544051
L-苯基丁氨酸 盐酸盐
97%
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关于此项目
线性分子式:
C6H5CH2CH2CH(NH2)CO2H · HCl
化学文摘社编号:
分子量:
215.68
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352209
MDL number:
Quality Level
assay
97%
optical activity
[α]20/D +38°, c = 1 in 3 M HCl
reaction suitability
reaction type: solution phase peptide synthesis
mp
262-265 °C (dec.) (lit.)
application(s)
peptide synthesis
SMILES string
Cl.N[C@@H](CCc1ccccc1)C(O)=O
InChI
1S/C10H13NO2.ClH/c11-9(10(12)13)7-6-8-4-2-1-3-5-8;/h1-5,9H,6-7,11H2,(H,12,13);1H/t9-;/m0./s1
InChI key
CHBMONIBOQCTCF-FVGYRXGTSA-N
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Sonja Nordhoff et al.
Bioorganic & medicinal chemistry letters, 19(16), 4818-4823 (2009-07-07)
A series of highly potent and selective inhibitors of DPP-4 was optimized for ADMET properties. The effort resulted in the discovery of inhibitor 1g, that exhibits excellent efficacy in an oral glucose tolerance test and an attractive pharmacokinetic profile.
Kento Koketsu et al.
Applied and environmental microbiology, 79(7), 2201-2208 (2013-01-29)
L-Homophenylalanine (L-Hph) is a useful chiral building block for synthesis of several drugs, including angiotensin-converting enzyme inhibitors and the novel proteasome inhibitor carfilzomib. While the chemoenzymatic route of synthesis is fully developed, we investigated microbial production of L-Hph to explore
Sonja Nordhoff et al.
Bioorganic & medicinal chemistry letters, 19(22), 6340-6345 (2009-10-17)
For a series of beta-homophenylalanine based inhibitors of dipeptidyl peptidase IV ADME properties were improved by the incorporation of amide replacements. These efforts led to a novel series of potent and selective inhibitors of DPP-4 that exhibit an attractive pharmacokinetic
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 544051-1G | 04061826095379 |