Home >> Signaling Pathways >> Cell Cycle/Checkpoint

Cell Cycle/Checkpoint(细胞周期/检查点)

Cell Cycle

Cells undergo a complex cycle of growth and division that is referred to as the cell cycle. The cell cycle consists of four phases, G1 (GAP 1), S (synthesis), G2 (GAP 2) and M (mitosis). DNA replication occurs during S phase. When cells stop dividing temporarily or indefinitely, they enter a quiescent state called G0. read more

Products for  Cell Cycle/Checkpoint

  1. Cat.No. 产品名称 Information
  2. GC15922 LEE011 hydrochloride

    瑞博西尼盐酸盐; LEE011 hydrochloride

    A selective cyclin D1/CDK4 and cyclin D3/CDK6 inhibitor
  3. GC16225 IPA-3 An allosteric inhibitor of PAK1
  4. GC11785 CDK4 inhibitor

    瑞博西尼

    An antiproliferative cyclin D1/Cdk4 inhibitor
  5. GC14517 KPT-185 An inhibitor of XPO1/CRM1
  6. GC16273 Dolastatin 10

    DLS 10; NSC 376128

    Dolastatin 10 (DLS 10) 是一种有效的抗有丝分裂肽,可抑制微管蛋白聚合。
  7. GC12261 FRAX597 A PAK1, PAK2, and PAK3 inhibitor
  8. GC11765 Cabazitaxel

    卡巴他赛,XRP6258; RPR-116258A; taxoid XRP6258

    A semisynthetic taxane
  9. GC13328 XL413 hydrochloride

    BMS-863233 hydrochloride

    A potent inhibitor of Cdc7
  10. GC18117 XL413 A potent inhibitor of Cdc7
  11. GC16607 Mesalamine

    5-氨基水杨酸; Mesalamine; 5-ASA; Mesalazine

    An NSAID and active metabolite of sulfasalazine, balsalazide, and olsalazine
  12. GC10235 Plinabulin (NPI-2358)

    普那布林; NPI-2358

    A tubulin depolymerizing agent
  13. GC15745 Mps1-IN-2

    9-环戊基-2-[[2-乙氧基-4-(4-羟基哌啶-1-基)苯基]氨基]-5-甲基-8,9-二氢-5H-嘧啶并[4,5-B][1,4]二氮杂卓-6(7H)-酮

    An inhibitor of Mps1
  14. GC11648 BML-277

    Chk2 Inhibitor II

    A selective DNA damage control kinase inhibitor
  15. GC10722 SR-3677

    N-[2-[2-(二甲基氨基)乙氧基]-4-(1H-吡唑-4-基)苯基]-2,3-二氢-1,4-苯并二恶烷-2-甲酰胺

    A ROCK1 and ROCK2 inhibitor
  16. GC17801 PYZD-4409 PYZD-4409 是泛素激活酶 UBA1 的特异性抑制剂,IC50 为 20 μM(无细胞酶测定)。 PYZD-4409 在恶性细胞中诱导细胞死亡并优先抑制原发性急性髓细胞白血病细胞的克隆形成。
  17. GC14600 SB743921 An Eg5 inhibitor
  18. GC12415 Rigosertib

    瑞格色替; ON-01910

    Rigosertib (ON-01910) 是一种多激酶抑制剂和选择性抗癌剂,通过抑制 PI3 激酶/Akt 通路诱导细胞凋亡,促进组蛋白 H2AX 的磷酸化并诱导细胞周期 G2/M 停滞。 Rigosertib 是一种选择性和非 ATP 竞争性的 PLK1 抑制剂,IC50 为 9 nM。
  19. GC13580 Rigosertib sodium

    瑞格色替钠,ON-01910 sodium

    Rigosertib sodium (ON-01910 sodium) 是一种多激酶抑制剂和选择性抗癌剂,通过抑制 PI3K/Akt 通路诱导细胞凋亡,促进组蛋白 H2AX 的磷酸化并诱导细胞周期 G2/M 停滞。 Rigosertib sodium 是一种选择性和非 ATP 竞争性的 PLK1 抑制剂,IC50 为 9 nM。
  20. GC14288 KX2-391

    5-[4-[2-(4-吗啉基)乙氧基]苯基]-N-(苯基甲基)-2-吡啶乙酰胺,KX2-391; KX-01

    A Src kinase inhibitor
  21. GC15712 Y-27632 A ROCK inhibitor
  22. GC13423 Y-39983 dihydrochloride ROCK family inhibitor
  23. GC14234 PF-477736

    PF 00477736

    A selective inhibitor of checkpoint kinase 1
  24. GC17994 Kif15-IN-2

    (ALPHAS)-1,4-二氢-ALPHA-异丙基-N-[4-甲基-5-(5-甲基-1,3,4-恶二唑-2-基)-2-噻唑基]-2,4-二氧代-3(2H)-喹唑啉乙酰胺

