03764
L-β-高亮氨酸 盐酸盐
≥98.0%
别名:
(S)-3-氨基-5-甲基己酸 盐酸盐
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关于此项目
经验公式（希尔记法）:
C7H15NO2 · HCl
化学文摘社编号:
分子量:
181.66
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
8073252
InChI
1S/C7H15NO2.ClH/c1-5(2)3-6(8)4-7(9)10;/h5-6H,3-4,8H2,1-2H3,(H,9,10);1H/t6-;/m0./s1
SMILES string
Cl.CC(C)C[C@H](N)CC(O)=O
InChI key
NXVYPYHWONGEFQ-RGMNGODLSA-N
assay
≥98.0%
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
color
beige
application(s)
peptide synthesis
Quality Level
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
Jaime A Espinoza et al.
Cell death and differentiation, 27(2), 773-789 (2019-07-10)
Pharmacological inhibition of ribosome biogenesis is a promising avenue for cancer therapy. Herein, we report a novel activity of the FDA-approved antimalarial drug amodiaquine which inhibits rRNA transcription, a rate-limiting step for ribosome biogenesis, in a dose-dependent manner. Amodiaquine triggers
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