Ciclo celular/Ponto de verificação
Os inibidores do ciclo celular/ponto de verificação são compostos que interrompem a progressão normal do ciclo celular, particularmente em pontos de verificação regulatórios chave. Esses inibidores são cruciais para estudar a divisão celular, entender a proliferação de células cancerígenas e desenvolver terapias anticâncer. Ao direcionar fases específicas do ciclo celular, esses inibidores podem induzir a parada do ciclo celular, levando à apoptose ou senescência em células de divisão rápida. Na CymitQuimica, oferecemos uma ampla gama de inibidores de alta qualidade do ciclo celular/ponto de verificação para apoiar sua pesquisa em biologia do câncer, biologia celular e desenvolvimento de medicamentos.
Subcategorias de "Ciclo celular/Ponto de verificação"
- Aurora Quinase(116 produtos)
- CDK(548 produtos)
- Ciclo celular/Parada(5 produtos)
- Chk(48 produtos)
- DYRK(46 produtos)
- Dinamina(27 produtos)
- Ferroptose(233 produtos)
- HSP(180 produtos)
- Integrinas(276 produtos)
- Cinesina(87 produtos)
- LIM Quinase(21 produtos)
- Microtúbulo associado(273 produtos)
- PKC(128 produtos)
- PLK(25 produtos)
- ROCK(61 produtos)
- Rho(6 produtos)
- Wee1(14 produtos)
- c-Myc(77 produtos)
Exibir 10 mais subcategorias
Foram encontrados 3936 produtos de "Ciclo celular/Ponto de verificação"
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HMN-214
CAS:HMN-214 (IVX-214) is a potent PLK1 inhibitor with an average IC50 of 0.12 μM.Fórmula:C22H20N2O5SPureza:98% - >99.99%Cor e Forma:SolidPeso molecular:424.47Ref: TM-T2438
1mg38,00€2mg50,00€5mg80,00€1mL*10mM (DMSO)87,00€10mg117,00€25mg207,00€50mg333,00€100mg477,00€500mg1.063,00€TAK-960
CAS:TAK-960 is an orally bioavailable, selective inhibitor of Plks with IC50 values of 0.8, 16.9, and 50.2 nM for Plk1, Plk2, and Plk3, respectively.Fórmula:C27H34F3N7O3Pureza:97.06%Cor e Forma:SolidPeso molecular:561.6Ref: TM-T7200
1mg60,00€2mg85,00€5mg114,00€10mg161,00€1mL*10mM (DMSO)161,00€25mg279,00€50mg464,00€100mg672,00€Cyclo(-RGDfK) TFA
CAS:Cyclo(-RGDfK) is a selective αvβ3 integrin inhibitor(IC50 : 0.94 nM).Fórmula:C29H42F3N9O9Pureza:98.99% - 99.54%Cor e Forma:SolidPeso molecular:717.69TH588 hydrochloride
CAS:TH588 hydrochloride is first-in-class inhibitor of nudix hydrolase family that selectively and effectively bind and inhibit the MTH1 with IC50 value of 5 nM.Fórmula:C13H13Cl3N4Cor e Forma:SolidPeso molecular:331.63Seliciclib
CAS:Seliciclib (Roscovitine) is a potent inhibitor of Cdk2/cyclin E, also inhibits Cdk7, Cdk5 and Cdc2. Seliciclib has antitumor effect. Cost-effective, quality assurance.Fórmula:C19H26N6OPureza:97.15% - 99.89%Cor e Forma:White To Off-White SolidPeso molecular:354.45InhA-IN-2
CAS:N-[3-(Aminomethyl)phenyl]-5-chloro-3-methyl-benzo[b]thiophene-2-sulfonamide inhibits InhA without KatG activation.Fórmula:C16H15ClN2O2S2Pureza:98.4%Cor e Forma:SolidPeso molecular:366.89Ref: TM-T9734
1mg93,00€5mg182,00€1mL*10mM (DMSO)187,00€10mg269,00€25mg429,00€50mg610,00€100mg820,00€200mg1.071,00€Zoliflodacin
CAS:Zoliflodacin (ETX0914) (ETX0914, AZD0914) is a new bacterial DNA gyrase/topoisomerase inhibitor.Fórmula:C22H22FN5O7Pureza:99.82% - 99.93%Cor e Forma:SolidPeso molecular:487.44Ref: TM-TQ0063
1mg105,00€5mg245,00€1mL*10mM (DMSO)264,00€10mg389,00€25mg645,00€50mg888,00€100mg1.234,00€500mg2.457,00€360A
CAS:360A is a stabilizing G-Quadruplex ligand, and also inhibits telomerase activity for telomerase in TRAP-G4 assay(IC50 : 300 nM).
