(3E)-3-Hepten-1-ol

Details

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Internal ID ef5be3bd-76d5-426e-9026-d53dffd2af4a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (E)-hept-3-en-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H14O/c1-2-3-4-5-6-7-8/h4-5,8H,2-3,6-7H2,1H3/b5-4+
InChI Key SDZQUCJFTUULJX-SNAWJCMRSA-N
Popularity 9 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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(3E)-3-Hepten-1-ol
3-Hepten-1-ol, (3E)-
3-Hepten-1-ol, (E)-
81C6I6M8QZ
DTXSID20883796
RefChem:1050208
DTXCID20909586
218-292-5
3-Hepten-1-ol
(E)-Hept-3-en-1-ol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (3E)-3-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 + 0.9927 99.27%
Caco-2 + 0.9497 94.97%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.4428 44.28%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.8566 85.66%
OATP1B3 inhibitior + 0.9197 91.97%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8994 89.94%
P-glycoprotein inhibitior - 0.9836 98.36%
P-glycoprotein substrate - 0.9713 97.13%
CYP3A4 substrate - 0.7600 76.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9301 93.01%
CYP2C9 inhibition - 0.9195 91.95%
CYP2C19 inhibition - 0.9196 91.96%
CYP2D6 inhibition - 0.9460 94.60%
CYP1A2 inhibition - 0.6264 62.64%
CYP2C8 inhibition - 0.9830 98.30%
CYP inhibitory promiscuity - 0.8527 85.27%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.6793 67.93%
Eye corrosion + 0.9093 90.93%
Eye irritation + 0.9669 96.69%
Skin irritation + 0.7946 79.46%
Skin corrosion - 0.9862 98.62%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6231 62.31%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5495 54.95%
skin sensitisation + 0.8014 80.14%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.5811 58.11%
Acute Oral Toxicity (c) III 0.8324 83.24%
Estrogen receptor binding - 0.9785 97.85%
Androgen receptor binding - 0.9412 94.12%
Thyroid receptor binding - 0.8706 87.06%
Glucocorticoid receptor binding - 0.8779 87.79%
Aromatase binding - 0.9119 91.19%
PPAR gamma - 0.8361 83.61%
Honey bee toxicity - 0.9817 98.17%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.8848 88.48%
Fish aquatic toxicity - 0.4579 45.79%

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 83.98% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 83.60% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.48% 96.09%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 5318018
NPASS NPC281486