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Endet am 31. Dez.( 7 verbleibende Tage )
TROX-1
CAS:TROX-1 is the activation state-dependent Cav2 channel antagonist.Formel:C22H16ClFN6OReinheit:98%Farbe und Form:SolidMolekulargewicht:434.85TRP-601
CAS:<p>TRP-601 is a caspase inhibitor.</p>Formel:C40H48F2N6O11Reinheit:98%Farbe und Form:SolidMolekulargewicht:826.852TSI-01
CAS:TSI-01,Pro-inflammatory phospholipid mediator. Inhibits LPCAT2 (IC50=0.47 μM). Suppresses PAF biosynthesis in macrophages.Formel:C14H11Cl2NO4Reinheit:99.87%Farbe und Form:SolidMolekulargewicht:328.15TT01001
CAS:<p>TT01001, a mitoNEET agonist, may treat type II diabetes by reducing oxidative stress and preventing neuronal death.</p>Formel:C15H19Cl2N3O2SReinheit:99.93%Farbe und Form:SolidMolekulargewicht:376.3Tuna AI
CAS:Tuna AI is an inhibitor of the angiotensin-converting enzyme. Tuna AI is a bioactive chemical.Formel:C44H64N12O12Reinheit:98%Farbe und Form:SolidMolekulargewicht:953.06Tuna AI acetate
<p>Tuna AI acetate is an inhibitor of angiotensin-converting enzyme (ACE) in non-competitive manner derived from tuna muscle.</p>Formel:C46H68N12O14Reinheit:98.49%Farbe und Form:SolidMolekulargewicht:1013.1Tunicamine
CAS:Tunicamine is a reversible polyprenol-phosphate inhibitor.Formel:C11H21NO9Reinheit:98%Farbe und Form:SolidMolekulargewicht:311.29Tyrphostin 47
CAS:Tyrphostin 47 inhibits the protein-tyrosine kinase activity of EGF-R.Formel:C10H8N2O2SFarbe und Form:SolidMolekulargewicht:220.25Tyrphostin 51
CAS:Tyrphostin 51 is an effective inhibitor of EGFR kinase.Formel:C13H8N4O3Reinheit:98%Farbe und Form:SolidMolekulargewicht:268.23AZ-5104
CAS:AZ5104 is a potent EGFR inhibitor.Formel:C27H31N7O2Reinheit:98.40% - 99.59%Farbe und Form:Solid PowderMolekulargewicht:485.58Tyrphostin A46
CAS:Tyrphostin A46 is an antagonist of the epidermal growth factor-urogastrone receptor.Formel:C10H8N2O3Reinheit:98%Farbe und Form:Off-White SolidMolekulargewicht:204.18Tyrphostin AG 1112
CAS:Tyrphostin AG 1112 is a Bcr-Abl kinase blocker. It can activate the terminal differentiation of K562 cells and the purging of Ph+ cells.Formel:C15H10N6Farbe und Form:SolidMolekulargewicht:274.28Tyrphostin AG 568
CAS:Tyrphostin AG 568 promotes Tyrphostin-induced inhibition of p210bcr-abl tyrosine kinase activity. It also induces K562 to differentiate.Formel:C13H9N5O2Reinheit:98%Farbe und Form:SolidMolekulargewicht:267.24U 89360E
CAS:U 89360E is a peptidic inhibitor.Formel:C28H52N8O6Reinheit:98%Farbe und Form:SolidMolekulargewicht:596.76UBP512
CAS:UBP512 is a NMDA receptor modulator.Formel:C15H9IO2Reinheit:98%Farbe und Form:SolidMolekulargewicht:348.14UBP618
CAS:UBP618 is a GluN1/GluN2 receptors pan-inhibitor.Formel:C17H11BrO3Reinheit:98%Farbe und Form:SolidMolekulargewicht:343.17UBP646
CAS:UBP646 is a GluN1/GluN2 receptors potentiator.Formel:C21H22O2Reinheit:98%Farbe und Form:SolidMolekulargewicht:306.4UBP684
CAS:UBP684 enhances NMDAR responses, boosts l-glutamate/glycine, and mildly affects subunit agonist potency.Formel:C17H20O2Reinheit:98%Farbe und Form:SolidMolekulargewicht:256.34UBP710
