3-Hydroxyphthalic acid

Details

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Internal ID d1c9363c-c9be-4295-89ca-bc4a914a5e42
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Salicylic acid and derivatives > Salicylic acids
IUPAC Name 3-hydroxyphthalic acid
SMILES (Canonical) C1=CC(=C(C(=C1)O)C(=O)O)C(=O)O
SMILES (Isomeric) C1=CC(=C(C(=C1)O)C(=O)O)C(=O)O
InChI InChI=1S/C8H6O5/c9-5-3-1-2-4(7(10)11)6(5)8(12)13/h1-3,9H,(H,10,11)(H,12,13)
InChI Key MNUOZFHYBCRUOD-UHFFFAOYSA-N
Popularity 28 references in papers

Physical and Chemical Properties

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Molecular Formula C8H6O5
Molecular Weight 182.13 g/mol
Exact Mass 182.02152329 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP 1.10
Atomic LogP (AlogP) 0.79
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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601-97-8
3-hydroxybenzene-1,2-dicarboxylic acid
Phthalic acid, 3-hydroxy-
U8LUD5V352
CHEMBL2420930
NSC-2436
MFCD17000078
1,2-Benzenedicarboxylic acid, 3-hydroxy-
EINECS 210-011-4
3-Hydroxyphthalicacid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Hydroxyphthalic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9200 92.00%
Caco-2 + 0.5067 50.67%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.8536 85.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9785 97.85%
OATP1B3 inhibitior + 0.9361 93.61%
MATE1 inhibitior + 0.6800 68.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9683 96.83%
P-glycoprotein inhibitior - 0.9787 97.87%
P-glycoprotein substrate - 0.9815 98.15%
CYP3A4 substrate - 0.8170 81.70%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8985 89.85%
CYP3A4 inhibition - 0.8608 86.08%
CYP2C9 inhibition - 0.7515 75.15%
CYP2C19 inhibition - 0.9107 91.07%
CYP2D6 inhibition - 0.9504 95.04%
CYP1A2 inhibition - 0.9753 97.53%
CYP2C8 inhibition - 0.9019 90.19%
CYP inhibitory promiscuity - 0.9463 94.63%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7346 73.46%
Carcinogenicity (trinary) Non-required 0.8203 82.03%
Eye corrosion - 0.8586 85.86%
Eye irritation + 0.9918 99.18%
Skin irritation + 0.8330 83.30%
Skin corrosion - 0.9074 90.74%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9186 91.86%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation + 0.6696 66.96%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.6734 67.34%
Acute Oral Toxicity (c) III 0.5586 55.86%
Estrogen receptor binding - 0.6878 68.78%
Androgen receptor binding - 0.6899 68.99%
Thyroid receptor binding - 0.7196 71.96%
Glucocorticoid receptor binding - 0.5796 57.96%
Aromatase binding - 0.8251 82.51%
PPAR gamma + 0.6268 62.68%
Honey bee toxicity - 0.9797 97.97%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity + 0.9547 95.47%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.43% 95.56%
CHEMBL2581 P07339 Cathepsin D 87.31% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.34% 95.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.48% 91.11%
CHEMBL3194 P02766 Transthyretin 83.47% 90.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.01% 93.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.58% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.95% 96.09%

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 69039
LOTUS LTS0172278
wikiData Q77383908