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P5874

Sigma-Aldrich

PTACH

≥98% (HPLC), solid

Synonym(s):

Cpd 51, S-[6-(4-Phenyl-2-thiazolylcarbamoyl)hexyl] thioisobutyrate

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About This Item

Empirical Formula (Hill Notation):
C20H26N2O2S2
CAS Number:
848354-66-5
Molecular Weight:
390.56
MDL number:
MFCD08705329
UNSPSC Code:
12352202
PubChem Substance ID:
24724582
NACRES:
NA.77

Assay

≥98% (HPLC)

form

solid

solubility

DMSO: 26 mg/mL

storage temp.

2-8°C

SMILES string

CC(C)C(=O)SCCCCCCC(=O)Nc1nc(cs1)-c2ccccc2

InChI

1S/C20H26N2O2S2/c1-15(2)19(24)25-13-9-4-3-8-12-18(23)22-20-21-17(14-26-20)16-10-6-5-7-11-16/h5-7,10-11,14-15H,3-4,8-9,12-13H2,1-2H3,(H,21,22,23)

InChI key

MDYDGUOQFUQOGE-UHFFFAOYSA-N

Biochem/physiol Actions

HDAC inhibitor; more potent than the majority of HDAC inhibitors except for SAHA (gold standard).

Features and Benefits

This compound is a featured product for Gene Regulation research. Click here to discover more featured Gene Regulation products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Minghui Wang et al.
Neuron, 109(2), 257-272 (2020-11-26)
To identify the molecular mechanisms and novel therapeutic targets of late-onset Alzheimer's Disease (LOAD), we performed an integrative network analysis of multi-omics profiling of four cortical areas across 364 donors with varying cognitive and neuropathological phenotypes. Our analyses revealed thousands

Articles

Histone Modification and Chromatin Remodeling | Epigenetics

Epigenetic modifications are thought to occur through two key interconnected processes—DNA methylation and the covalent modification of histones.

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