메뉴 건너뛰기




Volumn 69, Issue 3, 2015, Pages 255-266

Targeting cancer with sesterterpenoids: The new potential antitumor drugs

Author keywords

Cancer therapy; Sesterterpenoids; Structure activity relationship; Terpenoids

Indexed keywords

ANTINEOPLASTIC AGENT; FURAN DERIVATIVE; GAMMA HYDROXYBUTENOLIDE; HYPOXIA INDUCIBLE FACTOR 1; PYRROLE DERIVATIVE; SARCOTIN A; SESTERTERPENOID; TETRACARBOCYCLIC SESTERTERPENOID; TRICARBOCYCLIC SESTERTERPENOID; UNCLASSIFIED DRUG; SESTERTERPENE;

EID: 84930762344     PISSN: 13403443     EISSN: 18610293     Source Type: Journal    
DOI: 10.1007/s11418-015-0911-y     Document Type: Review
Times cited : (30)

References (65)
  • 1
    • 0032168167 scopus 로고    scopus 로고
    • Etoposide: Four decades of development of a topoisomerase II inhibitor
    • 1:CAS:528:DyaK1cXmvVSku7k%3D 9893622
    • Hande KR (1998) Etoposide: four decades of development of a topoisomerase II inhibitor. Eur J Cancer 34:1514-1521
    • (1998) Eur J Cancer , vol.34 , pp. 1514-1521
    • Hande, K.R.1
  • 2
    • 84894449156 scopus 로고    scopus 로고
    • Treatment with rituximab, cyclophosphamide, doxorubicin, vincristine and prednisolone is beneficial but toxic in very elderly patients with diffuse large B-cell lymphoma: A population-based cohort study on treatment, toxicity and outcome
    • 1:CAS:528:DC%2BC2cXivFensL8%3D 23734653
    • Boslooper K, Kibbelaar R, Storm H, Veeger NJ, Hovenga S, Woolthuis G, van Rees B, de Graaf E, van Roon E, Kluin-Nelemans HC (2014) Treatment with rituximab, cyclophosphamide, doxorubicin, vincristine and prednisolone is beneficial but toxic in very elderly patients with diffuse large B-cell lymphoma: a population-based cohort study on treatment, toxicity and outcome. Leuk Lymphoma 55:526-532
    • (2014) Leuk Lymphoma , vol.55 , pp. 526-532
    • Boslooper, K.1    Kibbelaar, R.2    Storm, H.3    Veeger, N.J.4    Hovenga, S.5    Woolthuis, G.6    Van Rees, B.7    De Graaf, E.8    Van Roon, E.9    Kluin-Nelemans, H.C.10
  • 3
    • 84892518941 scopus 로고    scopus 로고
    • A phase II window study of irinotecan (CPT-11) in high risk Ewing sarcoma: A Euro-E.W.I.N.G. study
    • 1:STN:280:DC%2BC3sbmsFOjsA%3D%3D 24019263
    • Morland B, Platt K, Whelan JS (2014) A phase II window study of irinotecan (CPT-11) in high risk Ewing sarcoma: a Euro-E.W.I.N.G. study. Pediatr Blood Cancer 61:442-445
    • (2014) Pediatr Blood Cancer , vol.61 , pp. 442-445
    • Morland, B.1    Platt, K.2    Whelan, J.S.3
  • 4
    • 84896984353 scopus 로고    scopus 로고
    • Phase II study on dose escalating schedule of paclitaxel concurrent with radiotherapy in treating patients with locally advanced non-small cell lung cancer
    • 24641393
    • Cui L, Liu XX, Jiang Y, Liu JJ, Zhou XR, He XJ, Chen J, Huang XE (2014) Phase II study on dose escalating schedule of paclitaxel concurrent with radiotherapy in treating patients with locally advanced non-small cell lung cancer. Asian Pac J Cancer Prev 15:1699-1702
    • (2014) Asian Pac J Cancer Prev , vol.15 , pp. 1699-1702
    • Cui, L.1    Liu, X.X.2    Jiang, Y.3    Liu, J.J.4    Zhou, X.R.5    He, X.J.6    Chen, J.7    Huang, X.E.8
  • 5
    • 34250785114 scopus 로고    scopus 로고
    • The function of terpene natural products in the natural world
    • 1:CAS:528:DC%2BD2sXms1SrsLc%3D 17576428
    • Gershenzon J, Dudareva N (2007) The function of terpene natural products in the natural world. Nat Chem Biol 3:408-414
    • (2007) Nat Chem Biol , vol.3 , pp. 408-414
    • Gershenzon, J.1    Dudareva, N.2
  • 6
    • 70350731753 scopus 로고    scopus 로고
    • Monoterpene and sesquiterpene synthases and the origin of terpene skeletal diversity in plants
    • 1:CAS:528:DC%2BD1MXhsVWls7bL 19793600
