1-Hepten-3-OL

Details

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Internal ID 9753e76d-874e-441c-952e-212cbc38cf23
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name hept-1-en-3-ol
SMILES (Canonical) CCCCC(C=C)O
SMILES (Isomeric) CCCCC(C=C)O
InChI InChI=1S/C7H14O/c1-3-5-6-7(8)4-2/h4,7-8H,2-3,5-6H2,1H3
InChI Key PZKFYTOLVRCMOA-UHFFFAOYSA-N
Popularity 31 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 2.00
Atomic LogP (AlogP) 1.72
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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4938-52-7
hept-1-en-3-ol
heptene-1-ol-3
NSC 93797
UNII-39TWV35509
EINECS 225-579-9
NSC-93797
(+/-)-1-HEPTEN-3-OL
39TWV35509
AI3-28621
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-Hepten-3-OL

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9895 98.95%
Caco-2 + 0.7702 77.02%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.3584 35.84%
OATP2B1 inhibitior - 0.8516 85.16%
OATP1B1 inhibitior + 0.9248 92.48%
OATP1B3 inhibitior + 0.9072 90.72%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9627 96.27%
P-glycoprotein inhibitior - 0.9853 98.53%
P-glycoprotein substrate - 0.9397 93.97%
CYP3A4 substrate - 0.6980 69.80%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6917 69.17%
CYP3A4 inhibition - 0.9156 91.56%
CYP2C9 inhibition - 0.8902 89.02%
CYP2C19 inhibition - 0.8188 81.88%
CYP2D6 inhibition - 0.9103 91.03%
CYP1A2 inhibition + 0.6453 64.53%
CYP2C8 inhibition - 0.9733 97.33%
CYP inhibitory promiscuity - 0.7754 77.54%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.6991 69.91%
Eye corrosion + 0.8046 80.46%
Eye irritation + 0.9780 97.80%
Skin irritation + 0.8460 84.60%
Skin corrosion + 0.6375 63.75%
Ames mutagenesis - 0.8937 89.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6368 63.68%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5909 59.09%
skin sensitisation + 0.8886 88.86%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.6277 62.77%
Acute Oral Toxicity (c) II 0.7203 72.03%
Estrogen receptor binding - 0.8859 88.59%
Androgen receptor binding - 0.9367 93.67%
Thyroid receptor binding - 0.8043 80.43%
Glucocorticoid receptor binding - 0.8058 80.58%
Aromatase binding - 0.9179 91.79%
PPAR gamma - 0.9064 90.64%
Honey bee toxicity - 0.9710 97.10%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.6768 67.68%
Fish aquatic toxicity + 0.6773 67.73%

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
CHEMBL2581 P07339 Cathepsin D 94.81% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 93.41% 93.31%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.85% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.62% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.42% 96.09%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.05% 85.94%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.96% 93.56%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.93% 92.86%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 84.16% 91.81%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 82.60% 97.34%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 81.87% 96.00%
CHEMBL2885 P07451 Carbonic anhydrase III 81.77% 87.45%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.57% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 80.47% 94.73%

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.
Aspalathus linearis
Litchi chinensis
Melissa officinalis
Mentha arvensis
Mentha canadensis
Mentha suaveolens
Monarda fistulosa

Cross-Links

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PubChem 21057
NPASS NPC276839
LOTUS LTS0139882
wikiData Q27256927