3,4-Dimethylthiophene

Details

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Internal ID 04b241ff-d286-4ca4-9b8e-3b03e1c6cb36
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 3,4-dimethylthiophene
SMILES (Canonical) CC1=CSC=C1C
SMILES (Isomeric) CC1=CSC=C1C
InChI InChI=1S/C6H8S/c1-5-3-7-4-6(5)2/h3-4H,1-2H3
InChI Key GPSFYJDZKSRMKZ-UHFFFAOYSA-N
Popularity 66 references in papers

Physical and Chemical Properties

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Molecular Formula C6H8S
Molecular Weight 112.19 g/mol
Exact Mass 112.03467143 g/mol
Topological Polar Surface Area (TPSA) 28.20 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.36
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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632-15-5
Thiophene, 3,4-dimethyl-
3,4-dimethyl-thiophene
UNII-96Q084Q43E
96Q084Q43E
FEMA NO. 4645
CHEBI:89511
DTXSID40212549
RefChem:91229
FEMA 4645
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,4-Dimethylthiophene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 + 0.8693 86.93%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8714 87.14%
Subcellular localzation Mitochondria 0.5393 53.93%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9737 97.37%
OATP1B3 inhibitior + 0.9606 96.06%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9137 91.37%
P-glycoprotein inhibitior - 0.9824 98.24%
P-glycoprotein substrate - 0.9906 99.06%
CYP3A4 substrate - 0.8057 80.57%
CYP2C9 substrate - 0.7829 78.29%
CYP2D6 substrate - 0.7756 77.56%
CYP3A4 inhibition - 0.9623 96.23%
CYP2C9 inhibition - 0.7391 73.91%
CYP2C19 inhibition + 0.5075 50.75%
CYP2D6 inhibition - 0.7925 79.25%
CYP1A2 inhibition - 0.5442 54.42%
CYP2C8 inhibition - 0.9779 97.79%
CYP inhibitory promiscuity + 0.7106 71.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Warning 0.3817 38.17%
Eye corrosion + 0.8449 84.49%
Eye irritation + 0.9902 99.02%
Skin irritation + 0.7662 76.62%
Skin corrosion - 0.9409 94.09%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7819 78.19%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.9085 90.85%
skin sensitisation + 0.7904 79.04%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.5671 56.71%
Acute Oral Toxicity (c) III 0.7273 72.73%
Estrogen receptor binding - 0.9107 91.07%
Androgen receptor binding - 0.8873 88.73%
Thyroid receptor binding - 0.8163 81.63%
Glucocorticoid receptor binding - 0.8686 86.86%
Aromatase binding - 0.8366 83.66%
PPAR gamma - 0.9224 92.24%
Honey bee toxicity - 0.9599 95.99%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.8400 84.00%
Fish aquatic toxicity + 0.9098 90.98%

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
CHEMBL3401 O75469 Pregnane X receptor 85.39% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.17% 93.65%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.97% 95.56%
CHEMBL2581 P07339 Cathepsin D 80.76% 98.95%

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.
Allium cepa

Cross-Links

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PubChem 79089
NPASS NPC221178