Fórmula:C27H23N5O2Pureza:98.68%Cor e Forma:SolidPeso molecular:449.5TH5487
CAS:TH5487 is an potent inhibitor of 8-oxoguanine DNA glycosylase 1 (OGG1)( IC50 of 342 nM)Fórmula:C19H18BrIN4O2Pureza:98.38% - 98.73%Cor e Forma:SolidPeso molecular:541.18Mogroside I E1
CAS:Mogroside I E1 is a triterpenoid glycoside isolated from the extracts of Luo Han Guo, is a nonsugar sweetener.Fórmula:C36H62O9Pureza:98.62% - 99.71%Cor e Forma:SolidPeso molecular:638.87Protein kinase inhibitor 6
CAS:Protein kinase inhibitor 6 is a protein kinase inhibitor.Fórmula:C13H9FN2SPureza:98.01%Cor e Forma:SolidPeso molecular:244.29Ref: TM-T9779
2mg34,00€5mg52,00€1mL*10mM (DMSO)52,00€10mg86,00€25mg163,00€50mg222,00€100mg324,00€200mg440,00€MLN0905
CAS:MLN0905 (PLK1 Inhibitor) is an effective PLK1 inhibitor(IC50=2 nM).Fórmula:C24H25F3N6SPureza:98% - 99.92%Cor e Forma:SolidPeso molecular:486.56AZD-5438
CAS:AZD-5438 is an effective inhibitor of CDK, for CDK1(IC50=16 nM), CDK2(IC50=6 nM), CDK9(IC50=20 nM).Fórmula:C18H21N5O2SPureza:99.73% - 99.87%Cor e Forma:SolidPeso molecular:371.46PF-06873600
CAS:PF-06873600: oral CDK inhibitor (CDK2/4/6), Ki 0.09-0.16 nM, potential anticancer drug.Fórmula:C20H27F2N5O4SPureza:98.77% - 99.55%Cor e Forma:SolidPeso molecular:471.52Ref: TM-T8463
1mg54,00€5mg114,00€1mL*10mM (DMSO)118,00€10mg178,00€25mg334,00€50mg557,00€100mg888,00€200mg1.198,00€2'-Deoxy-2'-fluorocytidine
CAS:2'-Deoxy-2'-fluorocytidine is an nucleoside analog and inhibits of Crimean-Congo hemorrhagic fever virus (CCHFV) replication potently.Fórmula:C9H12FN3O4Pureza:99.90%Cor e Forma:White Or Almost White Crystalline PowderPeso molecular:245.21DMT-2′Fluoro-dU Phosphoramidite
CAS:DMT-2′Fluoro-dU Phosphoramidite (2'-F-dU Phosphoramidite) can be used to modify nucleosides.Fórmula:C39H46FN4O8PPureza:99.5%Cor e Forma:SolidPeso molecular:748.78GLPG0187
CAS:GLPG0187, a broad spectrum integrin receptor antagonist, inhibits αvβ1-integrin (IC50: 1.3 nM).Fórmula:C29H37N7O5SPureza:99.4% - 99.70%Cor e Forma:SolidPeso molecular:595.71Ref: TM-T4259
1mg44,00€5mg98,00€1mL*10mM (DMSO)129,00€10mg144,00€25mg236,00€50mg350,00€100mg522,00€500mg1.134,00€Roniciclib
CAS:Roniciclib (BAY 1000394) is a potent pan-CDK inhibitor and a novel oral cytotoxic agent. Roniciclib inhibits the activity of cell-cycle CDKs CDK1, CDK2, CDK3, CDK4, and of transcriptional CDKs CDK7 and CDK9 with IC(50) values in the range between 5 and 25 nmol/L.Fórmula:C18H21F3N4O3SPureza:98% - 98.63%Cor e Forma:SolidPeso molecular:430.44PKD-IN-1 dihydrochloride (956121-30-5 free base)
CAS:CRT0066101 dihydrochloride is an inhibitor of PKD.Fórmula:C18H21Cl3N4OPureza:99.5%Cor e Forma:SolidPeso molecular:415.75SCH900776
CAS:SCH900776 (MK-8776) is an agent targeting cell cycle checkpoint kinase 1 (Chk1) with potential radiosensitization and chemosensitization activities.Fórmula:C15H18BrN7Pureza:96.69% - 99.6%Cor e Forma:SolidPeso molecular:376.25Eprociclovir potassium
CAS:Eprociclovir potassium, 15x stronger than acyclovir, inhibits EHV1 and human herpesviruses, also treats herpetic keratitis effectively with eyedrops.Fórmula:C11H15KN5O3Cor e Forma:SolidPeso molecular:304.37DMTr-LNA-5MeU-3-CED-phosphoramidite
