3-(Methylthio)propanoic acid

Details

Top
Internal ID 522efd2f-6482-4bf7-8c68-a84e074f353b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Straight chain fatty acids
IUPAC Name 3-methylsulfanylpropanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C4H8O2S/c1-7-3-2-4(5)6/h2-3H2,1H3,(H,5,6)
InChI Key CAOMCZAIALVUPA-UHFFFAOYSA-N
Popularity 123 references in papers

Physical and Chemical Properties

Top
Molecular Formula C4H8O2S
Molecular Weight 120.17 g/mol
Exact Mass 120.02450067 g/mol
Topological Polar Surface Area (TPSA) 62.60 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.82
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
646-01-5
3-methylthiopropionate
4-Thiapentanoic acid
3-(Methylthio)propanoic acid
Propanoic acid, 3-(methylthio)-
3-methylsulfanylpropanoic acid
3-methylthiopropionic acid
3-(Methylsulfanyl)propanoic acid
Propanoic acid 3-(methylthio)-
Propionic acid, 3-(methylthio)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 3-(Methylthio)propanoic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.6266 62.66%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6288 62.88%
OATP2B1 inhibitior - 0.8458 84.58%
OATP1B1 inhibitior + 0.9146 91.46%
OATP1B3 inhibitior + 0.9132 91.32%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9384 93.84%
P-glycoprotein inhibitior - 0.9788 97.88%
P-glycoprotein substrate - 0.9834 98.34%
CYP3A4 substrate - 0.7492 74.92%
CYP2C9 substrate + 0.6329 63.29%
CYP2D6 substrate - 0.8641 86.41%
CYP3A4 inhibition - 0.9890 98.90%
CYP2C9 inhibition - 0.9627 96.27%
CYP2C19 inhibition - 0.9684 96.84%
CYP2D6 inhibition - 0.9588 95.88%
CYP1A2 inhibition - 0.7941 79.41%
CYP2C8 inhibition - 0.9838 98.38%
CYP inhibitory promiscuity - 0.9957 99.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6035 60.35%
Carcinogenicity (trinary) Non-required 0.7674 76.74%
Eye corrosion + 0.9797 97.97%
Eye irritation + 0.9749 97.49%
Skin irritation + 0.8641 86.41%
Skin corrosion + 0.9370 93.70%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8217 82.17%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.5717 57.17%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.7769 77.69%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.5647 56.47%
Acute Oral Toxicity (c) III 0.8316 83.16%
Estrogen receptor binding - 0.9181 91.81%
Androgen receptor binding - 0.9628 96.28%
Thyroid receptor binding - 0.9095 90.95%
Glucocorticoid receptor binding - 0.9405 94.05%
Aromatase binding - 0.9031 90.31%
PPAR gamma - 0.8724 87.24%
Honey bee toxicity - 0.9715 97.15%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.7299 72.99%

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
CHEMBL4040 P28482 MAP kinase ERK2 93.28% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.76% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.85% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.90% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 82.80% 90.17%

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.
There are no matching plants.

Cross-Links

Top
PubChem 563
LOTUS LTS0225227
wikiData Q27105456