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Details

Stereochemistry ABSOLUTE
Molecular Formula C30H44O6
Molecular Weight 500.6668
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GANOLUCIDIC ACID A

SMILES

C[C@H](CC(=O)C[C@@H](C)C(O)=O)[C@H]1C[C@H](O)[C@@]2(C)C3=C(C(=O)C[C@]12C)[C@@]4(C)CCC(=O)C(C)(C)[C@@H]4CC3

InChI

InChIKey=XRXBNTYHQXKSAO-WRRQQOFWSA-N
InChI=1S/C30H44O6/c1-16(12-18(31)13-17(2)26(35)36)20-14-24(34)30(7)19-8-9-22-27(3,4)23(33)10-11-28(22,5)25(19)21(32)15-29(20,30)6/h16-17,20,22,24,34H,8-15H2,1-7H3,(H,35,36)/t16-,17-,20-,22+,24+,28+,29-,30-/m1/s1

HIDE SMILES / InChI

Molecular Formula C30H44O6
Molecular Weight 500.6668
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 8
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 22:49:19 GMT 2025
Edited
by admin
on Mon Mar 31 22:49:19 GMT 2025
Record UNII
M4J768CY9D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GANOLUCIDIC ACID A
Common Name English
Lanost-8-en-26-oic acid, 15-hydroxy-3,11,23-trioxo-, (15?,25R)-
Preferred Name English
(2r,6r)-6-[(5r,10s,13r,14r,15s,17r)-15-hydroxy-4,4,10,13,14-pentamethyl-3,11-dioxo-2,5,6,7,12,15,16,17-octahydro-1h-cyclopenta[a]phenanthren-17-yl]-2-methyl-4-oxoheptanoic acid
Systematic Name English
(15?,25R)-15-Hydroxy-3,11,23-trioxolanost-8-en-26-oic acid
Systematic Name English
Code System Code Type Description
CAS
1253643-85-4
Created by admin on Mon Mar 31 22:49:19 GMT 2025 , Edited by admin on Mon Mar 31 22:49:19 GMT 2025
PRIMARY
CAS
98665-21-5
Created by admin on Mon Mar 31 22:49:19 GMT 2025 , Edited by admin on Mon Mar 31 22:49:19 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
EPA CompTox
DTXSID30913139
Created by admin on Mon Mar 31 22:49:19 GMT 2025 , Edited by admin on Mon Mar 31 22:49:19 GMT 2025
PRIMARY
PUBCHEM
475412
Created by admin on Mon Mar 31 22:49:19 GMT 2025 , Edited by admin on Mon Mar 31 22:49:19 GMT 2025
PRIMARY
FDA UNII
M4J768CY9D
Created by admin on Mon Mar 31 22:49:19 GMT 2025 , Edited by admin on Mon Mar 31 22:49:19 GMT 2025
PRIMARY