9-Methyloctadec-9-ene

Details

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Internal ID 4fe52b30-b7ea-46db-9d81-32206d4b457e
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 9-methyloctadec-9-ene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H38/c1-4-6-8-10-12-14-16-18-19(3)17-15-13-11-9-7-5-2/h18H,4-17H2,1-3H3
InChI Key RCKXFWRCJBTHNQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C19H38
Molecular Weight 266.50 g/mol
Exact Mass 266.297351212 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 9.70
Atomic LogP (AlogP) 7.43
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 14

Synonyms

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SCHEMBL9545734

2D Structure

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2D Structure of 9-Methyloctadec-9-ene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9914 99.14%
Caco-2 + 0.9693 96.93%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Nucleus 0.4351 43.51%
OATP2B1 inhibitior - 0.8463 84.63%
OATP1B1 inhibitior + 0.8908 89.08%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5908 59.08%
P-glycoprotein inhibitior - 0.8424 84.24%
P-glycoprotein substrate - 0.9133 91.33%
CYP3A4 substrate - 0.6615 66.15%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.9582 95.82%
CYP2C9 inhibition - 0.9151 91.51%
CYP2C19 inhibition - 0.9179 91.79%
CYP2D6 inhibition - 0.9301 93.01%
CYP1A2 inhibition - 0.6093 60.93%
CYP2C8 inhibition - 0.9080 90.80%
CYP inhibitory promiscuity - 0.5282 52.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.4651 46.51%
Eye corrosion + 0.7853 78.53%
Eye irritation + 0.9764 97.64%
Skin irritation + 0.8332 83.32%
Skin corrosion - 0.9673 96.73%
Ames mutagenesis - 0.9423 94.23%
Human Ether-a-go-go-Related Gene inhibition - 0.4087 40.87%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5058 50.58%
skin sensitisation + 0.9369 93.69%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.4874 48.74%
Acute Oral Toxicity (c) III 0.8795 87.95%
Estrogen receptor binding - 0.7218 72.18%
Androgen receptor binding - 0.7782 77.82%
Thyroid receptor binding - 0.6459 64.59%
Glucocorticoid receptor binding - 0.8308 83.08%
Aromatase binding - 0.7578 75.78%
PPAR gamma + 0.7000 70.00%
Honey bee toxicity - 0.9852 98.52%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity + 0.8593 85.93%
Fish aquatic toxicity + 0.9930 99.30%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 98.95% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.30% 99.17%
CHEMBL2581 P07339 Cathepsin D 92.88% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 92.04% 92.86%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.23% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.99% 96.09%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 86.35% 85.94%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.14% 91.11%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.88% 91.81%
CHEMBL3401 O75469 Pregnane X receptor 82.24% 94.73%
CHEMBL2885 P07451 Carbonic anhydrase III 82.08% 87.45%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.49% 100.00%
CHEMBL299 P17252 Protein kinase C alpha 80.71% 98.03%

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.
Cissus quadrangularis

Cross-Links

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PubChem 54259429
LOTUS LTS0252581
wikiData Q105233755