JAK3 选择性抑制剂

目录号 产品名 产品描述 Selective / Pan IC50 / Ki
S5904 WHI-P97

WHI-P97 is a potent inhibitor of JAK-3 with an estimated Ki value of 0.09 μM in modeling studies and a measured IC50 value of 2.5 μM in EGFR kinase inhibition assays.

Selective
S8684 Selective JAK3 inhibitor 1

Selective JAK3 inhibitor 1 is an irreversible JAK3 inhibitor with Ki values of 0.07 nM, 320 nM, 740 nM for JAK3, JAK1 and JAK2 respectively. It is also selective over the other kinases possessing a cysteine in the same region as JAK3, such as BMX, EGFR, ITK, and BTK.

Selective JAK3, Ki: 0.07 nM
S8541 FM-381

FM-381 is a JAK3 specific reversible covalent inhibitor with IC50 of 127 pM for JAK3 and demonstrates 400-, 2,700- and 3,600-fold selectivity over JAK1, JAK2, and TYK2, respectively.

Selective JAK3, IC50: 127 pM
S2789 Tofacitinib (CP-690550)

Tofacitinib (CP-690550,Tasocitinib)是一种新型JAK3抑制剂,在无细胞试验中IC50为1 nM,作用于JAK2和JAK1选择性低20到100倍。

Selective JAK3, IC50: 1 nM
S5001 Tofacitinib (CP-690550) Citrate

Tofacitinib (CP-690550) Citrate是一种新型JAK抑制剂,对JAK3,JAK2,JAK1的IC50分别为1 nM, 20 nM 和112 nM。

Selective JAK3, IC50: 1 nM
S8538 Ritlecitinib (PF-06651600)

Ritlecitinib (PF-06651600) is a potent and irreversible JAK3-selective inhibitor with an IC50 of 33.1 nM but without activity (IC50 > 10 000 nM) against JAK1, JAK2, and TYK2.

Selective JAK3, IC50: 33.1 nM
S8004 ZM 39923 HCl

ZM 39923 HCl是一种JAK1/3抑制剂,pIC50为4.4/7.1,对JAK2没有作用活性,适度有效作用于EFGR;对转谷氨酰胺酶敏感。

Selective JAK3, pIC50: 7.1
S2867 WHI-P154

WHI-P154是一种有效的JAK3抑制剂,IC50为1.8 μM,对JAK1和JAK2没有抑制活性,也抑制EGFR, Src, Abl, VEGFR和MAPK,抑制Stat3而非Stat5磷酸化。

Selective JAK3, IC50: 1.8 μM
S6521 WHI-P258

WHI-P258 is an inhibitor of JAK3 with Ki value of 72 μM.

Selective JAK3, Ki: 72 μM
S5903 JANEX-1

JANEX-1 (WHI-P131) is a small molecule inhibitor of JAK3 that selectively inhibits JAK3 at an IC50 of 78 µM without altering the activity of JAK1 or JAK2, or any other protein tyrosine kinases (IC50 ≥ 350 µM).

Selective JAK3, IC50: 78 μM
S0981 BD750

BD750 is an effective immunosuppressant and a JAK3/STAT5 inhibitor that inhibits IL-2-induced JAK3/STAT5-dependent T cell proliferation with IC50 of 1.5 μM and 1.1 μM in mouse and human T cells, respectively.

Selective
S1134 AT9283

AT9283是一种有效的JAK2/3抑制剂,无细胞试验中IC50为1.2 nM/1.1 nM;对Aurora A/B,Abl(T315I)也有效。Phase 2。

Pan JAK3, IC50: 1.1 nM
S7541 Decernotinib (VX-509)

Decernotinib (VX-509)是一种有效的且选择性的JAK3抑制剂,Ki 为 2.5 nM,分别比作用于JAK1,JAK2,和 TYK2的选择性高4倍以上。Phase 2/3。

Pan JAK3, Ki: 2.5 nM
S6789 JAK Inhibitor I (Pyridone 6)

JAK Inhibitor I (Pyridone 6, CMP 6, Compound 6) is a pan-JAK inhibitor with IC50s of 1 nM, 1 nM, 5 nM and 15 nM for JAK2, TYK2, JAK3 and JAK1, respectively.

