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Termina em 31 de dez.( faltam 7 dias )
BI 1015550
CAS:Nerandomilast (BI 1015550) is an orally active PDE4B inhibitor with IC50 of 7.2 nM.Cost-effective and quality-assured.Fórmula:C20H25ClN6O2SPureza:98.06% - 99.96%Cor e Forma:SoildPeso molecular:448.97PI5P4Ks-IN-2
CAS:<p>PI5P4Ks-IN-2 inhibits PI5P4K isoforms α, β, γ, γ+ with IC50 <4.3, <4.6, 6.2, 0.32 µM, respectively.</p>Fórmula:C22H23N5Pureza:98.36% - 99.02%Cor e Forma:SoildPeso molecular:357.45pCDPK1/TgCDPK1-IN-3
CAS:<p>CpCDPK1/TgCDPK1-IN-3 inhibits Cp/TgCDPK1; IC50: 0.003/0.0036 µM. It's used to research Toxoplasma, Cryptosporidium diseases.</p>Fórmula:C17H18N6Pureza:99.63%Cor e Forma:SoildPeso molecular:306.36LI-2242
CAS:<p>LI-2242: Potent IP6K inhibitor, IC50s - IP6K1: 31nM, IP6K2: 42nM, IP6K3: 8.7nM, IPMK: 1944nM; improves hepatic steatosis and diabetes.</p>Fórmula:C20H18Cl2N2O3Pureza:98%Cor e Forma:SoildPeso molecular:405.27HPK1-IN-36
CAS:<p>HPK1-IN-36 (compound 2) is a potent inhibitor of hematopoietic progenitor kinase 1 (HPK1), demonstrating an inhibitory concentration 50 (IC50) of 0.5 nM [1].</p>Fórmula:C22H24ClF3N6O2Pureza:98%Cor e Forma:SoildPeso molecular:496.91Anti-Influenza agent 4
CAS:Anti-Influenza agent 4 selectively inhibits A/Parma (EC50: 62 nM) and A/Roma (EC50: 150 nM) influenza strains.Fórmula:C19H18N2O5SPureza:99.82% - 99.86%Cor e Forma:SolidPeso molecular:386.42YM-58790
CAS:YM-58790 is a potent mAChR blocker with Ki values of 28 nM (M1), 260 nM (M2), 15 nM (M3), and reduces bladder contractions in rats.Fórmula:C27H31N3O2Pureza:99.87%Cor e Forma:SoildPeso molecular:429.55CLK1-IN-3
CAS:Clk1-in-3 is a + selective and highly potent sexual Clk1 inhibitor with an IC50 of 5 nM and 300 pairs higher affinity than Dyrk1A.Fórmula:C24H23FN6OPureza:98.46% - 99.76%Cor e Forma:SoildPeso molecular:430.48PNU-74654
CAS:<p>PNU 74654 blocks β-catenin/Tcf4, disrupting Wnt signaling (Kd = 450 nM).</p>Fórmula:C19H16N2O3Pureza:97.27%Cor e Forma:SolidPeso molecular:320.34c-Myc inhibitor 7
CAS:c-Myc inhibitor 7 degrades c-MYC, CK1α, GSPT1, IKZF1/2/3 proteins in tumors, for research on related diseases.Fórmula:C35H30N6O5Cor e Forma:SoildPeso molecular:614.65Flaviviruses-IN-2
CAS:<p>Flaviviruses-IN-2 is a potent flaviviruses inhibitor. Flaviviruses-IN-2 reduces West Nile virus (WNV) protease activity and inhibits WNV by 56%.</p>Fórmula:C21H20N2O3SPureza:99.68%Cor e Forma:SoildPeso molecular:380.46Acetylsulfamerazine
CAS:<p>Acetylsulfamerazine, a metabolite of sulphamethazine, slightly inhibits cellulose digestion and rumen endocrine, with anti-microbial properties.</p>Fórmula:C13H14N4O3SPureza:99.88%Cor e Forma:SolidPeso molecular:306.34SCFSkp2-IN-2
