“abl”的搜索结果

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  1. CHMFL-ABL/KIT-155

    Catalog No. A12421
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    ABL/c-KIT dual kinase inhibitor
    CHMFL-ABL/KIT-155 (CHMFL-ABL-KIT-155; compound 34) is a highly potent and orally active type II ABL/c-KIT dual kinase inhibitor. 了解更多
  2. CHMFL-ABL-039

    Catalog No. A13182
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    BCR-ABL inhibitor
    CHMFL-ABL-039 is a type II native ABL kinase and drug-resistant V299L mutant BCR-ABL inhibitor with the IC50s of 7.9 nM and 27.9 nM, respectively. CHMFL-ABL-039 is used in the research of chronic myeloid leukemia. 了解更多
  3. SNIPER(ABL)-039

    Catalog No. A19588
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    SNIPER(ABL)-039, conjugating Dasatinib (ABL inhibitor) to LCL161 derivative (IAP ligand) with a linker, induces the reduction of BCR-ABL protein with a DC50 of 10 nM. IC50s are 0.54 nM, 10 nM, 12 nM, and 50 nM for ABL, cIAP1, cIAP2, XIAP, respectively. 了解更多
  4. BCR-ABL-IN-1

    Catalog No. A12496
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    BCR-ABL inhibitor
    BCR-ABL-IN-1 is an inhibitor of BCR-ABL tyrosine kinase, with a pIC50 of 6.46, and may be used in the research of chronic myelogenous leukemia. 了解更多
  5. SNIPER(ABL)-062

    Catalog No. A18567
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    ABL inhibitor
    SNIPER(ABL)-062, in which an ABL inhibitor is linked to a ligand of cIAP1 via a linker containing a variable polyethylene glycol (PEG) unit, shows a potent activity to degrade the BCR-ABL protein. 了解更多
  6. SNIPER(ABL)-058

    Catalog No. A19616
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    SNIPER(ABL)-058, conjugating Imatinib (ABL inhibitor) to LCL161 derivative (IAP ligand) with a linker, induces the reduction of BCR-ABL protein with a DC50 of 10 μM. 了解更多
  7. SNIPER(ABL)-024

    Catalog No. A19607
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    SNIPER(ABL)-024, conjugating GNF5 (ABL inhibitor) to LCL161 derivative (IAP ligand) with a linker, induces the reduction of BCR-ABL protein with a DC50 of 5μM. 了解更多
  8. SNIPER(ABL)-033

    Catalog No. A19597
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    SNIPER(ABL)-033, conjugating HG-7-85-01 (ABL inhibitor) to LCL161 derivative (IAP ligand) with a linker, induces the reduction of BCR-ABL protein with a DC50 of 0.3 μM. 了解更多
  9. CHMFL-ABL-121

    Catalog No. A19079
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    ABL2 inhibitor
    CHMFL-ABL-121 is a highly potent type II ABL kinase inhibitor with IC50s of 2 nM and 0.2 nM against purified inactive ABL wt and T315I kinase protein, respectively. 了解更多
  10. BCR-ABL-IN-2

    Catalog No. A21043
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    inhibitor of BCR-ABL1 tyrosine kinase
    BCR-ABL-IN-2 is an inhibitor of BCR-ABL1 tyrosine kinase, with IC50s of 57 nM, 773 nm for ABL1native and ABL1T315I, respectively. 了解更多
  11. Asciminib

    Catalog No. A19658
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    Bcr-Abl inhibitor
    Asciminib (ABL001) is a potent and selective allosteric Bcr-Abl inhibitor; inhibits Ba/F3 cells grown with an IC50 of 0.25 nM. 了解更多
  12. KW-2449

    Catalog No. A10508
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    FLT3/FGFR/Bcr-Abl/Aurora 抑制剂
    KW-2449是FLT3、ABl、ABl-T315I和Aurora激酶的多激酶抑制剂。 了解更多
  13. CT-721