    • Degenhardt J, Kollner TG, Gershenzon J (2009) Monoterpene and sesquiterpene synthases and the origin of terpene skeletal diversity in plants. Phytochemistry 70:1621-1637
    • (2009) Phytochemistry , vol.70 , pp. 1621-1637
    • Degenhardt, J.1    Kollner, T.G.2    Gershenzon, J.3
  • 7
  • 10
    • 67349264062 scopus 로고    scopus 로고
    • Terpenoids and breast cancer chemoprevention
    • 1:CAS:528:DC%2BD1MXmsVGjsrc%3D 18636327
    • Rabi T, Bishayee A (2009) Terpenoids and breast cancer chemoprevention. Breast Cancer Res Treat 115:223-239
    • (2009) Breast Cancer Res Treat , vol.115 , pp. 223-239
    • Rabi, T.1    Bishayee, A.2
  • 11
    • 84861024238 scopus 로고    scopus 로고
    • Terpenoids as potential chemopreventive and therapeutic agents in liver cancer
    • 3182282 21969877
    • Thoppil RJ, Bishayee A (2011) Terpenoids as potential chemopreventive and therapeutic agents in liver cancer. World J Hepatol 3:228-249
    • (2011) World J Hepatol , vol.3 , pp. 228-249
    • Thoppil, R.J.1    Bishayee, A.2
  • 12
    • 43049100156 scopus 로고    scopus 로고
    • Natural health products that inhibit angiogenesis: A potential source for investigational new agents to treat cancer - Part 1
    • 1:STN:280:DC%2BD2szmt1Whtg%3D%3D 1891166 17576437
    • Sagar SM, Yance D, Wong RK (2006) Natural health products that inhibit angiogenesis: a potential source for investigational new agents to treat cancer - Part 1. Curr Oncol 13:14-26
    • (2006) Curr Oncol , vol.13 , pp. 14-26
    • Sagar, S.M.1    Yance, D.2    Wong, R.K.3
  • 13
    • 80053088605 scopus 로고    scopus 로고
    • Inhibition of tumor progression by naturally occurring terpenoids
    • 1:CAS:528:DC%2BC3MXht1WqtLbI 21936626
    • Kuttan G, Pratheeshkumar P, Manu KA, Kuttan R (2011) Inhibition of tumor progression by naturally occurring terpenoids. Pharm Biol 49:995-1007
    • (2011) Pharm Biol , vol.49 , pp. 995-1007
    • Kuttan, G.1    Pratheeshkumar, P.2    Manu, K.A.3    Kuttan, R.4
  • 14
    • 77953533803 scopus 로고    scopus 로고
    • Targeting apoptosis pathway with natural terpenoids: Implications for treatment of breast and prostate cancer
    • 1:CAS:528:DC%2BC3cXmsF2qt7Y%3D 3306610 20298150
    • Yang H, Dou QP (2010) Targeting apoptosis pathway with natural terpenoids: implications for treatment of breast and prostate cancer. Curr Drug Targets 11:733-744
    • (2010) Curr Drug Targets , vol.11 , pp. 733-744
    • Yang, H.1    Dou, Q.P.2
  • 15
    • 77649213543 scopus 로고    scopus 로고
    • Bioactive sesterterpenes and triterpenes from marine sponges: Occurrence and pharmacological significance
    • 1:CAS:528:DC%2BC3cXis1Ght7c%3D 2852841 20390108
    • Ebada SS, Lin W, Proksch P (2010) Bioactive sesterterpenes and triterpenes from marine sponges: occurrence and pharmacological significance. Mar Drugs 8:313-346
    • (2010) Mar Drugs , vol.8 , pp. 313-346
    • Ebada, S.S.1    Lin, W.2    Proksch, P.3
  • 16
    • 24744438666 scopus 로고    scopus 로고
    • Sesterterpenoids, terretonins A-D, and an alkaloid, asterrelenin, from Aspergillus terreus
    • 1:CAS:528:DC%2BD2MXmsFWmsrw%3D 16124769
    • Li GY, Li BG, Yang T, Yin JH, Qi HY, Liu GY, Zhang GL (2005) Sesterterpenoids, terretonins A-D, and an alkaloid, asterrelenin, from Aspergillus terreus. J Nat Prod 68:1243-1246
    • (2005) J Nat Prod , vol.68 , pp. 1243-1246
    • Li, G.Y.1    Li, B.G.2    Yang, T.3    Yin, J.H.4    Qi, H.Y.5    Liu, G.Y.6    Zhang, G.L.7
  • 17
    • 84862549632 scopus 로고    scopus 로고
    • Synthetic approaches toward sesterterpenoids
    • 1:CAS:528:DC%2BC38XosFSlu74%3D 22652980
    • Hog DT, Webster R, Trauner D (2012) Synthetic approaches toward sesterterpenoids. Nat Prod Rep 29:752-779
