메뉴 건너뛰기




Volumn 23, Issue 7, 2014, Pages 3528-3538

Antioxidant and antibacterial evaluation of synthetic furomollugin and its diverse analogs

Author keywords

Antibacterial; Antioxidant; CAN; Furomollugin

Indexed keywords

1,1 DIPHENYL 2 PICRYLHYDRAZYL; AMMONIUM NITRATE; AMPICILLIN; ANTIINFECTIVE AGENT; ANTIOXIDANT; CIS METHYL 2 ETHOXY 5 HYDROXY 3 METHYL 2,3 DIHYDRONAPHTHO[1,2 B]FURAN 4 CARBOXYLATE; FUROMOLLUGIN; FUROMOLLUGIN DERIVATIVE; HYDROGEN PEROXIDE; METHYL 2 BUTOXY 5 HYDROXY 2,3 DIHYDRONAPHTHO[1,2 B]FURAN 4 CARBOXYLATE; METHYL 2 ETHOXY 5 HYDROXY 2,3 DIHYDRONAPHTHO[1,2 B]FURAN 4 CARBOXYLATE; METHYL 2 ETHOXY 5 HYDROXY 3 METHYL 2,3 DIHYDRONAPHTHO[1,2 B]FURAN 4 CARBOXYLATE; METHYL 5 HYDROXY 2 (2 OXOPYRROLIDIN 1 YL) 2,3 DIHYDRONAPHTHO[1,2 B]FURAN 4 CARBOXYLATE; METHYL 5 HYDROXY 2 (4 METHOXYPHENYL) 2,3 DIHYDRONAPHTHO[1,2 B]FURAN 4 CARBOXYLATE; METHYL 5 HYDROXY 2 METHOXY 2 METHYL 2,3 DIHYDRONAPHTHO[1,2 B]FURAN 4 CARBOXYLATE; METHYL 5 HYDROXY 2 METHYL 2 PHENYL 2,3 DIHYDRONAPHTHO[1,2 B]FURAN 4 CARBOXYLATE; METHYL 5 HYDROXY 2 METHYLNAPHTHO[1,2 B]FURAN 4 CARBOXYLATE; METHYL 5 HYDROXY 2 PROPOXY 2,3 DIHYDRONAPHTHO[1,2B]FURAN 4 CARBOXYLATE; METHYL 5 HYDROXY 7,8,9,10A TETRAHYDRO 6BH NAPHTHO[2',1':4,5]FURO[2,3 B]PYRAN 6 CARBOXYLATE; METHYL 5 HYDROXY 8,9 DIHYDRO 7H NAPHTHO[2',1':4,5]FURO[2,3 B]PYRAN 6 CARBOXYLATE; NITRIC OXIDE; UNCLASSIFIED DRUG;

EID: 84902359800     PISSN: 10542523     EISSN: 15548120     Source Type: Journal    
DOI: 10.1007/s00044-014-0929-9     Document Type: Article
Times cited : (27)

References (48)
  • 1
    • 0027741358 scopus 로고
    • Chain-breaking phenolic antioxidants: Steric and electronic effects in polyalkylchromanols, tocopherol analogs, hydroquinones, and superior antioxidants of the polyalkylbenzochromanol and naphthofuran class
    • Barclay LRC, Vinqvist MR, Mukai K, Itoh S, Morimoto H (1993) Chain-breaking phenolic antioxidants: steric and electronic effects in polyalkylchromanols, tocopherol analogs, hydroquinones, and superior antioxidants of the polyalkylbenzochromanol and naphthofuran class. J Org Chem 58:7416-7420. doi:10.1021/jo00078a020 (Pubitemid 24065028)
    • (1993) Journal of Organic Chemistry , vol.58 , Issue.26 , pp. 7416-7420
    • Barclay, L.R.C.1    Vinqvist, M.R.2    Mukai, K.3    Itoh, S.4    Morimoto, H.5
  • 2
    • 0029076614 scopus 로고
    • Chain-breaking naphtholic antioxidants: Antioxidant activities of a polyalkylbenzochromanol, a polyalkylbenzochromenol, and 2,3-dihydro-5-hydroxy-2, 2,4-trimethylnaphtho[1,2-b]furan compared to an a-tocopherol model in sodium dodecyl sulfate micelles
    • doi:10.1021/jo00114a022
    • Barclay LRC, Edwards CD, Mukai K, Egawa Y, Nishi T (1995) Chain-breaking naphtholic antioxidants: antioxidant activities of a polyalkylbenzochromanol, a polyalkylbenzochromenol, and 2,3-dihydro-5-hydroxy-2,2,4-trimethylnaphtho[1,2-b] furan compared to an a-tocopherol model in sodium dodecyl sulfate micelles. J Org Chem 60:2739-2744. doi:10.1021/jo00114a022
    • (1995) J Org Chem , vol.60 , pp. 2739-2744
    • Barclay, L.R.C.1    Edwards, C.D.2    Mukai, K.3    Egawa, Y.4    Nishi, T.5
  • 4
    • 0013902668 scopus 로고