    Catalog No. A19742
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    Bcr-Abl kinase inhibitor
    CT-721 is a potent and time-dependent Bcr-Abl kinase inhibitor with an IC50 of 21.3 nM for wild-type Bcr-Abl kinase, and possesses anti-chronic myeloid leukemia (CML) activities. 了解更多
  14. 1-Naphthyl PP1 hydrochloride

    Catalog No. A21790
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    Src/c-Abl inhibitor
    1-Naphthyl PP1 hydrochloride is a selective inhibitor of src family kinases v-Src and c-Fyn as well as the tyrosine kinase c-Abl (IC50 values are 1.0, 0.6, 0.6, 18 and 22 μM for v-Src, c-Fyn, c-Abl, CDK2 and CAMK II respectively). 了解更多
  15. GZD824 Dimesylate

    Catalog No. A15849
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    Bcr-Abl 抑制剂
    GZD824 Dimesylate是Bcr-Abl(WT)和Bcr-Abl(T315I)的新型生物可用Bcr-Abl抑制剂,IC50分别为0.34 nM和0.68 nM。 了解更多
  16. XL-228

    Catalog No. A13069
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    IGF-1R, Aurora, FGFR, ABL, SRC 抑制剂
    XL228是靶向IGF1R,AURORA激酶,FGFR1-3,ABL和SRC家族激酶的蛋白激酶抑制剂。XL228是一种Aurora A抑制剂(IC50,f3 nmol/L),对ABL1(Ki,5 nmol/L)以及BCR-ABL1 T315I(Ki,1.4 nmol/L)激酶显示出有效的生化活性。 了解更多
  17. Imatinib carbaldehyde

    Catalog No. A19670
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    Imatinib carbaldehyde (CGP-57148B carbaldehyde), the Imatinib (ABL inhibitor) based moiety, binds to IAP ligand via a linker to form SNIPER. 了解更多
  18. GNF5-amido-Me

    Catalog No. A19651
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    GNF5-amido-Me, the GNF5 (ABL inhibitor) based moiety, binds to IAP ligand via a linker to form SNIPER. 了解更多
  19. Dasatinib carbaldehyde

    Catalog No. A19627
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    Dasatinib carbaldehyde (BMS-354825 carbaldehyde), the Dasatinib (ABL inhibitor) based moiety, binds to IAP ligand via a linker to form SNIPER . 了解更多
  20. AZD0424

    Catalog No. A19488
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    Src/Abl kinase inhibitor
    AZD0424 is an orally active, and dual selective Src/Abl kinase inhibitor with potential antineoplastic activity. AZD0424 induces apoptosis and cell cycle arrest in lymphoma cells. 了解更多
  21. ABL127

    Catalog No. A19208
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    PME-1 inhibitor
    ABL127 is a selective and covalent inhibitor of protein methylesterase 1 (PME-1) with IC50s of 6.4 nM and 4.2 nM in HEK293T and MDA-MB-231 cells, respectively. 了解更多
  22. CZC-8004

    Catalog No. A19444
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    ABL inhibitor
    CZC-8004 is a pan-kinase inhibitor and binds a range of tyrosine kinases, including ABL kinase. 了解更多
  23. Lyn-IN-1

    Catalog No. A16265
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    dual Bcr-Abl/Lyn 抑制剂
    Lyn-IN-1是一种有效的选择性Bcr-Abl/Lyn双重抑制剂,摘自专利WO2014169128A1。 了解更多
  24. GNF-7

    Catalog No. A15887
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    Bcr-Abl 抑制剂
    GNF-7是一种有效的II型激酶Bcr-Abl抑制剂,对于M351T,T315I,E255 V,G250E和c-Abl,IC50分别<5 nM,61 nM,122 nM,136 nM和133 nM。 了解更多
  25. AG 957

    Catalog No. A13589
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    p210 tyrosine kinase 抑制剂
    AG 957是有效的酪氨酸激酶抑制剂。与p140c-abl(Ki = 10μM)相比,选择性阻断人p210bcr-abl(Ki = 750 nM)的酪氨酸激酶活性。 了解更多
  26. Dasatinib (BMS-354825)