CAS:DMTr-LNA-5MeU-3-CED-phosphoramidite is a derivative of nucleoside.Fórmula:C41H49N4O9PPureza:98.28%Cor e Forma:SolidPeso molecular:772.82SEL120-34A HCl
CAS:SEL120-34A HCl is a selective, orally available and ATP-competitive inhibitor of CDK8(CDK8/CycC and CDK19/CycC with IC50s of 4.4 nM and 10.4 nM , respectivelyFórmula:C15H19Br2ClN4Pureza:98.13% - 98.47%Cor e Forma:SolidPeso molecular:450.6Amenamevir
CAS:Amenamevir (ASP2151) is a novel helicase-primase inhibitor that is active against varicella-zoster virus and herpes simplex virus types 1 and 2 (EC50: 14 ng/mLFórmula:C24H26N4O5SPureza:99.00% - 99.86%Cor e Forma:SolidPeso molecular:482.55Ref: TM-T4226
1mg34,00€1mL*10mM (DMSO)52,00€5mg71,00€10mg92,00€25mg152,00€50mg222,00€100mg334,00€200mg494,00€Temozolomide Acid
CAS:TMZA, a TMZ metabolite, shows in vitro anticancer effects. TMZ, an oral alkylator, treats GBM and astrocytomas.Fórmula:C6H5N5O3Pureza:99.28%Cor e Forma:SolidPeso molecular:195.14Dalpiciclib
CAS:Dalpiciclib (SHR-6390) selectively inhibits CDK4/6 (IC50: 12.4/9.9 nM), is orally available, and impedes esophageal cancer growth.Fórmula:C25H30N6O2Pureza:99.69%Cor e Forma:SolidPeso molecular:446.54CYC-116
CAS:CYC116 is a potent inhibitor of Aurora A/B with Ki of 8.0 nM/9.2 nM, is less potent to VEGFR2 (Ki of 44 nM), with 50-fold greater potency than CDKs, not activeFórmula:C18H20N6OSPureza:97.36% - 97.59%Cor e Forma:SolidPeso molecular:368.46Acelarin
CAS:Acelarin (NUC-1031) (NUC-1031) is a ProTide enhancement and transformation of the nucleoside analog, gemcitabine.Fórmula:C25H27F2N4O8PPureza:99.26%Cor e Forma:SolidPeso molecular:580.47Ref: TM-T4060
200mgA consultar1mg43,00€2mg56,00€1mL*10mM (DMSO)92,00€5mg93,00€10mg137,00€25mg259,00€50mg398,00€100mg555,00€CDK9-IN-30
CAS:CDK9-IN-30 is one of the Tat peptide derivatives and inhibits HIV-1 long terminal repeat-activated transcription.Fórmula:C16H20FNO3Pureza:99.75%Cor e Forma:SolidPeso molecular:293.33POL1-IN-1
CAS:POL1-IN-1 (Compound 3A) 是一种RNA 聚合酶 1 POL1抑制剂，IC50值低于 0.5 uM。 它能有效抑制A375恶性黑色素瘤细胞系中RNA 聚合酶I 的转录。
Fórmula:C21H20N6Pureza:98% - 98.01%Cor e Forma:SolidPeso molecular:356.42MLS-573151
CAS:MLS-573151 is a selective inhibitor of GTPase Cdc42(EC50 of 2 μM).Fórmula:C21H19N3O2SPureza:98.80%Cor e Forma:SolidPeso molecular:377.46Ref: TM-T22106
2mg34,00€5mg50,00€1mL*10mM (DMSO)55,00€10mg86,00€25mg161,00€50mg245,00€100mg363,00€200mg515,00€LXW7
CAS:LXW7 is an octamer disulfide cyclic peptide and αvβ3 integrin ligand, acts as a potent and specific endothelial progenitor cells (EPCs) and endothelial cells (Fórmula:C29H48N12O12S2Pureza:>99.99%Cor e Forma:SolidPeso molecular:820.891,4-Anthraquinone
CAS:1,4-Anthraquinone: anticancer, hinders nucleoside transport, inhibits synthesis, fragments DNA, curbs L1210 cell growth; aids HPLC analysis of NAC, CAP.Fórmula:C14H8O2Pureza:95.96% - 97.01%Cor e Forma:Orange Brown SolidPeso molecular:208.21BMS-3
CAS:BMS-3 is a potent LIMK inhibitor with IC50s of 5 nM and 6 nM for LIMK1 and LIMK2, respectively.Fórmula:C17H12Cl2F2N4OSPureza:99.31% - 99.81%Cor e Forma:SolidPeso molecular:429.276-O-Methyl Guanosine
