5-(4-Isovaleryloxy-1-butynyl)-2,2'-bithiophene

Details

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Internal ID 24c78425-0902-456a-84bb-a872ec0af33d
Taxonomy Organoheterocyclic compounds > Bi- and oligothiophenes
IUPAC Name 4-(5-thiophen-2-ylthiophen-2-yl)but-3-ynyl 3-methylbutanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H18O2S2/c1-13(2)12-17(18)19-10-4-3-6-14-8-9-16(21-14)15-7-5-11-20-15/h5,7-9,11,13H,4,10,12H2,1-2H3
InChI Key APLQBKOCISXZRF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18O2S2
Molecular Weight 318.50 g/mol
Exact Mass 318.07482216 g/mol
Topological Polar Surface Area (TPSA) 82.80 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.81
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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CHEMBL2252905
APLQBKOCISXZRF-UHFFFAOYSA-N
5-(4-isovaleryloxy-1-butynyl)-2,2'-bithiophene

2D Structure

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2D Structure of 5-(4-Isovaleryloxy-1-butynyl)-2,2'-bithiophene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.5143 51.43%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7949 79.49%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.8853 88.53%
OATP1B3 inhibitior + 0.9334 93.34%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5460 54.60%
P-glycoprotein inhibitior - 0.7584 75.84%
P-glycoprotein substrate - 0.8498 84.98%
CYP3A4 substrate + 0.5320 53.20%
CYP2C9 substrate - 0.7846 78.46%
CYP2D6 substrate - 0.8486 84.86%
CYP3A4 inhibition - 0.9193 91.93%
CYP2C9 inhibition - 0.6321 63.21%
CYP2C19 inhibition - 0.5664 56.64%
CYP2D6 inhibition - 0.8703 87.03%
CYP1A2 inhibition - 0.5866 58.66%
CYP2C8 inhibition - 0.6255 62.55%
CYP inhibitory promiscuity + 0.5745 57.45%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.5971 59.71%
Eye corrosion - 0.8781 87.81%
Eye irritation - 0.8613 86.13%
Skin irritation - 0.8286 82.86%
Skin corrosion - 0.9568 95.68%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8291 82.91%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.5910 59.10%
skin sensitisation - 0.6246 62.46%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.5053 50.53%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.6451 64.51%
Acute Oral Toxicity (c) III 0.5907 59.07%
Estrogen receptor binding + 0.5579 55.79%
Androgen receptor binding + 0.6325 63.25%
Thyroid receptor binding + 0.5533 55.33%
Glucocorticoid receptor binding - 0.5740 57.40%
Aromatase binding + 0.6244 62.44%
PPAR gamma - 0.6917 69.17%
Honey bee toxicity - 0.9340 93.40%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5650 56.50%
Fish aquatic toxicity + 0.9923 99.23%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.60% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.52% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 93.27% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.34% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.53% 91.11%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 88.48% 92.95%
CHEMBL3401 O75469 Pregnane X receptor 87.14% 94.73%
CHEMBL226 P30542 Adenosine A1 receptor 85.85% 95.93%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.38% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.91% 86.33%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.07% 100.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.61% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.13% 99.17%
CHEMBL4208 P20618 Proteasome component C5 81.88% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.17% 95.56%

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 ritro

Cross-Links

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PubChem 9840009
NPASS NPC80036
LOTUS LTS0234148
wikiData Q104916394