JBJ-09-063 hydrochloride

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本产品不向个人销售，仅用作科学研究，不用于任何人体实验及非科研性质的动物实验。

包装与价格：

包装	价格(元)
5mg	电议
10mg	电议
50mg	电议
100mg	电议

产品介绍

JBJ-09-063 hydrochloride 是一种突变选择性变构EGFR抑制剂，对 EGFR L858R、EGFR L858R/T790M、EGFR L858R/T790M/C797S 和 EGFRLT/L747S 的IC₅₀分别为 0.147 nM、0.063 nM、0.083 nM 和 0.396 nM。JBJ-09-063 hydrochloride 有效降低 EGFR、Akt 和 ERK1/2 磷酸化。JBJ-09-063 hydrochloride 对 EGFR 酪氨酸激酶抑制剂 (TKI) 敏感和耐药模型均有效。JBJ-09-063 hydrochloride 可用于 EGFR 突变型肺癌研究。

生物活性

JBJ-09-063 hydrochloride is a mutant-selective allostericEGFRinhibitor withIC₅₀s of 0.147 nM, 0.063 nM, 0.083 nM and 0.396 nM forEGFRL858R,EGFRL858R/T790M,EGFRL858R/T790M/C797S and EGFRLT/L747S. JBJ-09-063 hydrochloride effectively reducesEGFR,Aktand ERK1/2 phosphorylation. JBJ-09-063 hydrochloride is effective acrossEGFRtyrosine kinase inhibitor (TKI)-sensitive and resistant models. JBJ-09-063 hydrochloride can be used for researching EGFR-mutant lungcancer^[1].

IC₅₀& Target^[1]

EGFR L858R

0.147 nM (IC₅₀)

EGFR L858R/T790M

0.063 nM (IC₅₀)

EGFR L858R/T790M/C797S

0.083 nM (IC₅₀)

EGFRLT/L747S

0.396 nM (IC₅₀)

体外研究
(In Vitro)

JBJ-09-063 is remarkably effective at inhibiting cell growth and leads to a significant increase in apoptosis, even though H3255GR cells are resistant to gefitinib as a single agent, as they contain an EGFR T790M mutation^[1].
JBJ-09-063 is effective in H1975 cells exogenously expressing the osimertinib-resistant mutations^[1].
JBJ-09-063 exhibits IC₅₀s of 50 nM and 6 nM in Ba/F3 cell when use alone or combination withCetuximab(HY-P9905)^[2].

体内研究
(In Vivo)

JBJ-09-063 (3 mg/kg i.v., 20 mg/kg p.o.) exhibits favorable pharmacokinetics properties and is sufficiently stable to deliver good efficacy upon oral dosing^[2].

Animal Model:

Mice^[2]

Dosage:

3 mg/kg for i.v., 20 mg/kg for p.o.

Administration:

i.v. and p.o.; single dosage

Result:

Pharmacokinetic Parameters of JBJ-09-063 in mice^[2].

Cl (mL/min/kg), i.v.	T_1/2(h)	V_ss(L/kg)	F (%)	AUC 8h (ng·h/mL)
15.7	2.3	2.5	15	2398

分子量

593.11

性状

Solid

Formula

C₃₁H₃₀ClFN₄O₃S

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	6 months
	-20°C	1 month

溶解性数据

In Vitro:

DMSO : ≥ 230 mg/mL(387.79 mM)

*"≥" means soluble, but saturation unknown.

配制储备液

浓度溶剂体积质量

1 mg

5 mg

10 mg

1 mM	1.6860 mL	8.4301 mL	16.8603 mL
5 mM	0.3372 mL	1.6860 mL	3.3721 mL
10 mM	0.1686 mL	0.8430 mL	1.6860 mL

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℃, 6 months; -20℃, 1 month。-80℃ 储存时，请在 6 个月内使用，-20℃ 储存时，请在 1 个月内使用。