CymitQuimica ha oltre 25 partner, tra i quali spicca il fornitore TargetMol
We have reached an agreement with TargetMol: CymitQuimica clients will benefit for a 20% discount on all TargetMol products until the end of the year.On our website you can find the products offered by this partner, which has become one of the world's most recognised compound libraries and small molecule inhibitors supplier. TargetMol offers approximately 120 compound libraries and a wide range of chemical products and kits for life sciences.
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pCDPK1/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>Formula:C17H18N6Purezza:99.63%Colore e forma:SoildPeso molecolare: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>Formula:C20H18Cl2N2O3Purezza:98%Colore e forma:SoildPeso molecolare: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>Formula:C22H24ClF3N6O2Purezza:98%Colore e forma:SoildPeso molecolare: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.Formula:C19H18N2O5SPurezza:99.82% - 99.86%Colore e forma:SolidPeso molecolare: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.Formula:C27H31N3O2Purezza:99.87%Colore e forma:SoildPeso molecolare: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.Formula:C24H23FN6OPurezza:98.46% - 99.76%Colore e forma:SoildPeso molecolare:430.48PNU-74654
CAS:<p>PNU 74654 blocks β-catenin/Tcf4, disrupting Wnt signaling (Kd = 450 nM).</p>Formula:C19H16N2O3Purezza:97.27%Colore e forma:SolidPeso molecolare: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.Formula:C35H30N6O5Colore e forma:SoildPeso molecolare: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>Formula:C21H20N2O3SPurezza:99.68%Colore e forma:SoildPeso molecolare:380.46Acetylsulfamerazine
CAS:<p>Acetylsulfamerazine, a metabolite of sulphamethazine, slightly inhibits cellulose digestion and rumen endocrine, with anti-microbial properties.</p>Formula:C13H14N4O3SPurezza:99.88%Colore e forma:SolidPeso molecolare:306.34SCFSkp2-IN-2
CAS:<p>SCFSkp2-IN-2, a Skp2 inhibitor, exhibits a dissociation constant (K_D) of 28.77 μM.</p>Formula:C17H20N4O2Purezza:99.86%Colore e forma:SolidPeso molecolare:312.37Fmoc-N-methyl-L-alloisoleucine
CAS:<p>Fmoc-N-methyl-L-alloisoleucine is a biochemical reagent for biosynthesis.</p>Formula:C22H25NO4Purezza:99.41%Colore e forma:SoildPeso molecolare: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.Formula:C21H28N4O5SPurezza:99.96%Colore e forma:SoildPeso molecolare: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>Formula:C15H11ClN2OPurezza:98.45%Colore e forma:SoildPeso molecolare: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.Formula:C21H20ClN3O2Purezza:98.55% - 99.22%Colore e forma:SoildPeso molecolare:381.864-N-Nonyloxyphenol
CAS:<p>4-N-Nonyloxyphenol, kaolinite nanotube photosensitizer, degrades phenolic pesticides, and disrupts endocrine.</p>Formula:C15H24O2Purezza:99.94%Colore e forma:SoildPeso molecolare: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>Formula:C12H14FNOPurezza:98.34% - 99.75%Colore e forma:SolidPeso molecolare: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>Formula:C18H30O2Purezza:99.88%Colore e forma:SolidPeso molecolare:278.43LabMol-319
CAS:LabMol-319 is a potent Zika virus (ZIKV) NS5 RdRp inhibitor with antiviral activity for the study of ZIKV virus.Formula:C22H16N2O5Purezza:99.92%Colore e forma:SolidPeso molecolare: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.Formula:C25H28N4O2SPurezza:99.39%Colore e forma:SolidPeso molecolare:448.58PERK-IN-6
CAS:<p>PERK-IN-6 is a novel and highly potent PERK inhibitor (IC50:2.5 nM).</p>Formula:C23H22N6OPurezza:99.62% - 99.92%Colore e forma:SolidPeso molecolare:398.46SLC26A3-IN-1
CAS:"SLC26A3-IN-1 inhibits SLC26A3, an anion transporter linked to diarrhea, with 340 nM IC50."Formula:C23H18O4Purezza:99.02%Colore e forma:SolidPeso molecolare:358.39FM04
