DNA Damage

产品 1 到 50 共 416个

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  1. Romidepsin (FK228 ,Depsipeptide)

    Catalog No. A11920
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    HDAC 抑制剂
    Romidepsin (FK228,Depsipeptide)抑制HDAC1和HDAC2,IC50分别为1.6 nM和3.9 nM,但相对较弱地分别抑制HDAC4和HDAC6,IC50值为25 nM和79 nM。 了解更多
  2. LBH589 (Panobinostat)

    Catalog No. A10518
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    HDAC 抑制剂
    LBH589是异羟肟酸,用作非选择性HDAC抑制剂,HDAC1的IC5o为0.23 nM。 了解更多
  3. Trichostatin-A (TSA)

    Catalog No. A10947
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    HDAC 抑制剂
    Trichostatin-A (TSA)是抑制HDAC 1、3、4、6和10,IC50值约为20 nM。 了解更多
  4. MC1568

    Catalog No. A10560
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    HDAC 抑制剂
    MC1568是HDAC抑制剂的成员,它通过修饰细胞周期的各种重要基因的基因表达(主要在G1期)来抑制II类组蛋白脱乙酰基酶,从而导致细胞凋亡导致乳腺癌细胞死亡。 了解更多
  5. Vorinostat (SAHA)

    Catalog No. A10979
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    HDAC 抑制剂
    Vorinostat (SAHA)是HDAC的抑制剂,抑制脱乙酰和导致双方超乙酰化组蛋白和转录因子的积累。 了解更多
  6. JNJ-26481585 (Quisinostat)

    Catalog No. A10492
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    HDAC 抑制剂
    JNJ-26481585 (Quisinostat)是一种pan-HDAC抑制剂,对HDAC1具有显著的效力(IC(50),0.16 nmol/L)。 了解更多
  7. MS-275 (Entinostat)

    Catalog No. A10611
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    HDAC 抑制剂
    MS-275 (Entinostat)是一种有效的HDAC抑制剂,对HDAC1和HDAC3的IC50分别为0.3和8uM。 了解更多
  8. Belinostat (PXD101)

    Catalog No. A10122
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    HDAC 抑制剂
    Belinostat(PXD101)是一种HDAC抑制剂,可抑制HeLa细胞提取物中的HDAC活性,IC50为27 nM。 了解更多
  9. MGCD0103 (Mocetinostat)

    Catalog No. A10586
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    HDAC 抑制剂
    MGCD0103 (Mocetinostat)是一种苯甲酰胺组蛋白脱乙酰基酶抑制剂,主要抑制组蛋白脱乙酰基酶1(HDAC1),但也抑制HDAC2,HDAC3和HDAC11。 了解更多
  10. AR-42 (HDAC-42)

    Catalog No. A11037
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    HDAC 抑制剂
    AR-42 (HDAC-42)是一种新型的HDAC抑制剂,通过下调本构激活的Kit表现出对恶性肥大细胞系的生物学活性。 了解更多
  11. SB939 ( Pracinostat )

    Catalog No. A10830
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    HDAC 抑制剂
    SB939 (Pracinostat)是HDAC的口服抑制剂,对I,II和IV类HDAC具有选择性,在体外HDAC1活性测定中显示IC50值为77 nM。 了解更多
  12. CUDC-907 (Fimepinostat)

    Catalog No. A11153
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    PI3K/HDAC 抑制剂
    CUDC-907 (Fimepinostat)是针对PI3K和HDAC的单一小分子抑制剂,作用于PI3Kα和HDAC1/2/3/10,IC50分别为19 nM和1.7 nM/5 nM/1.8 nM/2.8 nM。 了解更多
  13. 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
  14. Citarinostat (ACY-241)

    Catalog No. A12758
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    HDAC6 抑制剂
    ACY-241是HDAC6的新型,选择性和口服抑制剂。对HDAC6和HDAC3的IC50分别为2.6 nM和46 nM。 了解更多
  15. 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
  16. TMP 269

    Catalog No. A14128
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    HDAC 抑制剂
    TMP 269是一种有效的选择性IIa类HDAC抑制剂,对HDAC4,HDAC5,HDAC7和HDAC9的IC50分别为157 nM,97 nM,43 nM和23 nM。 了解更多
  17. RG2833 (RGFP109)

    Catalog No. A13139
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    HDAC 抑制剂
    RG2833 (RGFP109)是一种脑渗透性HDAC抑制剂,IC50为60 nM,HDAC1和HDAC3为50 nM。 了解更多
  18. Resminostat hydrochloride

    Catalog No. A15220
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    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
  19. KD 5170

    Catalog No. A15354
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    HDAC 抑制剂
    KD 5170是一种新型的基于巯基酮的组蛋白脱乙酰基酶抑制剂,在体外和体内均表现出广谱的抗肿瘤活性。 了解更多
  20. NCH 51

    Catalog No. A15355
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    HDAC 抑制剂
    NCH 51是细胞可渗透的前药,可在细胞内转化为有效的HDAC抑制剂,IC50为48 nM。 了解更多
  21. NSC 3852

    Catalog No. A15356
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    HDAC 抑制剂
    NSC 3852是HDAC(组蛋白脱乙酰基酶)抑制剂。 了解更多
  22. 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
  23. 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
  24. 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
  25. 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
  26. 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
  27. 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
  28. CRA-026440

    Catalog No. A12179
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    HDAC inhibitor
    CRA-026440 is a potent, broad-spectrum HDAC inhibitor. 了解更多
  29. Valproic acid sodium salt

    Catalog No. A10855
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    HDAC inhibitor
    Valproic acid sodium salt (Sodium Valproate) 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. 了解更多
  30. JAK/HDAC-IN-1

    Catalog No. A13362
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    JAK2/HDAC dual inhibitor
    JAK/HDAC-IN-1 is a potent JAK2/HDAC dual inhibitor, exhibits antiproliferative and proapoptotic activities in several hematological cell lines. 了解更多
  31. Sodium phenylbutyrate

    Catalog No. A16714
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    HDAC/ER stress inhibitor
    Sodium phenylbutyrate is an inhibitor of HDAC and endoplasmic reticulum (ER) stress, used in cancer and infection research. 了解更多
  32. Tubastatin A

    Catalog No. A16770
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    HDAC6 inhibitor
    Tubastatin A is a potent and selective HDAC6 inhibitor with IC50 of 15 nM in a cell-free assay, and is selective (1000-fold more) against all other isozymes except HDAC8 (57-fold more). 了解更多
  33. CG-200745

    Catalog No. A20939
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    HDAC inhibitor
    CG-200745 is a potent HDAC inhibitor which has the hydroxamic acid moiety to bind zinc at the bottom of catalytic pocket. 了解更多
  34. Givinostat

    Catalog No. A21126
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    HDAC inhibitor
    Givinostat (ITF-2357) is a HDAC inhibitor with an IC50 of 198 and 157 nM for HDAC1 and HDAC3, respectively. 了解更多
  35. HDAC-IN-7

    Catalog No. A21252
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    HDAC1/2/3/10 inhibitor
    HDAC-IN-7 (Chidamide impurity) is an impurity of Chidamide. Chidamide is a potent and orally bioavailable HDAC enzymes class I (HDAC1/2/3) and class IIb (HDAC10) inhibitor. 了解更多
  36. Givinostat hydrochloride

    Catalog No. A21487
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    HDAC inhibitor
    Givinostat hydrochloride (ITF-2357 hydrochloride) is a HDAC inhibitor with an IC50 of 198 and 157 nM for HDAC1 and HDAC3, respectively. 了解更多
  37. Nanatinostat

    Catalog No. A21625
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    HDAC inhibitor
    Nanatinostat (CHR-3996) is a potent, class I selective and orally active histone deacetylase (HDAC) inhibitor with an IC50 of 8 nM. 了解更多
  38. Belinostat

    Catalog No. A21772
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    HDAC inhibitor
    Belinostat (PXD101; PX105684) is a potent HDAC inhibitor with an IC50 of 27 nM in HeLa cell extracts. 了解更多
  39. HDAC-IN-5

    Catalog No. A20972
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    HDAC inhibitor
    HDAC-IN-5 is a histone deacetylase (HDAC) inhibitor. 了解更多
  40. Domatinostat tosylate

    Catalog No. A20986
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    HDAC1 inhibitor
    Domatinostat tosylate (4SC-202) is a selective class I HDAC inhibitor with IC50 of 1.20 μM, 1.12 μM, and 0.57 μM for HDAC1, HDAC2, and HDAC3, respectively. It also displays inhibitory activity against Lysine specific demethylase 1 (LSD1). 了解更多
  41. J22352

    Catalog No. A19174
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    HDAC6 inhibitor
    J22352 is a PROTAC (proteolysis-targeting chimeras)-like and highly selective HDAC6 inhibitor with an IC50 value of 4.7 nM. 了解更多
  42. BRD 4354

    Catalog No. A19532
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    HDAC5/HDAC9 inhibitor
    BRD 4354 is a moderately potent inhibitor of HDAC5 and HDAC9, with IC50s of 0.85 and 1.88 μM, respectively. 了解更多
  43. FT895

    Catalog No. A19615
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    HDAC11 inhibitor
    FT895 is a potent and selective HDAC11 inhibitor with an IC50 of 3 nM. 了解更多
  44. ACY-957

    Catalog No. A19666
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    HDAC1 /HDAC2 inhibitor
    ACY-957 is an orally active and selective inhibitor of HDAC1 and HDAC2, with IC50s of 7 nM, 18 nM, and 1300 nM against HDAC1/2/3, respectively, and shows no inhibition on HDAC4/5/6/7/8/9. 了解更多
  45. TH34

    Catalog No. A19873
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    HDAC6/8/10 inhibitor
    TH34, an HDAC6/8/10 inhibitor with IC50s of 4.6 μM, 1.9 μM, and 7.7 μM respectively, shows high selectivity over HDAC1/2/3. 了解更多
  46. ACY-1083

    Catalog No. A19985
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    HDAC6 inhibitor
    ACY-1083 is a selective and brain-penetrating HDAC6 inhibitor with an IC50 of 3 nM and is 260-fold more selective for HDAC6 than all other classes of HDAC isoforms. 了解更多
  47. RTS-V5

    Catalog No. A20099
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    HDAC/proteasome inhibitor
    RTS-V5 is a dual HDAC/proteasome inhibitor with IC50s of 6.9, 18, 15, 0.27, 0.53 μM for HDAC1, HDAC2, HDAC3, HDAC6, HDAC8, respectively. 了解更多
  48. Tefinostat

    Catalog No. A20258
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    pan HDAC inhibitor
    Tefinostat (CHR-2845) is a monocyte/macrophage-targeted pan HDAC inhibitor, cleaved into active acid CHR-2847 by the intracellular esterase human carboxylesterase-1 (hCE-1). Anti-monocytoid lineage leukaemias activity. 了解更多
  49. Oxamflatin

    Catalog No. A20265
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    HDAC inhibitor
    Oxamflatin (Metacept-3) is a potent HDAC inhibitor with an IC50 of 15.7 nM. 了解更多
  50. WT-161

    Catalog No. A20432
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    HDAC6 inhibitor
    WT-161 is a potent and selective HDAC6 inhibitor with an IC50 of 0.40 nM. 了解更多

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