4-Carbamoyl-2-methylbenzoate

Details

Top
Internal ID 45e37940-e8bf-4a19-8638-3f94957496e1
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzamides
IUPAC Name 4-carbamoyl-2-methylbenzoate
SMILES (Canonical) CC1=C(C=CC(=C1)C(=O)N)C(=O)[O-]
SMILES (Isomeric) CC1=C(C=CC(=C1)C(=O)N)C(=O)[O-]
InChI InChI=1S/C9H9NO3/c1-5-4-6(8(10)11)2-3-7(5)9(12)13/h2-4H,1H3,(H2,10,11)(H,12,13)/p-1
InChI Key LGEPNRWKNPFLJQ-UHFFFAOYSA-M
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H8NO3-
Molecular Weight 178.16 g/mol
Exact Mass 178.050418117 g/mol
Topological Polar Surface Area (TPSA) 83.20 Ų
XlogP 1.30
Atomic LogP (AlogP) -0.54
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 4-Carbamoyl-2-methylbenzoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9738 97.38%
Caco-2 + 0.8011 80.11%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7239 72.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9790 97.90%
OATP1B3 inhibitior + 0.9636 96.36%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8990 89.90%
P-glycoprotein inhibitior - 0.9740 97.40%
P-glycoprotein substrate - 0.9250 92.50%
CYP3A4 substrate - 0.7546 75.46%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate - 0.9046 90.46%
CYP3A4 inhibition - 0.9839 98.39%
CYP2C9 inhibition - 0.9469 94.69%
CYP2C19 inhibition - 0.9074 90.74%
CYP2D6 inhibition - 0.9412 94.12%
CYP1A2 inhibition - 0.8802 88.02%
CYP2C8 inhibition - 0.8188 81.88%
CYP inhibitory promiscuity - 0.9809 98.09%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5604 56.04%
Carcinogenicity (trinary) Non-required 0.6647 66.47%
Eye corrosion - 0.9298 92.98%
Eye irritation + 0.9654 96.54%
Skin irritation - 0.7037 70.37%
Skin corrosion - 0.9733 97.33%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8642 86.42%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation - 0.9243 92.43%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.5919 59.19%
Acute Oral Toxicity (c) III 0.5874 58.74%
Estrogen receptor binding - 0.8829 88.29%
Androgen receptor binding - 0.6320 63.20%
Thyroid receptor binding - 0.8536 85.36%
Glucocorticoid receptor binding - 0.8460 84.60%
Aromatase binding - 0.8140 81.40%
PPAR gamma - 0.7826 78.26%
Honey bee toxicity - 0.9884 98.84%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.8252 82.52%
Fish aquatic toxicity + 0.8285 82.85%

Targets

Top

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.43% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.00% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.98% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.79% 96.09%
CHEMBL2535 P11166 Glucose transporter 81.68% 98.75%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.56% 96.95%
CHEMBL4208 P20618 Proteasome component C5 81.55% 90.00%
CHEMBL3902 P09211 Glutathione S-transferase Pi 81.44% 93.81%
CHEMBL3401 O75469 Pregnane X receptor 80.97% 94.73%

Plants that contains it

Top
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.
Asarum heterotropoides
Asarum sieboldii
Capsicum annuum

Cross-Links

Top
PubChem 90475391
NPASS NPC97128