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DNA Damage/DNA Repair(DNA损伤/DNA修复)

  1. Cat.No. 产品名称 Information
  2. GC15033 Azathioprine

    硫唑嘌呤; BW 57-322

    An immunosuppressive purine analog
  3. GC14106 Adenosine

    腺苷; Adenine riboside; D-Adenosine

    A purine nucleoside
  4. GC12423 Mycophenolate mofetil hydrochloride

    RS 61443 hydrochloride; TM-MMF hydrochloride

    A prodrug form of mycophenolic acid
  5. GC13729 Cytidine

    胞苷; Cytosine β-D-riboside; Cytosine-1-β-D-ribofuranoside

    A pyrimidine nucleoside
  6. GC13432 Adenine

    腺嘌呤; 6-Aminopurine; Vitamin B4

    腺嘌呤(6-氨基嘌呤)是一种嘌呤,是DNA核酸中的四种核碱基之一。腺嘌呤是DNA和RNA的化学成分。腺嘌呤还在涉及细胞呼吸、ATP 和辅因子(NAD 和 FAD)的形式以及蛋白质合成的生物化学中发挥重要作用。
  7. GC11099 Doxifluridine

    去氧氟尿苷; Ro 21-9738; 5-Fluoro-5'-deoxyuridine; 5'-DFUR

    An antitumor prodrug of 5-fluorouracil
  8. GC13401 SJB3-019A SJB3-019A 是一种有效的新型 USP1 抑制剂,在促进 K562 细胞中 ID1 降解和细胞毒性方面的作用是 SJB2-043 的 5 倍,IC50 为 0.0781 μM。
  9. GC15663 LY2606368

    5-[[5-[2-(3-氨基丙氧基)-6-甲氧基苯基]-1H-吡唑-3-基]氨基]-2-吡嗪甲腈,LY2606368

    LY2606368 是一种 ATP 竞争性 CHK1 抑制剂,目前处于临床阶段,Ki 为 0.9 nM,IC50 <1 nM。
  10. GC17635 ML-323 A selective USP1-UAF1 deubiquitinase complex inhibitor
  11. GC17848 Penciclovir

    喷昔洛韦; BRL 39123; VSA 671

    An antiviral guanosine analog
  12. GC10637 Zidovudine

    叠氮胸苷; Azidothymidine; AZT; ZDV

    A nucleoside reverse transcriptase inhibitor
  13. GC13831 FT-207 (NSC 148958)

    替加氟; FT 207; NSC 148958

    A prodrug form of 5-fluorouracil
  14. GC13667 Temozolomide

    替莫唑胺; NSC 362856; CCRG 81045; TMZ

    替莫唑胺是一种口服活性烷化剂,可诱导 DNA 中 O6-甲基鸟嘌呤的形成,其在随后的 DNA 复制周期中与胸腺嘧啶错配,从而激活细胞凋亡途径,替莫唑胺可穿过血脑屏障并适用于恶性神经胶质瘤和转移性黑色素瘤。
  15. GC11048 Irinotecan HCl Trihydrate

    盐酸伊立替康三水合物; (+)-Irinotecan hydrochloride trihydrate; CPT-11 hydrochloride trihydrate

    A potent inhibitor of DNA topoisomerase I
  16. GC15377 LEE011 succinate

    瑞博西尼琥珀酸盐; LEE011 succinate

    A selective cyclin D1/CDK4 and cyclin D3/CDK6 inhibitor
  17. GC15922 LEE011 hydrochloride

    瑞博西尼盐酸盐; LEE011 hydrochloride

    A selective cyclin D1/CDK4 and cyclin D3/CDK6 inhibitor
  18. GC17466 LH846 A selective inhibitor of CK1δ
  19. GC13328 XL413 hydrochloride

    BMS-863233 hydrochloride

    A potent inhibitor of Cdc7
  20. GC18117 XL413 A potent inhibitor of Cdc7
  21. GC12350 T 705

    法匹拉韦; T-705

    An antiviral agent
  22. GC11648 BML-277

    Chk2 Inhibitor II

    A selective DNA damage control kinase inhibitor
  23. GC13359 Topotecan HCl

    盐酸拓扑替康; SKF 104864A Hydrochloride; NSC 609669 Hydrochloride

    A potent inhibitor of DNA topoisomerase I
  24. GC17522 LY2334737

    2'-脱氧-2',2'-二氟-N-(1-氧代-2-丙基戊基)胞苷

    LY2334737 是一种核苷类似物,是吉西他滨的口服活性前药。
  25. GC17865 Lomustine

    洛莫司汀; CCNU; NSC 79037

    A DNA alkylating agent
  26. GC14961 Cytarabine hydrochloride

    盐酸阿糖胞苷; Cytosine β-D-arabinofuranoside hydrochloride; Cytosine Arabinoside hydrochloride; Ara-C hydrochloride

    A nucleoside analog and prodrug form of ara-CTP
  27. GC11747 Amsacrine hydrochloride