Pan JAK3, IC50: 5 nM
S3566 Cerdulatinib (PRT062070)

Cerdulatinib (PRT062070, PRT2070) is an oral active, multi-targeted tyrosine kinase inhibitor with IC50 of 12 nM/6 nM/8 nM/0.5 nM and 32 nM for JAK1/JAK2/JAK3/TYK2 and Syk, respectively. Also inhibits 19 other tested kinases with IC50 less than 200 nM.

Pan JAK3, IC50: 8 nM
S7634 Cerdulatinib (PRT062070) hydrochloride

Cerdulatinib (PRT-062070)是一种具有口服活性的多靶点酪氨酸激酶抑制剂,对JAK1/JAK2/JAK3/TYK2SykIC50分别为12 nM/6 nM/8 nM/0.5 nM和32 nM。也能够抑制测试的其他19种激酶,IC50均低于200 nM。

Pan JAK3, IC50: 8 nM
S2686 NVP-BSK805 2HCl

NVP-BSK805 2HCl是一种有效的,选择性的,ATP竞争性的JAK2抑制剂,IC50为0.5 nM,比作用于JAK1, JAK3和TYK2选择性高20倍以上。

Pan JAK3, IC50: 18.68 nM
S0437 SAR-20347

SAR-20347 is a potent inhibitor of TYK2, JAK1, JAK2 and JAK3 with IC50 of 0.6 nM, 23 nM, 26 nM and 41 nM, respectively.

Pan JAK3, IC50: 41 nM
S2179 Gandotinib (LY2784544)

Gandotinib (LY2784544)是一种有效的JAK2抑制剂,IC50为3 nM,作用于JAK2V617F有效,比作用于JAK1和JAK3选择性高8和20倍。Phase 2。

Pan JAK3, IC50: 48.0 nM
S7144 BMS-911543

BMS-911543是一种有效的、选择性JAK2小分子抑制剂,IC50为1.1 nM。

Pan JAK3, IC50: 75 nM
S8195 Oclacitinib maleate

Oclacitinib(PF 03394197)是一种新型的JAK family members以及JAK1-dependent cytokines抑制剂,IC50分别为10-99 nM(JAK family members)和36-249 nM(JAK1-dependent cytokines)。

Pan JAK3, IC50: 99nM
S2219 Momelotinib (CYT387)

Momelotinib (CYT387)是一种ATP竞争性JAK1/JAK2抑制剂,IC50为11 nM/18 nM,比作用于JAK3选择性约高10倍左右。Phase 3。

Pan JAK3, IC50: 155 nM
S2692 TG101209

TG101209是一种选择性的JAK2抑制剂,无细胞试验中IC50为6 nM,对Flt3和RET作用效果稍弱,IC50分别为25 nM和17 nM,作用于JAK2比作用于JAK3选择性高30倍左右,对JAK2V617F和MPLW515L/K突变型敏感。

Pan JAK3, IC50: 169 nM
S7036 XL019

XL019是一种有效的,选择性的JAK2抑制剂,IC50为2.2 nM,比作用于JAK1, JAK3和TYK2.选择性高50倍。Phase 1。

Pan JAK3, IC50: 214.2 nM
S0374 GDC046

GDC046 is a potent lead analog with good kinase selectivity, physicochemical properties and pharmacokinetic profile.

Pan JAK3, Ki: 253 nM
S7198 BIO

BIO是一种特异性的GSK-3抑制剂,无细胞试验中作用于GSK-3α/β的IC50为5 nM,比作用于CDK5选择性高16倍以上,也是一种泛JAK抑制剂。

Pan JAK3, IC50: 0.5 μM
S8057 Pacritinib (SB1518)

Pacritinib (SB1518)是有效的选择性Janus Kinase 2 (JAK2)Fms-Like Tyrosine Kinase-3 (FLT3)抑制剂,无细胞试验中IC50分别为23和22 nM。Phase 3。

Pan JAK3, IC50: 520 nM
S7605 Filgotinib (GLPG0634)

Filgotinib(GLPG0634)是一个选择性JAK1抑制剂,其对JAK1, JAK2, JAK3,和TYK2的IC50分别为10 nM, 28 nM, 810 nM,和116 nM。Phase 2。

Pan JAK3, IC50: 810 nM
S5917 Solcitinib

Solcitinib (GLPG0778, GSK2586184) is an inhibitor of JAK1 with an IC50 of 8-9 nM, and shows 11-, 55- and 23-fold selectivity over JAK2, JAK3 and TYK2, respectively.

Pan