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Safety Information

SML2189

Sigma-Aldrich

L-Moses

≥98% (HPLC)

Synonym(s):

(1S,2S)-N1,N1-Dimethyl-N2-(3-methyl-1,2,4-triazolo[3,4-a]phthalazin-6-yl)-1-phenyl-1,2-propanediamine, L-45

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About This Item

Empirical Formula (Hill Notation):
C21H24N6
CAS Number:
Molecular Weight:
360.46
MDL number:
UNSPSC Code:
12352200

Assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

2-8°C

SMILES string

CC1=NN=C2N1N=C(N[C@@H](C)[C@@H](N(C)C)C3=CC=CC=C3)C4=CC=CC=C42

Biochem/physiol Actions

L-Moses is a cell penetrant, potent and selective PCAF bromodomain (Brd) inhibitor.
PCAF Bromodomain inhibitor

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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Andre Richters et al.
Current medicinal chemistry, 24(37), 4121-4150 (2017-02-28)
Histone acetyltransferases (HATs) are epigenetic drivers that catalyze the acetyl transfer from acetyl-CoA to lysines of both histone and non-histone substrates and thereby induce transcription either by chromatin remodeling or direct transcription factor activation. Histone deacetylases (HDACs) conduct the reverse
Moses Moustakim et al.
Angewandte Chemie (International ed. in English), 56(3), 827-831 (2016-12-15)
The p300/CBP-associated factor (PCAF) and related GCN5 bromodomain-containing lysine acetyl transferases are members of subfamily I of the bromodomain phylogenetic tree. Iterative cycles of rational inhibitor design and biophysical characterization led to the discovery of the triazolopthalazine-based L-45 (dubbed L-Moses) as

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