H-Ala-Gly-OH

CAS: 687-69-4

Ref. 3D-FA107962

Produktinformation

• Name: H-Ala-Gly-OH
• Synonyme: (S)-2-(2-Aminopropanamido)acetic acid, (S)-Alanylglycine, 113: PN: US20130123467 SEQID: 137 claimed protein, 1: PN: US20180169179 SEQID: 1 claimed protein, 2-[(2S)-2-Aminopropanamido]acetic acid, 33: PN: WO03052099 PAGE: 84 claimed protein, 52: PN: WO2009086116 SEQID: 27 unclaimed protein, <span class="text-smallcaps">L</span>-Alanylglycine, <span class="text-smallcaps">L</span>-α-Alanylglycine, Alanylglycine, Glycine, <span class="text-smallcaps">L</span>-alanyl-, Glycine, N-<span class="text-smallcaps">L</span>-alanyl-, Glycine, N-L-alanyl- (8CI)(9CI), H-Ala-Gly-Oh, L-Alanylglycine, N-<span class="text-smallcaps">L</span>-Alanylglycine, Nsc 89597
• CAS: 687-69-4

Beschreibung

H-Ala-Gly-OH is a synthetic amino acid that is used to produce the peptide hormone luteinizing hormone (LH). It has been shown that H-Ala-Gly-OH is an antigen specific antibody response and has a hydrogen bond. The functional groups of H-Ala-Gly-OH include amine, carboxyl, and hydroxyl. Structural analysis of this compound was completed using a kinetic method. The conformational properties of H-Ala-Gly-OH were determined by nmr spectra and titration method. This synthetic amino acid may inhibit protein synthesis in vivo through treatment with carbohydrate.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 146.14 g/mol
• Formel: C₅H₁₀N₂O₃
• Reinheit: Min. 95%
• InChl: InChI=1S/C5H10N2O3/c1-3(6)5(10)7-2-4(8)9/h3H,2,6H2,1H3,(H,7,10)(H,8,9)/t3-/m0/s1
• InChI Key: InChIKey=CXISPYVYMQWFLE-VKHMYHEASA-N
• SMILES: C[C@H](N)C(=O)NCC(=O)O