4-(3-Methylbut-2-enyl)benzoic acid

Details

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Internal ID b536b0e9-5a93-4f2b-af57-323f6db19d9b
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acids
IUPAC Name 4-(3-methylbut-2-enyl)benzoic acid
SMILES (Canonical) CC(=CCC1=CC=C(C=C1)C(=O)O)C
SMILES (Isomeric) CC(=CCC1=CC=C(C=C1)C(=O)O)C
InChI InChI=1S/C12H14O2/c1-9(2)3-4-10-5-7-11(8-6-10)12(13)14/h3,5-8H,4H2,1-2H3,(H,13,14)
InChI Key DQZXUWDSZIQTIS-UHFFFAOYSA-N
Popularity 0 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 4.00
Atomic LogP (AlogP) 2.89
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(3-Methylbut-2-enyl)benzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9225 92.25%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.6875 68.75%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9554 95.54%
OATP1B3 inhibitior + 0.9284 92.84%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7886 78.86%
P-glycoprotein inhibitior - 0.9707 97.07%
P-glycoprotein substrate - 0.9372 93.72%
CYP3A4 substrate - 0.7650 76.50%
CYP2C9 substrate - 0.8204 82.04%
CYP2D6 substrate - 0.8856 88.56%
CYP3A4 inhibition - 0.9423 94.23%
CYP2C9 inhibition - 0.8362 83.62%
CYP2C19 inhibition - 0.9435 94.35%
CYP2D6 inhibition - 0.8957 89.57%
CYP1A2 inhibition - 0.9434 94.34%
CYP2C8 inhibition - 0.8855 88.55%
CYP inhibitory promiscuity - 0.8370 83.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5371 53.71%
Carcinogenicity (trinary) Non-required 0.8041 80.41%
Eye corrosion - 0.7061 70.61%
Eye irritation + 0.9831 98.31%
Skin irritation + 0.8425 84.25%
Skin corrosion + 0.5745 57.45%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7963 79.63%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5749 57.49%
skin sensitisation + 0.9058 90.58%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.5014 50.14%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.5910 59.10%
Acute Oral Toxicity (c) III 0.8786 87.86%
Estrogen receptor binding - 0.7479 74.79%
Androgen receptor binding - 0.8284 82.84%
Thyroid receptor binding - 0.7905 79.05%
Glucocorticoid receptor binding - 0.7296 72.96%
Aromatase binding + 0.7741 77.41%
PPAR gamma - 0.5468 54.68%
Honey bee toxicity - 0.9665 96.65%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity + 0.9869 98.69%

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 92.22% 98.95%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 90.70% 87.67%
CHEMBL221 P23219 Cyclooxygenase-1 90.33% 90.17%
CHEMBL3492 P49721 Proteasome Macropain subunit 89.79% 90.24%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.72% 86.33%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.98% 89.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.25% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 85.04% 94.73%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.92% 93.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.60% 95.50%
CHEMBL4208 P20618 Proteasome component C5 83.49% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.29% 96.09%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.83% 81.11%

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.
Citrus × aurantium

Cross-Links

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PubChem 129924919
LOTUS LTS0090601
wikiData Q104987307