12alpha-Hydroxy-3-ketocholanic acid

Details

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Internal ID bb9eb15a-39f8-481b-8e1d-486bb7ef552d
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Bile acids, alcohols and derivatives > Hydroxy bile acids, alcohols and derivatives > Monohydroxy bile acids, alcohols and derivatives
IUPAC Name (4R)-4-[(10S,12S,13R)-12-hydroxy-10,13-dimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]pentanoic acid
SMILES (Canonical) CC(CCC(=O)O)C1CCC2C1(C(CC3C2CCC4C3(CCC(=O)C4)C)O)C
SMILES (Isomeric) C[C@H](CCC(=O)O)C1CCC2[C@@]1([C@H](CC3C2CCC4[C@@]3(CCC(=O)C4)C)O)C
InChI InChI=1S/C24H38O4/c1-14(4-9-22(27)28)18-7-8-19-17-6-5-15-12-16(25)10-11-23(15,2)20(17)13-21(26)24(18,19)3/h14-15,17-21,26H,4-13H2,1-3H3,(H,27,28)/t14-,15?,17?,18?,19?,20?,21+,23+,24-/m1/s1
InChI Key WMUMZOAFCDOTRW-AWTZCYDRSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C24H38O4
Molecular Weight 390.60 g/mol
Exact Mass 390.27700969 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.69
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 12alpha-Hydroxy-3-ketocholanic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9811 98.11%
Caco-2 - 0.6562 65.62%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8301 83.01%
OATP2B1 inhibitior - 0.5915 59.15%
OATP1B1 inhibitior + 0.8617 86.17%
OATP1B3 inhibitior + 0.9393 93.93%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.6794 67.94%
P-glycoprotein inhibitior + 0.5822 58.22%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6950 69.50%
CYP2C9 substrate - 0.8363 83.63%
CYP2D6 substrate - 0.8429 84.29%
CYP3A4 inhibition - 0.8262 82.62%
CYP2C9 inhibition - 0.9626 96.26%
CYP2C19 inhibition - 0.9763 97.63%
CYP2D6 inhibition - 0.9777 97.77%
CYP1A2 inhibition - 0.9366 93.66%
CYP2C8 inhibition - 0.7265 72.65%
CYP inhibitory promiscuity - 0.9718 97.18%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7550 75.50%
Eye corrosion - 0.9957 99.57%
Eye irritation - 0.9068 90.68%
Skin irritation + 0.7373 73.73%
Skin corrosion - 0.9322 93.22%
Ames mutagenesis - 0.6076 60.76%
Human Ether-a-go-go-Related Gene inhibition - 0.7463 74.63%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.5967 59.67%
skin sensitisation - 0.8539 85.39%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity - 0.9312 93.12%
Acute Oral Toxicity (c) III 0.6888 68.88%
Estrogen receptor binding + 0.7092 70.92%
Androgen receptor binding + 0.7684 76.84%
Thyroid receptor binding + 0.6364 63.64%
Glucocorticoid receptor binding + 0.8870 88.70%
Aromatase binding + 0.6424 64.24%
PPAR gamma + 0.5994 59.94%
Honey bee toxicity - 0.7963 79.63%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9896 98.96%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.89% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.26% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.42% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.63% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 92.36% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.22% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.20% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.86% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.81% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 87.53% 93.04%
CHEMBL237 P41145 Kappa opioid receptor 87.04% 98.10%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 86.93% 94.62%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 86.82% 85.11%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.36% 93.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.31% 95.56%
CHEMBL220 P22303 Acetylcholinesterase 86.01% 94.45%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.89% 95.89%
CHEMBL238 Q01959 Dopamine transporter 84.02% 95.88%
CHEMBL340 P08684 Cytochrome P450 3A4 83.79% 91.19%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.66% 93.56%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.79% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.95% 82.69%
CHEMBL1871 P10275 Androgen Receptor 80.94% 96.43%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 80.51% 89.05%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 80.39% 94.23%
CHEMBL1914 P06276 Butyrylcholinesterase 80.00% 95.00%

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 139587819
LOTUS LTS0269310
wikiData Q77624784