(4Z,6E)-9-thiophen-2-ylnona-4,6-dien-8-yn-3-one

Details

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Internal ID 980b06b7-8702-411f-8f27-f3c64a81c156
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name (4Z,6E)-9-thiophen-2-ylnona-4,6-dien-8-yn-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H12OS/c1-2-12(14)8-5-3-4-6-9-13-10-7-11-15-13/h3-5,7-8,10-11H,2H2,1H3/b4-3+,8-5-
InChI Key ORPQKHRFJCPNBE-LHOHZTISSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12OS
Molecular Weight 216.30 g/mol
Exact Mass 216.06088618 g/mol
Topological Polar Surface Area (TPSA) 45.30 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.19
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4Z,6E)-9-thiophen-2-ylnona-4,6-dien-8-yn-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.6020 60.20%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Plasma membrane 0.4084 40.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9024 90.24%
OATP1B3 inhibitior + 0.9544 95.44%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5064 50.64%
P-glycoprotein inhibitior - 0.9672 96.72%
P-glycoprotein substrate - 0.9217 92.17%
CYP3A4 substrate - 0.5678 56.78%
CYP2C9 substrate - 0.6019 60.19%
CYP2D6 substrate - 0.8516 85.16%
CYP3A4 inhibition - 0.8780 87.80%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.6474 64.74%
CYP2D6 inhibition - 0.8763 87.63%
CYP1A2 inhibition + 0.6216 62.16%
CYP2C8 inhibition - 0.7018 70.18%
CYP inhibitory promiscuity + 0.8755 87.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.3735 37.35%
Eye corrosion + 0.5871 58.71%
Eye irritation + 0.8238 82.38%
Skin irritation + 0.6103 61.03%
Skin corrosion - 0.7421 74.21%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4606 46.06%
Micronuclear - 0.7300 73.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.8362 83.62%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.7999 79.99%
Acute Oral Toxicity (c) III 0.8023 80.23%
Estrogen receptor binding - 0.5333 53.33%
Androgen receptor binding - 0.7131 71.31%
Thyroid receptor binding - 0.6315 63.15%
Glucocorticoid receptor binding + 0.5853 58.53%
Aromatase binding + 0.6631 66.31%
PPAR gamma - 0.7460 74.60%
Honey bee toxicity - 0.9500 95.00%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.7856 78.56%

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
CHEMBL221 P23219 Cyclooxygenase-1 95.19% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.99% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.72% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.86% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.87% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.62% 86.33%
CHEMBL226 P30542 Adenosine A1 receptor 81.98% 95.93%
CHEMBL3401 O75469 Pregnane X receptor 81.81% 94.73%
CHEMBL4208 P20618 Proteasome component C5 80.51% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.27% 96.00%

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.
Cota tinctoria

Cross-Links

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PubChem 101416675
LOTUS LTS0048707
wikiData Q105198142