Cell Cycle/Checkpoint
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.
Targets for Cell Cycle/Checkpoint
- ATM/ATR(26)
- Aurora Kinase(47)
- Cdc42(4)
- Cdc7(4)
- Chk(16)
- c-Myc(20)
- CRM1(8)
- Cyclin-Dependent Kinases(91)
- E1 enzyme(1)
- G-quadruplex(14)
- Haspin(7)
- HMTase(1)
- Kinesin(26)
- Ksp(6)
- Microtubule/Tubulin(243)
- Mps1(15)
- Mitotic(11)
- RAD51(18)
- ROCK(71)
- Rho(13)
- PERK(11)
- PLK(37)
- PTEN(8)
- Wee1(7)
- PAK(21)
- Arp2/3 Complex(8)
- Dynamin(12)
- ECM & Adhesion Molecules(40)
- Cholesterol Metabolism(3)
- Endomembrane System & Vesicular Trafficking(26)
- G1(38)
- G2/M(26)
- G2/S(10)
- Genotoxic Stress(18)
- Inositol Phosphates(18)
- Proteolysis(99)
- Cytoskeleton & Motor Proteins(53)
- Cellular Chaperones(8)
Products for Cell Cycle/Checkpoint
- Cat.No. Product Name Information
- GC48470 Ac-DEVD-CHO (trifluoroacetate salt) A dual caspase3/caspase7 inhibitor
- GC42689 Ac-DNLD-AMC Ac-WLA-AMC is a fluorogenic substrate of caspase-3.
- GC49704 Ac-FLTD-CMK (trifluoroacetate salt) An inhibitor of caspase-1, -4, -5, and -11
- GC18226 Ac-LEHD-AMC (trifluoroacetate salt) Ac-LEHD-AMC (trifluoroacetate salt) is a fluorogenic substrate for caspase-9 (Excitation: 341 nm; Emission: 441 nm).
- GC40556 Ac-LETD-AFC Ac-LETD-AFC is a fluorogenic substrate that can be cleaved specifically by caspase-8.
- GC15171 Ac-LEVD-AFC A fluorogenic substrate for caspase-4
- GC13400 Ac-VDVAD-AFC Ac-VDVAD-AFC is a caspase-specific fluorescent substrate. Ac-VDVAD-AFC can measure caspase-3-like activity and caspase-2 activity and can be used for the research of tumor and cancer.
- GC52372 Ac-VDVAD-AFC (trifluoroacetate salt) A fluorogenic substrate for caspase-2
- GC48974 Ac-VEID-AMC (ammonium acetate salt) A caspase-6 fluorogenic substrate
- GC18021 Ac-YVAD-CHO Selective inhibitor of interleukin-1β converting enzyme (ICE; Caspase-1)
- GC42721 Ac-YVAD-CMK Ac-YVAD-CMK is a selective irreversible inhibitor of caspase-1 (Ki=0.8nM), which can prevent the proinflammatory cytokine IL-1β activation. Ac-YVAD-CMK can reduce the inflammatory response and induce a long-lasting neuroprotective effect.
- GC10244 Ac2-12 inhibitor of leukocyte extravasation
- GC15598 Ac2-26 inhibitor of leukocyte extravasation
- GC46786 Acetyl Hexapeptide-3 (acetate) A synthetic hexapeptide
- GC42701 Acetyl Tetrapeptide-3 Acetyl tetrapeptide-3 is a biomimetic peptide.
- GC49699 Acetyl Tetrapeptide-9 (acetate) A synthetic signal peptide
- GC46790 Acibenzolar-S-methyl A fungicide inducer of systemic acquired resistance
- GC49804 Acridine An azaarene
- GC41242 Acridine Orange Acridine Orange is a cell-permeable fluorescent dye that stains organisms (bacteria, parasites, viruses, etc.
