广告:热烈庆祝【宁波康贝生化有限公司】成为全球资源网"战略合作伙伴关系企业"!

inhibitor- (MAPK))

点击图片查看原图
品牌: karebay biochem
纯度: 粗品-98%
报告: ESI-MS&HPLC
单价: 1.00元/mg
起订: 1 mg
供货总量: 1000 mg
发货期限: 自买家付款之日起 3 天内发货
所在地: 浙江 宁波市
有效期至: 长期有效
最后更新: 2014-12-18 14:19
购买
公司基本资料信息
 
 
产品详细说明
 
AS703026 1236699-92-5 AS703026 is a novel, selective, orally bioavailable mitogen-activated protein kinase (MEK) 1/2 inhibitor, in human multiple myeloma (MM)....
AS703026 1236699-92-5 AS703026 is a novel, selective, orally bioavailable mitogen-activated protein kinase (MEK) 1/2 inhibitor, in human multiple myeloma (MM)....
AS703026 1236699-92-5 AS703026 is a novel, selective, orally bioavailable mitogen-activated protein kinase (MEK) 1/2 inhibitor, in human multiple myeloma (MM)....
AS703026 1236699-92-5 AS703026 is a novel, selective, orally bioavailable mitogen-activated protein kinase (MEK) 1/2 inhibitor, in human multiple myeloma (MM)....
AZD6244 606143-52-6 AZD6244 is a potent, selective, and ATP-uncompetitive inhibitor of MEK1/2 kinases....
AZD6244 606143-52-6 AZD6244 is a potent, selective, and ATP-uncompetitive inhibitor of MEK1/2 kinases....
AZD6244 606143-52-6 AZD6244 is a potent, selective, and ATP-uncompetitive inhibitor of MEK1/2 kinases....
AZD6244 606143-52-6 AZD6244 is a potent, selective, and ATP-uncompetitive inhibitor of MEK1/2 kinases....
BIX 02188 1094614-84-2 BIX02188 is a selective and potent MEK5 inhibitor....
BIX 02188 1094614-84-2 BIX02188 is a selective and potent MEK5 inhibitor....
BIX 02188 1094614-84-2 BIX02188 is a selective and potent MEK5 inhibitor....
BIX 02188 1094614-84-2 BIX02188 is a selective and potent MEK5 inhibitor....
BIX 02189 1094614-85-3 BIX02189 is a selective and potent MEK5 inhibitor....
BIX 02189 1094614-85-3 BIX02189 is a selective and potent MEK5 inhibitor....
BIX 02189 1094614-85-3 BIX02189 is a selective and potent MEK5 inhibitor....
BIX 02189 1094614-85-3 BIX02189 is a selective and potent MEK5 inhibitor....
CCT239065 1163719-51-4 CCT239065 is a BRAFV600E inhibitor....
CEP-32496 1188910-76-0 CEP-32496 is a potent BRAF inhibitor....
CEP-32496 1188910-76-0 CEP-32496 is a potent BRAF inhibitor....
CEP-32496 1188910-76-0 CEP-32496 is a potent BRAF inhibitor....
CI-1040 212631-79-3 CI-1040 is a small-molecule with highly selective adenosine triphosphate (ATP) non-competitive inhibition activity against MEK1/2....
CI-1040 212631-79-3 CI-1040 is a small-molecule with highly selective adenosine triphosphate (ATP) non-competitive inhibition activity against MEK1/2....
CI-1040 212631-79-3 CI-1040 is a small-molecule with highly selective adenosine triphosphate (ATP) non-competitive inhibition activity against MEK1/2....
CI-1040 212631-79-3 CI-1040 is a small-molecule with highly selective adenosine triphosphate (ATP) non-competitive inhibition activity against MEK1/2....
CI-1040 212631-79-3 CI-1040 is a small-molecule with highly selective adenosine triphosphate (ATP) non-competitive inhibition activity against MEK1/2....
CPI-613 95809-78-2 CPI-613 is a non-redox active lipoate derivative that selectively inhibits mitochondrial enzymes pyruvate dehydrogenase (PDH) and α-ketoglutarate dehydrogenase....
