Coibanol B

Details

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Internal ID f61b278c-dc7f-4bcc-830d-1454cadb2603
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name (1R,3aS,5S,7S,9aR)-7-hydroxy-5-methoxy-3a-methyl-1-prop-1-en-2-yl-1,2,3,5,6,7,9,9a-octahydrocyclopenta[b]chromen-8-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H24O4/c1-9(2)10-5-6-17(3)12(10)7-11-15(19)13(18)8-14(20-4)16(11)21-17/h10,12-14,18H,1,5-8H2,2-4H3/t10-,12+,13-,14-,17-/m0/s1
InChI Key OICVSQXUNLEFRY-QWKMPEQISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H24O4
Molecular Weight 292.40 g/mol
Exact Mass 292.16745924 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.37
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Coibanol B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9844 98.44%
Caco-2 + 0.6780 67.80%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6083 60.83%
OATP2B1 inhibitior - 0.8547 85.47%
OATP1B1 inhibitior + 0.9120 91.20%
OATP1B3 inhibitior + 0.9515 95.15%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8151 81.51%
P-glycoprotein inhibitior - 0.8122 81.22%
P-glycoprotein substrate - 0.7353 73.53%
CYP3A4 substrate + 0.6458 64.58%
CYP2C9 substrate - 0.7896 78.96%
CYP2D6 substrate - 0.8615 86.15%
CYP3A4 inhibition - 0.6915 69.15%
CYP2C9 inhibition - 0.8829 88.29%
CYP2C19 inhibition - 0.8098 80.98%
CYP2D6 inhibition - 0.9341 93.41%
CYP1A2 inhibition - 0.5622 56.22%
CYP2C8 inhibition - 0.6135 61.35%
CYP inhibitory promiscuity - 0.9329 93.29%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6345 63.45%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.8149 81.49%
Skin irritation + 0.5812 58.12%
Skin corrosion - 0.9336 93.36%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6100 61.00%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.5682 56.82%
skin sensitisation - 0.8333 83.33%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 1.0000 100.00%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity + 0.7223 72.23%
Acute Oral Toxicity (c) III 0.3833 38.33%
Estrogen receptor binding + 0.7993 79.93%
Androgen receptor binding + 0.5985 59.85%
Thyroid receptor binding + 0.6352 63.52%
Glucocorticoid receptor binding + 0.7984 79.84%
Aromatase binding - 0.7044 70.44%
PPAR gamma - 0.5996 59.96%
Honey bee toxicity - 0.7395 73.95%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9525 95.25%

Targets

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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 97.14% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.46% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.60% 94.45%
CHEMBL1871 P10275 Androgen Receptor 89.64% 96.43%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.63% 85.14%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.22% 96.95%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.04% 97.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.90% 97.09%
CHEMBL2581 P07339 Cathepsin D 84.85% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.33% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.04% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 83.97% 91.19%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.41% 99.23%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.19% 92.94%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.60% 96.77%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.58% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.27% 95.56%
CHEMBL1902 P62942 FK506-binding protein 1A 82.17% 97.05%
CHEMBL221 P23219 Cyclooxygenase-1 81.47% 90.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.17% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.91% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.32% 100.00%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 80.01% 97.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139587154
LOTUS LTS0113997
wikiData Q77559318