RIPK2 Inhibitor OD36 (hydrochloride)

目录号: GC92293纯度: >98.00%同义词: OD36; Receptor-interacting Serine/Threonine Kinase 2 Inhibitor OD36
RIPK2 inhibitor OD36 is an inhibitor of receptor-interacting serine/threonine kinase 2 (RIPK2; IC50 = 5.3 nM).

RIPK2 Inhibitor OD36 (hydrochloride)
Cas No.: 2387510-88-3
规格价格库存数量操作
1mg¥601.00现货
1
5mg¥2,556.00现货
1
10mg¥4,512.00现货
1
25mg¥7,515.00现货
1

文献被引

本产品暂无引用记录;以下为 GlpBio 产品在 Nature / Cell / Science 等顶刊的客户引用样例
  • Nature cover
    Nature
    641, 529–536 (2025)
  • Nature cover
    Nature
    628, 630–638 (2024)
  • Nature cover
    Nature
    632, 686–694 (2024)
  • Nature cover
    Nature
    618, 1017–1023 (2023)
  • Nature cover
    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
  • Cell cover
    Cell
    183(7):1867-1883 (2020)
  • Science cover
    Science
    388(6745) (2025)
  • Science cover
    Science
    387(6739) (2025)
  • Science cover
    Science
    387(6734) (2025)
  • Cell Research cover
    Cell Research
    35, 97–116 (2025)
  • Cell Research cover
    Cell Research
    34, 683–706 (2024)
  • Cell Research cover
    Cell Research
    33, 273–287 (2023)
  • Cell Research cover
    Cell Research
    33, 546–561 (2023)
  • Cell Research cover
    Cell Research
    33, 904–922 (2023)
  • Cell Research cover
    Cell Research
    31, 1291–1307 (2021)

产品描述 Description

RIPK2 inhibitor OD36 is an inhibitor of receptor-interacting serine/threonine kinase 2 (RIPK2; IC50 = 5.3 nM). It also inhibits wild-type and R206H mutant activin receptor-like kinase 2 (ALK2; IC50s = 47 and 22 nM, respectively). RIPK2 inhibitor OD36 (0.5 µM) inhibits activin A-induced chondrogenic and osteogenic differentiation in ATDC-5 cells overexpressing ALKR206H, an activating mutation found in patients with fibrodysplasia ossificans progressiva (FOP), which is characterized by progressive heterotopic ossification, or diffuse intrinsic pontine glioma (DIPG), a type of pediatric brain stem cancer. In vivo, RIPK2 inhibitor OD36 (6.25 mg/kg) reduces the number of peritoneal lavage neutrophils and lymphocytes in a mouse model of muramyl dipeptide-induced peritonitis.

产品文档 Product Documents

Purity:>98.00%

化学性质Chemical Properties

CAS 号
2387510-88-3
同义词
OD36; Receptor-interacting Serine/Threonine Kinase 2 Inhibitor OD36
化学名
(13Z)-25-chloro-14,15-dihydro-3,6-dioxa-9-aza-1(3,5)-pyrazolo[1,5-a]pyrimidina-2(1,3)-benzenacyclononaphane, monohydrochloride
SMILES
ClC1=CC2=CC(C3=C4N(C=CC(N4)=NCCOCCO2)N=C3)=C1.Cl
分子式
C16H15ClN4O2 • HCl
分子量
367.2 g/mol
溶解性
DMSO: Soluble: ≥10 mg/ml; Ethanol: Slightly Soluble: 0.1-1 mg/ml
保存条件
-20°C
General tips
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol