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BRD6688

Product Name
BRD6688
CAS No.
1404562-17-9
Chemical Name
BRD6688
Synonyms
BRD6688;N-[2-Amino-5-(4-pyridinyl)phenyl]-1-pyrrolidinecarboxamide;N-(2-Amino-5-(pyridin-4-yl)phenyl)pyrrolidine-1-carboxamide;1-Pyrrolidinecarboxamide, N-[2-amino-5-(4-pyridinyl)phenyl]-
CBNumber
CB73152567
Molecular Formula
C16H18N4O
Formula Weight
282.34
MOL File
1404562-17-9.mol
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BRD6688 Property

Boiling point:
528.2±50.0 °C(Predicted)
Density 
1.288±0.06 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
≤2mg/ml in ethanol;30mg/ml in DMSO;30mg/ml in dimethyl formamide
form 
crystalline solid
pka
12.22±0.70(Predicted)
color 
Off-white to light yellow
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
19836
Product name
BRD6688
Purity
≥98%
Packaging
1mg
Price
$54
Updated
2024/03/01
Cayman Chemical
Product number
19836
Product name
BRD6688
Purity
≥98%
Packaging
5mg
Price
$231
Updated
2024/03/01
Cayman Chemical
Product number
19836
Product name
BRD6688
Purity
≥98%
Packaging
10mg
Price
$308
Updated
2024/03/01
AK Scientific
Product number
9710DS
Product name
N-(2-Amino-5-pyridin-4-ylphenyl)pyrrolidine-1-carboxamide
Packaging
5mg
Price
$355
Updated
2021/12/16
ApexBio Technology
Product number
C5334
Product name
BRD6688
Packaging
10mg
Price
$432
Updated
2021/12/16
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BRD6688 Chemical Properties,Usage,Production

Biological Activity

brd6688 is an hdac inhibitor.a few chromatin modifying enzymes have been implicated in the neurobiology of learning and memory, especially, histone deacetylases (hdacs). hdacs are responsible for catalyzing the posttranslational hydrolysis of acetyl groups from the 3-nitrogen of lysine residues of histone and non-histone proteins.

in vitro

brd6688 was found to demonstrate kinetic selectivity for hdac2 against hdac1, an isoform with 95% similarity within the catalytic binding domain. moreover, brd6688 could increase histone acetylation (h4k12 and h3k9) in primary mouse neuronal cultures [1].

in vivo

mouse in-vivo study showed that brd6688 was able to increase the histone acetylation (h4k12 and h3k9) in hippocampal ca1 neurons of ck-p25 mice. moreove, the increased histone acetylation in brain served as a surrogate pharmacodynamic marker of hdac engagement and was consistent with previously observed brain pharmacokinetic properties. in addition, brd6688 rescued the cognitive deficits in ck-p25 mice, a model of neurodegeneration, in a pavlovian fear conditioning behavioral assay [1].

IC 50

21 nm, 100 nm, and 11.48 μm for hdac1, 2, and 3, respectively

References

[1] wagner, f. f.,zhang, y.-l.,fass, d.m., et al. kinetically selective inhibitors of histone deacetylase 2 (hdac2) as cognition enhancers. chem.sci. 6(1), 804-815 (2015).

BRD6688 Preparation Products And Raw materials

Raw materials

Preparation Products

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BRD6688 Suppliers

BOC Sciences
Tel
16314854226
Email
info@bocsci.com
Country
United States
ProdList
9923
Advantage
65
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32165
Advantage
58
ApexBio Technology
Tel
--
Fax
--
Email
sales@apexbt.com
Country
United States
ProdList
6251
Advantage
58
Cayman Chemical Company
Tel
--
Fax
--
Email
cayman@caymanchem.com
Country
United States
ProdList
6213
Advantage
81

1404562-17-9, BRD6688Related Search:


  • BRD6688
  • N-[2-Amino-5-(4-pyridinyl)phenyl]-1-pyrrolidinecarboxamide
  • 1-Pyrrolidinecarboxamide, N-[2-amino-5-(4-pyridinyl)phenyl]-
  • N-(2-Amino-5-(pyridin-4-yl)phenyl)pyrrolidine-1-carboxamide
  • 1404562-17-9