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GSK-3 inhibitor 1是GSK-3抑制剂。

价格￥2170

品牌medchemexpress(MCE)
产地美国
货号HY-13973A
更新日期2025年07月14日

杭州昊鑫生物科技股份有限公司

代理商

10 年钻石会员

kb NB 142-70

kb NB 142-70 是一种有效的 PKD 抑制剂，对 PKD1，PKD2 和 PKD3 的 IC₅₀ 值分别为 28.3 nM，58.7 nM 和 53.2 nM；kb NB 142-70 同时具有抗肿瘤活性。
GSK-3 inhibitor 1是GSK-3抑制剂。

美国medchemexpress（MCE)浙江省一级代理:杭州昊鑫生物科技股份有限公司
MCE中国是全球领先的科研化学品和生物活性化合物供应商，总部位于美国新泽西。我们的产品范围覆盖各种抑制剂、激动剂、API和化合物库。专业、高效的企业灵魂铸造了在行业的卓越地位。热情和充满活力的研发团队拥有着大量的化学和生物科学家。专注于生物活性化合物，拥有着多年的发展历程和丰富的行业经验。从产品的HNMR数据解析到生物活性数据，从客户的询价到产品的售后服务，我们拥有着完善的管理体系，从而保证我们的服务更加高效、准确。努力为中国的医药行业发展注入新的活力，我们将成为您研发工作值得信赖的伙伴。
GSK-3 inhibitor 1是GSK-3抑制剂。

生物活性

kb NB 142-70 is a potent PKD inhibitor, with IC₅₀s of 28.3, 58.7 and 53.2 nM for PKD1, PKD2, and PKD3, respectively. kb NB 142-70 also has antitumor activity.

IC₅₀ & Target^[1]

PKD1

28.3 nM (IC₅₀)

PKD3

53.2 nM (IC₅₀)

PKD2

58.7 nM (IC₅₀)

体外研究 (In Vitro)	kb NB 142-70 is a potent PKD inhibitor, with IC₅₀s of 28.3, 58.7 and 53.2 nM for PKD1, PKD2, and PKD3, respectively. kb NB 142-70 also inhibits Ser⁹¹⁶ phosphorylation of PKD1 (IC₅₀, 2.2 ± 0.6 μM) in LNCaP cells. Moreover, kb NB 142-70 is cytotoxic against PC3 cells with an EC₅₀ of 8.025 μM^[1]. kb NB 142-70 (0-5 μM) concentration-dependently prevents ANG II-induced phosphorylation of HDAC4 at Ser²⁴⁶ and Ser⁶³², HDAC5 at Ser²⁵⁹ and Ser⁴⁹⁸, and HDAC7 at Ser¹⁵⁵ in IEC-18 cells. In addition, kb NB 142-70 (3.5 μM) also suppresses HDAC4, HDAC5, and HDAC7 phosphorylation in IEC-18 cells stimulated with ANG II for 0-240 min or with vasopressin, lysophosphatidic acid (LPA), or phorbol 12,13-dibutyrate (PDBu)^[2].

体外研究
(In Vitro)

kb NB 142-70 is a potent PKD inhibitor, with IC₅₀s of 28.3, 58.7 and 53.2 nM for PKD1, PKD2, and PKD3, respectively. kb NB 142-70 also inhibits Ser⁹¹⁶ phosphorylation of PKD1 (IC₅₀, 2.2 ± 0.6 μM) in LNCaP cells. Moreover, kb NB 142-70 is cytotoxic against PC3 cells with an EC₅₀ of 8.025 μM^[1]. kb NB 142-70 (0-5 μM) concentration-dependently prevents ANG II-induced phosphorylation of HDAC4 at Ser²⁴⁶ and Ser⁶³², HDAC5 at Ser²⁵⁹ and Ser⁴⁹⁸, and HDAC7 at Ser¹⁵⁵ in IEC-18 cells. In addition, kb NB 142-70 (3.5 μM) also suppresses HDAC4, HDAC5, and HDAC7 phosphorylation in IEC-18 cells stimulated with ANG II for 0-240 min or with vasopressin, lysophosphatidic acid (LPA), or phorbol 12,13-dibutyrate (PDBu)^[2].

分子量

251.32

Formula

C₁₁H₉NO₂S₂

CAS 号

1233533-04-4

性状

固体

颜色

White to gray

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Powder	-20°C	3 years
	4°C	2 years
In solvent	-80°C	2 years
	-20°C	1 year

参考文献	[1]. Lavalle CR, et al. Novel protein kinase D inhibitors cause potent arrest in prostate cancer cell growth and motility. BMC Chem Biol. 2010 May 5;10:5. [Content Brief] [2]. James Sinnett-Smith, et al. Protein kinase D1 mediates class IIa histone deacetylase phosphorylation and nuclear extrusion in intestinal epithelial cells: role in mitogenic signaling. Am J Physiol Cell Physiol. 2014 May 15; 306(10): C961-C971. [Content Brief]

参考文献

[1]. Lavalle CR, et al. Novel protein kinase D inhibitors cause potent arrest in prostate cancer cell growth and motility. BMC Chem Biol. 2010 May 5;10:5. [Content Brief]

[2]. James Sinnett-Smith, et al. Protein kinase D1 mediates class IIa histone deacetylase phosphorylation and nuclear extrusion in intestinal epithelial cells: role in mitogenic signaling. Am J Physiol Cell Physiol. 2014 May 15; 306(10): C961-C971. [Content Brief]

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文献和实验

该产品被引用文献

参考文献	[1]. Lavalle CR, et al. Novel protein kinase D inhibitors cause potent arrest in prostate cancer cell growth and motility. BMC Chem Biol. 2010 May 5;10:5. [Content Brief] [2]. James Sinnett-Smith, et al. Protein kinase D1 mediates class IIa histone deacetylase phosphorylation and nuclear extrusion in intestinal epithelial cells: role in mitogenic signaling. Am J Physiol Cell Physiol. 2014 May 15; 306(10): C961-C971. [Content Brief]

参考文献

[1]. Lavalle CR, et al. Novel protein kinase D inhibitors cause potent arrest in prostate cancer cell growth and motility. BMC Chem Biol. 2010 May 5;10:5. [Content Brief]

[2]. James Sinnett-Smith, et al. Protein kinase D1 mediates class IIa histone deacetylase phosphorylation and nuclear extrusion in intestinal epithelial cells: role in mitogenic signaling. Am J Physiol Cell Physiol. 2014 May 15; 306(10): C961-C971. [Content Brief]

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GSK-3 inhibitor 1是GSK-3抑制剂。

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GSK-3 inhibitor 1是GSK-3抑制剂。

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Tyloxapol (Triton WR1339) 是一种烷基芳基聚醚醇型非离子液体聚合物，用作表面活性稳定剂

PF-670462 dihydrochloride 是一种有效的，选择性的 casein kinase (CKIε/CKIδ) 抑制剂，IC50 值分别为 7.7 nM 和 14 nM。

Molindone hydrochloride (EN-1733A) 是一种抗精神病药，有潜力用于精神分裂症的研究，可以通过阻断大脑中多巴胺的作用，从而降低精神病。

Alisol B (泽泻醇B) 是一种潜在的新型治疗骨科疾病的化合物，通过对破骨细胞的分化以其功能发挥作用。

Pyridostigmine bromide 是可逆的胆碱酯酶抑制剂。

万千商家帮你免费找货

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kb NB 142-70

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