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Documenti fondamentali

C9873

Sigma-Aldrich

CPTH2

≥98% (HPLC), powder

Sinonimo/i:

Cyclopentylidene-[4-(4-chlorophenyl)thiazol-2-yl)hydrazone

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5 MG
CHF 166.00
25 MG
CHF 667.00

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Spedizione prevista il29 maggio 2025


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5 MG
CHF 166.00
25 MG
CHF 667.00

About This Item

Formula empirica (notazione di Hill):
C14H14ClN3S
Numero CAS:
Peso molecolare:
291.80
Numero MDL:
Codice UNSPSC:
12352200
ID PubChem:
NACRES:
NA.77

CHF 166.00


Spedizione prevista il29 maggio 2025


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Livello qualitativo

Saggio

≥98% (HPLC)

Stato

powder

Colore

white to beige

Solubilità

DMSO: >10 mg/mL

Temperatura di conservazione

2-8°C

Stringa SMILE

Clc1ccc(cc1)-c2csc(N\N=C3\CCCC3)n2

InChI

1S/C14H14ClN3S/c15-11-7-5-10(6-8-11)13-9-19-14(16-13)18-17-12-3-1-2-4-12/h5-9H,1-4H2,(H,16,18)
YYTHPXHGWSAKIZ-UHFFFAOYSA-N

Categorie correlate

Descrizione generale

CPTH2 ((3-methylcyclopentylidene-[4-(4′-chlorophenyl)thiazol-2-yl]hydrazone)) inhibits histone acetyltransferase functionality and reduces acetylation of histone H3 [1] and H4.[2] CPTH2 promotes apoptosis in lymphoma cell lines.[2] It may serve as an anticancer agent. CPTH2 inhibits α-tubulin acetylation and modulates autophagic pathway in human acute myeloid leukemia cell lines.[3]

Applicazioni

CPTH2 has been used for the inhibition of histone acetyltransferase in cortical cultures,[4] bud cells[5] and natural killer T cells (iNKT).[6]

Azioni biochim/fisiol

CPTH2 is a histone acetyltransferase (HAT) inhibitor modulating the Gcn5 network.
CPTH2 is a histone acetyltransferase (HAT) inhibitor modulating the Gcn5 network. Histone Acetyltransferase (HAT) inhibitor modulating Gcn5 network. Histone acetyltransferases (HATs) act as transcriptional coactivators. Histone acetylation plays an important role in regulating the chromatin structure and is tightly regulated by two classes of enzyme, histone acetyltransferases (HAT) and histone deacetylases (HDAC). Deregulated HAT and HDAC activity plays a role in the development of a range of cancers. Consequently, inhibitors of these enzymes have potential as anticancer agents.

Caratteristiche e vantaggi

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.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

nwg

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Sodium butyrate ≥98.5% (GC)

Sigma-Aldrich

B5887

Sodium butyrate

The lysine acetyltransferase GCN5 is required for iNKT cell development through EGR2 acetylation
Wang Y, et al.
Cell Reports, 20(3), 600-612 (2017)
The thiazole derivative CPTH6 impairs autophagy
Ragazzoni Y, et al.
Cell Death & Disease, 4(3), e524-e524 (2013)
A novel histone acetyltransferase inhibitor modulating Gcn5 network: cyclopentylidene-[4-(4?-chlorophenyl) thiazol-2-yl) hydrazone
Chimenti F, et al.
Journal of Medicinal Chemistry, 52(2), 530-536 (2008)
Interactive histone acetylation and methylation in regulating transdifferentiation-related genes during tunicate budding and regeneration
Shibuya M, et al.
Developmental Dynamics, 244(1), 10-20 (2015)
CPTH6, a thiazole derivative, induces histone hypoacetylation and apoptosis in human leukemia cells
Trisciuoglio D, et al.
Clinical Cancer Research, 18(2), 475-486 (2012)

Articoli

We offer a variety of small molecule research tools, such as transcription factor modulators, inhibitors of chromatin modifying enzymes, and agonists/antagonists for target identification and validation in gene regulation research; a selection of these research tools is shown below.

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