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

研究方向

Cell Cycle/Checkpoint 相关产品(1379)

  • GC16167 structure
    GC16167K 858
    CAS: 72926-24-0
    纯度: >99.50%

    An inhibitor of Eg5

  • GC16265 structure
    GC16265RS-1
    CAS: 312756-74-4
    纯度: >98.50%

    A RAD51 activator

  • GC16268 structure
    GC16268Purvalanol B
    CAS: 212844-54-7
    纯度: >98.50%

    A CDK inhibitor

  • GC16289 structure
    GC16289SAR407899 hydrochloride
    CAS: 923262-96-8
    纯度: >98.00%

    A ROCK1 and ROCK2 inhibitor

  • GC16374 structure
    GC16374MK-8776(SCH-900776)
    CAS: 891494-63-6
    纯度: >99.50%

    MK-8776(SCH-900776) 是一种新型、选择性更高的Chk1抑制剂,旨在通过废除细胞周期阻滞来增强DNA损伤剂和抗代谢物的细胞毒性。

  • GC16391 structure
    GC16391Amuvatinib (MP-470, HPK 56)
    CAS: 850879-09-3
    纯度: >98.00%

    A multi-targeted RTK inhibitor

  • GC16413 structure
    GC16413TMCB
    CAS: 905105-89-7
    纯度: >98.00%

    A dual inhibitor of CK2 and ERK8

  • GC16420 structure
    GC16420THZ531
    CAS: 1702809-17-3
    纯度: >98.00%

    An inhibitor of Cdk12 and Cdk13

  • GC16425 structure
    GC16425Flavopiridol hydrochloride
    CAS: 131740-09-5
    纯度: >98.00%

    An inhibitor of cyclin-dependent kinases

  • GC16429 structure
    GC16429(R)-DRF053 dihydrochloride
    CAS: 1241675-76-2

    cdk/CK1 inhibitor,potent and ATP-competitive

  • GC16472 structure
    GC16472ARQ 621
    CAS: 1095253-39-6

    An Eg5 inhibitor

  • GC16475 structure
    GC16475Afuresertib
    CAS: 1047644-62-1
    纯度: >99.50%

    A pan-Akt inhibitor

  • GC16520 structure
    GC16520Olomoucine
    CAS: 101622-51-9
    纯度: >99.50%

    An inhibitor of cyclin-dependent kinases

  • GC16545 structure
    GC16545GX-674
    CAS: 1432913-36-4

    GX-674是一种芳基磺酰胺类拮抗剂,可抑制Nav1.7通道,IC 50 值为0.1nM。

  • GC16607 structure
    GC16607Mesalamine
    CAS: 89-57-6
    纯度: >98.00%

    An NSAID and active metabolite of sulfasalazine, balsalazide, and olsalazine

  • GC16692 structure
    GC16692Casin
    CAS: 425399-05-9
    纯度: >98.00%

    A Cdc42 GTPase inhibitor

  • GC16727 structure
    GC16727Flutax 1
    CAS: 191930-58-2
    纯度: >98.00%

    荧光紫杉醇衍生物;微管染色

  • GC16741 structure
    GC16741UNC0379
    CAS: 1620401-82-2
    纯度: >99.50%

    A selective SET8 inhibitor

  • GC16822 structure
    GC16822LY2835219
    CAS: 1231930-82-7
    纯度: >99.00%

    LY2835219是 CDK4 和 CDK6 的强效选择性抑制剂,在非细胞实验中的 IC 50 分别为 2nM 和 10nM。

  • GC16827 structure
    GC16827ELR510444
    CAS: 1233948-35-0
    纯度: >98.00%

    An inhibitor of tubulin polymerization

  • GC16869 structure
    GC16869Ixabepilone
    CAS: 219989-84-1
    纯度: >99.50%

    A broad-spectrum anticancer agent

  • GC16941 structure
    GC16941AZD6738
    CAS: 1352226-88-0
    纯度: >98.50%

    AZD6738是一种具有口服活性和高效选择性的共济失调毛细血管扩张和Rad3相关蛋白(ATR)激酶抑制剂,IC 50 值为1nM。

  • GC16959 structure
    GC16959NVP-LCQ195
    CAS: 902156-99-4
    纯度: >99.50%

    NVP-LCQ195 (AT9311; LCQ195) 是 CDK1、CDK2、CDK3 和 CDK5 的小分子杂环抑制剂,IC50 为 1-42 nM。

  • GC17105 structure
    GC17105CCT241533 hydrochloride
    CAS: 1431697-96-9
    纯度: >99.00%

    A selective Chk2 inhibitor