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Epigenetics

产品 51 到 100 共 474个

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  1. Nexturastat A
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    Nexturastat A

    Catalog No. A14032
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    HDAC6 抑制剂
    Nexturastat A是一种芳基脲衍生物，可作为组蛋白脱乙酰基酶6（HDAC6）的有效且高度选择性的抑制剂（IC50 = 5.02+/-0.60 nM）。 了解更多
  2. HPOB
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    HPOB

    Catalog No. A14197
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    HDAC6 抑制剂
    HPOB是组蛋白去乙酰化酶6(HDAC6；IC50 = 56 nM)。 了解更多
  3. Splitomicin
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    Splitomicin

    Catalog No. A14221
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    NAD(+)-dependent histone deacetylase Sir2p 抑制剂
    Splitomicin是一种选择性的NAD(+)-依赖性组蛋白脱乙酰基酶Sir2p抑制剂，IC50为60 uM，在基于细胞的测定中显示出更高的活性。 了解更多
  4. Tasquinimod
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    Tasquinimod

    Catalog No. A12616
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    HDAC4 抑制剂
    Tasquinimod是一种变构抑制HDAC4信号传导的口服活性抗血管生成剂。 了解更多
  5. Santacruzamate A
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    Santacruzamate A

    Catalog No. A14236
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    HDAC 抑制剂
    Santacruzamate A (CAY10683)是一种有效的选择性HDAC抑制剂，对HDAC2的IC50为119 pM，选择性是其他HDAC的3600倍以上。 了解更多
  6. LMK-235
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    LMK-235

    Catalog No. A14341
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    HDAC4/5 抑制剂
    LMK-235是选择性组蛋白脱乙酰基酶(HDAC) 4和HDAC5抑制剂。 了解更多
  7. ST7612AA1
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    ST7612AA1

    Catalog No. A14418
    HDAC 抑制剂
    ST7612AA1是新型的有效HDAC抑制剂，具有潜在的抗癌活性。 了解更多
  8. Domatinostat (4SC-202)
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    Domatinostat (4SC-202)

    Catalog No. A14354
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    HDAC 抑制剂
    4SC-202是生物利用的苯甲酰胺和人I类组蛋白脱乙酰基酶（HDACs）同工酶1、2和3的抑制剂，具有潜在的抗肿瘤活性。 了解更多
  9. TMP 195
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    TMP 195

    Catalog No. A14326
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    HDAC 抑制剂
    TMP195是最有效和选择性的IIa类HDAC抑制剂。 了解更多
  10. UF010
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    UF010

    Catalog No. A15781
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    HADC 抑制剂
    UF010是一种有效的选择性HADC抑制剂，对于HDAC 3、2、1和8分别具有IC50?0.06 uM，0.1 uM，0.5 uM和1.5 uM。它的选择性是其他HDAC的6倍以上。 了解更多
  11. HDAC inhibitor
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    HDAC inhibitor

    Catalog No. A13405
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    HDAC 抑制剂
    N/A 了解更多
  12. SR-4370
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    SR-4370

    Catalog No. A16899
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    HDAC 抑制剂
    SR-4370是HDAC抑制剂。SR-4370对HDAC1，HDAC2和HDAC3的IC50值分别为0.5 uM，0.1 uM和0.06 uM。 了解更多
  13. HDAC8-IN-1
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    HDAC8-IN-1

    Catalog No. A17091
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    HDAC8 抑制剂
    HDAC8-IN-1是一种HDAC8抑制剂，在癌细胞系中的IC50为27.2 nM。 了解更多
  14. Tinostamustine (EDO-S101)
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    Tinostamustine (EDO-S101)

    Catalog No. A18342
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    HDAC inhibitor
    EDO-S101 is a pan HDAC inhibitor; inhibits HDAC1, HDAC2 and HDAC3 with IC50 values of 9, 9 and 25 nM, respectively. 了解更多
  15. SKLB-23bb
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    SKLB-23bb

    Catalog No. A18339
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    HDAC6 inhibitor
    SKLB-23bb is a potent and selective inhibitor for HDAC6 with an IC50 of 17 nM and shows 25-fold and 200-fold selectivity relative to HDAC1 (IC50=422 nM) and HDAC8 (IC50=3398 nM), respectively. 了解更多
  16. Valproic acid
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    Valproic acid

    Catalog No. A17323
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    HDAC inhibitor
    Valproic acid is an HDAC inhibitor, with IC50 in the range of 0.5 and 2 mM, also inhibits HDAC1 (IC50, 400 μM), and induces proteasomal degradation of HDAC2; Valproic acid sodium salt is used in the treatment of epilepsy, bipolar disorder and prevention of migraine headaches. 了解更多
  17. Tucidinostat (Chidamide)
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    Tucidinostat (Chidamide)

    Catalog No. A17861
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    HDAC inhibitor
    Tucidinostat is a potent and orally bioavailable HDAC enzymes class I (HDAC1/2/3) and class IIb (HDAC10) inhibitor, with IC50s of 95, 160, 67 and 78 nM, less active on HDAC8 and HDAC11 (IC50s, 733 nM, 432 nM, respectively), and shows no effect on HDAC4/5/6/7/9. 了解更多
  18. CM-675
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    CM-675

    Catalog No. A18741
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    PDE5/HDAC-1 inhibitor
    CM-675 is a dual phosphodiesterase 5 (PDE5) and class I histone deacetylases-selective inhibitor, with IC50 values of 114 nM and 673 nM for PDE5 and HDAC1, respectively. CM-675 has potential to treat Alzheimer??s disease. 了解更多
  19. SIS-17
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    SIS-17

    Catalog No. A18463
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    HDAC 11 inhibitor
    SIS17 is a potent and selective HDAC 11 inhibitor with an IC50 value of 0.83 μM. SIS17, is active in cells and inhibited the demyristoylation of a known HDAC11 substrate, serine hydroxymethyl transferase 2, without inhibiting other HDACs. 了解更多
  20. AES-135
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    AES-135

    Catalog No. A19087
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    HDAC inhibitor
    AES-135 is a potent HDAC inhibitor, inhibits HDAC3, HDAC6, HDAC11 with IC50s of 654, 190, and 636 nM, respectively. Anti-tumor activity. 了解更多
  21. MPT0E028
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    MPT0E028

    Catalog No. A18982
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    HDAC inhibitor
    MPT0E028 is an orally active and selective HDAC inhibitor with IC50s of 53.0 nM, 106.2 nM, 29.5 nM for HDAC1, HDAC2 and HDAC6, respectively. 了解更多
  22. SS-208
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    SS-208

    Catalog No. A18952
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    HDAC6 inhibitor
    SS-208 is a selective HDAC6 inhibitor, with an IC50 of 12 nM. SS-208 possesses anti-tumor activity in melanoma. 了解更多
  23. SW-100
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    SW-100

    Catalog No. A18947
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    HDAC6 inhibitor
    SW-100, a selective histone deacetylase 6 (HDAC6) inhibitor with an IC50 of 2.3 nM, shows at least 1000-fold selectivity for HDAC6 relative to all other HDAC isozymes. 了解更多
  24. CHDI-390576
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    CHDI-390576

    Catalog No. A18899
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    HDAC inhibitor
    CHDI-390576, a potent, cell permeable and CNS penetrant class IIa histonedeacetylase (HDAC) inhibitor with IC50s of 54 nM, 60 nM, 31 nM, 50 nM for class IIa HDAC4, HDAC5, HDAC7, HDAC9, respectively, shows >500-fold selectivity over class I HDACs (1, 2, 3) and ~150-fold selectivity over HDAC8 and the class IIb HDAC6 isoform. 了解更多
  25. ACY-775
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    ACY-775

    Catalog No. A12456
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    HDAC6 inhibitor
    ACY-775 is a potent and selective inhibitor of the of histone deacetylase 6 (HDAC6) with an IC50 of 7.5?nM. 了解更多
  26. Remetinostat
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    Remetinostat

    Catalog No. A12149
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    HDAC inhibitor
    Remetinostat (SHP-141) is a hydroxamic acid-based inhibitor of histone deacetylase enzymes (HDAC) which is under development for the treatment of cutaneous T-cell lymphoma. 了解更多
  27. CXD101
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    CXD101

    Catalog No. A12253
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    HDAC inhibitor
    CXD101 is a class I-selective HDAC inhibitor (HDAC1 (IC50, 63 nM), HDAC2 (IC50, 570 nM), HDAC3 (IC50, 550 nM). CXD101 has no activity against HDAC class II. 了解更多
  28. BRD-6929
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    BRD-6929

    Catalog No. A12511
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    HDAC1/HDAC2 inhibitor
    BRD-6929 (Cpd-60) is a brain-penetrant, selective inhibitor of HDAC1 and HDAC2 (IC50=?1 and 8 nM), extracted from patent US2018360927. 了解更多
  29. HDACs/mTOR Inhibitor 1
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    HDACs/mTOR Inhibitor 1

    Catalog No. A13462
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    HDACs/mTOR Inhibitor 1
    HDACs/mTOR Inhibitor 1 is a dual Histone Deacetylases (HDACs) and mammalian target of Rapamycin (mTOR) target inhibitor for treating hematologic malignancies. 了解更多
  30. TC-H 106
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    TC-H 106

    Catalog No. A15357
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    HDAC 抑制剂
    TC-H 106是一种慢速，紧密结合的I类HDAC（组蛋白脱乙酰基酶）抑制剂。 了解更多
  31. TCS HDAC6 20b
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    TCS HDAC6 20b

    Catalog No. A15387
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    HDAC6 抑制剂
    TCS HDAC6 20b是组蛋白脱乙酰基酶6（HDAC6）的选择性抑制剂。与紫杉醇联合抑制HCT116的生长。还抑制雌激素刺激的MCF-7细胞的生长。 了解更多
  32. R306465
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    R306465

    Catalog No. A15437
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    HDAC 抑制剂
    R306465是一种新型的基于异羟肟酸酯的组蛋白脱乙酰基酶（HDAC）抑制剂，在临床前模型中具有针对实体和血液恶性肿瘤的广谱抗肿瘤活性。 了解更多
  33. ACY-738
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    ACY-738

    Catalog No. A15934
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    HDAC6 抑制剂
    ACY-738是一种有效的选择性HDAC6抑制剂，具有改善的脑生物利用度。ACY-738抑制HDAC6的纳摩尔浓度低，选择性比I类HDAC高60到1500倍。 了解更多
  34. BML-210
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    BML-210

    Catalog No. A15935
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    HDAC 抑制剂?
    BML-210是HDAC抑制剂。BML-210诱导宫颈癌细胞中的生长抑制和凋亡并调节HDAC和DAPC复合物的表达水平。 了解更多
  35. M344
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    M344

    Catalog No. A11355
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    HDAC 抑制剂
    M344是HDAC的有效抑制剂，IC50为100 nM，能够诱导细胞分化。 了解更多
  36. BG45
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    BG45

    Catalog No. A11361
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    HDAC 抑制剂
    BG45是一种HDAC I类抑制剂，对HDAC3具有选择性（IC50 = 289 nM）。它抑制HDAC1，HDAC2和HDAC6的效力大大降低（IC50分别为2、2和> 20μM）。 了解更多
  37. ITSA-1
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    ITSA-1

    Catalog No. A16127
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    HDAC 抑制剂
    ITSA-1具有膜渗透性，可以特异性抑制TSA对HDAC（组蛋白脱乙酰基酶）的抑制，但不能抑制其他HDAC抑制剂。 了解更多
  38. CAY10603
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    CAY10603

    Catalog No. A16431
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    HDAC6 抑制剂
    CAY10603是一种有效的选择性HDAC6抑制剂，IC50为2 pM，选择性是其他HDAC的200倍以上。 了解更多
  39. JW 55
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    JW 55

    Catalog No. A13731
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    TNKS1/2 抑制剂
    JW 55是端锚聚合酶1和2（TNKS1/2）的PARP域的抑制剂。 了解更多
  40. 4-HQN
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    4-HQN

    Catalog No. A15370
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    PARP 抑制剂
    4-HQN已显示抑制PARP（聚（ADP-核糖）合成酶），该酶催化NAD+的ADP-核糖部分与各种蛋白质的共价结合。 了解更多
  41. BYK 204165
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    BYK 204165

    Catalog No. A15371
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    PARP-1 抑制剂
    BYK204165是一种可渗透细胞的异喹啉二酮化合物，可有效并选择性地抑制聚（ADP-核糖）聚合酶1（PARP1）。 了解更多
  42. BYK 49187
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    BYK 49187

    Catalog No. A15372
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    PARP-1/PARP-2 抑制剂
    BYK 49187，PARP-1和PARP-2抑制剂（无细胞重组PARP-1和鼠PARP-2的pIC50值分别为8.36和7.50）。 了解更多
  43. DR 2313
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    DR 2313

    Catalog No. A15373
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    PARP 抑制剂
    DR 2313是一种水溶性嘧啶酮化合物，起PARP（聚（ADP-核糖）聚合酶）抑制剂的作用。 了解更多
  44. EB 47
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    EB 47

    Catalog No. A15374
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    PARP1 抑制剂
    EB 47是PARP1的有效抑制剂，IC50为45 nM。 了解更多
  45. NU 1025
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    NU 1025

    Catalog No. A15375
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    PARP 抑制剂
    NU 1025是一种有效的聚（ADP-核糖）聚合酶（PARP）抑制剂，可增强L1210细胞中一系列机制多样的抗癌药的细胞毒性。 了解更多
  46. G007-LK
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    G007-LK

    Catalog No. A15528
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    TNKS 抑制剂
    G007-LK对坦科聚合酶1和2具有很高的选择性，生化IC50值分别为46 nM和25 nM，细胞IC50值为50 nM，并具有出色的小鼠药代动力学特征， 了解更多
  47. NVP-TNKS656
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    NVP-TNKS656

    Catalog No. A15786
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    TNKS2 抑制剂
    NVP-TNKS656是一种高效，选择性和活性的TNKS2抑制剂，IC50为6 nM。对PARP1和PARP2的选择性> 300倍。 了解更多
  48. MN-64
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    MN-64

    Catalog No. A15927
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    TNKS 抑制剂
    MN-64是Tankyrase 1和2的有效和选择性抑制剂（IC50分别为6和72 nM）。 了解更多
  49. AZ6102
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    AZ6102

    Catalog No. A15873
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    TNKS1/2 抑制剂
    AZ6102是有效的TNKS1/2抑制剂，对其他PARP家族酶具有100倍的选择性，对DLD-1细胞中Wnt途径的抑制作用的IC50为5 nM。 了解更多
  50. ABT-888 (Veliparib)
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    ABT-888 (Veliparib)

    Catalog No. A10026
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    PARP 抑制剂
    ABT-888 (Veliparib)是一种潜在的抗癌药物，可作为PARP抑制剂。 了解更多

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