Suc-Gly-NH2

Suc-Gly-NH2 contains a glycine amino acid residue bearing an N-terminal succinyl (Suc) acyl group and a free C-terminal primary amide (-CONH2), classifying it as an amino acid amide derivative rather than a free amino acid. The molecule retains the glycine backbone with an amide-linked carboxyl equivalent and an acylated nitrogen, featuring an N-succinyl protecting/activating motif that modulates chemoselectivity by reducing the nucleophilicity of the amino group while maintaining the terminal amide functionality. Suc-Gly-NH2 is used in peptide and amide bond synthesis and in substrate or standard preparation for analytical method development where a defined glycine amide structure is required.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: CP26668

CAS No:200863-20-3

Synonyms/Alias:SUC-GLY-NH2;200863-20-3;3-(carbamoylmethylcarbamoyl)propanoicAcid;SCHEMBL9870186;ZINC2561166;7728AH;STK024414;AKOS009558304;AM019635;K-5868;4-[(2-amino-2-oxoethyl)amino]-4-oxobutanoicacid

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M.F/Formula
C6H10N2O4
M.W/Mr.
174.16
Size
1 g;5 g;
InChI
1S/C6H10N2O4/c7-4(9)3-8-5(10)1-2-6(11)12/h1-3H2,(H2,7,9)(H,8,10)(H,11,12)
InChI Key
BBUFVFQEJADKHT-UHFFFAOYSA-N
Canonical SMILES
C(CC(=O)O)C(=O)NCC(=O)N

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