BTK
信号通路图
研究领域
抑制剂选择性比较
BTK产品
| 目录号 | 产品描述 | 文献引用 | 实验数据 |
|---|---|---|---|
| S7173 |
Spebrutinib (CC-292)Spebrutinib (CC-292, AVL-292)是一个通过共价结合的，可以口服，并且具有高度选择性的BTK抑制剂，其IC50小于0.5 nM，展示了比其他被测激酶至少1400倍的选择性。Phase 1. |
Effects of AVL-292, CNX-774 and dasatinib on IgE-mediated histamine release in human basophils. Basophils (BA) obtained from three nonallergic donors (A). |
|
| S7257 |
CNX-774CNX-774是不可逆的，口服有效的高选择性BTK抑制剂，IC50<1 nM。 |
Effects of AVL-292, CNX-774 and dasatinib on IgE-mediated histamine release in human basophils. Basophils (BA) obtained from three nonallergic donors (A), three patients allergic to Der p 2, and three patients allergic to Phl p 5 (B and C) were preincubated in control medium (Co) or medium containing various concentrations of AVL-292, CNX-774, or dasatinib (0.001-1 μmol/L) at 37°C for 30 minutes. Then, cells were exposed to anti-IgE antibody E-124.2.8 (1 μg/mL; nonallergic donors) or recombinant allergens (1 μg/mL of rDer p 2 or rPhl p 5 in allergic patients) at 37°C for 30 minutes. After centrifugation, histamine concentrations were determined in cell-free supernatants and cell lysates. Histamine release is expressed as percentage of total histamine. Results show the percentage of control and represent mean SD from three independent experiments (three donors). Asterisk (*): P<0.05 by Student's t test with Bonferroni correction |
|
| S8832 |
Branebrutinib (BMS-986195)Branebrutinib (BMS-986195)是有效的BTK抑制剂，对BTK, TEC, BMX, TXK的IC50值分别为0.1 nM, 0.9 nM, 1.5 nM, 5 nM。 |
||
| S7080 |
RN486RN486是一种有效的选择性BTK 抑制剂，IC50为4 nM。 |
||
| S9825New |
Pirtobrutinib (LOXO-305)Pirtobrutinib (LOXO-305, LY 3527727, RXC-005) 是一种高选择性、非共价、下一代 BTK 抑制剂，在 WT BTK HEK 细胞中的 IC50 为 5.69 nM。Pirtobrutinib 对 BTK 的选择性超过 370 种其他激酶的 98% 的 300 倍以上。 |
||
| E0041New |
Tolebrutinib (SAR442168)Tolebrutinib (SAR442168, PRN2246, BTKi'168, BTKi('168)) 是一种口服的、CNS 渗透性的、不可逆的BTK抑制剂，在 Ramos B 细胞和 HMC microglia 细胞中的 IC50 分别为 0.4 nM 和 0.7 nM。 |
||
| S6966New |
MT-802MT-802 是一种有效的 PROTAC，可诱导 Bruton's tyrosine kinase (BTK) 的降解。MT-802 可将BTK募集到 cereblon E3 ubiquitin ligase complex 中，以通过蛋白酶体触发BTK泛素化和降解。MT-802 具有治疗C481S突变型慢性淋巴细胞白血病(CLL)的潜力。 |
||
| S8679 |
BTK inhibitor 1 (Compound 27)BTK inhibitor 1 (compound 27) is an inhibitor of BTK with an IC50 of 0.11 nM for Btk and inhibits B cell activation in hWB with an IC50 of 2 nM. |
||
| S7734 |
LFM-A13LFM-A13是一种特异性布鲁顿氏酪氨酸激酶(BTK)抑制剂，IC50为2.5 μM,选择性比其他蛋白激酶，包括JAK1，JAK2，HCK，EGFR，和 IRK高100多倍。 |
Cell-free kinase assay of IFN-gR2 phosphorylation at Y289 by constitutively active BTK with or without BTK inhibitor LFM-A13 (100 mM). WCL, whole-cell lysate; DIC, differential interference contrast microscopy.
