    • 18544400971 scopus 로고    scopus 로고
    • Tetrahydrofuran-type sesquiterpenes from Artemisia lobelii All var canescens(DC.) Briqu and Artemisia lobelii All var biasolettiana(Vis.) K. Maly
    • Tesevic, V.; Milosavljevic, S.; Vajs, V.; Janackovic, P.; Jovic, D.L.; Vujisic, L. Tetrahydrofuran-type sesquiterpenes from Artemisia lobelii All. var. canescens(DC.) Briqu. and Artemisia lobelii All. var. biasolettiana(Vis.) K. Maly. Biochem. Syst. Ecol., 2004, 32(5), 525-527.
    • (2004) Biochem. Syst. Ecol. , vol.32 , Issue.5 , pp. 525-527
    • Tesevic, V.1    Milosavljevic, S.2    Vajs, V.3    Janackovic, P.4    Jovic, D.L.5    Vujisic, L.6
  • 32
    • 52649120927 scopus 로고    scopus 로고
    • The bisabolane sesquiterpenoid endoperoxide 3,6-epidioxy-1,10-bisaboladiene, isolated from Cacalia delphiniifolia inhibits the growth of human cancer cells and induces apoptosis
    • Nishikawa, K.; Aburai, N.; Yamada, K.; Koshino, H.; Tsuchiya, E.; Kimura, K.I. The bisabolane sesquiterpenoid endoperoxide, 3,6-epidioxy-1,10-bisaboladiene, isolated from Cacalia delphiniifolia inhibits the growth of human cancer cells and induces apoptosis. Biosci. Biotechnol. Biochem., 2008, 72(9), 2463-2466.
    • (2008) Biosci. Biotechnol. Biochem. , vol.72 , Issue.9 , pp. 2463-2466
    • Nishikawa, K.1    Aburai, N.2    Yamada, K.3    Koshino, H.4    Tsuchiya, E.5    Kimura, K.I.6
  • 34
    • 84915750580 scopus 로고    scopus 로고
    • 3,6-Epidioxy-1,10-bisaboladiene inhibits G1-specific transcription through Swi4/Swi6 and Mbp1/Swi6 via the Hog1 stress pathway in yeast
    • Imamura, Y.; Yukawa, M.; Ueno, M.; Kimura, K.; Tsuchiya, E. 3,6-Epidioxy-1,10-bisaboladiene inhibits G1-specific transcription through Swi4/Swi6 and Mbp1/Swi6 via the Hog1 stress pathway in yeast. FEBS J., 2014, 281(20), 4612-4621
    • (2014) FEBS J. , vol.281 , Issue.20 , pp. 4612-4621
    • Imamura, Y.1    Yukawa, M.2    Ueno, M.3    Kimura, K.4    Tsuchiya, E.5
  • 36
    • 0034703382 scopus 로고    scopus 로고
    • Novel guaiane endoperoxides, nardoguaianone A-D, from Nardostachys chinensis roots and their antinociceptive andantimalarial activities
    • Takaya, Y.; Takeuji, Y.; Akasaka, M.; Nakagawasai, O.; Tadano, T.; Kisara, K.; Kim, H.; Wataya, Y.; Niwa, M.; Oshima, Y. Novel guaiane endoperoxides, nardoguaianone A-D, from Nardostachys chinensis roots and their antinociceptive andantimalarial activities. Tetrahedron, 2000, 56(39), 7673-7678.
    • (2000) Tetrahedron , vol.56 , Issue.39 , pp. 7673-7678
    • Takaya, Y.1    Takeuji, Y.2    Akasaka, M.3    Nakagawasai, O.4    Tadano, T.5    Kisara, K.6    Kim, H.7    Wataya, Y.8    Niwa, M.9    Oshima, Y.10
  • 38
    • 84865113257 scopus 로고    scopus 로고
    • Combined receptor-based and ligand-based approach to delineate the modeof binding of guaianolide-endoperoxides to PfATP6
    • Helal, M.A.; Avery, M.A. Combined receptor-based and ligand-based approach to delineate the modeof binding of guaianolide-endoperoxides to PfATP6. Bioorg. Med. Chem. Lett., 2012, 22(17), 5410-5414.
    • (2012) Bioorg. Med. Chem. Lett. , vol.22 , Issue.17 , pp. 5410-5414
    • Helal, M.A.1    Avery, M.A.2
  • 39
    • 80053393925 scopus 로고    scopus 로고
    • Isolation of artediffusin(tehranolide) as a new antimalarial agent
    • Rustaiyan, A.; Nahrevanian, H.; Kazemi, M. Isolation of artediffusin(tehranolide) as a new antimalarial agent. Asian J. Chem., 2011, 23(11), 4810-4814.
    • (2011) Asian J. Chem. , vol.23 , Issue.11 , pp. 4810-4814
    • Rustaiyan, A.1    Nahrevanian, H.2    Kazemi, M.3
  • 40
    • 84859491411 scopus 로고    scopus 로고
    • Tehranolide inhibits proliferation of MCF-7 human breast cancer cells by inducing G0/G1 arrest and apoptosis
    • Noori, S.; Hassan, Z.M. Tehranolide inhibits proliferation of MCF-7 human breast cancer cells by inducing G0/G1 arrest and apoptosis. Free. Radic. Biol. Med., 2012, 52(9), 1987-1999.
    • (2012) Free. Radic. Biol. Med. , vol.52 , Issue.9 , pp. 1987-1999
    • Noori, S.1    Hassan, Z.M.2
  • 41
    • 77950629650 scopus 로고    scopus 로고
    • Tehranolide molecule modulates the immune response reduce regulatory T cell and inhibits tumor growth in vivo
    • Noori, S.; Taghikhani, M.; Hassan, Z.M.; Allameha, A.; Mostafaei, A. Tehranolide molecule modulates the immune response, reduce regulatory T cell and inhibits tumor growth in vivo. Mol. Immunol., 2010, 47(7-8), 1579-1584.
    • (2010) Mol. Immunol. , vol.47 , Issue.7-8 , pp. 1579-1584
    • Noori, S.1    Taghikhani, M.2    Hassan, Z.M.3    Allameha, A.4    Mostafaei, A.5
  • 42
    • 77951934024 scopus 로고    scopus 로고
    • Tehranolide could shift the immune response towards Th1 and modulate the intra-tumor infiltrated T regulatory cells
    • Noori, S.; Taghikhani, M.; Hassan, Z.M.; Allameh, A.; Mostafaei, A. Tehranolide could shift the immune response towards Th1 and modulate the intra-tumor infiltrated T regulatory cells. Iran J. Immunol., 2009, 6(4), 216-224.
    • (2009) Iran J. Immunol. , vol.6 , Issue.4 , pp. 216-224
    • Noori, S.1    Taghikhani, M.2    Hassan, Z.M.3    Allameh, A.4    Mostafaei, A.5
  • 43
    • 84873856866 scopus 로고    scopus 로고
    • Development of artemisinin compounds for cancer treatment
    • Singh, N.P.; Sasaki, T. Development of artemisinin compounds for cancer treatment. Invest. New Drug, 2013, 31(1), 230-246.
    • (2013) Invest. New Drug , vol.31 , Issue.1 , pp. 230-246
    • Singh, N.P.1    Sasaki, T.2
  • 45
    • 80055091470 scopus 로고    scopus 로고
    • Antiangiogenic effect of chamigrane endoperoxides from a Thai Mangrove-derived fungus
    • Chokpaiboon, S.; Sommit, D.; Bunyapaiboonsri, T.; Matsubara, K.; Pudhom, K. Antiangiogenic effect of chamigrane endoperoxides from a Thai Mangrove-derived fungus. J. Nat. Fungus., 2012, 74(10), 2290-2294.
    • (2012) J. Nat. Fungus. , vol.74 , Issue.10 , pp. 2290-2294
    • Chokpaiboon, S.1    Sommit, D.2    Bunyapaiboonsri, T.3    Matsubara, K.4    Pudhom, K.5
  • 47
    • 77953123169 scopus 로고    scopus 로고
    • Two novelnorsesquiterpene peroxides from basidiomycete Steccherinum ochraceum
    • Liu, D.Z.; Dong, Z.J.; Wang, F.; Liu, J.K. Two novelnorsesquiterpene peroxides from basidiomycete Steccherinum ochraceum. Tetrahedron Lett., 2010, 51(23), 3152-3153.
    • (2010) Tetrahedron Lett. , vol.51 , Issue.23 , pp. 3152-3153
    • Liu, D.Z.1    Dong, Z.J.2    Wang, F.3    Liu, J.K.4
  • 48
    • 80055091470 scopus 로고    scopus 로고
    • Antiangiogenic effect of chamigrane endoperoxides from a Thai mangrove-derived fungus
    • Chokpaiboon, S.; Sommit, D.; Bunyapaiboonsri, T.; Matsubara, K.; Pudhom, K. Antiangiogenic effect of chamigrane endoperoxides from a Thai mangrove-derived fungus. J. Nat. Prod., 2011, 74(10), 2290-2294.
    • (2011) J. Nat. Prod. , vol.74 , Issue.10 , pp. 2290-2294
    • Chokpaiboon, S.1    Sommit, D.2    Bunyapaiboonsri, T.3    Matsubara, K.4    Pudhom, K.5
  • 49
    • 84922637400 scopus 로고    scopus 로고
    • Expeditious entry to the chamigrane endoperoxide family of natural products
    • Chen, H.J.; Wu, Y.K. Expeditious entry to the chamigrane endoperoxide family of natural products. Org. Lett., 2015, 17(3), 592-595.
    • (2015) Org. Lett. , vol.17 , Issue.3 , pp. 592-595
    • Chen, H.J.1    Wu, Y.K.2
  • 50
    • 79957841774 scopus 로고    scopus 로고
    • Cytotoxic norsesquiterpene peroxides from the endophytic fungusTalaromyces flavus isolated from the mangrove plant Sonneratia apetala
    • Li, H.X.; Huang, H.B.; Shao, C.L.; Huang, H.R.; Jiang, J.Y.; Zhu, X.; Liu, Y.Y.; Liu, L.; Lu, Y.J.; Li, M.F.; Lin, Y.C.; She, Z.G. Cytotoxic norsesquiterpene peroxides from the endophytic fungusTalaromyces flavus isolated from the mangrove plant Sonneratia apetala. J. Nat. Prod., 2011, 74(5), 1230-1235.
