Phthalic acid

Details

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Internal ID 1b488f39-4fd0-4d31-8b97-bd933c543b16
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acids
IUPAC Name phthalic acid
SMILES (Canonical) C1=CC=C(C(=C1)C(=O)O)C(=O)O
SMILES (Isomeric) C1=CC=C(C(=C1)C(=O)O)C(=O)O
InChI InChI=1S/C8H6O4/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4H,(H,9,10)(H,11,12)
InChI Key XNGIFLGASWRNHJ-UHFFFAOYSA-N
Popularity 8,600 references in papers

Physical and Chemical Properties

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Molecular Formula C8H6O4
Molecular Weight 166.13 g/mol
Exact Mass 166.02660867 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 0.70
Atomic LogP (AlogP) 1.08
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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88-99-3
1,2-benzenedicarboxylic acid
o-phthalic acid
benzene-1,2-dicarboxylic acid
Pathalic acid
o-dicarboxybenzene
o-benzenedicarboxylic acid
Acide phtalique
Kyselina ftalova
ortho-phthalic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Phthalic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9041 90.41%
Caco-2 + 0.6084 60.84%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.9000 90.00%
Subcellular localzation Mitochondria 0.9213 92.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9790 97.90%
OATP1B3 inhibitior + 0.9565 95.65%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9708 97.08%
P-glycoprotein inhibitior - 0.9849 98.49%
P-glycoprotein substrate - 0.9975 99.75%
CYP3A4 substrate - 0.9066 90.66%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8854 88.54%
CYP3A4 inhibition - 0.9863 98.63%
CYP2C9 inhibition - 0.9808 98.08%
CYP2C19 inhibition - 0.9753 97.53%
CYP2D6 inhibition - 0.9344 93.44%
CYP1A2 inhibition - 0.9621 96.21%
CYP2C8 inhibition - 0.9601 96.01%
CYP inhibitory promiscuity - 0.9839 98.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5753 57.53%
Carcinogenicity (trinary) Non-required 0.7773 77.73%
Eye corrosion - 0.5796 57.96%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8622 86.22%
Skin corrosion - 0.7665 76.65%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9394 93.94%
Micronuclear - 0.5400 54.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation + 0.6273 62.73%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.5760 57.60%
Acute Oral Toxicity (c) IV 0.7284 72.84%
Estrogen receptor binding - 0.8939 89.39%
Androgen receptor binding - 0.7617 76.17%
Thyroid receptor binding - 0.7533 75.33%
Glucocorticoid receptor binding - 0.8164 81.64%
Aromatase binding - 0.8539 85.39%
PPAR gamma - 0.5111 51.11%
Honey bee toxicity - 0.9840 98.40%
Biodegradation + 0.9250 92.50%
Crustacea aquatic toxicity - 0.9400 94.00%
Fish aquatic toxicity + 0.9769 97.69%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3577 P00352 Aldehyde dehydrogenase 1A1 28183.8 nM
Potency
via CMAUP
CHEMBL2903 P16050 Arachidonate 15-lipoxygenase 39810.7 nM
Potency
via CMAUP

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.21% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.18% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.87% 95.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.51% 93.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 84.44% 81.11%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 83.57% 87.67%
CHEMBL5847 P52895 Aldo-keto reductase family 1 member C2 82.47% 92.50%
CHEMBL2581 P07339 Cathepsin D 81.33% 98.95%

Cross-Links

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PubChem 1017
NPASS NPC282895
ChEMBL CHEMBL1045
LOTUS LTS0167476
wikiData Q423876