2-Amino-3-(2-amino-2-carboxyethyl)sulfanylbutanoic acid

Details

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Internal ID d2af050c-4ba3-4936-835b-03aead7bfe86
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Cysteine and derivatives
IUPAC Name 2-amino-3-(2-amino-2-carboxyethyl)sulfanylbutanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H14N2O4S/c1-3(5(9)7(12)13)14-2-4(8)6(10)11/h3-5H,2,8-9H2,1H3,(H,10,11)(H,12,13)
InChI Key NSGOABPZARPCFM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H14N2O4S
Molecular Weight 222.26 g/mol
Exact Mass 222.06742811 g/mol
Topological Polar Surface Area (TPSA) 152.00 Ų
XlogP -5.90
Atomic LogP (AlogP) -1.07
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Amino-3-(2-amino-2-carboxyethyl)sulfanylbutanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8129 81.29%
Caco-2 - 0.9390 93.90%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.4552 45.52%
OATP2B1 inhibitior - 0.8603 86.03%
OATP1B1 inhibitior + 0.9525 95.25%
OATP1B3 inhibitior + 0.9482 94.82%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9506 95.06%
P-glycoprotein inhibitior - 0.9727 97.27%
P-glycoprotein substrate - 0.9562 95.62%
CYP3A4 substrate - 0.7071 70.71%
CYP2C9 substrate + 0.5973 59.73%
CYP2D6 substrate - 0.8334 83.34%
CYP3A4 inhibition - 0.8925 89.25%
CYP2C9 inhibition - 0.9299 92.99%
CYP2C19 inhibition - 0.9481 94.81%
CYP2D6 inhibition - 0.9524 95.24%
CYP1A2 inhibition - 0.8811 88.11%
CYP2C8 inhibition - 0.9816 98.16%
CYP inhibitory promiscuity - 0.9964 99.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.7584 75.84%
Eye corrosion - 0.9823 98.23%
Eye irritation - 0.6419 64.19%
Skin irritation - 0.7987 79.87%
Skin corrosion - 0.7365 73.65%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7456 74.56%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.9167 91.67%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6542 65.42%
Acute Oral Toxicity (c) III 0.6369 63.69%
Estrogen receptor binding - 0.7277 72.77%
Androgen receptor binding - 0.6237 62.37%
Thyroid receptor binding - 0.8230 82.30%
Glucocorticoid receptor binding - 0.7080 70.80%
Aromatase binding - 0.8767 87.67%
PPAR gamma - 0.8057 80.57%
Honey bee toxicity - 0.9499 94.99%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity + 0.6844 68.44%

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 96.80% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.65% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 88.14% 83.82%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 86.10% 92.29%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.63% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 82.74% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.68% 99.17%
CHEMBL226 P30542 Adenosine A1 receptor 81.44% 95.93%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.04% 96.95%

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 13894881
LOTUS LTS0201869
wikiData Q105185026