2-Hydroxyterephthalic acid

Details

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Internal ID 1c876dfe-b0ad-4bb2-aa52-70ed72372435
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Phthalic acid and derivatives > P-phthalic acid and derivatives
IUPAC Name 2-hydroxyterephthalic acid
SMILES (Canonical) C1=CC(=C(C=C1C(=O)O)O)C(=O)O
SMILES (Isomeric) C1=CC(=C(C=C1C(=O)O)O)C(=O)O
InChI InChI=1S/C8H6O5/c9-6-3-4(7(10)11)1-2-5(6)8(12)13/h1-3,9H,(H,10,11)(H,12,13)
InChI Key CDOWNLMZVKJRSC-UHFFFAOYSA-N
Popularity 378 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 1.50
Atomic LogP (AlogP) 0.79
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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636-94-2
2-hydroxybenzene-1,4-dicarboxylic acid
Hydroxyterephthalic acid
1,4-Benzenedicarboxylic acid, 2-hydroxy-
MFCD09835368
2-Hydroxy-1,4-benzenedicarboxylic acid
2-hydroxyterephthalicacid
2-hydroxyterephthalate
2-HYDROXYBENZENE-1,4-DIOIC ACID
2-hydroxy terephthalic 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 2-Hydroxyterephthalic 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 + 0.5477 54.77%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Mitochondria 0.8536 85.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9671 96.71%
OATP1B3 inhibitior + 0.9361 93.61%
MATE1 inhibitior + 0.6800 68.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9697 96.97%
P-glycoprotein inhibitior - 0.9839 98.39%
P-glycoprotein substrate - 0.9868 98.68%
CYP3A4 substrate - 0.8496 84.96%
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 - 0.7824 78.24%
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 + 0.9967 99.67%
Skin irritation + 0.8330 83.30%
Skin corrosion - 0.9074 90.74%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9466 94.66%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation + 0.6696 66.96%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.5616 56.16%
Acute Oral Toxicity (c) III 0.5586 55.86%
Estrogen receptor binding - 0.8744 87.44%
Androgen receptor binding - 0.6554 65.54%
Thyroid receptor binding - 0.7440 74.40%
Glucocorticoid receptor binding - 0.7911 79.11%
Aromatase binding - 0.8203 82.03%
PPAR gamma - 0.6157 61.57%
Honey bee toxicity - 0.9787 97.87%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.9600 96.00%
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
CHEMBL3194 P02766 Transthyretin 96.26% 90.71%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 94.30% 87.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 91.54% 81.11%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 89.70% 94.42%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.04% 86.33%
CHEMBL1811 P34995 Prostanoid EP1 receptor 87.32% 95.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.19% 91.11%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 85.80% 89.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.45% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.77% 93.40%
CHEMBL4208 P20618 Proteasome component C5 82.56% 90.00%
CHEMBL2535 P11166 Glucose transporter 81.22% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.11% 99.17%

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.
Gentiana lutea

Cross-Links

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PubChem 97257
LOTUS LTS0262443
wikiData Q72481869