2,2'-Bithiophene-5-carboxylic acid

Details

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Internal ID ff294818-01f4-4730-a861-10b09574b93d
Taxonomy Organoheterocyclic compounds > Bi- and oligothiophenes
IUPAC Name 5-thiophen-2-ylthiophene-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H6O2S2/c10-9(11)8-4-3-7(13-8)6-2-1-5-12-6/h1-5H,(H,10,11)
InChI Key PTNWHEHDBNNKEO-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C9H6O2S2
Molecular Weight 210.30 g/mol
Exact Mass 209.98092178 g/mol
Topological Polar Surface Area (TPSA) 93.80 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.17
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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2,2'-Bithiophene-5-carboxylic acid
[2,2'-Bithiophene]-5-carboxylic acid
5-thiophen-2-ylthiophene-2-carboxylic acid
2,2-Bithiophene-5-carboxylic acid
5-(thiophen-2-yl)thiophene-2-carboxylic acid
MFCD00159571
[2,2']Bithiophenyl-5-carboxylic acid
C9H6O2S2
[2,2'-Bithiophene]-5-carboxylicacid
2,2'-Bithiophene-5-CA
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'-Bithiophene-5-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 + 0.9930 99.30%
Caco-2 + 0.6869 68.69%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6784 67.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9605 96.05%
OATP1B3 inhibitior + 0.9398 93.98%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9017 90.17%
P-glycoprotein inhibitior - 0.9825 98.25%
P-glycoprotein substrate - 0.9865 98.65%
CYP3A4 substrate - 0.7302 73.02%
CYP2C9 substrate - 0.5896 58.96%
CYP2D6 substrate - 0.9006 90.06%
CYP3A4 inhibition - 0.9758 97.58%
CYP2C9 inhibition - 0.8671 86.71%
CYP2C19 inhibition - 0.8507 85.07%
CYP2D6 inhibition - 0.8877 88.77%
CYP1A2 inhibition - 0.8914 89.14%
CYP2C8 inhibition - 0.8496 84.96%
CYP inhibitory promiscuity - 0.8672 86.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6917 69.17%
Carcinogenicity (trinary) Non-required 0.5449 54.49%
Eye corrosion - 0.6807 68.07%
Eye irritation + 0.9833 98.33%
Skin irritation - 0.5235 52.35%
Skin corrosion - 0.9152 91.52%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8238 82.38%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.8625 86.25%
skin sensitisation - 0.6445 64.45%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6108 61.08%
Acute Oral Toxicity (c) III 0.5530 55.30%
Estrogen receptor binding - 0.5473 54.73%
Androgen receptor binding - 0.6278 62.78%
Thyroid receptor binding - 0.8074 80.74%
Glucocorticoid receptor binding + 0.5432 54.32%
Aromatase binding + 0.5380 53.80%
PPAR gamma + 0.6148 61.48%
Honey bee toxicity - 0.9816 98.16%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9065 90.65%

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
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 88.48% 85.30%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.31% 95.50%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.90% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.93% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.54% 95.56%
CHEMBL4578 Q14680 Maternal embryonic leucine zipper kinase 82.53% 81.58%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.46% 94.62%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.32% 81.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.26% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 80.09% 90.17%

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.
Echinops grijsii

Cross-Links

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PubChem 150965
LOTUS LTS0006021
wikiData Q83044704