    • (2012) Nat Prod Rep , vol.29 , pp. 752-779
    • Hog, D.T.1    Webster, R.2    Trauner, D.3
  • 18
    • 33646683781 scopus 로고    scopus 로고
    • Isolation of aureol from Smenospongia sp. and cytotoxic activity of some aureol derivatives
    • 1:CAS:528:DC%2BD28XlvVChurw%3D 16835091
    • Shen YC, Liaw CC, Ho JR, Khalil AT, Kuo YH (2006) Isolation of aureol from Smenospongia sp. and cytotoxic activity of some aureol derivatives. Nat Prod Res 20:578-585
    • (2006) Nat Prod Res , vol.20 , pp. 578-585
    • Shen, Y.C.1    Liaw, C.C.2    Ho, J.R.3    Khalil, A.T.4    Kuo, Y.H.5
  • 19
    • 80053213572 scopus 로고    scopus 로고
    • Cytotoxic C21 and C22 terpenoid-derived metabolites from the sponge Ircinia sp.
    • 1:CAS:528:DC%2BC3MXhtFCgs7vL 21902186
    • Su JH, Tseng SW, Lu MC, Liu LL, Chou Y, Sung PJ (2011) Cytotoxic C21 and C22 terpenoid-derived metabolites from the sponge Ircinia sp. J Nat Prod 74:2005-2009
    • (2011) J Nat Prod , vol.74 , pp. 2005-2009
    • Su, J.H.1    Tseng, S.W.2    Lu, M.C.3    Liu, L.L.4    Chou, Y.5    Sung, P.J.6
  • 20
    • 0035937606 scopus 로고    scopus 로고
    • Effects of temperature on polyunsaturation in cytostatic lipids of Haslea ostrearia
    • 1:CAS:528:DC%2BD3MXhvFKisLc%3D 11281137
    • Rowland SJ, Belt ST, Wraige EJ, Masse G, Roussakis C, Robert JM (2001) Effects of temperature on polyunsaturation in cytostatic lipids of Haslea ostrearia. Phytochemistry 56:597-602
    • (2001) Phytochemistry , vol.56 , pp. 597-602
    • Rowland, S.J.1    Belt, S.T.2    Wraige, E.J.3    Masse, G.4    Roussakis, C.5    Robert, J.M.6
  • 21
    • 0035849146 scopus 로고    scopus 로고
    • Tetra-unsaturated sesterterpenoids (Haslenes) from Haslea ostrearia and related species
    • 1:CAS:528:DC%2BD3MXisVWjs70%3D 11324906
    • Allard WG, Belt ST, Masse G, Naumann R, Robert JM, Rowland S (2001) Tetra-unsaturated sesterterpenoids (Haslenes) from Haslea ostrearia and related species. Phytochemistry 56:795-800
    • (2001) Phytochemistry , vol.56 , pp. 795-800
    • Allard, W.G.1    Belt, S.T.2    Masse, G.3    Naumann, R.4    Robert, J.M.5    Rowland, S.6
  • 22
    • 27644587861 scopus 로고    scopus 로고
    • Ircinin-1 induces cell cycle arrest and apoptosis in SK-MEL-2 human melanoma cells
    • 1:CAS:528:DC%2BD2MXht1WrurrE 16163705
    • Choi HJ, Choi YH, Yee SB, Im E, Jung JH, Kim ND (2005) Ircinin-1 induces cell cycle arrest and apoptosis in SK-MEL-2 human melanoma cells. Mol Carcinog 44:162-173
    • (2005) Mol Carcinog , vol.44 , pp. 162-173
    • Choi, H.J.1    Choi, Y.H.2    Yee, S.B.3    Im, E.4    Jung, J.H.5    Kim, N.D.6
  • 23
    • 0037794367 scopus 로고    scopus 로고
    • Three new metabolites from marine-derived fungi of the genera coniothyrium and microsphaeropsis
    • 9917295
    • Holler U, Konig GM, Wright AD (1999) Three new metabolites from marine-derived fungi of the genera coniothyrium and microsphaeropsis. J Nat Prod 62:114-118
    • (1999) J Nat Prod , vol.62 , pp. 114-118
    • Holler, U.1    Konig, G.M.2    Wright, A.D.3
  • 24
    • 78349278859 scopus 로고    scopus 로고
    • Hypoxia-selective growth inhibition of cancer cells by furospinosulin-1, a furanosesterterpene isolated from an Indonesian marine sponge
    • 1:CAS:528:DC%2BC3cXhtlClu7zF 20839272
    • Arai M, Kawachi T, Setiawan A, Kobayashi M (2010) Hypoxia-selective growth inhibition of cancer cells by furospinosulin-1, a furanosesterterpene isolated from an Indonesian marine sponge. Chem Med Chem 5:1919-1926
    • (2010) Chem Med Chem , vol.5 , pp. 1919-1926
    • Arai, M.1    Kawachi, T.2    Setiawan, A.3    Kobayashi, M.4
  • 25
    • 33745074127 scopus 로고    scopus 로고
    • Manoalide derivatives from a sponge, Luffariella sp.
