Withacoagulin G

Details

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Internal ID ada146da-6da3-4198-a497-23fee8aeffb6
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Withanolides and derivatives
IUPAC Name (2R)-2-[(1S)-1-hydroxy-1-[(8S,9S,10R,13S,14S,17R)-17-hydroxy-10,13-dimethyl-1-oxo-7,8,9,11,12,14,15,16-octahydro-4H-cyclopenta[a]phenanthren-17-yl]ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H38O6/c1-16-14-23(34-24(31)19(16)15-29)27(4,32)28(33)13-11-20-18-9-8-17-6-5-7-22(30)26(17,3)21(18)10-12-25(20,28)2/h5,7-8,18,20-21,23,29,32-33H,6,9-15H2,1-4H3/t18-,20-,21-,23+,25-,26-,27-,28+/m0/s1
InChI Key CHNXPBONLRCQFD-VOQRJTHWSA-N
Popularity 3 references 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 2.80
Atomic LogP (AlogP) 3.40
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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CHEMBL2333671

2D Structure

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2D Structure of Withacoagulin G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9316 93.16%
Caco-2 - 0.6436 64.36%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8506 85.06%
OATP2B1 inhibitior - 0.8645 86.45%
OATP1B1 inhibitior + 0.8803 88.03%
OATP1B3 inhibitior + 0.9104 91.04%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5438 54.38%
BSEP inhibitior + 0.8585 85.85%
P-glycoprotein inhibitior + 0.6092 60.92%
P-glycoprotein substrate + 0.5767 57.67%
CYP3A4 substrate + 0.7194 71.94%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9107 91.07%
CYP3A4 inhibition - 0.6702 67.02%
CYP2C9 inhibition - 0.9207 92.07%
CYP2C19 inhibition - 0.9298 92.98%
CYP2D6 inhibition - 0.9592 95.92%
CYP1A2 inhibition - 0.8394 83.94%
CYP2C8 inhibition + 0.5854 58.54%
CYP inhibitory promiscuity - 0.9718 97.18%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5841 58.41%
Eye corrosion - 0.9922 99.22%
Eye irritation - 0.9659 96.59%
Skin irritation + 0.6992 69.92%
Skin corrosion - 0.9395 93.95%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6658 66.58%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.9315 93.15%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.5967 59.67%
Acute Oral Toxicity (c) III 0.5786 57.86%
Estrogen receptor binding + 0.8735 87.35%
Androgen receptor binding + 0.7849 78.49%
Thyroid receptor binding + 0.6142 61.42%
Glucocorticoid receptor binding + 0.8573 85.73%
Aromatase binding + 0.7749 77.49%
PPAR gamma + 0.6322 63.22%
Honey bee toxicity - 0.8432 84.32%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9684 96.84%

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 98.55% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.09% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.46% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.17% 93.99%
CHEMBL1937 Q92769 Histone deacetylase 2 91.68% 94.75%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 91.00% 97.14%
CHEMBL2581 P07339 Cathepsin D 90.01% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.40% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.32% 100.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 88.89% 90.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.10% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.60% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.38% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.80% 86.33%
CHEMBL3310 Q96DB2 Histone deacetylase 11 83.19% 88.56%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.92% 93.04%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.79% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 81.62% 94.73%
CHEMBL1871 P10275 Androgen Receptor 81.57% 96.43%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.88% 89.00%

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 71524297
LOTUS LTS0208112
wikiData Q104959076