Ganodermalactone B

Details

Top
Internal ID 86e4b5b0-10fa-440f-9cae-fd3d487bbd7b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name [(1R,3aR,5aR,10aR,12aR)-3a,6,6,12a-tetramethyl-1-[(1S)-1-[(2S)-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8-oxo-1,2,3,4,5,5a,9,10,11,12-decahydroindeno[5,4-g][2]benzoxepin-10a-yl]methyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H46O6/c1-19-8-10-25(37-28(19)35)20(2)22-12-15-31(7)23-9-11-26-29(4,5)38-27(34)14-17-32(26,18-36-21(3)33)24(23)13-16-30(22,31)6/h8,20,22,25-26H,9-18H2,1-7H3/t20-,22+,25-,26-,30+,31-,32-/m0/s1
InChI Key PKHFZHSYUYWRMN-UANBTYQASA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C32H46O6
Molecular Weight 526.70 g/mol
Exact Mass 526.32943918 g/mol
Topological Polar Surface Area (TPSA) 78.90 Ų
XlogP 6.00
Atomic LogP (AlogP) 6.47
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Ganodermalactone B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9866 98.66%
Caco-2 - 0.6599 65.99%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8606 86.06%
OATP2B1 inhibitior - 0.8640 86.40%
OATP1B1 inhibitior + 0.8024 80.24%
OATP1B3 inhibitior + 0.8963 89.63%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.9436 94.36%
P-glycoprotein inhibitior + 0.8164 81.64%
P-glycoprotein substrate - 0.5247 52.47%
CYP3A4 substrate + 0.6962 69.62%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9122 91.22%
CYP3A4 inhibition - 0.8374 83.74%
CYP2C9 inhibition - 0.8056 80.56%
CYP2C19 inhibition - 0.9061 90.61%
CYP2D6 inhibition - 0.9305 93.05%
CYP1A2 inhibition - 0.8351 83.51%
CYP2C8 inhibition + 0.6709 67.09%
CYP inhibitory promiscuity - 0.8040 80.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6543 65.43%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.9208 92.08%
Skin irritation - 0.6061 60.61%
Skin corrosion - 0.9402 94.02%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3889 38.89%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.6590 65.90%
skin sensitisation - 0.7891 78.91%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.6922 69.22%
Acute Oral Toxicity (c) III 0.6714 67.14%
Estrogen receptor binding + 0.8048 80.48%
Androgen receptor binding + 0.7463 74.63%
Thyroid receptor binding + 0.5911 59.11%
Glucocorticoid receptor binding + 0.8202 82.02%
Aromatase binding + 0.7822 78.22%
PPAR gamma + 0.6284 62.84%
Honey bee toxicity - 0.7821 78.21%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9946 99.46%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.55% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 96.21% 94.75%
CHEMBL2581 P07339 Cathepsin D 95.81% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.18% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.25% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.81% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.45% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.04% 89.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 86.15% 90.08%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.95% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 85.38% 90.17%
CHEMBL2782 P35610 Acyl coenzyme A:cholesterol acyltransferase 1 85.31% 91.65%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.75% 97.14%
CHEMBL5028 O14672 ADAM10 84.74% 97.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.48% 99.23%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.92% 93.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.75% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.94% 95.89%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.61% 96.77%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.11% 100.00%

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.
There are no matching plants.

Cross-Links

Top
PubChem 139043749
LOTUS LTS0249457
wikiData Q77625160