Cell Cycle/DNA Damage

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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C5041 3'-DeoxyguanosineSummary: An antitumor drug targeting purine nucleoside phosphorylase. -
C4939 Cytochalasin BSummary: A cell-permeable actin polymerization inhibitor -
C4399 2,4-Dichlorophenoxy Acetic AcidSummary: A selective herbicide with plant hormone regulatory activity that can induce apoptosis. -
C4055 2-Aminopurine (hydrochloride)Summary: A fluorescent probe used to study nucleic acid structure and dynamics. -
C3612 BRD32048Summary: Directly targets the ETV1 protein, inhibits acetylation, and promotes its degradation. -
C3513 5'-deoxy-5-FluorocytidineSummary: A cytidine analog that can interfere with DNA methyltransferase activity. -
B8758 SR-4835Summary: Highly selective CDK12/CDK13 dual inhibitor, promotes apoptosis of TNBC cells -
B8570 SPHINX31Summary: Selectively inhibits SRPK1 activity, modulating SRSF1 splicing and VEGF expression. -
B8549 (R)-CR8 (CR8)Summary: A second-generation analog of (R)-roscovitin and a potent cyclin-dependent kinase (CDK) inhibitor. -
B8548 RA-9Summary: A potent, selective, and cell-permeable inhibitor of proteasome-associated DUBs

