Methyl 3-(3,4-dimethyl-5-pentylfuran-2-yl)propanoate

Details

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Internal ID e53b0a7f-858d-4bdb-8d39-286d0de1dbe8
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Heterocyclic fatty acids > Furanoid fatty acids
IUPAC Name methyl 3-(3,4-dimethyl-5-pentylfuran-2-yl)propanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O3/c1-5-6-7-8-13-11(2)12(3)14(18-13)9-10-15(16)17-4/h5-10H2,1-4H3
InChI Key VYNYUKYQVKAEQP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O3
Molecular Weight 252.35 g/mol
Exact Mass 252.17254462 g/mol
Topological Polar Surface Area (TPSA) 39.40 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.73
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 3-(3,4-dimethyl-5-pentylfuran-2-yl)propanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.9271 92.71%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.5959 59.59%
OATP2B1 inhibitior - 0.8534 85.34%
OATP1B1 inhibitior + 0.8546 85.46%
OATP1B3 inhibitior + 0.9503 95.03%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.6255 62.55%
P-glycoprotein inhibitior - 0.7716 77.16%
P-glycoprotein substrate - 0.7425 74.25%
CYP3A4 substrate - 0.5321 53.21%
CYP2C9 substrate - 0.5963 59.63%
CYP2D6 substrate - 0.8442 84.42%
CYP3A4 inhibition - 0.8513 85.13%
CYP2C9 inhibition - 0.6937 69.37%
CYP2C19 inhibition - 0.6081 60.81%
CYP2D6 inhibition - 0.9215 92.15%
CYP1A2 inhibition - 0.5781 57.81%
CYP2C8 inhibition - 0.6990 69.90%
CYP inhibitory promiscuity - 0.6183 61.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.6212 62.12%
Eye corrosion - 0.9345 93.45%
Eye irritation + 0.8644 86.44%
Skin irritation - 0.7908 79.08%
Skin corrosion - 0.9775 97.75%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4757 47.57%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.6351 63.51%
skin sensitisation - 0.7070 70.70%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.5479 54.79%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.6136 61.36%
Acute Oral Toxicity (c) III 0.5895 58.95%
Estrogen receptor binding - 0.8006 80.06%
Androgen receptor binding - 0.6104 61.04%
Thyroid receptor binding - 0.5645 56.45%
Glucocorticoid receptor binding - 0.4634 46.34%
Aromatase binding - 0.7637 76.37%
PPAR gamma + 0.6476 64.76%
Honey bee toxicity - 0.9801 98.01%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6783 67.83%
Fish aquatic toxicity + 0.9765 97.65%

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 94.31% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 94.15% 96.95%
CHEMBL230 P35354 Cyclooxygenase-2 91.79% 89.63%
CHEMBL2581 P07339 Cathepsin D 91.69% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.73% 92.08%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 89.63% 97.21%
CHEMBL3401 O75469 Pregnane X receptor 88.75% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.53% 91.11%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.89% 94.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.04% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.31% 93.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.31% 99.23%

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 162971343
LOTUS LTS0035496
wikiData Q105299107