6-Hepten-1-ol

Details

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Internal ID 7622f7f2-8ec3-407f-967b-4d02fb4e4808
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name hept-6-en-1-ol
SMILES (Canonical) C=CCCCCCO
SMILES (Isomeric) C=CCCCCCO
InChI InChI=1S/C7H14O/c1-2-3-4-5-6-7-8/h2,8H,1,3-7H2
InChI Key UFULDTPDHIRNGS-UHFFFAOYSA-N
Popularity 10 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 5

Synonyms

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hept-6-en-1-ol
4117-10-6
6-heptenol
6-heptene-1-ol
(z)-6-hepten-1-ol
SCHEMBL129386
UFULDTPDHIRNGS-UHFFFAOYSA-
AMY7500
DTXSID40337504
MFCD00229167
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 6-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 + 0.9763 97.63%
Caco-2 + 0.8332 83.32%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.4411 44.11%
OATP2B1 inhibitior - 0.8580 85.80%
OATP1B1 inhibitior + 0.9429 94.29%
OATP1B3 inhibitior + 0.9424 94.24%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9358 93.58%
P-glycoprotein inhibitior - 0.9877 98.77%
P-glycoprotein substrate - 0.9840 98.40%
CYP3A4 substrate - 0.7109 71.09%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7062 70.62%
CYP3A4 inhibition - 0.9330 93.30%
CYP2C9 inhibition - 0.8635 86.35%
CYP2C19 inhibition - 0.9172 91.72%
CYP2D6 inhibition - 0.9458 94.58%
CYP1A2 inhibition - 0.7265 72.65%
CYP2C8 inhibition - 0.9348 93.48%
CYP inhibitory promiscuity - 0.8900 89.00%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.7087 70.87%
Eye corrosion + 0.9273 92.73%
Eye irritation + 0.9927 99.27%
Skin irritation + 0.7438 74.38%
Skin corrosion - 0.8982 89.82%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6468 64.68%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5281 52.81%
skin sensitisation + 0.8187 81.87%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.5781 57.81%
Acute Oral Toxicity (c) III 0.7938 79.38%
Estrogen receptor binding - 0.9521 95.21%
Androgen receptor binding - 0.8774 87.74%
Thyroid receptor binding - 0.8507 85.07%
Glucocorticoid receptor binding - 0.6854 68.54%
Aromatase binding - 0.8798 87.98%
PPAR gamma - 0.8915 89.15%
Honey bee toxicity - 0.8959 89.59%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.7478 74.78%
Fish aquatic toxicity - 0.5000 50.00%

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
CHEMBL2885 P07451 Carbonic anhydrase III 90.22% 87.45%
CHEMBL1829 O15379 Histone deacetylase 3 88.26% 95.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.58% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.96% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.13% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.43% 96.09%
CHEMBL1977 P11473 Vitamin D receptor 81.25% 99.43%

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.
Citrus × aurantium
Citrus deliciosa

Cross-Links

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PubChem 543123
NPASS NPC92918