CAS:UBP710 is an effective and selective NMDA receptor modulator.Formel:C18H14O2Reinheit:98.05%Farbe und Form:SolidMolekulargewicht:262.3UBP714
CAS:UBP714, derived from UBP608, boosts NMDAR in CA1 hippocampus, promising for schizophrenia and cognitive deficits treatment.Formel:C11H7BrO4Reinheit:98%Farbe und Form:SolidMolekulargewicht:283.07Perifosine
CAS:Perifosine (KRX-0401) is an oral-active, alkyl-phosphocholine Akt inhibitor with potential antineoplastic activity.Formel:C25H52NO4PReinheit:99.80 - >99.99%Farbe und Form:SolidMolekulargewicht:461.66UCD38B HCl
CAS:UCD38B HCl, a cell-permeable uPA inhibitor, induces programmed necrosis in high-grade glioma cells.Formel:C15H17Cl2N7O3Reinheit:98%Farbe und Form:SolidMolekulargewicht:414.25UK-88947 HCl
CAS:UK 88947 is a protease inhibitor.Formel:C41H63ClN6O6Reinheit:98%Farbe und Form:SolidMolekulargewicht:771.44UMB-136
CAS:UMB-136 is a bromodomain BRD4 inhibitor that acts by significantly inducing HIV-1 reactivation.Formel:C24H27N5O2Reinheit:98%Farbe und Form:SolidMolekulargewicht:417.5Umespirone
CAS:Umespirone is a potential antipsychotic/anxiolytic drug of the azapirone class. It possesses anxiolytic and antipsychotic properties.Formel:C28H40N4O5Reinheit:98%Farbe und Form:SolidMolekulargewicht:512.64UNC-2170
CAS:UNC-2170 (UNC2170 Maleate) is the methyl-lysine binding protein, 53BP1 ligand.Formel:C14H21BrN2OReinheit:97.44%Farbe und Form:SolidMolekulargewicht:313.23UNC2327
CAS:<p>UNC2327 is a potent and selective inhibitor of protein arginine methyltransferase 3 (PRMT3) (IC50:230 nM).</p>Formel:C14H17N5O2SReinheit:98%Farbe und Form:SolidMolekulargewicht:319.38Undecylprodigiosin
CAS:Undecylprodigiosin is a classical cytotoxic immunosuppressant, suppressing immune functions. It also inhibits DNA synthesis.Formel:C25H35N3OFarbe und Form:SolidMolekulargewicht:393.56UPR-IN-17#
CAS:UPR-IN-17# is an effective pan-inhibitor of the unfolded protein response.Formel:C23H22ClN3O3SReinheit:98%Farbe und Form:SolidMolekulargewicht:455.96V-06-018
CAS:V-06-018 is a quorum-sensing modulator. It also acts as a LasR antagonist.Formel:C18H27NO2Reinheit:98%Farbe und Form:SolidMolekulargewicht:289.41PD 151746
CAS:<p>PD151746: calpain inhibitor, Ki μ-calpain=0.26μM, Ki m-calpain=5.33μM; reduces oxLDL cytotoxicity.</p>Formel:C11H8FNO2SReinheit:98.63% - ≥95%Farbe und Form:SolidMolekulargewicht:237.25Valone
CAS:Valone is an anticoagulant.Formel:C14H14O3Reinheit:98%Farbe und Form:Yellow Crystalline Solid SolidMolekulargewicht:230.26Vapiprost
CAS:Vapiprost is an antagonist of the thromboxane receptor and a prostaglandin receptor.Formel:C30H39NO4Reinheit:98%Farbe und Form:SolidMolekulargewicht:477.64Vatanidipine
CAS:Vatanidipine (AE0047) is a novel dihydropyridine (DHP)-type calcium channel blocker with slow-onset pharmacological actions.A slow-onset and long-lastingFormel:C41H42N4O6Reinheit:99.95%Farbe und Form:SolidMolekulargewicht:686.8VCC234718
CAS:VCC234718 is a molecule with growth inhibitory activity against Mycobacterium tuberculosis (Mtb).Formel:C20H25N3O3SReinheit:99.35% - 99.82%Farbe und Form:SolidMolekulargewicht:387.5Vesamicol