CAS:<p>SCFSkp2-IN-2, a Skp2 inhibitor, exhibits a dissociation constant (K_D) of 28.77 μM.</p>Fórmula:C17H20N4O2Pureza:99.86%Cor e Forma:SolidPeso molecular:312.37Fmoc-N-methyl-L-alloisoleucine
CAS:<p>Fmoc-N-methyl-L-alloisoleucine is a biochemical reagent for biosynthesis.</p>Fórmula:C22H25NO4Pureza:99.41%Cor e Forma:SoildPeso molecular:367.44PF-17
CAS:1-[6-(4-methoxysulfonylphenoxy)-4-pyrimidinyl]piperidine-4-carbamic acid tert-butyl ester is a PUF60 inhibitor potentially for ovarian cancer treatment.Fórmula:C21H28N4O5SPureza:99.96%Cor e Forma:SoildPeso molecular:448.54Antibacterial agent 125
CAS:<p>Antibacterial agent 125 shows strong activity against Gram-positive pathogens; MICs: 0.25-8 μM; used in antimicrobial resistance research.</p>Fórmula:C15H11ClN2OPureza:98.45%Cor e Forma:SoildPeso molecular:270.71CDK8-IN-12
CAS:CDK8-IN-12: selective CDK8 inhibitor (Ki 14 nM), oral anticancer, blocks GSK-3α/β, PCK-θ, halts MV4-11 cell growth.Fórmula:C21H20ClN3O2Pureza:98.55% - 99.22%Cor e Forma:SoildPeso molecular:381.864-N-Nonyloxyphenol
CAS:<p>4-N-Nonyloxyphenol, kaolinite nanotube photosensitizer, degrades phenolic pesticides, and disrupts endocrine.</p>Fórmula:C15H24O2Pureza:99.94%Cor e Forma:SoildPeso molecular:236.35A-967079
CAS:<p>A 967079 is a potent, selective, and bioavailable inhibitor of the TRPA1 channel, with IC50 values of 67 and 289 nM for the human and rat isoforms, respectively</p>Fórmula:C12H14FNOPureza:98.34% - 99.75%Cor e Forma:SolidPeso molecular:207.244-N-Dodecyloxyphenol
CAS:<p>4-N-Dodecyloxyphenol is an additive for ferroelectric crystals without chiral groups, aiding in the SmC phase display.</p>Fórmula:C18H30O2Pureza:99.88%Cor e Forma:SolidPeso molecular:278.43LabMol-319
CAS:LabMol-319 is a potent Zika virus (ZIKV) NS5 RdRp inhibitor with antiviral activity for the study of ZIKV virus.Fórmula:C22H16N2O5Pureza:99.92%Cor e Forma:SolidPeso molecular:388.37HPK1-IN-34
CAS:HPK1-IN-34 (Compound 143) is an inhibitor of HPK1 (Haematopoietic progenitor kinase 1) with an IC₅₀ < 0.1 μM, suitable for cancer and immunology research.Fórmula:C25H28N4O2SPureza:99.39%Cor e Forma:SolidPeso molecular:448.58PERK-IN-6
CAS:<p>PERK-IN-6 is a novel and highly potent PERK inhibitor (IC50:2.5 nM).</p>Fórmula:C23H22N6OPureza:99.62% - 99.92%Cor e Forma:SolidPeso molecular:398.46SLC26A3-IN-1
CAS:"SLC26A3-IN-1 inhibits SLC26A3, an anion transporter linked to diarrhea, with 340 nM IC50."Fórmula:C23H18O4Pureza:99.02%Cor e Forma:SolidPeso molecular:358.39FM04
CAS:FM04 is a potent oral P-gp inhibitor (EC50: 83 nM), disrupting human P-gp NBD2 to enhance cancer treatment.Fórmula:C26H25NO4Pureza:99.87%Cor e Forma:SolidPeso molecular:415.48KYN-101
