(2R)-2-(propan-2-ylsulfanylamino)-3-sulfanylpropanoic acid

Details

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Internal ID 128e40f4-ea2f-444c-bb81-f5ce6260abbe
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Cysteine and derivatives
IUPAC Name (2R)-2-(propan-2-ylsulfanylamino)-3-sulfanylpropanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H13NO2S2/c1-4(2)11-7-5(3-10)6(8)9/h4-5,7,10H,3H2,1-2H3,(H,8,9)/t5-/m0/s1
InChI Key IIZXHUBOMBDZGJ-YFKPBYRVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C6H13NO2S2
Molecular Weight 195.30 g/mol
Exact Mass 195.03877100 g/mol
Topological Polar Surface Area (TPSA) 75.60 Ų
XlogP -1.30
Atomic LogP (AlogP) 1.02
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R)-2-(propan-2-ylsulfanylamino)-3-sulfanylpropanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9767 97.67%
Caco-2 - 0.9185 91.85%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Lysosomes 0.5095 50.95%
OATP2B1 inhibitior - 0.8524 85.24%
OATP1B1 inhibitior + 0.9257 92.57%
OATP1B3 inhibitior + 0.9407 94.07%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9550 95.50%
P-glycoprotein inhibitior - 0.9776 97.76%
P-glycoprotein substrate - 0.9395 93.95%
CYP3A4 substrate - 0.7115 71.15%
CYP2C9 substrate + 0.6165 61.65%
CYP2D6 substrate - 0.8901 89.01%
CYP3A4 inhibition - 0.9274 92.74%
CYP2C9 inhibition - 0.8339 83.39%
CYP2C19 inhibition - 0.8550 85.50%
CYP2D6 inhibition - 0.8993 89.93%
CYP1A2 inhibition - 0.7381 73.81%
CYP2C8 inhibition - 0.9881 98.81%
CYP inhibitory promiscuity - 0.9639 96.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.6737 67.37%
Eye corrosion - 0.9601 96.01%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.6635 66.35%
Skin corrosion - 0.8050 80.50%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7973 79.73%
Micronuclear + 0.6200 62.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.8691 86.91%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.5568 55.68%
Acute Oral Toxicity (c) III 0.6771 67.71%
Estrogen receptor binding - 0.8168 81.68%
Androgen receptor binding - 0.8050 80.50%
Thyroid receptor binding - 0.7797 77.97%
Glucocorticoid receptor binding - 0.8233 82.33%
Aromatase binding - 0.8385 83.85%
PPAR gamma - 0.8706 87.06%
Honey bee toxicity - 0.9454 94.54%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity - 0.5953 59.53%

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
CHEMBL4040 P28482 MAP kinase ERK2 94.89% 83.82%
CHEMBL2581 P07339 Cathepsin D 91.97% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.90% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 89.80% 90.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 88.62% 100.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 86.64% 96.47%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.39% 99.17%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 85.37% 92.29%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.48% 93.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.09% 85.14%

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 53918855
LOTUS LTS0238834
wikiData Q105113853