CAS:Vesamicol is an experimental drug. It acting presynaptically by inhibiting acetylcholine uptake into synaptic vesicles and reducing its release.Formel:C17H25NOReinheit:98%Farbe und Form:SolidMolekulargewicht:259.39Vif-A3G Inhibitor N.41
CAS:Vif-A3G Inhibitor N.41 is a HIV-1 inhibitor-targeting drug. It causes Vif-dependent degradation of human APOBEC3G, thereby inhibiting the Vif-A3G interaction.Formel:C15H14N2O2Reinheit:98%Farbe und Form:SolidMolekulargewicht:254.28Viminol
CAS:Viminol is an opioid analgesic. Viminol is based on the α-pyrryl-2-aminoethanol structure, unlike any other class of opioids.Formel:C21H31ClN2OReinheit:98%Farbe und Form:SolidMolekulargewicht:362.94Viprostol
CAS:Viprostol is an agent of prostaglandin antihypertensive.Formel:C23H36O5Reinheit:98%Farbe und Form:SolidMolekulargewicht:392.53Virodhamine trifluoroacetate
CAS:Virodhamine trifluoroacetate: full GPR55 & CB2 agonist, partial CB1 antagonist, cannabinoid receptor mixed antagonist.Formel:C24H38F3NO4Reinheit:98%Farbe und Form:SolidMolekulargewicht:461.56Cilengitide
CAS:Cilengitide (EMD 121974) is a potent integrin inhibitor for the αvβ3/5 receptor (IC50: 4.1/79 nM, in cell-free assays); ~10-fold selectivity against gpIIbIIIa.Formel:C27H40N8O7Reinheit:98% - 99.8%Farbe und Form:SolidMolekulargewicht:588.66Vitacoxib
CAS:Vitacoxib is a selective inhibitor of COX-2. It is used as a novel nonsteroidal anti-inflammatory agent.Formel:C16H14ClN3O2SReinheit:98%Farbe und Form:SolidMolekulargewicht:347.82VMAT2-IN-I HCl
CAS:VMAT2-IN-I HCl is an inhibitor of vesicular monoamine transporter-2. It also has 15- fold greater affinity than GZ- 793A.Formel:C25H32ClF4NO4Reinheit:98%Farbe und Form:SolidMolekulargewicht:521.97VPC-14228
CAS:VPC-14228 is a specific AR-DBD inhibitor that acts by inhibiting both Y594A and Q592A mutants.Formel:C13H14N2OSReinheit:99.96%Farbe und Form:SolidMolekulargewicht:246.33VPC-14449
CAS:VPC-14449 is a selective androgen receptor DNA-binding domain (AR-DBD) inhibitor, useful in prostate cancer research.Formel:C10H10Br2N4OSReinheit:99.56%Farbe und Form:SolidMolekulargewicht:394.09VU0410425
CAS:VU0410425 is a metabotropic glutamate receptor subtype 1 negative allosteric modulator.Formel:C19H16ClN3O3Reinheit:98%Farbe und Form:SolidMolekulargewicht:369.8VU0415374
CAS:VU0415374 is a positive allosteric modulator of mGlu4.Formel:C20H16ClN3O3Reinheit:98%Farbe und Form:SolidMolekulargewicht:381.81VU0431316
CAS:VU0431316 is a negative mGlu5 allosteric modulator. It has activity in a mouse model of anxiety.Formel:C14H9ClN6O2Reinheit:98%Farbe und Form:SolidMolekulargewicht:328.71VU625
CAS:<p>VU625 (VU007625) is an AeKir1 inhibitor (IC50: 96.8nM) that acts as a mosquito killer and inhibits AeKir1-mediated currents.</p>Formel:C19H22N2O4SReinheit:99.08%Farbe und Form:SolidMolekulargewicht:374.45VUF10132
CAS:<p>VUF10132 is a full inverse CXCR3 N3.35A agonist.</p>Formel:C19H13BrCl4N2O2Reinheit:98%Farbe und Form:SolidMolekulargewicht:523.03
