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WP1066,JAK / STAT3抑制剂

JAK / STAT3抑制剂; AG 490模拟
规格或纯度: ≥98%
有货

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货号 (SKU) 包装规格 是否现货 价格 数量
W129459-10mg
10mg 现货 Stock Image
W129459-50mg
50mg 现货 Stock Image
W129459-250mg
250mg 现货 Stock Image
W129459-1g
1g 现货 Stock Image

基本描述

英文别名 WP1066|857064-38-1|(S,E)-3-(6-Bromopyridin-2-yl)-2-cyano-N-(1-phenylethyl)acrylamide|WP 1066|WP-1066|wp1066STAT Inhibitor III|63V8AIE65T|2-Propenamide, 3-(6-bromo-2-pyridinyl)-2-cyano-N-((1S)-1-phenylethyl)-, (2E)-|UNII-63V8AIE65T|MLS006010178|GTPL7972|SC
规格或纯度 ≥98%
英文名称 WP1066
生化机理 WP1066 (WP10666) is a cell permeable AG 490 tyrphostin analog that effectively inhibits the STAT3 pathway. The inhibitor is a potent antitumor agent as displayed in the growth inhibition of malignant glioma cell and acute myelogenous leukemia cells. Stat3 Inhibitor III, WP1066 has shown more potency as an antitumor agent than AG 490 when inhibiting malignant glioma growth in vitro. WP1066 also acts as an immune adjuvant by inducing proliferation of effector T cells and upregulating CD86 and CD80. In addition WP1066 has displayed inhibition of JAK2 protein tyrosine kinase as well as sμggested activation of Bax.JAK/STAT3 inhibitor (IC 50 = 2.3 μM). More potent analog of AG 490 . Antitumor activity in vitro and in vivo . Cell-permeable. Blood-brain barrier permeable.
储存温度 2-8°C储存
运输条件 冰袋运输
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产品介绍

WP1066是一种新型JAK2和STAT3抑制剂,在HEL细胞中IC50分别为2.30 μM和2.43 μM;对JAK2,STAT3,STAT5和ERK1/2具有抑制活性,而对JAK1和JAK3没有作A cell permeable inhibitor of Stat3 and JAK2 protein tyrosine kinase.

WP1066 is a novel inhibitor of JAK2 and STAT3 with IC50 of 2.30 μM and 2.43 μM in HEL cells; shows activity to JAK2, STAT3, STAT5, and ERK1/2 not JAK1 and JAK3.
A cell permeable inhibitor of Stat3 and JAK2 protein tyrosine kinase.

名称和标识符

PubChem SID 488197282
IUPAC Name (E)-3-(6-bromopyridin-2-yl)-2-cyano-N-[(1S)-1-phenylethyl]prop-2-enamide
INCHI InChI=1S/C17H14BrN3O/c1-12(13-6-3-2-4-7-13)20-17(22)14(11-19)10-15-8-5-9-16(18)21-15/h2-10,12H,1H3,(H,20,22)/b14-10+/t12-/m0/s1
InChi Key VFUAJMPDXIRPKO-LQELWAHVSA-N
Canonical SMILES CC(C1=CC=CC=C1)NC(=O)C(=CC2=NC(=CC=C2)Br)C#N
Isomeric SMILES C[C@@H](C1=CC=CC=C1)NC(=O)/C(=C/C2=NC(=CC=C2)Br)/C#N
PubChem CID 11210478
分子量 356.22

化学和物理性质

溶解性 DMSO 72 mg/mL Water <1 mg/mL Ethanol <1 mg/mL

安全和危险性(GHS)

象形图
ghs07

Harmful

信号词 Warning
危险声明 H302: Harmful if swallowed
预防措施声明 P501,P264,P270,P330,P301+P317

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参考文献

1. Ferrajoli A, Faderl S, Van Q, Koch P, Harris D, Liu Z, Hazan-Halevy I, Wang Y, Kantarjian HM, Priebe W et al..  (2007)  WP1066 disrupts Janus kinase-2 and induces caspase-dependent apoptosis in acute myelogenous leukemia cells..  Cancer Res,  67  (23):  (11291-9).  [PMID:18056455]
2. Verstovsek S, Manshouri T, Quintás-Cardama A, Harris D, Cortes J, Giles FJ, Kantarjian H, Priebe W, Estrov Z.  (2008)  WP1066, a novel JAK2 inhibitor, suppresses proliferation and induces apoptosis in erythroid human cells carrying the JAK2 V617F mutation..  Clin Cancer Res,  14  (3):  (788-96).  [PMID:18245540]
3. Bill MA, Fuchs JR, Li C, Yui J, Bakan C, Benson Jr DM, Schwartz EB, Abdelhamid D, Lin J, Hoyt DG et al..  (2010)  The small molecule curcumin analog FLLL32 induces apoptosis in melanoma cells via STAT3 inhibition and retains the cellular response to cytokines with anti-tumor activity..  Mol Cancer,  (13):  (165).  [PMID:20576164]
4. Tsujita Y, Horiguchi A, Tasaki S, Isono M, Asano T, Ito K, Asano T, Mayumi Y, Kushibiki T.  (2017)  STAT3 inhibition by WP1066 suppresses the growth and invasiveness of bladder cancer cells..  Oncol Rep,  38  (4):  (2197-2204).  [PMID:28849140]
5. Li M, Yu H.  (2021)  Identification of WP1066, an inhibitor of JAK2 and STAT3, as a KV 1.3 potassium channel blocker..  Br J Pharmacol,  178  (13):  (2617-2631).  [PMID:33689167]
6. Allaf A, Victoria B, Rosario R, Misztal C, Humayun Gultekin S, Dinh CT, Fernandez-Valle C.  (2022)  WP1066 induces cell death in a schwannomatosis patient-derived schwannoma cell line..  Cold Spring Harb Mol Case Stud,  (4):  (1755-70).  [PMID:35732500]