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Merck

U4885

Sigma-Aldrich

UNC0638 hydrate

≥98% (HPLC)

Sinónimos:

2-Cyclohexyl-N-(1-isopropylpiperidin-4-yl)-6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy) quinazolin-4-amine

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5 MG
142,80 €
25 MG
808,00 €

142,80 €

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5 MG
142,80 €
25 MG
808,00 €

About This Item

Fórmula empírica (notación de Hill):
C30H47N5O2 · xH2O
Número de CAS:
Peso molecular:
509.73 (anhydrous basis)
Número MDL:
Código UNSPSC:
12352200
ID de la sustancia en PubChem:
NACRES:
NA.77

142,80 €

Precio de catálogo204,00 €Ahorre 30 %

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Nivel de calidad

Ensayo

≥98% (HPLC)

Formulario

solid

condiciones de almacenamiento

protect from light

color

off-white

solubilidad

DMSO: >10 mg/mL

temp. de almacenamiento

−20°C

cadena SMILES

O.COc1cc2c(NC3CCN(CC3)C(C)C)nc(nc2cc1OCCCN4CCCC4)C5CCCCC5

InChI

1S/C30H47N5O2.H2O/c1-22(2)35-17-12-24(13-18-35)31-30-25-20-27(36-3)28(37-19-9-16-34-14-7-8-15-34)21-26(25)32-29(33-30)23-10-5-4-6-11-23;/h20-24H,4-19H2,1-3H3,(H,31,32,33);1H2

Clave InChI

LLJGACAJGYXBTL-UHFFFAOYSA-N

Descripción general

UNC0638 enhances the E-cadherin expression in gemcitabine-resistant cell line (PANC-1-R).[1]

Aplicación

UNC0638 has been used to block G9a (a lysine methyltransferase) function in C2C12 cells[2]. UNC0638 has also been reported to decrease H3K9 dimethylation (H3K9me2) levels and inhibit cell death in hair cells[3].
UNC0638 hydrate has been used:
  • in fractionation and isolation of human blood cells and cell nuclei[4]
  • in the analysis of human immunodeficiency virus (HIV) reactivation in latently infected cell line[5]
  • to determine the effect of G9a and its enzymatic activity on cisplatin resistance[6]

Acciones bioquímicas o fisiológicas

Histone methyltransferase inhibitor (HMT); G9a/GLP selective methyltransferase chemical probe.
UNC0638 hydrate is a histone methyltransferase (HMT) inhibitor. UNC0638 shows selectivity for G9a (EHMT2) and GLP (EHMT1) methyltransferases, which catalyze the methylation of lysine 9 of histone 3 (H3K9) as well as other non-histone substrates. For full characterization details, please visit the UNC0638 probe summary on the Structural Genomics Consortium (SGC) website.

To learn about other SGC chemical probes for epigenetic targets, visit sigma.com/sgc

Características y beneficios

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.
UNC0638 is an epigenetic chemical probe available through a partnership with the Structural Genomics Consortium (SGC). To learn more and view other SGC epigenetic probes, visit sigma.com/SGC.

Otras notas

UNC0638 has been expertly reviewed and recommended by the Chemical Probes Portal. For more information, please visit the UNC0638 probe summary on the Chemical Probes Portal website.

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Pictogramas

Skull and crossbones

Palabra de señalización

Danger

Frases de peligro

Clasificaciones de peligro

Acute Tox. 2 Oral - Aquatic Chronic 4

Código de clase de almacenamiento

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Histone methyltransferase G9a drives chemotherapy resistance by regulating the glutamate-cysteine ligase catalytic subunit in head and neck squamous cell carcinoma
Liu CW, et al.
Molecular Cancer Therapeutics, molcanther-molcan0567 (2017)
Genome-wide mapping of histone H3K9me2 in acute myeloid leukemia reveals large chromosomal domains associated with massive gene silencing and sites of genome instability
Salzberg AC, et al.
PLoS ONE, 12(3), e0173723-e0173723 (2017)
G9a orchestrates PCL3 and KDM7A to promote histone H3K27 methylation
Pan MR, et al.
Scientific Reports, 5, 18709-18709 (2015)
HIV-1 infection of microglial cells in a reconstituted humanized mouse model and identification of compounds that selectively reverse HIV latency
Llewellyn GN, et al.
Journal of Neurovirology, 1-12 (2017)
Tie-Gang Meng et al.
International journal of biological sciences, 18(11), 4513-4531 (2022-07-23)
During oocyte growth, various epigenetic modifications are gradually established, accompanied by accumulation of large amounts of mRNAs and proteins. However, little is known about the relationship between epigenetic modifications and meiotic progression. Here, by using Gdf9-Cre to achieve oocyte-specific ablation

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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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