gamma-Glutamylaspartic acid

Details

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Internal ID a2bd32ee-b5d6-4158-ba8d-92bb13ab2507
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Dipeptides
IUPAC Name (2S)-2-[[(4S)-4-amino-4-carboxybutanoyl]amino]butanedioic acid
SMILES (Canonical) C(CC(=O)NC(CC(=O)O)C(=O)O)C(C(=O)O)N
SMILES (Isomeric) C(CC(=O)N[C@@H](CC(=O)O)C(=O)O)[C@@H](C(=O)O)N
InChI InChI=1S/C9H14N2O7/c10-4(8(15)16)1-2-6(12)11-5(9(17)18)3-7(13)14/h4-5H,1-3,10H2,(H,11,12)(H,13,14)(H,15,16)(H,17,18)/t4-,5-/m0/s1
InChI Key JTJZAUVWVBUZAU-WHFBIAKZSA-N
Popularity 24 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14N2O7
Molecular Weight 262.22 g/mol
Exact Mass 262.08010079 g/mol
Topological Polar Surface Area (TPSA) 167.00 Ų
XlogP -4.60
Atomic LogP (AlogP) -1.78
H-Bond Acceptor 5
H-Bond Donor 5
Rotatable Bonds 8

Synonyms

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gamma-Glutamylaspartic acid
gamma-Glu-asp
16804-55-0
LGLA
(2S)-2-[[(4S)-4-amino-4-carboxybutanoyl]amino]butanedioic acid
SCHEMBL6021265
gamma-l-glutamyl-l-aspartic acid
DTXSID60937429
CHEBI:169907
N-L-gamma-Glutamyl-L-aspartic 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-Glutamylaspartic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7600 76.00%
Caco-2 - 0.9464 94.64%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7124 71.24%
OATP2B1 inhibitior - 0.8538 85.38%
OATP1B1 inhibitior + 0.9454 94.54%
OATP1B3 inhibitior + 0.9445 94.45%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9822 98.22%
BSEP inhibitior - 0.9754 97.54%
P-glycoprotein inhibitior - 0.9734 97.34%
P-glycoprotein substrate - 0.9486 94.86%
CYP3A4 substrate - 0.6610 66.10%
CYP2C9 substrate - 0.6329 63.29%
CYP2D6 substrate - 0.7783 77.83%
CYP3A4 inhibition - 0.9273 92.73%
CYP2C9 inhibition - 0.9596 95.96%
CYP2C19 inhibition - 0.9713 97.13%
CYP2D6 inhibition - 0.9526 95.26%
CYP1A2 inhibition - 0.9598 95.98%
CYP2C8 inhibition - 0.9788 97.88%
CYP inhibitory promiscuity - 0.9930 99.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.7306 73.06%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.9498 94.98%
Skin irritation - 0.8927 89.27%
Skin corrosion - 0.9272 92.72%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7904 79.04%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.5077 50.77%
skin sensitisation - 0.9566 95.66%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7042 70.42%
Acute Oral Toxicity (c) IV 0.5268 52.68%
Estrogen receptor binding - 0.7040 70.40%
Androgen receptor binding - 0.8349 83.49%
Thyroid receptor binding - 0.7428 74.28%
Glucocorticoid receptor binding + 0.5943 59.43%
Aromatase binding - 0.7895 78.95%
PPAR gamma - 0.6515 65.15%
Honey bee toxicity - 0.9274 92.74%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity - 0.8788 87.88%

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 98.51% 83.82%
CHEMBL236 P41143 Delta opioid receptor 96.03% 99.35%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.00% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 94.25% 90.17%
CHEMBL2581 P07339 Cathepsin D 94.21% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 94.13% 90.20%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 91.97% 92.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.54% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.40% 91.11%
CHEMBL3776 Q14790 Caspase-8 87.62% 97.06%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 87.36% 100.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.31% 97.21%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 84.83% 95.17%
CHEMBL2334 P42574 Caspase-3 84.49% 98.25%
CHEMBL3784 Q09472 Histone acetyltransferase p300 83.89% 93.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.72% 96.95%
CHEMBL340 P08684 Cytochrome P450 3A4 83.31% 91.19%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.33% 90.71%
CHEMBL3437 Q16853 Amine oxidase, copper containing 82.04% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.41% 99.15%
CHEMBL2413 P32246 C-C chemokine receptor type 1 81.31% 89.50%
CHEMBL4801 P29466 Caspase-1 80.86% 96.85%

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.
Vigna radiata

Cross-Links

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PubChem 161197
LOTUS LTS0104761
wikiData Q82913657