    • (2011) J. Nat. Prod. , vol.74 , Issue.5 , pp. 1230-1235
    • Li, H.X.1    Huang, H.B.2    Shao, C.L.3    Huang, H.R.4    Jiang, J.Y.5    Zhu, X.6    Liu, Y.Y.7    Liu, L.8    Lu, Y.J.9    Li, M.F.10    Lin, Y.C.11    She, Z.G.12
  • 51
    • 0242352589 scopus 로고    scopus 로고
    • Nardosinone the first enhancer of neurite outgrowth-promoting activity of staurosporine and dibutyryl cyclic AMP in PC12D cells
    • Li, P.; Matsunaga, K.; Yamakuni, T.; Ohizumi, Y. Nardosinone, the first enhancer of neurite outgrowth-promoting activity of staurosporine and dibutyryl cyclic AMP in PC12D cells. Dev. Brain Res., 2003, 145(2), 177-183.
    • (2003) Dev. Brain Res. , vol.145 , Issue.2 , pp. 177-183
    • Li, P.1    Matsunaga, K.2    Yamakuni, T.3    Ohizumi, Y.4
  • 54
    • 27744585070 scopus 로고    scopus 로고
    • Structure of a new diterpene alcohol from Pinus sibirica buds
    • Khamidullina, E.A.; Vereshchagin, A.L.; Medvedeva, S.A. Structure of a new diterpene alcohol from Pinus sibirica buds. Chem. Nat. Compd., 2005, 41(4), 426-428.
    • (2005) Chem. Nat. Compd. , vol.41 , Issue.4 , pp. 426-428
    • Khamidullina, E.A.1    Vereshchagin, A.L.2    Medvedeva, S.A.3
  • 56
    • 33646253681 scopus 로고    scopus 로고
    • A diterpene endoperoxide from Microtoena insuavis(Hance) Prain ex Dunn
    • Li, C.Q.; Li, B.G.; Wang, F.P.; Zhang, G.L. A diterpene endoperoxide from Microtoena insuavis(Hance) Prain ex Dunn. J. Integr. Plant. Biol., 2006, 48(5), 613-616.
    • (2006) J. Integr. Plant. Biol. , vol.48 , Issue.5 , pp. 613-616
    • Li, C.Q.1    Li, B.G.2    Wang, F.P.3    Zhang, G.L.4
  • 58
    • 84986289918 scopus 로고    scopus 로고
    • Isolation of cytotoxic diterpenoids from the chilean medicinal plant azorella compacta phil from the atacama desert by highspeed counter-current chromatography
    • [ Epub ahead of print]
    • Borquez, J.; Bartolucci, N.L.; Echiburu-Chau, C.; Winterhalter, P.; Vallejos, J.; Jerz, G.; Simirgiotis, M.J. Isolation of cytotoxic diterpenoids from the Chilean medicinal plant Azorella compacta Phil from the Atacama Desert by highspeed counter-current chromatography. J. Sci. Food Agr., 2015, [Epub ahead of print].
    • (2015) J. Sci. Food Agr.
    • Borquez, J.1    Bartolucci, N.L.2    Echiburu-Chau, C.3    Winterhalter, P.4    Vallejos, J.5    Jerz, G.6    Simirgiotis, M.J.7
  • 60
    • 2342654179 scopus 로고    scopus 로고
    • New triterpene peroxide from Pseudolarix kaempferi
    • Zhou, T.X.; Zhang, H.P.; Zhu, N.Y.; Chiu, P.L. New triterpene peroxide from Pseudolarix kaempferi. Tetrahedron, 2004, 60(22), 4931-4936.
    • (2004) Tetrahedron , vol.60 , Issue.22 , pp. 4931-4936
    • Zhou, T.X.1    Zhang, H.P.2    Zhu, N.Y.3    Chiu, P.L.4
  • 61
    • 80052839823 scopus 로고    scopus 로고
    • Three new peroxy triterpene lactones from Pseudolarix kaempferi
    • Tan, J.M.; Qiu, Y.H.; Tan, X.Q.; Tan, C.H. Three new peroxy triterpene lactones from Pseudolarix kaempferi. Helv. Chim. Acta., 2011, 94(9), 1697-1702.
    • (2011) Helv. Chim. Acta. , vol.94 , Issue.9 , pp. 1697-1702
    • Tan, J.M.1    Qiu, Y.H.2    Tan, X.Q.3    Tan, C.H.4
  • 62
    • 81855161812 scopus 로고    scopus 로고
    • Antimicrobial cytotoxic lignans and terpenoids from the twigs of Pseudolarix kaempferi
    • He, W.J.; Chu, H.B.; Zhang, Y.M.; Han, H.J.; Yan, H.; Zeng, G.Z.; Fu, Z.H.; Olubanke, O.; Tan, N.H. Antimicrobial, cytotoxic lignans and terpenoids from the twigs of Pseudolarix kaempferi. Planta Med., 2011, 77(17), 1924-1931.
    • (2011) Planta Med. , vol.77 , Issue.17 , pp. 1924-1931
    • He, W.J.1    Chu, H.B.2    Zhang, Y.M.3    Han, H.J.4    Yan, H.5    Zeng, G.Z.6    Fu, Z.H.7    Olubanke, O.8    Tan, N.H.9
  • 63
    • 77949794864 scopus 로고    scopus 로고
    • SChinalacton A a new cytotoxic triterpenoid from Schisandra sphenanthera
    • He, F.; Pu, J.X.; Huang, S.X.; Sun, H.D. SChinalacton A, a new cytotoxic triterpenoid from Schisandra sphenanthera. Org. Lett., 2010, 12(6), 1208-1211.
    • (2010) Org. Lett. , vol.12 , Issue.6 , pp. 1208-1211
    • He, F.1    Pu, J.X.2    Huang, S.X.3    Sun, H.D.4
  • 64
    • 55549145037 scopus 로고    scopus 로고
    • The structure and absolute configuration of Shuangkangsu: A novel natural cyclic peroxide from Lonicera japonica(Thunb.)
    • Yu, D.Q.; Chen, R.Y.; Huang, L.J.; Tong, K.M. The structure and absolute configuration of Shuangkangsu: A novel natural cyclic peroxide from Lonicera japonica(Thunb.). J. Asian. Nat. Prod. Res., 2008, 10(9), 851-856.
    • (2008) J. Asian. Nat. Prod. Res. , vol.10 , Issue.9 , pp. 851-856
    • Yu, D.Q.1    Chen, R.Y.2    Huang, L.J.3    Tong, K.M.4
  • 68
    • 77954074797 scopus 로고    scopus 로고
    • Manadoperoxides A-D from the Indonesian sponge Plakortis cfr simplex. Further insights on the structure-activity relationships of simple 1, 2-dioxane antimalarials
    • Fattorusso, C.; Persico, M.; Calcinai, B.; Cerrano, C.; Parapini, S.; Taramelli, D.; Novellino, E.; Romano, A.; Scala, F.; Fattorusso, E. Manadoperoxides A-D from the Indonesian sponge Plakortis cfr. simplex. Further insights on the structure-activity relationships of simple 1,2-dioxane antimalarials. J. Nat. Prod., 2010, 73(6), 1138-1145.
    • (2010) J. Nat. Prod. , vol.73 , Issue.6 , pp. 1138-1145
    • Fattorusso, C.1    Persico, M.2    Calcinai, B.3    Cerrano, C.4    Parapini, S.5    Taramelli, D.6    Novellino, E.7    Romano, A.8    Scala, F.9    Fattorusso, E.10
  • 69
    • 84885027251 scopus 로고    scopus 로고
    • Natural and semisynthetic analogues of manadoperoxide Breveal new structural requirements for trypanocidal activity
    • Chianese, G.; Scala, F.; Calcinai, B.; Cerrano, C.; Dien, H.A.; Kaiser, M.; Tasdemir, D.; Taglialatela-Scafati, O. Natural and semisynthetic analogues of manadoperoxide Breveal new structural requirements for trypanocidal activity. Mar. Drugs, 2013, 11(9), 3297-3308.
    • (2013) Mar. Drugs , vol.11 , Issue.9 , pp. 3297-3308
    • Chianese, G.1    Scala, F.2    Calcinai, B.3    Cerrano, C.4    Dien, H.A.5    Kaiser, M.6    Tasdemir, D.7    Taglialatela-Scafati, O.8
  • 71
    • 33846805634 scopus 로고    scopus 로고
    • Eupalmerin acetate, a novel anticancer agent from Caribbean gorgonian octocorals, induces apoptosis in malignant glioma cells via the c-Jun NH2-terminal kinase pathway
    • Iwamaru, A.; Iwado, E.; Kondo, S.; Newman, R.A.; Vera, B.; Rodriguez, A.D.; Kondo, Y. Eupalmerin acetate, a novel anticancer agent from Caribbean gorgonian octocorals, induces apoptosis in malignant glioma cells via the c-Jun NH2-terminal kinase pathway. Mol. Cancer Ther., 2007, 6(1), 184-192.
    • (2007) Mol. Cancer Ther. , vol.6 , Issue.1 , pp. 184-192
    • Iwamaru, A.1    Iwado, E.2    Kondo, S.3    Newman, R.A.4    Vera, B.5    Rodriguez, A.D.6    Kondo, Y.7
  • 73
    • 77951605067 scopus 로고    scopus 로고
    • Antitrypanosomal cyclic polyketide from the Australian marine sponge Plakortis sp
    • Feng, Y.J.; Davis, R.A.; Sykes, M.; Avery, V.M.; Camp, D.; Quinn, R.J. Antitrypanosomal cyclic polyketide from the Australian marine sponge Plakortis sp. J. Nat. Prod., 2010, 73(4), 716-719.
    • (2010) J. Nat. Prod. , vol.73 , Issue.4 , pp. 716-719
    • Feng, Y.J.1    Davis, R.A.2    Sykes, M.3    Avery, V.M.4    Camp, D.5    Quinn, R.J.6
  • 75
    • 84875439523 scopus 로고    scopus 로고
    • New antimalarial polyketide endoperoxides from the marine sponge Plakinastrella mamillaris collected at Fiji Islands
    • Festa, C.; De Marino, S.; D'Auria, M.V.; Taglialatela-Scafati, O.; Deharo, E.; Petek, S.; Zampella, A. New antimalarial polyketide endoperoxides from the marine sponge Plakinastrella mamillaris collected at Fiji Islands. Tetrahedron, 2013, 69(18), 3706-3713.
