3025-95-4
3025-95-4
Chemical Structure
Ac-β-Ala-OH
- CAS No.: 3025-95-4
- Formula:C5H9NO3
- Molecular Weight:131.13
IUPAC Name: 3-acetamidopropanoic acid
InChIKey: LJLLAWRMBZNPMO-UHFFFAOYSA-N
SMILES: O=C(O)CCNC(C)=O
Biological Activity: Ac-β-Ala-OH is an abnormal amino acid metabolite and also serves as a mono-N-protected amino acid (MPAA) ligand. Ac-β-Ala-OH supports the β-C (sp3)-H arylation of aliphatic carboxylic acids and also serves as a starting building block for the reverse MAP core in the construction of the gonorrhea vaccine candidate TMCP2[1][2][3].
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Ac-β-Ala-OH | 98.0% | Ac-β-Ala-OH is an abnormal amino acid metabolite and also serves as a mono-N-protected amino acid (MPAA) ligand. Ac-β-Ala-OH supports the β-C (sp3)-H arylation of aliphatic carboxylic acids and also serves as a starting building block for the reverse MAP core in the construction of the gonorrhea vaccine candidate TMCP2. | ||||||||||||||||||||
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References
- [1]. Park HS, et al. Distal γ-C(sp3 )-H Olefination of Ketone Derivatives and Free Carboxylic Acids. Angew Chem Int Ed Engl. 2020 Jul 27;59(31):12853-12859. [Content Brief]
- [2]. Mal S. Design of Reagents and Ligands for Direct Palladium-Catalyzed C (sp3)-H Functionalization of Aliphatic Carboxylic Acids[D]. Universitätsbibliothek Kiel, 2026.
- [3]. Gulati S, et al. Preclinical Efficacy of a Lipooligosaccharide Peptide Mimic Candidate Gonococcal Vaccine. mBio. 2019 Nov 05;10(6):e02552-19.
