3-Hydroxy-2-methoxybenzoic acid

Details

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Internal ID a166add8-8603-4202-bb4c-d24ba4f64bed
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Methoxybenzoic acids and derivatives > O-methoxybenzoic acids and derivatives
IUPAC Name 3-hydroxy-2-methoxybenzoic acid
SMILES (Canonical) COC1=C(C=CC=C1O)C(=O)O
SMILES (Isomeric) COC1=C(C=CC=C1O)C(=O)O
InChI InChI=1S/C8H8O4/c1-12-7-5(8(10)11)3-2-4-6(7)9/h2-4,9H,1H3,(H,10,11)
InChI Key DSMHCSBCMFQGAZ-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C8H8O4
Molecular Weight 168.15 g/mol
Exact Mass 168.04225873 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.10
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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2169-28-0
Benzoic acid, 3-hydroxy-2-methoxy-
SCHEMBL470708
DTXSID90540687
MFCD03840538
AKOS006276445
MB03017
5-Phenyloxazole-4-carboxylicacidethylester
BS-25405
CS-0196009
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-Hydroxy-2-methoxybenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9739 97.39%
Caco-2 + 0.6770 67.70%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.8793 87.93%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9716 97.16%
OATP1B3 inhibitior + 0.9785 97.85%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9495 94.95%
P-glycoprotein inhibitior - 0.9761 97.61%
P-glycoprotein substrate - 0.9762 97.62%
CYP3A4 substrate - 0.7428 74.28%
CYP2C9 substrate - 0.7957 79.57%
CYP2D6 substrate - 0.8545 85.45%
CYP3A4 inhibition - 0.9683 96.83%
CYP2C9 inhibition - 0.8918 89.18%
CYP2C19 inhibition - 0.8554 85.54%
CYP2D6 inhibition - 0.9692 96.92%
CYP1A2 inhibition - 0.8799 87.99%
CYP2C8 inhibition - 0.7775 77.75%
CYP inhibitory promiscuity - 0.8885 88.85%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7009 70.09%
Carcinogenicity (trinary) Non-required 0.6679 66.79%
Eye corrosion + 0.5790 57.90%
Eye irritation + 0.9897 98.97%
Skin irritation + 0.7696 76.96%
Skin corrosion - 0.9011 90.11%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8020 80.20%
Micronuclear + 0.7400 74.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.8166 81.66%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.4933 49.33%
Acute Oral Toxicity (c) III 0.4790 47.90%
Estrogen receptor binding - 0.8384 83.84%
Androgen receptor binding - 0.8344 83.44%
Thyroid receptor binding - 0.7934 79.34%
Glucocorticoid receptor binding - 0.8761 87.61%
Aromatase binding - 0.8842 88.42%
PPAR gamma - 0.5844 58.44%
Honey bee toxicity - 0.9825 98.25%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity + 0.8805 88.05%

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 93.13% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.78% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.84% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.03% 95.50%
CHEMBL2535 P11166 Glucose transporter 87.95% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.16% 86.33%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.39% 93.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.14% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.11% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 80.92% 91.19%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.49% 99.15%

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.
Populus euphratica

Cross-Links

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PubChem 13434501
LOTUS LTS0060754
wikiData Q82416771