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Merck
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主要文件

C6499

Sigma-Aldrich

CTB

≥98% (HPLC)

别名:

CTPB, N-（4-氯-3-三氟甲基-苯基）-2-乙氧基-苯甲酰胺

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About This Item

经验公式（希尔记法）:
C16H13ClF3NO2
CAS号:
451491-47-7
分子量:
343.73
分類程式碼代碼:
12352200
NACRES:
NA.77

品質等級

100

化驗

≥98% (HPLC)

形狀

powder

顏色

white to off-white

溶解度

DMSO: >10 mg/mL

儲存溫度

2-8°C

一般說明

CTB（N-（4-氯-3-三氟甲基-苯基）-2-乙氧基-苯甲酰胺）来源于漆树酸。

應用

CTB 已用于研究其P53 蛋白乙酰化的凋亡作用。

生化／生理作用

CTPB 是第一个已知的组蛋白乙酰转移酶 p300 的小分子激活剂。CTB 是 CTPB 的一种简化类似物，具有相当或更高的活性。该化合物激活 p300/EP300/E1A 结合蛋白的组蛋白乙酰转移酶 (HAT) 活性。
HAT 的小分子激活剂如 CTB（N-（4-氯-3-三氟甲基-苯基）-2-乙氧基-苯甲酰胺）可直接改变染色质乙酰化。可作为治疗神经精神、神经发育和神经退行性疾病等认知功能障碍并发症的药物。

特點和優勢

这种化合物是基因调控研究的特色产品。点击此处发现更多特色基因调控产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 2

分析证书(COA)

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Cory Chew et al.
Neurorehabilitation and neural repair, 33(8), 656-667 (2019-07-10)
Background. Motoneuron loss is a severe medical problem that can result in loss of motor control and eventually death. We have previously demonstrated that partial motoneuron loss can result in dendritic atrophy and functional deficits in nearby surviving motoneurons, and
The effect of CTB on P53 protein acetylation and consequence apoptosis on MCF-7 and MRC-5 cell lines
Dastjerdi MN, et al.
Advanced Biomedical Research, 2 (2013)
DeMetris D Reed et al.
Meat science, 123, 205-210 (2016-10-19)
Palatability attributes of beef striploin steaks mechanically enhanced with pork fat were evaluated. Striploins were collected from USDA Standard steer carcasses, longitudinally cut into halves (lateral or medial) and assigned randomly to pork fat injection (PFI) or non-injected control (CON).
Franklin D Echevarria et al.
Frontiers in neuroscience, 11, 318-318 (2017-06-18)
The pleotropic cytokine interleukin-6 (IL-6) is implicated in retinal ganglion cell (RGC) survival and degeneration, including that associated with glaucoma. IL-6 protects RGCs from pressure-induced apoptosis
Willian S Korim et al.
Cardiovascular research, 115(6), 1092-1101 (2018-10-26)
Neuroinflammation is a common feature in renovascular, obesity-related, and angiotensin II mediated hypertension. There is evidence that increased release of the pro-inflammatory cytokine tumour necrosis factor-α (TNF-α) contributes to the development of the hypertension, but the underlying neural mechanisms are
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