3-Mercaptopropionic acid

Details

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Internal ID 2f07d13e-07d9-473f-a4a4-b8659f6b0336
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acids
IUPAC Name 3-sulfanylpropanoic acid
SMILES (Canonical) C(CS)C(=O)O
SMILES (Isomeric) C(CS)C(=O)O
InChI InChI=1S/C3H6O2S/c4-3(5)1-2-6/h6H,1-2H2,(H,4,5)
InChI Key DKIDEFUBRARXTE-UHFFFAOYSA-N
Popularity 2,384 references in papers

Physical and Chemical Properties

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Molecular Formula C3H6O2S
Molecular Weight 106.15 g/mol
Exact Mass 106.00885060 g/mol
Topological Polar Surface Area (TPSA) 38.30 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.39
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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107-96-0
3-Mercaptopropanoic acid
3-Sulfanylpropanoic acid
3-Thiopropionic acid
3-Thiopropanoic acid
beta-Mercaptopropionic acid
Mercaptopropionic acid
Propanoic acid, 3-mercapto-
3MPA
2-Mercaptoethanecarboxylic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Mercaptopropionic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9387 93.87%
Caco-2 - 0.5795 57.95%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6613 66.13%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9451 94.51%
OATP1B3 inhibitior + 0.9407 94.07%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9432 94.32%
P-glycoprotein inhibitior - 0.9850 98.50%
P-glycoprotein substrate - 0.9946 99.46%
CYP3A4 substrate - 0.8038 80.38%
CYP2C9 substrate + 0.8121 81.21%
CYP2D6 substrate - 0.8574 85.74%
CYP3A4 inhibition - 0.9577 95.77%
CYP2C9 inhibition - 0.9300 93.00%
CYP2C19 inhibition - 0.9679 96.79%
CYP2D6 inhibition - 0.9600 96.00%
CYP1A2 inhibition - 0.7736 77.36%
CYP2C8 inhibition - 0.9938 99.38%
CYP inhibitory promiscuity - 0.9689 96.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7020 70.20%
Carcinogenicity (trinary) Non-required 0.7346 73.46%
Eye corrosion + 0.8308 83.08%
Eye irritation + 0.9583 95.83%
Skin irritation + 0.8026 80.26%
Skin corrosion + 0.9671 96.71%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8191 81.91%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation + 0.6316 63.16%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.7508 75.08%
Acute Oral Toxicity (c) II 0.7558 75.58%
Estrogen receptor binding - 0.9368 93.68%
Androgen receptor binding - 0.9559 95.59%
Thyroid receptor binding - 0.9084 90.84%
Glucocorticoid receptor binding - 0.9042 90.42%
Aromatase binding - 0.8899 88.99%
PPAR gamma - 0.8310 83.10%
Honey bee toxicity - 0.9540 95.40%
Biodegradation + 0.9750 97.50%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity - 0.9207 92.07%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.53% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 85.13% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 81.41% 90.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 6514
LOTUS LTS0220146
wikiData Q11751618