Unter den Marken unserer mehr als 25 Partner sticht TargetMol hervor
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.
Endet am 31. Dez.( 8 verbleibende Tage )
UNC2025
CAS:<p>UNC2025 (mrx-6313)(IC50 of 0.74 nM and 0.8 nM) is a potent and orally bioavailable dual MER/FLT3 inhibitor.</p>Formel:C28H40N6OReinheit:99.53% - 99.74%Farbe und Form:SolidMolekulargewicht:476.66Cisapride tartrate
CAS:Cisapride tartrate is chemically related to metoclopramide, but unlike metoclopramide, it does not cross the blood-brain barrier or have antidopaminergicFormel:C27H35ClFN3O10Farbe und Form:SolidMolekulargewicht:616.04SLM6031434 (free base)
CAS:SLM6031434 (free base) is an inhibitor of sphingosine kinase type 2 (SphK2). It consists of pedant 1-guanidino-2-phenyloxadiazolylpyrrolidine group.Formel:C22H30F3N5O2Farbe und Form:SolidMolekulargewicht:453.5Aplindore
CAS:<p>Aplindore is a dopamine receptor agonist used in the therapeutic treatment of Parkinson's Disease.</p>Formel:C18H18N2O3Farbe und Form:SolidMolekulargewicht:310.35Fabomotizole dihydrochloride
CAS:<p>Fabomotizole (Afobazole, Obenoxazine, CM346) is a non-sedative anxiolytic with neuroprotective properties, launched in Russia 2000s; exact mechanism unclear.</p>Formel:C15H23Cl2N3O2SFarbe und Form:SolidMolekulargewicht:380.33SB1-F-21
CAS:SB1-F-21 is an UCHL1 inhibitor.Formel:C15H14N4OSFarbe und Form:SolidMolekulargewicht:298.36KDS2010 mesylate
CAS:<p>KDS2010: potent, reversible MAO-B inhibitor with 12,500x selectivity vs. MAO-A; enhances memory in APP/PS1 mice.</p>Formel:C18H21F3N2O4SFarbe und Form:SolidMolekulargewicht:418.43NOSO-95C
CAS:<p>NOSO-95C, an antibacterial, targets bacterial ribosomes, halting translation, and is effective against Enterobacteriaceae in vitro/in vivo.</p>Formel:C54H101N23O12Farbe und Form:SolidMolekulargewicht:1264.53Fadolmidine HCl
CAS:<p>Fadolmidine (MPV-2426) is a potent alpha2-adrenoceptor agonist for spinal analgesia with high affinity across human subtypes and efficacy in vivo.</p>Formel:C13H15ClN2OFarbe und Form:SolidMolekulargewicht:250.72Fadolmidine
CAS:Fadolmidine is a novel and potent alpha2 -adrenoceptor (alpha2) -AR) agonist developed for spinal analgesia.Formel:C13H14N2OFarbe und Form:SolidMolekulargewicht:214.26MPV-1306
CAS:MPV-1306 is a metabolite of Dexmedetomidine -- a novel alpha 2-adrenergic receptor agonist.Formel:C13H14N2O2Farbe und Form:SolidMolekulargewicht:230.26Vacquinol-1
CAS:Vacquinol-1 is an MKK4 activator, which rapidly and selectively induces glioma cell death.Formel:C21H21ClN2OReinheit:99.92%Farbe und Form:SolidMolekulargewicht:352.86Methasquin
CAS:<p>Methasquin is a folic acid antagonist that has been used in the treatment of experimental leukemia; acts by inhibiting the dihydrofolate reductase in the cell.</p>Formel:C21H22N6O5Farbe und Form:SolidMolekulargewicht:438.44Pd 158771
CAS:Pd 158771 is a D2 and 5-HT1A agonist.Formel:C22H31N5Farbe und Form:SolidMolekulargewicht:365.52Pyrithione cadmium
CAS:Pyrithione cadmium suppresses tumor growth in vitro and in vivo through inhibition of proteasomal deubiquitinaseFormel:C10H8CdN2O2S2Farbe und Form:SolidMolekulargewicht:364.73Cilengitide hydrochloride