    • 1:CAS:528:DC%2BD28XmtFKksLc%3D 16753777
    • Zhou GX, Molinski TF (2006) Manoalide derivatives from a sponge, Luffariella sp. J Asian Nat Prod Res 8:15-20
    • (2006) J Asian Nat Prod Res , vol.8 , pp. 15-20
    • Zhou, G.X.1    Molinski, T.F.2
  • 26
    • 0031881662 scopus 로고    scopus 로고
    • Isolation and cytotoxic evaluation of marine sponge-derived norterpene peroxides
    • 1:CAS:528:DyaK1cXovVWntw%3D%3D 9514009
    • Sperry S, Valeriote FA, Corbett TH, Crews P (1998) Isolation and cytotoxic evaluation of marine sponge-derived norterpene peroxides. J Nat Prod 61:241-247
    • (1998) J Nat Prod , vol.61 , pp. 241-247
    • Sperry, S.1    Valeriote, F.A.2    Corbett, T.H.3    Crews, P.4
  • 27
    • 33847036644 scopus 로고    scopus 로고
    • Hypoxia-selective antitumor agents: Norsesterterpene peroxides from the marine sponge Diacarnus levii preferentially suppress the growth of tumor cells under hypoxic conditions
    • 1:CAS:528:DC%2BD2sXlt1CltQ%3D%3D 2910712 17253866
    • Dai J, Liu Y, Zhou YD, Nagle DG (2007) Hypoxia-selective antitumor agents: norsesterterpene peroxides from the marine sponge Diacarnus levii preferentially suppress the growth of tumor cells under hypoxic conditions. J Nat Prod 70:130-133
    • (2007) J Nat Prod , vol.70 , pp. 130-133
    • Dai, J.1    Liu, Y.2    Zhou, Y.D.3    Nagle, D.G.4
  • 28
    • 35048875691 scopus 로고    scopus 로고
    • Evaluation of HIF-1 inhibitors as anticancer agents
    • 1:CAS:528:DC%2BD2sXhtFKit77O 17933687
    • Semenza GL (2007) Evaluation of HIF-1 inhibitors as anticancer agents. Drug Discov Today 12:853-859
    • (2007) Drug Discov Today , vol.12 , pp. 853-859
    • Semenza, G.L.1
  • 29
    • 47549094913 scopus 로고    scopus 로고
    • Aplysinoplides A-C, cytotoxic sesterterpenes from the marine sponge Aplysinopsis digitata
    • 1:CAS:528:DC%2BD1cXls1WhtLc%3D 18461996
    • Ueoka R, Nakao Y, Fujii S, van Soest RW, Matsunaga S (2008) Aplysinoplides A-C, cytotoxic sesterterpenes from the marine sponge Aplysinopsis digitata. J Nat Prod 71:1089-1091
    • (2008) J Nat Prod , vol.71 , pp. 1089-1091
    • Ueoka, R.1    Nakao, Y.2    Fujii, S.3    Van Soest, R.W.4    Matsunaga, S.5
  • 30
    • 0027468008 scopus 로고
    • Luffariolides F and G, new manoalide derivatives from the Okinawan marine sponge Luffariella sp.