CAS:<p>KYN-101 is an and aryl hydrocarbon receptor (AHR) inhibitor with anticancer activity. KYN-101 is used for the study of breast cancer and acute myeloid leukemia.</p>Fórmula:C22H19FN6Pureza:98.35%Cor e Forma:SolidPeso molecular:386.43H1k
<p>H1k is an eudistomin Y fluorescent derivative and lysosome-targeted antiproliferative agent that downregulates the expression of cell cycle protein B1.</p>Fórmula:C27H22N2OPureza:98.13%Cor e Forma:SoildPeso molecular:390.48CDD-1102 HCl
CDD-1102 HCl is a novel BRDT-BD4 / BRD2-BD1302 selective inhibitor that shows non-hormonal contraceptive potential in ex vivo experiments.Fórmula:C32H31ClN6O3Pureza:98.30%Cor e Forma:SoildPeso molecular:583.08S1R agonist 2
CAS:S1R agonist 2 is a selective S1R agonist with a Ki of 88 nM for S2R and 1.1 nM for S1R and is protective against ROS and NMDA-induced neurotoxicity.Fórmula:C21H27NOPureza:99.66%Cor e Forma:SolidPeso molecular:309.452-Iminobiotin
CAS:2-Iminobiotin inhibits iNOS/nNOS; Ki: 21.8 μM (mouse iNOS), 37.5 μM (rat nNOS).Fórmula:C10H17N3O2SPureza:98%Cor e Forma:SolidPeso molecular:243.33Myosin V-IN-1
CAS:<p>Myosin V-IN-1: potent, selective Myosin V inhibitor, Ki of 6 μM; hinders actin-activated ATPase by blocking ADP release.</p>Fórmula:C29H26N6O3SPureza:98.64% - 98.64%Cor e Forma:SolidPeso molecular:538.62BI-2493
CAS:BI-2493 is a highly selective pan-KRAS inhibitor and structural analog of BI-2865.BI-2493 exhibits antitumor activity and inhibits tumor cell growth.Cost-effective and quality-assured.Fórmula:C24H27N7OSPureza:97.74% - 99.88%Cor e Forma:SoildPeso molecular:461.58BI-2865
CAS:BI-2865 is a non-covalent pan-KRAS inhibitor.Cost-effective and quality-assured.Fórmula:C23H27N7O2SPureza:99.29% - 99.39%Cor e Forma:SoildPeso molecular:465.57PDCD4-IN-1
CAS:<p>PDCD4-IN-1, a PDCD4 inhibitor (Kd : 350 nM), promotes BDNF expression in hippocampal neuronal cells HT-22.</p>Fórmula:C12H9BrClN3OPureza:99.21%Cor e Forma:SoildPeso molecular:326.58TASK-1-IN-1
CAS:<p>TASK-1-IN-1: Potent, selective TASK-1 blocker (IC50: 148 nM), weaker on TASK-3 (IC50: 1750 nM), anticancer properties.</p>Fórmula:C22H20N2O2Pureza:99.57%Cor e Forma:SoildPeso molecular:344.41CHET3
CAS:CHET3 is a highly selective allosteric activator for TASK-3-containing K2P channels. CHET3 has shown potent in vivo analgesic effects. Cost-effective and quality-assured.Fórmula:C21H21N5O3SPureza:98.28% - 99.92%Cor e Forma:SoildPeso molecular:423.49DPTN dihydrochloride
CAS:DPTN dihydrochloride is a potent and selective A3AR antagonist with Ki values of 1.65, 9.61 and 8.53 nM in human, mouse and rat, respectively.Fórmula:C22H20Cl2N4OSPureza:99.95%Cor e Forma:SoildPeso molecular:459.39SFI003
