CID 11969584

Details

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Internal ID df5b0a10-0948-4eea-a893-3844cf710a6f
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Hydroxysteroids > 18-hydroxysteroids
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C54H76N2O10/c1-26-45-40(63-52(26)14-13-46(3,4)65-52)17-35-31-12-10-29-16-37-39(22-49(29,7)33(31)19-42(60)51(35,45)25-58)56-36-15-28-9-11-30-32(48(28,6)21-38(36)55-37)18-41(59)50(8)34(30)20-44-53(50,62)27(2)54(64-44)43(61)23-47(5,24-57)66-54/h17,20,26-33,40-45,57-62H,9-16,18-19,21-25H2,1-8H3/t26?,27?,28?,29?,30?,31?,32?,33?,40-,41+,42+,43?,44-,45-,47-,48-,49-,50+,51+,52+,53+,54-/m1/s1
InChI Key AWYLYACMGLGJJG-LKODHQLJSA-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) 184.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 5.30
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 11969584

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9674 96.74%
Caco-2 - 0.8598 85.98%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.4410 44.10%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8394 83.94%
OATP1B3 inhibitior + 0.9206 92.06%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.9471 94.71%
P-glycoprotein inhibitior + 0.7519 75.19%
P-glycoprotein substrate + 0.6934 69.34%
CYP3A4 substrate + 0.7383 73.83%
CYP2C9 substrate - 0.8114 81.14%
CYP2D6 substrate - 0.8001 80.01%
CYP3A4 inhibition - 0.8571 85.71%
CYP2C9 inhibition - 0.8676 86.76%
CYP2C19 inhibition - 0.8528 85.28%
CYP2D6 inhibition - 0.9007 90.07%
CYP1A2 inhibition - 0.6695 66.95%
CYP2C8 inhibition + 0.7931 79.31%
CYP inhibitory promiscuity - 0.7499 74.99%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5141 51.41%
Eye corrosion - 0.9865 98.65%
Eye irritation - 0.9025 90.25%
Skin irritation - 0.7074 70.74%
Skin corrosion - 0.9305 93.05%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7331 73.31%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8447 84.47%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.6062 60.62%
Acute Oral Toxicity (c) III 0.6738 67.38%
Estrogen receptor binding + 0.7936 79.36%
Androgen receptor binding + 0.7760 77.60%
Thyroid receptor binding + 0.5770 57.70%
Glucocorticoid receptor binding + 0.7398 73.98%
Aromatase binding + 0.6380 63.80%
PPAR gamma + 0.7994 79.94%
Honey bee toxicity - 0.7336 73.36%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.8815 88.15%

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 98.56% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.30% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.00% 97.09%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 91.11% 89.05%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.26% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.63% 86.33%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.61% 86.92%
CHEMBL2243 O00519 Anandamide amidohydrolase 86.14% 97.53%
CHEMBL259 P32245 Melanocortin receptor 4 85.30% 95.38%
CHEMBL2094135 Q96BI3 Gamma-secretase 85.18% 98.05%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.64% 100.00%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 83.53% 97.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.31% 92.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.03% 85.14%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.80% 96.95%
CHEMBL4040 P28482 MAP kinase ERK2 81.88% 83.82%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 81.47% 98.46%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 81.42% 100.00%
CHEMBL1914 P06276 Butyrylcholinesterase 80.92% 95.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.72% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.57% 99.23%

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.
There are no matching plants.

Cross-Links

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PubChem 11969584
LOTUS LTS0158284
wikiData Q105100267