PTACH, 98%, a SAHA-based novel inhibitor of human HDAC

Name: PTACH, 98%, a SAHA-based novel inhibitor of human HDAC | 848354-66-5
Brand: J&K Chemical
SKU: JK786110_10_MG
Price: 136.8 USD
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Cat. No JK786110_10_MG

Vendor: J&K Chemical

Product Information

Product Name

PTACH, 98%, a SAHA-based novel inhibitor of human HDAC

Brand Name

J&K

Product Number

786110

CAS

848354-66-5

SDS Document

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Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

11395181

IUPAC Name

S-7-oxo-7-(4-phenyl-1,3-thiazol-2-yl)aminoheptyl 2-methylpropanethioate

InChI Key

MDYDGUOQFUQOGE-UHFFFAOYSA-N

SMILES

CC(C)C(=O)SCCCCCCC(=O)NC1=NC(=CS1)C2=CC=CC=C2

Safety Information

Storage Condition

Freezer -20℃

References Data Source From Pubchem

Target Class Profiling of Small-Molecule Methyltransferases

Publication Name: ACS Chemical Biology

Publication Date: 2023-03-28

DOI: 10.1021/acschembio.3c00124

Modern Improvements in the Digital Logic Laboratory

Publication Name: Technological Developments in Networking, Education and Automation

Publication Date: 2010

DOI: 10.1007/978-90-481-9151-2_19

Histone Deacetylase Inhibitors: From Bench to Clinic

Publication Name: Journal of Medicinal Chemistry

Publication Date: 2008-02-05

DOI: 10.1021/jm7011408|10.1021/jm800398r

Identification of a potent and stable antiproliferative agent by the prodrug formation of a thiolate histone deacetylase inhibitor

Publication Name: Bioorganic & Medicinal Chemistry Letters

Publication Date: 2007-03-15

DOI: 10.1016/j.bmcl.2006.12.117

Highly Potent and Selective Histone Deacetylase 6 Inhibitors Designed Based on a Small-Molecular Substrate

Publication Name: Journal of Medicinal Chemistry

Publication Date: 2006-07-18

DOI: 10.1021/jm060554y

PTACH, 98%, a SAHA-based novel inhibitor of human HDAC

Product Information

General Information

Safety Information

References Data Source From Pubchem

Target Class Profiling of Small-Molecule Methyltransferases

Modern Improvements in the Digital Logic Laboratory

Histone Deacetylase Inhibitors: From Bench to Clinic

Identification of a potent and stable antiproliferative agent by the prodrug formation of a thiolate histone deacetylase inhibitor

Highly Potent and Selective Histone Deacetylase 6 Inhibitors Designed Based on a Small-Molecular Substrate