2-Methylpent-2-en-1-oic acid

Details

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Internal ID 7fb481f2-0e19-4026-a3ff-6899c00946e5
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Branched fatty acids > Methyl-branched fatty acids
IUPAC Name 2-methylpent-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H10O2/c1-3-4-5(2)6(7)8/h4H,3H2,1-2H3,(H,7,8)
InChI Key JJYWRQLLQAKNAD-UHFFFAOYSA-N
Popularity 27 references in papers

Physical and Chemical Properties

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Molecular Formula C6H10O2
Molecular Weight 114.14 g/mol
Exact Mass 114.068079557 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.43
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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2-methylpent-2-enoic acid
2-Pentenoic acid, 2-methyl-
Pentenoic acid, 2-methyl-
methylpent-2-enoic acid
2-methyl-pent-2-enoic acid
DTXSID0051998
JJYWRQLLQAKNAD-UHFFFAOYSA-N
FT-0608332
FT-0658729
FT-0700012

2D Structure

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2D Structure of 2-Methylpent-2-en-1-oic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 + 0.7903 79.03%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5565 55.65%
OATP2B1 inhibitior - 0.8526 85.26%
OATP1B1 inhibitior + 0.9181 91.81%
OATP1B3 inhibitior + 0.9272 92.72%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9054 90.54%
P-glycoprotein inhibitior - 0.9846 98.46%
P-glycoprotein substrate - 0.9899 98.99%
CYP3A4 substrate - 0.7558 75.58%
CYP2C9 substrate + 0.6145 61.45%
CYP2D6 substrate - 0.9169 91.69%
CYP3A4 inhibition - 0.9336 93.36%
CYP2C9 inhibition - 0.8587 85.87%
CYP2C19 inhibition - 0.9312 93.12%
CYP2D6 inhibition - 0.9119 91.19%
CYP1A2 inhibition - 0.9212 92.12%
CYP2C8 inhibition - 0.9816 98.16%
CYP inhibitory promiscuity - 0.8251 82.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5758 57.58%
Carcinogenicity (trinary) Non-required 0.7060 70.60%
Eye corrosion + 0.9158 91.58%
Eye irritation + 0.9693 96.93%
Skin irritation + 0.8450 84.50%
Skin corrosion + 0.9102 91.02%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8442 84.42%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6948 69.48%
skin sensitisation + 0.7986 79.86%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.5754 57.54%
Acute Oral Toxicity (c) III 0.8407 84.07%
Estrogen receptor binding - 0.9670 96.70%
Androgen receptor binding - 0.8536 85.36%
Thyroid receptor binding - 0.9404 94.04%
Glucocorticoid receptor binding - 0.9616 96.16%
Aromatase binding - 0.9345 93.45%
PPAR gamma - 0.8487 84.87%
Honey bee toxicity - 0.9773 97.73%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity + 0.9052 90.52%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.67% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.19% 96.95%
CHEMBL2581 P07339 Cathepsin D 84.18% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 80.16% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.08% 99.17%

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 18458
LOTUS LTS0188946
wikiData Q72494448