Homophthalic acid

Details

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Internal ID e0b5b169-de6f-44d8-944f-8bac23377af4
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acids
IUPAC Name 2-(carboxymethyl)benzoic acid
SMILES (Canonical) C1=CC=C(C(=C1)CC(=O)O)C(=O)O
SMILES (Isomeric) C1=CC=C(C(=C1)CC(=O)O)C(=O)O
InChI InChI=1S/C9H8O4/c10-8(11)5-6-3-1-2-4-7(6)9(12)13/h1-4H,5H2,(H,10,11)(H,12,13)
InChI Key ZHQLTKAVLJKSKR-UHFFFAOYSA-N
Popularity 105 references in papers

Physical and Chemical Properties

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Molecular Formula C9H8O4
Molecular Weight 180.16 g/mol
Exact Mass 180.04225873 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.01
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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89-51-0
2-(Carboxymethyl)benzoic acid
Benzeneacetic acid, 2-carboxy-
2-Carboxybenzeneacetic acid
2-Carboxyphenylacetic acid
alpha-Carboxy-o-toluic acid
(o-Carboxymethyl)benzoic acid
(2-Carboxyphenyl)acetic acid
o-Toluic acid, alpha-carboxy-
Homophthalicacid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Homophthalic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8038 80.38%
Caco-2 + 0.7058 70.58%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.9000 90.00%
Subcellular localzation Mitochondria 0.9115 91.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9580 95.80%
OATP1B3 inhibitior + 0.9616 96.16%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9676 96.76%
P-glycoprotein inhibitior - 0.9923 99.23%
P-glycoprotein substrate - 0.9865 98.65%
CYP3A4 substrate - 0.8502 85.02%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.8825 88.25%
CYP3A4 inhibition - 0.9632 96.32%
CYP2C9 inhibition - 0.9821 98.21%
CYP2C19 inhibition - 0.9756 97.56%
CYP2D6 inhibition - 0.9238 92.38%
CYP1A2 inhibition - 0.9365 93.65%
CYP2C8 inhibition - 0.8839 88.39%
CYP inhibitory promiscuity - 0.9760 97.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6961 69.61%
Carcinogenicity (trinary) Non-required 0.7847 78.47%
Eye corrosion - 0.8204 82.04%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.6547 65.47%
Skin corrosion - 0.6908 69.08%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8789 87.89%
Micronuclear - 0.5982 59.82%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation + 0.5416 54.16%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.5948 59.48%
Acute Oral Toxicity (c) III 0.6732 67.32%
Estrogen receptor binding - 0.9208 92.08%
Androgen receptor binding - 0.9099 90.99%
Thyroid receptor binding - 0.8522 85.22%
Glucocorticoid receptor binding - 0.6890 68.90%
Aromatase binding - 0.8595 85.95%
PPAR gamma + 0.5416 54.16%
Honey bee toxicity - 0.9684 96.84%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity + 0.9351 93.51%

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 90.63% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.31% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.29% 95.56%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.53% 93.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.94% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.88% 95.50%
CHEMBL221 P23219 Cyclooxygenase-1 84.73% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.39% 94.62%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 80.95% 87.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.73% 86.33%

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.
Drynaria coronans
Garcinia morella

Cross-Links

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PubChem 66643
NPASS NPC284477
ChEMBL CHEMBL1229545