| Identification | Back Directory | [Name]
Spiro[azuleno[4,5-b]furan-9(2H),3'-[3H]benz[1,8]azuleno[4,5-b]furan]-2,2',8,9'(1'H,3H,4'H)-tetrone, 3a,4,5,5',5'a,6,6',6a,7,7',7'a,8',9a,9b,10'a,10'b-hexadecahydro-5'a-hydroxy-1',3,6,8'-tetrakis(methylene)-, (3'R,3aS,5'aS,6aR,7'aS,9aR,9bS,10'aS,10'bR)- | [CAS]
87606-12-0 | [Synonyms]
Spiro[azuleno[4,5-b]furan-9(2H),3'-[3H]benz[1,8]azuleno[4,5-b]furan]-2,2',8,9'(1'H,3H,4'H)-tetrone, 3a,4,5,5',5'a,6,6',6a,7,7',7'a,8',9a,9b,10'a,10'b-hexadecahydro-5'a-hydroxy-1',3,6,8'-tetrakis(methylene)-, (3'R,3aS,5'aS,6aR,7'aS,9aR,9bS,10'aS,10'bR)- | [Molecular Formula]
C30H30O7 | [MOL File]
87606-12-0.mol | [Molecular Weight]
502.55 |
| Hazard Information | Back Directory | [Uses]
Gochnatiolide A is a dimeric sesquiterpene that can be found in Ainsliaea henryi. Gochnatiolide A exhibits antiproliferative activity against the kidney, melanoma, ovarian-resistant and glioma cell lines[1][2]. | [References]
[1] Xiong HP, et, al. A dimeric sesquiterpene, gochnatiolide A. Acta Crystallogr Sect E Struct Rep Online. 2009 Oct 23;65(Pt 11):o2847. DOI:10.1107/S1600536809042743
[2] Strapasson RLB, et, al. Bioactivity-guided isolation of cytotoxic sesquiterpene lactones of Gochnatia polymorpha ssp. Floccose. Phytother Res. 2012 Jul;26(7):1053-6. DOI:10.1002/ptr.3693 |
| Spectrum Detail | Back Directory | [Spectrum Detail]
Spiro[azuleno[4,5-b]furan-9(2H),3'-[3H]benz[1,8]azuleno[4,5-b]furan]-2,2',8,9'(1'H,3H,4'H)-tetrone, 3a,4,5,5',5'a,6,6',6a,7,7',7'a,8',9a,9b,10'a,10'b-hexadecahydro-5'a-hydroxy-1',3,6,8'-tetrakis(methylene)-, (3'R,3aS,5'aS,6aR,7'aS,9aR,9bS,10'aS,10'bR)-(87606-12-0)1HNMR
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