    Catalog No. A10290
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    Abl-Src 抑制剂
    Dasatinib (BMS-354825)是一种口服多BCR/ABL和Src家族酪氨酸激酶抑制剂。Dasatinib (BMS-354825)的主要靶标是BCR/ABL,Src,c-Kit,ephrin受体和其他几种酪氨酸激酶,但不是erbB激酶,例如EGFR或Her2。 了解更多
  27. Bafetinib (INNO-406)

    Catalog No. A10119
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    Bcr-Abl 抑制剂
    Bafetinib (INNO-406)是一种双重Bcr-Abl/Lyn酪氨酸激酶抑制剂。 了解更多
  28. AP24534 (Ponatinib)

    Catalog No. A10080
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    BCR-ABL 抑制剂
    AP24534 (Ponatinib)是有效的多激酶和pan-BCR-ABL抑制剂。 了解更多
  29. JNJ-10198409

    Catalog No. A22554
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    PDGFRα/PDGFRβ inhbitor
    JNJ 10198409 is a potent platelet-derived growth factor receptor (PDGFR) inhibitor (IC50 values are 4.2 and 45 nM for PDGFRβ and PDGFRα, respectively). Also inhibits c-Abl, Lck, c-Src and Fyn kinases (IC50 values are 22, 100, 185 and 378 nM respectively). 了解更多
  30. Multi-kinase inhibitor 1

    Catalog No. A22645
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    multi-kinase inhibitor
    Multi-kinase inhibitor 1 is a potent multi-kinase inhibitor. Multi-kinase inhibitor 1 has the potential for diseases or disorders associated with abnormal or deregulated tyrosine kinase activity, particularly diseases associated with the activity of PDGF-R, c-Kit and Bcr-abl. 了解更多
  31. N-Deshydroxyethyl Dasatinib

    Catalog No. A20125
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    N-Deshydroxyethyl Dasatinib (N-Deshydroxyethyl BMS-354825), the Dasatinib-based moiety, binds to IAP ligand via a linker to form SNIPER to degrade ABL. 了解更多
  32. KB SRC 4

    Catalog No. A20111
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    c-Src inhibitor
    KB SRC 4 is a potent, and highly selective c-Src inhibitor, with a Ki of 44 nM and a Kd of 86 nM, and shows no inhibition on c-Abl up to 125 μM; KB SRC 4 has antitumor activity. 了解更多
  33. Bestatin-amido-Me

    Catalog No. A19661
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    Bestatin-amido-Me, the Bestatin-based IAP ligand, binds to ABL inhibitor via a linker to form SNIPER. 了解更多
  34. MV-1-NH-Me

    Catalog No. A19642
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    MV-1-NH-Me, the MV-1 based IAP ligand, binds to ABL inhibitor via a linker to form SNIPER. 了解更多
  35. cIAP1 ligand 2

    Catalog No. A19034
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    cIAP1 ligand 2 is the LCL161 derivative based IAP ligand. cIAP1 ligand 2 can be connected to the ABL ligand for protein by a linker to form SNIPER. 了解更多
  36. cIAP1 ligand 1

    Catalog No. A19040
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    cIAP1 ligand 1 is the LCL161 derivative based IAP ligand. cIAP1 ligand 1 can be connected to the ABL ligand for protein by a linker to form SNIPER. 了解更多
  37. Mcl1-IN-9

    Catalog No. A18372
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    Mcl-1 Inhibitor
    Mcl1-IN-9 is a potent myeloid cell leukemia-1 (Mcl-1) Inhibitor with an IC50 of 446 nM in reengineered BCR-ABL+ B-ALL cells and a Ki of 0.03 nM. 了解更多
  38. ON 146040

    Catalog No. A16266
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    dual PI3K and BCR-ABL 抑制剂
    ON 146040是第一个靶向STAT3和STAT5途径的PI3K和BCR-ABL双重抑制剂;抑制PI3Kα/δ同工型,IC50为14/20 nM。 了解更多
  39. GZD824