CPI-613 95809-78-2 CPI-613 is a non-redox active lipoate derivative that selectively inhibits mitochondrial enzymes pyruvate dehydrogenase (PDH) and α-ketoglutarate dehydrogenase....
CPI-613 95809-78-2 CPI-613 is a non-redox active lipoate derivative that selectively inhibits mitochondrial enzymes pyruvate dehydrogenase (PDH) and α-ketoglutarate dehydrogenase....
CPI-613 95809-78-2 CPI-613 is a non-redox active lipoate derivative that selectively inhibits mitochondrial enzymes pyruvate dehydrogenase (PDH) and α-ketoglutarate dehydrogenase....
Dabrafenib 1195765-45-7 ....
Dabrafenib Mesylate 1195768-06-9 Dabrafenib mesylate is a mutant-BRAF kinase inhibitor....
Dabrafenib Mesylate 1195768-06-9 Dabrafenib mesylate is a mutant-BRAF kinase inhibitor....
Dabrafenib Mesylate 1195768-06-9 Dabrafenib mesylate is a mutant-BRAF kinase inhibitor....
Dabrafenib Mesylate 1195768-06-9 Dabrafenib mesylate is a mutant-BRAF kinase inhibitor....
GDC-0879 905281-76-7 GDC-0879 is a highly selective and orally bioavailable RAF small-molecule inhibitor....
GSK1120212 871700-17-3 GSK1120212 is a selective and highly potent MEK1 and MEK2 inhibitor with IC50 values of 1.8 and 0.92 nM, respectively....
GSK1120212 871700-17-3 GSK1120212 is a selective and highly potent MEK1 and MEK2 inhibitor with IC50 values of 1.8 and 0.92 nM, respectively....
GSK1120212 871700-17-3 GSK1120212 is a selective and highly potent MEK1 and MEK2 inhibitor with IC50 values of 1.8 and 0.92 nM, respectively....
JNK-IN-8 1410880-22-6 ....
LY2228820 862507-23-1 LY2228820 is a novel p38 mitogen-activated protein kinase (p38MAPK) inhibitor....
Nilotinib 641571-10-0 Nilotinib inhibits the kinases BCR-ABL, KIT, LCK, EPHA3, EPHA8, DDR1, DDR2, PDGFRB, MAPK11 and ZAK....
Nilotinib 641571-10-0 Nilotinib inhibits the kinases BCR-ABL, KIT, LCK, EPHA3, EPHA8, DDR1, DDR2, PDGFRB, MAPK11 and ZAK....
Nilotinib 641571-10-0 Nilotinib inhibits the kinases BCR-ABL, KIT, LCK, EPHA3, EPHA8, DDR1, DDR2, PDGFRB, MAPK11 and ZAK....
PD0325901 391210-10-9 PD0325901 is selective and non ATP-competitive mitogenic extracellular kinase 1/2 (MEK1/2) inhibitor with an IC50 of 0.33 nM....
PD0325901 391210-10-9 PD0325901 is selective and non ATP-competitive mitogenic extracellular kinase 1/2 (MEK1/2) inhibitor with an IC50 of 0.33 nM....
PD0325901 391210-10-9 PD0325901 is selective and non ATP-competitive mitogenic extracellular kinase 1/2 (MEK1/2) inhibitor with an IC50 of 0.33 nM....
PD0325901 391210-10-9 PD0325901 is selective and non ATP-competitive mitogenic extracellular kinase 1/2 (MEK1/2) inhibitor with an IC50 of 0.33 nM....
PD318088 391210-00-7 PD318088 is a non-ATP competitive MEK inhibitor....
PD98059 167869-21-8 PD98059 is a specific inhibitor of mitogen-activated protein kinase kinase (MEK)....
PD98059 167869-21-8 PD98059 is a specific inhibitor of mitogen-activated protein kinase kinase (MEK)....
PD98059 167869-21-8 PD98059 is a specific inhibitor of mitogen-activated protein kinase kinase (MEK)....
Pelitinib 257933-82-7 ....
Pelitinib 257933-82-7 ....
Pelitinib 257933-82-7 ....
     
