2-Propynal, 3-(2-thienyl)-

Details

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Internal ID 848e469e-9741-43ff-852e-aeaea7ab718c
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 3-thiophen-2-ylprop-2-ynal
SMILES (Canonical) C1=CSC(=C1)C#CC=O
SMILES (Isomeric) C1=CSC(=C1)C#CC=O
InChI InChI=1S/C7H4OS/c8-5-1-3-7-4-2-6-9-7/h2,4-6H
InChI Key UAYNIWKGZIESFI-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C7H4OS
Molecular Weight 136.17 g/mol
Exact Mass 135.99828592 g/mol
Topological Polar Surface Area (TPSA) 45.30 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.30
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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13781-33-4
3-(2-Thienyl)propynal
SCHEMBL3834463
DTXSID10415787
AKOS006373708

2D Structure

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2D Structure of 2-Propynal, 3-(2-thienyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.7955 79.55%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.4912 49.12%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9328 93.28%
OATP1B3 inhibitior + 0.9585 95.85%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9323 93.23%
P-glycoprotein inhibitior - 0.9815 98.15%
P-glycoprotein substrate - 0.9843 98.43%
CYP3A4 substrate - 0.7164 71.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8000 80.00%
CYP3A4 inhibition - 0.9505 95.05%
CYP2C9 inhibition - 0.7384 73.84%
CYP2C19 inhibition - 0.5612 56.12%
CYP2D6 inhibition - 0.8525 85.25%
CYP1A2 inhibition - 0.5506 55.06%
CYP2C8 inhibition - 0.9384 93.84%
CYP inhibitory promiscuity + 0.6185 61.85%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6317 63.17%
Carcinogenicity (trinary) Danger 0.3871 38.71%
Eye corrosion + 0.9618 96.18%
Eye irritation + 0.9450 94.50%
Skin irritation + 0.7765 77.65%
Skin corrosion - 0.5000 50.00%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5609 56.09%
Micronuclear + 0.5900 59.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.7743 77.43%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.4636 46.36%
Acute Oral Toxicity (c) III 0.7290 72.90%
Estrogen receptor binding - 0.8110 81.10%
Androgen receptor binding - 0.8759 87.59%
Thyroid receptor binding - 0.7589 75.89%
Glucocorticoid receptor binding - 0.6014 60.14%
Aromatase binding - 0.6000 60.00%
PPAR gamma - 0.6565 65.65%
Honey bee toxicity - 0.8668 86.68%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.7904 79.04%

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 91.21% 95.56%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 84.33% 85.30%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 83.78% 96.42%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.10% 94.62%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 80.98% 94.23%
CHEMBL4578 Q14680 Maternal embryonic leucine zipper kinase 80.29% 81.58%

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.
Achillea millefolium

Cross-Links

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PubChem 5321944
NPASS NPC42579