2-(2-Methyl-1-piperidinyl)isonicotinic+acid
Supplier:
AMBEED, INC
Description:
3-(tert-Butoxycarbonylamino)-1-propanol 97%
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
4-(tert-Butoxycarbonylamino)-1-butanol 98%
Supplier:
APOLLO SCIENTIFIC
Description:
1-(tert-Butoxycarbonyl)piperidine-2-carboxylic acid
Supplier:
AMBEED, INC
Description:
N-(tert-Butoxycarbonyl)-D-threonine 95%
Catalog Number:
(TCD2849-500MG)
Supplier:
TCI America
Description:
CAS Number: 51325-91-8
Molecular Formula: C19H17N3O Molecular Weight: 303.37 Purity/Analysis Method: >95.0% (HPLC) Form: Crystal Melting point (°C): 220 Flash Point (°C): 43 Lambda max.: 468 nm
Supplier:
AMBEED, INC
Description:
4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]aminomethyl]benzoic acid 97%
Supplier:
Matrix Scientific
Description:
(S)-2-Amino-4-(tert-butoxy)-4-oxobutanoic acid ≥95%
Supplier:
AMBEED, INC
Description:
(S)-2-((tert-Butoxycarbonyl)amino)-4-phenylbutanoic acid 97%
Supplier:
AMBEED, INC
Description:
1-Boc-3-carbamoylpiperidine 95%
Supplier:
ALADDIN SCIENTIFIC
Description:
Acipimox is a niacin derivative.
Catalog Number:
(76997-462)
Supplier:
AMBEED, INC
Description:
2-Piperidineethanol, Purity: 97%, CAS number: 1484-84-0, Appearance: Solid or Semi-solid or liquid or lump, Storage: Keep in dark place, Sealed in dry, Room Temperature, Size: 5G
Catalog Number:
(89359-226)
Supplier:
Genetex
Description:
The basic repeating unit of chromatin is the nucleosome, which is composed of a protein octamer containing two each of the core histones H2A, H2B, H3, and H4, surrounded by approximately 146 base pairs of DNA. Reversible acetylation of highly conserved lysine residues in the N-terminal tail domains of core histones plays an important role in transcriptional regulation, cell cycle progression, and development events. Several histone acetyltransferases (HATs) catalyze this acetylation reaction (e.g. GCN5, PCAF, p300/CBP, TAFII250, P/CAF, SRC-1, BRCA-2). Acetylation of the core histones is generally considered to be associated with gene activation, probably through maintenance of the unfolded structure of transcribing nucleosomes. Histone acetylation is a dynamic process in which levels are determined by the net activities of HATs and the competing enzymes histone deacetylases (HDACs). Both activities are associated with the nuclear matrix. Eleven different mammalian HDACs have been described. HDACs 1-3 & 8 (Class I) are similar to yeast Rpd3 protein, while HDACs 4-7, 9 & 10 (Class II) are similar to yeast Hda1 protein. The activities of the histone deacetylases are often, but not always, associated with transcriptional repression and nucleosome condensation. HDAC1, HDAC2 and several others are the catalytic subunits of different multiprotein regulatory complexes. Other components of such complexes may include: corepressors such as mSin3, N-CoR, SMRT, associated proteins such as SAP18, SAP30, RbAp46, RbAp48, and c-Ski oncogenic protein (involved in DNA methylation). Nucleosome remodeling and deacetylation (NRD) complexes containing HDAC1, HDAC2, Mi-2 (CH3, CH4) dermatomyositis specific autoantigen, and MAT2 (metastasis-associated protein) (related to MAT1) have been described. It is therefore assumed that ATP-dependent nucleosome remodeling activity and histone deacetylation may be interconnected or interdependent. Recruitment of the multiprotein complexes to promoter sites occurs by many sequence specific DNA-binding proteins such as unliganded nuclear hormone receptors, DP1-E2F, YY1, and Rb family of transcription factors, transcriptional repressors, and tumor suppressors (e.g. BRCA1). Aberrant recruitment of HDACs by various oncoproteins may occur in certain neoplastic diseases. It has been found that inhibition ofHDAC2 activity by valporic acid induces proteosomal degradation of HDAC2.
Supplier:
Thermo Scientific Chemicals
Description:
5g CAS: 142253-55-2, MDL: MFCD01860897
Supplier:
Matrix Scientific
Description:
MF=C6H6N2O3 MW=154.13 CAS=51037-30-0 MDL=MFCD00865757 5G
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