|
|
| S7877 |
ONO-4059 analogueONO-4059 analogue (ONO-WG-307)是一种ONO-4059类似物，其是一种高度有效的选择性口服BTK抑制剂，IC50为23.9 nM。Phase 1。 |
||
| S8294 |
Olmutinib (BI 1482694)Olmutinib (BI 1482694) 是一种新型的EGFR突变特效性酪氨酸激酶抑制剂、布鲁顿氏酪氨酸激酶抑制剂。 |
||
| S8777 |
Evobrutinib (M-2951)Evobrutinib (M-2951, MSC-2364447C) 是一种高度选择性的BTK抑制剂，IC50为37.9 nM，具有潜在的抗肿瘤活性。 |
||
| S8348 |
BMS-935177BMS-935177是一种有效的、可逆的BTK抑制剂，IC50为2.8 nM，具有良好的激酶选择性。它对BTK比对其他激酶如TEC, BMX, ITK, and TXK更有效力，选择性是其5-67倍。 |
||
| S8381 |
BMS-986142BMS-986142是一种有效、高选择性的、可逆的BTK小分子抑制剂，IC50为0.5 nM。在384种激酶试验中，BMS-986142对BTK的选择性相较于对TEC、ITK、BLK、TXK和BMX的选择性在100倍以内。 |
||
| S8116 |
Acalabrutinib (ACP-196)Acalabrutinib (ACP-196) 是选择性的第二代BTK抑制剂，抑制B细胞表面原抗体信号通路的激活，IC50为3 nM。它具有很好的靶标特异性，对BTK的选择性比对其他TEC激酶家族成员如ITK、TXK、BMK和TEC的选择性高323-, 94-, 19-, 9-倍。对EGFR没有活性。 |
Comparison of the impairment of ADCC against primary CLL cells by different irreversible BTK inhibitors. The antibody-dependent increase in the percentages of minimal calcein retention was determined with 3-fold excess of 1708-LC3E11 effector cells over CLL target cells in seven independent experiments. (a) Asterisks above the boxes and whiskers denote the significance of enhanced cytotoxicity compared to the control without addition of antibodies and inhibitors as determined by paired t-tests. Furthermore combination treatment was compared to that with anti-CD20 antibodies as single agents. (b) The mean differences ± SEM in the cytotoxicity against CLL cells in the presence and absence of rituximab and obinutuzumab were calculated from the data shown in (a). The ADCC of rituximab and obinutuzumab was compared by paired two-tailed t-test. *p<0.05; **p<0.01; ***p<0.001.
|
|
| S9660 |
Remibrutinib (LOU064)Remibrutinib (LOU064) 是一种有效的、高选择性的 bruton tyrosine kinase (BTK) 的抑制剂，对BTK、FcγR-induced IL8 和 anti-IgM/IL4-induced CD69的IC50值分别为1.3 nM、2.5 nM和18 nM。Remibrutinib (LOU064) 表现出出色的激酶选择性，其可与BTK的非活性构象结合，并具有治疗自身免疫性疾病的潜力。 |
||
| S8421 |
Fenebrutinib (GDC-0853)Fenebrutinib (GDC-0853)是一种有效的、选择性的非共价BTK抑制剂，对BRK的Ki值为0.91 nM。对BTK的IC50值是对其他3种脱靶激酶的100倍以上。（Bmx :153倍, Fgr: 168倍, Src:131倍）。 |
||
| S8791 |
Zanubrutinib (BGB-3111)Zanubrutinib (BGB-3111)是一种有效的、特异的不可逆性型BTK抑制剂，对其他激酶如ITK、JAK3和EGFR仅具有微弱的脱靶抑制效应。 |
||
| S6725 |
PCI 29732PCI 29732是一种选择性的、不可逆的Btk抑制剂，IC50为0.5 nM。 |
||
| S9600 |
Orelabrutinib (ICP-022)Orelabrutinib (ICP-022)是一种有效的、口服活性的且不可逆的 Bruton's tyrosine kinase (BTK) 的抑制剂。Orelabrutinib 具有潜在的抗肿瘤活性。 |
||
| S7051 |
CGI1746CGI1746 是强效的高度选择性的小分子Btk抑制剂，其IC50为1.9 nM。 |
Cleaved IL-1β and caspase-1 from primed and nigericin-treated human primary MoMacs pretreated with DMSO (mock), ibrutinib, or CGI-1746 for 10 minutes. Pro-IL-1β and caspase-1 processing in primary MoMacs was strongly reduced by both ibrutinib and CGI1746.
