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Cat. No. Product Name Target Signaling Pathways
T22349 JNJ-38158471

CS-2660

VEGFR; c-RET; c-Kit Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors
JNJ-38158471 (CS-2660) 是一种耐受性好的,有口服活性的、高效的、选择性的 VEGFR-2抑制剂 (IC50:40 nM),还能抑制 Ret (IC50:180 nM) 和 Kit (IC50:500 nM)。
T2516 Amuvatinib

MP470,HPK 56

Apoptosis; FLT; c-Met/HGFR; c-RET; DNA/RNA Synthesis; PDGFR; c-Kit Angiogenesis; Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Tyrosine Kinase/Adaptors
Amuvatinib (MP470) 是一种多靶点酪氨酸激酶抑制剂,对突变 c-Kit,PDGFRα,Flt3,c-Met 和 c-Ret 具有活性。它还是一种 DNA 修复抑制剂,靶向蛋白 DNA 修复 RAD51,从而破坏 DNA 损伤修复,具有抗肿瘤活性。
T0520 Lenvatinib

仑伐替尼,E7080

VEGFR; FGFR; c-RET; PDGFR; c-Kit Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors
Lenvatinib (E7080) 是一种多靶点受体酪氨酸激酶抑制剂,抑制 VEGFR1-3、FGFR1-4、KIT、PDGFR 和 RET 等,具有口服活性。Lenvatinib 对 VEGFR2 和 VEGFR3 的抑制活性最强 (IC50=4/5.2 nM)。Lenvatinib 具有强效抗肿瘤活性。
T4053 AST 487

NVP-AST 487

VEGFR; FLT; c-RET; Bcr-Abl; c-Kit Angiogenesis; Apoptosis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors
AST 487 (NVP-AST 487) 是 RET 激酶抑制剂 (IC50:880 nM),能够抑制 RET 自磷酸化,及下游效应器激活,也抑制 Flt-3 (IC50:520 nM)。
T8541 Lenvatinib mesylate

仑伐替尼甲酸盐,E7080 (mesylate),乐伐替尼

VEGFR; FGFR; c-RET; PDGFR; c-Kit Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors
Lenvatinib mesylate (E7080 (mesylate)) 是一种口服具有活力的,多靶点酪氨酸激酶抑制剂,能够抑制血管内皮生长因子受体(VEGFR1-3),成纤维细胞生长因子受体(FGFR1-4),干细胞因子受体(KIT),血小板衍生生长因子受体(PDGFR),转染期间重排(RET),具有效抗癌作用。
T1792 Regorafenib

BAY 73-4506,瑞戈非尼,Fluoro-Sorafenib,瑞格非尼

Raf; VEGFR; c-RET; PDGFR; c-Kit; Autophagy Angiogenesis; Apoptosis; Autophagy; MAPK; Tyrosine Kinase/Adaptors
Regorafenib (BAY 73-4506) 是一种多靶点受体酪氨酸激酶抑制剂,抑制 RETC-RAF、VEGFR2、c-Kit、VEGFR1 和 PDGFRβ (IC50=1.5/2.5/4.2/7/13/22 nM),具有口服活性。Regorafenib 具有抗肿瘤和抗血管生成活性。
T6028 PF 477736

PF 00477736,PF-477736,PF-736,PF-00477736,PF477736

c-Fms; VEGFR; FGFR; FLT; c-RET; Chk; CDK; Src; Aurora Kinase Angiogenesis; Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Tyrosine Kinase/Adaptors
PF 477736 (PF-736,PF-00477736) 是一种特异性、有效且具有 ATP 竞争性的 Chk1 抑制剂,Ki 值为0.49 nM。它也是Chk2抑制剂,Ki 值为 47 nM。它还抑制VEGFR2、Fms、Yes、Aurora-A、FGFR3、Flt3和Ret
T11638 Ilorasertib hydrochloride