    盐酸胺苯吖啶,m-AMSA hydrochloride; acridinyl anisidide hydrochloride

    A topoisomerase II poison
  28. GC12326 Amsacrine

    安吖啶; m-AMSA; acridinyl anisidide

    A topoisomerase II poison
  29. GC12828 Daunorubicin

    柔红霉素; Daunomycin; RP 13057; Rubidomycin

    Daunorubicin (Daunomycin) 是一种拓扑异构酶 II 抑制剂,具有有效的抗肿瘤活性。

  30. GC10354 Daunorubicin HCl

    盐酸柔红霉素; Daunomycin hydrochloride; RP 13057 hydrochloride; Rubidomycin hydrochloride

    Antitumor antibiotic used in the treatment of acute myeloid leukemias
  31. GC13858 Torin 2

    9-(6-氨基-3-吡啶基)-1-[3-(三氟甲基)苯基]苯并[H]-1,6-萘啶-2(1H)-酮

    Selective inhibitor of mTOR
  32. GC11537 MK-4827 tosylate

    尼拉帕尼对苯甲磺酸盐; MK-4827 tosylate

    An orally bioavailable PARP1/2 inhibitor
  33. GC12756 MK-4827 hydrochloride

    MK-4827 hydrochloride

    MK-4827 hydrochloride (MK-4827 hydrochloride) 是一种高效且具有口服生物利用度的 PARP1 和 PARP2 抑制剂,IC50 分别为 3.8 和 2.1 nM。 MK-4827 hydrochloride 抑制 DNA 损伤的修复,激活细胞凋亡并显示出抗肿瘤活性。
  34. GC11424 Valproic acid

    丙戊酸; VPA; 2-Propylpentanoic Acid

    A class I HDAC inhibitor
  35. GC17651 Sunitinib

    舒尼替尼; SU 11248

    舒尼替尼Sunitinib(SU 11248)是一种具口服活性的多靶点受体酪氨酸激酶抑制剂,对血管内皮生长因子受体(VEGFR2)和血小板衍生生长因子受体(PDGFRβ)的IC50分别为80nM和2nM。
  36. GC14234 PF-477736

    PF 00477736

    A selective inhibitor of checkpoint kinase 1
  37. GC16143 Varenicline Hydrochloride

    6,7,8,9-四氢-6,10-甲桥-6H-吡嗪并[2,3-H][3]苯并氮杂卓盐酸盐,CP 526555 hydrochloride

    Varenicline Hydrochloride (CP 526555 hydrochloride) 是一种高亲和力、选择性的 α4β2 尼古丁乙酰胆碱受体 (nAChR) 部分激动剂和完整的 α7 nAChR 激动剂。
  38. GC15306 Calcium N5-methyltetrahydrofolate

    N5-甲基四氢叶酸钙; NSC173328

    N5-甲基四氢叶酸钙 (NSC173328) 是左旋叶酸的钙盐,已被提议用于治疗心血管疾病和晚期癌症,如乳腺癌和结肠直肠癌。
  39. GC17139 APY29 A modulator of IRE1α function
  40. GC14974 AMG 925 A dual inhibitor of FLT3 and Cdk4
  41. GC10734 Beta-Lapachone

    3,4-二氢-2,2-二甲基-2H-萘并[1,2-B]吡喃-5,6-二酮,ARQ-501; NSC-26326

    An anti-cancer quinone
  42. GC14364 SGI-1027

    DNA Methyltransferase Inhibitor II

    A DNA methyltransferase inhibitor
  43. GC13013 TCID

    4,5,6,7-四氯茚满-1,3-二酮,4,5,6,7-Tetrachloroindan-1,3-dione

    A potent, selective inhibitor of UCH-L3
  44. GC12011 P276-00

    P276-00

    P276-00 (P276-00) 是一种有效的细胞周期蛋白依赖性激酶 (CDK) 抑制剂,可抑制 CDK9-cyclinT1、CDK4-cyclin D1 和 CDK1-cyclinB,IC50 分别为 20 nM、63 nM 和 79 nM。 P276-00 (P276-00) 对顺铂耐药细胞具有抗肿瘤活性。
  45. GC15337 VE-822 ATR抑制剂
  46. GC17897 Triapine

    [(3-氨基吡啶-2-基)亚甲基氨基]硫脲

    核糖核苷酸还原酶抑制剂
  47. GC17231 CRT0044876

    7-硝基吲哚-2-甲酸

    A cell-permeable inhibitor of Ape-1
  48. GC13419 ME0328 A selective PARP3 inhibitor
  49. GC17703 TMP269

    TMP 269;TMP-269

    A selective class IIa HDAC inhibitor
  50. GC14285 RGFP966

    RGFP 966;RGFP-966

    RGFP966是一种N-(o-aminophenyl)carboxamide HDAC抑制剂,对HDAC3的IC50为0.08 μM,是一类针对HDAC3的慢开/慢关竞争性紧密结合抑制剂。
  51. GC13136 (S)-Crizotinib An MTH1 inhibitor

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