    Kif15-IN-2 是有丝分裂驱动蛋白 Kif15 的抑制剂,用于细胞增殖性疾病的研究。
  25. GC16603 Kif15-IN-1

    2-[[(2S)-2-(1,4-二氢-2,4-二氧代-3(2H)-喹唑啉基)-3-甲基-1-氧代丁基]氨基]-4-甲基-5-噻唑羧酸乙酯

    Kif15-IN-1 是有丝分裂驱动蛋白家族成员 15 (Kif15) 的抑制剂,用于细胞增殖性疾病的研究。
  26. GC14974 AMG 925 A dual inhibitor of FLT3 and Cdk4
  27. GC10034 MMAF

    一甲基澳瑞他汀F,Monomethylauristatin F

    An auristatin with anticancer activity
  28. GC10030 EHop-016 A Rac1 and Rac3 inhibitor
  29. GC11068 GSK2656157 A PERK inhibitor
  30. GC15337 VE-822 ATR抑制剂
  31. GC11252 CW069 An inhibitor of KIFC/HSET
  32. GC15894 CK-636

    CK-0944636

    An inhibitor of Arp2/3 complex action
  33. GC10442 MK-8745 An Aurora A kinase inhibitor
  34. GC13903 Ro3280 A selective Plk1 inhibitor
  35. GC10163 MLN0905

    2-[[5-[3-(二甲基氨基)丙基]-2-甲基-3-吡啶基]氨基]-5,7-二氢-9-(三氟甲基)-6H-嘧啶并[5,4-D][1]苯并氮杂卓-6-硫酮,PLK1 Inhibitor

    A Plk1 inhibitor
  36. GC16000 WHI-P180

    3-[(6,7-二甲氧基-4-喹唑啉基)氨基]苯酚,Janex 3

    A multi-kinase inhibitor
  37. GC17400 R547

    [4-氨基-2-[(1-甲磺酰基哌啶-4-基)氨基]嘧啶-5-基](2,3-二氟-6-甲氧基苯基)甲酮

    A selective Cdk inhibitor
  38. GC10842 LEE011

    瑞博西尼; LEE011

    A selective cyclin D1/CDK4 and cyclin D3/CDK6 inhibitor
  39. GC16425 Flavopiridol hydrochloride

    (-)-2-(2-氯苯基)-5,7-二羟基-8-[(3S,4R)-3-羟基-1-甲基-4-哌啶基]-4H-1-苯并吡喃-4-酮盐酸盐,Alvocidib Hydrochloride; L86-8275 Hydrochloride; HMR-1275 Hydrochloride

    An inhibitor of cyclin-dependent kinases
  40. GC11835 Deferasirox

    地拉罗司; ICL 670

    Deferasirox是一种具口服活性的铁螯合剂,用于治疗铁过载疾病。
  41. GC15741 LY2603618

    LY2603618; IC-83

    A Chk1 inhibitor
  42. GC10196 ETP-46464

    ATM Inhibitor III, ATR Inhibitor III

    An ATR inhibitor
  43. GC16489 CP-466722 An ATM kinase inhibitor
  44. GC14526 CGK733

    ATM/ATR Kinase Inhibitor

    An anticancer compound
  45. GC16268 Purvalanol B

    (2R)-2-[[6-[(3-氯-4-羧基苯基)氨基]-9-(1-甲基乙基)-9H-嘌呤-2-基]氨基]-3-甲基-1-丁醇,NG 95; NG95; NG-95

    A CDK inhibitor
  46. GC11224 BI6727(Volasertib)

    伏拉塞替; BI 6727

    A polo-like kinase inhibitor
  47. GC14807 Fingolimod (FTY720) HCl

    盐酸芬戈莫德; FTY720

    芬戈莫德(FTY720)是一种免疫抑制剂,通常用于治疗多发性硬化症,也有抗癌作用,可以作为HDACi(组蛋白脱乙酰酶抑制剂)。
  48. GC17648 Dinaciclib(SCH727965)

    (2S)-1-[3-乙基-7-[[(1-氧代-3-吡啶基)甲基]氨基]吡唑并[1,5-A]嘧啶-5-基]-2-哌啶乙醇,SCH 727965

    A CDK inhibitor
  49. GC15739 CHIR-124

    4-[((3S)-1-氮杂双环[2,2,2]辛-3-基)氨基]-3-(1H-苯并咪唑-2-基)-6-氯喹啉-2(1H)-酮

    A selective Chk1 inhibitor
  50. GC12865 BMS265246 A cell-permeable inhibitor of Cdk1 and Cdk2
  51. GC12338 Wortmannin

    渥曼青霉素; SL-2052; KY-12420

    渥曼青霉素是一种高效的 PI3 激酶特异性直接抑制剂,最初源自真菌 (1,2)。

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