Withacoagulin I

Details

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Internal ID a8bfef7c-2ee3-4216-b857-e9eb7c936426
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Withanolides and derivatives
IUPAC Name (2R)-2-[(1S)-1-[(8R,9S,10R,13S,14S,17R)-14,17-dihydroxy-10,13-dimethyl-1-oxo-2,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-17-yl]-1-hydroxyethyl]-4,5-dimethyl-2,3-dihydropyran-6-one
SMILES (Canonical) CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC=C5C4(C(=O)CC=C5)C)C)O)O)O)C
SMILES (Isomeric) CC1=C(C(=O)O[C@H](C1)[C@@](C)([C@]2(CC[C@]3([C@@]2(CC[C@H]4[C@H]3CC=C5[C@@]4(C(=O)CC=C5)C)C)O)O)O)C
InChI InChI=1S/C28H38O6/c1-16-15-22(34-23(30)17(16)2)26(5,31)28(33)14-13-27(32)20-10-9-18-7-6-8-21(29)25(18,4)19(20)11-12-24(27,28)3/h6-7,9,19-20,22,31-33H,8,10-15H2,1-5H3/t19-,20+,22+,24-,25-,26-,27-,28+/m0/s1
InChI Key HYSIDFWCYWFQMQ-IMANIDBLSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C28H38O6
Molecular Weight 470.60 g/mol
Exact Mass 470.26683893 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 3.54
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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CHEMBL2333673

2D Structure

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2D Structure of Withacoagulin I

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9129 91.29%
Caco-2 - 0.6035 60.35%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7508 75.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8942 89.42%
OATP1B3 inhibitior + 0.9021 90.21%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6124 61.24%
BSEP inhibitior + 0.8940 89.40%
P-glycoprotein inhibitior + 0.6082 60.82%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6988 69.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9124 91.24%
CYP3A4 inhibition - 0.8102 81.02%
CYP2C9 inhibition - 0.9188 91.88%
CYP2C19 inhibition - 0.9084 90.84%
CYP2D6 inhibition - 0.9525 95.25%
CYP1A2 inhibition - 0.8466 84.66%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.9794 97.94%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5917 59.17%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.9505 95.05%
Skin irritation + 0.6663 66.63%
Skin corrosion - 0.9078 90.78%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7422 74.22%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.6499 64.99%
skin sensitisation - 0.8497 84.97%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.7985 79.85%
Acute Oral Toxicity (c) I 0.4263 42.63%
Estrogen receptor binding + 0.8458 84.58%
Androgen receptor binding + 0.7593 75.93%
Thyroid receptor binding + 0.6699 66.99%
Glucocorticoid receptor binding + 0.8090 80.90%
Aromatase binding + 0.7856 78.56%
PPAR gamma + 0.6105 61.05%
Honey bee toxicity - 0.8639 86.39%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9797 97.97%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.77% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.46% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.76% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.06% 91.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.57% 93.56%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 88.10% 93.04%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.55% 86.33%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 87.06% 93.03%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.97% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.63% 85.14%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.29% 97.14%
CHEMBL3401 O75469 Pregnane X receptor 85.61% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.29% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.48% 97.09%
CHEMBL1907 P15144 Aminopeptidase N 82.89% 93.31%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.35% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.08% 95.89%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 81.55% 82.38%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.17% 100.00%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 80.86% 85.11%

Plants that contains it

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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.
Withania coagulans

Cross-Links

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PubChem 71720665
LOTUS LTS0122883
wikiData Q105035453