CAS:FM04 is a potent oral P-gp inhibitor (EC50: 83 nM), disrupting human P-gp NBD2 to enhance cancer treatment.Formula:C26H25NO4Purezza:99.87%Colore e forma:SolidPeso molecolare: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>Formula:C22H19FN6Purezza:98.35%Colore e forma:SolidPeso molecolare: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>Formula:C27H22N2OPurezza:98.13%Colore e forma:SoildPeso molecolare: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.Formula:C32H31ClN6O3Purezza:98.30%Colore e forma:SoildPeso molecolare:583.08S1R agonist 2
CAS:<p>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.</p>Formula:C21H27NOPurezza:98.85%Colore e forma:SolidPeso molecolare:309.452-Iminobiotin
CAS:2-Iminobiotin inhibits iNOS/nNOS; Ki: 21.8 μM (mouse iNOS), 37.5 μM (rat nNOS).Formula:C10H17N3O2SPurezza:98%Colore e forma:SolidPeso molecolare: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>Formula:C29H26N6O3SPurezza:98.64% - 98.64%Colore e forma:SolidPeso molecolare: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.Formula:C24H27N7OSPurezza:97.74% - 99.88%Colore e forma:SoildPeso molecolare:461.58BI-2865
CAS:BI-2865 is a non-covalent pan-KRAS inhibitor.Cost-effective and quality-assured.Formula:C23H27N7O2SPurezza:99.29% - 99.39%Colore e forma:SoildPeso molecolare: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>Formula:C12H9BrClN3OPurezza:99.21%Colore e forma:SoildPeso molecolare: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>Formula:C22H20N2O2Purezza:99.57%Colore e forma:SoildPeso molecolare: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.Formula:C21H21N5O3SPurezza:98.28% - 99.92%Colore e forma:SoildPeso molecolare: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.Formula:C22H20Cl2N4OSPurezza:99.95%Colore e forma:SoildPeso molecolare: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 inFormula:C19H17N5OSPurezza:99.44%Colore e forma:SoildPeso molecolare: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.Formula:C16H15ClN4O2S2Purezza:97.65%Colore e forma:SolidPeso molecolare: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>Formula:C10H18BrN3O2SPurezza:98.13%Colore e forma:SolidPeso molecolare: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>Formula:C15H13F2NO4SPurezza:97.98%Colore e forma:SolidPeso molecolare:341.33B-Raf IN 14
CAS:B-Raf IN 14 is a BRAF inhibitor.Formula:C15H14BrN5O3SPurezza:98.38%Colore e forma:SolidPeso molecolare:424.27WAY-299017
CAS:WAY-299017 is a potent and selective UPPS inhibitor for the treatment of bacterial infections.Formula:C17H14N2O3Purezza:97.01%Colore e forma:SolidPeso molecolare: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>Formula:C17H16N2OSPurezza:99.49%Colore e forma:SolidPeso molecolare:296.39AKOS037652256
CAS:<p>AKOS037652256 modulates TRPML, treating TRPML-linked diseases like lysosomal disorders, muscular dystrophy, neurodegeneration, and oxidative stress.</p>Formula:C24H26ClFN4O4S2Purezza:98.81%Colore e forma:SolidPeso molecolare:553.07BTA-EG4 hydrate
CAS:<p>BTA-EG4 hydrate aids in diagnosing and mitigating Alzheimer's, enhancing cognitive abilities.</p>Formula:C22H28N2O4SColore e forma:SolidPeso molecolare:416.53HyT36
CAS:<p>HyT36: hydrophobic tag that destabilizes fusion proteins & Her3 pseudokinase; treats cells with acute erht.</p>Formula:C25H44ClNO3Purezza:99.86%Colore e forma:SolidPeso molecolare:442.07H2-Gamendazole
CAS:<p>H2-Gamendazole: inhibits spermatogenesis, cancer therapy, targets heat shock proteins & EF1α, regulates Hsp90.</p>Formula:C18H13Cl2F3N2O2Purezza:97.36%Colore e forma:SolidPeso molecolare:417.21Imidacloprid-urea
CAS:<p>Imidacloprid-urea, a byproduct of imidacloprid, may alter its environmental behavior by competing for soil binding sites.</p>Formula:C9H10ClN3OPurezza:99.89%Colore e forma:SolidPeso molecolare:211.65Xanthine oxidoreductase-IN-4
CAS:Xanthine oxidoreductase-IN-4: oral XOR inhibitor, IC50 of 29.3 nM, potential for hyperuricemia research.Formula:C16H15N5O2Purezza:98.93%Colore e forma:SoildPeso molecolare:309.32Biotin-aniline
CAS:<p>Biotin-aniline is a probe that reacts strongly to RNA and DNA.</p>Formula:C18H26N4O2SPurezza:99.23%Colore e forma:SolidPeso molecolare:362.49AMD 3465 hexahydrobromide
CAS:AMD 3465 hexahydrobromide (GENZ-644494 (hexahydrobromide)) is a CXCR4 receptor antagonist with potential anticancer and anti-HIV activity.Formula:C24H44Br6N6Purezza:99.39%Colore e forma:SolidPeso molecolare:896.07
