trans-2-Hepten-1-ol

Details

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Internal ID baccf4db-98b9-42cb-8827-eaaec1909f51
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (E)-hept-2-en-1-ol
SMILES (Canonical) CCCCC=CCO
SMILES (Isomeric) CCCC/C=C/CO
InChI InChI=1S/C7H14O/c1-2-3-4-5-6-7-8/h5-6,8H,2-4,7H2,1H3/b6-5+
InChI Key ASFYPVGAALGVNR-AATRIKPKSA-N
Popularity 30 references in papers

Physical and Chemical Properties

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Molecular Formula C7H14O
Molecular Weight 114.19 g/mol
Exact Mass 114.104465066 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.73
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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33467-76-4
(E)-2-Hepten-1-ol
(E)-Hept-2-en-1-ol
2-Hepten-1-ol
2-Hepten-1-ol, (E)-
2-HEPTENOL
2-Hepten-1-ol, (2E)-
22104-77-4
(2E)-2-Hepten-1-ol
UNII-Q989YFO10I
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of trans-2-Hepten-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9890 98.90%
Caco-2 + 0.9489 94.89%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.4882 48.82%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.8452 84.52%
OATP1B3 inhibitior + 0.9227 92.27%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9138 91.38%
P-glycoprotein inhibitior - 0.9886 98.86%
P-glycoprotein substrate - 0.9552 95.52%
CYP3A4 substrate - 0.7101 71.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9465 94.65%
CYP2C9 inhibition - 0.8838 88.38%
CYP2C19 inhibition - 0.8991 89.91%
CYP2D6 inhibition - 0.9241 92.41%
CYP1A2 inhibition - 0.5867 58.67%
CYP2C8 inhibition - 0.9664 96.64%
CYP inhibitory promiscuity - 0.7249 72.49%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.6793 67.93%
Eye corrosion + 0.9463 94.63%
Eye irritation + 0.9628 96.28%
Skin irritation + 0.7383 73.83%
Skin corrosion - 0.9653 96.53%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6344 63.44%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5914 59.14%
skin sensitisation + 0.9122 91.22%
Respiratory toxicity - 0.9889 98.89%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.5562 55.62%
Acute Oral Toxicity (c) III 0.7183 71.83%
Estrogen receptor binding - 0.9766 97.66%
Androgen receptor binding - 0.8627 86.27%
Thyroid receptor binding - 0.8573 85.73%
Glucocorticoid receptor binding - 0.8783 87.83%
Aromatase binding - 0.9200 92.00%
PPAR gamma - 0.8329 83.29%
Honey bee toxicity - 0.9940 99.40%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.6728 67.28%
Fish aquatic toxicity + 0.9241 92.41%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 91.13% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.51% 97.29%
CHEMBL2581 P07339 Cathepsin D 87.69% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.18% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.59% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 84.40% 87.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.96% 96.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 82.53% 92.86%

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.
Camellia sinensis

Cross-Links

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PubChem 5318017
NPASS NPC308696