Thiophene

Details

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Internal ID c0183820-ea2a-4fca-b2ce-b390a86f4d3b
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name thiophene
SMILES (Canonical) C1=CSC=C1
SMILES (Isomeric) C1=CSC=C1
InChI InChI=1S/C4H4S/c1-2-4-5-3-1/h1-4H
InChI Key YTPLMLYBLZKORZ-UHFFFAOYSA-N
Popularity 29,426 references in papers

Physical and Chemical Properties

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Molecular Formula C4H4S
Molecular Weight 84.14 g/mol
Exact Mass 84.00337130 g/mol
Topological Polar Surface Area (TPSA) 28.20 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.75
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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110-02-1
Thiofuran
Thiole
Thiophen
Thiacyclopentadiene
Thiotetrole
Thiofurfuran
Divinylene sulfide
Thiaphene
Thiofuram
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Thiophene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9914 99.14%
Caco-2 + 0.8139 81.39%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.4702 47.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9732 97.32%
OATP1B3 inhibitior + 0.9607 96.07%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9211 92.11%
P-glycoprotein inhibitior - 0.9866 98.66%
P-glycoprotein substrate - 0.9958 99.58%
CYP3A4 substrate - 0.8157 81.57%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7557 75.57%
CYP3A4 inhibition - 0.9825 98.25%
CYP2C9 inhibition - 0.7629 76.29%
CYP2C19 inhibition - 0.5662 56.62%
CYP2D6 inhibition - 0.7520 75.20%
CYP1A2 inhibition - 0.7243 72.43%
CYP2C8 inhibition - 0.9895 98.95%
CYP inhibitory promiscuity + 0.6139 61.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6417 64.17%
Carcinogenicity (trinary) Warning 0.4863 48.63%
Eye corrosion + 0.9843 98.43%
Eye irritation + 0.9945 99.45%
Skin irritation + 0.9162 91.62%
Skin corrosion - 0.7216 72.16%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7567 75.67%
Micronuclear - 0.6900 69.00%
Hepatotoxicity + 0.9000 90.00%
skin sensitisation + 0.7837 78.37%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.6194 61.94%
Acute Oral Toxicity (c) III 0.8448 84.48%
Estrogen receptor binding - 0.8947 89.47%
Androgen receptor binding - 0.7721 77.21%
Thyroid receptor binding - 0.8164 81.64%
Glucocorticoid receptor binding - 0.8389 83.89%
Aromatase binding - 0.8877 88.77%
PPAR gamma - 0.8332 83.32%
Honey bee toxicity - 0.8184 81.84%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.7444 74.44%

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
No predicted targets yet!

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.
Arnebia euchroma
Arnebia guttata
Lithospermum erythrorhizon

Cross-Links

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PubChem 8030
NPASS NPC108375