CID 73835853

Details

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Internal ID 385a855f-823a-4916-9b4b-2e9fc1477dd0
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Oxosteroids
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C54H76N2O10/c1-26-44-39(64-52(26)14-12-45(3,4)66-52)24-51(61)30-11-10-28-16-34-36(22-47(28,6)31(30)19-41(59)50(44,51)9)56-35-17-29-18-38(57)43-32(48(29,7)23-37(35)55-34)20-40(58)49(8)33(43)21-42-54(49,62)27(2)53(65-42)15-13-46(5,60)25-63-53/h21,26-32,38-40,42-44,57-58,60-62H,10-20,22-25H2,1-9H3
InChI Key VXYJPRLVLXYUAE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C54H76N2O10
Molecular Weight 913.20 g/mol
Exact Mass 912.54999663 g/mol
Topological Polar Surface Area (TPSA) 181.00 Ų
XlogP 3.80
Atomic LogP (AlogP) 5.73
H-Bond Acceptor 12
H-Bond Donor 5
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 73835853

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9876 98.76%
Caco-2 - 0.8577 85.77%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5218 52.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8438 84.38%
OATP1B3 inhibitior + 0.9300 93.00%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9662 96.62%
P-glycoprotein inhibitior + 0.7541 75.41%
P-glycoprotein substrate + 0.7661 76.61%
CYP3A4 substrate + 0.7510 75.10%
CYP2C9 substrate - 0.8111 81.11%
CYP2D6 substrate - 0.8265 82.65%
CYP3A4 inhibition - 0.8767 87.67%
CYP2C9 inhibition - 0.8640 86.40%
CYP2C19 inhibition - 0.8764 87.64%
CYP2D6 inhibition - 0.8948 89.48%
CYP1A2 inhibition - 0.5243 52.43%
CYP2C8 inhibition + 0.7266 72.66%
CYP inhibitory promiscuity - 0.7819 78.19%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5221 52.21%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.9025 90.25%
Skin irritation - 0.6847 68.47%
Skin corrosion - 0.9294 92.94%
Ames mutagenesis - 0.5974 59.74%
Human Ether-a-go-go-Related Gene inhibition + 0.6626 66.26%
Micronuclear - 0.6200 62.00%
Hepatotoxicity + 0.5075 50.75%
skin sensitisation - 0.8282 82.82%
Respiratory toxicity + 0.9444 94.44%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.7597 75.97%
Acute Oral Toxicity (c) III 0.6563 65.63%
Estrogen receptor binding + 0.7862 78.62%
Androgen receptor binding + 0.7775 77.75%
Thyroid receptor binding + 0.5855 58.55%
Glucocorticoid receptor binding + 0.7775 77.75%
Aromatase binding + 0.6450 64.50%
PPAR gamma + 0.8062 80.62%
Honey bee toxicity - 0.6631 66.31%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9576 95.76%

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 96.69% 96.09%
CHEMBL220 P22303 Acetylcholinesterase 94.98% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.26% 99.23%
CHEMBL204 P00734 Thrombin 92.56% 96.01%
CHEMBL1914 P06276 Butyrylcholinesterase 91.50% 95.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.50% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.92% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.64% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.34% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.14% 97.09%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 87.82% 96.39%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.68% 94.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.54% 82.69%
CHEMBL259 P32245 Melanocortin receptor 4 85.76% 95.38%
CHEMBL325 Q13547 Histone deacetylase 1 85.31% 95.92%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.67% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 84.11% 94.75%
CHEMBL1871 P10275 Androgen Receptor 83.98% 96.43%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.27% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.77% 92.94%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 81.14% 98.99%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.88% 96.90%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.83% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.54% 95.89%

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 73835853
LOTUS LTS0006752
wikiData Q105298838