Home >> Signaling Pathways >> Tyrosine Kinase

Tyrosine Kinase(酪氨酸激酶)

  1. Cat.No. 产品名称 Information
  2. GC48840 9-Methoxyellipticine

    Methoxy-9-ellipticine, NSC 69187

    An alkaloid with anticancer activity
  3. GC48800 SU 4942 A modulator of tyrosine kinase signaling
  4. GC48614 IMP-1710 A clickable UCH-L1 inhibitor
  5. GC48387 Inostamycin A A bacterial metabolite with anticancer activity
  6. GC48332 RR-Src (trifluoroacetate salt)

    Arg-Arg-Leu-Ile-Glu-Asp-Ala-Glu-Tyr-Ala-Ala-Arg-Gly, RRLIEDAEYAARG, Src-Peptide

    A synthetic peptide substrate
  7. GC50706 JBJ-03-142-02 Highly potent epidermal growth factor receptor (EGFR) and ErbB2 (human epidermal growth factor receptor; HER2) inhibitor
  8. GC50660 HIOC HIOC 是 TrkB(原肌球蛋白相关激酶 B)受体的有效和选择性激活剂。
  9. GC48118 Sunitinib-d10

    舒尼替尼-D10,SU 11248-d10

    An internal standard for the quantification of sunitinib
  10. GC48070 SB-431542 (hydrate) Inhibitor of receptors ALK4, ALK5, and ALK7
  11. GC48022 Radotinib-d6

    IY-5511

    Radotinib-d6 是氘标记的 Radotinib。
  12. GC47938 Pericosine A

    (+)-Pericosine A

    A fungal metabolite with anticancer activity
  13. GC47771 NG 25 (hydrochloride hydrate) An inhibitor of MAP4K2 and TAK1
  14. GC47697 Mobocertinib

    莫博替尼; TAK-788; AP32788

    An inhibitor of mutant EGFR and HER2 receptors
  15. GC47687 ML-209 An RORγt antagonist
  16. GC47570 Lipoxygenin An inhibitor of 5-LO
  17. GC47452 Imatinib-d3

    STI571-d3 hydrochloride; CGP-57148B-d3 hydrochloride

    An internal standard for the quantification of imatinib
  18. GC47398 Genistein-d4

    金雀异黄酮-D4,NPI 031L-d4

    An internal standard for the quantification of genistein
  19. GC47395 Gefitinib-d6

    D6-吉非替尼,ZD1839-d6

    An internal standard for the quantification of gefitinib
  20. GC47393 Ganglioside GM1 Mixture (porcine brain) (ammonium salt)

    GM1, Monosialoganglioside GM1

    A sphingolipid
  21. GC47392 Ganglioside GM1 Mixture (ovine) (ammonium salt)

    GM1, Monosialoganglioside GM1

    A sphingolipid
  22. GC47350 Finasteride-d9

    非那雄胺-D9,MK-906-d9

    An internal standard for the quantification of finasteride
  23. GC47321 Etifoxine-13C-d3

    艾替伏辛 13C-d3

    A neuropeptide with diverse biological activities
  24. GC47303 Erlotinib-d6 (hydrochloride)

    埃罗替尼-D6盐酸盐,CP-358774-d6 hydrochloride; NSC 718781-d6 hydrochloride; OSI-774-d6 hydrochloride

    An internal standard for the quantification of erlotinib
  25. GC47182 Dehydrolithocholic Acid

    3-Ketolithocholic Acid

    A major metabolite of lithocholic acid
  26. GC46924 BIBF 1120-13C-d3

    Nintedanib-13C-d3

    A neuropeptide with diverse biological activities
  27. GC46899 Axitinib-13C-d3

    阿昔替尼杂质,AG-013736 13CD3

    An internal standard for the quantification of axitinib
  28. GC46809 Afatinib-d6

    BIBW 2992 D6

    An internal standard for the quantification of afatinib
  29. GC46628 4-Chloro-6,7-bis(2-methoxyethoxy)quinazoline

    4-氯-6,7-二(2-甲氧基乙氧基)喹唑啉

    A building block and synthetic intermediate
  30. GC46490 1-Palmitoyl-d3-2-hydroxy-sn-glycero-3-PC

    1-Hexadecanoyl-sn-glycero-3-Phosphatidylcholine-d3, 1-Hexadecanoyl-sn-glycero-3-Phosphocholine-d3, LPC-d3, 16:0/0:0(d3) Lyso-PC, 1-Palmitoyl-sn-glycero-3-Phosphocholine-d3, PC(16:0/0:0)-d3, 16:0/0:0-PC-d3

    A neuropeptide with diverse biological activities
  31. GC46474 18-Deoxyherboxidiene