    • (2013) Tetrahedron , vol.69 , Issue.18 , pp. 3706-3713
    • Festa, C.1    De Marino, S.2    D'Auria, M.V.3    Taglialatela-Scafati, O.4    Deharo, E.5    Petek, S.6    Zampella, A.7
  • 77
    • 84868027456 scopus 로고    scopus 로고
    • Plakortolide stereochemistry revisited: The checkered history of Plakortolides e and i
    • Yong, K.W.L.; Barnych, B.; De Voss, J.J.; Vatele, J.M.; Garson, M.J. Plakortolide stereochemistry revisited: The checkered history of Plakortolides E and I. J. Nat. Prod., 2012, 75(10), 1792-1797.
    • (2012) J. Nat. Prod. , vol.75 , Issue.10 , pp. 1792-1797
    • Yong, K.W.L.1    Barnych, B.2    De Voss, J.J.3    Vatele, J.M.4    Garson, M.J.5
  • 78
    • 77958548626 scopus 로고    scopus 로고
    • Bioactive cycloperoxides isolated from the Puerto Rican sponge Plakortis halichondrioides
    • Jimenez-Romero, C.; Ortiz, I.; Vicente, J.; Vera, B.; Rodriguez, A.D.; Nam, S.; Jove, R. Bioactive cycloperoxides isolated from the Puerto Rican sponge Plakortis halichondrioides. J. Nat. Prod., 2010, 73(10), 1694-1700.
    • (2010) J. Nat. Prod. , vol.73 , Issue.10 , pp. 1694-1700
    • Jimenez-Romero, C.1    Ortiz, I.2    Vicente, J.3    Vera, B.4    Rodriguez, A.D.5    Nam, S.6    Jove, R.7
  • 79
    • 0035906015 scopus 로고    scopus 로고
    • New peroxylactones from the Jamaican sponge Plakinastrella onkodes, with inhibitory activity against the AIDS opportunistic parasitic infection Toxoplasma gondii
    • Tony, L.P.; Amiee, D.; Anis, A.K.; Rama, K.K.; David, N.B.; Peter, W.; Michelle K.; Mark, T.H. New peroxylactones from the Jamaican sponge Plakinastrella onkodes, with inhibitory activity against the AIDS opportunistic parasitic infection Toxoplasma gondii. Tetrahedron, 2001, 57(8), 1483-1487.
    • (2001) Tetrahedron , vol.57 , Issue.8 , pp. 1483-1487
    • Tony, L.P.1    Amiee, D.2    Anis, A.K.3    Rama, K.K.4    David, N.B.5    Peter, W.6    Michelle, K.7    Mark, T.H.8
  • 81
    • 79952289533 scopus 로고    scopus 로고
    • Configurational assignment of cyclic peroxy metabolites provides an insight into their biosynthesis: Isolation of Plakortolides seco-Plakortolides, and Plakortones from the Australian marine sponge Plakinastrella clathrata
    • Yong, K.W.L.; De Voss, J.J.; Hooper, J.N.A.; Garson, M.J. Configurational assignment of cyclic peroxy metabolites provides an insight into their biosynthesis: Isolation of Plakortolides, seco-Plakortolides, and Plakortones from the Australian marine sponge Plakinastrella clathrata. J. Nat. Prod., 2011, 74(2), 194-207.
    • (2011) J. Nat. Prod. , vol.74 , Issue.2 , pp. 194-207
    • Yong, K.W.L.1    De Voss, J.J.2    Hooper, J.N.A.3    Garson, M.J.4
  • 82
    • 76049100214 scopus 로고    scopus 로고
    • Stolonoxides e and F cytotoxic metabolites from the marine ascidian Stolonica Socialis
    • Reyes, F.; Rodriguez-Acebes, R.; Fernandez, R.; Bueno, S.; Francesch, A.; Cuevas, C. Stolonoxides E and F, cytotoxic metabolites from the marine ascidian Stolonica Socialis. J. Nat. Prod., 2010, 73(1), 83-85.
    • (2010) J. Nat. Prod. , vol.73 , Issue.1 , pp. 83-85
    • Reyes, F.1    Rodriguez-Acebes, R.2    Fernandez, R.3    Bueno, S.4    Francesch, A.5    Cuevas, C.6
  • 83
    • 84936792028 scopus 로고    scopus 로고
    • Catalytic enantioselective peroxidation of ?,?-unsaturatedaldehydes for the asymmetric synthesis of biologically important chiral endoperoxides
    • Hu, L.; Lu, X.J.; Deng, L. Catalytic enantioselective peroxidation of ?,?-unsaturatedaldehydes for the asymmetric synthesis of biologically important chiral endoperoxides. J. Am. Chem. Soc., 2015, 137(26), 8400-8403.
    • (2015) J. Am. Chem. Soc. , vol.137 , Issue.26 , pp. 8400-8403
    • Hu, L.1    Lu, X.J.2    Deng, L.3
  • 84
    • 0942269013 scopus 로고    scopus 로고
    • Tasnemoxides A-C new cytotoxic cyclic norsesterterpene peroxides from the Red Sea sponge Diacarnus erythraenus
    • Youssef, D.T.A. Tasnemoxides A-C, new cytotoxic cyclic norsesterterpene peroxides from the Red Sea sponge Diacarnus erythraenus. J. Nat. Prod., 2004, 67(1), 112-114.
    • (2004) J. Nat. Prod. , vol.67 , Issue.1 , pp. 112-114
    • Youssef, D.T.A.1
  • 85
    • 77952519885 scopus 로고    scopus 로고
    • Inhibition of nitric oxide(NO) production inlipopolysaccharide( LPS)-activated murine macrophage RAW 264.7 cells by the norsesterterpene peroxide epimuqubilin A
    • Cheenpracha, S.; Park, E.J.; Rostama, B.; Pezzuto, J.M.; Chang, L.C. Inhibition of nitric oxide(NO) production inlipopolysaccharide( LPS)-activated murine macrophage RAW 264.7 cells by the norsesterterpene peroxide, epimuqubilin A. Mar. Drugs, 2010, 8, 429-437
    • (2010) Mar. Drugs , vol.8 , pp. 429-437
    • Cheenpracha, S.1    Park, E.J.2    Rostama, B.3    Pezzuto, J.M.4    Chang, L.C.5
  • 86
    • 81855197030 scopus 로고    scopus 로고
    • Suppression of cyclooxygenase-2 and inducible nitric oxide synthase expressionby epimuqubilin A via IKK/I?B/NF-?B pathways in lipopolysaccharide-stimulated RAW 264.7 cells
    • Park, E.J.; Cheenpracha, S.; Chang, L.C.; Pezzuto, J.M. Suppression of cyclooxygenase-2 and inducible nitric oxide synthase expressionby epimuqubilin A via IKK/I?B/NF-?B pathways in lipopolysaccharide-stimulated RAW 264.7 cells. Phytochem. Lett., 2011, 4(4), 426-431.
    • (2011) Phytochem. Lett. , vol.4 , Issue.4 , pp. 426-431
    • Park, E.J.1    Cheenpracha, S.2    Chang, L.C.3    Pezzuto, J.M.4
  • 88
    • 0034758908 scopus 로고    scopus 로고
    • Cytotoxic cyclic norterpene peroxides from a Red Sea sponge Diacarnus erythraenus
    • Youssef, D.T.A.; Yoshida, W.Y.; Kelly, M.; Scheuer, P.J. Cytotoxic cyclic norterpene peroxides from a Red Sea sponge Diacarnus erythraenus. J. Nat. Prod., 2001, 64(10), 1332-1335.
    • (2001) J. Nat. Prod. , vol.64 , Issue.10 , pp. 1332-1335
    • Youssef, D.T.A.1    Yoshida, W.Y.2    Kelly, M.3    Scheuer, P.J.4
  • 89
    • 77957223342 scopus 로고    scopus 로고
    • Norterpenoids and related peroxides from the Formosan marine sponge Negombata corticata
    • Chao, C.H.; Chou, K.J.; Wang, G.H.; Wu, Y.C.; Wang, L.H.; Chen, J.P.; Sheu, J.H.; Sung, P.J. Norterpenoids and related peroxides from the Formosan marine sponge Negombata corticata. J. Nat. Prod., 2010, 73(9), 1538-1543.
    • (2010) J. Nat. Prod. , vol.73 , Issue.9 , pp. 1538-1543
    • Chao, C.H.1    Chou, K.J.2    Wang, G.H.3    Wu, Y.C.4    Wang, L.H.5    Chen, J.P.6    Sheu, J.H.7    Sung, P.J.8
  • 91
    • 84863416237 scopus 로고    scopus 로고
    • Towards thetotal synthesis of mycaperoxide B: Probing biosynthetic rationale
    • Silva, E.M.P.; Pye, R.J.; Brown, G.D.; Harwood, L.M. Towards thetotal synthesis of mycaperoxide B: Probing biosynthetic rationale. Eur. J. Org. Chem., 2012, 2012(6), 1209-1216.
    • (2012) Eur. J. Org. Chem. , vol.2012 , Issue.6 , pp. 1209-1216
    • Silva, E.M.P.1    Pye, R.J.2    Brown, G.D.3    Harwood, L.M.4
  • 93
    • 51849109849 scopus 로고    scopus 로고
    • Diacarperoxides norterpene cyclic peroxides from the sponge Diacarnus megaspinorhabdosa
    • Ibrahim, S.R.M.; Eble, R.; Wray, V.; Muller, W.E.G.; Edrada-Ebel, R.A.; Prolsch, P. Diacarperoxides, norterpene cyclic peroxides from the sponge Diacarnus megaspinorhabdosa. J. Nat. Prod., 2008, 71(8), 1358-1364.
    • (2008) J. Nat. Prod. , vol.71 , Issue.8 , pp. 1358-1364
    • Ibrahim, S.R.M.1    Eble, R.2    Wray, V.3    Muller, W.E.G.4    Edrada-Ebel, R.A.5    Prolsch, P.6
  • 94
    • 84867352661 scopus 로고    scopus 로고
    • Plakilactones from the marine sponge Plakinastrella mamillaris. Discovery of a new class of marine ligands of peroxisome proliferator-activated receptor ?
    • Festa, C.; Lauro, G.; De Marino, S.; D'Auria, M.V.; Monti, M.C.; Casapullo, A.; D'Amore, C.; Renga, B.; Mencarelli, A.; Petek, S. Plakilactones from the marine sponge Plakinastrella mamillaris. Discovery of a new class of marine ligands of peroxisome proliferator-activated receptor ? . J. Med. Chem., 2012, 55(19), 8303-8317.
