Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Chemical & Pharmaceutical Bulletin called Synthesis of stereoisomeric alanine containing peptide derivatives, Author is Okada, Yoshio; Tani, Shohei; Yawatari, Yuko; Yagyu, Masami, which mentions a compound: 61302-99-6, SMILESS is N[C@H](C)C(NC)=O.[H]Cl, Molecular C4H11ClN2O, Recommanded Product: D-Alanine methylamide hydrochloride.
D-alanine derivatives and their stereoisomers and D-alanyl-D-alanine derivatives and their stereoisomers (R1-Ala-R2, R1-Ala-Ala-R2: R1 = PhCH2O2C, H; R2 = NHNH2, NHCH3, NHCH2CH2OH) were synthesized. All compounds obtained did not show antibacterial activity against Staphylococcus aureus, Sarcina lutea, Pseudomonas aeruginosa and Escherichia coli.
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Reference:
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem