“rasgap ras p21”的搜索结果

产品 1 到 50 共 312个

每页
页面:
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5

设置降序顺序
    • 最新产品

    Ras-IN-3144

    Catalog No. A17222
    Quick View
    pan-RAS inhibitor
    Ras-IN-3144 is a pan-RAS inhibitor which inhibits RAS signaling pathways in cancer cells and prevents the growth of RAS mutant mouse cancer xenografts. 了解更多
  1. K-Ras-IN-1

    Catalog No. A20875
    Quick View
    K-Ras inhibitor
    K-Ras-IN-1 is a K-Ras inhibitor, by binding to K-Ras in a hydrophobic pocket that is occupied by Tyr-71 in the apo-Ras crystal structure.(the detailed information refer to the reference). 了解更多
  2. K-Ras G12C-IN-1

    Catalog No. A20937
    Quick View
    K-ras G12C inhibitor
    K-Ras G12C-IN-1 is a novel and irreversible inhibitor of mutant K-ras G12C extracted from patent WO 2014152588 A1. 了解更多
  3. K-Ras G12C-IN-2

    Catalog No. A20936
    Quick View
    covalent K-Ras G12C inhibitor
    K-Ras G12C-IN-2 is an irreversible covalent K-Ras G12C inhibitor. 了解更多
  4. K-Ras G12C-IN-3

    Catalog No. A20931
    Quick View
    K-ras G12C inhibitor
    K-Ras G12C-IN-3 is a novel and irreversible inhibitor of mutant K-ras G12C. 了解更多
  5. K-Ras(G12C) inhibitor 9

    Catalog No. A14250
    Quick View
    K-Ras(G12C) 抑制剂
    K-Ras(G12C) inhibitor 9是致癌性K-Ras(G12C)的变构抑制剂。 了解更多
  6. Pluripotin (SC-1)

    Catalog No. A11225
    Quick View
    ERK1/RasGAP 抑制剂
    Pluripotin (SC-1)的活性是通过联合抑制RasGAP和ERK1介导的,其Kd值分别为98和212 nM。 了解更多
  7. K-Ras(G12C) inhibitor 12

    Catalog No. A14227
    Quick View
    K-Ras(G12C) 抑制剂
    K-Ras(G12C) inhibitor 12 是致癌性K-Ras(G12C)的变构抑制剂。 了解更多
  8. K-Ras(G12C) inhibitor 6

    Catalog No. A14103
    Quick View
    K-Ras(G12C) 抑制剂
    K-Ras(G12C) inhibitor 6 是致癌性K-Ras(G12C)的不可逆抑制剂,颠覆了天然核苷酸的偏爱性,使GDP优于GTP。 了解更多
  9. WS-383

    Catalog No. A21483
    Quick View
    DCN1-UBC12 interaction inhibitor
    WS-383 is a potent, selective and reversible inhibitor of DCN1-UBC12 interaction, with an IC50 of 11 nM. WS-383 inhibits Cul3/1 neddylation, induces accumulation of p21, p27 and NRF2. 了解更多
  10. Pifithrin-alpha

    Catalog No. A12451
    Quick View
    p53 抑制剂
    Pifithrin-alpha是p53介导的细胞凋亡和p53依赖性基因转录(如细胞周期蛋白G,p21/waf1和mdm2表达)的可逆抑制剂。 了解更多
  11. 6H05

    Catalog No. A16097
    Quick View
    K-Ras 抑制剂
    6H05是致癌突变体K-Ras(G12C)的选择性变构抑制剂。 了解更多
  12. (Rac)-Antineoplaston A10

    Catalog No. A21689
    Quick View
    Ras inhibitor
    (rac)-Antineoplaston A10 is the racemate of Antineoplaston A10. Antineoplaston A10 is a Ras inhibitor potentially for the treatment of glioma, lymphoma, astrocytoma and breast cancer. 了解更多
  13. 6H05 (TFA)

    Catalog No. A21377
    Quick View
    K-Ras(G12C) inhibitor
    6H05 TFA is a selective, and allosteric inhibitor of oncogenic mutant K-Ras(G12C). 了解更多
  14. ARS-1323

    Catalog No. A17060
    Quick View
    mutant K-ras G12C 抑制剂
    ARS-1323是突变K-ras G12C的新型抑制剂。 了解更多
  15. ARS-1630

    Catalog No. A17061
    Quick View
    mutant K-ras G12C 抑制剂
    ARS-1630是突变K-ras G12C的新型抑制剂。 了解更多
  16. APS-2-79 HCl

    Catalog No. A16175
    Quick View
    KSR/Ras 抑制剂
    APS-2-79 HCl,稳定KSR(Ras激酶抑制剂)失活状态并拮抗致癌性Ras信号(IC50值为120 nM,对抗KSR2的ATP-生物素探针标记)的小分子。 了解更多
  17. Resminostat hydrochloride

    Catalog No. A15220
    Quick View
    HDAC 抑制剂
    Resminostat hydrochloride是HDAC1/3/6的有效抑制剂(IC50 = 43-72 nM);对HDAC8的效力较低,IC50为877 nM。 了解更多
  18. 6H05 (trifluoroacetate salt)

    Catalog No. A14235
    Quick View
    K-Ras 抑制剂
    6H05 (trifluoroacetate salt)是致癌性K-Ras(G12C)的选择性变构抑制剂。 了解更多
  19. Kobe2602

    Catalog No. A12578
    Quick View
    Ras–Raf 抑制剂
    Kobe2602是Kobe0065的类似物。表现出有效的活性以竞争性抑制Ki-值为149±55 μM的H-Ras·GTP与c-Raf-1 RBD的结合。 了解更多
  20. FTI 277

    Catalog No. A12368
    Quick View
    FTase 抑制剂
    FTI 277是一种抑制法呢基转移酶(FTase)的抑制剂(IC50 = 0.5 nM)。抑制全细胞的 H-Ras 和 K-Ras 加工(IC50值分别为0.1和10 nM),破坏mapk的组成型H-Ras特异性激活。在人恶性胶质瘤细胞和许多其他肿瘤细胞系中引起显著的抗增殖作用。 了解更多
  21. Lonafarnib (SCH66336)

    Catalog No. A12328
    Quick View
    FPTase 抑制剂
    Lonafarnib (SCH66336)是H-ras、K-ras-4B和N-ras的选择性FPTase抑制剂,IC50分别为1.9 nM、5.2 nM和2.8 nM。 了解更多
  22. CID-1067700

    Catalog No. A21560
    Quick View
    pan GTPase inhibitor
    CID-1067700 (ML282) is a pan GTPase inhibitor, and competitively inhibits Ras-related in brain 7 (Rab7) with a Ki of 13 nM. 了解更多
  23. GGTI298 Trifluoroacetate

    Catalog No. A16560
    Quick View
    GGTase I inhibitor
    GGTI298 Trifluoroacetate is a CAAZ peptidomimetic geranylgeranyltransferase I (GGTase I) inhibitor, which can inhibit Rap1A with IC50 of 3 μM; little effect on Ha-Ras with IC50 of >20 μM. 了解更多
  24. PHT-7.3

    Catalog No. A18473
    Quick View
    Cnk1 inhibitor
    PHT-7.3 is a selective inhibitor of connector enhancer of kinase suppressor of Ras 1 (Cnk1) pleckstrin homology (PH) domain, which inhibits mut-KRas, but not wild-type KRas cancer cell and tumor growth and signaling. 了解更多
  25. FGTI-2734

    Catalog No. A18578
    Quick View
    FT/GGT dual inhibitor
    FGTI-2734 is a RAS C-terminal mimetic dual farnesyl transferase (FT) and geranylgeranyl transferase-1 (GGT) inhibitor with IC50s of 250 nM and 520 nM for FT and GGT, respectively. 了解更多
  26. Antineoplaston A10

    Catalog No. A17183
    Quick View
    Ras 抑制剂
    Antineoplaston A 10是Ras抑制剂,可能用于治疗神经胶质瘤,淋巴瘤,星形细胞瘤和乳腺癌。 了解更多
  27. APS-2-79

    Catalog No. A16231
    Quick View
    KSR/Ras 抑制剂
    APS-2-79是RAF通过直接结合KSR活性位点而使MEK磷酸化的拮抗剂。 了解更多
  28. XRP44X

    Catalog No. A16049
    Quick View
    Ras-Net 抑制剂
    XRP44X是Ras-Net(Elk-3)途径抑制剂(IC50 = 10-20 nM)。间接抑制Erk1/2激活上游的净磷酸化。 了解更多
  29. RSL3

    Catalog No. A15865
    Quick View
    Ferroptosis inhibitor
    RSL3 is a ferroptosis activator in a VDAC-independent manner,exhibiting selectivity for tumor cells bearing oncogenic RAS. 了解更多
  30. Kobe0065

    Catalog No. A13135
    Quick View
    Ras-Raf interaction 抑制剂
    Kobe0065抑制锚定依赖性和非依赖性生长,阻断MEK / ERK活性并诱导H-rasG12V转化的NIH3T3细胞凋亡。 了解更多
  31. Balamapimod (MKI-833)

    Catalog No. A13119
    Quick View
    Ras/Raf/MEK 抑制剂
    Balamapimod (MKI-833)是Ras/Raf/MEK抑制剂。 了解更多
  32. Diazepinomicin

    Catalog No. A12891
    Quick View
    RAS/RAF/MAPK 抑制剂
    Diazepinomicin,也称为TLN-4601,是具有潜在抗肿瘤活性的RAS/RAF/MAPK信号传导途径的小分子抑制剂。 了解更多
    • 最新产品

    AMG-510 (Sotorasib)

    Catalog No. A19021
    Quick View
    KRAS G12C covalent inhibitor
    AMG-510 is a potent, orally bioavailable, and selective KRAS G12C covalent inhibitor with anti-tumor activity. 了解更多
  33. (±)-Huperzine A

    Catalog No. A21003
    Quick View
    AChE inhibitor
    (??)-Huperzine A, an active Lycopodium alkaloid extracted from traditional Chinese herb, is a potent, selective and reversible acetylcholinesterase (AChE) inhibitor and has been widely used in China for the treatment of Alzheimer's disease (AD). 了解更多
  34. (+)-Phenserine

    Catalog No. A20993
    Quick View
    cholinesterase noncompetitive inhibitor
    (+)-Phenserine is a novel selective cholinesterase noncompetitive inhibitor with an IC50 of 45.3 μM. 了解更多
  35. Ilorasertib

    Catalog No. A20982
    Quick View
    ATP-competitive multitargeted kinase inhibitor
    Ilorasertib (ABT-348) is a potent and ATP-competitive multitargeted kinase inhibitor, which inhibits Aurora C, Aurora B, and Aurora A with IC50s of 1 nM, 7 nM, 120 nM, respectively. 了解更多
  36. Indotecan

    Catalog No. A20979
    Quick View
    Top1 inhibitor
    Indotecan (LMP-400) is a potent topoisomerase 1(Top1) inhibitor with IC50 values of 300, 1200, 560 nM for P388, HCT116, MCF-7 cell lines, respectively. 了解更多
  37. MF-438

    Catalog No. A20963
    Quick View
    SCD1 inhibitor
    MF-438 is a potent and orally bioavailable stearoyl-CoA desaturase 1 (SCD1) inhibitor with an EC50 of 2.3 nM for rSCD1. 了解更多
  38. BMS-214662

    Catalog No. A20948
    Quick View
    farnesyl transferase inhibitor
    BMS-214662 is a potent and selective farnesyl transferase inhibitor with potent antitumor activity with an IC50 of 1.35 nM. 了解更多
  39. Remodelin

    Catalog No. A21985
    Quick View
    acetyl-transferase protein NAT10 inhibitor
    Remodelin is a novel potent and selective inhibitor of the acetyl-transferase protein NAT10. 了解更多
  40. Raltegravir potassium

    Catalog No. A21403
    Quick View
    integrase (IN) inhibitor
    Raltegravir is a potent integrase (IN) inhibitor, used to treat HIV infection. 了解更多
  41. BTZ043

    Catalog No. A21263
    Quick View
    DprE1 inhibitor
    BTZ043 is an inhibitor of decaprenyl-phosphoribose-epimerase (DprE1), with MICs of of 2.3 nM and 9.2 nM for M. tuberculosis H37Rv and Mycobacterium smegmatis, respectively. 了解更多
  42. Carotegrast

    Catalog No. A21997
    α4 integrin receptor inhibitor
    Carotegrast is an orally available α4 integrin receptor inhibitor with anti-inflammatories activities. 了解更多
  43. TAS-103

    Catalog No. A21954
    Quick View
    DNA topoisomerase I/II inhibitor
    TAS-103 is a dual inhibitor of DNA topoisomerase I/II, used for cancer research. 了解更多
  44. LY309887

    Catalog No. A21905
    Quick View
    GARFT inhibitor
    LY309887 is a potent inhibitor of glycinamide ribonucleotide formyltransferase (GARFT), with a Ki of 6.5 nM, and has antitumor activity. 了解更多
  45. Daunorubicin

    Catalog No. A21903
    Quick View
    topoisomerase II inhibitor
    Daunorubicin (Daunomycin; RP 13057; Rubidomycin) is a topoisomerase II inhibitor with potent antineoplastic activities. 了解更多
  46. Entacapone sodium salt

    Catalog No. A21888
    Quick View
    COMT inhibitor
    Entacapone is a specific, potent, peripherally acting catechol-O-methyltransferase (COMT) inhibitor with IC50 of 151 nM for PD treatment. 了解更多
  47. Olprinone

    Catalog No. A21869
    Quick View
    PDE3 inhibitor
    Olprinone(Loprinone) is a selective phosphodiesterase 3 (PDE3) inhibitor. 了解更多
  48. IBMX

    Catalog No. A21847
    Quick View
    PDE inhibitor
    IBMX is a broad-spectrum phosphodiesterase (PDE) inhibitor, with IC50s of 6.5, 26.3 and 31.7 μM for PDE3, PDE4 and PDE5, respectively. 了解更多

产品 1 到 50 共 312个

每页
页面:
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5

设置降序顺序
Rewards