    • 1:CAS:528:DyaK3sXitlSntbY%3D 8482949
    • Kobayashi J, Zeng CM, Ishibashi M, Sasaki T (1993) Luffariolides F and G, new manoalide derivatives from the Okinawan marine sponge Luffariella sp. J Nat Prod 56:436-439
    • (1993) J Nat Prod , vol.56 , pp. 436-439
    • Kobayashi, J.1    Zeng, C.M.2    Ishibashi, M.3    Sasaki, T.4
  • 31
    • 0036773605 scopus 로고    scopus 로고
    • Luffariolides H and J, new sesterterpenes from a marine sponge Luffariella species
    • 1:CAS:528:DC%2BD38XmtlSktro%3D 12398555
    • Tsuda M, Endo T, Mikami Y, Fromont J, Kobayashi J (2002) Luffariolides H and J, new sesterterpenes from a marine sponge Luffariella species. J Nat Prod 65:1507-1508
    • (2002) J Nat Prod , vol.65 , pp. 1507-1508
    • Tsuda, M.1    Endo, T.2    Mikami, Y.3    Fromont, J.4    Kobayashi, J.5
  • 33
    • 79251481487 scopus 로고    scopus 로고
    • DNA polymerases and cancer
    • 1:CAS:528:DC%2BC3MXps1Wqug%3D%3D 3739438 21258395
    • Lange SS, Takata K, Wood RD (2011) DNA polymerases and cancer. Nat Rev Cancer 11:96-110
    • (2011) Nat Rev Cancer , vol.11 , pp. 96-110
    • Lange, S.S.1    Takata, K.2    Wood, R.D.3
  • 35
    • 0035015067 scopus 로고    scopus 로고
    • Thorectandrols A and B, new cytotoxic sesterterpenes from the marine sponge Thorectandra species
    • 1:CAS:528:DC%2BD3MXivFymsLs%3D 11374971
    • Charan RD, McKee TC, Boyd MR (2001) Thorectandrols A and B, new cytotoxic sesterterpenes from the marine sponge Thorectandra species. J Nat Prod 64:661-663
    • (2001) J Nat Prod , vol.64 , pp. 661-663
    • Charan, R.D.1    McKee, T.C.2    Boyd, M.R.3
  • 36
    • 0036240214 scopus 로고    scopus 로고
    • Thorectandrols C, D, and E, new sesterterpenes from the marine sponge Thorectandra sp.
    • 1:CAS:528:DC%2BD38XhslGluro%3D 11975486
    • Charan RD, McKee TC, Boyd MR (2002) Thorectandrols C, D, and E, new sesterterpenes from the marine sponge Thorectandra sp. J Nat Prod 65:492-495
    • (2002) J Nat Prod , vol.65 , pp. 492-495
    • Charan, R.D.1    McKee, T.C.2    Boyd, M.R.3
  • 37
    • 0029955176 scopus 로고    scopus 로고
    • Palauolol, a new anti-inflammatory sesterterpene from the sponge Fascaplysinopsis sp. from Palau
    • 1:CAS:528:DyaK28XjsFKis70%3D
    • Schmidt EW, Faulkner DJ (1996) Palauolol, a new anti-inflammatory sesterterpene from the sponge Fascaplysinopsis sp. from Palau. Tetrahedron Lett 37:3951-3954
    • (1996) Tetrahedron Lett , vol.37 , pp. 3951-3954
    • Schmidt, E.W.1    Faulkner, D.J.2
  • 38
    • 84881407991 scopus 로고    scopus 로고
    • Bioactive substances with anti-neoplastic efficacy from marine invertebrates: Porifera and Coelenterata
    • 3212816 22087433
    • Sima P, Vetvicka V (2011) Bioactive substances with anti-neoplastic efficacy from marine invertebrates: Porifera and Coelenterata. World J Clin Oncol 2:355-361
    • (2011) World J Clin Oncol , vol.2 , pp. 355-361
    • Sima, P.1    Vetvicka, V.2
  • 39
    • 80052176402 scopus 로고    scopus 로고
    • Sesterterpenes from the tropical sponge Coscinoderma sp.
