ganoderol B

Details

Top
Internal ID cc7859fa-6db4-45d8-9296-e690fd507442
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (3S,5R,10S,13R,14R,17R)-17-[(E,2R)-7-hydroxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-3-ol
SMILES (Canonical) CC(CCC=C(C)CO)C1CCC2(C1(CC=C3C2=CCC4C3(CCC(C4(C)C)O)C)C)C
SMILES (Isomeric) C[C@H](CC/C=C(\C)/CO)[C@H]1CC[C@@]2([C@@]1(CC=C3C2=CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)C)C
InChI InChI=1S/C30H48O2/c1-20(19-31)9-8-10-21(2)22-13-17-30(7)24-11-12-25-27(3,4)26(32)15-16-28(25,5)23(24)14-18-29(22,30)6/h9,11,14,21-22,25-26,31-32H,8,10,12-13,15-19H2,1-7H3/b20-9+/t21-,22-,25+,26+,28-,29-,30+/m1/s1
InChI Key AOXXVRDKZLRGTJ-AZIDVCJLSA-N
Popularity 9 references in papers

Physical and Chemical Properties

Top
Molecular Formula C30H48O2
Molecular Weight 440.70 g/mol
Exact Mass 440.365430770 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 7.40
Atomic LogP (AlogP) 7.23
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

Top
(+)-Ganoderol B
104700-96-1
Ganodermadiol
Z99BBB5WR6
Lanosta-7,9(11),24-triene-3,26-diol
Ganodermadiol; Ganoderol B
(3beta,24E)-Lanosta-7,9(11),24-trien-3,26-diol
(3S,5R,10S,13R,14R,17R)-17-((E,2R)-7-HYDROXY-6-METHYLHEPT-5-EN-2-YL)-4,4,10,13,14-PENTAMETHYL-2,3,5,6,12,15,16,17-OCTAHYDRO-1H-CYCLOPENTA(A)PHENANTHREN-3-OL
(3S,5R,10S,13R,14R,17R)-17-[(E,2R)-7-hydroxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-3-ol
UNII-Z99BBB5WR6
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of ganoderol B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.6807 68.07%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.5908 59.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8831 88.31%
OATP1B3 inhibitior + 0.9728 97.28%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5885 58.85%
BSEP inhibitior + 0.8567 85.67%
P-glycoprotein inhibitior + 0.5799 57.99%
P-glycoprotein substrate - 0.5457 54.57%
CYP3A4 substrate + 0.6542 65.42%
CYP2C9 substrate - 0.8350 83.50%
CYP2D6 substrate - 0.7620 76.20%
CYP3A4 inhibition - 0.8815 88.15%
CYP2C9 inhibition - 0.9103 91.03%
CYP2C19 inhibition - 0.9029 90.29%
CYP2D6 inhibition - 0.9235 92.35%
CYP1A2 inhibition - 0.9024 90.24%
CYP2C8 inhibition - 0.6135 61.35%
CYP inhibitory promiscuity - 0.6166 61.66%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6228 62.28%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.9681 96.81%
Skin irritation - 0.5875 58.75%
Skin corrosion - 0.9653 96.53%
Ames mutagenesis - 0.8181 81.81%
Human Ether-a-go-go-Related Gene inhibition + 0.8089 80.89%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.7237 72.37%
skin sensitisation - 0.6794 67.94%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity - 0.7274 72.74%
Acute Oral Toxicity (c) III 0.7930 79.30%
Estrogen receptor binding + 0.7469 74.69%
Androgen receptor binding + 0.7239 72.39%
Thyroid receptor binding + 0.8003 80.03%
Glucocorticoid receptor binding + 0.8541 85.41%
Aromatase binding + 0.7632 76.32%
PPAR gamma + 0.6803 68.03%
Honey bee toxicity - 0.7810 78.10%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9704 97.04%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL220 P22303 Acetylcholinesterase 26780 nM
IC50
PMID: 21924611

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 96.64% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.89% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.33% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.74% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.95% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.95% 97.25%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.85% 93.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.19% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 86.26% 95.93%
CHEMBL325 Q13547 Histone deacetylase 1 85.49% 95.92%
CHEMBL4227 P25090 Lipoxin A4 receptor 84.50% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.98% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.96% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 83.85% 94.75%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.91% 95.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.89% 92.62%
CHEMBL2996 Q05655 Protein kinase C delta 80.54% 97.79%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.37% 96.61%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Glycine max
Juniperus occidentalis
Vigna mungo

Cross-Links

Top
PubChem 13934286
NPASS NPC202389
ChEMBL CHEMBL240972
LOTUS LTS0185048
wikiData Q65689742