    • (2012) J. Med. Chem. , vol.55 , Issue.19 , pp. 8303-8317
    • Festa, C.1    Lauro, G.2    De Marino, S.3    D'Auria, M.V.4    Monti, M.C.5    Casapullo, A.6    D'Amore, C.7    Renga, B.8    Mencarelli, A.9    Petek, S.10
  • 96
    • 4644224274 scopus 로고    scopus 로고
    • Antineoplastic agents.535. Isolation and structure of plakorstatins 1 and 2 from the Indo-Pacific sponge Plakortis nigra
    • Pettit, G.R.; Nogawa, T.; Knight, J.C.; Doubek, D.L.; Hooper, J.N.A. Antineoplastic agents.535. Isolation and structure of plakorstatins 1 and 2 from the Indo-Pacific sponge Plakortis nigra. J. Nat. Prod., 2004, 67(9), 1611-1613.
    • (2004) J. Nat. Prod. , vol.67 , Issue.9 , pp. 1611-1613
    • Pettit, G.R.1    Nogawa, T.2    Knight, J.C.3    Doubek, D.L.4    Hooper, J.N.A.5
  • 97
    • 84885027251 scopus 로고    scopus 로고
    • Natural and semisynthetic analogues of manadoperoxide B reveal new structural requirements for trypanocidal activity
    • Chianese, G.; Scala, F.; Calcinai, B.; Cerrano, C.; Dien, H.A.; Kaiser, M.; Tasdemir, D.; Taglialatela-Scafati, O. Natural and semisynthetic analogues of manadoperoxide B reveal new structural requirements for trypanocidal activity. Mar. Drugs, 2013, 11(9), 3297-3308.
    • (2013) Mar. Drugs , vol.11 , Issue.9 , pp. 3297-3308
    • Chianese, G.1    Scala, F.2    Calcinai, B.3    Cerrano, C.4    Dien, H.A.5    Kaiser, M.6    Tasdemir, D.7    Taglialatela-Scafati, O.8
  • 98
    • 84906938551 scopus 로고    scopus 로고
    • Endoperoxide polyketides from a Chinese Plakortis simplex: Further evidence of the impact of stereochemistry on antimalarial activity ofsimple 1,2-dioxanes
    • Chianese, G.; Persico, M.; Yang, F.; Lin, H.W.; Guo, Y.W.; Basilico, N.; Parapini, S.; Taramelli, D.; Taglialatela-Scafati, O.; Fattorusso, C. Endoperoxide polyketides from a Chinese Plakortis simplex: Further evidence of the impact of stereochemistry on antimalarial activity ofsimple 1,2-dioxanes. Bio. Med. Chem., 2014, 22(17), 4572-4580
    • (2014) Bio. Med. Chem. , vol.22 , Issue.17 , pp. 4572-4580
    • Chianese, G.1    Persico, M.2    Yang, F.3    Lin, H.W.4    Guo, Y.W.5    Basilico, N.6    Parapini, S.7    Taramelli, D.8    Taglialatela-Scafati, O.9    Fattorusso, C.10
  • 100
    • 0036741295 scopus 로고    scopus 로고
    • Cytotoxic ?-carbolines and cyclic peroxides from the Palauan sponge Plakortis nigra
    • Sandler, J.S.; Colin, P.L.; Hooper, J.N.A.; Faulkner, D.J. Cytotoxic ?-carbolines and cyclic peroxides from the Palauan sponge Plakortis nigra. J. Nat. Prod., 2002, 65(9), 1258-1261.
    • (2002) J. Nat. Prod. , vol.65 , Issue.9 , pp. 1258-1261
    • Sandler, J.S.1    Colin, P.L.2    Hooper, J.N.A.3    Faulkner, D.J.4
  • 102
    • 77958548626 scopus 로고    scopus 로고
    • Bioactivecy cloperoxides isolated from the Puerto Rican sponge Plakortis halichondrioides
    • Jimenez-Romero, C.; Ortiz, I.; Vicente, J.; Vera, B.; Rodriguez, A.D.; Nam, S.; Jove, R. Bioactivecy cloperoxides isolated from the Puerto Rican sponge Plakortis halichondrioides. J. Nat. Prod., 2010, 73(10), 1694-1700.
    • (2010) J. Nat. Prod. , vol.73 , Issue.10 , pp. 1694-1700
    • Jimenez-Romero, C.1    Ortiz, I.2    Vicente, J.3    Vera, B.4    Rodriguez, A.D.5    Nam, S.6    Jove, R.7
  • 104
    • 77954485187 scopus 로고    scopus 로고
    • Osteoclastforming suppressing compounds from the medicinal mushroom Agrocybe chaxingu Huang(Agaricomycetidea)
    • Choi, J.H.; Abe, N.; Kodani, S.; Masuda, K.; Koyama, T.; Yazawa, K.; Takahashi, M.; Kawagishi, H. Osteoclastforming suppressing compounds from the medicinal mushroom Agrocybe chaxingu Huang(Agaricomycetidea). Int. J. Med. Mushrooms., 2010, 12(2), 151-155.
    • (2010) Int. J. Med. Mushrooms. , vol.12 , Issue.2 , pp. 151-155
    • Choi, J.H.1    Abe, N.2    Kodani, S.3    Masuda, K.4    Koyama, T.5    Yazawa, K.6    Takahashi, M.7    Kawagishi, H.8
  • 107
    • 54249085827 scopus 로고    scopus 로고
    • Chemical constituents of Antrodia camphorata submerged whole broth
    • Shao, Y.Y.; Chen, C.C.; Wang, H.Y.; Chiu, H.L.; Hseu, T.H.; Kuo, Y.H. Chemical constituents of Antrodia camphorata submerged whole broth. Nat. Prod. Res., 2008, 22(13), 1151-1157.
    • (2008) Nat. Prod. Res. , vol.22 , Issue.13 , pp. 1151-1157
    • Shao, Y.Y.1    Chen, C.C.2    Wang, H.Y.3    Chiu, H.L.4    Hseu, T.H.5    Kuo, Y.H.6
  • 108
    • 34748834195 scopus 로고    scopus 로고
    • Triterpenes and steroids from Armillaria mellea Vahl ex Fr
    • Guo, W.J.; Guo, S.X.; Yang, J.S.; Chen, X.M.; Xiao, P.G. Triterpenes and steroids from Armillaria mellea Vahl. ex Fr. Biochem. Syst. Ecolo., 2007, 35(11), 790-793.
    • (2007) Biochem. Syst. Ecolo. , vol.35 , Issue.11 , pp. 790-793
    • Guo, W.J.1    Guo, S.X.2    Yang, J.S.3    Chen, X.M.4    Xiao, P.G.5
  • 110
    • 33845474327 scopus 로고    scopus 로고
    • A new perylenequinone from the fruit bodies of Bulgaria inquinans
    • Xian Li, P.Z.; Jing Xu, N.L.; Meng, D.L.; Sha, Y. A new perylenequinone from the fruit bodies of Bulgaria inquinans. J. Asian. Nat. Prod. Res., 2006, 8(8), 743-746.
    • (2006) J. Asian. Nat. Prod. Res. , vol.8 , Issue.8 , pp. 743-746
    • Xian Li, P.Z.1    Jing Xu, N.L.2    Meng, D.L.3    Sha, Y.4
  • 111
    • 82355164549 scopus 로고    scopus 로고
    • Cytotoxic and Antimalarial Azaphilones from Chaetomium longirostre
    • Panthama, N.; Kanokmedhakul, S.; Kanokmedhakul, K.; Soytong, K. Cytotoxic and Antimalarial Azaphilones from Chaetomium longirostre. J. Nat. Prod., 2011, 74(11), 2395-2399.
    • (2011) J. Nat. Prod. , vol.74 , Issue.11 , pp. 2395-2399
    • Panthama, N.1    Kanokmedhakul, S.2    Kanokmedhakul, K.3    Soytong, K.4
  • 112
    • 67650330853 scopus 로고    scopus 로고
    • Suwanborirux K.8-Isocyanoamphilecta-11(20),15-diene, a new antimalarial isonitrile diterpene from the sponge Ciocalapata sp
    • Wattanapiromsakul, C.; Chanthathamrongsiri, N.; Bussarawit, S.; Yuenyongsawad, S.; Plubrukarn, A.; Suwanborirux, K.8-Isocyanoamphilecta-11(20),15-diene, a new antimalarial isonitrile diterpene from the sponge Ciocalapata sp. Can. J. Chem., 2009, 87(5), 612-618.
    • (2009) Can. J. Chem. , vol.87 , Issue.5 , pp. 612-618
    • Wattanapiromsakul, C.1    Chanthathamrongsiri, N.2    Bussarawit, S.3    Yuenyongsawad, S.4    Plubrukarn, A.5
  • 113
    • 84896493213 scopus 로고    scopus 로고
    • Ergosterol peroxide from Cordyceps cicadae ameliorates TGF-?1-induced activation of kidney fibroblasts
    • Zhu, R.; Zheng, R.; Deng, Y.; Chen, Y.; Zhang, S. Ergosterol peroxide from Cordyceps cicadae ameliorates TGF-?1-induced activation of kidney fibroblasts. Phytomedicine, 2013, 21(3), 372-378.
    • (2013) Phytomedicine , vol.21 , Issue.3 , pp. 372-378
    • Zhu, R.1    Zheng, R.2    Deng, Y.3    Chen, Y.4    Zhang, S.5
  • 114
    • 77956264611 scopus 로고    scopus 로고
    • Constituents isolated from Cordyceps militaris suppress enhanced inflammatory mediator's production and human cancer cell proliferation
    • Rao, Y.K.; Fang, S.H.; Wu, W.S.; Tzeng, Y.M. Constituents isolated from Cordyceps militaris suppress enhanced inflammatory mediator's production and human cancer cell proliferation. J. Ethnopharmacol., 2010, 131(2), 363-367.
    • (2010) J. Ethnopharmacol. , vol.131 , Issue.2 , pp. 363-367
    • Rao, Y.K.1    Fang, S.H.2    Wu, W.S.3    Tzeng, Y.M.4
  • 115
    • 84888433375 scopus 로고    scopus 로고
    • Two new with anolides from the halophyte Datura stramonium L
    • Fang, S.T.; Liu, X.; Kong, N.N.; Liu, S.J.; Xia, C.H. Two new with anolides from the halophyte Datura stramonium L. Nat. Prod. Res., 2013, 27(21), 1965-1970.