    • 1:CAS:528:DC%2BC3MXhtVSrt7fJ 21827183
    • Bae J, Jeon JE, Lee YJ, Lee HS, Sim CJ, Oh KB, Shin J (2011) Sesterterpenes from the tropical sponge Coscinoderma sp. J Nat Prod 74:1805-1811
    • (2011) J Nat Prod , vol.74 , pp. 1805-1811
    • Bae, J.1    Jeon, J.E.2    Lee, Y.J.3    Lee, H.S.4    Sim, C.J.5    Oh, K.B.6    Shin, J.7
  • 40
  • 42
    • 0034701596 scopus 로고    scopus 로고
    • New cytotoxic isomalabaricane-type sesterterpenes from the New Caledonian marine sponge Rhabdastrella globostellata
    • 1:CAS:528:DC%2BD3cXjt1CitLk%3D
    • Bourguet-Kondracki ML, Longeon A, Debitus C, Guyot M (2000) New cytotoxic isomalabaricane-type sesterterpenes from the New Caledonian marine sponge Rhabdastrella globostellata. Tetrahedron Lett 41:3087-3091
    • (2000) Tetrahedron Lett , vol.41 , pp. 3087-3091
    • Bourguet-Kondracki, M.L.1    Longeon, A.2    Debitus, C.3    Guyot, M.4
  • 43
    • 0030825329 scopus 로고    scopus 로고
    • New cytotoxic sesterterpenes from the New Caledonian marine sponge Petrosaspongia nigra (Bergquist)
    • Paloma LG, Randazzo A, Minale L, Debitus C, Roussakis C (1997) New cytotoxic sesterterpenes from the New Caledonian marine sponge Petrosaspongia nigra (Bergquist). Tetrahedron 53:10451-10454
    • (1997) Tetrahedron , vol.53 , pp. 10451-10454
    • Paloma, L.G.1    Randazzo, A.2    Minale, L.3    Debitus, C.4    Roussakis, C.5
  • 44
    • 33646474115 scopus 로고    scopus 로고
    • Sesterterpene metabolites from the sponge Hyatella intestinalis
    • 1:CAS:528:DC%2BD28XksFeku7c%3D
    • Hernandez-Guerrero CJ, Zubia E, Ortega MJ, Luis Carballo J (2006) Sesterterpene metabolites from the sponge Hyatella intestinalis. Tetrahedron 62:5392-5400
    • (2006) Tetrahedron , vol.62 , pp. 5392-5400
    • Hernandez-Guerrero, C.J.1    Zubia, E.2    Ortega, M.J.3    Luis Carballo, J.4
  • 45
    • 77954217513 scopus 로고    scopus 로고
    • Globostelletins A-I, cytotoxic isomalabaricane derivatives from the marine sponge Rhabdastrella globostellata
    • 1:CAS:528:DC%2BC3cXnsVals7c%3D 20627740
    • Li J, Xu B, Cui J, Deng Z, de Voogd NJ, Proksch P, Lin W (2010) Globostelletins A-I, cytotoxic isomalabaricane derivatives from the marine sponge Rhabdastrella globostellata. Bioorg Med Chem 18:4639-4647
    • (2010) Bioorg Med Chem , vol.18 , pp. 4639-4647
    • Li, J.1    Xu, B.2    Cui, J.3    Deng, Z.4    De Voogd, N.J.5    Proksch, P.6    Lin, W.7
  • 47
    • 0036928421 scopus 로고    scopus 로고
    • New scalarane class sesterterpenes from an Indonesian sponge, Phyllospongia sp.
    • 1:CAS:528:DC%2BD38XotFSqsrY%3D 12502324
    • Roy MC, Tanaka J, de Voogd N, Higa T (2002) New scalarane class sesterterpenes from an Indonesian sponge, Phyllospongia sp. J Nat Prod 65:1838-1842
    • (2002) J Nat Prod , vol.65 , pp. 1838-1842
    • Roy, M.C.1    Tanaka, J.2    De Voogd, N.3    Higa, T.4
  • 48
    • 24744432700 scopus 로고    scopus 로고
    • Antineoplastic agents. 542. Isolation and structure of sesterstatin 6 from the Indian Ocean sponge Hyrtios erecta
    • 1:CAS:528:DC%2BD2MXmt1Krtb0%3D 3335338 16124771
    • Pettit GR, Tan R, Cichacz ZA (2005) Antineoplastic agents. 542. Isolation and structure of sesterstatin 6 from the Indian Ocean sponge Hyrtios erecta. J Nat Prod 68:1253-1255
    • (2005) J Nat Prod , vol.68 , pp. 1253-1255
    • Pettit, G.R.1    Tan, R.2    Cichacz, Z.A.3
  • 49
    • 84862860095 scopus 로고    scopus 로고
    • Cytotoxic sesterterpenoids from a sponge Hippospongia sp.