    Catalog No. A16264
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    Bcr-Abl 抑制剂
    GZD824是一种新型的口服生物利用型抑制剂,可抵抗包括T315I在内的各种Bcr-Abl突变体。 了解更多
  40. Flumatinib

    Catalog No. A16258
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    multi-kinase 抑制剂
    Flumatinib是一种多激酶抑制剂,对c-Abl,PDGFRbeta和c-Kit的IC50值分别为1.2 nM,307.6 nM和2662 nM。 了解更多
  41. DPH

    Catalog No. A11379
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    c-ABL activitor
    DPH是一种有效的细胞渗透性c-Abl激活剂,在刺激c-Abl激活中显示出强大的酶和细胞活性。 了解更多
  42. NVP-BAW2881

    Catalog No. A12693
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    VEGFR 抑制剂
    NVP-BAW2881是有效的选择性VEGFR抑制剂(血管内皮生长因子受体酪氨酸激酶抑制剂),IC50 为值9 nM,具有抑制慢性和急性皮肤炎症的作用。 了解更多
  43. Radotinib (IY-5511)

    Catalog No. A13029
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    Bcr-Abl tyrosine 抑制剂?
    Radotinib是一种新型的选择性Bcl-Abl酪氨酸激酶抑制剂。 了解更多
  44. Nilotinib monohydrochloride monohydrate

    Catalog No. A15186
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    Bcr-Abl 抑制剂
    Nilotinib monohydrochloride monohydrate是一种Bcr-Abl抑制剂,IC50小于30 nM。 了解更多
  45. NRC-AN-019

    Catalog No. A13562
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    Bcr-Abl 抑制剂
    NRC-AN-019是Bcr-Abl蛋白-酪氨酸激酶的口服酪氨酸激酶抑制剂(TKI)。NRC-AN-019在抑制MDAMB231和HTB20/BT474细胞的血管生成潜力和增殖方面更有效。 了解更多
  46. Flumatinib mesylate

    Catalog No. A13530
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    c-Abl/c-Kit/PDGRFβ 抑制剂
    Flumatinib mesylate以时间和剂量依赖性的方式降低U266细胞中C-MYC,HIF-1a和VEGF的表达,因此甲磺酸氟马替尼可能成为MM治疗的新药。 了解更多
  47. GNF-5

    Catalog No. A13237
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    Bcr-Abl 抑制剂
    GNF-5是BCR-ABL的选择性变构抑制剂。 了解更多
  48. PD173955

    Catalog No. A13120
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    Bcr-Abl 抑制剂
    PD-173955是src酪氨酸激酶抑制剂。PD173955抑制Bcr-Abl依赖的细胞生长。PD173955显示G(1)中的细胞周期停滞。PD173955在Bcr-Abl的激酶抑制测定中的IC(50)为1-2 nM,在细胞生长测定中,其抑制Bcr-Abl依赖性底物酪氨酸磷酸化。 PD173955抑制试剂盒配体依赖性c-kit自磷酸化(IC(50)=约25 nM)和试剂盒配体依赖性M07e细胞增殖(IC(50)= 40 nM),但对白介素3依赖性(IC (50)= 250 nM)或粒细胞巨噬细胞集落刺激因子(IC(50)= 1 microM)依赖性细胞生长。 了解更多
  49. PP1

    Catalog No. A12724
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    Src 抑制剂
    PP1是Src家族酪氨酸激酶的有效抑制剂。抑制p56lck和p59fynT(IC50值分别为5和6 nM)。在ZAP-70和JAK2上显示的选择性> 8000倍。还适度抑制p38,CSK,PDGF受体,RET衍生的癌蛋白,c-Kit和Bcr-Abl。 了解更多
  50. GNF 2

    Catalog No. A11439
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    Bcr-Abl 抑制剂
    GNF 2是一种Bcr-abl抑制剂,在表达Bcr-abl的细胞中抑制增殖并诱导凋亡。 了解更多

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