gamma-GLUTAMYL-S-ALLYLCYSTEINE

Details

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Internal ID ee70d40a-bcf8-4830-8210-fe622709fabc
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Dipeptides
IUPAC Name (2S)-2-amino-5-[[(1R)-1-carboxy-2-prop-2-enylsulfanylethyl]amino]-5-oxopentanoic acid
SMILES (Canonical) C=CCSCC(C(=O)O)NC(=O)CCC(C(=O)O)N
SMILES (Isomeric) C=CCSC[C@@H](C(=O)O)NC(=O)CC[C@@H](C(=O)O)N
InChI InChI=1S/C11H18N2O5S/c1-2-5-19-6-8(11(17)18)13-9(14)4-3-7(12)10(15)16/h2,7-8H,1,3-6,12H2,(H,13,14)(H,15,16)(H,17,18)/t7-,8-/m0/s1
InChI Key FUTHBNRZCFKVQZ-YUMQZZPRSA-N
Popularity 59 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18N2O5S
Molecular Weight 290.34 g/mol
Exact Mass 290.09364285 g/mol
Topological Polar Surface Area (TPSA) 155.00 Ų
XlogP -2.80
Atomic LogP (AlogP) -0.33
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 10

Synonyms

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91216-95-4
UNII-1O5QGM20NB
1O5QGM20NB
gamma-Glutamyl-S-2-propenylcysteine
gamma-Glutamyl-S-prop-2-en-1-ylcysteine
Glutamine, N-(2-(allylthio)-1-carboxyethyl)-, L-
GAMMA-GLUTAMYL-
L-Cysteine, L-gamma-glutamyl-S-2-propenyl-
L-gamma-Glutamyl-(S)-Allyl-Cysteine
(2S)-2-amino-5-[[(1R)-1-carboxy-2-prop-2-enylsulfanylethyl]amino]-5-oxopentanoic 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 gamma-GLUTAMYL-S-ALLYLCYSTEINE

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6702 67.02%
Caco-2 - 0.9251 92.51%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7171 71.71%
OATP2B1 inhibitior - 0.8554 85.54%
OATP1B1 inhibitior + 0.9004 90.04%
OATP1B3 inhibitior + 0.9450 94.50%
MATE1 inhibitior - 0.9031 90.31%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8881 88.81%
P-glycoprotein inhibitior - 0.9368 93.68%
P-glycoprotein substrate - 0.9189 91.89%
CYP3A4 substrate - 0.5595 55.95%
CYP2C9 substrate - 0.6211 62.11%
CYP2D6 substrate - 0.8054 80.54%
CYP3A4 inhibition - 0.7495 74.95%
CYP2C9 inhibition - 0.9043 90.43%
CYP2C19 inhibition - 0.9045 90.45%
CYP2D6 inhibition - 0.9295 92.95%
CYP1A2 inhibition - 0.9150 91.50%
CYP2C8 inhibition - 0.8827 88.27%
CYP inhibitory promiscuity - 0.9952 99.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6253 62.53%
Eye corrosion - 0.9771 97.71%
Eye irritation - 0.9886 98.86%
Skin irritation - 0.8126 81.26%
Skin corrosion - 0.9167 91.67%
Ames mutagenesis - 0.5178 51.78%
Human Ether-a-go-go-Related Gene inhibition - 0.6812 68.12%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.5052 50.52%
skin sensitisation - 0.9054 90.54%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.7980 79.80%
Acute Oral Toxicity (c) III 0.7099 70.99%
Estrogen receptor binding + 0.6301 63.01%
Androgen receptor binding - 0.8257 82.57%
Thyroid receptor binding - 0.5827 58.27%
Glucocorticoid receptor binding + 0.6173 61.73%
Aromatase binding - 0.6892 68.92%
PPAR gamma + 0.7845 78.45%
Honey bee toxicity - 0.8274 82.74%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.5231 52.31%

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 97.14% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.64% 99.17%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 96.40% 92.29%
CHEMBL236 P41143 Delta opioid receptor 94.28% 99.35%
CHEMBL221 P23219 Cyclooxygenase-1 91.57% 90.17%
CHEMBL2581 P07339 Cathepsin D 91.26% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 89.71% 91.19%
CHEMBL1255126 O15151 Protein Mdm4 89.14% 90.20%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.35% 96.09%
CHEMBL233 P35372 Mu opioid receptor 87.91% 97.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.65% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.94% 94.45%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 86.55% 100.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.94% 89.34%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 83.65% 96.00%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 83.46% 82.05%
CHEMBL2413 P32246 C-C chemokine receptor type 1 83.15% 89.50%
CHEMBL226 P30542 Adenosine A1 receptor 82.04% 95.93%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.01% 96.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 81.92% 95.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.85% 97.21%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.52% 90.71%

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 sativum
Aniba megaphylla
Berberis integerrima
Calocedrus decurrens
Digitalis sceptrum
Herbertus sakuraii
Nauclea latifolia
Orthopappus angustifolius
Scurrula parasitica

Cross-Links

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PubChem 11346811
NPASS NPC51920
LOTUS LTS0055613
wikiData Q27252677