    • Antibiotic susceptibility testing by a standardized single disk method
    • Bauer AW, Kirby WM, Sherris JC, Turck M (1966) Antibiotic susceptibility testing by a standardized single disk method. Am J Clin Pathol 45:493-496
    • (1966) Am J Clin Pathol , vol.45 , pp. 493-496
    • Bauer, A.W.1    Kirby, W.M.2    Sherris, J.C.3    Turck, M.4
  • 5
    • 2942516293 scopus 로고    scopus 로고
    • Synthesis of pyrrolo[3,2-b]benzofurans and pyrrolo[3,2-b]naphthofurans via addition of a silyloxypyrrole to activated quinones
    • DOI 10.1016/j.tet.2004.05.008, PII S0040402004006817
    • Brimble MA, Burgess C, Halim R, Petersson M, Ray J (2004) Synthesis of pyrrolo[3,2-b]benzofurans and pyrrolo[3,2-b]naphthofurans via addition of a silyloxypyrrole to activated quinones. Tetrahedron 60:5751-5758. doi:10.1016/j.tet.2004.05.008 (Pubitemid 38757717)
    • (2004) Tetrahedron , vol.60 , Issue.27 , pp. 5751-5758
    • Brimble, M.A.1    Burgess, C.2    Halim, R.3    Petersson, M.4    Ray, J.5
  • 6
    • 0033837710 scopus 로고    scopus 로고
    • Antioxidant activity of Nigella sativa essential oil
    • DOI 10.1002/1099-1573(200008)14:5<323::AID-PTR621
    • Burits M, Bucar F (2000) Antioxidant activity of Nigella sativa essential oil. Phytother Res 14:323-328. doi:10.1002/1099-1573(200008)14:5〈323:aid- ptr621〉3.0.co;2-q (Pubitemid 30655515)
    • (2000) Phytotherapy Research , vol.14 , Issue.5 , pp. 323-328
    • Burits, M.1    Bucar, F.2
  • 7
    • 33845377128 scopus 로고
    • Autoxidation of biological molecules. 4. Maximizing the antioxidant activity of phenols
    • doi:10.1021/ja00310a049
    • Burton GW, Doba T, Gabe E, Hughes L, Lee FL, Prasad L, Ingold KU (1985) Autoxidation of biological molecules. 4. Maximizing the antioxidant activity of phenols. J Am Chem Soc 107:7053-7065. doi:10.1021/ja00310a049
    • (1985) J Am Chem Soc , vol.107 , pp. 7053-7065
    • Burton, G.W.1    Doba, T.2    Gabe, E.3    Hughes, L.4    Lee, F.L.5    Prasad, L.6    Ingold, K.U.7
  • 9
    • 84857543380 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of chalcones of naphtho[2,1-b]furan condensed with barbituric acid
    • Chandrashekhar CH, Latha KP, Vagdevi HM, Vaidya VP (2011) Synthesis and antimicrobial activity of chalcones of naphtho[2,1-b]furan condensed with barbituric acid. Der Pharm Chem 3:365-369
    • (2011) Der Pharm Chem , vol.3 , pp. 365-369
    • Chandrashekhar, C.H.1    Latha, K.P.2    Vagdevi, H.M.3    Vaidya, V.P.4
  • 10
    • 33745943653 scopus 로고    scopus 로고
    • Synthesis of mollugin
    • DOI 10.1016/j.tet.2006.06.014, PII S0040402006009288
    • Claessens S, Kesteleyn B, Van Nguyen T, De Kimpe N (2006) Synthesis of mollugin. Tetrahedron 62(35):8419-8424. doi:10.1016/j.tet.2006.06.014 (Pubitemid 44062626)
    • (2006) Tetrahedron , vol.62 , Issue.35 , pp. 8419-8424
    • Claessens, S.1    Kesteleyn, B.2    Nguyen, V.T.3    De Kimpe, N.4
  • 11
    • 0027266850 scopus 로고
    • Mechanistic interpretation of the genotoxicity of nitrofurans (antibacterial agents) using quantitative structure-activity relationships and comparative molecular field analysis
