2-Pent-2-enylbenzoic acid

Details

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Internal ID a2cab530-b373-4888-abac-de6de6041d9f
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acids
IUPAC Name 2-pent-2-enylbenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H14O2/c1-2-3-4-7-10-8-5-6-9-11(10)12(13)14/h3-6,8-9H,2,7H2,1H3,(H,13,14)
InChI Key RWMKYKAUOZVIIN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O2
Molecular Weight 190.24 g/mol
Exact Mass 190.099379685 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.80
Atomic LogP (AlogP) 2.89
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Pent-2-enylbenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9953 99.53%
Caco-2 + 0.9171 91.71%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.5884 58.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9021 90.21%
OATP1B3 inhibitior + 0.9356 93.56%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8166 81.66%
P-glycoprotein inhibitior - 0.9891 98.91%
P-glycoprotein substrate - 0.9547 95.47%
CYP3A4 substrate - 0.7984 79.84%
CYP2C9 substrate - 0.5992 59.92%
CYP2D6 substrate - 0.8931 89.31%
CYP3A4 inhibition - 0.9324 93.24%
CYP2C9 inhibition - 0.8077 80.77%
CYP2C19 inhibition - 0.8831 88.31%
CYP2D6 inhibition - 0.9300 93.00%
CYP1A2 inhibition - 0.7784 77.84%
CYP2C8 inhibition - 0.8043 80.43%
CYP inhibitory promiscuity - 0.7176 71.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5640 56.40%
Carcinogenicity (trinary) Non-required 0.6386 63.86%
Eye corrosion - 0.6676 66.76%
Eye irritation + 0.9801 98.01%
Skin irritation + 0.7793 77.93%
Skin corrosion - 0.7060 70.60%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7270 72.70%
Micronuclear - 0.8377 83.77%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.8813 88.13%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.5053 50.53%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.6439 64.39%
Acute Oral Toxicity (c) III 0.8917 89.17%
Estrogen receptor binding - 0.5880 58.80%
Androgen receptor binding - 0.9017 90.17%
Thyroid receptor binding - 0.6484 64.84%
Glucocorticoid receptor binding - 0.6831 68.31%
Aromatase binding - 0.6348 63.48%
PPAR gamma + 0.5716 57.16%
Honey bee toxicity - 0.9696 96.96%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.9940 99.40%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.85% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.82% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.13% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.37% 86.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.38% 93.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.30% 95.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.91% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.07% 99.17%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 83.00% 87.67%
CHEMBL3401 O75469 Pregnane X receptor 82.92% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 82.74% 90.17%

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.
Delphinium elatum

Cross-Links

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PubChem 54289479
LOTUS LTS0222554
wikiData Q105246578