CID 73835673

Details

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Internal ID adb962ee-5e1e-477b-aa19-12fa9456fa99
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Hydroxysteroids > 18-hydroxysteroids
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C55H78N2O10/c1-26-20-53(66-47(26,4)5)27(2)46-41(64-53)16-36-32-13-11-30-15-38-40(22-50(30,8)34(32)18-43(61)52(36,46)25-59)57-37-14-29-10-12-31-33(49(29,7)21-39(37)56-38)17-42(60)51(9)35(31)19-45-54(51,63)28(3)55(65-45)44(62)23-48(6,24-58)67-55/h16,19,26-34,41-46,58-63H,10-15,17-18,20-25H2,1-9H3
InChI Key XNTXQZOYRVJULO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C55H78N2O10
Molecular Weight 927.20 g/mol
Exact Mass 926.56564669 g/mol
Topological Polar Surface Area (TPSA) 184.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 5.54
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 73835673

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 - 0.8608 86.08%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.4410 44.10%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8351 83.51%
OATP1B3 inhibitior + 0.9206 92.06%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.9388 93.88%
P-glycoprotein inhibitior + 0.7505 75.05%
P-glycoprotein substrate + 0.7316 73.16%
CYP3A4 substrate + 0.7296 72.96%
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 + 0.8047 80.47%
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 - 0.9019 90.19%
Skin irritation - 0.7074 70.74%
Skin corrosion - 0.9305 93.05%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7270 72.70%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8447 84.47%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.6127 61.27%
Acute Oral Toxicity (c) III 0.6738 67.38%
Estrogen receptor binding + 0.7986 79.86%
Androgen receptor binding + 0.7754 77.54%
Thyroid receptor binding + 0.5861 58.61%
Glucocorticoid receptor binding + 0.7490 74.90%
Aromatase binding + 0.6477 64.77%
PPAR gamma + 0.8063 80.63%
Honey bee toxicity - 0.7466 74.66%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5500 55.00%
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 98.38% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.62% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.47% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.78% 96.95%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 87.29% 89.05%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.91% 100.00%
CHEMBL226 P30542 Adenosine A1 receptor 85.94% 95.93%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 84.33% 98.46%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.26% 85.14%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.83% 86.92%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.74% 86.33%
CHEMBL4040 P28482 MAP kinase ERK2 83.72% 83.82%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.71% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.49% 95.89%
CHEMBL259 P32245 Melanocortin receptor 4 82.18% 95.38%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 81.19% 97.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.73% 92.62%

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 73835673
LOTUS LTS0247721
wikiData Q105331960