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N(α)-Boc-L-2,3-二氨丙酸

N(α)-Boc-L-2,3-二氨丙酸结构式
N(α)-Boc-L-2,3-二氨丙酸结构式
品牌特惠专场
常用名 N(α)-Boc-L-2,3-二氨丙酸 英文名 N(Alpha)-Boc-L-2,3-Diaminopropionic Acid
CAS号 73259-81-1 分子量 204.22
密度 1.2±0.1 g/cm3 沸点 364.4±37.0 °C at 760 mmHg
分子式 C8H16N2O4 熔点 210ºC (dec.)
MSDS 美版 闪点 174.2±26.5 °C

Glucosamine-6-phosphate synthase from Escherichia coli: determination of the mechanism of inactivation by N3-fumaroyl-L-2,3-diaminopropionic derivatives.

Biochemistry 29 , 3668, (1990)

A mechanistic investigation of the inactivation of Escherichia coli glucosamine-6-phosphate synthase by N3-(4-methoxyfumaroyl)-L-2,3-diaminopropionate (FMDP) was undertaken. On the basis of the known participation of the N-terminal cysteine residue in this pr...

Antimicrobial properties of N3-(iodoacetyl)-L-2,3-diaminopropanoic acid-peptide conjugates.

J. Med. Chem. 33 , 2755, (1990)

Six peptide conjugates consisting of either norvaline, methionine, or lysine and N3-(iodoacetyl)-L-2,3-diaminopropanoic acid--a strong, irreversible inactivator of bacterial and fungal glucosamine-6-phosphate synthase--were synthesized and their antibacterial...

Minimum requirements for inhibition of smooth-muscle myosin light-chain kinase by synthetic peptides.

Biochem. J. 257 , 73, (1989)

Although the amino acid residues that are important for peptide substrates of myosin light-chain kinase have been reported, those that are important for peptide inhibitors of this enzyme have not previously been investigated. Synthetic peptides based on the s...

F. Ruan et al.

J. Org. Chem. 56 , 4347, (1991)