15-(5-Hydroxy-6-methyl-4-methylideneheptan-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol

Details

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Internal ID c7fdefa4-c5ce-4edb-8fa7-dc8e8f51cc95
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cycloartanols and derivatives
IUPAC Name 15-(5-hydroxy-6-methyl-4-methylideneheptan-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H52O2/c1-19(2)26(33)21(4)17-20(3)22-11-13-29(8)24-10-9-23-27(5,6)25(32)12-14-30(23)18-31(24,30)16-15-28(22,29)7/h19-20,22-26,32-33H,4,9-18H2,1-3,5-8H3
InChI Key CROIFUIXDDBNGA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H52O2
Molecular Weight 456.70 g/mol
Exact Mass 456.396730897 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 9.10
Atomic LogP (AlogP) 7.39
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 15-(5-Hydroxy-6-methyl-4-methylideneheptan-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 - 0.6102 61.02%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.4630 46.30%
OATP2B1 inhibitior - 0.5771 57.71%
OATP1B1 inhibitior + 0.8866 88.66%
OATP1B3 inhibitior + 0.9086 90.86%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.5594 55.94%
P-glycoprotein inhibitior - 0.6847 68.47%
P-glycoprotein substrate - 0.6631 66.31%
CYP3A4 substrate + 0.6140 61.40%
CYP2C9 substrate - 0.6284 62.84%
CYP2D6 substrate - 0.6829 68.29%
CYP3A4 inhibition - 0.8029 80.29%
CYP2C9 inhibition - 0.8126 81.26%
CYP2C19 inhibition - 0.7380 73.80%
CYP2D6 inhibition - 0.9382 93.82%
CYP1A2 inhibition - 0.7885 78.85%
CYP2C8 inhibition - 0.6849 68.49%
CYP inhibitory promiscuity - 0.5608 56.08%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6392 63.92%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9348 93.48%
Skin irritation - 0.5346 53.46%
Skin corrosion - 0.9451 94.51%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4196 41.96%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.4818 48.18%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity - 0.7411 74.11%
Acute Oral Toxicity (c) III 0.4308 43.08%
Estrogen receptor binding + 0.7568 75.68%
Androgen receptor binding + 0.7453 74.53%
Thyroid receptor binding + 0.6595 65.95%
Glucocorticoid receptor binding + 0.7303 73.03%
Aromatase binding + 0.7001 70.01%
PPAR gamma + 0.5783 57.83%
Honey bee toxicity - 0.7363 73.63%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9936 99.36%

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 98.31% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.67% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 92.68% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.63% 91.11%
CHEMBL2581 P07339 Cathepsin D 90.22% 98.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.54% 95.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.87% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.46% 97.09%
CHEMBL206 P03372 Estrogen receptor alpha 85.14% 97.64%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.43% 93.00%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 83.95% 96.38%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.06% 90.24%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.05% 95.89%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 82.84% 98.75%
CHEMBL1937 Q92769 Histone deacetylase 2 82.73% 94.75%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 82.58% 92.86%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.16% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.06% 82.69%
CHEMBL1977 P11473 Vitamin D receptor 81.65% 99.43%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.49% 96.61%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.08% 100.00%
CHEMBL2095194 P08709 Coagulation factor VII/tissue factor 80.89% 99.17%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.83% 91.03%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.44% 90.08%

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 esula

Cross-Links

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PubChem 162881080
LOTUS LTS0168868
wikiData Q104968628