    • (2013) Nat. Prod. Res. , vol.27 , Issue.21 , pp. 1965-1970
    • Fang, S.T.1    Liu, X.2    Kong, N.N.3    Liu, S.J.4    Xia, C.H.5
  • 116
    • 34447558018 scopus 로고    scopus 로고
    • Antibacterial activity of ergosterol peroxide against Mycobacterium tuberculosis: Dependence upon system and medium employed
    • Duarte, N.; Ferreira, M.J.U.; Martins, M.; Viveiros, M.; Amaral, L. Antibacterial activity of ergosterol peroxide against Mycobacterium tuberculosis: Dependence upon system and medium employed. Phytother. Res., 2007, 21(7), 601-604.
    • (2007) Phytother. Res. , vol.21 , Issue.7 , pp. 601-604
    • Duarte, N.1    Ferreira, M.J.U.2    Martins, M.3    Viveiros, M.4    Amaral, L.5
  • 117
    • 77954748531 scopus 로고    scopus 로고
    • Secondary metabolites and antimycobacterial activities from the roots of Ficus nervosa
    • Chen, L.W.; Cheng, M.J.; Peng, C.F.; Chen, I.S. Secondary metabolites and antimycobacterial activities from the roots of Ficus nervosa. Chem. Biodivers., 2010, 7(7), 1814-1821.
    • (2010) Chem. Biodivers. , vol.7 , Issue.7 , pp. 1814-1821
    • Chen, L.W.1    Cheng, M.J.2    Peng, C.F.3    Chen, I.S.4
  • 118
    • 80052354527 scopus 로고    scopus 로고
    • Polyoxygenated ergostane-type sterols from the liquid culture of Ganoderma applanatum
    • Lee, S.Y.; Kim, J.S.; Lee, S.Y.; Kang, S.S. Polyoxygenated ergostane-type sterols from the liquid culture of Ganoderma applanatum. Nat. Prod. Res., 2011, 25(14), 1304-1311.
    • (2011) Nat. Prod. Res. , vol.25 , Issue.14 , pp. 1304-1311
    • Lee, S.Y.1    Kim, J.S.2    Lee, S.Y.3    Kang, S.S.4
  • 119
    • 84865583196 scopus 로고    scopus 로고
    • Ergosterol peroside isolated from Ganoderma lucidum abolishes microRNA miR-378-mediated tumor cells on chemoresistance
    • Wu, Q.P.; Xie, Y.Z.; Deng, Z.Q.; Li, X.M.; Yang, W.N.; Jiao, C.W.; Fang, L.; Yang, B.B. Ergosterol peroside isolated from Ganoderma lucidum abolishes microRNA miR-378-mediated tumor cells on chemoresistance. Plos One, 2012, 7(8), 1-14.
    • (2012) Plos One , vol.7 , Issue.8 , pp. 1-14
    • Wu, Q.P.1    Xie, Y.Z.2    Deng, Z.Q.3    Li, X.M.4    Yang, W.N.5    Jiao, C.W.6    Fang, L.7    Yang, B.B.8
  • 121
    • 67649880855 scopus 로고    scopus 로고
    • Cytotoxic activities of 9,11-dehydroergosterol peroxide and ergosterol peroxide from the fermentation mycelia of Ganoderma lucidum cultivated in the medium containing leguminous plant on Hep3B cells
    • Chen, Y.K.; Kuo, Y.H.; Chiang, B.H.; Lo, J.M.; Sheen, L.Y. Cytotoxic activities of 9,11-dehydroergosterol peroxide and ergosterol peroxide from the fermentation mycelia of Ganoderma lucidum cultivated in the medium containing leguminous plant on Hep3B cells. J. Agr. Food. Chem., 2009, 57(13), 5713-5719.
    • (2009) J. Agr. Food. Chem. , vol.57 , Issue.13 , pp. 5713-5719
    • Chen, Y.K.1    Kuo, Y.H.2    Chiang, B.H.3    Lo, J.M.4    Sheen, L.Y.5
  • 122
    • 70349656465 scopus 로고    scopus 로고
    • Anti-human immunodeficiency virus-1 protease activity of new lanostane-type triterpenoids from Ganoderma sinense
    • Sato, N.; Zhang, Q.; Ma, C.M.; Hattori, M. Anti-human immunodeficiency virus-1 protease activity of new lanostane-type triterpenoids from Ganoderma sinense. Chem. Pharm. Bull., 2009, 57(10), 1076-1080.
    • (2009) Chem. Pharm. Bull. , vol.57 , Issue.10 , pp. 1076-1080
    • Sato, N.1    Zhang, Q.2    Ma, C.M.3    Hattori, M.4
  • 124
    • 84872930901 scopus 로고    scopus 로고
    • Immunomodulatory activities of medicinal mushroom Grifola frondosa extract and its bioactive constituent
    • Wu, S.J.; Lu, T.M.; Lai, M.N.; Ng, L.T. Immunomodulatory activities of medicinal mushroom Grifola frondosa extract and its bioactive constituent. Am. J. Chinese. Med., 2013, 41(1), 131-144.
    • (2013) Am. J. Chinese. Med. , vol.41 , Issue.1 , pp. 131-144
    • Wu, S.J.1    Lu, T.M.2    Lai, M.N.3    Ng, L.T.4
  • 126
    • 80054953476 scopus 로고    scopus 로고
    • Two new epoxysteroids from Helianthus tuberosus
    • Li, X.D.; Miao, F.P.; Ji, N.Y. Two new epoxysteroids from Helianthus tuberosus. Molecules, 2011, 16(10), 8646-8653.
    • (2011) Molecules , vol.16 , Issue.10 , pp. 8646-8653
    • Li, X.D.1    Miao, F.P.2    Ji, N.Y.3
  • 127
    • 52949148931 scopus 로고    scopus 로고
    • Isolation and quantitative determination of ergosterol peroxide in various edible mushroom species
    • Krzyczkowski, W.; Malinowska, E.; Suchocki, P.; Kleps, J.; Olejnik, M.; Herold, F. Isolation and quantitative determination of ergosterol peroxide in various edible mushroom species. Food Chem., 2009, 113(1), 351-355.
    • (2009) Food Chem. , vol.113 , Issue.1 , pp. 351-355
    • Krzyczkowski, W.1    Malinowska, E.2    Suchocki, P.3    Kleps, J.4    Olejnik, M.5    Herold, F.6
  • 130
    • 81855227116 scopus 로고    scopus 로고
    • Cytotoxicity of ergosterol derivatives from the fruiting bodies of Hygrophorus russula
    • Lee, I.S.; Min, B.S.; Jung, H.J.; Kim, J.P.; Na, M.K.; Bae, K.H. Cytotoxicity of ergosterol derivatives from the fruiting bodies of Hygrophorus russula. Nat. Prod. Sci., 2011, 17(2), 85-89.
    • (2011) Nat. Prod. Sci. , vol.17 , Issue.2 , pp. 85-89
    • Lee, I.S.1    Min, B.S.2    Jung, H.J.3    Kim, J.P.4    Na, M.K.5    Bae, K.H.6
  • 131
    • 46249085719 scopus 로고    scopus 로고
    • Chemical constituents of Melandrium firmum Rohrbach and their anti-inflammatory activity
    • Zheng, M.S.; Hwang, N.K.; Kim, D.H.; Moon, T.C.; Son, J.K.; Chang, H.W. Chemical constituents of Melandrium firmum Rohrbach and their anti-inflammatory activity. Arch. Pharm. Res., 2008, 31(3), 318-322.
    • (2008) Arch. Pharm. Res. , vol.31 , Issue.3 , pp. 318-322
    • Zheng, M.S.1    Hwang, N.K.2    Kim, D.H.3    Moon, T.C.4    Son, J.K.5    Chang, H.W.6
  • 132
  • 133
    • 35549005010 scopus 로고    scopus 로고
    • Ergosterol peroxides as phospholipase A2 inhibitors from the fungus Lactarius hatsudake
    • Gao, J.M.; Wang, M.; Liu, L.P.; Wei, G.H.; Zhang, A.L.; Draghici, C.; Konishi, Y. Ergosterol peroxides as phospholipase A2 inhibitors from the fungus Lactarius hatsudake. Phytomedicine, 2007, 14(12), 821-824.
    • (2007) Phytomedicine , vol.14 , Issue.12 , pp. 821-824
    • Gao, J.M.1    Wang, M.2    Liu, L.P.3    Wei, G.H.4    Zhang, A.L.5    Draghici, C.6    Konishi, Y.7
  • 134
    • 68349125518 scopus 로고    scopus 로고
    • Sterol composition of the macromycete fungus Laetiporus sulphureus
    • Ericsson, D.C.B.; Ivonne, J.N.R. Sterol composition of the macromycete fungus Laetiporus sulphureus. Chem. Nat. Compd., 2009, 45(2), 193-196.
    • (2009) Chem. Nat. Compd. , vol.45 , Issue.2 , pp. 193-196
    • Ericsson, D.C.B.1    Ivonne, J.N.R.2
  • 135
    • 62249172216 scopus 로고    scopus 로고
    • 22E-ergosta-6,22-diene-3?,5?,8?-triol: A new polyhydroxysterol isolated from Lentinus edodes(Shiitake)
    • Rivera, A.; Benavides, O.L.; Rios-Motta, J. (22E)-ergosta-6,22-diene-3?,5?,8?-triol: A new polyhydroxysterol isolated from Lentinus edodes(Shiitake). Nat. Prod. Res., 2009, 23(3), 293-300.
    • (2009) Nat. Prod. Res. , vol.23 , Issue.3 , pp. 293-300
    • Rivera, A.1    Benavides, O.L.2    Rios-Motta, J.3
  • 136
    • 84884288573 scopus 로고    scopus 로고
    • Bioactive ergostanoids and a new polyhydroxyoctane from Lentinus polychrous mycelia and their inhibitory effects on E2-enhanced cell proliferation of T47D cells
    • Fangkrathok, N.; Sripanidkulchai, B.; Umehara, K.; Noguchi, H. Bioactive ergostanoids and a new polyhydroxyoctane from Lentinus polychrous mycelia and their inhibitory effects on E2-enhanced cell proliferation of T47D cells. Nat. Prod. Res., 2013, 27(18), 1611-1619.
    • (2013) Nat. Prod. Res. , vol.27 , Issue.18 , pp. 1611-1619
    • Fangkrathok, N.1    Sripanidkulchai, B.2    Umehara, K.3    Noguchi, H.4
  • 138
    • 68149165609 scopus 로고    scopus 로고
    • Macrolepiotin a new indole alkaloid from Macrolepiota neomastoidea
    • Kim, K.H.; Park, K.M.; Choi, S.U.; Lee, K.R. Macrolepiotin, a new indole alkaloid from Macrolepiota neomastoidea. J. Antibiot., 2009, 62(6), 335-338.
