ANDILESIN A

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C25H32O6
Molecular Weight	428.518
Optical Activity	UNSPECIFIED
Defined Stereocenters	9 / 9
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

C[C@@]12C[C@@H]3[C@]5(CC[C@@H]4[C@]3(C)C=CC(=O)OC4(C)C)C[C@@](C)([C@H](O)[C@@H]6C(=O)OC[C@@]156)C2=O

InChI

InChIKey=SJSNDUDHAXBERS-ABGUQTIISA-N

InChI=1S/C25H32O6/c1-20(2)13-6-9-24-11-22(4)17(27)16-18(28)30-12-25(16,24)23(5,19(22)29)10-14(24)21(13,3)8-7-15(26)31-20/h7-8,13-14,16-17,27H,6,9-12H2,1-5H3/t13-,14-,16+,17+,21-,22-,23-,24-,25+/m0/s1

HIDE SMILES / InChI

Molecular Formula	C25H32O6
Molecular Weight	428.518
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	9 / 9
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Mon Mar 31 23:19:22 GMT 2025` Edited by `admin` on `Mon Mar 31 23:19:22 GMT 2025`
Record UNII	KR1MLA877F
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

ANDILESIN

Preferred Name

English

ANDILESIN A

Common Name

English

DIHYDROANDIBENIN

Common Name

English

(3AR-(3A.ALPHA.,4.BETA.,5.ALPHA.,6A.BETA.,7A.ALPHA.,7B.ALPHA.,12A.BETA.,14A.ALPHA.,14BR*))-4,5,6A,7,7A,7B,12,12A,13,14-DECAHYDRO-4-HYDROXY-5,6A,7B,12,12-PENTAMETHYL-5,14A-METHANO-1H,14AH-FURO(3',4':4B,5)FLUORENO(2,1-C)OXEPIN-3,6,10(3AH)-TRIONE

Systematic Name

English

5,14A-METHANO-1H,14AH-FURO(3',4':4B,5)FLUORENO(2,1-C)OXEPIN-3,6,10(3AH)-TRIONE, 4,5,6A,7,7A,7B,12,12A,13,14-DECAHYDRO-4-HYDROXY-5,6A,7B,12,12-PENTAMETHYL-, (3AR,4R,5S,6AR,7AS,7BR,12AR,14AS,14BR)-

Systematic Name

English

5,15-METHANO-1H,3H,11H-FURO(3',4':3A,4)INDENO(1,7A-G)(2)BENZOXEPIN-3,11,16-TRIONE, 3A,4,5,6,7,8,8A,9,13A,13B,14,15-DODECAHYDRO-4-HYDROXY-5,9,9,13A,15-PENTAMETHYL-, (3AR,4R,5S,6AS,8AR,13AR,13BS,15R,15AR)-

Systematic Name

English

Code System Code Type Description

PUBCHEM

91819930

Created by admin on Mon Mar 31 23:19:22 GMT 2025 , Edited by admin on Mon Mar 31 23:19:22 GMT 2025

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FDA UNII

KR1MLA877F

Created by admin on Mon Mar 31 23:19:22 GMT 2025 , Edited by admin on Mon Mar 31 23:19:22 GMT 2025

PRIMARY

CAS

60451-43-6

Created by admin on Mon Mar 31 23:19:22 GMT 2025 , Edited by admin on Mon Mar 31 23:19:22 GMT 2025

PRIMARY