(3beta,5alpha)-3-Hydroxypregnane-2,16-dione

Details

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Internal ID 625c1fd4-146f-4a17-aff8-5e5044f2844f
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Pregnane steroids > Gluco/mineralocorticoids, progestogins and derivatives
IUPAC Name (3R,5S,8R,9S,10S,13S,14S,17R)-17-ethyl-3-hydroxy-10,13-dimethyl-3,4,5,6,7,8,9,11,12,14,15,17-dodecahydro-1H-cyclopenta[a]phenanthrene-2,16-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H32O3/c1-4-14-17(22)10-16-13-6-5-12-9-18(23)19(24)11-21(12,3)15(13)7-8-20(14,16)2/h12-16,18,23H,4-11H2,1-3H3/t12-,13+,14-,15-,16-,18+,20+,21-/m0/s1
InChI Key AYTMEYVBLXAHPT-LZUXVWQXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H32O3
Molecular Weight 332.50 g/mol
Exact Mass 332.23514488 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.77
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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DTXSID101291405
183172-90-9

2D Structure

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2D Structure of (3beta,5alpha)-3-Hydroxypregnane-2,16-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.7486 74.86%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7553 75.53%
OATP2B1 inhibitior - 0.8709 87.09%
OATP1B1 inhibitior + 0.8863 88.63%
OATP1B3 inhibitior + 0.9771 97.71%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior + 0.8431 84.31%
P-glycoprotein inhibitior - 0.4773 47.73%
P-glycoprotein substrate - 0.6468 64.68%
CYP3A4 substrate + 0.6638 66.38%
CYP2C9 substrate - 0.8408 84.08%
CYP2D6 substrate - 0.7400 74.00%
CYP3A4 inhibition - 0.6660 66.60%
CYP2C9 inhibition - 0.8259 82.59%
CYP2C19 inhibition - 0.8096 80.96%
CYP2D6 inhibition - 0.9569 95.69%
CYP1A2 inhibition - 0.9088 90.88%
CYP2C8 inhibition - 0.7998 79.98%
CYP inhibitory promiscuity - 0.9225 92.25%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6728 67.28%
Eye corrosion - 0.9927 99.27%
Eye irritation - 0.9403 94.03%
Skin irritation + 0.6399 63.99%
Skin corrosion - 0.8981 89.81%
Ames mutagenesis - 0.8170 81.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4856 48.56%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5928 59.28%
skin sensitisation - 0.7590 75.90%
Respiratory toxicity + 0.9111 91.11%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.8361 83.61%
Acute Oral Toxicity (c) II 0.4589 45.89%
Estrogen receptor binding + 0.8710 87.10%
Androgen receptor binding + 0.8160 81.60%
Thyroid receptor binding + 0.7686 76.86%
Glucocorticoid receptor binding + 0.9167 91.67%
Aromatase binding + 0.5399 53.99%
PPAR gamma - 0.7193 71.93%
Honey bee toxicity - 0.7873 78.73%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9789 97.89%

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 94.79% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.57% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.29% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.84% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.20% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 88.79% 90.17%
CHEMBL1902 P62942 FK506-binding protein 1A 88.42% 97.05%
CHEMBL1871 P10275 Androgen Receptor 86.94% 96.43%
CHEMBL2581 P07339 Cathepsin D 86.11% 98.95%
CHEMBL299 P17252 Protein kinase C alpha 85.58% 98.03%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.62% 82.69%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.51% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.63% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.31% 90.71%
CHEMBL226 P30542 Adenosine A1 receptor 80.93% 95.93%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.15% 93.04%

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.
Trichilia hirta

Cross-Links

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PubChem 11484381
LOTUS LTS0194592
wikiData Q104921370