    • (2009) J. Antibiot. , vol.62 , Issue.6 , pp. 335-338
    • Kim, K.H.1    Park, K.M.2    Choi, S.U.3    Lee, K.R.4
  • 139
    • 79954506270 scopus 로고    scopus 로고
    • Secondary metabolites from magnolia kachirachirai
    • Chang, H.S.; Chen, M.J.; Chen, I.S. Secondary metabolites from magnolia kachirachirai. Helv. Chim. Acta., 2011, 94(4), 703-710.
    • (2011) Helv. Chim. Acta. , vol.94 , Issue.4 , pp. 703-710
    • Chang, H.S.1    Chen, M.J.2    Chen, I.S.3
  • 141
    • 70449561244 scopus 로고    scopus 로고
    • Steroids produced by Penicillium herquei. An endophytic fungus isolated from the fruits of Melia azedarach( MELIACEAE)
    • Do Rosario Marinho, A.M.; Marinho, P.S.B.; Filho, E.R. Steroids produced by Penicillium herquei. An endophytic fungus isolated from the fruits of Melia azedarach( MELIACEAE). Quim. Nova., 2009, 32(7), 1710-1712.
    • (2009) Quim. Nova. , vol.32 , Issue.7 , pp. 1710-1712
    • Do Rosario Marinho, A.M.1    Marinho, P.S.B.2    Filho, E.R.3
  • 142
    • 80053008178 scopus 로고    scopus 로고
    • Antioxidant and NF-?B inhibitory constituents isolated from Morchella esculenta
    • Kim, J.A.; Lau, E.; Tay, D.; De Blanco, E.J. Antioxidant and NF-?B inhibitory constituents isolated from Morchella esculenta. Nat. Prod. Res., 2011, 25(15), 1412-1417.
    • (2011) Nat. Prod. Res. , vol.25 , Issue.15 , pp. 1412-1417
    • Kim, J.A.1    Lau, E.2    Tay, D.3    De Blanco, E.J.4
  • 144
    • 70849125117 scopus 로고    scopus 로고
    • Antitumor components from Naematoloma fasciculare
    • Ding, Y.; Bao, H.Y.; Bau, T.; Li, Y.; Kim, Y.H. Antitumor components from Naematoloma fasciculare. J. Microbiol. Biotechn., 2009, 19(10), 1135-1138.
    • (2009) J. Microbiol. Biotechn. , vol.19 , Issue.10 , pp. 1135-1138
    • Ding, Y.1    Bao, H.Y.2    Bau, T.3    Li, Y.4    Kim, Y.H.5
  • 145
    • 33746563455 scopus 로고    scopus 로고
    • Neoplaether a new cytotoxic and antifungal endophyte metabolite from Neoplaconema napellum IFB-E016
    • Wang, F.W.; Ye, Y.H.; Chen, J.R.; Wang, X.T.; Zhu, H.L.; Song, Y.C.; Tan, R.X. Neoplaether, a new cytotoxic and antifungal endophyte metabolite from Neoplaconema napellum IFB-E016. FEMS. Microbiol. Lett., 2006, 261(2), 218-223.
    • (2006) FEMS. Microbiol. Lett. , vol.261 , Issue.2 , pp. 218-223
    • Wang, F.W.1    Ye, Y.H.2    Chen, J.R.3    Wang, X.T.4    Zhu, H.L.5    Song, Y.C.6    Tan, R.X.7
  • 146
    • 54849438091 scopus 로고    scopus 로고
    • Isolation of ergosterol peroxide from Nomuraea rileyi infected larvae of tobacco cutworm
    • Prompiboon, P.; Bhumiratana, A.; Ruchirawat, S.; Boucias, D.G.; Wiwat, C. Isolation of ergosterol peroxide from Nomuraea rileyi infected larvae of tobacco cutworm. World J. Microb. Biot., 2008, 24(12), 2909-2917.
    • (2008) World J. Microb. Biot. , vol.24 , Issue.12 , pp. 2909-2917
    • Prompiboon, P.1    Bhumiratana, A.2    Ruchirawat, S.3    Boucias, D.G.4    Wiwat, C.5
  • 147
    • 84871420395 scopus 로고    scopus 로고
    • Structural characterization and metabolite profiling of the facultative marine fungus Paecilomyces variotii
    • Marante, F.J.T.; Mioso, R.; Barrera, J.B.; Gonzalez, J.E.G.; Rodriguez, J.J.S.; De Laguna, I.H.B. Structural characterization and metabolite profiling of the facultative marine fungus Paecilomyces variotii. Ann. Microbiol., 2012, 62(4), 1601-1607.
    • (2012) Ann. Microbiol. , vol.62 , Issue.4 , pp. 1601-1607
    • Marante, F.J.T.1    Mioso, R.2    Barrera, J.B.3    Gonzalez, J.E.G.4    Rodriguez, J.J.S.5    De Laguna, I.H.B.6
  • 148
    • 30844439671 scopus 로고    scopus 로고
    • C25 steroid epimers produced by Penicillium janthinellum a fungus isolated from fruits of Melia azedarach
    • Do Rosario Marinho, A.M.; Rodrigues-Filho, E.; Ferreira, A.G.; Santos, L.S. C25 steroid epimers produced by Penicillium janthinellum, a fungus isolated from fruits of Melia azedarach. J. Brazil. Chem. Soc., 2005, 16(6B), 1342-1346.
    • (2005) J. Brazil. Chem. Soc. , vol.16 , Issue.6 B , pp. 1342-1346
    • Do Rosario Marinho, A.M.1    Rodrigues-Filho, E.2    Ferreira, A.G.3    Santos, L.S.4
  • 150
    • 79957855410 scopus 로고    scopus 로고
    • Antitubercular chromones and flavonoids from Pisonia aculeate
    • Wu, M.C.; Peng, C.F.; Chen, I.S.; Tsai, I.L. Antitubercular chromones and flavonoids from Pisonia aculeate. J. Nat. Prod., 2011, 74(5), 976-982.
    • (2011) J. Nat. Prod. , vol.74 , Issue.5 , pp. 976-982
    • Wu, M.C.1    Peng, C.F.2    Chen, I.S.3    Tsai, I.L.4
  • 151
    • 84866757365 scopus 로고    scopus 로고
    • Osteoclastogenesis inhibitory effect of ergosterol peroxide isolated from Pleurotus eryngii
    • Chen, Y.C.; Kuo, Y.H. Osteoclastogenesis inhibitory effect of ergosterol peroxide isolated from Pleurotus eryngii. Nat. Prod. Commun., 2012, 7(9), 1163-1164.
    • (2012) Nat. Prod. Commun. , vol.7 , Issue.9 , pp. 1163-1164
    • Chen, Y.C.1    Kuo, Y.H.2
  • 152
    • 84861803642 scopus 로고    scopus 로고
    • Trigos, Á Trypanocidal activity of ergosterol peroxide from Pleurotus ostreatus
    • Ramos-Ligonio, A.; López-Monteon, A.; Trigos, Á. Trypanocidal activity of ergosterol peroxide from Pleurotus ostreatus. Phytother. Res., 2012, 26(6), 938-943.
    • (2012) Phytother. Res. , vol.26 , Issue.6 , pp. 938-943
    • Ramos-Ligonio, A.1    López-Monteon, A.2
  • 154
    • 67650581615 scopus 로고    scopus 로고
    • HPLC and NMR studies of phenoxazone alkaloids from Pycnoporus cinnabarinus
    • Dias, D.A.; Urban, S. HPLC and NMR studies of phenoxazone alkaloids from Pycnoporus cinnabarinus. Nat. Prod. Commun., 2009, 4(4), 489-498.
    • (2009) Nat. Prod. Commun. , vol.4 , Issue.4 , pp. 489-498
    • Dias, D.A.1    Urban, S.2
  • 156
    • 49349083002 scopus 로고    scopus 로고
    • A new ceramide from Ramaria botrytis(Pers.) Ricken
    • Yaoita, Y.; Satoh, Y.; Kikuchi, M. A new ceramide from Ramaria botrytis(Pers.) Ricken. J. Nat. Med., 2007, 61(2), 205-207.
    • (2007) J. Nat. Med. , vol.61 , Issue.2 , pp. 205-207
    • Yaoita, Y.1    Satoh, Y.2    Kikuchi, M.3
  • 157
    • 36849081268 scopus 로고    scopus 로고
    • Six new ergosterols from the marine-derived fungus Rhizopus sp
    • Wang, F.; Fang, Y.; Zhang, M.; Lin, A.; Zhu, T.; Gu, Q.; Zhu, W. Six new ergosterols from the marine-derived fungus Rhizopus sp. Steroids, 2008, 73(1), 19-26.
    • (2008) Steroids , vol.73 , Issue.1 , pp. 19-26
    • Wang, F.1    Fang, Y.2    Zhang, M.3    Lin, A.4    Zhu, T.5    Gu, Q.6    Zhu, W.7
  • 158
    • 33645540156 scopus 로고    scopus 로고
    • 5?,8?-epidioxy-22E-ergosta-6,9(11),22-trien-3b-ol from an edible mushroom suppresses growth of HL60 Leukemia and HT29 colon adenocarcinoma cells
    • Kobori, M.; Yoshida, M.; Ohnishi-Kameyama, M.; Takei, T.; Shinmoto, H. 5?,8?-epidioxy-22E-ergosta-6,9(11),22-trien-3b-ol from an edible mushroom suppresses growth of HL60 Leukemia and HT29 colon adenocarcinoma cells. Biol. Pharm. Bull., 2006, 29(4), 755-759.
    • (2006) Biol. Pharm. Bull. , vol.29 , Issue.4 , pp. 755-759
    • Kobori, M.1    Yoshida, M.2    Ohnishi-Kameyama, M.3    Takei, T.4    Shinmoto, H.5
  • 159
    • 15244350525 scopus 로고    scopus 로고
    • Ergosterol peroxide an apoptosis-inducing component isolated from Sarcodon aspratus(Berk.) S. Ito
    • Takei, T.; Yoshida, M.; Ohnishi-Kameyama, M.; Kobori, M. Ergosterol peroxide, an apoptosis-inducing component isolated from Sarcodon aspratus(Berk.) S. Ito. Biosic. Biotechem. Biochem., 2005, 69(1), 212-215.