|
|
| S8542 |
Btk inhibitor 2Btk inhibitor 2是BTK抑制剂。 |
||
| S8166 |
tirabrutinib(ONO-4059) hydrochlorideTirabrutinib Hydrochloride (ONO-4059, GS-4059) 是一种高度有效的、选择性的BTK抑制剂，IC50为2.2 nM。 |
||
| S8711 |
Nemtabrutinib (ARQ 531)Nemtabrutinib (ARQ 531, MK-1026) 是一种ATP竞争性的酪氨酸激酶抑制剂，靶向BTK，IC50为0.85 nM。它具有明显的激酶选择性，对几种关键的致瘤因子（如TEC、Trk和Src中的一些家族成员）具有强抑制活性。 |
||
| S2680 |
Ibrutinib (PCI-32765)Ibrutinib (PCI-32765)是一种有效的，高选择性的Brutons tyrosine kinase (Btk)抑制剂，无细胞试验中IC50为0.5 nM，对Bmx， CSK， FGR， BRK及HCK适度有效，对EGFR， Yes， ErbB2， JAK3等作用效果较弱。Ibrutinib 可作为Btk配体用于合成包括P13I在内的一系列PROTAC。 |
Identification of Btk as a potent kinase for WIP tyrosine phosphorylation. Total protein lysates were prepared from THP-1 cells that were stably transfected with wild-type WIP-EGFP and treated with PCI-32765 at the concentration specified on the blots for 2h before pervanadate treatment for 30 min. In all cases WIP-EGFP was immunoprecipitated from cell lysates using anti-EGFP antibody and membranes subsequently blotted with the pY (4G10) antibody, EGFP antibody and β-Tubulin.
|
| 目录号 | 产品描述 | 文献引用 | 实验数据 |
|---|---|---|---|
| S7173 |
Spebrutinib (CC-292)Spebrutinib (CC-292, AVL-292)是一个通过共价结合的，可以口服，并且具有高度选择性的BTK抑制剂，其IC50小于0.5 nM，展示了比其他被测激酶至少1400倍的选择性。Phase 1. |
Effects of AVL-292, CNX-774 and dasatinib on IgE-mediated histamine release in human basophils. Basophils (BA) obtained from three nonallergic donors (A). |
|
| S7257 |
CNX-774CNX-774是不可逆的，口服有效的高选择性BTK抑制剂，IC50<1 nM。 |
Effects of AVL-292, CNX-774 and dasatinib on IgE-mediated histamine release in human basophils. Basophils (BA) obtained from three nonallergic donors (A), three patients allergic to Der p 2, and three patients allergic to Phl p 5 (B and C) were preincubated in control medium (Co) or medium containing various concentrations of AVL-292, CNX-774, or dasatinib (0.001-1 μmol/L) at 37°C for 30 minutes. Then, cells were exposed to anti-IgE antibody E-124.2.8 (1 μg/mL; nonallergic donors) or recombinant allergens (1 μg/mL of rDer p 2 or rPhl p 5 in allergic patients) at 37°C for 30 minutes. After centrifugation, histamine concentrations were determined in cell-free supernatants and cell lysates. Histamine release is expressed as percentage of total histamine. Results show the percentage of control and represent mean SD from three independent experiments (three donors). Asterisk (*): P<0.05 by Student's t test with Bonferroni correction |
|
| S8832 |
Branebrutinib (BMS-986195)Branebrutinib (BMS-986195)是有效的BTK抑制剂，对BTK, TEC, BMX, TXK的IC50值分别为0.1 nM, 0.9 nM, 1.5 nM, 5 nM。 |
||
| S7080 |
RN486RN486是一种有效的选择性BTK 抑制剂，IC50为4 nM。 |
||
| S9825New |
