2-Hydroxy-3,6-dimethylbenzoic acid

Details

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Internal ID b8e72b9e-fa67-403f-a4e6-0062fa74bab1
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Salicylic acid and derivatives > Salicylic acids
IUPAC Name 2-hydroxy-3,6-dimethylbenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H10O3/c1-5-3-4-6(2)8(10)7(5)9(11)12/h3-4,10H,1-2H3,(H,11,12)
InChI Key SDQFDFFLPQFIHQ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O3
Molecular Weight 166.17 g/mol
Exact Mass 166.062994177 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 2.40
Atomic LogP (AlogP) 1.71
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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3921-12-8
3,6-dimethylsalicylic acid
CHEBI:70733
DTXSID00294109
RefChem:473107
DTXCID10245248
820-676-8
MFCD00156975
Benzoic acid, 2-hydroxy-3,6-dimethyl-
JBIR-26
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-Hydroxy-3,6-dimethylbenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9861 98.61%
Caco-2 + 0.9075 90.75%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.9125 91.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9434 94.34%
OATP1B3 inhibitior + 0.9731 97.31%
MATE1 inhibitior + 0.5600 56.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8858 88.58%
P-glycoprotein inhibitior - 0.9640 96.40%
P-glycoprotein substrate - 0.9878 98.78%
CYP3A4 substrate - 0.7530 75.30%
CYP2C9 substrate - 0.6663 66.63%
CYP2D6 substrate - 0.9078 90.78%
CYP3A4 inhibition - 0.8132 81.32%
CYP2C9 inhibition - 0.7115 71.15%
CYP2C19 inhibition - 0.8478 84.78%
CYP2D6 inhibition - 0.9568 95.68%
CYP1A2 inhibition - 0.8862 88.62%
CYP2C8 inhibition - 0.9042 90.42%
CYP inhibitory promiscuity - 0.8269 82.69%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7282 72.82%
Carcinogenicity (trinary) Non-required 0.8201 82.01%
Eye corrosion + 0.6887 68.87%
Eye irritation + 0.9790 97.90%
Skin irritation + 0.8518 85.18%
Skin corrosion - 0.5894 58.94%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8147 81.47%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation + 0.7870 78.70%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6236 62.36%
Acute Oral Toxicity (c) III 0.8327 83.27%
Estrogen receptor binding - 0.7798 77.98%
Androgen receptor binding - 0.7275 72.75%
Thyroid receptor binding - 0.8004 80.04%
Glucocorticoid receptor binding - 0.8509 85.09%
Aromatase binding - 0.8875 88.75%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.9950 99.50%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.9371 93.71%

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 87.15% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.86% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 84.05% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.31% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.28% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.26% 86.33%

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 261630
LOTUS LTS0155937
wikiData Q27139050