    • Debnath AK, Hansch C, Kim KH, Martin YC (1993) Mechanistic interpretation of the genotoxicity of nitrofurans (antibacterial agents) using quantitative structure-activity relationships and comparative molecular field analysis. J Med Chem 36: 1007-1016. doi:10.1021/jm00060a008 (Pubitemid 23143613)
    • (1993) Journal of Medicinal Chemistry , vol.36 , Issue.8 , pp. 1007-1016
    • Debnath, A.K.1    Hansch, C.2    Kim, K.H.3    Martin, Y.C.4
  • 12
    • 0021687238 scopus 로고
    • EFFET D'UN SUBSTITUANT EN POSITION 2b DE L'HETEROCYCLE SUR LES PROPRIETES ANTIBACTERIENNES ET PARSITICIDES DES NITRO-2 NAPHTO[2,1-b] FURANNES
    • Einhorn J, Demerseman P, Royer R, Cavier R, Gayral P (1984) Effect of a substituent in the β position of the heterocycle on the antibacterial and parasiticidal properties of 2-nitronaphtho[2.1-b]furans. Eur J Med Chem Chim Ther 19:405-410 (Pubitemid 15202642)
    • (1984) European Journal of Medicinal Chemistry , vol.19 , Issue.5 , pp. 405-410
    • Einhorn, J.1    Demerseman, P.2    Royer, R.3
  • 13
    • 0030272214 scopus 로고    scopus 로고
    • Stereoselective syntheses of substituted pterocarpans with anti-HIV activity, and 5-aza-/5-thia-pterocarpan and 2-aryl-2,3-dihydrobenzofuran analogues
    • DOI 10.1016/0968-0896(96)00192-7, PII S0968089696001927
    • Engler TA, LaTessa KO, Iyengar R, Chai W, Agrios K (1996) Stereoselective syntheses of substituted pterocarpans with anti-HIV activity, and 5-aza-/5-thia-pterocarpan and 2-aryl-2,3-dihydrobenzofuran analogs. Bioorg Med Chem 4:1755-1769. doi:10.1016/0968-0896(96)00192-7 (Pubitemid 26361881)
    • (1996) Bioorganic and Medicinal Chemistry , vol.4 , Issue.10 , pp. 1755-1769
    • Engler, T.A.1    LaTessa, K.O.2    Iyengar, R.3    Chai, W.4    Agrios, K.5
  • 14
    • 0020081811 scopus 로고
    • SULL'ATTIVITA beta-ADRENOLITICA DI ALCUNI DERIVATI DEL NAFTO[2,1-b]FURANO
    • Gaggi R, Giovanninetti G, Garuti L (1982) β-Adrenolytic activity of some naphtho[2,1-b]furan derivatives. Farm Ed Sci 37:149-150 (Pubitemid 12126543)
    • (1982) Farmaco, Edizione Scientifica , vol.37 , Issue.2 , pp. 149-150
    • Gaggi, R.1    Giovanninetti, G.2    Garuti, L.3
  • 15
    • 0016157911 scopus 로고
    • Substances with antiviral activity. I. Naphtho[2,1-b]furan-1(2H)-one, 1H-benz[e]indene-2,3-dihydro-1-one, and 1H-benz[ e]indene-1,3(2H)-dione derivatives
    • Giovanninetti G, Cavrini V, Chiarini A, Garuti L, Mannini-Palenzona A (1974) Substances with antiviral activity. I. Naphtho[2,1-b]furan-1(2H)-one, 1H-benz[e]indene-2,3-dihydro-1-one, and 1H-benz[ e]indene-1,3(2H)-dione derivatives. Farm Ed Sci 29:375-385
    • (1974) Farm Ed Sci , vol.29 , pp. 375-385
    • Giovanninetti, G.1    Cavrini, V.2    Chiarini, A.3    Garuti, L.4    Mannini-Palenzona, A.5
  • 16
    • 33749321036 scopus 로고    scopus 로고
    • Efficient syntheses of mollugin
    • doi:10.1055/s-2006-950441
    • Habonimana P, Claessens S, De Kimpe N (2006) Efficient syntheses of mollugin. Synlett 2472-2475. doi:10.1055/s-2006-950441
    • (2006) Synlett , vol.2472-2475
    • Habonimana, P.1    Claessens, S.2    De Kimpe, N.3
  • 17
    • 0029897985 scopus 로고    scopus 로고
