Trimethylthiophene-2-carboxylicacid

Details

Top
Internal ID 6bec12b5-e7c9-451e-91a5-fd22e5bdb1be
Taxonomy Organoheterocyclic compounds > Thiophenes > Thiophene carboxylic acids and derivatives > Thiophene carboxylic acids
IUPAC Name 3,4,5-trimethylthiophene-2-carboxylic acid
SMILES (Canonical) CC1=C(SC(=C1C)C(=O)O)C
SMILES (Isomeric) CC1=C(SC(=C1C)C(=O)O)C
InChI InChI=1S/C8H10O2S/c1-4-5(2)7(8(9)10)11-6(4)3/h1-3H3,(H,9,10)
InChI Key ZHSGKMPXEWBKBM-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C8H10O2S
Molecular Weight 170.23 g/mol
Exact Mass 170.04015073 g/mol
Topological Polar Surface Area (TPSA) 65.50 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.37
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
trimethylthiophene-2-carboxylic acid
3,4,5-trimethyl-2-thiophenecarboxylic acid
EN300-7706788
Z1262515566
90953-80-3

2D Structure

Top
2D Structure of Trimethylthiophene-2-carboxylicacid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 + 0.5756 57.56%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7452 74.52%
OATP2B1 inhibitior - 0.8570 85.70%
OATP1B1 inhibitior + 0.9621 96.21%
OATP1B3 inhibitior + 0.9515 95.15%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9091 90.91%
P-glycoprotein inhibitior - 0.9490 94.90%
P-glycoprotein substrate - 0.9875 98.75%
CYP3A4 substrate - 0.7485 74.85%
CYP2C9 substrate - 0.7560 75.60%
CYP2D6 substrate - 0.9281 92.81%
CYP3A4 inhibition - 0.9533 95.33%
CYP2C9 inhibition - 0.8907 89.07%
CYP2C19 inhibition - 0.9192 91.92%
CYP2D6 inhibition - 0.9433 94.33%
CYP1A2 inhibition - 0.8474 84.74%
CYP2C8 inhibition - 0.9783 97.83%
CYP inhibitory promiscuity - 0.7921 79.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.5892 58.92%
Eye corrosion - 0.5574 55.74%
Eye irritation + 0.9343 93.43%
Skin irritation - 0.5379 53.79%
Skin corrosion - 0.8915 89.15%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7424 74.24%
Micronuclear - 0.6926 69.26%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation - 0.5302 53.02%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.4734 47.34%
Acute Oral Toxicity (c) III 0.6271 62.71%
Estrogen receptor binding - 0.8328 83.28%
Androgen receptor binding - 0.8213 82.13%
Thyroid receptor binding - 0.8418 84.18%
Glucocorticoid receptor binding - 0.8187 81.87%
Aromatase binding - 0.7908 79.08%
PPAR gamma - 0.7604 76.04%
Honey bee toxicity - 0.9843 98.43%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9324 93.24%

Targets

Top

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
CHEMBL1293294 P51151 Ras-related protein Rab-9A 93.62% 87.67%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 90.70% 93.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 86.96% 81.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.03% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.29% 95.50%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.60% 96.09%
CHEMBL1811 P34995 Prostanoid EP1 receptor 80.41% 95.71%
CHEMBL2581 P07339 Cathepsin D 80.37% 98.95%

Plants that contains it

Top
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.
Ferula assa-foetida

Cross-Links

Top
PubChem 10877558
LOTUS LTS0210154
wikiData Q105375969