PDGFR
PDGFR(血小板衍生生长因子受体)
PDGFR (platelet-derived growth factor receptor) is a group of cell surface tyrosine kinase receptors for members of the PDGF (platelet-derived growth factor) family.
PDGFR 相关产品(107)
- GC12216Axitinib (AG 013736)CAS: 319460-85-0纯度: >99.50% / >98.00%
Axitinib (AG 013736)是一种具有口服活性的特异性血管内皮生长因子受体(VEGFR)抑制剂,主要靶向VEGFR-1、VEGFR-2和VEGFR-3,IC 50 值分别为 0.1nM、0.2nM和0.1-0.3nM。
- GC13547Dovitinib (TKI-258, CHIR-258)CAS: 405169-16-6纯度: >98.00%
Dovitinib (TKI-258, CHIR-258)是一种高效,具有口服活性和安全药代动力学特性的小分子多激酶抑制剂,作用于FLT3、KIT和FGFR等靶点,IC 50 值分别为1、2和8-9nM。
- GC14396Ponatinib (AP24534)CAS: 943319-70-8纯度: >99.00%
Ponatinib (AP24534)是一种多靶点酪氨酸激酶抑制剂,可抑制Abl(IC 50 =0.37nM),PDGFRα(IC 50 =1.1nM),VEGFR2(IC 50 =1.5nM),FGFR1(IC 50 =2.2nM)和Src(IC 50 =5.4nM)的活性。
- GC15454Lenvatinib (E7080)CAS: 417716-92-8纯度: >99.50%
E7080,称为乐伐替尼,是一种口服多靶点酪氨酸激酶抑制剂,包括 VEGF、FGF 和 SCF 受体,已被证明可以提高放射性碘难治性甲状腺癌患者的生存率。
- GC16732TSU-68 (SU6668,Orantinib)CAS: 252916-29-3纯度: >98.50%
An inhibitor of select receptor tyrosine kinases
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC12216 | Axitinib (AG 013736) | 319460-85-0 | >99.50% / >98.00% | |
Axitinib (AG 013736)是一种具有口服活性的特异性血管内皮生长因子受体(VEGFR)抑制剂,主要靶向VEGFR-1、VEGFR-2和VEGFR-3,IC 50 值分别为 0.1nM、0.2nM和0.1-0.3nM。 | ||||
| GC12686 | SU 16f | 251356-45-3 | >98.00% / >99.50% | |
SU 16f是一种有效的酪氨酸激酶抑制剂,可抑制VEGF-R2、FGF-R1和PDGFRβ,IC 50 值分别为0.14、2.29和0.01μM。 | ||||
| GC12730 | Pazopanib Hydrochloride | 635702-64-6 | >99.50% | |
A multi-kinase inhibitor | ||||
| GC12980 | CP-673451 | 343787-29-1 | >99.50% | |
A selective PDGFRα/β kinase inhibitor | ||||
| GC13264 | Ki20227 | 623142-96-1 | >98.00% | |
A c-Fms kinase inhibitor | ||||
| GC13547 | Dovitinib (TKI-258, CHIR-258) | 405169-16-6 | >98.00% | |
Dovitinib (TKI-258, CHIR-258)是一种高效,具有口服活性和安全药代动力学特性的小分子多激酶抑制剂,作用于FLT3、KIT和FGFR等靶点,IC 50 值分别为1、2和8-9nM。 | ||||
| GC14315 | SU14813 maleate | 849643-15-8 | >99.50% | |
A dual VEGFR and PDGFR family kinase inhibitor | ||||
| GC14396 | Ponatinib (AP24534) | 943319-70-8 | >99.00% | |
Ponatinib (AP24534)是一种多靶点酪氨酸激酶抑制剂,可抑制Abl(IC 50 =0.37nM),PDGFRα(IC 50 =1.1nM),VEGFR2(IC 50 =1.5nM),FGFR1(IC 50 =2.2nM)和Src(IC 50 =5.4nM)的活性。 | ||||
| GC14534 | Regorafenib monohydrate | 1019206-88-2 | >99.50% | |
A multi-kinase inhibitor | ||||
| GC14544 | JNJ-10198409 | 627518-40-5 | >97.00% | |
A potent PDGF tyrosine kinase inhibitor | ||||
| GC14606 | Regorafenib hydrochloride | 835621-07-3 | >99.50% | |
A multi-kinase inhibitor | ||||
| GC14660 | SU 5402 | 215543-92-3 | >98.00% | |
SU 5402是一种多靶点受体酪氨酸激酶抑制剂,对血管内皮生长因子受体2(VEGF-R2)和成纤维细胞生长因子受体1(FGF-R1)酪氨酸激酶活性的IC 50 分别为20nM和30nM。 | ||||
| GC14676 | Pacritinib (SB1518) | 937272-79-2 | - | |
An equipotent inhibitor of FLT3 and JAK2 | ||||
| GC14733 | SU14813 | 627908-92-3 | >98.50% | |
A dual VEGFR and PDGFR family kinase inhibitor | ||||
| GC14906 | Crenolanib (CP-868596) | 670220-88-9 | >99.50% | |
An inhibitor of PDGFRα/β and FLT3 | ||||
| GC15254 | Tandutinib (MLN518) | 387867-13-2 | >99.00% | |
An antagonist of PDGFRβ, FLT3, and c-Kit | ||||
| GC15454 | Lenvatinib (E7080) | 417716-92-8 | >99.50% | |
E7080,称为乐伐替尼,是一种口服多靶点酪氨酸激酶抑制剂,包括 VEGF、FGF 和 SCF 受体,已被证明可以提高放射性碘难治性甲状腺癌患者的生存率。 | ||||
| GC15739 | CHIR-124 | 405168-58-3 | >98.00% | |
A selective Chk1 inhibitor | ||||
| GC16235 | AG-1295 | 71897-07-9 | >99.50% | |
A selective inhibitor of PDGF receptor kinase | ||||
| GC16421 | Cediranib (AZD217) | 288383-20-0 | >99.50% | |
An inhibitor of VEGF receptor tyrosine kinases | ||||
| GC16499 | Sorafenib Tosylate | 475207-59-1 | >99.50% | |
A multi-kinase inhibitor | ||||
| GC16519 | ENMD-2076 | 934353-76-1 | >98.00% | |
A multi-kinase inhibitor | ||||
| GC16732 | TSU-68 (SU6668,Orantinib) | 252916-29-3 | >98.50% | |
An inhibitor of select receptor tyrosine kinases | ||||
| GC17024 | DMPQ dihydrochloride | 1123491-15-5 | - | |
An potent inhibitor of PDGFRβ | ||||
