ganoderic acid Q
IUPAC name: (E,5S,6S)-5-acetyloxy-6-[(3R,5R,10S,13R,14R,15S,17R)-3-acetyloxy-15-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid
CAS Number: 112790-45-1
Class: Terpenoid
Mushrooms contain this compound
1 mushrooms
MushID |
Thai name |
Common name |
Scientific name |
Family |
1 |
เห็ดหลินจือ |
Lingzhi |
Ganoderma lucidum ( Curtis ) P. Karst. |
Ganodermataceae |
2D Structure
Compound Properties
SMILES
CC(=O)O[C@H]([C@H]([C@H]1C[C@@H]([C@@]2([C@]1(C)CC=C1C2=CC[C@@H]2[C@]1(C)CC[C@H](C2(C)C)OC(=O)C)C)O)C)C/C=C(/C(=O)O)\C
Physicochemical Properties
Formula |
C34H50O7 |
Molecular wieght(g/mol) |
570.76 |
Num. of Heavy atoms |
41 |
Num. of Aromatic Heavy atoms |
0 |
Fraction Csp3 |
0.74 |
Num. of Rotatable bonds |
9 |
Num. of H-bond acceptors |
7 |
Num. of H-bonds donors |
2 |
Molar Refractivity |
160.14 |
TPSA (square Angstrom) |
110.13 |
Lipophilicity
iLOGP |
3.95 |
XLOGP3 |
5.96 |
WLOGP |
6.40 |
MLOGP |
4.54 |
Silicos-IT LOGP |
5.77 |
Consensus LOGP |
5.33 |
Water Solubility
ESOL |
|
LogS |
-6.54 |
Solubility(mg/ml) |
1.65E-04 |
Solubility(mol/l) |
2.89E-07 |
Class |
Poorly soluble |
Ali |
|
LogS |
-8.05 |
Solubility(mg/ml) |
5.10E-06 |
Solubility(mol/l) |
8.94E-09 |
Class |
Poorly soluble |
Silicos-IT |
|
LogS |
-5.12 |
Solubility(mg/ml) |
4.33E-03 |
Solubility(mol/l) |
7.59E-06 |
Class |
Moderately soluble |
Pharmacokinetics
GI absorbtion |
Low |
BBB permeant |
No |
Pgp substrate |
Yes |
CYP1A2 inhibitor |
No |
CYP2C19 inhibitor |
No |
CYP2C9 inhibitor |
No |
CYP2D6 inhibitor |
No |
CYP3A4 inhibitor |
Yes |
Log Kp (skin permeation) (cm/s) |
-5.55 |
Druglikeness
Lipinski Num. violations |
2 |
Ghose Num. violations |
4 |
Veber Num. violations |
0 |
Egan Num. violations |
1 |
Muegge Num. violations |
1 |
Bioavailability Score |
0.56 |
Medicinal Chemistry
PAINS Num. of alerts |
0 |
Brenk Num. of alerts |
2 |
Leadlikeness Num. of violations |
3 |
Synthetic Accessibility |
6.91 |
Biological Activity
Biological Activity |
JID |
Anticancer |
8 |
Cytotoxicity |
8 |
Anti-HIV |
8 |
Antitumour |
8 |
Hypotensive |
8 |
Antiplatelet aggregation |
8 |
Antihypertension |
8 |
Hypocholesterolemic |
8 |
Antioxidant |
8 |
Antibacterial |
8 |
Hepatoprotective |
8 |
Antiallergic |
8 |
Enzyme inhibitors |
8 |