CAS:6-O-Methyl Guanosine inhibit colony-forming ability in a malignant xeroderma pigmentosum cell line.Fórmula:C11H15N5O5Pureza:97.5%Cor e Forma:SolidPeso molecular:297.27TH588
CAS:TH588 is nudix hydrolase family inhibitor that effectively and selectively engages and inhibits the MTH1(IC50: 5 nM) in cells.Fórmula:C13H12Cl2N4Pureza:96.05% - 99.82%Cor e Forma:SolidPeso molecular:295.17Ispinesib
CAS:Ispinesib (SB-715992), a selective, effectvie and reversible inhibitor of kinesin spindle protein (KSP), is derived from quinazolinone, with antineoplasticFórmula:C30H33ClN4O2Pureza:98% - 99.09%Cor e Forma:SolidPeso molecular:517.06Ref: TM-T2103
2mg46,00€5mg74,00€1mL*10mM (DMSO)85,00€10mg112,00€25mg200,00€50mg320,00€100mg528,00€200mg755,00€Saccharin 1-methylimidazole
CAS:Saccharin 1-methylimidazole (SMI) is a general-purpose activator used for DNA and RNA synthesis.Fórmula:C7H5NO3S·C4H6N2Pureza:98.21%Cor e Forma:SolidPeso molecular:265.29AZD-5597
CAS:AZD-5597 ((S)-(4-((5-Fluoro-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidin-2-yl)amino)phenyl)(3-(methylamino)pyrrolidin-1-yl)methanone) is a potent
Fórmula:C23H28FN7OPureza:98.01%Cor e Forma:SolidPeso molecular:437.51SP-146
SP-146 is a selective, potent and non-ATP-competitive Aurora B inhibitor(IC50 : 0.316 nM).Fórmula:C25H20FN7OPureza:97.82%Cor e Forma:SolidPeso molecular:453.47Ref: TM-T8685
1mg84,00€5mg166,00€1mL*10mM (DMSO)168,00€10mg245,00€25mg404,00€50mg567,00€100mg767,00€200mg1.018,00€3-AP
CAS:3-AP (Triapine) is a novel inhibitor of the M2 subunit of ribonucleotide reductase (RR).Fórmula:C7H9N5SPureza:97.33% - 99.87%Cor e Forma:SolidPeso molecular:195.24Ref: TM-T1982
2mg37,00€5mg54,00€1mL*10mM (DMSO)54,00€10mg65,00€25mg142,00€50mg250,00€100mg379,00€500mg862,00€5-BrdU
CAS:5-BrdU (Broxuridine) is a nucleoside analogue, detect proliferating cells and compete with thymidine for incorporation into DNA. High-Quality, Low-Cost!Fórmula:C9H11BrN2O5Pureza:99.54% - 99.87%Cor e Forma:Crystals From Absolute Ethanol Physical Description White Crystalline Powder (Ntp 1992)Peso molecular:307.1ILK-IN-2
CAS:ILK-IN-2 (OSU-T315) is a novel potent, orally active ILK (integrin-linked kinase) inhibitor with IC50 of 0.6 μM.Fórmula:C30H30F3N5OPureza:99.30%Cor e Forma:SolidPeso molecular:533.59Ref: TM-T5488
1mg46,00€5mg92,00€10mg122,00€1mL*10mM (DMSO)130,00€25mg154,00€50mg182,00€100mg266,00€200mg386,00€GSK461364
CAS:GSK461364 (GSK461364A)(Ki=2.2 nM) inhibits purified Plk1 .The specificity of GSK461364 for Plk1 is more than 1000-fold over Plk2/3.Fórmula:C27H28F3N5O2SPureza:99% - 99.73%Cor e Forma:SolidPeso molecular:543.6Ref: TM-T6282
1mg34,00€2mg49,00€5mg71,00€10mg117,00€25mg195,00€50mg354,00€100mg528,00€200mg755,00€500mg1.153,00€UNC10217938A
CAS:UNC10217938A is a 3-deazapteridine analog, has strong oligonucleotide enhancing effects.Fórmula:C26H28N6O2Pureza:98%Cor e Forma:SolidPeso molecular:456.54WNK463
CAS:WNK463 is a pan-WNK-kinase inhibitor. It effectively inhibits the in vitro kinase activity of all four WNK family members (WNK1/2/3/4).Fórmula:C21H24F3N7O2Pureza:>99.99% - ≥95%Cor e Forma:SolidPeso molecular:463.46RCM-1
