Determine the necessary mass, volume, or concentration for preparing a solution.
≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Protected from light,Desiccated Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Ganoderic acid I is a triterpenoid found in ganoderma lucidum.
Form:Solid
| Canonical Smiles | CC(CC(=O)CC(C)(C1CC(=O)C2(C1(CC(=O)C3=C2C(CC4C3(CCC(C4(C)C)O)C)O)C)C)O)C(=O)O |
|---|---|
| IUPAC Name | 6-[(3S,5R,7S,10S,13R,14R,17S)-3,7-dihydroxy-4,4,10,13,14-pentamethyl-11,15-dioxo-2,3,5,6,7,12,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-4-oxoheptanoic acid |
| InChIKey | ZWMMEKXOLCCKLA-XDKAHJIMSA-N |
| INCHI | 1S/C30H44O8/c1-15(25(36)37)10-16(31)13-29(6,38)20-12-22(35)30(7)24-17(32)11-19-26(2,3)21(34)8-9-27(19,4)23(24)18(33)14-28(20,30)5/h15,17,19-21,32,34,38H,8-14H2,1-7H3,(H,36,37)/t15?,17-,19-,20-,21-,27-,28+,29?,30-/m0/s1 |
| Isomeric SMILES | CC(CC(=O)CC(C)([C@H]1CC(=O)[C@@]2([C@@]1(CC(=O)C3=C2[C@H](C[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)O)C)C)O)C(=O)O |
| Molecular Weight | 532.67 |
| Reaxy-Rn | 30110219 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=30110219&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Prenol lipids |
| Subclass | Triterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Triterpenoids |
| Alternative Parents | Trihydroxy bile acids, alcohols and derivatives Steroid acids 11-oxosteroids 14-alpha-methylsteroids 3-beta-hydroxysteroids 7-alpha-hydroxysteroids Medium-chain keto acids and derivatives Gamma-keto acids and derivatives Cyclohexenones Beta-hydroxy ketones Tertiary alcohols Cyclic alcohols and derivatives Secondary alcohols Carboxylic acids Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homopolycyclic compounds |
| Substituents | Triterpenoid - Trihydroxy bile acid, alcohol, or derivatives - Hydroxy bile acid, alcohol, or derivatives - 23-oxosteroid - Bile acid, alcohol, or derivatives - 20-hydroxysteroid - Steroid acid - 3-hydroxysteroid - Hydroxysteroid - 11-oxosteroid - 14-alpha-methylsteroid - 15-oxosteroid - Oxosteroid - 7-hydroxysteroid - 3-beta-hydroxysteroid - 7-alpha-hydroxysteroid - Steroid - Medium-chain keto acid - Gamma-keto acid - Cyclohexenone - Beta-hydroxy ketone - Keto acid - Tertiary alcohol - Cyclic alcohol - Secondary alcohol - Ketone - Carboxylic acid - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Alcohol - Organic oxide - Organooxygen compound - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Aliphatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. |
| External Descriptors | Not available |
| Solubility | DMSO : 100 mg/mL (187.73 mM; Need ultrasonic) |
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