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Merck
CN

03764

L-β-Homoleucine hydrochloride

≥98.0%

Synonym(s):

(S)-3-Amino-5-methylhexanoic acid hydrochloride

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About This Item

Empirical Formula (Hill Notation):
C7H15NO2 · HCl
CAS Number:
Molecular Weight:
181.66
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
8073252
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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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Certificates of Analysis (COA)

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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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