2-Hepten-4-ol

Details

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Internal ID 98820117-09d0-42a1-8a25-3d199714afa1
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name (E)-hept-2-en-4-ol
SMILES (Canonical) CCCC(C=CC)O
SMILES (Isomeric) CCCC(/C=C/C)O
InChI InChI=1S/C7H14O/c1-3-5-7(8)6-4-2/h3,5,7-8H,4,6H2,1-2H3/b5-3+
InChI Key DODCYMXUZOEOQF-HWKANZROSA-N
Popularity 6 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 1.70
Atomic LogP (AlogP) 1.72
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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4798-59-8
hept-2-en-4-ol
(E)-hept-2-en-4-ol
(2E)-2-Hepten-4-ol
2-Heptene-4-ol
(2E)-2-Hepten-4-ol #
SCHEMBL3418051
2-Hepten-4-ol, (E)+(Z)
DODCYMXUZOEOQF-HWKANZROSA-N
MFCD00021932
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Hepten-4-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.8389 83.89%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.3386 33.86%
OATP2B1 inhibitior - 0.8470 84.70%
OATP1B1 inhibitior + 0.8943 89.43%
OATP1B3 inhibitior + 0.9215 92.15%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9375 93.75%
P-glycoprotein inhibitior - 0.9850 98.50%
P-glycoprotein substrate - 0.9568 95.68%
CYP3A4 substrate - 0.7317 73.17%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7129 71.29%
CYP3A4 inhibition - 0.9560 95.60%
CYP2C9 inhibition - 0.9310 93.10%
CYP2C19 inhibition - 0.8888 88.88%
CYP2D6 inhibition - 0.9269 92.69%
CYP1A2 inhibition + 0.5132 51.32%
CYP2C8 inhibition - 0.9846 98.46%
CYP inhibitory promiscuity - 0.8287 82.87%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.6498 64.98%
Eye corrosion + 0.6373 63.73%
Eye irritation + 0.9046 90.46%
Skin irritation + 0.6489 64.89%
Skin corrosion - 0.8823 88.23%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6441 64.41%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.9181 91.81%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.4541 45.41%
Acute Oral Toxicity (c) III 0.7493 74.93%
Estrogen receptor binding - 0.9239 92.39%
Androgen receptor binding - 0.9694 96.94%
Thyroid receptor binding - 0.8149 81.49%
Glucocorticoid receptor binding - 0.8194 81.94%
Aromatase binding - 0.9415 94.15%
PPAR gamma - 0.9135 91.35%
Honey bee toxicity - 0.9588 95.88%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity - 0.7142 71.42%

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
CHEMBL4040 P28482 MAP kinase ERK2 95.60% 83.82%
CHEMBL2581 P07339 Cathepsin D 91.33% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.00% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.69% 99.17%
CHEMBL1907 P15144 Aminopeptidase N 82.63% 93.31%
CHEMBL230 P35354 Cyclooxygenase-2 81.11% 89.63%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.88% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.74% 85.14%
CHEMBL301 P24941 Cyclin-dependent kinase 2 80.35% 91.23%

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.
Dendrobium chrysanthum

Cross-Links

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PubChem 5366235
NPASS NPC164135