关于 "FGFR" 的结果23+ 个结果
- FGFR3-IN-5CAS: 2446664-72-6
FGFR3-IN-5 是一种有效的选择性 FGFR3 抑制剂,对 FGFR3、FGFR2 和 FGFR1 的 IC50 值分别为 3、44、和 289 nM。FGFR3-IN-5 可用于癌症的研究。
- FGFR4-IN-5CAS: 1628793-01-0
FGFR4-IN-5 是一种有效的选择性共价 FGFR4 抑制剂,IC50 为 6.5 nM。FGFR4-IN-5 具有较强的抗肿瘤活性,可用于肝癌研究。
- FGFR1/DDR2 inhibitor 1CAS: 2308497-58-5
FGFR1/DDR2 inhibitor 1 is an inhibitor of fibroblast growth factor receptor 1 (FGFR1) and discoidin domain receptor 2 (DDR2).
- FGFR2-IN-2CAS: 2677709-81-6
FGFR2-IN-2 (Compound 38) 是一种选择性 FGFR2 抑制剂,对 FGFR1、FGFR2 和 FGFR3 的 IC50 分别为 389、29 和 758 nM。
- FGFR1 Human, (22-285)
Fibroblast Growth Factor Receptor-1 Human Recombinant, (22-285 a.a.)
- FGFR1 Human, (22-374)
Fibroblast Growth Factor Receptor-1, (22-374 a.a.) Human Recombinant
- FGFR2 Human, (22-289)
FGFR2 produced in Sf9 Baculovirus cells is a single, glycosylated polypeptide chain containing 507 amino acids (22-289a
- FIIN 1 hydrochlorideCAS: 1256152-35-8
FIIN 1 hydrochloride 是一种有效的、不可逆的、选择性的 FGFR 抑制剂。 FIIN 1 hydrochloride 与 FGFR1/2/3/4 和 Flt1/4 结合,Kd 分别为 2.8/6.9/5.4/120 nM 和 32/120 nM。 FIIN 1 hydrochloride 对 FGFR1/2/3/4 的生化 IC50 分别为 9.2、6.2、11.9 和 189 nM。
| 货号 | 产品名称 | CAS号 | 靶点 / 通路 | 引用 | 结构 |
|---|---|---|---|---|---|
| GC63395 | FGFR-IN-1 | 1513860-41-7 | FGFR | ||
FGFR-IN-1 是一种有效的 FGFR 抑制剂,对 FGFR1、FGFR2 和 FGFR3 的IC50 分别小于 100 nM。 | |||||
| GP22499 | FGFR1OP Human | - | FGF Receptors | ||
FGFR1 Oncogene Partner Human Recombinant | |||||
| GP22502 | FGFR3 Human | - | FGF Receptors | ||
Fibroblast Growth Factor Receptor 3 Fc Chimera Human Recombinant | |||||
| GP22504 | FGFR4 Human | - | FGF Receptors | ||
Fibroblast Growth Factor Receptor 4 Fc Chimera Human Recombinant | |||||
| GP22503 | FGFR3 Human, His | - | FGF Receptors | ||
Fibroblast Growth Factor Receptor-3 Human Recombinant, His Tag | |||||
| GC69106 | FGFR3-IN-5 | 2446664-72-6 | FGFR | ||
FGFR3-IN-5 是一种有效的选择性 FGFR3 抑制剂,对 FGFR3、FGFR2 和 FGFR1 的 IC50 值分别为 3、44、和 289 nM。FGFR3-IN-5 可用于癌症的研究。 | |||||
| GC19155 | FGFR4-IN-1 | 1708971-72-5 | FGFR | ||
An inhibitor of FGFR4 | |||||
| GP22505 | FGFR4 Human, His | - | FGF Receptors | ||
Fibroblast Growth Factor Receptor-4 Human Recombinant, His Tag | |||||
| GP22495 | FGFR1 Human | - | FGF Receptors | ||
Fibroblast Growth Factor Receptor 1 Fc Chimera Human Recombinant | |||||
| GP22500 | FGFR2 Human | - | FGF Receptors | ||
Fibroblast Growth Factor Receptor 2 Fc Chimera Human Recombinant | |||||
| GC62602 | FGFR4-IN-5 | 1628793-01-0 | FGFR | ||
FGFR4-IN-5 是一种有效的选择性共价 FGFR4 抑制剂,IC50 为 6.5 nM。FGFR4-IN-5 具有较强的抗肿瘤活性,可用于肝癌研究。 | |||||
| GP22496 | FGFR1 Human, His | - | FGF Receptors | ||
Fibroblast Growth Factor Receptor-1 Human Recombinant, His Tag | |||||
| GP22501 | FGFR2 Human, His | - | FGF Receptors | ||
Fibroblast Growth Factor Receptor-2 Human Recombinant, His Tag | |||||
| GC65992 | FGFR2-IN-3 | 2549174-42-5 | EGFR | ||
FGFR2-IN-3 是一种具有口服活性的 FGFR2 选择性抑制剂。 | |||||
| GC65212 | FGFR1/DDR2 inhibitor 1 | 2308497-58-5 | Discoidin Domain Receptor | ||
FGFR1/DDR2 inhibitor 1 is an inhibitor of fibroblast growth factor receptor 1 (FGFR1) and discoidin domain receptor 2 (DDR2). | |||||
| GC70914 | FGFR2-IN-1 | 2677709-76-9 | FGFR | ||
FGFR2-IN-1是一种选择性FGFR2抑制剂,IC50为140 nM。 | |||||
| GC64475 | FGFR2-IN-2 | 2677709-81-6 | FGFR | ||
FGFR2-IN-2 (Compound 38) 是一种选择性 FGFR2 抑制剂,对 FGFR1、FGFR2 和 FGFR3 的 IC50 分别为 389、29 和 758 nM。 | |||||
| GP22497 | FGFR1 Human, (22-285) | - | FGF Receptors | ||
Fibroblast Growth Factor Receptor-1 Human Recombinant, (22-285 a.a.) | |||||
| GP22498 | FGFR1 Human, (22-374) | - | FGF Receptors | ||
Fibroblast Growth Factor Receptor-1, (22-374 a.a.) Human Recombinant | |||||
| GC73608 | FGFR1 inhibitor-10 | 2426769-76-6 | FGFR | ||
FGFR1 inhibitor-10(化合物4i)是FGFR1抑制剂(IC50:28nM)。 | |||||
| GP26188 | FGFR2 Human, (22-289) | - | FGF Receptors | ||
FGFR2 produced in Sf9 Baculovirus cells is a single, glycosylated polypeptide chain containing 507 amino acids (22-289a | |||||
| GC65991 | FGFR2-IN-3 hydrochloride | 2688040-45-9 | EGFR | ||
FGFR2-IN-3 hydrochloride 是一种具有口服活性的 FGFR2 选择性抑制剂。 | |||||
| GC50051 | FIIN 1 hydrochloride | 1256152-35-8 | FGFR | ||
FIIN 1 hydrochloride 是一种有效的、不可逆的、选择性的 FGFR 抑制剂。 FIIN 1 hydrochloride 与 FGFR1/2/3/4 和 Flt1/4 结合,Kd 分别为 2.8/6.9/5.4/120 nM 和 32/120 nM。 FIIN 1 hydrochloride 对 FGFR1/2/3/4 的生化 IC50 分别为 9.2、6.2、11.9 和 189 nM。 | |||||