    • 1:CAS:528:DC%2BC38XnvFWntL4%3D 3397461 22822351
    • Chang YC, Tseng SW, Liu LL, Chou Y, Ho YS, Lu MC, Su JH (2012) Cytotoxic sesterterpenoids from a sponge Hippospongia sp. Mar Drugs 10:987-997
    • (2012) Mar Drugs , vol.10 , pp. 987-997
    • Chang, Y.C.1    Tseng, S.W.2    Liu, L.L.3    Chou, Y.4    Ho, Y.S.5    Lu, M.C.6    Su, J.H.7
  • 51
    • 0030698069 scopus 로고    scopus 로고
    • A simple enantioselective synthesis of the biologically active tetracyclic marine sesterterpene scalarenedial
    • 1:CAS:528:DyaK2sXms1OnsL4%3D
    • Corey EJ, Luo G, Lin LS (1997) A simple enantioselective synthesis of the biologically active tetracyclic marine sesterterpene scalarenedial. J Am Chem Soc 119:9927-9928
    • (1997) J Am Chem Soc , vol.119 , pp. 9927-9928
    • Corey, E.J.1    Luo, G.2    Lin, L.S.3
  • 52
    • 0034637608 scopus 로고    scopus 로고
    • Mangicols: Structures and biosynthesis of a new class of sesterterpene polyols from a marine fungus of the genus Fusarium
    • 1:CAS:528:DC%2BD3cXkslWmtro%3D 10956462
    • Renner MK, Jensen PR, Fenical W (2000) Mangicols: structures and biosynthesis of a new class of sesterterpene polyols from a marine fungus of the genus Fusarium. J Org Chem 65:4843-4852
    • (2000) J Org Chem , vol.65 , pp. 4843-4852
    • Renner, M.K.1    Jensen, P.R.2    Fenical, W.3
  • 53
    • 71349086366 scopus 로고    scopus 로고
    • Heteronemin, a spongean sesterterpene, inhibits TNF alpha-induced NF-kappa B activation through proteasome inhibition and induces apoptotic cell death
    • 1:CAS:528:DC%2BD1MXhsFGgtL3O 19814997
    • Schumacher M, Cerella C, Eifes S, Chateauvieux S, Morceau F, Jaspars M, Dicato M, Diederich M (2010) Heteronemin, a spongean sesterterpene, inhibits TNF alpha-induced NF-kappa B activation through proteasome inhibition and induces apoptotic cell death. Biochem Pharmacol 79:610-622
    • (2010) Biochem Pharmacol , vol.79 , pp. 610-622
    • Schumacher, M.1    Cerella, C.2    Eifes, S.3    Chateauvieux, S.4    Morceau, F.5    Jaspars, M.6    Dicato, M.7    Diederich, M.8
  • 56
    • 0032514839 scopus 로고    scopus 로고
    • Neomangicols: Structures and absolute stereochemistries of unprecedented halogenated sesterterpenes from a marine fungus of the genus Fusarium
    • 1:CAS:528:DyaK1cXmslKjsLo%3D
    • Renner MK, Jensen PR, Fenical WJ (1998) Neomangicols: structures and absolute stereochemistries of unprecedented halogenated sesterterpenes from a marine fungus of the genus Fusarium. J Org Chem 63:8346-8354
    • (1998) J Org Chem , vol.63 , pp. 8346-8354
    • Renner, M.K.1    Jensen, P.R.2    Fenical, W.J.3
  • 57
    • 84859235771 scopus 로고    scopus 로고
    • Cacospongionolide and scalaradial, two marine sesterterpenoids as potent apoptosis-inducing factors in human carcinoma cell lines
    • 3317917 22509253
    • De Stefano D, Tommonaro G, Malik SA, Iodice C, De Rosa S, Maiuri MC, Carnuccio R (2012) Cacospongionolide and scalaradial, two marine sesterterpenoids as potent apoptosis-inducing factors in human carcinoma cell lines. PLoS One 7:e33031
    • (2012) PLoS One , vol.7
    • De Stefano, D.1    Tommonaro, G.2    Malik, S.A.3    Iodice, C.4    De Rosa, S.5    Maiuri, M.C.6    Carnuccio, R.7
  • 58
    • 0036163649 scopus 로고    scopus 로고
    • Salmahyrtisol A, a novel cytotoxic sesterterpene from the Red Sea sponge Hyrtios erecta
    • 1:CAS:528:DC%2BD3MXovV2hu78%3D 11809054
