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PTACH

CAS No.
848354-66-5
Chemical Name:
PTACH
Synonyms
NCH 51;NCH51, >98%;PTACH?, >98%;PTACH (NCH-51);HDAC Inhibitor XXII, NCH51;HDAC Inhibitor XXII, NCH51 - CAS 848354-66-5 - Calbiochem;Cpd 51, S-[6-(4-Phenyl-2-thiazolylcarbamoyl)hexyl] thioisobutyrate;S-(7-Oxo-7-((4-phenylthiazol-2-yl)amino)-heptyl) 2-methylpropanethioate;S-[7-oxo-7-[(4-phenyl-1,3-thiazol-2-yl)amino]heptyl] 2-methylpropanethioate;2-MethylpropanethioicacidS-[7-oxo-7-[(4-phenyl-2-thiazolyl)amino]heptyl]ester
CBNumber:
CB8972794
Molecular Formula:
C20H26N2O2S2
Molecular Weight:
390.56
MDL Number:
MFCD08705329
MOL File:
848354-66-5.mol
Last updated:2023-09-04 15:51:00

PTACH Properties

Melting point 127-128 °C(Solv: hexane (110-54-3); ethyl acetate (141-78-6))
Density 1.181±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMSO: soluble26mg/mL
form White powder
pka 9.52±0.50(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS05
Signal word  Danger
Hazard statements  H318-H413
Precautionary statements  P280-P305+P351+P338
Hazard Codes  Xi
Risk Statements  41
Safety Statements  26-39
WGK Germany  3
NFPA 704
0
3 0

PTACH price More Price(26)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 382185 HDAC Inhibitor XXII, NCH51 848354-66-5 2mg $140 2023-01-07 Buy
Sigma-Aldrich P5874 PTACH ≥98% (HPLC), solid 848354-66-5 2mg $286 2022-05-15 Buy
Cayman Chemical 21234 NCH-51 ≥98% 848354-66-5 1 mg $26 2024-03-01 Buy
Cayman Chemical 21234 NCH-51 ≥98% 848354-66-5 5mg $96 2024-03-01 Buy
Cayman Chemical 21234 NCH-51 ≥98% 848354-66-5 10mg $153 2024-03-01 Buy
Product number Packaging Price Buy
382185 2mg $140 Buy
P5874 2mg $286 Buy
21234 1 mg $26 Buy
21234 5mg $96 Buy
21234 10mg $153 Buy

PTACH Chemical Properties,Uses,Production

Uses

NCH 51 is a Histone deacetylase inhibitor.

Definition

ChEBI: 2-methylpropanethioic acid S-[7-oxo-7-[(4-phenyl-2-thiazolyl)amino]heptyl] ester is an aromatic amide.

General Description

A cell-permeable S-isobutyryl prodrug that is processed intracellularly to form the potent HDAC inhibitor NCH-31 (IC50 = 48 and 170 nM, respectively, using partially purified HDAC1 or HeLa nuclear extract) that is predicted to exhibit a similar HADC binding mode as that of SAHA with its sulfhydryl replacing SAHA′s hydroxamate as the active-site zinc-targeting group. NCH-51 is shown to exhibit comparable antiproliferative (mean IC50 = 3.8 μM vs. 3.7 μM for SAHA; 48 h treatment) and apoptotic activity as SAHA against various cancer cell lines, but not PBMCs from 4 healthy individuals (IC50 >30 μM with either drug), and the antioxidant N-Acetyl-L-Cysteine (NAC; Cat. No. 106425) at 2 mM is reported to abolish the cell-growth inhibition caused by either 3 μM NCH-51 or SAHA in the Multiple Myeloma U266 cultures. Half-life in human plasma at 37 °C = 24 h.

Biological Activity

Histone deacetylase (HDAC) inhibitor. Inhibits growth of various cancer cells in vitro (EC 50 = 1.1-9.1 μ M).

Biochem/physiol Actions

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

References

[1]. suzuki t, hisakawa s, itoh y, et al. identification of a potent and stable antiproliferative agent by the prodrug formation of a thiolate histone deacetylase inhibitor. bioorg med chem lett, 2007, 17(6): 1558-1561.
[2]. suzuki t, nagano y, kouketsu a, et al. novel inhibitors of human histone deacetylases: design, synthesis, enzyme inhibition, and cancer cell growth inhibition of saha-based non-hydroxamates. j med chem, 2005, 48(4): 1019-1032.
[3]. sanda t, okamoto t, uchida y, et al. proteome analyses of the growth inhibitory effects of nch-51, a novel histone deacetylase inhibitor, on lymphoid malignant cells. leukemia, 2007, 21(11): 2344-2353.
[4]. victoriano af, imai k, togami h, et al. novel histone deacetylase inhibitor nch-51 activates latent hiv-1 gene expression. febs lett, 2011, 585(7): 1103-1111.

PTACH Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 78)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471 sales@sarms4muscle.com China 10523 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6393 58
Nanjing Doge Biomedical Technology Co., Ltd
+86-25-58227606 +86-15305155328 sales@dogechemical.com China 4128 58
LEAP CHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 24738 58
TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58
ShenZhen Trendseen Biological Technology Co.,Ltd.
13417589054 trendseenbio@gmail.com China 11681 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 57511 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131981 58
Changzhou Borl Biotechnology Co.,LTD 13606124132;13656121842 luyan0021@163.com China 219 58

848354-66-5(PTACH)Related Search:

Cpd 51, S-[6-(4-Phenyl-2-thiazolylcarbamoyl)hexyl] thioisobutyrate 2-MethylpropanethioicacidS-[7-oxo-7-[(4-phenyl-2-thiazolyl)amino]heptyl]ester S-(7-Oxo-7-((4-phenylthiazol-2-yl)amino)-heptyl) 2-methylpropanethioate PTACH (NCH-51) HDAC Inhibitor XXII, NCH51 Propanethioic acid,2-methyl-, S-[7-oxo-7-[(4-phenyl-2-thiazolyl)amino]heptyl] ester NCH51, >98% PTACH?, >98% HDAC Inhibitor XXII, NCH51 - CAS 848354-66-5 - Calbiochem NCH 51 HIV-1,inhibit,NCH 51,PTACH,HIV,Inhibitor,Histone deacetylases,hyperacetylation,NCH51,Anti-cancer,p21WAF1/CIP1,Human immunodeficiency virus,HDAC,SAHA S-[7-oxo-7-[(4-phenyl-1,3-thiazol-2-yl)amino]heptyl] 2-methylpropanethioate 848354-66-5