S-propyl thioacetate

Details

Top
Internal ID a85ecc03-5c80-490e-a312-905ecade27b5
Taxonomy Organic acids and derivatives > Thiocarboxylic acids and derivatives > Thioesters
IUPAC Name S-propyl ethanethioate
SMILES (Canonical) CCCSC(=O)C
SMILES (Isomeric) CCCSC(=O)C
InChI InChI=1S/C5H10OS/c1-3-4-7-5(2)6/h3-4H2,1-2H3
InChI Key SBWFWBJCYMBZEY-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

Top
Molecular Formula C5H10OS
Molecular Weight 118.20 g/mol
Exact Mass 118.04523611 g/mol
Topological Polar Surface Area (TPSA) 42.40 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.68
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
S-N-PROPYL THIOACETATE
Ethanethioic acid, S-propyl ester
Propyl thioacetate
S-N-Propylthioacetate
FEMA No. 3385
1-(propylsulfanyl)ethan-1-one
UNII-Y7284NZ6EP
N-PROPYL THIO ACETATE
Y7284NZ6EP
EINECS 218-984-7
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of S-propyl thioacetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.7624 76.24%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4811 48.11%
OATP2B1 inhibitior - 0.8480 84.80%
OATP1B1 inhibitior + 0.9532 95.32%
OATP1B3 inhibitior + 0.9387 93.87%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9128 91.28%
P-glycoprotein inhibitior - 0.9805 98.05%
P-glycoprotein substrate - 0.9743 97.43%
CYP3A4 substrate - 0.7454 74.54%
CYP2C9 substrate - 0.6084 60.84%
CYP2D6 substrate - 0.8528 85.28%
CYP3A4 inhibition - 0.9855 98.55%
CYP2C9 inhibition - 0.8817 88.17%
CYP2C19 inhibition - 0.9004 90.04%
CYP2D6 inhibition - 0.9322 93.22%
CYP1A2 inhibition - 0.5393 53.93%
CYP2C8 inhibition - 0.9875 98.75%
CYP inhibitory promiscuity - 0.8645 86.45%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.7144 71.44%
Eye corrosion + 0.9863 98.63%
Eye irritation + 0.9623 96.23%
Skin irritation + 0.7667 76.67%
Skin corrosion - 0.7369 73.69%
Ames mutagenesis - 0.7170 71.70%
Human Ether-a-go-go-Related Gene inhibition - 0.7987 79.87%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.9420 94.20%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.7267 72.67%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.5644 56.44%
Acute Oral Toxicity (c) III 0.8142 81.42%
Estrogen receptor binding - 0.9378 93.78%
Androgen receptor binding - 0.9496 94.96%
Thyroid receptor binding - 0.8551 85.51%
Glucocorticoid receptor binding - 0.9324 93.24%
Aromatase binding - 0.9295 92.95%
PPAR gamma - 0.8673 86.73%
Honey bee toxicity - 0.9777 97.77%
Biodegradation + 0.9750 97.50%
Crustacea aquatic toxicity - 0.8232 82.32%
Fish aquatic toxicity + 0.8892 88.92%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.15% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.34% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.08% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.14% 99.17%

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.
Allium cepa

Cross-Links

Top
PubChem 61295
NPASS NPC176510
LOTUS LTS0234460
wikiData Q27294326