CAS:RCM-1 is an inhibitor of FOXM1.Fórmula:C20H12N2OS4Pureza:98.08%Cor e Forma:SolidPeso molecular:424.58Palmatine chloride
CAS:Palmatine chloride an isoquinoline alkaloid, is an important medicinal herbal extract with diverse pharmacological and biological properties.Fórmula:C21H22ClNO4Pureza:97.9% - 99.47%Cor e Forma:SolidPeso molecular:387.86TH-263
CAS:TH-263 is inactive toward both LIMK1 and LIMK2 and thus can be used as negative control for TH-257, and is a diaryl sulfonamide derivative.Fórmula:C21H20N2O3SPureza:99.54%Cor e Forma:SolidPeso molecular:380.46Ref: TM-T19578
2mg34,00€5mg49,00€1mL*10mM (DMSO)54,00€10mg75,00€25mg137,00€50mg192,00€100mg281,00€200mg419,00€Cetraxate hydrochloride
CAS:Cetraxate hydrochloride (DV10062) is an oral gastrointestinal medication. It has a cytoprotective effect.Fórmula:C17H24ClNO4Pureza:99.75%Cor e Forma:SolidPeso molecular:341.83AT-9283 HCl
CAS:AT-9283, a multi-targeted kinase inhibitor, is used potentially for the treatment of multiple myeloma.Fórmula:C19H24ClN7O2Cor e Forma:SolidPeso molecular:417.89BS-181 dihydrochloride
CAS:BS-181 dihydrochloride: Potent CDK7 inhibitor (IC50: 21 nM), less effective on CDK2/5/9, no impact on CDK1/4/6, halts cancer cell growth, triggers apoptosis.Fórmula:C22H34Cl2N6Cor e Forma:SolidPeso molecular:453.46GPRP acetate (67869-62-9 free base)
CAS:GPRP acetate (Pefabloc FG) is fibrinogen-related peptides, which inhibit the interaction of fibrinogen with the platelet membrane glycoprotein IIbIIIa complex.
Fórmula:C20H35N7O7Pureza:>99.99%Cor e Forma:SolidPeso molecular:485.535-Chloro-2'-deoxyuridine
CAS:5-Chloro-2'-deoxyuridine (5-Chlorodeoxyuridine) is a thymine analog.Fórmula:C9H11ClN2O5Pureza:99.54%Cor e Forma:SolidPeso molecular:262.65Vidofludimus
CAS:Vidofludimus (SC12267) (4SC-101, SC12267) is a novel small molecule inhibitor of dihydroorotate dehydrogenase (DHODH).Fórmula:C20H18FNO4Pureza:98.33% - 99.58%Cor e Forma:SolidPeso molecular:355.36EG1
CAS:EG1, a novel specific inhibitor of Pax2 transcription activation, targets the DNA binding domain and inhibits embryonic kidney development.Fórmula:C22H18N2O5Pureza:97.48%Cor e Forma:SolidPeso molecular:390.39Ref: TM-T27246
1mL*10mM (DMSO)33,00€2mg34,00€5mg54,00€10mg86,00€25mg130,00€50mg187,00€100mg260,00€200mg370,00€BAY-1816032
CAS:BAY-1816032 is a benzimidazole budding inhibition relieved homolog protein 1 kinase (BUB1) inhibitor.Cost-effective and quality-assured.Fórmula:C27H24F2N6O4Pureza:98.02% - 99.81%Cor e Forma:SolidPeso molecular:534.51Ref: TM-T10467
1mg35,00€5mg80,00€1mL*10mM (DMSO)95,00€10mg119,00€25mg230,00€50mg339,00€100mg485,00€200mg665,00€Longdaysin
CAS:Longdaysin is an inhibitor of CK1α and CK1δ (IC50s: 5.6/8.8 μM). It also can inhibit ERK2 (IC50: 52 μM).Fórmula:C16H16F3N5Pureza:99.97%Cor e Forma:SolidPeso molecular:335.335-Fluorocytidine
CAS:5-Fluorocytidine with antiviral activityFórmula:C9H12FN3O5Pureza:99.23%Cor e Forma:White PowderPeso molecular:261.21Adefovir dipivoxil