    • Inhibition of hepatitis B surface antigen secretion on human hepatoma cells. Components from Rubia cordifolia
    • DOI 10.1021/np960200h
    • Ho L-K, Don M-J, Chen H-C, Yeh S-F, Chen J-M (1996) Inhibition of hepatitis B surface antigen secretion on human hepatoma cells. Components from Rubia cordifolia. J Nat Prod 59:330-333. doi:10.1021/np960200h (Pubitemid 26112730)
    • (1996) Journal of Natural Products , vol.59 , Issue.3 , pp. 330-333
    • Ho, L.-K.1    Don, M.-J.2    Chen, H.-C.3    Yeh, S.-F.4    Chen, J.-M.5
  • 18
    • 0242468134 scopus 로고    scopus 로고
    • Synthesis and antitumor evaluation of some new substituted amidino-benzimidazolyl-furyl-phenyl-acrylates and naphtho[2,1-b]furan- carboxylates
    • doi:10.1016/s0014-827x(03)00197-6
    • Hranjec M, Grdisa M, Pavelic K, Boykin DW, Karminski-Zamola G (2003) Synthesis and antitumor evaluation of some new substituted amidino- benzimidazolyl-furyl-phenyl-acrylates and naphtho[2,1-b]furan-carboxylates. Farmaco 58:1319-1324. doi:10.1016/s0014-827x(03)00197-6
    • (2003) Farmaco , vol.58 , pp. 1319-1324
    • Hranjec, M.1    Grdisa, M.2    Pavelic, K.3    Boykin, D.W.4    Karminski-Zamola, G.5
  • 19
    • 0000262655 scopus 로고
    • Quinones and related compounds in higher plants. Part 19. Biosynthesis of anthraquinones and related compounds in Galium mollugo cell suspension cultures
    • doi:10.1016/s0031-9422(00)80323-4
    • Inoue K, Shiobara Y, Nayeshiro H, Inouye H, Wilson G, Zenk MH (1984) Quinones and related compounds in higher plants. Part 19. Biosynthesis of anthraquinones and related compounds in Galium mollugo cell suspension cultures. Phytochemistry 23:307-311. doi:10.1016/s0031-9422(00)80323-4
    • (1984) Phytochemistry , vol.23 , pp. 307-311
    • Inoue, K.1    Shiobara, Y.2    Nayeshiro, H.3    Inouye, H.4    Wilson, G.5    Zenk, M.H.6
  • 20
    • 58149152847 scopus 로고    scopus 로고
    • New and highly efficient synthesis of 3-substituted 1-hydroxybenz[g] isoquinoline-5,10-diones
    • doi:10.1016/j.tet.2008.11.070
    • Jacobs J, Claessens S, Mbala BM, Huygen K, De Kimpe N (2009) New and highly efficient synthesis of 3-substituted 1-hydroxybenz[g]isoquinoline-5,10- diones. Tetrahedron 65:1193-1199. doi:10.1016/j.tet.2008.11.070
    • (2009) Tetrahedron , vol.65 , pp. 1193-1199
    • Jacobs, J.1    Claessens, S.2    Mbala, B.M.3    Huygen, K.4    De Kimpe, N.5
  • 21
    • 84862835703 scopus 로고    scopus 로고
    • Bioassay-guided isolation of fatty acid synthase inhibitory diterpenoids from the roots of Salvia miltiorrhiza Bunge
    • doi:10.1007/s12272-012-0311-8
    • Jang T-S, Zhang HY, Kim GJ, Kim DW, Min B-S, Kang W, Son KH, Na MK, Lee SH (2012) Bioassay-guided isolation of fatty acid synthase inhibitory diterpenoids from the roots of Salvia miltiorrhiza Bunge. Arch Pharm Res 35:481-486. doi:10.1007/s12272-012-0311-8
    • (2012) Arch Pharm Res , vol.35 , pp. 481-486
    • Jang, T.-S.1    Zhang, H.Y.2    Kim, G.J.3    Kim, D.W.4    Min, B.-S.5    Kang, W.6    Son, K.H.7    Na, M.K.8    Lee, S.H.9
  • 22
    • 84864563661 scopus 로고    scopus 로고
    • Recent development on the synthesis of benzo[b]- and naphtho[b]furans: A review