    • (2005) Biosic. Biotechem. Biochem. , vol.69 , Issue.1 , pp. 212-215
    • Takei, T.1    Yoshida, M.2    Ohnishi-Kameyama, M.3    Kobori, M.4
  • 160
    • 33846512747 scopus 로고    scopus 로고
    • Ergosterol peroxide from an edible mushroom suppresses inflammatory responses in RAW264.7 macrophages and growth of HT29 colon adenocarcinoma cells
    • Kobori, M.; Yoshida, M.; Ohnishi-Kameyama, M.; Shinmoto, H. Ergosterol peroxide from an edible mushroom suppresses inflammatory responses in RAW264.7 macrophages and growth of HT29 colon adenocarcinoma cells. Brit. J. Pharmacol., 2007, 150(2), 209-219.
    • (2007) Brit. J. Pharmacol. , vol.150 , Issue.2 , pp. 209-219
    • Kobori, M.1    Yoshida, M.2    Ohnishi-Kameyama, M.3    Shinmoto, H.4
  • 162
    • 84872559159 scopus 로고    scopus 로고
    • Steroids and phenolic constituents from the fruiting bodies of the basidiomycete Sarcodon joedes
    • Liu, H.W.; Hu, L.; Zhang, A.L.; Gao, J.M. Steroids and phenolic constituents from the fruiting bodies of the basidiomycete Sarcodon joedes. Nat. Prod. Res., 2013, 27(1), 80-84.
    • (2013) Nat. Prod. Res. , vol.27 , Issue.1 , pp. 80-84
    • Liu, H.W.1    Hu, L.2    Zhang, A.L.3    Gao, J.M.4
  • 163
    • 84878860629 scopus 로고    scopus 로고
    • Eremophilane-type sesquiterpenes from cultured lichen mycobionts of Sarcographa tricosa
    • Le, D.H.; Takenaka, Y.; Hamada, N.; Tanahashi, T. Eremophilane-type sesquiterpenes from cultured lichen mycobionts of Sarcographa tricosa. Phytochemistry, 2013, 91, 242-248.
    • (2013) Phytochemistry , vol.91 , pp. 242-248
    • Le, D.H.1    Takenaka, Y.2    Hamada, N.3    Tanahashi, T.4
  • 165
    • 78449244854 scopus 로고    scopus 로고
    • Structural implication in cytotoxic effects of sterolsfrom Sellaginella tamariscina
    • Roh, E.M.; Jin, Q.; Jin, H.G.; Shin, J.E.; Choi, E.J.; Moon, Y.H.; Woo, E.R. Structural implication in cytotoxic effects of sterolsfrom Sellaginella tamariscina. Arch. Pharm. Res., 2010, 33(9), 1347-1353.
    • (2010) Arch. Pharm. Res. , vol.33 , Issue.9 , pp. 1347-1353
    • Roh, E.M.1    Jin, Q.2    Jin, H.G.3    Shin, J.E.4    Choi, E.J.5    Moon, Y.H.6    Woo, E.R.7
  • 166
    • 33750014500 scopus 로고    scopus 로고
    • 5,8-Epidioxysterols and related derivatives from a Chinese Soft Coral Sinularia flexibilis
    • Yu, S.; Deng, Z.; Van Ofwegen, L.; Proksch, P.; Lin, W. 5,8-Epidioxysterols and related derivatives from a Chinese Soft Coral Sinularia flexibilis. Steroids, 2006, 71(11-12), 955-959.
    • (2006) Steroids , vol.71 , Issue.11-12 , pp. 955-959
    • Yu, S.1    Deng, Z.2    Van Ofwegen, L.3    Proksch, P.4    Lin, W.5
  • 170
    • 49649123343 scopus 로고    scopus 로고
    • Chemical constituents of Stereum subtomentosum and two other birch-associated basidiomycetes: An interspecies comparative study
    • Hybelbauerova, S.; Sejbal, J.; Dracinsky, M.; Hahnova, A.; Koutek, B. Chemical constituents of Stereum subtomentosum and two other birch-associated basidiomycetes: An interspecies comparative study. Chem. Biodivers., 2008, 5(5), 743-750.
    • (2008) Chem. Biodivers. , vol.5 , Issue.5 , pp. 743-750
    • Hybelbauerova, S.1    Sejbal, J.2    Dracinsky, M.3    Hahnova, A.4    Koutek, B.5
  • 172
    • 84894093656 scopus 로고    scopus 로고
    • Chemical constituents of Penicillium chrysogenum an endophytic fungus from Strychnos toxifera
    • Koolen, H.H.; Soares, E.R.; Araujo da Silva, F.M.; Lima De Souza, A.Q. Chemical constituents of Penicillium chrysogenum, an endophytic fungus from Strychnos toxifera. Chem. Nat. Compd., 2014, 49(6), 1164-1165.
    • (2014) Chem. Nat. Compd. , vol.49 , Issue.6 , pp. 1164-1165
    • Koolen, H.H.1    Soares, E.R.2    Araujo da Silva, F.M.3    Lima De Souza, A.Q.4
  • 173
    • 38849104877 scopus 로고    scopus 로고
    • A new ceramide from Suillus luteus and its cytotoxic activity against human melanoma cells
    • Leon, F.; Brouard, I.; Torres, F.; Quintana, J.; Rivera, A.; Estevez, F.; Bermejo, J. A new ceramide from Suillus luteus and its cytotoxic activity against human melanoma cells. Chem. Biodivers., 2008, 5(1), 120-125.
    • (2008) Chem. Biodivers. , vol.5 , Issue.1 , pp. 120-125
    • Leon, F.1    Brouard, I.2    Torres, F.3    Quintana, J.4    Rivera, A.5    Estevez, F.6    Bermejo, J.7
  • 174
    • 33846460394 scopus 로고    scopus 로고
    • 26, 27-Cyclosterols and other polyoxygenated sterols from a marine sponge topsentia sp
    • Luo, X.; Li, F.; Shinde, P.B.; Hong, J.; Lee, C.O.; Im, K.S.; Jung, J.H. 26, 27-Cyclosterols and other polyoxygenated sterols from a marine sponge Topsentia sp. J. Nat. Prod., 2006, 69(12), 1760-1768.
    • (2006) J. Nat. Prod. , vol.69 , Issue.12 , pp. 1760-1768
    • Luo, X.1    Li, F.2    Shinde, P.B.3    Hong, J.4    Lee, C.O.5    Im, K.S.6    Jung, J.H.7
  • 175
    • 80055024287 scopus 로고    scopus 로고
    • A new peroxy-multiflorane triterpene ester from the processed seeds of Trichosanthes kirilowii
    • Ma, Y.P.; Li, N.; Gao, J.; Fu, K.L.; Qin, Y.; Li, G.Y.; Wang, J.H. A new peroxy-multiflorane triterpene ester from the processed seeds of Trichosanthes kirilowii. Helv. Chim. Acta, 2011, 94(10), 1881-1887.
    • (2011) Helv. Chim. Acta , vol.94 , Issue.10 , pp. 1881-1887
    • Ma, Y.P.1    Li, N.2    Gao, J.3    Fu, K.L.4    Qin, Y.5    Li, G.Y.6    Wang, J.H.7
  • 176
    • 67349243084 scopus 로고    scopus 로고
    • Antifungal secondary metabolites from endophytic Verticillium sp
    • You, F.; Han, T.; Wu, J.Z.; Huang, B.K.; Qin, L.P. Antifungal secondary metabolites from endophytic Verticillium sp. Biochem. Syst. Ecol., 2009, 37(3), 162-165.
    • (2009) Biochem. Syst. Ecol. , vol.37 , Issue.3 , pp. 162-165
    • You, F.1    Han, T.2    Wu, J.Z.3    Huang, B.K.4    Qin, L.P.5
  • 177
    • 75849162485 scopus 로고    scopus 로고
    • Secondary metabolites of Volvariella bombycina and their inhibitory effects on melanogenesis
    • Xu, G.H.; Choo, S.J.; Kim, Y.H.; Ryoo, I.J.; Seok, S.J.; Ahn, J.S.; Yoo, I.D. Secondary metabolites of Volvariella bombycina and their inhibitory effects on melanogenesis. J. Microbiol. Biotechnol., 2010, 20(1), 78-81.
    • (2010) J. Microbiol. Biotechnol. , vol.20 , Issue.1 , pp. 78-81
    • Xu, G.H.1    Choo, S.J.2    Kim, Y.H.3    Ryoo, I.J.4    Seok, S.J.5    Ahn, J.S.6    Yoo, I.D.7
  • 178
    • 33646399186 scopus 로고    scopus 로고
    • Three new pentacyclic triterpenes and some flavonoids from the fruits of an Indian ayurvedic plant Dendrophthoe falcata and their estrogen receptor binding activity
    • Mallavadhani, U.V.; Narasimhan, K.; Sudhakar, A.V.S.; Mahapatra, A.; Li, W.; Van Breemen, R.B. Three new pentacyclic triterpenes and some flavonoids from the fruits of an Indian ayurvedic plant Dendrophthoe falcata and their estrogen receptor binding activity. Chem. Pharm. Bull., 2006, 54(5), 740-744.
    • (2006) Chem. Pharm. Bull. , vol.54 , Issue.5 , pp. 740-744
    • Mallavadhani, U.V.1    Narasimhan, K.2    Sudhakar, A.V.S.3    Mahapatra, A.4    Li, W.5    Van Breemen, R.B.6
  • 179
    • 84855992638 scopus 로고    scopus 로고
    • Inhibiton of STAT3 signaling and induction of SHP1 mediate antiangiogenic and antitumor activities of ergosterol peroxide in U266 multiple myeloma cells
    • Rhee, Y.H.; Jeong, S.J.; Lee, H.J.; Lee, H.J.; Koh, W.; Jung, J.H.; Kim, S.H. Inhibiton of STAT3 signaling and induction of SHP1 mediate antiangiogenic and antitumor activities of ergosterol peroxide in U266 multiple myeloma cells. BMC. Cancer., 2012, 12(1), 28-38.
    • (2012) BMC. Cancer. , vol.12 , Issue.1 , pp. 28-38
    • Rhee, Y.H.1    Jeong, S.J.2    Lee, H.J.3    Lee, H.J.4    Koh, W.5    Jung, J.H.6    Kim, S.H.7
  • 180
    • 15244350525 scopus 로고    scopus 로고
    • Ergosterol peroxide an apoptosis-induced component isolated from Sarcodon aspratus(Berk.) S. Ito
    • Takei, T.; Yoshida, M.; Ohnishi-Kameyama, M.; Kobori, M. Ergosterol peroxide, an apoptosis-induced component isolated from Sarcodon aspratus(Berk.) S. Ito. Biosci. Biotech. Bioch., 2005, 69(1), 212-215.
