6-Methylsalicylic Acid

Details

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Internal ID 1bd4651c-76de-4edd-8894-c82c56e6d97e
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Salicylic acid and derivatives > Salicylic acids
IUPAC Name 2-hydroxy-6-methylbenzoic acid
SMILES (Canonical) CC1=C(C(=CC=C1)O)C(=O)O
SMILES (Isomeric) CC1=C(C(=CC=C1)O)C(=O)O
InChI InChI=1S/C8H8O3/c1-5-3-2-4-6(9)7(5)8(10)11/h2-4,9H,1H3,(H,10,11)
InChI Key HCJMNOSIAGSZBM-UHFFFAOYSA-N
Popularity 262 references in papers

Physical and Chemical Properties

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Molecular Formula C8H8O3
Molecular Weight 152.15 g/mol
Exact Mass 152.047344113 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.40
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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567-61-3
6-Methylsalicylic acid
2,6-Cresotic acid
6-Hydroxy-o-toluic acid
Benzoic acid, 2-hydroxy-6-methyl-
6-MSA
6-MS
MFCD01194284
NSC 403256
BRN 2208693
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 6-Methylsalicylic Acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9880 98.80%
Caco-2 + 0.9393 93.93%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.9052 90.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9730 97.30%
OATP1B3 inhibitior + 0.9763 97.63%
MATE1 inhibitior + 0.5600 56.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9334 93.34%
P-glycoprotein inhibitior - 0.9851 98.51%
P-glycoprotein substrate - 0.9798 97.98%
CYP3A4 substrate - 0.7363 73.63%
CYP2C9 substrate - 0.6663 66.63%
CYP2D6 substrate - 0.9078 90.78%
CYP3A4 inhibition - 0.8585 85.85%
CYP2C9 inhibition - 0.6743 67.43%
CYP2C19 inhibition - 0.8282 82.82%
CYP2D6 inhibition - 0.9694 96.94%
CYP1A2 inhibition - 0.9129 91.29%
CYP2C8 inhibition - 0.8937 89.37%
CYP inhibitory promiscuity - 0.8396 83.96%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7282 72.82%
Carcinogenicity (trinary) Non-required 0.8005 80.05%
Eye corrosion + 0.6475 64.75%
Eye irritation + 0.9937 99.37%
Skin irritation + 0.9147 91.47%
Skin corrosion + 0.5316 53.16%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8480 84.80%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.8311 83.11%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.4814 48.14%
Acute Oral Toxicity (c) III 0.6729 67.29%
Estrogen receptor binding - 0.8933 89.33%
Androgen receptor binding - 0.8489 84.89%
Thyroid receptor binding - 0.7550 75.50%
Glucocorticoid receptor binding - 0.8949 89.49%
Aromatase binding - 0.9286 92.86%
PPAR gamma - 0.6841 68.41%
Honey bee toxicity - 0.9949 99.49%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity + 0.9190 91.90%

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 94.26% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.54% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 87.58% 94.73%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.64% 93.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.22% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.67% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.10% 99.23%

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.
Aster bellidiastrum
Caragana halodendron
Davallia divaricata
Dolomiaea souliei
Eucalyptus camaldulensis
Garcinia mangostana
Leibnitzia anandria
Ligularia vellerea
Lonicera hypoleuca
Mutisia spinosa
Nicotiana sylvestris
Serpocaulon triseriale

Cross-Links

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PubChem 11279
NPASS NPC125252
LOTUS LTS0079350
wikiData Q6172528