5-(5-Methylthiophen-2-yl)pent-2-en-4-ynyl acetate

Details

Top
Internal ID 07e6a43e-100a-4331-9a4a-79f7ccddfaaf
Taxonomy Organoheterocyclic compounds > Thiophenes > 2,5-disubstituted thiophenes
IUPAC Name 5-(5-methylthiophen-2-yl)pent-2-en-4-ynyl acetate
SMILES (Canonical) CC1=CC=C(S1)C#CC=CCOC(=O)C
SMILES (Isomeric) CC1=CC=C(S1)C#CC=CCOC(=O)C
InChI InChI=1S/C12H12O2S/c1-10-7-8-12(15-10)6-4-3-5-9-14-11(2)13/h3,5,7-8H,9H2,1-2H3
InChI Key JGEJBLJJKCJGQP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H12O2S
Molecular Weight 220.29 g/mol
Exact Mass 220.05580079 g/mol
Topological Polar Surface Area (TPSA) 54.50 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.53
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 5-(5-Methylthiophen-2-yl)pent-2-en-4-ynyl acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.6214 62.14%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6225 62.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9119 91.19%
OATP1B3 inhibitior + 0.9438 94.38%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5809 58.09%
P-glycoprotein inhibitior - 0.9816 98.16%
P-glycoprotein substrate - 0.9433 94.33%
CYP3A4 substrate - 0.5243 52.43%
CYP2C9 substrate + 0.6083 60.83%
CYP2D6 substrate - 0.8701 87.01%
CYP3A4 inhibition - 0.8198 81.98%
CYP2C9 inhibition - 0.6904 69.04%
CYP2C19 inhibition - 0.6572 65.72%
CYP2D6 inhibition - 0.8901 89.01%
CYP1A2 inhibition + 0.5263 52.63%
CYP2C8 inhibition - 0.8231 82.31%
CYP inhibitory promiscuity + 0.7318 73.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6917 69.17%
Carcinogenicity (trinary) Non-required 0.6156 61.56%
Eye corrosion - 0.5550 55.50%
Eye irritation - 0.5873 58.73%
Skin irritation + 0.5641 56.41%
Skin corrosion - 0.8767 87.67%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3952 39.52%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.7338 73.38%
skin sensitisation + 0.7100 71.00%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.5583 55.83%
Acute Oral Toxicity (c) III 0.7503 75.03%
Estrogen receptor binding - 0.6499 64.99%
Androgen receptor binding - 0.6321 63.21%
Thyroid receptor binding - 0.7587 75.87%
Glucocorticoid receptor binding - 0.4878 48.78%
Aromatase binding - 0.5565 55.65%
PPAR gamma - 0.6242 62.42%
Honey bee toxicity - 0.9207 92.07%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6555 65.55%
Fish aquatic toxicity + 0.9827 98.27%

Targets

Top

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 93.77% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.09% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.78% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 86.00% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.98% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.62% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.84% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.36% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.97% 96.00%
CHEMBL4208 P20618 Proteasome component C5 81.05% 90.00%
CHEMBL1951 P21397 Monoamine oxidase A 80.61% 91.49%
CHEMBL240 Q12809 HERG 80.16% 89.76%

Plants that contains it

Top
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.
Osmitopsis asteriscoides

Cross-Links

Top
PubChem 162988834
LOTUS LTS0052417
wikiData Q105127293