    • doi:10.2174/157017912802651393
    • Kwiecien H, Smist M, Kowalewska M (2012) Recent development on the synthesis of benzo[b]- and naphtho[b]furans: a review. Curr Org Synth 9:529-560. doi:10.2174/157017912802651393
    • (2012) Curr Org Synth , vol.9 , pp. 529-560
    • Kwiecien, H.1    Smist, M.2    Kowalewska, M.3
  • 23
    • 69949171195 scopus 로고    scopus 로고
    • Identification of small molecule regulators of the nuclear receptor HNF4α based on naphthofuran scaffolds
    • doi:10.1016/j.bmc.2009.07.079
    • Le GR, Oger F, Lecorgne A, Dudasova Z, Chevance S, Bondon A, Barath P, Simonneaux G, Salbert G (2009) Identification of small molecule regulators of the nuclear receptor HNF4α based on naphthofuran scaffolds. Bioorg Med Chem 17:7021-7030. doi:10.1016/j.bmc.2009.07.079
    • (2009) Bioorg Med Chem , vol.17 , pp. 7021-7030
    • Le, G.R.1    Oger, F.2    Lecorgne, A.3    Dudasova, Z.4    Chevance, S.5    Bondon, A.6    Barath, P.7    Simonneaux, G.8    Salbert, G.9
  • 24
    • 0035085221 scopus 로고    scopus 로고
    • Efficient synthesis of cytotoxic furonaphthoquinone natural products
    • DOI 10.1081/SCC-100000527
    • Lee YR, Kim BS (2001) Efficient synthesis of cytotoxic furonaphthoquinone natural products. Synth Commun 31:381-386. doi:10.1081/scc-100000527 (Pubitemid 32231817)
    • (2001) Synthetic Communications , vol.31 , Issue.3 , pp. 381-386
    • Lee, Y.R.1    Kim, B.S.2
  • 25
    • 0005613723 scopus 로고    scopus 로고
    • Efficient One-Step Synthesis of 2-Arylfurans by Ceric Ammonium Nitrate (CAN)-Mediated Cycloaddition of 1,3-Dicarbonyl Compounds to Alkynes
    • Lee YR, Byun MW, Kim BS (1998) Efficient one-step synthesis of 2-arylfurans by ceric ammonium nitrate (CAN)-mediated cycloaddition of 1,3-dicarbonyl compounds to alkynes. Bull Korean Chem Soc 19:1080-1083 (Pubitemid 128473413)
    • (1998) Bulletin of the Korean Chemical Society , vol.19 , Issue.10 , pp. 1080-1083
    • Lee, Y.R.1    Byun, M.W.2    Kim, B.S.3
  • 26
    • 0034602142 scopus 로고    scopus 로고
    • Ceric ammonium nitrate (CAN)-mediated oxidative cycloaddition of 1,3-dicarbonyls to conjugated compounds.Efficient synthesis of dihydrofurans, dihydrofurocoumarins, dihydrofuroquinolinones, dihydrofurophenalenones, and furonaphthoquinone natural products
    • doi:10.1016/s0040-4020(00)00839-5
    • Lee YR, Kim BS, Kim DH (2000) Ceric ammonium nitrate (CAN)-mediated oxidative cycloaddition of 1,3-dicarbonyls to conjugated compounds.Efficient synthesis of dihydrofurans, dihydrofurocoumarins, dihydrofuroquinolinones, dihydrofurophenalenones, and furonaphthoquinone natural products. Tetrahedron 56:8845-8853. doi:10.1016/s0040-4020(00)00839-5
    • (2000) Tetrahedron , vol.56 , pp. 8845-8853
    • Lee, Y.R.1    Kim, B.S.2    Kim, D.H.3
  • 27
    • 0037145601 scopus 로고    scopus 로고
    • Ceric ammonium nitrate(CAN)-mediated oxidative cycloaddition of 1,3-dicarbonyls to vinyl sulfides. Application to the synthesis of evodone and avicequinone-B
    • doi:10.5012/bkcs.2002.23.10.1477