    • Youssef DT, Yamaki RK, Kelly M, Scheuer PJ (2002) Salmahyrtisol A, a novel cytotoxic sesterterpene from the Red Sea sponge Hyrtios erecta. J Nat Prod 65:2-6
    • (2002) J Nat Prod , vol.65 , pp. 2-6
    • Youssef, D.T.1    Yamaki, R.K.2    Kelly, M.3    Scheuer, P.J.4
  • 59
    • 77951241278 scopus 로고    scopus 로고
    • Terpestacin inhibits tumor angiogenesis by targeting UQCRB of mitochondrial complex III and suppressing hypoxia-induced reactive oxygen species production and cellular oxygen sensing
    • 1:CAS:528:DC%2BC3cXktFGltLw%3D 2857036 20145250
    • Jung HJ, Shim JS, Lee J, Song YM, Park KC, Choi SH, Kim ND, Yoon JH, Mungai PT (2010) Terpestacin inhibits tumor angiogenesis by targeting UQCRB of mitochondrial complex III and suppressing hypoxia-induced reactive oxygen species production and cellular oxygen sensing. J Biol Chem 285:11584-11595
    • (2010) J Biol Chem , vol.285 , pp. 11584-11595
    • Jung, H.J.1    Shim, J.S.2    Lee, J.3    Song, Y.M.4    Park, K.C.5    Choi, S.H.6    Kim, N.D.7    Yoon, J.H.8    Mungai, P.T.9
  • 60
    • 84875825774 scopus 로고    scopus 로고
    • Exploring the role of mitochondrial UQCRB in angiogenesis using small molecules
    • 1:CAS:528:DC%2BC3sXltVOlsr0%3D 23475074
    • Jung HJ, Kwon HJ (2013) Exploring the role of mitochondrial UQCRB in angiogenesis using small molecules. Mol BioSyst 9:930-939
    • (2013) Mol BioSyst , vol.9 , pp. 930-939
    • Jung, H.J.1    Kwon, H.J.2
  • 61
    • 0036742135 scopus 로고    scopus 로고
    • Cytotoxic pyrrolo- and furanoterpenoids from the sponge sarcotragus species
    • 1:CAS:528:DC%2BD38Xmt1Cksrg%3D 12350153
    • Liu Y, Hong J, Lee CO, Im KS, Kim ND, Choi JS, Jung JH (2002) Cytotoxic pyrrolo- and furanoterpenoids from the sponge sarcotragus species. J Nat Prod 65:1307-1314
    • (2002) J Nat Prod , vol.65 , pp. 1307-1314
    • Liu, Y.1    Hong, J.2    Lee, C.O.3    Im, K.S.4    Kim, N.D.5    Choi, J.S.6    Jung, J.H.7
  • 62
    • 3242742750 scopus 로고    scopus 로고
    • Cytotoxic furanosesterterpenes from a marine sponge Psammocinia sp.
    • 1:CAS:528:DC%2BD2cXlsFemsLs%3D 15270579
    • Choi K, Hong J, Lee CO, Kim DK, Sim CJ, Im KS, Jung JH (2004) Cytotoxic furanosesterterpenes from a marine sponge Psammocinia sp. J Nat Prod 67:1186-1189
    • (2004) J Nat Prod , vol.67 , pp. 1186-1189
    • Choi, K.1    Hong, J.2    Lee, C.O.3    Kim, D.K.4    Sim, C.J.5    Im, K.S.6    Jung, J.H.7
  • 63
    • 0030720972 scopus 로고    scopus 로고
    • Further bioactive sesterterpenes from the Tyrrhenian sponge Fasciospongia cavernosa
    • De Rosa S, de Giulio A, Crispino A, Iodice C, Tommonaro G (1997) Further bioactive sesterterpenes from the Tyrrhenian sponge Fasciospongia cavernosa. Nat Prod Lett 10:267-274
    • (1997) Nat Prod Lett , vol.10 , pp. 267-274
    • De Rosa, S.1    De Giulio, A.2    Crispino, A.3    Iodice, C.4    Tommonaro, G.5
  • 64
    • 0344550324 scopus 로고    scopus 로고
    • New cytotoxic sesterterpenoids and norsesterterpenoids from two sponges of the genus Sarcotragus
    • 1:CAS:528:DC%2BD3sXot1OisL8%3D 14640517
    • Liu Y, Mansoor TA, Hong J, Lee CO, Sim CJ, Im KS, Kim ND, Jung JH (2003) New cytotoxic sesterterpenoids and norsesterterpenoids from two sponges of the genus Sarcotragus. J Nat Prod 66:1451-1456
    • (2003) J Nat Prod , vol.66 , pp. 1451-1456
    • Liu, Y.1    Mansoor, T.A.2    Hong, J.3    Lee, C.O.4    Sim, C.J.5    Im, K.S.6    Kim, N.D.7    Jung, J.H.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.