CAS:Cilengitide hydrochloride is a salt that may combat cancer by blocking specific integrins, disrupting cell interactions and angiogenesis.Formel:C27H41ClN8O7Farbe und Form:SolidMolekulargewicht:625.12Dersalazine
CAS:<p>Dersalazine, a PAF inhibitor, reduces IL-17 to treat colitis in rodents, potentially aiding ulcerative colitis patients.</p>Formel:C35H32N6O4Reinheit:99.62%Farbe und Form:SolidMolekulargewicht:600.67IND 1316
CAS:<p>IND 1316 is an activator of AMP-activated protein kinase (AMPK).</p>Formel:C22H17NO3Farbe und Form:SolidMolekulargewicht:343.38EPZ033294
CAS:EPZ033294 has potential anticancer and antiproliferative activity.Formel:C20H22ClN7OReinheit:99.95%Farbe und Form:SolidMolekulargewicht:411.89EPZ032597
CAS:EPZ032597 is a novel selective inhibitor of SMYD2 with an IC50 of 16 nM. EPZ032597 has anticancer activity and prevent and treat pancreatic cancerFormel:C20H23N7OReinheit:99.70%Farbe und Form:SolidMolekulargewicht:377.44Grp94-IN-2
CAS:Grp94-IN-2 is a inhibitor of Grp94.Formel:C22H23ClN2O5Farbe und Form:SolidMolekulargewicht:430.88Colterol (free base)
CAS:Colterol: short-acting β2 agonist; Bitolterol prodrug treats asthma, COPD bronchospasm.Formel:C12H19NO3Farbe und Form:SolidMolekulargewicht:225.28Soyacerebroside II
CAS:Soyacerebroside II is a Ca2+ ionophore; both I and II inhibit IL-18 in PBMCs and modulate immune responses.Formel:C40H75NO9Reinheit:98%Farbe und Form:SolidMolekulargewicht:714.02Nizatidine amide
CAS:Nizatidine amide blocks H2 receptors, reducing stomach acid to treat ulcers and GERD.Formel:C11H18N4O3S2Farbe und Form:SolidMolekulargewicht:318.42IACS-4759
CAS:<p>IACS-4759 is a novel potent and selective MTH1 inhibitor with excellent cell permeability and good metabolic stability in microsomes.</p>Formel:C10H17N3O2Farbe und Form:SolidMolekulargewicht:211.26ent-Entecavir
CAS:Ent-Entecavir, an enantiomeric impurity of Entecavir (an oral HBV drug), inhibits HBV replication as a reverse transcriptase inhibitor.Formel:C12H15N5O3Farbe und Form:SolidMolekulargewicht:277.28JTP 103237
CAS:<p>JTP 103237 is a potent and selective monoacyglycerol acyltransferase 2 (MOGAT2) inhibitor.</p>Formel:C24H29F3N6OFarbe und Form:SolidMolekulargewicht:474.52MS-049 oxalate salt
CAS:MS-049 oxalate salt is a potent and selective inhibitor of protein arginine methyltransferases (PRMTs) PRMT 4 and PRMT6.Formel:C17H26N2O5Farbe und Form:SolidMolekulargewicht:338.4Mps1-IN-1 dihydrochloride
CAS:Mps1-IN-1 dihydrochloride, a potent ATP-competitive inhibitor of Mps1 kinase, exhibits an IC50 of 367 nM.Formel:C28H35Cl2N5O4SFarbe und Form:SolidMolekulargewicht:608.58AEG40730 HCl
CAS:<p>AEG40730: A potent, selective IAP inhibitor, induces cIAP1/2 degradation, reduces RIP1 ubiquitination, and depletes XIAP, c-IAP1.</p>Formel:C52H70Cl2F6N8O8Farbe und Form:SolidMolekulargewicht:1120.0704Acefylline piperazine
CAS:<p>Acefylline piperazine, a less toxic theophylline derivative, treats asthma and bronchitis by bronchodilation, stimulating respiration and CNS.</p>Formel:C9H10N4O4·xC4H10N2Farbe und Form:SolidMolekulargewicht:562.54CDK8-IN-18
CAS:CDK8-IN-18, also known as ZINC584617986, is a potent and selective inhibitor of CDK8, also modulating CDK19.Formel:C18H17N5OFarbe und Form:SolidMolekulargewicht:319.36Methylsilanol ascorbate