ABT-348 hydrochloride

Aurora Kinase Cell Cycle/Checkpoint; Chromatin/Epigenetic
Ilorasertib hydrochloride (ABT-348 hydrochloride) is an ATP-competitive multitargeted kinase inhibitor, which inhibits Aurora C, Aurora B, and Aurora A (IC50s: 1 nM, 7 nM, 120 nM). It also suppresses RET tyrosine kinase, PDGFRβ, and Flt1 (IC50s: 7 nM, 3 nM, and 32 nM).
T14363 AZ-23

AZ 23,AZ23

Trk receptor Tyrosine Kinase/Adaptors
AZ-23是一种 ATP-竞争性的,口服具有活性的 Trk 激酶 A/B/C 抑制剂,IC50值分别为2 nM (TrkA),8 nM (TrkB),24 nM (FGFR1),52 nM (Flt3),55 nM (Ret),84 nM (MuSk),99 nM (Lck)。
TQ0059 Ilorasertib

ABT-348

VEGFR; FLT; c-RET; PDGFR; Aurora Kinase Angiogenesis; Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Tyrosine Kinase/Adaptors
Ilorasertib (ABT-348) 是一种 ATP 竞争性多靶点激酶抑制剂,可抑制 Aurora A、Aurora B 和Aurora C,IC50值为120 nM、7 nM 和1 nM。它还抑制 RET 酪氨酸激酶、PDGFRβ 和 Flt1,IC50为7 nM、3 nM 和 32 nM。
T70382 KBP-7018 HCl

KBP-7018 Hydrochloride is a novel, tyrosine kinase-selective inhibitor with potent effects on three fibrotic kinases (c-KIT, PDGFR, and RET).
T27715 KBP-7018

KBP 7018

KBP-7018 is a potent, selective tyrosine kinase inhibitor with effects on three fibrotic kinases c-KIT, RET, and PDGFR (IC50 values are 10nM, 7.6 nM and 25nM respectively).
T1792L Regorafenib monohydrate

Raf; VEGFR; c-RET; PDGFR; c-Kit; Autophagy Angiogenesis; Apoptosis; Autophagy; MAPK; Tyrosine Kinase/Adaptors
Regorafenib monohydrate 是一种新型口服多激酶抑制剂,对VEGFR1/2/3、PDGFRβ、Kit、RET 和Raf-1的IC50分别为 13、4.2、46、22、7、1.5 和 2.5 nM。
T14282 Amuvatinib hydrochloride

HPK 56 hydrochloride,MP470 hydrochloride

Others Others
Amuvatinib hydrochloride (MP470 hydrochloride) is an orally bioavailable multi-targeted tyrosine kinase inhibitor with potent activity against mutant c-Kit, PDGFRα, Flt3, c-Met and c-Ret and is also a DNA repair suppressor through suppression of DNA repai
T10157 Regorafénib N-oxyde (M2)

瑞戈非尼杂质 13

Raf; VEGFR; c-RET; PDGFR; c-Kit; Drug Metabolite Angiogenesis; Apoptosis; MAPK; Metabolism; Tyrosine Kinase/Adaptors
Regorafénib N-oxyde M2 是 Regorafenib 的活性代谢物。Regorafenib 是多靶点抑制剂,包括VEGFR1/2/3,PDGFRβ,Kit,RET 和 Raf-1 , IC50分别是 13/4.2/46,22,7,1.5 和 2.5 nM。
T2070 Agerafenib

RXDX-105,CEP 32496,CEP-32496,CEP32496

Raf; c-RET; Bcr-Abl; PDGFR; Src; c-Kit Angiogenesis; Apoptosis; Cytoskeletal Signaling; MAPK; Tyrosine Kinase/Adaptors
Agerafenib (CEP32496) 是口服高效的 BRAFV600E 抑制剂,Kd 为 14 nM。
T73033 TRK II-IN-1

Trk receptor Tyrosine Kinase/Adaptors
TRKII-IN-1 是一种有效的 II 型TRK抑制剂,对TRKA/B/C及TRKAG667C的IC50分别为3.3、6.4、4.3 和 9.4 nM。此外,TRKII-IN-1 对FLT3、RET和VEGFR2也具有抑制作用,其IC50分别为1.3、9.9 和 71.1 nM。TRKII-IN-1 主要用于TRK驱动的癌症研究。
T37582 Ganglioside GM1 Mixture (ovine) (ammonium salt)

