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Glycyl-glycyl-glycine

PubChem CID: 11161

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Compound Synonyms 556-33-2, Glycylglycylglycine, Triglycine, Glycyl-glycyl-glycine, H-Gly-Gly-Gly-OH, Gly-Gly-Gly, Diglycylglycine, N-(N-Glycylglycyl)glycine, Glycine, glycylglycyl-, GlyGlyGly, 2-(2-(2-Aminoacetamido)acetamido)acetic acid, 2-[[2-[(2-aminoacetyl)amino]acetyl]amino]acetic acid, Glycine, N-(N-glycylglycyl)-, UNII-CVK73ZDQ8B, MFCD00036223, CHEBI:63961, (Gly)3, EINECS 209-122-0, NSC 46707, NSC-46707, CVK73ZDQ8B, TRIGLYCINE [USP-RS], CHEMBL54278, DTXSID80204140, Gly-Gly-Gly-OH, TRIGLYCINE (USP-RS), [2-(2-Amino-acetylamino)-acetylamino]-acetic acid, 2-[[2-[(2-Aminoacetyl)amino]acetyl]amino]acetic Acid (Triglycine), 2-[2-(2-aminoacetamido)acetamido]acetic acid, 2-((2-((2-aminoacetyl)amino)acetyl)amino)acetic acid, 2-((2-((2-azaniumylacetyl)amino)acetyl)amino)acetate, 2-[[2-[(2-azaniumylacetyl)amino]acetyl]amino]acetate, Glycylpeptide, 2-({2-[(2-AMINOACETYL)AMINO]ACETYL}AMINO)ACETIC ACID, diglycyl-glycine, GGG peptide, Triglycine (van), NSC46707, N(NGlycylglycyl)glycine, Maybridge1_006812, SCHEMBL98565, N-(N-GLYCYLGLYCYL)-Glycine, HMS560N14, DTXCID80126631, Glycine, N(Nglycylglycyl) (8CI), OGG-3061, BDBM50188484, Glycine, N-(N-glycylglycyl)-(8CI), AKOS005207234, CS-W015952, DS-7430, FG39666, HY-W015236, BP-31100, Glycine, N(Nglycylglycyl) (8CI)(9CI), SY025319, Glycine, N-(N-glycylglycyl)-(8CI)(9CI), G0126, Gly-Gly-Gly, BioUltra, >=99.0% (NT), NS00033358, Glycine, N-(N-glycylglycyl)- (8CI)(9CI), (([(Aminoacetyl)amino]acetyl)amino)acetic acid, 3,6-Diazaoctanoic acid, 8-amino-4,7-dioxo-, EN300-176110, F17230, Glycylglycylglycine, 98+% (H-Gly-Gly-Gly-OH), (([(Aminoacetyl)amino]acetyl)amino)acetic acid #, Q27132936, Triglycine, United States Pharmacopeia (USP) Reference Standard
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 122.0
Hydrogen Bond Donor Count 4.0
Pfizer 3 75 Rule True
Np Classifier Class Tripeptides
Deep Smiles NCC=O)NCC=O)NCC=O)O
Heavy Atom Count 13.0
Classyfire Class Carboxylic acids and derivatives
Classyfire Subclass Amino acids, peptides, and analogues
Isotope Atom Count 0.0
Molecular Complexity 216.0
Database Name hmdb_chem_all;imppat_phytochem;pubchem
Defined Atom Stereocenter Count 0.0
Iupac Name 2-[[2-[(2-aminoacetyl)amino]acetyl]amino]acetic acid
Class Carboxylic acids and derivatives
Veber Rule True
Classyfire Superclass Organic acids and derivatives
Xlogp -3.6
Superclass Organic acids and derivatives
Subclass Amino acids, peptides, and analogues
Gsk 4 400 Rule True
Molecular Formula C6H11N3O4
Inchi Key XKUKSGPZAADMRA-UHFFFAOYSA-N
Silicos It Class Soluble
Rotatable Bond Count 5.0
State Solid
Synonyms (Gly)3, Diglycylglycine, GGG, Gly-gly-gly, GlyGlyGly, N-(N-Glycylglycyl)glycine, Triglycine, (([(Aminoacetyl)amino]acetyl)amino)acetic acid, Glycine, N-(N-glycylglycyl)- (8ci)(9ci), GLYCYL-glycyl-glycine, Glycylpeptide, N-(N-GLYCYLGLYCYL)-glycine, GGG Peptide, Triglycine sulfate, Diglycyl-glycine, diglycylglycine, glycylglycylglycine
Esol Class Highly soluble
Functional Groups CC(=O)O, CN, CNC(C)=O
Compound Name Glycyl-glycyl-glycine
Kingdom Organic compounds
Exact Mass 189.075
Formal Charge 0.0
Monoisotopic Mass 189.075
Hydrogen Bond Acceptor Count 5.0
Molecular Weight 189.17
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 0.0
Total Bond Stereocenter Count 0.0
Molecular Framework Aliphatic acyclic compounds
Lipinski Rule Of 5 True
Inchi InChI=1S/C6H11N3O4/c7-1-4(10)8-2-5(11)9-3-6(12)13/h1-3,7H2,(H,8,10)(H,9,11)(H,12,13)
Smiles C(C(=O)NCC(=O)NCC(=O)O)N
Np Classifier Biosynthetic Pathway Amino acids and Peptides
Defined Bond Stereocenter Count 0.0
Egan Rule False
Taxonomy Direct Parent Oligopeptides
Np Classifier Superclass Small peptides

  • 1. Outgoing r'ship FOUND_IN to/from Blighia Sapida (Plant) Rel Props:Reference:https://doi.org/10.15482/usda.adc/1239279