CAS:Methylsilanol ascorbate is a silanol analogue and inhibitor of angiotensin-converting enzyme.Formel:C7H12O8SiFarbe und Form:SolidMolekulargewicht:252.25VER-155008
CAS:<p>VER-155008 is a potent Hsp70 family inhibitor with IC50 of 0.5 μM, 2.6 μM, and 2.6 μM in cell-free assays for HSP70, HSC70, and GRP78, respectively.</p>Formel:C25H23Cl2N7O4Reinheit:97.03% - 99.55%Farbe und Form:SolidMolekulargewicht:556.4SG3-179
CAS:SG3-179 is a BET inhibitor.Formel:C28H35ClFN7O3SFarbe und Form:SolidMolekulargewicht:604.14EMD-66684
CAS:EMD-66684 is a non-peptide angiotensin II receptor antagonist.Formel:C28H31ClN8O2Farbe und Form:SolidMolekulargewicht:547.06KFP-H008
CAS:KFP-H008 is a potassium-competitive acid blocker.Formel:C19H18N4O2SFarbe und Form:SolidMolekulargewicht:366.44KSK213
CAS:KSK213: Strongly inhibits C. trachomatis (EC50=60 nM); non-toxic to commensals/host cells at 25 μM.Formel:C28H25N3O2SFarbe und Form:SolidMolekulargewicht:467.58Verubecestat tosylate
CAS:Verubecestat (MK-8931/SCH 900931) is a potent BACE1 inhibitor, promising for Alzheimer’s, reducing Aβ in CSF by up to 92%.Formel:C25H26N4O4S2Farbe und Form:SolidMolekulargewicht:510.627Chlorpromazine Sulfone Hydrochloride
CAS:Chlorpromazine Sulfone Hydrochloride: metabolite of anti-psychotic, may inhibit N-methyltransferase.Formel:C17H20Cl2N2O2SFarbe und Form:SolidMolekulargewicht:387.32F-050
CAS:F-050 inhibits platelet aggregation, potentially treating thrombosis in guinea pigs, rabbits, and rats.Formel:C21H20OFarbe und Form:SolidMolekulargewicht:288.38Olcorolimus
CAS:Olcorolimus blocks specific allergen-induced inflammation, reducing eosinophil, lymphocyte infiltration, and IL-4/IL-5 mRNA expression.Formel:C51H81NO12Farbe und Form:SolidMolekulargewicht:900.19Fasudil hydrochloride hydrate
CAS:Fasudil HCl hydrate is a ROCK inhibitor that hinders mature CCM development and lowers portal pressure in cirrhotic rats.Formel:C28H38Cl2N6O5S2Farbe und Form:SolidMolekulargewicht:673.67Delucemine Free Base
CAS:Delucemine Free Base is an NMDA Receptor AntagonistFormel:C16H17F2NFarbe und Form:SolidMolekulargewicht:261.31Verubecestat
CAS:<p>Verubecestat (MK-8931) (MK-8931) is an effective and specific β-secretase inhibitor and β-site APP-cleaving enzyme 1 inhibitor or BACE1 protein inhibitor.</p>Formel:C17H17F2N5O3SReinheit:92.24% - 99.55%Farbe und Form:SolidMolekulargewicht:409.41CVS-1578
CAS:CVS-1578 is a potent serine protease inhibitor, targeting the S2S3 thrombin and FXa subsites.Formel:C20H30N6O5SFarbe und Form:SolidMolekulargewicht:466.55GT-2394
CAS:GT-2394 is a histamine H3 receptor agonist.Formel:C14H21N3O2Farbe und Form:SolidMolekulargewicht:263.34GT-2227
CAS:<p>GT-2227 is a histamine H3 receptor antagonist.</p>Formel:C15H24N2Farbe und Form:SolidMolekulargewicht:232.36ATM-1001
CAS:ATM-1001 is an inhibitor of the cancer-associated tropomyosin 3.1 (Tpm3.1), suppressing glucose-stimulated insulin secretion (GSIS) from the pancreatic islets.Formel:C30H36N4OFarbe und Form:SolidMolekulargewicht:468.63Paclitaxel Ceribate
CAS:<p>Paclitaxel Ceribate is a mitotic inhibitor used in cancer chemotherapy.</p>Formel:C51H57NO18Farbe und Form:SolidMolekulargewicht:971.99