- GC46810 Aflatoxin B1-13C17 An internal standard for the quantification of aflatoxin B1
- GC46811 Aflatoxin B2-13C17 An internal standard for the quantification of aflatoxin B2
- GC16475 Afuresertib pan-AKT inhibitor
- GC42747 Afuresertib (hydrochloride) Afuresertib is a selective, orally bioavailable inhibitor of Akt1, 2, and 3 with Ki values of 0.08, 2, and 2.6 nM, respectively.
- GC35262 Afzelin A polyphenolic glycoside flavone with diverse biological activities
- GC46825 Alachlor An herbicide
- GC49773 Albendazole sulfone-d3 An internal standard for the quantification of albendazole sulfone
- GC48848 Albendazole-d7 An internal standard for the quantification of albendazole
- GC49393 all-trans-13,14-Dihydroretinol A metabolite of all-trans retinoic acid
- GC18539 all-trans-4-hydroxy Retinoic Acid all-trans-4-hydroxy Retinoic acid is a metabolite of all-trans retinoic acid formed by the cytochrome P450 (CYP) isoforms CYP26A1, B1, and C1.
- GC40476 Allethrin Allethrin is a pyrethroid insecticide and modulator of voltage-gated sodium channels (NaV).
- GC45379 Alloxan (hydrate)
- GC18386 Aloisine RP106 Aloisine is an inhibitor of Cdk1/cyclin B, Cdk5/p25, and GSK3 (IC50s = 0.70, 1.5, and 0.92 uM, respectively).
- GC15841 Alsterpaullone CDKs and GSK3β inhibitor
- GC18437 Alternariol monomethyl ether Alternariol monomethyl ether, isolated from the roots of Anthocleista djalonensis (Loganiaceae), is an important taxonomic marker of the plant species.
- GC64698 AM-5308 AM-5308 is a potent kinesin KIF18A inhibitor (WO2021211549A1, C13).
- GC14974 AMG 925 FLT3/CDK4 inhibitor,potent and selective
- GC39156 AMG PERK 44 AMG PERK 44 is an orally active and highly selective PERK inhibitor with an IC50 of 6 nM. AMG PERK 44 has 1000-fold and 160-fold selectivity over GCN2 (IC50=7300 nM) and B-Raf (IC50 >1000 nM), respectively. AMG PERK 44 induces autophagy.
- GC45809 AMG-Tie2-1 A Tie2 and VEGFR2 inhibitor
- GC65578 Aminobenzenesulfonic auristatin E TFA Aminobenzenesulfonic auristatin E TFA is a drug-linker conjugate for ADC. Aminobenzenesulfonic auristatin E TFA has potent antitumor activity by using Auristatin E (a cytotoxic tubulin modifier), linked via the ADC linker Aminobenzenesulfonic.
- GC42788 Aminopeptidase N Inhibitor Aminopeptidase N (AP-N) inhibitor is a reversible inhibitor of AP-N/CD13 (IC50 = 25 μM).
- GC11410 Aminopurvalanol A cyclin-dependent kinase inhibitor
- GC18274 Amiprofos-methyl Amiprofos-methyl (APM) is a phosphoric amide herbicide.
- GC33370 Amphethinile (Amphetinile) Amphethinile (Amphetinile) is an anti-tubulin agent. The affinity constant for the association (Ka) of Amphethinile (Amphetinile) with tubulin is 1.3 μM.
- GC16391 Amuvatinib (MP-470, HPK 56) A multi-targeted RTK inhibitor
- GC33362 Amuvatinib hydrochloride (MP470 hydrochloride) Amuvatinib hydrochloride (MP470 hydrochloride) (MP470 hydrochloride) is an orally bioavailable multi-targeted tyrosine kinase inhibitor with potent activity against mutant c-Kit, PDGFRα, Flt3, c-Met and c-Ret. Amuvatinib hydrochloride (MP470 hydrochloride) (MP470 hydrochloride) is also a DNA repair suppressor through suppression of DNA repair protein RAD51, thereby disrupting DNA damage repair. Antineoplastic activity.
