2-Butyl-5-propan-2-ylthiophene

Details

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Internal ID faa66dce-37f0-41f6-a5de-30bd2f5529f7
Taxonomy Organoheterocyclic compounds > Thiophenes > 2,5-disubstituted thiophenes
IUPAC Name 2-butyl-5-propan-2-ylthiophene
SMILES (Canonical) CCCCC1=CC=C(S1)C(C)C
SMILES (Isomeric) CCCCC1=CC=C(S1)C(C)C
InChI InChI=1S/C11H18S/c1-4-5-6-10-7-8-11(12-10)9(2)3/h7-9H,4-6H2,1-3H3
InChI Key UNXLEMAVNRUZHN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18S
Molecular Weight 182.33 g/mol
Exact Mass 182.11292175 g/mol
Topological Polar Surface Area (TPSA) 28.20 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.21
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Butyl-5-propan-2-ylthiophene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 + 0.8490 84.90%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.3410 34.10%
OATP2B1 inhibitior - 0.8558 85.58%
OATP1B1 inhibitior + 0.9026 90.26%
OATP1B3 inhibitior + 0.9488 94.88%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8954 89.54%
P-glycoprotein inhibitior - 0.9677 96.77%
P-glycoprotein substrate - 0.8454 84.54%
CYP3A4 substrate - 0.6350 63.50%
CYP2C9 substrate - 0.6092 60.92%
CYP2D6 substrate - 0.6859 68.59%
CYP3A4 inhibition - 0.9505 95.05%
CYP2C9 inhibition - 0.6626 66.26%
CYP2C19 inhibition - 0.6276 62.76%
CYP2D6 inhibition - 0.8149 81.49%
CYP1A2 inhibition - 0.5374 53.74%
CYP2C8 inhibition - 0.8319 83.19%
CYP inhibitory promiscuity + 0.5681 56.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.4520 45.20%
Eye corrosion + 0.5370 53.70%
Eye irritation + 0.6645 66.45%
Skin irritation + 0.5464 54.64%
Skin corrosion - 0.9097 90.97%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4621 46.21%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation + 0.8141 81.41%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.5167 51.67%
Acute Oral Toxicity (c) III 0.7415 74.15%
Estrogen receptor binding - 0.9133 91.33%
Androgen receptor binding - 0.5430 54.30%
Thyroid receptor binding - 0.7206 72.06%
Glucocorticoid receptor binding - 0.7676 76.76%
Aromatase binding - 0.8719 87.19%
PPAR gamma - 0.8743 87.43%
Honey bee toxicity - 0.9832 98.32%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9743 97.43%

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 97.11% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 93.19% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.28% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.71% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 89.21% 94.73%
CHEMBL255 P29275 Adenosine A2b receptor 89.09% 98.59%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 88.40% 95.00%
CHEMBL226 P30542 Adenosine A1 receptor 85.98% 95.93%
CHEMBL1907 P15144 Aminopeptidase N 85.04% 93.31%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 82.85% 92.08%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.10% 90.71%

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.
Basella alba

Cross-Links

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PubChem 23057999
LOTUS LTS0003910
wikiData Q105276198