    • Lee YR, Lee GJ, Kang KY (2002) Ceric ammonium nitrate(CAN)-mediated oxidative cycloaddition of 1,3-dicarbonyls to vinyl sulfides. Application to the synthesis of evodone and avicequinone-B. Bull Korean Chem Soc 23:1477-1480. doi:10.5012/bkcs.2002.23.10.1477
    • (2002) Bull Korean Chem Soc , vol.23 , pp. 1477-1480
    • Lee, Y.R.1    Lee, G.J.2    Kang, K.Y.3
  • 28
    • 0141618326 scopus 로고    scopus 로고
    • Efficient synthesis of dihydrofurans with sulfide groups by ceric(IV) ammonium nitrate-mediated oxidative cycloaddition of 1,3-dicarbonyl compounds to vinyl sulfides. Application to the synthesis of benzo[b]naphtho[2,3-d ]furan-6,11-dione and first total synthesis of millettocalyxins C and pongamol methyl ether
    • doi:10.1055/s-2003-41023
    • Lee YR, Kang KY, Lee GJ, Lee WK (2003) Efficient synthesis of dihydrofurans with sulfide groups by ceric(IV) ammonium nitrate-mediated oxidative cycloaddition of 1,3-dicarbonyl compounds to vinyl sulfides. Application to the synthesis of benzo[b]naphtho[2,3-d ]furan-6,11-dione and first total synthesis of millettocalyxins C and pongamol methyl ether. Synthesis 1977-1988. doi:10.1055/s-2003-41023
    • (2003) Synthesis , pp. 1977-1988
    • Lee, Y.R.1    Kang, K.Y.2    Lee, G.J.3    Lee, W.K.4
  • 29
    • 47749100518 scopus 로고    scopus 로고
    • ortho-quinone methides from para-quinones: Total synthesis of rubioncolin B
    • DOI 10.1021/ja803498r
    • Lumb J-P, Choong KC, Trauner D (2008) ortho-Quinone Methides from para-quinones: total Synthesis of Rubioncolin B. J Am Chem Soc 130:9230-9231. doi:10.1021/ja803498r (Pubitemid 352031123)
    • (2008) Journal of the American Chemical Society , vol.130 , Issue.29 , pp. 9230-9231
    • Lumb, J.-P.1    Choong, K.C.2    Trauner, D.3
  • 30
    • 7444236690 scopus 로고    scopus 로고
    • Synthesis and pharmacological evaluation of some potent naphtho[2,1-b]furopyrazolyl, -oxadiazolyl, and -coumaryl derivatives
    • Mahadevan KM, Vaidya VP (2003) Synthesis and pharmacological evaluation of some potent naphtho[2,1-b]furopyrazolyl, -oxadiazolyl, and -coumaryl derivatives. Indian J Pharm Sci 65:128-134
    • (2003) Indian J Pharm Sci , vol.65 , pp. 128-134
    • Mahadevan, K.M.1    Vaidya, V.P.2
  • 31
    • 0035565504 scopus 로고    scopus 로고
    • Studies in naphthofurans: Part V-synthesis of 2-aryl-1,2,3,4- tetrahydropyrido (naphtho [2,1-b] furan)-4-ones and their biological activity
    • Mahadevan KM, Padmashali B, Vaidya VP (2001) Studies in naphthofurans: Part V - synthesis of 2-aryl-1,2,3,4-tetrahydropyrido(naphtho[2,1-b]furan)-4- ones and their biological activity. Indian J Heterocycl Chem 11:15-20 (Pubitemid 33690822)
    • (2001) Indian Journal of Heterocyclic Chemistry , vol.11 , Issue.1 , pp. 15-20
    • Mahadevan, K.M.1    Padmashali, B.2    Vaidya, V.P.3
  • 34
    • 0037128499 scopus 로고    scopus 로고
    • A facile three-component reaction involving [4+1] cycloaddition leading to furan annulated heterocycles
    • DOI 10.1016/S0040-4039(02)00226-5, PII S0040403902002265
    • Nair V, Menon RS, Vinod AU, Viji S (2002) A facile three-component reaction involving [4 + 1] cycloaddition leading to furan annulated heterocycles. Tetrahedron Lett 43:2293-2295. doi:10.1016/s0040-4039(02)00226-5 (Pubitemid 34214916)
