(E)-5-(5-but-3-en-1-ynylthiophen-2-yl)pent-2-en-4-ynal

Details

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Internal ID 0cf316f1-c2ff-4fa4-a817-8eaae42985e8
Taxonomy Organoheterocyclic compounds > Thiophenes > 2,5-disubstituted thiophenes
IUPAC Name (E)-5-(5-but-3-en-1-ynylthiophen-2-yl)pent-2-en-4-ynal
SMILES (Canonical) C=CC#CC1=CC=C(S1)C#CC=CC=O
SMILES (Isomeric) C=CC#CC1=CC=C(S1)C#C/C=C/C=O
InChI InChI=1S/C13H8OS/c1-2-3-7-12-9-10-13(15-12)8-5-4-6-11-14/h2,4,6,9-11H,1H2/b6-4+
InChI Key FTPBGNZLXXGRQB-GQCTYLIASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H8OS
Molecular Weight 212.27 g/mol
Exact Mass 212.02958605 g/mol
Topological Polar Surface Area (TPSA) 45.30 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.39
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E)-5-(5-but-3-en-1-ynylthiophen-2-yl)pent-2-en-4-ynal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9931 99.31%
Caco-2 + 0.6734 67.34%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Plasma membrane 0.3682 36.82%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9315 93.15%
OATP1B3 inhibitior + 0.9538 95.38%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7346 73.46%
P-glycoprotein inhibitior - 0.9248 92.48%
P-glycoprotein substrate - 0.9565 95.65%
CYP3A4 substrate - 0.6057 60.57%
CYP2C9 substrate + 0.8028 80.28%
CYP2D6 substrate - 0.8350 83.50%
CYP3A4 inhibition - 0.8737 87.37%
CYP2C9 inhibition - 0.6972 69.72%
CYP2C19 inhibition + 0.5396 53.96%
CYP2D6 inhibition - 0.8743 87.43%
CYP1A2 inhibition - 0.5639 56.39%
CYP2C8 inhibition - 0.8644 86.44%
CYP inhibitory promiscuity + 0.7317 73.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6217 62.17%
Carcinogenicity (trinary) Danger 0.3845 38.45%
Eye corrosion + 0.9302 93.02%
Eye irritation + 0.7523 75.23%
Skin irritation + 0.6956 69.56%
Skin corrosion + 0.5441 54.41%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7162 71.62%
Micronuclear - 0.5100 51.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.8315 83.15%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.5761 57.61%
Acute Oral Toxicity (c) III 0.6075 60.75%
Estrogen receptor binding + 0.5352 53.52%
Androgen receptor binding - 0.5489 54.89%
Thyroid receptor binding - 0.5175 51.75%
Glucocorticoid receptor binding + 0.5943 59.43%
Aromatase binding + 0.7865 78.65%
PPAR gamma + 0.6877 68.77%
Honey bee toxicity - 0.7512 75.12%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9606 96.06%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.00% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 86.31% 91.49%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.23% 93.40%
CHEMBL4578 Q14680 Maternal embryonic leucine zipper kinase 84.08% 81.58%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.51% 91.11%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 83.04% 96.42%
CHEMBL3401 O75469 Pregnane X receptor 81.24% 94.73%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 80.55% 82.05%

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.
Lepidaploa cotoneaster

Cross-Links

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PubChem 101415941
LOTUS LTS0083734
wikiData Q105001187