    RQN-18690A

    A bacterial metabolite with antiangiogenic activity
  32. GC46304 (±)-Nebivolol-d4 (hydrochloride) A neuropeptide with diverse biological activities
  33. GC61217 Protein kinase inhibitors 1 hydrochloride Proteinkinaseinhibitors1hydrochloride是一种有效的HIPK2抑制剂,对HIPK1和HIPK2的IC50值分别为136和74nM,对HIPK2的Kd值为9.5nM。
  34. GC61161 Osimertinib D6

    AZD-9291-d6; Mereletinib-d6

    OsimertinibD6(AZD-9291D6)是Osimertinib的一种氘代化合物。Osimertinib是一种不可逆和突变的选择性的EGFR抑制剂,抑制EGFRL858R和EGFRL858R/T790M的IC50分别为12和1nM。
  35. GC61111 NBI-31772 hydrate A nonpeptide ligand that releases IGF-1 from IGFBP
  36. GC60930 Imatinib D4

    [2H4]-伊马替尼,STI571 D4; CGP-57148B D4

    ImatinibD4(STI571D4)是Imatinib(STI571)的氘代物。Imatinib是一种口服生物可用的酪氨酸激酶抑制剂,可选择性抑制BCR/ABL,v-Abl,PDGFR,c-kit激酶活性。
  37. GC60868 Gefitinib D8

    吉非替尼杂质-D8,ZD1839-d8

    GefitinibD8(ZD1839D8)是Gefitinib的氘代物。Gefitinib是一种有效的(EGFR)抑制剂,在NR6wtEGFR细胞中IC50值为2-37nM。
  38. GC60805 EMI48 EMI48是EMI1的衍生物,EMI48比EMI1对突变型EGFR具有更大的效力。EMI48抑制EGFR三重突变体。
  39. GC60726 CP-547632 TFA A potent inhibitor of VEGFR2 and bFGF
  40. GC60629 BDTX-189

    BDTX-189

    An inhibitor of wild-type and mutant EGFR and HER2
  41. GC60601 ARRY-382 ARRY-382 is a highly selective, oral inhibitor of the CSF1R with an IC50 of 9 nM.
  42. GC60592 APS6-45 APS6-45(Compound 10) is an orally active tumor-calibrated inhibitor (TCI) that inhibits RAS/MAPK signaling and exhibits antitumor activity.
  43. GC60567 Afatinib impurity 11 Afatinib impurity 11 is an impurity of afatinib, an EGFR family inhibitor.
  44. GC60372 TrkA-IN-1 TrkA-IN-1 是一种有效的选择性肌球蛋白相关激酶 A (TrkA) 抑制剂,在基于细胞的测定中,IC50 为 99 nM。TrkA-IN-1 具有镇痛作用。
  45. GC60365 TIE-2/VEGFR-2 kinase-IN-1 TIE-2/VEGFR-2 kinase-IN-1 用于合成 TIE-2 或者 VEGFR-2 抑制剂,从专利 WO2003022852 中获得,例 14。TIE-2/VEGFR-2 kinase-IN-1 用于研究不适当的血管生成相关疾病。
  46. GC60283 Pentagamavunon-1

    PGV-1

    Pentagamavunon-1 (PGV-1) 是Curcumin 的类似物,具有口服活性,通过多个机制诱导凋亡信号,如抑制COX-2 和 VEGF。Pentagamavunon-1 (PGV-1) 可抑制 NF-κB 的激活。
  47. GC60270 Nilotinib D6

    尼罗替尼-D6,AMN107-d6

    An internal standard for the quantification of nilotinib
  48. GC60175 GIP (1-30) amide,Human acetate GIP (1-30) amide,Human acetate 是葡萄糖依赖性促胰岛素多肽 (GIP) 片段。葡萄糖依赖性促胰岛素多肽是一种肠降血糖素激素,可刺激胰岛素分泌并减少餐后血糖波动。GIP (1-30) amide (Human) 在 10-9-10-6 M 范围内剂量依赖性地促进胰岛素分泌。
  49. GC60154 Erlotinib D6

    CP-358774-d6; NSC 718781-d6; OSI-774-d6

    An internal standard for the quantification of erlotinib
  50. GC39689 3-Hydroxy Midostaurin

    CGP52421

    3-Hydroxy Midostaurin (CGP 52421) 是 PKC412 的代谢产物,可有效抑制 FMS 样酪氨酸激酶 3 (FLT3) 自磷酸化,在培养基和血浆中的 IC50 分别为 132 nM 和 9.8 μM。与 PKC412 相比,3-Hydroxy Midostaurin 的选择性较低,但细胞毒性更高。
  51. GC39623 DCC-3014

    DCC-3014

    Vimseltinib (DCC-3014) is a c-FMS (CSF-IR) and c-Kit dual inhibitor extracted from patent WO2014145025A2, Compound Example 10, has IC50s of <0.01 μM and 0.1-1 μM, respectively.

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