4-Methyloctadec-3-ene

Details

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Internal ID d22d8f24-a335-423a-9905-0f284cf09fc6
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 4-methyloctadec-3-ene
SMILES (Canonical) CCCCCCCCCCCCCCC(=CCC)C
SMILES (Isomeric) CCCCCCCCCCCCCCC(=CCC)C
InChI InChI=1S/C19H38/c1-4-6-7-8-9-10-11-12-13-14-15-16-18-19(3)17-5-2/h17H,4-16,18H2,1-3H3
InChI Key OKFARPKORSESQZ-UHFFFAOYSA-N
Popularity 0 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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495397-60-9
DTXSID60786217

2D Structure

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2D Structure of 4-Methyloctadec-3-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 + 0.9460 94.60%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Nucleus 0.4351 43.51%
OATP2B1 inhibitior - 0.8470 84.70%
OATP1B1 inhibitior + 0.8970 89.70%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.5700 57.00%
P-glycoprotein inhibitior - 0.8608 86.08%
P-glycoprotein substrate - 0.8882 88.82%
CYP3A4 substrate - 0.6555 65.55%
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 - 0.8847 88.47%
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 + 0.9784 97.84%
Skin irritation + 0.8332 83.32%
Skin corrosion - 0.9673 96.73%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4197 41.97%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5674 56.74%
skin sensitisation + 0.9369 93.69%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.5073 50.73%
Acute Oral Toxicity (c) III 0.8795 87.95%
Estrogen receptor binding - 0.8458 84.58%
Androgen receptor binding - 0.7606 76.06%
Thyroid receptor binding - 0.5644 56.44%
Glucocorticoid receptor binding - 0.8959 89.59%
Aromatase binding - 0.8099 80.99%
PPAR gamma + 0.6699 66.99%
Honey bee toxicity - 0.9832 98.32%
Biodegradation + 0.9750 97.50%
Crustacea aquatic toxicity + 0.8640 86.40%
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 96.70% 92.08%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 93.98% 92.86%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.31% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.74% 97.29%
CHEMBL2581 P07339 Cathepsin D 91.08% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.63% 96.09%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.05% 85.94%
CHEMBL240 Q12809 HERG 87.98% 89.76%
CHEMBL2885 P07451 Carbonic anhydrase III 86.41% 87.45%
CHEMBL230 P35354 Cyclooxygenase-2 85.97% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.49% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 85.10% 94.73%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.91% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.02% 97.25%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.06% 91.81%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.02% 93.56%

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.
Boerhavia diffusa

Cross-Links

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PubChem 71362601
LOTUS LTS0053660
wikiData Q82752353