PH-797804 586379-66-0 PH-797804 is an inhibitor of the α isoform of human p38 mitogen-active protein kinase (MAPK)....
PLX-4032 918504-65-1 PLX-4032 is a potent small-molecule B-Raf inhibitor for the potential treatment of malignant melanoma....
PLX-4032 918504-65-1 PLX-4032 is a potent small-molecule B-Raf inhibitor for the potential treatment of malignant melanoma....
PLX-4032 918504-65-1 PLX-4032 is a potent small-molecule B-Raf inhibitor for the potential treatment of malignant melanoma....
PLX4720 918505-84-7 PLX4720 inhibits B-RafV600E with an IC50 of 13 nM, defines a class of kinase inhibitor with marked selectivity in both biochemical and cellular assays....
PLX4720 918505-84-7 PLX4720 inhibits B-RafV600E with an IC50 of 13 nM, defines a class of kinase inhibitor with marked selectivity in both biochemical and cellular assays....
PLX4720 918505-84-7 PLX4720 inhibits B-RafV600E with an IC50 of 13 nM, defines a class of kinase inhibitor with marked selectivity in both biochemical and cellular assays....
R406(Free base) 841290-80-0 ....
RAF265 927880-90-8 RAF265 is a selective and potent inhibitor of RAF and VEGFR2....
RAF265 927880-90-8 RAF265 is a selective and potent inhibitor of RAF and VEGFR2....
SB 202190 152121-30-7 SB202190 is an effective and selective inhibitor of p38 with an IC50 of 30 nM....
SB 202190 152121-30-7 SB202190 is an effective and selective inhibitor of p38 with an IC50 of 30 nM....
SB 203580 152121-47-6 SB203580 is a selective cytokine suppressive binding protein/p38 kinase (p38 MAPK) inhibitor....
SB 203580 152121-47-6 SB203580 is a selective cytokine suppressive binding protein/p38 kinase (p38 MAPK) inhibitor....
SB 203580 152121-47-6 SB203580 is a selective cytokine suppressive binding protein/p38 kinase (p38 MAPK) inhibitor....
SB 203580 152121-47-6 SB203580 is a selective cytokine suppressive binding protein/p38 kinase (p38 MAPK) inhibitor....
Skepinone-L 1221485-83-1 ....
Skepinone-L 1221485-83-1 ....
Sorafenib 284461-73-0 Sorafenib is a small molecular inhibitor of several tyrosine protein kinases including VEGFR (vascular endothelial growth factor receptors) and PDGFR (platelet-derived growth factor receptors) and Raf kinases....
Sorafenib 284461-73-0 Sorafenib is a small molecular inhibitor of several tyrosine protein kinases including VEGFR (vascular endothelial growth factor receptors) and PDGFR (platelet-derived growth factor receptors) and Raf kinases....
Sorafenib 284461-73-0 Sorafenib is a small molecular inhibitor of several tyrosine protein kinases including VEGFR (vascular endothelial growth factor receptors) and PDGFR (platelet-derived growth factor receptors) and Raf kinases....
Sorafenib 284461-73-0 Sorafenib is a small molecular inhibitor of several tyrosine protein kinases including VEGFR (vascular endothelial growth factor receptors) and PDGFR (platelet-derived growth factor receptors) and Raf kinases....
Sorafenib tosylate 475207-59-1 ....
Sorafenib tosylate 475207-59-1 ....
Sorafenib tosylate 475207-59-1 ....
Sorafenib tosylate 475207-59-1 ....
SP600125 129-56-6 SP600125 is a selective inhibitor of Jun N-terminal kinase (JNK)....
SP600125 129-56-6 SP600125 is a selective inhibitor of Jun N-terminal kinase (JNK)....
SP600125 129-56-6 SP600125 is a selective inhibitor of Jun N-terminal kinase (JNK)....
TAK-632 1228591-30-7 TAK-632 is a potent pan-RAF inhibitor....
TAK-733 1035555-63-5 TAK-733 is a potent and selective MEK inhibitor....
TAK-733 1035555-63-5 TAK-733 is a potent and selective MEK inhibitor....
TAK-733 1035555-63-5 TAK-733 is a potent and selective MEK inhibitor....
TAK-733 1035555-63-5 TAK-733 is a potent and selective MEK inhibitor....
TAK715 303162-79-0 ....
TAK715 303162-79-0 ....
U0126 109511-58-2 U0126 is a highly selective inhibitor of both MEK1 and MEK2 which are human extracellular signal-regulated kinase activator kinases....
U0126 109511-58-2 U0126 is a highly selective inhibitor of both MEK1 and MEK2 which are human extracellular signal-regulated kinase activator kinases....
U0126 109511-58-2 U0126 is a highly selective inhibitor of both MEK1 and MEK2 which are human extracellular signal-regulated kinase activator kinases....
U0126 109511-58-2 U0126 is a highly selective inhibitor of both MEK1 and MEK2 which are human extracellular signal-regulated kinase activator kinases....
Vx-702 745833-23-2 VX-702 is a highly selective novel p38 MAPK inhibitor....
Vx-702 745833-23-2 VX-702 is a highly selective novel p38 MAPK inhibitor....
Vx-702 745833-23-2 VX-702 is a highly selective novel p38 MAPK inhibitor....
Vx-702 745833-23-2 VX-702 is a highly selective novel p38 MAPK inhibitor....
XMD 8-92 1234480-50-2 ....
ZM 336372 208260-29-1 ....

可以根据客户要求定制合成,并按要求分装,提供各项检测指标以确保产品质量。

联系电话18217049878;QQ:2578105091

更多详情可邮件至karebaybio2002@163.com

药物用中间体,不得直接用于人体,仅供科研使用


0条 [查看全部]  相关评论
 
更多»本企业其它产品

[ 产品搜索 ]  [ 加入收藏 ]  [ 告诉好友 ]  [ 打印本文 ]  [ 违规举报 ]  [ 关闭窗口 ]

 
网站首页 | 公益慈善栏目 赞助本站可以扫描支付 | 免费推广计划 | 全球资源网顾问团 | 帮助中心 | 企业文化 | 关于我们 | 全球信息中心 | 隐私政策 | 使用协议 | 版权隐私 | 网站地图 | 排名推广 | 广告服务 | 积分换礼 | 网站留言 | RSS订阅 | 本站对所有发布的信息不承担任何责任,用户应决定是否采用并承担风险。