    • (2002) Tetrahedron Letters , vol.43 , Issue.12 , pp. 2293-2295
    • Nair, V.1    Menon, R.S.2    Vinod, A.U.3    Viji, S.4
  • 35
    • 0003655628 scopus 로고    scopus 로고
    • NCCLS (National Committee for Clinical Laboratory Standards) National Committee for Clinical Laboratory Standards, Wayne, PA
    • NCCLS (National Committee for Clinical Laboratory Standards) (1997) Performance standards for antimicrobial disk susceptibility tests. Approved standard M2-A6. National Committee for Clinical Laboratory Standards, Wayne, PA
    • (1997) Performance Standards for Antimicrobial Disk Susceptibility Tests. Approved Standard M2-A6
  • 36
    • 0034065967 scopus 로고    scopus 로고
    • New Cdc25B tyrosine phosphatase inhibitors, nocardiones A and B, produced by Nocardia sp. TP-A0248: Taxonomy, fermentation, isolation, structural elucidation and biological properties
    • Otani T, Sugimoto Y, Aoyagi Y, Igarashi Y, Furumai T, Saito N, Yamada Y, Asao T, Oki T (2000) New Cdc25B tyrosine phosphatase inhibitors, nocardiones A and B, produced by Nocardia sp. TP-A0248: taxonomy, fermentation, isolation, structural elucidation and biological properties. J Antibiot 53:337-344. doi:10.7164/antibiotics.53.337 (Pubitemid 30265202)
    • (2000) Journal of Antibiotics , vol.53 , Issue.4 , pp. 337-344
    • Otani, T.1    Sugimoto, Y.2    Aoyagi, Y.3    Igarashi, Y.4    Furumai, T.5    Saito, N.6    Yamada, Y.7    Asao, T.8    Oki, T.9
  • 38
    • 0028445102 scopus 로고
    • The spectrum and antibacterial activity of naphthofurans and furans
    • Qian X, Zhang Y, Ni C (1994) The spectrum and antibacterial activity of naphthofurans and furans. J East China Inst Chem Technol 20:336-341
    • (1994) J East China Inst Chem Technol , vol.20 , pp. 336-341
    • Qian, X.1    Zhang, Y.2    Ni, C.3
  • 39
    • 0026741217 scopus 로고
    • Genotoxic effectivity. Comparison of 36 nitrated furan and arenofuran derivatives on a quantitative scale. Statistical comparison of T7 and other short-term tests
    • doi:10.1093/mutage/7.4.243
    • Rontó G, Gróf P, Buisson J-P, Einhorn J, Demerseman P (1992) Genotoxic effectivity. Comparison of 36 nitrated furan and arenofuran derivatives on a quantitative scale. Statistical comparison of T7 and other short-term tests. Mutagenesis 7:243-249. doi:10.1093/mutage/7.4.243
    • (1992) Mutagenesis , vol.7 , pp. 243-249
    • Rontó, G.1    Gróf, P.2    Buisson, J.-P.3    Einhorn, J.4    Demerseman, P.5
  • 40
    • 0024368805 scopus 로고
    • Prevention of cytotoxicity and inhibition of intercellular communication by antioxidant catechins isolated from Chinese green tea
    • Ruch RJ, Cheng S, Klaunig JE (1989) Prevention of cytotoxicity and inhibition of intercellular communication by antioxidant catechins isolated from Chinese green tea. Carcinogenesis (Lond) 10:1003-1008. doi:10.1093/carcin/10.6. 1003 (Pubitemid 19164833)
    • (1989) Carcinogenesis , vol.10 , Issue.6 , pp. 1003-1008
    • Ruch, R.J.1    Cheng, S.-J.2    Klaunig, J.E.3
  • 41
    • 77950323308 scopus 로고    scopus 로고
