CID 146684621

Details

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Internal ID 2673bfb5-46c5-4404-861f-24c20e50b9ac
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Acylaminobenzoic acid and derivatives
IUPAC Name 2-[2-[(2-carboxyacetyl)amino]propanoylamino]benzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H14N2O6/c1-7(14-10(16)6-11(17)18)12(19)15-9-5-3-2-4-8(9)13(20)21/h2-5,7H,6H2,1H3,(H,14,16)(H,15,19)(H,17,18)(H,20,21)
InChI Key LCKFAMIWUNBCPL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14N2O6
Molecular Weight 294.26 g/mol
Exact Mass 294.08518617 g/mol
Topological Polar Surface Area (TPSA) 133.00 Ų
XlogP 1.30
Atomic LogP (AlogP) 0.30
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 146684621

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7335 73.35%
Caco-2 - 0.6528 65.28%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7404 74.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9370 93.70%
OATP1B3 inhibitior + 0.9418 94.18%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8414 84.14%
P-glycoprotein inhibitior - 0.9744 97.44%
P-glycoprotein substrate - 0.7539 75.39%
CYP3A4 substrate - 0.7000 70.00%
CYP2C9 substrate - 0.5963 59.63%
CYP2D6 substrate - 0.8957 89.57%
CYP3A4 inhibition - 0.9674 96.74%
CYP2C9 inhibition - 0.8626 86.26%
CYP2C19 inhibition - 0.9114 91.14%
CYP2D6 inhibition - 0.9545 95.45%
CYP1A2 inhibition - 0.8937 89.37%
CYP2C8 inhibition - 0.7752 77.52%
CYP inhibitory promiscuity - 0.9629 96.29%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8211 82.11%
Carcinogenicity (trinary) Non-required 0.7863 78.63%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.9700 97.00%
Skin irritation - 0.8433 84.33%
Skin corrosion - 0.9787 97.87%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6046 60.46%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.5784 57.84%
skin sensitisation - 0.9060 90.60%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.7522 75.22%
Acute Oral Toxicity (c) IV 0.5002 50.02%
Estrogen receptor binding - 0.5596 55.96%
Androgen receptor binding - 0.5865 58.65%
Thyroid receptor binding - 0.6997 69.97%
Glucocorticoid receptor binding + 0.5676 56.76%
Aromatase binding + 0.6322 63.22%
PPAR gamma + 0.5261 52.61%
Honey bee toxicity - 0.9660 96.60%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.7477 74.77%

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 97.82% 98.95%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 94.09% 87.67%
CHEMBL3308 P55212 Caspase-6 92.03% 97.56%
CHEMBL221 P23219 Cyclooxygenase-1 92.03% 90.17%
CHEMBL1255126 O15151 Protein Mdm4 90.83% 90.20%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.48% 95.56%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 89.79% 93.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.20% 95.50%
CHEMBL2535 P11166 Glucose transporter 87.74% 98.75%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 87.60% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.45% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.33% 96.09%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 87.01% 81.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.65% 99.23%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.51% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 82.23% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.31% 91.11%
CHEMBL2321614 Q9NPC2 Potassium channel subfamily K member 9 80.14% 80.00%

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 146684621
LOTUS LTS0160171
wikiData Q105149876