CAS:Adefovir dipivoxil (GS 0840) is a dipivoxil formulation of adefovir, a nucleoside reverse transcriptase inhibitor analog of adenosine with activity againstFórmula:C20H32N5O8PPureza:98% - 99.80%Cor e Forma:It Has Broad-Spectrum Antiviral ActivityPeso molecular:501.47BTB-1
CAS:BTB-1 (NSC156750) is a novel small molecule inhibitor of the mitotic motor protein Kif18A.Fórmula:C12H8ClNO4SPureza:99.71%Cor e Forma:SolidPeso molecular:297.71XMD8-92
CAS:XMD8-92 is an effective and specific BMK1/ERK5 inhibitor (Kd: 80 nM).Fórmula:C26H30N6O3Pureza:98.21%Cor e Forma:SolidPeso molecular:474.55FUBP1-IN-1
CAS:FUBP1-in-1: Potent FUBP1 inhibitor with 11.0 M IC50, disrupts FUBP1-DNA binding.Fórmula:C19H14F3N3O2SPureza:99.7%Cor e Forma:SolidPeso molecular:405.39Ref: TM-T11332
1mg72,00€1mL*10mM (DMSO)144,00€5mg160,00€10mg245,00€25mg406,00€50mg572,00€100mg772,00€200mg1.035,00€Tipiracil
CAS:Tipiracil inhibits thymidine phosphorylase, enhancing trifluridine bioavailability, and is studied in colorectal and gastric cancer treatment.Fórmula:C9H11ClN4O2Pureza:99.815%Cor e Forma:SolidPeso molecular:242.66Besifloxacin Hydrochloride
CAS:Besifloxacin Hydrochloride (BOL-303224-A) is a fourth-generation fluoroquinolone antibiotic.Fórmula:C19H21ClFN3O3·HClPureza:99.20%Cor e Forma:Pale Yellow SolidPeso molecular:430.3Ref: TM-T6406
5mg38,00€1mL*10mM (DMSO)52,00€10mg57,00€25mg97,00€50mg172,00€100mg319,00€200mg470,00€500mg750,00€roxifiban
CAS:Roxifiban, a prodrug of XV459, is an antiplatelet agent with high affinity and specificity for platelet glycoprotein IIb/IIIa complex(GPIIb/IIIa) receptors.
Fórmula:C21H29N5O6Pureza:98%Cor e Forma:SolidPeso molecular:447.48Mps1-IN-3 hydrochloride
Mps1-IN-3 HCl: potent Mps1 inhibitor (IC50: 50 nM), hampers glioblastoma growth, enhances vincristine efficacy in vivo.Fórmula:C26H32ClN7O4SCor e Forma:SolidPeso molecular:574.09Eptifibatide acetate (148031-34-9 free base)
CAS:Eptifibatide acetate (148031-34-9), a cyclic heptapeptide GP IIb/IIIa inhibitor antiplatelet drug.Fórmula:C35H49N11O9S2·xC2H4O2Pureza:99.7% - 99.87%Cor e Forma:SolidPeso molecular:891.012-Chloropyrazine
CAS:2-Chloropyrazine is used in chemical industry.Fórmula:C4H3ClN2Pureza:98.98% - 99.89%Cor e Forma:Clear Colorless To Yellowish LiquidPeso molecular:114.53CB-6644
CAS:CB-6644 is a small molecule inhibitor of the ATPase activity of the RUVBL1/2 complex.Cost-effective and quality-assured.Fórmula:C29H34ClFN4O5Pureza:96.33% - 99.85%Cor e Forma:SolidPeso molecular:573.06Ref: TM-T10693
1mg205,00€5mg416,00€1mL*10mM (DMSO)525,00€10mg533,00€25mg748,00€50mg973,00€100mg1.260,00€VPC-80051 racemate
CAS:VPC-80051 is the first small molecule inhibitor of hnRNP A1 splicing activity by using a computer-aided drug discovery approach.Fórmula:C16H13F2N3OPureza:97.36%Cor e Forma:SolidPeso molecular:301.29C/EBPα inducer 1
CAS:C/EBPα inducer 1 (4(3H)-Quinazolinone, 6-fluoro-2-[(1E)-2-(5-nitro-2-furanyl)ethenyl]-3-phenyl-) is a potential inducer of myeloid differentiation viaFórmula:C20H12FN3O4Pureza:98.99%Cor e Forma:SolidPeso molecular:377.33MK-8745
CAS:MK-8745 is a potent and selective Aurora A inhibitor.Fórmula:C20H19ClFN5OSPureza:99.09% - 99.79%Cor e Forma:SolidPeso molecular:431.91TC-E 5003