    • (2005) Biosci. Biotech. Bioch. , vol.69 , Issue.1 , pp. 212-215
    • Takei, T.1    Yoshida, M.2    Ohnishi-Kameyama, M.3    Kobori, M.4
  • 181
    • 77949915554 scopus 로고    scopus 로고
    • Pro-apoptotic activity of ergosterol peroxide and(22E)-ergosta-7,22-dien-5?-hydroxy-3,6-dione in human prostate cancer cells
    • Russo, A.; Cardile, V.; Piovano, M.; Caggia, S.; Espinoza, C.L.; Garbarino, J.A. Pro-apoptotic activity of ergosterol peroxide and(22E)-ergosta-7,22-dien-5?-hydroxy-3,6-dione in human prostate cancer cells. Chem-Biol. Interact., 2010, 184(3), 352-358.
    • (2010) Chem-Biol. Interact. , vol.184 , Issue.3 , pp. 352-358
    • Russo, A.1    Cardile, V.2    Piovano, M.3    Caggia, S.4    Espinoza, C.L.5    Garbarino, J.A.6
  • 182
    • 84862206418 scopus 로고    scopus 로고
    • Antimycobacterial activity of steroids long-chain alcohols and lytic peptides
    • Rugutt, J.K.; Rugutt, K.J. Antimycobacterial activity of steroids, long-chain alcohols and lytic peptides. Nat. Prod. Res., 2012, 26(11), 1004-1011.
    • (2012) Nat. Prod. Res. , vol.26 , Issue.11 , pp. 1004-1011
    • Rugutt, J.K.1    Rugutt, K.J.2
  • 184
    • 57349182220 scopus 로고    scopus 로고
    • 5?,8?-Epidioxysterols from the gorgonian Eunicella cavolini and the ascidian Trididemnum inarmatum: Isolation and evaluation of their antiproliferative activity
    • Ioannou, E.; Abdel-Razik, A.F.; Zervou, M.; Christofidis, D.; Alexi, X.; Vagias, C.; Alexis, M.N.; Roussis V. 5?,8?-Epidioxysterols from the gorgonian Eunicella cavolini and the ascidian Trididemnum inarmatum: Isolation and evaluation of their antiproliferative activity. Steroids, 2009, 74(1), 73-80.
    • (2009) Steroids , vol.74 , Issue.1 , pp. 73-80
    • Ioannou, E.1    Abdel-Razik, A.F.2    Zervou, M.3    Christofidis, D.4    Alexi, X.5    Vagias, C.6    Alexis, M.N.7    Roussis, V.8
  • 185
    • 77955364604 scopus 로고    scopus 로고
    • New N-acyl taurine from the sea urchin Glyptocidaris crenularis
    • Zhou, X.; Xu, T.; Wen, K.; Yang, X.W.; Xu, S.H.; Liu, Y. New N-acyl taurine from the sea urchin Glyptocidaris crenularis. Biosci. Biotechnol. Biochem., 2010, 74(5), 1089-1091.
    • (2010) Biosci. Biotechnol. Biochem. , vol.74 , Issue.5 , pp. 1089-1091
    • Zhou, X.1    Xu, T.2    Wen, K.3    Yang, X.W.4    Xu, S.H.5    Liu, Y.6
  • 186
    • 3342885502 scopus 로고    scopus 로고
    • Chemical divergence between two sibling species of Oscarella(Porifera) from the Mediterranean Sea
    • Loukaci, A.; Muricy, G.; Brouard, J.P.; Guyot, M.; Vacelet, J.; Boury-Esnault, N. Chemical divergence between two sibling species of Oscarella(Porifera) from the Mediterranean Sea. Biochem. Syst. Ecol., 2004, 32(10), 893-899.
    • (2004) Biochem. Syst. Ecol. , vol.32 , Issue.10 , pp. 893-899
    • Loukaci, A.1    Muricy, G.2    Brouard, J.P.3    Guyot, M.4    Vacelet, J.5    Boury-Esnault, N.6
  • 187
    • 79958194491 scopus 로고    scopus 로고
    • Identification of epidioxysterol from South China Sea urchin Tripneustes gratilla Linnaeus and its cytotoxic activity
    • Liu, Y.H.; Yan, H.; Wen, K.W.; Zhang, J.; Xu, T.H.; Wang, L.S.; Zhou, X.F.; Yang, X.W. Identification of epidioxysterol from South China Sea urchin Tripneustes gratilla Linnaeus and its cytotoxic activity. J. Food. Biochem., 2011, 35(3), 932-938.
    • (2011) J. Food. Biochem. , vol.35 , Issue.3 , pp. 932-938
    • Liu, Y.H.1    Yan, H.2    Wen, K.W.3    Zhang, J.4    Xu, T.H.5    Wang, L.S.6    Zhou, X.F.7    Yang, X.W.8
  • 188
    • 33846185899 scopus 로고    scopus 로고
    • Apoptotic-inducing epidioxysterols identified in hard clam(Meretrix lusoria)
    • Pan, M.H.; Huang, Y.T.; Chang, C.I.; Ho, C.T.; Pan, B.S. Apoptotic-inducing epidioxysterols identified in hard clam(Meretrix lusoria). Food Chem., 2007, 102(3), 788-795.
    • (2007) Food Chem. , vol.102 , Issue.3 , pp. 788-795
    • Pan, M.H.1    Huang, Y.T.2    Chang, C.I.3    Ho, C.T.4    Pan, B.S.5
  • 189
    • 0033842160 scopus 로고    scopus 로고
    • Isolation of bioactive 5?,8?-epidioxy sterols from the marine sponge Luffariella cf variabilis
    • Gauvin, A.; Smadja, J.; Aknin, M.; Faure, R.; Gaydou, E.M. Isolation of bioactive 5?,8?-epidioxy sterols from the marine sponge Luffariella cf. variabilis. Can. J. Chem., 2000, 78(7), 986-992.
    • (2000) Can. J. Chem. , vol.78 , Issue.7 , pp. 986-992
    • Gauvin, A.1    Smadja, J.2    Aknin, M.3    Faure, R.4    Gaydou, E.M.5
  • 190
    • 0032909771 scopus 로고    scopus 로고
    • A new epidioxy sterol as an antifouling substance from a Palauan marine sponge Lendenfeldia chondrodes
    • Sera, Y.; Adachi, K.; Shizuri, Y. A new epidioxy sterol as an antifouling substance from a Palauan marine sponge Lendenfeldia chondrodes. J. Nat. Prod., 1999, 62(1), 152-154.
    • (1999) J. Nat. Prod. , vol.62 , Issue.1 , pp. 152-154
    • Sera, Y.1    Adachi, K.2    Shizuri, Y.3
  • 191
    • 57349182220 scopus 로고    scopus 로고
    • 5?,8?-Epidioxysterols from the gorgonian Eunicella cavolini and the ascidian Trididemnum inarmatum: Isolation andevaluation of their antiproliferative activity
    • Ioannou, E.; Abdel-Razika, A.F.; Zervou, M.; Christofidis, D.; Alexi, X.; Vagias, C.; Alexis, M.N.; Roussis, V. 5?,8?-Epidioxysterols from the gorgonian Eunicella cavolini and the ascidian Trididemnum inarmatum: Isolation andevaluation of their antiproliferative activity. Steroids, 2009, 74(1), 73-80.
    • (2009) Steroids , vol.74 , Issue.1 , pp. 73-80
    • Ioannou, E.1    Abdel-Razika, A.F.2    Zervou, M.3    Christofidis, D.4    Alexi, X.5    Vagias, C.6    Alexis, M.N.7    Roussis, V.8
  • 192
    • 0036730991 scopus 로고    scopus 로고
    • New biologically active marine sesquiterpenoid and steroid from the Okinawan sponge of the genus Axinyssa
    • Iwashima, M.; Terada, I.; Iguchi, K.; Yamori, T. New biologically active marine sesquiterpenoid and steroid from the Okinawan sponge of the genus Axinyssa. Chem. Pharm. Bull., 2002, 50(9), 1286-1289.
    • (2002) Chem. Pharm. Bull. , vol.50 , Issue.9 , pp. 1286-1289
    • Iwashima, M.1    Terada, I.2    Iguchi, K.3    Yamori, T.4
  • 193
    • 0033621674 scopus 로고    scopus 로고
    • A cytotoxic 5?,8?-epidioxysterol from a soft coral Sinularia species
    • Sheu, J.H.; Chang, K.C.; Duh, C.Y. A cytotoxic 5?,8?-epidioxysterol from a soft coral Sinularia species. J. Nat. Prod., 2000, 63(1), 149-151.
    • (2000) J. Nat. Prod. , vol.63 , Issue.1 , pp. 149-151
    • Sheu, J.H.1    Chang, K.C.2    Duh, C.Y.3
  • 195
    • 79960181442 scopus 로고    scopus 로고
    • Synthesis of 7-dehydrocholesterol through hexacarbonyl molybdenum catalyzed elimination reaction
    • Rahman, F; Tan, T.W. Synthesis of 7-dehydrocholesterol through hexacarbonyl molybdenum catalyzed elimination reaction. Bull. Chem. Soc. Ethiop., 2011, 25(2), 247-254.
    • (2011) Bull. Chem. Soc. Ethiop. , vol.25 , Issue.2 , pp. 247-254
    • Rahman, F.1    Tan, T.W.2
  • 196
    • 24944436271 scopus 로고    scopus 로고
    • New efficient and totally stereoselective copper allylic benzoyloxylation of sterol derivatives
    • Brunel, J.M.; Billottet, L.; Letourneux, Y. New efficient and totally stereoselective copper allylic benzoyloxylation of sterol derivatives. Tetrahedron: Asymmetr., 2005, 16(18), 3036-3041.
    • (2005) Tetrahedron: Asymmetr. , vol.16 , Issue.18 , pp. 3036-3041
    • Brunel, J.M.1    Billottet, L.2    Letourneux, Y.3
  • 198
  • 200
    • 33749655167 scopus 로고    scopus 로고
    • Synthesis of oxysterols and nitrogenous sterols with antileishmanial and trypanocidal activities
    • Loiseau, P.M.; Bories, C.; Letourneux, Y.; Rault, S.; Kihel, L.E. Synthesis of oxysterols and nitrogenous sterols with antileishmanial and trypanocidal activities. Eur. J. Med. Chem., 2006, 41(10), 1109-1116.
    • (2006) Eur. J. Med. Chem. , vol.41 , Issue.10 , pp. 1109-1116
    • Loiseau, P.M.1    Bories, C.2    Letourneux, Y.3    Rault, S.4    Kihel, L.E.5


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