Ganglioside GM1is a monosialylated ganglioside and the prototypic ganglioside for those containing one sialic acid residue.1,2It is found in a large variety of cells, including immune cells and neurons, and is enriched in lipid rafts in the cell membrane.3It associates with growth factor receptors, including TrkA, TrkB, and the GDNF receptor complex containing Ret and GFRα, and is required for TrkA expression on the cell surface. Ganglioside GM1interacts with other proteins to increase calcium i...
T14928 Agerafenib hydrochloride

RXDX-105 hydrochloride,CEP-32496 (hydrochloride)

c-RET; c-Kit Apoptosis; Tyrosine Kinase/Adaptors
Agerafenib hydrochloride is a highly potent inhibitor of BRAFV600E (Kd: 14 nM).

化合物

JNJ-38158471
Cat.No: T22349
Synonym: CS-2660
Target: VEGFR, c-RET, c-Kit
Amuvatinib
Cat.No: T2516
Synonym: MP470,HPK 56
Target: Apoptosis, FLT, c-Met/HGFR, c-RET, DNA/RNA Synthesis, PDGFR, c-Kit
Lenvatinib
Cat.No: T0520
Synonym: 仑伐替尼,E7080
Target: VEGFR, FGFR, c-RET, PDGFR, c-Kit
AST 487
Cat.No: T4053
Synonym: NVP-AST 487
Target: VEGFR, FLT, c-RET, Bcr-Abl, c-Kit
Lenvatinib mesylate
Cat.No: T8541
Synonym: 仑伐替尼甲酸盐,E7080 (mesylate),乐伐替尼
Target: VEGFR, FGFR, c-RET, PDGFR, c-Kit
Regorafenib
Cat.No: T1792
Synonym: BAY 73-4506,瑞戈非尼,Fluoro-Sorafenib,瑞格非尼
Target: Raf, VEGFR, c-RET, PDGFR, c-Kit, Autophagy
PF 477736
Cat.No: T6028
Synonym: PF 00477736,PF-477736,PF-736,PF-00477736,PF477736
Target: c-Fms, VEGFR, FGFR, FLT, c-RET, Chk, CDK, Src, Aurora Kinase
Ilorasertib hydrochloride
Cat.No: T11638
Synonym: ABT-348 hydrochloride
Target: Aurora Kinase
AZ-23
Cat.No: T14363
Synonym: AZ 23,AZ23
Target: Trk receptor
Ilorasertib
Cat.No: TQ0059
Synonym: ABT-348
Target: VEGFR, FLT, c-RET, PDGFR, Aurora Kinase
KBP-7018 HCl
Cat.No: T70382
Synonym:
Target:
KBP-7018
Cat.No: T27715
Synonym: KBP 7018
Target:
Regorafenib monohydrate
Cat.No: T1792L
Synonym:
Target: Raf, VEGFR, c-RET, PDGFR, c-Kit, Autophagy
Amuvatinib hydrochloride
Cat.No: T14282
Synonym: HPK 56 hydrochloride,MP470 hydrochloride
Target: Others
Regorafénib N-oxyde (M2)
Cat.No: T10157
Synonym: 瑞戈非尼杂质 13
Target: Raf, VEGFR, c-RET, PDGFR, c-Kit, Drug Metabolite
Agerafenib
Cat.No: T2070
Synonym: RXDX-105,CEP 32496,CEP-32496,CEP32496
Target: Raf, c-RET, Bcr-Abl, PDGFR, Src, c-Kit
TRK II-IN-1
Cat.No: T73033
Synonym:
Target: Trk receptor
Ganglioside GM1 Mixture (ovine) (ammonium salt)
Cat.No: T37582
Synonym:
Target:
Agerafenib hydrochloride
Cat.No: T14928
Synonym: RXDX-105 hydrochloride,CEP-32496 (hydrochloride)
Target: c-RET, c-Kit
TargetMol Loading
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