CAS:TC-E 5003 (NSC-30176) is a selective inhibitor of PRMT1 with IC50 of 1.5 μM.Fórmula:C16H14Cl2N2O4SPureza:97.01%Cor e Forma:SolidPeso molecular:401.26Antitumor agent-152
CAS:Organic compound, potential dCK inhibitor, with 2-ethyl-3-methoxyphenyl-1,3-thiazole and pyrimidine units.Fórmula:C17H19N5O2S2Pureza:95.00%Cor e Forma:SolidPeso molecular:389.5Ref: TM-T50079
1mg85,00€5mg170,00€1mL*10mM (DMSO)185,00€10mg253,00€25mg414,00€50mg583,00€100mg783,00€200mg1.054,00€CRT0066854
CAS:CRT-0066854 is a PKCι and PKCζ inhibitor. CRT0066854 was able to restore polarized morphogenesis in the dysplastic H-Ras spheroids.Fórmula:C24H25N5SCor e Forma:SolidPeso molecular:415.55Myoseverin
CAS:Myoseverin triggers myotube fission into single cells, influencing genes for growth, immunity, matrix remodeling, and stress, aiding healing and regeneration.Fórmula:C24H28N6O2Pureza:99.25%Cor e Forma:SolidPeso molecular:432.522-Amino-4-hydroxypyrrolo[2,3- d]pyrimidi
CAS:2-Amino-4-hydroxypyrrolo[2,3-d]pyrimidine serves as an intermediate.Fórmula:C6H6N4OPureza:99.21% - 99.42%Cor e Forma:SolidPeso molecular:150.14Pipobroman
CAS:Pipobroman (Vercyte) is an alkylating anti-cancer drug effective in PV and ET with low toxicity and thrombosis risk.Fórmula:C10H16Br2N2O2Pureza:97.08%Cor e Forma:SolidPeso molecular:356.059-Ethylguanine
CAS:9-Ethylguanine is a model nucleobase commonly used in the studies of DNA interactions with organometallic complexes.Fórmula:C7H9N5OPureza:98.6%Cor e Forma:SolidPeso molecular:179.18Spermine tetrahydrochloride
CAS:Spermine tetrahydrochloride, a polyamine in all eukaryotic cells, protects DNA from free radicals.Fórmula:C10H26N4·4HClPureza:99.75% - 99.82%Cor e Forma:SolidPeso molecular:348.18GJ103 sodium salt
CAS:GJ103 sodium salt, a GJ072 analog, lowers surface tension, viscosity, and pH in aqueous solutions, aiding molecular movement.Fórmula:C16H13N4NaO3SPureza:99.70% - 99.91%Cor e Forma:SolidPeso molecular:364.36Sovilnesib
CAS:Sovilnesib is a kinesin-like protein KIF18A inhibitor. Sovilnesib can be used for the cancer research.Fórmula:C26H34F2N6O4SPureza:99.57%Cor e Forma:SolidPeso molecular:564.65Ref: TM-T39994
1mg96,00€5mg235,00€1mL*10mM (DMSO)259,00€10mg376,00€25mg630,00€50mg898,00€100mg1.216,00€Gadodiamide
CAS:Gadodiamide is an MRI contrast agent, used in MR imaging procedures to assist in the visualization of blood vessels.Fórmula:C16H26GdN5O8Pureza:99.86% - 99.93%Cor e Forma:SolidPeso molecular:573.662,2'-Anhydrouridine
CAS:2,2'-Anhydrouridine (2,2'-Cyclouridine) is a research tool for antiviral and anticancer studies.Fórmula:C9H10N2O5Pureza:98.45%Cor e Forma:SolidPeso molecular:226.19PRT4165
CAS:PRT4165 (NSC600157) is a potent PRC1-mediated H2A ubiquitylation inhibitor.Fórmula:C15H9NO2Pureza:98.91% - 99.6%Cor e Forma:SolidPeso molecular:235.24Ref: TM-T3110
5mg43,00€10mg49,00€1mL*10mM (DMSO)50,00€25mg88,00€50mg112,00€100mg182,00€200mg254,00€500mg427,00€KIRA6
CAS:KIRA6 is an effective inhibitor of IRE1α RNase kinase (IC50: 0.6 μM). It can trigger an apoptotic response.