Pirtobrutinib (LOXO-305)Pirtobrutinib (LOXO-305, LY 3527727, RXC-005) 是一种高选择性、非共价、下一代 BTK 抑制剂，在 WT BTK HEK 细胞中的 IC50 为 5.69 nM。Pirtobrutinib 对 BTK 的选择性超过 370 种其他激酶的 98% 的 300 倍以上。 |
||
| E0041New |
Tolebrutinib (SAR442168)Tolebrutinib (SAR442168, PRN2246, BTKi'168, BTKi('168)) 是一种口服的、CNS 渗透性的、不可逆的BTK抑制剂，在 Ramos B 细胞和 HMC microglia 细胞中的 IC50 分别为 0.4 nM 和 0.7 nM。 |
||
| S6966New |
MT-802MT-802 是一种有效的 PROTAC，可诱导 Bruton's tyrosine kinase (BTK) 的降解。MT-802 可将BTK募集到 cereblon E3 ubiquitin ligase complex 中，以通过蛋白酶体触发BTK泛素化和降解。MT-802 具有治疗C481S突变型慢性淋巴细胞白血病(CLL)的潜力。 |
||
| S8679 |
BTK inhibitor 1 (Compound 27)BTK inhibitor 1 (compound 27) is an inhibitor of BTK with an IC50 of 0.11 nM for Btk and inhibits B cell activation in hWB with an IC50 of 2 nM. |
||
| S7734 |
LFM-A13LFM-A13是一种特异性布鲁顿氏酪氨酸激酶(BTK)抑制剂，IC50为2.5 μM,选择性比其他蛋白激酶，包括JAK1，JAK2，HCK，EGFR，和 IRK高100多倍。 |
Cell-free kinase assay of IFN-gR2 phosphorylation at Y289 by constitutively active BTK with or without BTK inhibitor LFM-A13 (100 mM). WCL, whole-cell lysate; DIC, differential interference contrast microscopy.
|
|
| S7877 |
ONO-4059 analogueONO-4059 analogue (ONO-WG-307)是一种ONO-4059类似物，其是一种高度有效的选择性口服BTK抑制剂，IC50为23.9 nM。Phase 1。 |
||
| S8294 |
Olmutinib (BI 1482694)Olmutinib (BI 1482694) 是一种新型的EGFR突变特效性酪氨酸激酶抑制剂、布鲁顿氏酪氨酸激酶抑制剂。 |
||
| S8777 |
Evobrutinib (M-2951)Evobrutinib (M-2951, MSC-2364447C) 是一种高度选择性的BTK抑制剂，IC50为37.9 nM，具有潜在的抗肿瘤活性。 |
||
| S8348 |
BMS-935177BMS-935177是一种有效的、可逆的BTK抑制剂，IC50为2.8 nM，具有良好的激酶选择性。它对BTK比对其他激酶如TEC, BMX, ITK, and TXK更有效力，选择性是其5-67倍。 |
||
| S8381 |
BMS-986142BMS-986142是一种有效、高选择性的、可逆的BTK小分子抑制剂，IC50为0.5 nM。在384种激酶试验中，BMS-986142对BTK的选择性相较于对TEC、ITK、BLK、TXK和BMX的选择性在100倍以内。 |
||
| S8116 |
Acalabrutinib (ACP-196)Acalabrutinib (ACP-196) 是选择性的第二代BTK抑制剂，抑制B细胞表面原抗体信号通路的激活，IC50为3 nM。它具有很好的靶标特异性，对BTK的选择性比对其他TEC激酶家族成员如ITK、TXK、BMK和TEC的选择性高323-, 94-, 19-, 9-倍。对EGFR没有活性。 |
Comparison of the impairment of ADCC against primary CLL cells by different irreversible BTK inhibitors. The antibody-dependent increase in the percentages of minimal calcein retention was determined with 3-fold excess of 1708-LC3E11 effector cells over CLL target cells in seven independent experiments. (a) Asterisks above the boxes and whiskers denote the significance of enhanced cytotoxicity compared to the control without addition of antibodies and inhibitors as determined by paired t-tests. Furthermore combination treatment was compared to that with anti-CD20 antibodies as single agents. (b) The mean differences ± SEM in the cytotoxicity against CLL cells in the presence and absence of rituximab and obinutuzumab were calculated from the data shown in (a). The ADCC of rituximab and obinutuzumab was compared by paired two-tailed t-test. *p<0.05; **p<0.01; ***p<0.001.
