3-Methylthiophene-2-carboxylic acid

Details

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Internal ID f824c1f5-0d89-46b3-8cf6-de2f03e2b234
Taxonomy Organoheterocyclic compounds > Thiophenes > Thiophene carboxylic acids and derivatives > Thiophene carboxylic acids
IUPAC Name 3-methylthiophene-2-carboxylic acid
SMILES (Canonical) CC1=C(SC=C1)C(=O)O
SMILES (Isomeric) CC1=C(SC=C1)C(=O)O
InChI InChI=1S/C6H6O2S/c1-4-2-3-9-5(4)6(7)8/h2-3H,1H3,(H,7,8)
InChI Key IFLKEBSJTZGCJG-UHFFFAOYSA-N
Popularity 16 references in papers

Physical and Chemical Properties

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Molecular Formula C6H6O2S
Molecular Weight 142.18 g/mol
Exact Mass 142.00885060 g/mol
Topological Polar Surface Area (TPSA) 65.50 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.75
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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3-Methylthiophene-2-carboxylic acid
3-Methyl-2-thiophenecarboxylic acid
3-Methyl-2-thenoic acid
3-methyl-2-thiophene carboxylic acid
2-Thiophenecarboxylic acid, 3-methyl-
MFCD00005438
AC30341
3-methyl-thiophene-2-carboxylic acid
3-methyl-2-thiophenecarboxylic
3-Methyl-2-thiophenecarboxylicacid
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-Methylthiophene-2-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.8367 83.67%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7338 73.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9687 96.87%
OATP1B3 inhibitior + 0.9591 95.91%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9414 94.14%
P-glycoprotein inhibitior - 0.9778 97.78%
P-glycoprotein substrate - 0.9921 99.21%
CYP3A4 substrate - 0.7363 73.63%
CYP2C9 substrate - 0.7560 75.60%
CYP2D6 substrate - 0.9281 92.81%
CYP3A4 inhibition - 0.9733 97.33%
CYP2C9 inhibition - 0.9122 91.22%
CYP2C19 inhibition - 0.9240 92.40%
CYP2D6 inhibition - 0.9406 94.06%
CYP1A2 inhibition - 0.9049 90.49%
CYP2C8 inhibition - 0.9822 98.22%
CYP inhibitory promiscuity - 0.8638 86.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.5965 59.65%
Eye corrosion + 0.7103 71.03%
Eye irritation + 0.9806 98.06%
Skin irritation + 0.6075 60.75%
Skin corrosion - 0.7568 75.68%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8048 80.48%
Micronuclear - 0.6226 62.26%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation + 0.4948 49.48%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.6430 64.30%
Acute Oral Toxicity (c) III 0.5025 50.25%
Estrogen receptor binding - 0.9622 96.22%
Androgen receptor binding - 0.9273 92.73%
Thyroid receptor binding - 0.9065 90.65%
Glucocorticoid receptor binding - 0.9098 90.98%
Aromatase binding - 0.8903 89.03%
PPAR gamma - 0.8140 81.40%
Honey bee toxicity - 0.9934 99.34%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity + 0.9140 91.40%

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 90.79% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.05% 98.95%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 87.58% 93.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.89% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.30% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 84.07% 94.73%
CHEMBL1811 P34995 Prostanoid EP1 receptor 83.71% 95.71%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.74% 81.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.02% 99.23%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 80.97% 87.67%

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.
Inula cappa

Cross-Links

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PubChem 90269
LOTUS LTS0141553
wikiData Q27456145