Tyrosine Kinase
Tyrosine Kinase(酪氨酸激酶)
- Bcr-Abl(73)
- Ack1(3)
- Axl(6)
- ALK(64)
- BMX Kinase(3)
- Broad Spectrum Protein Kinase Inhibitor(10)
- c-FMS(42)
- c-Kit(58)
- c-MET(99)
- c-RET(7)
- CSF-1R(3)
- DDR1/DDR2 Receptor(1)
- EGFR(278)
- EphB4(1)
- FAK(39)
- FGFR(104)
- FLT3(97)
- HER2(15)
- IGF1R(34)
- Insulin Receptor(46)
- IRAK(32)
- ITK(10)
- Lck(1)
- LRRK2(25)
- PDGFR(113)
- PTKs/RTKs(10)
- Pyk2(8)
- ROR(41)
- Spleen Tyrosine Kinase (Syk)(33)
- Src(108)
- Tie-2 (4)
- Trk(43)
- VEGFR(200)
- Kinase
- Discoidin Domain Receptor(16)
- DYRK(35)
- Ephrin Receptor(13)
- RET(30)
- ROS(14)
- TAM Receptor(33)
- IGFBR(1)
- Others(55)
Tyrosine Kinase 相关产品(1402)
- GC15568Dasatinib (BMS-354825)CAS: 302962-49-8纯度: >99.50% / >98.00%
Dasatinib (BMS-354825)是一种高效、口服生物利用度高的多靶点酪氨酸激酶抑制剂,对BCR-ABL、SRC家族激酶、c-KIT和PDGFR-β的IC₅₀分别为0.4nM、0.5nM、100nM和180nM。
- GC15709R788 disodium hexahydrateCAS: 914295-16-2纯度: >98.00%
Fostamatinib (R788) 二钠六水合物是活性化合物 R406 的口服前药。
- GC16021Lavendustin ACAS: 125697-92-9
A selective inhibitor of EGF receptor-associated tyrosine kinase
- GC16028NVP-BGJ398 phosphateCAS: 1310746-10-1
NVP-BGJ398 phosphate (BGJ-398 phosphate; NVP-BGJ398 phosphate) 是一种有效的 FGFR 家族抑制剂,对 FGFR1、FGFR2、FGFR3 和 FGFR4 的 IC50 分别为 0.9 nM、1.4 nM、1 nM 和 60 nM。
- GC16062VEGFR Tyrosine Kinase Inhibitor IICAS: 269390-69-4纯度: >98.00%
An inhibitor of KDR, FLT1, and c-Kit
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC15556 | UNC2025 | 1429881-91-3 | >99.50% | |
An orally bioavailable inhibitor of Mer and Flt3 | ||||
| GC15568 | Dasatinib (BMS-354825) | 302962-49-8 | >99.50% / >98.00% | |
Dasatinib (BMS-354825)是一种高效、口服生物利用度高的多靶点酪氨酸激酶抑制剂,对BCR-ABL、SRC家族激酶、c-KIT和PDGFR-β的IC₅₀分别为0.4nM、0.5nM、100nM和180nM。 | ||||
| GC15589 | WHI-P154 | 211555-04-3 | >99.00% | |
A JAK3 inhibitor | ||||
| GC15600 | Erlotinib Hydrochloride | 183319-69-9 | >99.50% | |
An EGFR tyrosine kinase inhibitor | ||||
| GC15647 | ID-8 | 147591-46-6 | >99.00% | |
A cell culture supplement for maintaining embryonic stem cell pluriotency | ||||
| GC15655 | AMG 337 | 1173699-31-4 | >99.00% | |
A selective c-Met inhibitor | ||||
| GC15658 | R406(free base) | 841290-80-0 | >99.50% | |
A potent and selective Syk inhibitor | ||||
| GC15664 | SGX-523 | 1022150-57-7 | >99.00% | |
A potent inhibitor of c-Met | ||||
| GC15674 | HDS 029 | 881001-19-0 | - | |
HDS 029 (compound 29) 是一种有效的酪氨酸激酶抑制剂,对 erbB1、erbB2、erbB4、EGF、HER 的 IC50 分别为 0.3、1.1、0.5、2.5、24 nM。 | ||||
| GC15709 | R788 disodium hexahydrate | 914295-16-2 | >98.00% | |
Fostamatinib (R788) 二钠六水合物是活性化合物 R406 的口服前药。 | ||||
| GC15739 | CHIR-124 | 405168-58-3 | >98.00% | |
A selective Chk1 inhibitor | ||||
| GC15801 | ACTB-1003 | 939805-30-8 | >98.00% | |
A multi-kinase inhibitor | ||||
| GC15818 | RAF265 | 927880-90-8 | >99.50% | |
A B-Raf and VEGFR2 inhibitor | ||||
| GC15925 | PD 158780 | 171179-06-9 | >99.50% | |
An ErbB receptor family inhibitor | ||||
| GC15927 | GW 583340 dihydrochloride | 1173023-85-2 | - | |
dual EGFR/ErbB2 tyrosine kinase inhibitor | ||||
| GC15936 | MSDC-0160 | 146062-49-9 | >99.00% | |
A thiazolidinedione | ||||
| GC15950 | CGP 52411 | 145915-58-8 | - | |
A phthalimide with diverse biological activities | ||||
| GC16000 | WHI-P180 | 211555-08-7 | >99.50% | |
A multi-kinase inhibitor | ||||
| GC16021 | Lavendustin A | 125697-92-9 | - | |
A selective inhibitor of EGF receptor-associated tyrosine kinase | ||||
| GC16025 | CH5424802 | 1256580-46-7 | >99.50% | |
An orally available inhibitor of ALK | ||||
| GC16028 | NVP-BGJ398 phosphate | 1310746-10-1 | - | |
NVP-BGJ398 phosphate (BGJ-398 phosphate; NVP-BGJ398 phosphate) 是一种有效的 FGFR 家族抑制剂,对 FGFR1、FGFR2、FGFR3 和 FGFR4 的 IC50 分别为 0.9 nM、1.4 nM、1 nM 和 60 nM。 | ||||
| GC16062 | VEGFR Tyrosine Kinase Inhibitor II | 269390-69-4 | >98.00% | |
An inhibitor of KDR, FLT1, and c-Kit | ||||
| GC16126 | INDY | 1169755-45-6 | >98.00% | |
A DYRK1A inhibitor | ||||
| GC16235 | AG-1295 | 71897-07-9 | >99.50% | |
A selective inhibitor of PDGF receptor kinase | ||||
