H-Gly-Pro-Gly-NH2

Category	Human immunodeficiency Virus (HIV)
CAS	141497-12-3
Description	H-Gly-Pro-Gly-NH2 inhibits HIV-1 replication through its metabolite α-hydroxyglycineamide. It increases the antiviral activity of zidovudine and ritonavir.

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Synonyms	H-Gly-Pro-Gly-NH2;141497-12-3;Glycinamide, glycyl-L-prolyl-;GPG-NH2;Glycylprolylglycine Amide;Glycyl-prolyl-glycyl amide;Glycinamide, glycyl-prolyl-;(2S)-1-(2-aminoacetyl)-N-(2-amino-2-oxoethyl)pyrrolidine-2-carboxamide;Gly-pro-gly-NH2;Glycyl-L-prolylglycinamide;glycyl-prolyl-glycine amide;73GV270Z6Z;(2s)-1-(aminoacetyl)-n-(carbamoylmethyl)pyrrolidine-2-carboxamide;H-Gly-Pro-Gly-NH2 . HCl;glycyl-prolyl-glycinamide;Glycinamide, glycyl-L-prolyl;UNII-73GV270Z6Z;SCHEMBL1046072;(S)-N-(2-Amino-2-oxoethyl)-1-(2-aminoacetyl)pyrrolidine-2-carboxamide;HY-P4292;Glycyl-prolyl-glycyl amide; GPG-NH2;DA-74147;PD161520;CS-0653409;Q27266174;
IUPAC Name	(2S)-1-(2-aminoacetyl)-N-(2-amino-2-oxoethyl)pyrrolidine-2-carboxamide
Molecular Weight	228.25
Molecular Formula	C9H16N4O3
Canonical SMILES	C1CC(N(C1)C(=O)CN)C(=O)NCC(=O)N
InChI	InChI=1S/C9H16N4O3/c10-4-8(15)13-3-1-2-6(13)9(16)12-5-7(11)14/h6H,1-5,10H2,(H2,11,14)(H,12,16)/t6-/m0/s1
InChIKey	JWWLMJFURJYNEX-LURJTMIESA-N
Boiling Point	618.0±55.0°C (Predicted)
Purity	≥95% by HPLC
Density	1.326±0.06 g/cm3 (Predicted)
Solubility	Soluble in Methanol
Appearance	White Powder
Storage	Please store the product under the recommended conditions in the Certificate of Analysis.