5-Methylsulfanyl-1-phenylpent-4-en-2-yn-1-one

Details

Top
Internal ID 8d31518d-d8d8-42f3-bf46-fa69744c85df
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoyl derivatives
IUPAC Name 5-methylsulfanyl-1-phenylpent-4-en-2-yn-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H10OS/c1-14-10-6-5-9-12(13)11-7-3-2-4-8-11/h2-4,6-8,10H,1H3
InChI Key FVLHLTHPRFIJEO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H10OS
Molecular Weight 202.27 g/mol
Exact Mass 202.04523611 g/mol
Topological Polar Surface Area (TPSA) 42.40 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.75
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 5-Methylsulfanyl-1-phenylpent-4-en-2-yn-1-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9953 99.53%
Caco-2 + 0.8837 88.37%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5035 50.35%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8995 89.95%
OATP1B3 inhibitior + 0.9703 97.03%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7954 79.54%
P-glycoprotein inhibitior - 0.9530 95.30%
P-glycoprotein substrate - 0.9703 97.03%
CYP3A4 substrate - 0.6667 66.67%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.7760 77.60%
CYP3A4 inhibition - 0.9465 94.65%
CYP2C9 inhibition - 0.7848 78.48%
CYP2C19 inhibition - 0.6572 65.72%
CYP2D6 inhibition - 0.9589 95.89%
CYP1A2 inhibition + 0.7018 70.18%
CYP2C8 inhibition - 0.6989 69.89%
CYP inhibitory promiscuity + 0.5384 53.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5366 53.66%
Carcinogenicity (trinary) Non-required 0.6539 65.39%
Eye corrosion + 0.8687 86.87%
Eye irritation + 0.9472 94.72%
Skin irritation + 0.8385 83.85%
Skin corrosion - 0.5821 58.21%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8498 84.98%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.5177 51.77%
skin sensitisation + 0.9425 94.25%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.5807 58.07%
Acute Oral Toxicity (c) II 0.4651 46.51%
Estrogen receptor binding - 0.5233 52.33%
Androgen receptor binding - 0.7959 79.59%
Thyroid receptor binding - 0.5734 57.34%
Glucocorticoid receptor binding - 0.7130 71.30%
Aromatase binding + 0.7645 76.45%
PPAR gamma - 0.5821 58.21%
Honey bee toxicity - 0.9182 91.82%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.8293 82.93%

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
CHEMBL221 P23219 Cyclooxygenase-1 95.53% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.24% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.87% 86.33%
CHEMBL4208 P20618 Proteasome component C5 82.26% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.13% 96.00%
CHEMBL2581 P07339 Cathepsin D 81.87% 98.95%
CHEMBL2535 P11166 Glucose transporter 81.42% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.42% 99.17%
CHEMBL5028 O14672 ADAM10 80.37% 97.50%

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.
Glebionis coronaria
Ismelia carinata

Cross-Links

Top
PubChem 140034686
LOTUS LTS0045425
wikiData Q105002529