CAS:SFI003 is a novel SRSF3 inhibitor that exerts anticancer activity against colorectal cancer by modulating the SRSF3 / DHCR24 / ROS axis and driving apoptosis inFórmula:C19H17N5OSPureza:99.44%Cor e Forma:SoildPeso molecular:363.44MMP-9-IN-7
CAS:N-[2-[(5-Cl-2-methoxyphenyl)amino]-4'-methyl[4,5'-bithiazol]-2'-yl]acetamide inhibits pro-MMP activation, treats MMP9/MMP13 syndromes.Fórmula:C16H15ClN4O2S2Pureza:97.65%Cor e Forma:SolidPeso molecular:394.92-Iminobiotin hydrobromide
CAS:<p>2-Iminobiotin hydrobromide (Guanidinobiotin) is a cyclic guanidino analog of biotin that acts as a reversible inhibitor of inducible nitric oxide synthase (iNOS</p>Fórmula:C10H18BrN3O2SPureza:98.13%Cor e Forma:SolidPeso molecular:324.24FK 3311
CAS:<p>FK 3311 (COX-2 Inhibitor V) is a cell permeable and orally available sulfonanilide that acts as a COX-2 inhibitor and non-steroidal anti-inflammatory drug (</p>Fórmula:C15H13F2NO4SPureza:97.98%Cor e Forma:SolidPeso molecular:341.33B-Raf IN 14
CAS:B-Raf IN 14 is a BRAF inhibitor.Fórmula:C15H14BrN5O3SPureza:98.38%Cor e Forma:SolidPeso molecular:424.27WAY-299017
CAS:WAY-299017 is a potent and selective UPPS inhibitor for the treatment of bacterial infections.Fórmula:C17H14N2O3Pureza:97.01%Cor e Forma:SolidPeso molecular:294.32-benzylsulfanyl-6-methoxy-4-methylquinazoline
CAS:<p>2-benzylsulfanyl-6-methoxy-4-methylquinazoline: a TRPML modulator for lysosomal and ROS-related ailments.</p>Fórmula:C17H16N2OSPureza:99.49%Cor e Forma:SolidPeso molecular:296.39AKOS037652256
CAS:<p>AKOS037652256 modulates TRPML, treating TRPML-linked diseases like lysosomal disorders, muscular dystrophy, neurodegeneration, and oxidative stress.</p>Fórmula:C24H26ClFN4O4S2Pureza:98.81%Cor e Forma:SolidPeso molecular:553.07BTA-EG4 hydrate
CAS:BTA-EG4 hydrate aids in diagnosing and mitigating Alzheimer's, enhancing cognitive abilities.Fórmula:C22H28N2O4SCor e Forma:SolidPeso molecular:416.53HyT36
CAS:<p>HyT36: hydrophobic tag that destabilizes fusion proteins & Her3 pseudokinase; treats cells with acute erht.</p>Fórmula:C25H44ClNO3Pureza:99.86%Cor e Forma:SolidPeso molecular:442.07H2-Gamendazole
CAS:<p>H2-Gamendazole: inhibits spermatogenesis, cancer therapy, targets heat shock proteins & EF1α, regulates Hsp90.</p>Fórmula:C18H13Cl2F3N2O2Pureza:97.36%Cor e Forma:SolidPeso molecular:417.21Imidacloprid-urea
CAS:<p>Imidacloprid-urea, a byproduct of imidacloprid, may alter its environmental behavior by competing for soil binding sites.</p>Fórmula:C9H10ClN3OPureza:99.89%Cor e Forma:SolidPeso molecular:211.65Xanthine oxidoreductase-IN-4
CAS:Xanthine oxidoreductase-IN-4: oral XOR inhibitor, IC50 of 29.3 nM, potential for hyperuricemia research.Fórmula:C16H15N5O2Pureza:98.93%Cor e Forma:SoildPeso molecular:309.32
