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ST7612AA1

Catalog No. T70692   CAS 1428535-92-5

ST7612AA1 is a novel potent and oral HDCA inhibitor that acts as an HIV-1 latency reactivator. ST7612AA1 showed significant antitumor activity at low concentrations in vitro and in vivo. ST7612AA1 has potential anticancer activity and can be used to study malaria.

All products from TargetMol are for Research Use Only. Not for Human or Veterinary or Therapeutic Use.
ST7612AA1 Chemical Structure
ST7612AA1, CAS 1428535-92-5
Pack Size Availability Price/USD Quantity
1 mg In stock $ 195.00
5 mg In stock $ 483.00
10 mg In stock $ 692.00
25 mg In stock $ 1,080.00
50 mg In stock $ 1,490.00
100 mg In stock $ 1,970.00
500 mg In stock $ 3,930.00
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Biological Description
Chemical Properties
Storage & Solubility Information
Description ST7612AA1 is a novel potent and oral HDCA inhibitor that acts as an HIV-1 latency reactivator. ST7612AA1 showed significant antitumor activity at low concentrations in vitro and in vivo. ST7612AA1 has potential anticancer activity and can be used to study malaria.
Molecular Weight 405.51
Formula C20H27N3O4S
CAS No. 1428535-92-5

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

TargetMolReferences and Literature

1. Vesci L,et al. Preclinical antitumor activity of ST7612AA1: a new oral thiol-based histone deacetylase (HDAC) inhibitor. Oncotarget. 2015 Mar 20;6(8):5735-48. 2. Giannini G,et al. ST7612AA1, a thioacetate-ω(γ-lactam carboxamide) derivative selected from a novel generation of oral HDAC inhibitors. J Med Chem. 2014 Oct 23;57(20):8358-77.

Related compound libraries

This product is contained In the following compound libraries:
Anti-Parasitic Compound Library Inhibitor Library

Related Products

Related compounds with same targets
Helichrysetin 3-Deazaadenosine hydrochloride HIV-1 inhibitor-53 Pepstatin Dextran sulfate sodium salt (MW 4500-5500) (-)-Epigallocatechin Gallate Emivirine DAPTA

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Keywords

ST7612AA1 1428535-92-5 Microbiology/Virology Proteases/Proteasome HIV Protease MRT 92 MRT92. inhibitor inhibit

 

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