Pent-1-EN-1-YL pentanoate

Details

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Internal ID a0fd867c-0a5d-4262-8810-c97891fe2d38
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name pent-1-enyl pentanoate
SMILES (Canonical) CCCCC(=O)OC=CCCC
SMILES (Isomeric) CCCCC(=O)OC=CCCC
InChI InChI=1S/C10H18O2/c1-3-5-7-9-12-10(11)8-6-4-2/h7,9H,3-6,8H2,1-2H3
InChI Key YCPDOSBDNBUOBD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O2
Molecular Weight 170.25 g/mol
Exact Mass 170.130679813 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.03
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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565165-36-8
DTXSID60850265

2D Structure

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2D Structure of Pent-1-EN-1-YL pentanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.9356 93.56%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Plasma membrane 0.6046 60.46%
OATP2B1 inhibitior - 0.8466 84.66%
OATP1B1 inhibitior + 0.7805 78.05%
OATP1B3 inhibitior + 0.9059 90.59%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7493 74.93%
P-glycoprotein inhibitior - 0.9765 97.65%
P-glycoprotein substrate - 0.9397 93.97%
CYP3A4 substrate - 0.6218 62.18%
CYP2C9 substrate - 0.7980 79.80%
CYP2D6 substrate - 0.8654 86.54%
CYP3A4 inhibition - 0.9576 95.76%
CYP2C9 inhibition - 0.9329 93.29%
CYP2C19 inhibition - 0.8926 89.26%
CYP2D6 inhibition - 0.9487 94.87%
CYP1A2 inhibition + 0.5599 55.99%
CYP2C8 inhibition - 0.8450 84.50%
CYP inhibitory promiscuity - 0.8284 82.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.6304 63.04%
Eye corrosion + 0.9850 98.50%
Eye irritation + 0.8832 88.32%
Skin irritation + 0.8296 82.96%
Skin corrosion - 0.6055 60.55%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7749 77.49%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5899 58.99%
skin sensitisation + 0.9248 92.48%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.5623 56.23%
Acute Oral Toxicity (c) III 0.7045 70.45%
Estrogen receptor binding - 0.9205 92.05%
Androgen receptor binding - 0.8654 86.54%
Thyroid receptor binding - 0.8699 86.99%
Glucocorticoid receptor binding - 0.8634 86.34%
Aromatase binding - 0.8574 85.74%
PPAR gamma - 0.7679 76.79%
Honey bee toxicity - 0.9833 98.33%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.8712 87.12%

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 94.76% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.20% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.34% 96.95%
CHEMBL2581 P07339 Cathepsin D 88.71% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.05% 86.33%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.78% 94.33%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.29% 92.08%

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.
Heracleum dissectum

Cross-Links

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PubChem 71441326
LOTUS LTS0023472
wikiData Q82843401