4,14-Dimethyl-9,19-cyclostigmast-25-en-3-ol

Details

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Internal ID 85667984-eb61-465f-b68a-0bd81e16290d
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cycloartanols and derivatives
IUPAC Name (6S,7S,8S,11S,15R,16R)-15-[(2R,5R)-5-ethyl-6-methylhept-6-en-2-yl]-7,12,16-trimethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H52O/c1-8-23(20(2)3)10-9-21(4)24-13-15-29(7)27-12-11-25-22(5)26(32)14-16-30(25)19-31(27,30)18-17-28(24,29)6/h21-27,32H,2,8-19H2,1,3-7H3/t21-,22+,23-,24-,25+,26+,27+,28-,29?,30?,31?/m1/s1
InChI Key IGSHUKWRIPUVMM-WXSVSFSUSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H52O
Molecular Weight 440.70 g/mol
Exact Mass 440.401816278 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 10.60
Atomic LogP (AlogP) 8.41
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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41507-26-0
4,14-Dimethyl-9,19-cyclostigmast-25-en-3-ol

2D Structure

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2D Structure of 4,14-Dimethyl-9,19-cyclostigmast-25-en-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.5233 52.33%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.7068 70.68%
OATP2B1 inhibitior - 0.5732 57.32%
OATP1B1 inhibitior + 0.8424 84.24%
OATP1B3 inhibitior + 0.9299 92.99%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.4661 46.61%
P-glycoprotein inhibitior - 0.6314 63.14%
P-glycoprotein substrate + 0.5234 52.34%
CYP3A4 substrate + 0.6519 65.19%
CYP2C9 substrate - 0.6284 62.84%
CYP2D6 substrate - 0.6829 68.29%
CYP3A4 inhibition - 0.6600 66.00%
CYP2C9 inhibition - 0.6730 67.30%
CYP2C19 inhibition - 0.6847 68.47%
CYP2D6 inhibition - 0.9255 92.55%
CYP1A2 inhibition - 0.7501 75.01%
CYP2C8 inhibition - 0.6500 65.00%
CYP inhibitory promiscuity - 0.5247 52.47%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6016 60.16%
Eye corrosion - 0.9878 98.78%
Eye irritation - 0.9018 90.18%
Skin irritation + 0.5097 50.97%
Skin corrosion - 0.9321 93.21%
Ames mutagenesis - 0.7404 74.04%
Human Ether-a-go-go-Related Gene inhibition - 0.4117 41.17%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.5892 58.92%
skin sensitisation - 0.5308 53.08%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.8559 85.59%
Acute Oral Toxicity (c) III 0.6978 69.78%
Estrogen receptor binding + 0.7516 75.16%
Androgen receptor binding + 0.7660 76.60%
Thyroid receptor binding + 0.5716 57.16%
Glucocorticoid receptor binding + 0.7445 74.45%
Aromatase binding + 0.6690 66.90%
PPAR gamma + 0.5753 57.53%
Honey bee toxicity - 0.6374 63.74%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9953 99.53%

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 98.78% 97.25%
CHEMBL218 P21554 Cannabinoid CB1 receptor 93.74% 96.61%
CHEMBL233 P35372 Mu opioid receptor 93.72% 97.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.65% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.51% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 92.92% 90.17%
CHEMBL240 Q12809 HERG 89.40% 89.76%
CHEMBL2095194 P08709 Coagulation factor VII/tissue factor 87.09% 99.17%
CHEMBL3837 P07711 Cathepsin L 86.65% 96.61%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 85.82% 92.86%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.07% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 84.92% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.90% 97.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.78% 93.56%
CHEMBL2996 Q05655 Protein kinase C delta 84.46% 97.79%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.27% 93.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 84.17% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.07% 82.69%
CHEMBL2581 P07339 Cathepsin D 83.96% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.41% 96.95%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 82.56% 97.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.25% 94.45%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 81.08% 96.38%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.60% 92.94%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.06% 99.18%

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.
Euphorbia caducifolia
Trichosanthes tricuspidata

Cross-Links

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PubChem 191060
LOTUS LTS0265982
wikiData Q82943274