Fórmula:C28H25F3N6OPureza:97.91%Cor e Forma:SolidPeso molecular:518.53N2-Methylguanosine
CAS:N2-methylguanosine is a modified nucleoside of tRNA that occurs at several specific locations in many tRNA's
Fórmula:C11H15N5O5Pureza:97.77%Cor e Forma:SolidPeso molecular:297.27Triciribine
CAS:Triciribine (NSC-154020) is a DNA synthesis inhibitor, and it also inhibits Akt and HIV-1/2.Fórmula:C13H16N6O4Pureza:99.01% - 99.87%Cor e Forma:SolidPeso molecular:320.3Ref: TM-T6065
1mg38,00€2mg49,00€5mg80,00€1mL*10mM (DMSO)88,00€10mg116,00€25mg207,00€50mg329,00€100mg512,00€200mg727,00€Rg3039
CAS:Rg3039 (PF-06687859) is a potent DcpS inhibitor. DcpS is a therapeutic target for spinal muscular atrophy (SMA). RG3039 improves motor function in SMA mice.Fórmula:C21H23Cl2N5OPureza:98.24% - 99.58%Cor e Forma:SolidPeso molecular:432.35VX-11e
CAS:VX-11e (TCS ERK 11e) is a potent, selective, and orally bioavailable ERK(Extracellular Signal-Regulated Kinase) inhibitor; antitumor agent.Fórmula:C24H20Cl2FN5O2Pureza:98.92% - ≥98%Cor e Forma:SolidPeso molecular:500.35Tirofiban hydrochloride monohydrate
CAS:Tirofiban（MK383） hydrochloride monohydrate is a non-peptide glycoprotein IIb/IIIa antagonist. Cost-effective and quality-assured.Fórmula:C22H39ClN2O6SPureza:98.81% - >99.99%Cor e Forma:White SolidPeso molecular:495.07GSK-923295
CAS:GSK923295 is a selective allosteric inhibitor of CENP-E kinesin motor ATPase(Ki=3.2 nM).Fórmula:C32H38ClN5O4Pureza:96.22% - 98.02%Cor e Forma:SolidPeso molecular:592.13Ref: TM-T2039
1mg49,00€5mg97,00€1mL*10mM (DMSO)136,00€10mg168,00€25mg283,00€50mg432,00€100mg605,00€200mg852,00€ON-013100
CAS:ON-013100 is an antineoplastic drug. ON-013100 also acts as a mitotic inhibitor that could inhibit Cyclin D1 expression.Fórmula:C19H22O7SPureza:98.27%Cor e Forma:SolidPeso molecular:394.44Ref: TM-T16391
1mg48,00€1mL*10mM (DMSO)60,00€5mg71,00€10mg100,00€25mg172,00€50mg268,00€100mg404,00€200mg570,00€Voruciclib
CAS:Voruciclib: oral, selective CDK inhibitor (Ki: 0.626-9.1 nM), reduces MCL-1, targets CDK9 in diffuse large B-cell lymphoma.Fórmula:C22H19ClF3NO5Pureza:99.89% - 99.99%Cor e Forma:SolidPeso molecular:469.84FDI-6
CAS:FDI-6 is an effective and selective inhibitor of FOXM1 that blocks DNA binding. FDI-6 binds to the FOXM1 protein and downregulates FOXM1-activated genes.Fórmula:C19H11F4N3OS2Pureza:98.92% - >99.99%Cor e Forma:SolidPeso molecular:437.43Ref: TM-T4005
1mg34,00€5mg74,00€1mL*10mM (DMSO)84,00€10mg114,00€25mg192,00€50mg274,00€100mg408,00€200mg597,00€CID-797718
CAS:CID-797718 is a protein kinase D1 (PKD1) inhibitor.Fórmula:C12H11NO3Pureza:98.91% - 99.21%Cor e Forma:SolidPeso molecular:217.22Ref: TM-T1858
1mg62,00€5mg138,00€1mL*10mM (DMSO)152,00€10mg200,00€25mg339,00€50mg482,00€100mg665,00€200mg893,00€MNS
CAS:MNS is a tyrosine kinases inhibitor, inhibits Syk, Src, p97 with IC50 of 2.5 μM, 29.3 μM and 1.7 μM, respectively.Fórmula:C9H7NO4Pureza:98.53%Cor e Forma:Yellow PowderPeso molecular:193.16URMC-099
CAS:URMC-099: oral, brain-accessible MLK/LRRK2 inhibitor; IC50 – MLK1/2/3/DLK: 19/42/14/150 nM, LRRK2: 11 nM.Fórmula:C27H27N5Pureza:99.32% - 99.98%Cor e Forma:SolidPeso molecular:421.54APY29
CAS:APY29 is an allosteric modulator of IRE1α; inhibits IRE1α autophosphorylation (IC50 = 280 nM) and activates IRE1α RNase activity.Fórmula:C17H16N8Pureza:96.51% - 98.46%Cor e Forma:SolidPeso molecular:332.36Ref: TM-T3654
2mg40,00€5mg62,00€1mL*10mM (DMSO)67,00€10mg90,00€25mg167,00€50mg285,00€100mg515,00€500mg1.071,00€
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