Cell Cycle/Checkpoint


The cell cycle is consisted of 4 main phases: Gap 1 (G1), DNA replication (S), Gap 2 (G2), and mitosis (M). There are “checkpoints” mechanism regulates the transition between these phases, at the G1/S boundary, in the S-phase and during G2/M phases. Cell can only pass through these checkpoints when signaling factors are activated and free of DNA damage. Important proteins that control cell cycle events and checkpoints are cullins, cyclins, cyclin-dependent kinases (Cdks), p53 and their inhibitors etc. Cdks family (Cdk2, Cdk3, Cdk4 and Cdk6) are Ser/Thr kinases that regulate cell cycle progression in association with cyclin binding partners (cyclin D, cyclin E and cyclin A) during all four phases. p53 halts the cell cycle if the DNA is damaged and allowing time for DNA repair to progress; it can also initiate apoptosis if DNA damage is too severe to be repaired.
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BA3984 PyrazofurinSummary: Pyrazofurin is a pyrimidine nucleoside analog with antitumor activity that inhibits cell proliferation and intracellular DNA synthesis through inhibition. -
BA3986 ERCC1-XPF-IN-2Summary: ERCC1-XPF-IN-2 is a potent inhibitor of ERCC1-XPF nucleic acid endonuclease. -
BA3988 EthynylcytidineSummary: Ethynylcytidine (ECyD) is a nucleoside analog that is a potent inhibitor of RNA synthesis, inhibiting RNA polymerases I, II and II. -
BA3992 NVS-SM2Summary: NVS-SM2 is a potent, orally active and splicing enhancer that crosses the blood-brain barrier. -
BA3994 BMVCSummary: BMVC is a potent G-quadruplex stabilizer and selective telomerase inhibitor. -
BA3995 3-DeazauridineSummary: 3-Deazauridine (NSC126849) is a uridine analog. -
BA3997 DHODH-IN-16Summary: DHODH-IN-16 is a potent dihydroorotic acid dehydrogenase inhibitor. -
BA4005 Brr2-IN-3Summary: Brr2-IN-3 is a potent and selective deconjugate inhibitor. -
BA4011 2-O-MOE-USummary: 2'-O-MOE-U is a phosphoramidite monomer. -
BA4013 BAY-707Summary: BAY-707 is a substrate-competitive, highly efficient and selective inhibitor.

