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9

抑制剂 & 化合物

2

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Cat. No. Product Name Target Signaling Pathways
T61304 FGFR2-IN-1

FGFR Angiogenesis; Tyrosine Kinase/Adaptors
FGFR2-IN-1是一种 FGFR 抑制剂,对 FGFR1FGFR2FGFR3具有抑制作用, IC50 分别为460、140和2200 nM。FGFR2-IN-1 可用于研究与 FGFR2 相关的癌症。
T60185 FGFR2-IN-3

FGFR Angiogenesis; Tyrosine Kinase/Adaptors
FGFR2-IN-3 是一种具有口服活性的选择性 FGFR2抑制剂。
T5044 Futibatinib

TAS120,FGFR-IN-1

FGFR Angiogenesis; Tyrosine Kinase/Adaptors
Futibatinib (FGFR-IN-1) 是口服具有活力的、选择性强的、高生物利用度的、不可逆的 FGFR 抑制剂。它抑制突变型和野生型 FGFR2,且 IC50相似(wild-type FGFR2=0.9 nM; V5651=1-3 nM; N550H=3.6 nM; E566G=2.4 nM)。
T62653 FGFR-IN-2

FGFR-IN-2 (compound 1) 是一种有效的 FGFR 抑制剂,能够作用于 FGFR1 (IC50: 7.3 nM)、FGFR2 (IC50: 4.3 nM)、FGFR3 (IC50: 7.6 nM) 和 FGFR4 (IC50: 11 nM)。FGFR-IN-2 具有潜力进行癌症研究。
T39001 FGFR-IN-1

FGFR-IN-1 is a highly effective inhibitor targeting the Fibroblast Growth Factor Receptor (FGFR) group, comprising FGFR1, FGFR2, and FGFR3, with an impressive inhibitory concentration (IC 50) of less than 100 nM (US20130338134A1, example 219).
T64107 FGFR3-IN-1

FGFR3-IN-1 (compound 1) 是一种成纤维细胞生长因子受体 (FGFR) 抑制剂,可抑制FGFR1 (IC50: 40 nM),FGFR2 (IC50: 5.1 nM) 和 FGFR3 (IC50: 12 nM)。FGFR3-IN-1 能够用于研究膀胱癌。
T77816 Deruxtecan analog 2

Deruxtecananalog 2(示例9 P3)是一种含活性分子-linker的Deruxtecan类似物,由Camptothecin(一种对多种癌症如结直肠癌、乳腺癌、肺癌和卵巢癌具有抗肿瘤活性的Topo I抑制剂)和linker组成,主要用于开发针对EGFR2的抗体药物偶联物(ADC)活性分子。
T69162 Ki23057

Ki23057 is a a FGFR2 inhibitor, which enhances the chemosensitivity of drug-resistant gastric cancer cell lines when used in combination with chemotherapeutic drugs. Ki23057 might be therapeutically promising for treating drug-resistant gastric cancer cells, especially when used in combination with SN38, PTX, or VP16. The apoptosis process might be the main mechanism underlying the synergistic effect of these combinations. The ERCC1 and p53 genes may play an integral role in the synergism betwee...
T79257 FGFR-IN-11

FGFR Angiogenesis; Tyrosine Kinase/Adaptors
FGFR-IN-11(compound I-5)是一款具备口服活性的共价pan-FGFR抑制剂,对FGFR1FGFR4的IC50值分别为9.9 nM、3.1 nM、16 nM和1.8 nM。该化合物能够在纳摩尔水平有效抑制多种肿瘤细胞的增殖,并在荷瘤小鼠模型中显著地抑制肿瘤生长。

化合物

FGFR2-IN-1
Cat.No: T61304
Synonym:
Target: FGFR
FGFR2-IN-3
Cat.No: T60185
Synonym:
Target: FGFR
Futibatinib
Cat.No: T5044
Synonym: TAS120,FGFR-IN-1
Target: FGFR
FGFR-IN-2
Cat.No: T62653
Synonym:
Target:
FGFR-IN-1
Cat.No: T39001
Synonym:
Target:
FGFR3-IN-1
Cat.No: T64107
Synonym:
Target:
Deruxtecan analog 2
Cat.No: T77816
Synonym:
Target:
Ki23057
Cat.No: T69162
Synonym:
Target:
FGFR-IN-11
Cat.No: T79257
Synonym:
Target: FGFR
Cat. No. Product Name Target Signaling Pathways
T2S0007 Ferulic acid sodium

阿魏酸钠,阿魏酸钠;3-甲氧基-4-羟基肉桂酸钠,Sodium ferulic,Ferulic acid sodium salt,Sodium ferulate

FGFR; Reactive Oxygen Species; 5-HT Receptor; Endogenous Metabolite Angiogenesis; GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience; NF-κB; Tyrosine Kinase/Adaptors
Ferulic acid sodium (Sodium ferulic) 是新型的成纤维细胞生长因子受体 1 (FGFR1) 抑制剂。它对于FGFR1FGFR2的IC50分别为 3.78 and 12.5 μM。
T2215 Ferulic Acid

Coniferic acid,Fumalic Acid,阿魏酸

FGFR; Endogenous Metabolite Angiogenesis; Metabolism; Tyrosine Kinase/Adaptors
Ferulic Acid (Coniferic acid) 是新型的成纤维细胞生长因子受体 1 (FGFR1)抑制剂, 在FGFR1FGFR2的IC50分别为 3.78 和 12.5 μM。

天然产物

Ferulic acid sodium
Cat.No: T2S0007
Synonym: 阿魏酸钠,阿魏酸钠;3-甲氧基-4-羟基肉桂酸钠,Sodium ferulic,Ferulic acid sodium salt,Sodium ferulate
Target: FGFR, Reactive Oxygen Species, 5-HT Receptor, Endogenous Metabolite
Ferulic Acid
Cat.No: T2215
Synonym: Coniferic acid,Fumalic Acid,阿魏酸
Target: FGFR, Endogenous Metabolite
TargetMol Loading
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