- GC64273 AMXI-5001 AMXI-5001 is a potent, orally active, and dual parp1/2 and microtubule polymerization inhibitor. MXI-5001 exhibits selective antitumor cytotoxicity across a wide variety of human cancer cells with much lower IC50s than existing clinical PARP1/2 inhibitors. AMXI-5001 induces complete regression of established tumors, including exceedingly large tumors.
- GC67900 AMXI-5001 hydrochloride
- GC49419 Aniline-d5 An internal standard for the quantification of aniline
- GC11947 Ansamitocin P-3 A microtubule depolymerizing agent
- GC25075 Ansamitocin p-3 (Maytansinol isobutyrate, NSC292222) Ansamitocin p-3 (Maytansinol isobutyrate, NSC292222, Antibiotic C 15003P3) is a potent inhibitor of tubulin polymerization with IC50 of 3.4 μM.
- GC66198 Anti-α-Tubulin Antibody, AF555 conjugate Anti-α-Tubulin Antibody, AF555 conjugate is a conjugate of mouse anti-α-tubulin monoclonal antibody and the red fluorescent dye Alexa Fluor 555. Anti-α-Tubulin Antibody, AF555 conjugate can be used for the detection of tubulin (Ex/Em: 554/567 nm).
- GC68024 Antiproliferative agent-14
- GC46867 Apremilast-d5 An internal standard for the quantification of apremilast
- GC32692 APTO-253 (LOR-253) APTO-253 (LOR-253) (LOR-253) is a small molecule that inhibits c-Myc expression, stabilizes G-quadruplex DNA, and induces cell cycle arrest and apoptosis in acute myeloid leukemia cells.
- GC34300 AR-13324 analog mesylate
- GC19034 AR-13324 mesylate AR-13324 is a potent inhibitor of ROCK I and ROCK II that has been shown to induce morphologic changes in cultured human and porcine TM cells at low concentration.
- GC45385 Ara-G
- GC46878 Aranciamycin A fungal metabolite with diverse biological activities
- GC13649 Arcyriaflavin A cdk4/cyclin D1 inhibitor
- GC52474 Arg-Gly-Asp (trifluoroacetate salt) A synthetic peptide corresponding to an integrin cell adhesion sequence
- GC52332 Arimoclomol A co-inducer of heat shock proteins
-
GC16472
ARQ 621
Eg5 inhibitor
- GC11656 ARRY 520 trifluoroacetate A potent Eg5 inhibitor
- GC13282 ARRY-520 R enantiomer
- GC46882 Artemisinin-d3 An internal standard for the quantification of artemisinin
- GC11754 AS 1892802 ROCK inhibitor,potent and ATP-competitive
- GC17712 AT13148 Multi-AGC kinase inhibitor,ATP-competitive
- GC15870 AT7519 Multi-CDK inhibitor
- GC13998 AT7519 Hydrochloride A Cdk inhibitor
- GC15597 AT7519 trifluoroacetate
- GC65327 ATM Inhibitor-5 ATM Inhibitor-5 [formula (1)] is a potent inhibitor of serine/threonine protein kinase ATM (extracted from patent WO2022058351A1).
- GC65514 ATR inhibitor 1 ATR inhibitor 1 is a ATR inhibitor extracted from patent WO2015187451A1, compound I-l, has a Ki value below 1 ?Μ.
-
GC68707
ATR-IN-4
ATR-IN-4 is an effective ATR inhibitor. ATR-IN-4 inhibits the growth of human prostate cancer cells DU145 and human lung cancer cells NCI-H460, with IC50 values of 130.9 nM and 41.33 nM, respectively (excerpted from patent CN112142744A, compound 13).
- GC46892 ATRA-BA Hybrid A prodrug form of all-trans retinoic acid and butyric acid
- GC46895 Aurintricarboxylic Acid (ammonium salt) A protein synthesis inhibitor with diverse biological activities
- GC35429 Auristatin E Auristatin E is a cytotoxic tubulin modifier with potent and selective antitumor activity; MMAE analog and cytotoxin in Antibody-drug conjugates. Auristatin E inhibits cell division by blocking the polymerisation of tubulin.
