(E)-5-thiophen-2-ylpent-2-en-4-ynoic acid

Details

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Internal ID 7df3ae98-052e-414d-81ba-ff87d7c4fbc7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name (E)-5-thiophen-2-ylpent-2-en-4-ynoic acid
SMILES (Canonical) C1=CSC(=C1)C#CC=CC(=O)O
SMILES (Isomeric) C1=CSC(=C1)C#C/C=C/C(=O)O
InChI InChI=1S/C9H6O2S/c10-9(11)6-2-1-4-8-5-3-7-12-8/h2-3,5-7H,(H,10,11)/b6-2+
InChI Key WWGWQEVARVAMOV-QHHAFSJGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H6O2S
Molecular Weight 178.21 g/mol
Exact Mass 178.00885060 g/mol
Topological Polar Surface Area (TPSA) 65.50 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.74
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E)-5-thiophen-2-ylpent-2-en-4-ynoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9929 99.29%
Caco-2 - 0.5803 58.03%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Plasma membrane 0.5379 53.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9433 94.33%
OATP1B3 inhibitior + 0.9506 95.06%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8880 88.80%
P-glycoprotein inhibitior - 0.9798 97.98%
P-glycoprotein substrate - 0.9815 98.15%
CYP3A4 substrate - 0.6806 68.06%
CYP2C9 substrate - 0.5765 57.65%
CYP2D6 substrate - 0.8741 87.41%
CYP3A4 inhibition - 0.9447 94.47%
CYP2C9 inhibition - 0.8368 83.68%
CYP2C19 inhibition - 0.8443 84.43%
CYP2D6 inhibition - 0.9082 90.82%
CYP1A2 inhibition - 0.8565 85.65%
CYP2C8 inhibition - 0.8538 85.38%
CYP inhibitory promiscuity - 0.7617 76.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6417 64.17%
Carcinogenicity (trinary) Non-required 0.4432 44.32%
Eye corrosion + 0.8635 86.35%
Eye irritation + 0.9249 92.49%
Skin irritation + 0.6920 69.20%
Skin corrosion - 0.6333 63.33%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7902 79.02%
Micronuclear - 0.6700 67.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.6425 64.25%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.6818 68.18%
Acute Oral Toxicity (c) III 0.4739 47.39%
Estrogen receptor binding - 0.6896 68.96%
Androgen receptor binding - 0.7809 78.09%
Thyroid receptor binding - 0.6892 68.92%
Glucocorticoid receptor binding - 0.5665 56.65%
Aromatase binding + 0.5302 53.02%
PPAR gamma - 0.5228 52.28%
Honey bee toxicity - 0.9342 93.42%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9362 93.62%

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 91.51% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.02% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 88.13% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.63% 91.11%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 85.04% 94.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.62% 86.33%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 82.48% 94.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.40% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.62% 95.50%

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.
Chamaemelum fuscatum

Cross-Links

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PubChem 14454666
LOTUS LTS0180359
wikiData Q105314016