5-Hydroxyisophthalic acid

Details

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Internal ID f68894ca-3c5e-4d94-a597-6d2c3847a104
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Phthalic acid and derivatives > M-phthalic acid and derivatives
IUPAC Name 5-hydroxybenzene-1,3-dicarboxylic acid
SMILES (Canonical) C1=C(C=C(C=C1C(=O)O)O)C(=O)O
SMILES (Isomeric) C1=C(C=C(C=C1C(=O)O)O)C(=O)O
InChI InChI=1S/C8H6O5/c9-6-2-4(7(10)11)1-5(3-6)8(12)13/h1-3,9H,(H,10,11)(H,12,13)
InChI Key QNVNLUSHGRBCLO-UHFFFAOYSA-N
Popularity 94 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 0.70
Atomic LogP (AlogP) 0.79
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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618-83-7
5-hydroxybenzene-1,3-dicarboxylic acid
5-Oxyisophthalic acid
Isophthalic acid, 5-hydroxy-
1,3-Benzenedicarboxylic acid, 5-hydroxy-
5-Hydoxyisophthalic acid
5-Hydroxy-1,3-benzenedicarboxylic acid
5-Hydroxyisosphthalic acid
EINECS 210-565-7
MFCD00002515
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 5-Hydroxyisophthalic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9679 96.79%
Caco-2 - 0.7026 70.26%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.9184 91.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9586 95.86%
OATP1B3 inhibitior + 0.9445 94.45%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9726 97.26%
P-glycoprotein inhibitior - 0.9820 98.20%
P-glycoprotein substrate - 0.9958 99.58%
CYP3A4 substrate - 0.8338 83.38%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.8731 87.31%
CYP3A4 inhibition - 0.9411 94.11%
CYP2C9 inhibition - 0.9522 95.22%
CYP2C19 inhibition - 0.9729 97.29%
CYP2D6 inhibition - 0.9618 96.18%
CYP1A2 inhibition - 0.9824 98.24%
CYP2C8 inhibition - 0.9126 91.26%
CYP inhibitory promiscuity - 0.9831 98.31%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6152 61.52%
Carcinogenicity (trinary) Non-required 0.6797 67.97%
Eye corrosion - 0.6111 61.11%
Eye irritation + 0.9973 99.73%
Skin irritation + 0.8339 83.39%
Skin corrosion - 0.8298 82.98%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8920 89.20%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation - 0.7156 71.56%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.6204 62.04%
Acute Oral Toxicity (c) III 0.5091 50.91%
Estrogen receptor binding - 0.8871 88.71%
Androgen receptor binding - 0.7011 70.11%
Thyroid receptor binding - 0.8830 88.30%
Glucocorticoid receptor binding - 0.7667 76.67%
Aromatase binding - 0.8376 83.76%
PPAR gamma - 0.8616 86.16%
Honey bee toxicity - 0.9698 96.98%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity + 0.9255 92.55%

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 90.19% 90.71%
CHEMBL1811 P34995 Prostanoid EP1 receptor 85.34% 95.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.70% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.47% 99.17%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 84.43% 87.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.72% 86.33%
CHEMBL4208 P20618 Proteasome component C5 80.77% 90.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.20% 94.42%

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.
Glycyrrhiza glabra
Vitex negundo

Cross-Links

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PubChem 69257
NPASS NPC230953
LOTUS LTS0238671
wikiData Q72484591