- GC35430 Auristatin F Auristatin F is a potent cytotoxin. Auristatin F, a potent microtubule inhibitor and vascular damaging agent (VDA), can be used in antibody-drug conjugates (ADC).
- GC33379 Aurora B inhibitor 1 Aurora B inhibitor 1 is an Aurora B (Aurora-1) inhibitor extracted from patent WO2007059299A1, compound 1-3, has a Ki value of <0.010 uM.
- GC38441 Aurora Kinase Inhibitor 3 A potent inhibitor of Aurora A kinase
- GC67899 Aurora kinase inhibitor-8
- GC63663 Avanbulin Avanbulin (BAL27862) is a potent, Colchicine site-binding, tubulin assembly inhibitor. Avanbulin inhibits tubulin assembly at 37 °C with an IC50 of 1.4 μM. Avanbulin binds to tubulin with an apparent Kd value of 244 nM. Avanbulin can be used for the research of cancer and cell division.
- GC50370 AZ 13705339 Highly potent PAK1 and PAK2 inhibitor
- GC66036 AZ13705339 hemihydrate AZ13705339 hemihydrate is a highly potent and selective PAK1 inhibitor with IC50s of 0.33 nM and 59 nM for PAK1 and pPAK1, respectively. AZ13705339 hemihydrate has binding affinities to PAK1 and PAK2, with Kds of 0.28 nM and 0.32 nM, respectively. AZ13705339 hemihydrate can be used in the research of cancers.
- GC15283 AZ3146 Mps1 inhibitor,potent and selective
- GC19047 AZ32 AZ32 is an orally bioavailable and blood-brain barrier-penetrating ATM inhibitor with an IC50 of <6.2 nM for ATM enzyme, and an IC50 of 0.31 uM for ATM in cell.
-
GC18956
AZ82
AZ82 is a small molecule inhibitor of KIFC1/HSET, a kinesin-14 family protein that is important for assembling bipolar spindles in cancer cells containing supernumerary centrosomes.
- GC35442 Azaindole 1 Azaindole 1 (Azaindole 1; TC-S 7001) is an orally active and ATP-competitive ROCK inhibitor with IC50s of 0.6 and 1.1nM for human ROCK-1 and ROCK-2, respectively.
- GC48971 AZD 1152 (hydrochloride) A prodrug for a potent Aurora B inhibitor
- GC12438 AZD-5438 Potent CDK1/2/9 inhibitor
-
GC12826
AZD-5597
Potent CDK inhibitor
- GC64938 AZD-7648 AZD-7648 is a potent, orally active, selective DNA-PK inhibitor with an IC50 of 0.6 nM. AZD-7648 induces apoptosis and shows antitumor activity.
- GC11593 AZD0156 ATM kinase inhibitor
-
GC19468
AZD1390
AZD1390 is a potent and selective ATM inhibitor
- GC16941 AZD6738 AZD6738 (AZD6738) is an orally active and bioavailable inhibitor of ATR kinase with an IC50 of 1 nM.
- GC10546 AZD7762 Checkpoint kinase inhibitor,ATP competitive
- GC60620 Batabulin Batabulin (T138067) is an antitumor agent, which binds covalently and selectively to a subset of the β-tubulin isotypes, thereby disrupting microtubule polymerization. Batabulin affects cell morphology and leads to cell-cycle arrest ultimately induces apoptotic cell death.
- GC60621 Batabulin sodium An inhibitor of tubulin polymerization
- GC42897 BAY 61-3606 (hydrochloride) BAY 61-3606 is a cell-permeable, reversible inhibitor of spleen tyrosine kinase (Syk; Ki = 7.5 nM; IC50 = 10 nM).
- GC33420 BAY-1895344 BAY-1895344 (BAY-1895344) is a potent, orally active and selective ATR inhibitor with an IC50 of 7 nM. BAY-1895344 has anti-tumor activity. BAY-1895344 can be used for the research of solid tumors and lymphomas.
- GC34374 BAY-1895344 hydrochloride An ATR inhibitor