    • Synthesis of the natural products 3-hydroxymollugin and 3-methoxymollugin
    • doi:10.1021/jo100024b
    • Sastry MNV, Claessens S, Habonimana P, De Kimpe N (2010) Synthesis of the natural products 3-hydroxymollugin and 3-methoxymollugin. J Org Chem 75:2274-2280. doi:10.1021/jo100024b
    • (2010) J Org Chem , vol.75 , pp. 2274-2280
    • Sastry, M.N.V.1    Claessens, S.2    Habonimana, P.3    De Kimpe, N.4
  • 42
    • 84916804742 scopus 로고
    • Structure and synthesis of furomollugin from rhizomes of Galium mollugo L. (Rubiaceae)
    • Schildknecht H, Straub F (1976) Structure and synthesis of furomollugin from rhizomes of Galium mollugo L. (Rubiaceae). Justus Liebigs Ann Chem 1976:1772-1776
    • (1976) Justus Liebigs Ann Chem , vol.1976 , pp. 1772-1776
    • Schildknecht, H.1    Straub, F.2
  • 43
    • 84863084691 scopus 로고    scopus 로고
    • Synthesis and analgesic activity of triazolothiadiazoles and triazolothiadiazines encompassing 3-nitronaphtho[2,1-b ]furan
    • Shashikala DK, Ramaiah M, Vanita GK, Veena K, Vaidya VP (2011) Synthesis and analgesic activity of triazolothiadiazoles and triazolothiadiazines encompassing 3-nitronaphtho[2,1-b ]furan. J Chem Pharm Res 3:445-451
    • (2011) J Chem Pharm Res , vol.3 , pp. 445-451
    • Shashikala, D.K.1    Ramaiah, M.2    Vanita, G.K.3    Veena, K.4    Vaidya, V.P.5
  • 46
    • 84861165464 scopus 로고    scopus 로고
    • Structure-based discovery of anti-viral compounds for hepatitis B & C, human immunodeficiency, and dengue viruses
    • doi:10.2174/157489312800604462
    • Velmurugan D, Selvi UM, Mythily U, Rao K, Rajarajeshwari R, Sangeetha (2012) Structure-based discovery of anti-viral compounds for hepatitis B & C, human immunodeficiency, and dengue viruses. Curr Bioinform 7:187-211. doi:10.2174/157489312800604462
    • (2012) Curr Bioinform , vol.7 , pp. 187-211
    • Velmurugan, D.1    Selvi, U.M.2    Mythily, U.3    Rao, K.4    Rajarajeshwari, R.S.5
  • 47
    • 2942712913 scopus 로고
    • 6-Methoxygeniposidic acid, and iridoid glycoside from Rubia cordifolia
    • doi:10.1016/0031-9422(91)84241-j
    • Wu L, Wang S, Hua H, Li X, Zhu t, Miyase T, Ueno A (1991) 6-Methoxygeniposidic acid, and iridoid glycoside from Rubia cordifolia. Phytochemistry 30:1710-1711. doi:10.1016/0031-9422(91)84241-j
    • (1991) Phytochemistry , vol.30 , pp. 1710-1711
    • Wu, L.1    Wang, S.2    Hua, H.3    Li, X.4    Zhu, T.5    Miyase, T.6    Ueno, A.7
  • 48
    • 84882986235 scopus 로고    scopus 로고
    • A novel and efficient synthesis of diverse dihydronaphtho[1,2-b]furans using the ceric ammonium nitrate-catalyzed formal [3 + 2] cycloaddition of 1,4-naphthoquinones to olefins and its application to furomollugin
    • doi:10.1039/c3ob40977e
    • Xia L, Lee YR (2013) A novel and efficient synthesis of diverse dihydronaphtho[1,2-b]furans using the ceric ammonium nitrate-catalyzed formal [3 + 2] cycloaddition of 1,4-naphthoquinones to olefins and its application to furomollugin. Org Biomol Chem 11:6097-6107. doi:10.1039/c3ob40977e
    • (2013) Org Biomol Chem , vol.11 , pp. 6097-6107
    • Xia, L.1    Lee, Y.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.