|
|
| S9660 |
Remibrutinib (LOU064)Remibrutinib (LOU064) 是一种有效的、高选择性的 bruton tyrosine kinase (BTK) 的抑制剂，对BTK、FcγR-induced IL8 和 anti-IgM/IL4-induced CD69的IC50值分别为1.3 nM、2.5 nM和18 nM。Remibrutinib (LOU064) 表现出出色的激酶选择性，其可与BTK的非活性构象结合，并具有治疗自身免疫性疾病的潜力。 |
||
| S8421 |
Fenebrutinib (GDC-0853)Fenebrutinib (GDC-0853)是一种有效的、选择性的非共价BTK抑制剂，对BRK的Ki值为0.91 nM。对BTK的IC50值是对其他3种脱靶激酶的100倍以上。（Bmx :153倍, Fgr: 168倍, Src:131倍）。 |
||
| S8791 |
Zanubrutinib (BGB-3111)Zanubrutinib (BGB-3111)是一种有效的、特异的不可逆性型BTK抑制剂，对其他激酶如ITK、JAK3和EGFR仅具有微弱的脱靶抑制效应。 |
||
| S6725 |
PCI 29732PCI 29732是一种选择性的、不可逆的Btk抑制剂，IC50为0.5 nM。 |
||
| S9600 |
Orelabrutinib (ICP-022)Orelabrutinib (ICP-022)是一种有效的、口服活性的且不可逆的 Bruton's tyrosine kinase (BTK) 的抑制剂。Orelabrutinib 具有潜在的抗肿瘤活性。 |
||
| S7051 |
CGI1746CGI1746 是强效的高度选择性的小分子Btk抑制剂，其IC50为1.9 nM。 |
Cleaved IL-1β and caspase-1 from primed and nigericin-treated human primary MoMacs pretreated with DMSO (mock), ibrutinib, or CGI-1746 for 10 minutes. Pro-IL-1β and caspase-1 processing in primary MoMacs was strongly reduced by both ibrutinib and CGI1746.
|
|
| S8542 |
Btk inhibitor 2Btk inhibitor 2是BTK抑制剂。 |
||
| S8166 |
tirabrutinib(ONO-4059) hydrochlorideTirabrutinib Hydrochloride (ONO-4059, GS-4059) 是一种高度有效的、选择性的BTK抑制剂，IC50为2.2 nM。 |
||
| S8711 |
Nemtabrutinib (ARQ 531)Nemtabrutinib (ARQ 531, MK-1026) 是一种ATP竞争性的酪氨酸激酶抑制剂，靶向BTK，IC50为0.85 nM。它具有明显的激酶选择性，对几种关键的致瘤因子（如TEC、Trk和Src中的一些家族成员）具有强抑制活性。 |
| 目录号 | 产品描述 | 文献引用 | 实验数据 |
|---|---|---|---|
| S2680 |
Ibrutinib (PCI-32765)Ibrutinib (PCI-32765)是一种有效的，高选择性的Brutons tyrosine kinase (Btk)抑制剂，无细胞试验中IC50为0.5 nM，对Bmx， CSK， FGR， BRK及HCK适度有效，对EGFR， Yes， ErbB2， JAK3等作用效果较弱。Ibrutinib 可作为Btk配体用于合成包括P13I在内的一系列PROTAC。 |
Identification of Btk as a potent kinase for WIP tyrosine phosphorylation. Total protein lysates were prepared from THP-1 cells that were stably transfected with wild-type WIP-EGFP and treated with PCI-32765 at the concentration specified on the blots for 2h before pervanadate treatment for 30 min. In all cases WIP-EGFP was immunoprecipitated from cell lysates using anti-EGFP antibody and membranes subsequently blotted with the pY (4G10) antibody, EGFP antibody and β-Tubulin.
|
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