2,2':3',2''-Terthiophene

Details

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Internal ID 5df35606-3994-4f91-b959-08c668049259
Taxonomy Organoheterocyclic compounds > Bi- and oligothiophenes
IUPAC Name 2,3-dithiophen-2-ylthiophene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H8S3/c1-3-10(13-6-1)9-5-8-15-12(9)11-4-2-7-14-11/h1-8H
InChI Key SBVKMIQOXJYJIM-UHFFFAOYSA-N
Popularity 406 references in papers

Physical and Chemical Properties

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Molecular Formula C12H8S3
Molecular Weight 248.40 g/mol
Exact Mass 247.97881378 g/mol
Topological Polar Surface Area (TPSA) 84.70 Ų
XlogP 4.30
Atomic LogP (AlogP) 5.21
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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2,3-dithiophen-2-ylthiophene
111744-23-1
CHEBI:50079
DTXSID90327899
105124-96-7
RefChem:80776
DTXCID80279010
NSC700222
2,3-di(2-thienyl)thiophene
SCHEMBL147273
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,2':3',2''-Terthiophene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.7932 79.32%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6552 65.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9390 93.90%
OATP1B3 inhibitior + 0.9498 94.98%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6488 64.88%
P-glycoprotein inhibitior - 0.9450 94.50%
P-glycoprotein substrate - 0.9811 98.11%
CYP3A4 substrate - 0.7040 70.40%
CYP2C9 substrate - 0.6129 61.29%
CYP2D6 substrate - 0.7353 73.53%
CYP3A4 inhibition - 0.9612 96.12%
CYP2C9 inhibition - 0.5305 53.05%
CYP2C19 inhibition + 0.6866 68.66%
CYP2D6 inhibition - 0.7112 71.12%
CYP1A2 inhibition + 0.5602 56.02%
CYP2C8 inhibition - 0.9172 91.72%
CYP inhibitory promiscuity + 0.8512 85.12%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.3609 36.09%
Eye corrosion - 0.7340 73.40%
Eye irritation + 0.9347 93.47%
Skin irritation + 0.6765 67.65%
Skin corrosion - 0.9040 90.40%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6359 63.59%
Micronuclear - 0.6900 69.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation + 0.5816 58.16%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6195 61.95%
Acute Oral Toxicity (c) III 0.6299 62.99%
Estrogen receptor binding + 0.8418 84.18%
Androgen receptor binding + 0.6657 66.57%
Thyroid receptor binding + 0.6731 67.31%
Glucocorticoid receptor binding + 0.7699 76.99%
Aromatase binding + 0.8716 87.16%
PPAR gamma + 0.6947 69.47%
Honey bee toxicity - 0.9098 90.98%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity + 0.9712 97.12%

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
CHEMBL2581 P07339 Cathepsin D 86.15% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 85.18% 85.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.99% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.82% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 80.80% 95.93%
CHEMBL3568 P29475 Nitric-oxide synthase, brain 80.44% 95.46%

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.
Eclipta prostrata
Olea europaea

Cross-Links

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PubChem 395532
LOTUS LTS0046449
wikiData Q105272599