(R)-2-Isopropylamino-3-mercapto-propionic acid

Details

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Internal ID 1d3bd47c-be72-47b3-8176-f7646ed21670
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Cysteine and derivatives
IUPAC Name (2R)-2-(propan-2-ylamino)-3-sulfanylpropanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H13NO2S/c1-4(2)7-5(3-10)6(8)9/h4-5,7,10H,3H2,1-2H3,(H,8,9)/t5-/m0/s1
InChI Key AIFYCUKWFYJXJO-YFKPBYRVSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C6H13NO2S
Molecular Weight 163.24 g/mol
Exact Mass 163.06669983 g/mol
Topological Polar Surface Area (TPSA) 50.30 Ų
XlogP -1.80
Atomic LogP (AlogP) 0.37
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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SCHEMBL1058215
BDBM50109595
(R)-2-Isopropylamino-3-mercapto-propionic acid

2D Structure

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2D Structure of (R)-2-Isopropylamino-3-mercapto-propionic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9753 97.53%
Caco-2 - 0.9186 91.86%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Lysosomes 0.6569 65.69%
OATP2B1 inhibitior - 0.8332 83.32%
OATP1B1 inhibitior + 0.9377 93.77%
OATP1B3 inhibitior + 0.9395 93.95%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9141 91.41%
P-glycoprotein inhibitior - 0.9800 98.00%
P-glycoprotein substrate - 0.9793 97.93%
CYP3A4 substrate - 0.7457 74.57%
CYP2C9 substrate + 0.6063 60.63%
CYP2D6 substrate - 0.8077 80.77%
CYP3A4 inhibition - 0.9630 96.30%
CYP2C9 inhibition - 0.9231 92.31%
CYP2C19 inhibition - 0.9544 95.44%
CYP2D6 inhibition - 0.9302 93.02%
CYP1A2 inhibition - 0.8500 85.00%
CYP2C8 inhibition - 0.9954 99.54%
CYP inhibitory promiscuity - 0.9803 98.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.7287 72.87%
Eye corrosion - 0.9395 93.95%
Eye irritation - 0.7109 71.09%
Skin irritation - 0.6270 62.70%
Skin corrosion - 0.6653 66.53%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8817 88.17%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.5056 50.56%
skin sensitisation - 0.8901 89.01%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.7721 77.21%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.7494 74.94%
Acute Oral Toxicity (c) III 0.7722 77.22%
Estrogen receptor binding - 0.9020 90.20%
Androgen receptor binding - 0.8516 85.16%
Thyroid receptor binding - 0.9061 90.61%
Glucocorticoid receptor binding - 0.9170 91.70%
Aromatase binding - 0.8534 85.34%
PPAR gamma - 0.6610 66.10%
Honey bee toxicity - 0.9612 96.12%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity - 0.8245 82.45%

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
CHEMBL2581 P07339 Cathepsin D 92.47% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 91.69% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.92% 96.09%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 89.63% 100.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 87.10% 96.47%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.08% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.55% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.16% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.23% 94.45%

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.
Allium cepa

Cross-Links

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PubChem 11062712
LOTUS LTS0027821
wikiData Q104912742