[12-acetyloxy-3,8,14-trihydroxy-17-(1-hydroxyethyl)-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate

Details

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Internal ID 78e8a728-2a74-4f9c-a8da-ac9eff763658
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Pregnane steroids > Gluco/mineralocorticoids, progestogins and derivatives
IUPAC Name [12-acetyloxy-3,8,14-trihydroxy-17-(1-hydroxyethyl)-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate
SMILES (Canonical) CC(C1CCC2(C1(C(C(C3C2(CC=C4C3(CCC(C4)O)C)O)OC(=O)C)OC(=O)C)C)O)O
SMILES (Isomeric) CC(C1CCC2(C1(C(C(C3C2(CC=C4C3(CCC(C4)O)C)O)OC(=O)C)OC(=O)C)C)O)O
InChI InChI=1S/C25H38O8/c1-13(26)18-8-11-25(31)23(18,5)21(33-15(3)28)19(32-14(2)27)20-22(4)9-7-17(29)12-16(22)6-10-24(20,25)30/h6,13,17-21,26,29-31H,7-12H2,1-5H3
InChI Key JBQVNTFIPFQJOW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H38O8
Molecular Weight 466.60 g/mol
Exact Mass 466.25666817 g/mol
Topological Polar Surface Area (TPSA) 134.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.62
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [12-acetyloxy-3,8,14-trihydroxy-17-(1-hydroxyethyl)-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9843 98.43%
Caco-2 - 0.6195 61.95%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8518 85.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9024 90.24%
OATP1B3 inhibitior + 0.8103 81.03%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7124 71.24%
BSEP inhibitior + 0.7179 71.79%
P-glycoprotein inhibitior - 0.5891 58.91%
P-glycoprotein substrate + 0.5483 54.83%
CYP3A4 substrate + 0.6600 66.00%
CYP2C9 substrate - 0.8092 80.92%
CYP2D6 substrate - 0.8650 86.50%
CYP3A4 inhibition - 0.8356 83.56%
CYP2C9 inhibition - 0.8477 84.77%
CYP2C19 inhibition - 0.8122 81.22%
CYP2D6 inhibition - 0.9582 95.82%
CYP1A2 inhibition - 0.6809 68.09%
CYP2C8 inhibition - 0.7085 70.85%
CYP inhibitory promiscuity - 0.9731 97.31%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5931 59.31%
Eye corrosion - 0.9934 99.34%
Eye irritation - 0.9385 93.85%
Skin irritation + 0.7198 71.98%
Skin corrosion - 0.9352 93.52%
Ames mutagenesis - 0.7670 76.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4899 48.99%
Micronuclear - 0.6900 69.00%
Hepatotoxicity + 0.5074 50.74%
skin sensitisation - 0.8508 85.08%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.9875 98.75%
Nephrotoxicity - 0.7872 78.72%
Acute Oral Toxicity (c) IV 0.5637 56.37%
Estrogen receptor binding + 0.7246 72.46%
Androgen receptor binding + 0.7213 72.13%
Thyroid receptor binding - 0.4930 49.30%
Glucocorticoid receptor binding + 0.6865 68.65%
Aromatase binding + 0.6384 63.84%
PPAR gamma + 0.6182 61.82%
Honey bee toxicity - 0.7380 73.80%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6850 68.50%
Fish aquatic toxicity + 0.9960 99.60%

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 99.00% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.36% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.06% 97.25%
CHEMBL2996 Q05655 Protein kinase C delta 90.88% 97.79%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.79% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.28% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.61% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.06% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.77% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.93% 89.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.79% 100.00%
CHEMBL4208 P20618 Proteasome component C5 83.51% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.36% 85.14%
CHEMBL340 P08684 Cytochrome P450 3A4 82.70% 91.19%
CHEMBL226 P30542 Adenosine A1 receptor 82.17% 95.93%
CHEMBL221 P23219 Cyclooxygenase-1 81.74% 90.17%
CHEMBL5255 O00206 Toll-like receptor 4 80.52% 92.50%
CHEMBL5028 O14672 ADAM10 80.47% 97.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.36% 95.89%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 80.31% 82.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.14% 93.56%

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.
Hoya carnosa

Cross-Links

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PubChem 622636
LOTUS LTS0056765
wikiData Q105124534