
Inhibidores
Los inhibidores son moléculas que se unen a enzimas, receptores u otras proteínas para reducir o bloquear su actividad biológica. Estos compuestos se utilizan ampliamente en la investigación para estudiar vías biológicas, comprender los mecanismos de las enfermedades y desarrollar fármacos terapéuticos. Los inhibidores desempeñan un papel crucial en el tratamiento de diversas enfermedades, incluyendo el cáncer, las enfermedades cardiovasculares y las infecciones. En CymitQuimica, ofrecemos una amplia gama de inhibidores de alta calidad para apoyar su investigación en bioquímica, biología celular y desarrollo farmacéutico.
Subcategorías de "Inhibidores"
- Angiogénesis(2.523 productos)
- Apoptosis(5.792 productos)
- Ciclo celular / Checkpoint(4.449 productos)
- Cromatina / Epigenética(2.238 productos)
- Señalización citoesquelética(1.383 productos)
- Daño al ADN / Reparación del ADN(2.825 productos)
- Endocrinología / Hormonas(3.507 productos)
- Enzima(3.640 productos)
- GPCR / proteína G(8.333 productos)
- Inmunología e inflamación(3.526 productos)
- Virus de la gripe(296 productos)
- Señalización JAK / STAT(404 productos)
- Señalización MAPK(1.202 productos)
- Transportador de membrana / canal de iones(2.790 productos)
- Metabolismo(9.448 productos)
- Microbiología / Virología(6.981 productos)
- Neurociencia(9.926 productos)
- Otros inhibidores(37.926 productos)
- Reducción de oxidación(41 productos)
- Señalización PI3K / Akt / mTOR(1.400 productos)
- Proteasas / Proteasoma(1.597 productos)
- Células madre y Derivados(831 productos)
- Tirosina quinasa / adaptadores(2.016 productos)
- Ubiquitinación(1.650 productos)
Mostrar 16 subcategorías más
Se han encontrado 66641 productos de "Inhibidores"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
GAL-021 sulfate
CAS:<p>GAL-021 sulfate is a BKCa channel blocker that inhibits the analgesic effects of opioids and is used in the study of respiratory control diseases.</p>Fórmula:C11H24N6O5SPureza:99.92%Forma y color:SolidPeso molecular:352.41Diprafenone Free Base
CAS:<p>Diprafenone Free Base is an antiarrhythmic beta adrenergic antagonist.</p>Fórmula:C23H31NO3Forma y color:SolidPeso molecular:369.5LX-3
CAS:<p>LX-3 activates p38 MAPK, enabling expression of genes normally silenced by DNA methylation.</p>Fórmula:C20H13BrN4OSForma y color:SolidPeso molecular:437.31M2WJ332
CAS:<p>M2WJ332 is a novel M2-S31N inhibitor, showing antiviral activity against Influenza A virus.</p>Fórmula:C18H22N2OSForma y color:SolidPeso molecular:314.45LH-708
CAS:<p>LH-708 is an inhibitor of cystine stone formation for treatment of cystinuria.</p>Fórmula:C16H36Cl4N6O2S2Forma y color:SolidPeso molecular:550.42SC 23133
CAS:<p>SC 23133 is an antimineralocorticoid that is known to induce a marked but reversible inhibition of aldosterone biosynthesis.</p>Fórmula:C23H30O3Forma y color:SolidPeso molecular:354.48CAY10568
CAS:<p>Most local anesthetics act by abolishing voltage gated sodium channel currents indiscriminately in all populations of neurons.</p>Fórmula:C11H17IN2OForma y color:SolidPeso molecular:320.174Anti-hyperglycemic agent-1
CAS:<p>Anti-hyperglycemic agent 1 is a potent inhibitor of alpha-glucosidase (IC50: 0.53 μM). anti-Hyperglycemic agent 1 can be used to study diabetes.</p>Fórmula:C20H15BrN2O3Forma y color:SolidPeso molecular:411.25Quinoprazine
CAS:<p>Quinoprazine: inhibits Vaccinia virus (IC50=10μM), antimalarial vs Plasmodium berghei, reduces PrPSc, antiprion.</p>Fórmula:C25H26N4Forma y color:SolidPeso molecular:382.5AY-16804
CAS:<p>AY-16804 is an inhibitor of platelet aggregation.</p>Fórmula:C12H18O3Forma y color:SolidPeso molecular:210.27(rel)-Oxaliplatin
CAS:<p>(rel)-Oxaliplatin, a DNA inhibitor, induces crosslinks, hinders replication/transcription, and triggers apoptosis; used in cancer studies.</p>Fórmula:C8H14N2O4PtForma y color:SolidPeso molecular:397.29Binifibrate
CAS:<p>Binifibrate is a hyperlipemiant drug used for the treatment of hyperlipidemia.</p>Fórmula:C25H23ClN2O7Forma y color:SolidPeso molecular:498.91EMI56
CAS:<p>EMI56, a derivative of EMI1, exhibits enhanced potency against mutant EGFR compared to EMI1. Additionally, EMI56 effectively inhibits EGFR triple mutants[1].</p>Fórmula:C21H20N2O3Forma y color:SolidPeso molecular:348.4Bexin-1
CAS:<p>Bexin-1 blocks Munc13-4 from binding to membranes, targeting its C2 domain and stopping ANF-EGFP release induced by ionomycin.</p>Fórmula:C20H26ClN5OSForma y color:SolidPeso molecular:419.97TM-9
CAS:<p>TM-9, an Alzheimer's drug, strongly inhibits both ChE and MAO-B.</p>Fórmula:C21H20N2O2Forma y color:SolidPeso molecular:332.4TEAD-IN-3
CAS:<p>TEAD-IN-3 (compound I-177) is a potent inhibitor of the TEAD transcription factor, which can be used to study proliferative diseases such as cancer.</p>Fórmula:C22H20F3N5O2Forma y color:SolidPeso molecular:443.42LY 81067
CAS:<p>LY 81067, a new anticonvulsant, prevents PTZ- and picrotoxin-induced seizures in mice via picrotoxin site interaction.</p>Fórmula:C22H24N4OForma y color:SolidPeso molecular:360.45As-358
CAS:<p>As-358 has inhibitory effects against Ebola virus (IC50 = 47.5 μM) and Marburg virus (IC50 = 3.7 μM) [1].</p>Fórmula:C18H31NO2Forma y color:SolidPeso molecular:293.44TCSA
CAS:<p>TCSA is an inhibitor of fungal morphogenesis, biofilm formation, and host cell invasion.</p>Fórmula:C13H8Cl3NO2Forma y color:SolidPeso molecular:316.57Azidobenzamidotaurocholate
CAS:<p>Azido Benzamido Taurocholate is a bile acid transporter.</p>Fórmula:C33H49N5O7SForma y color:SolidPeso molecular:659.84DHPCG
CAS:<p>DHPCG is an inhibitor of HIF-1α prolyl hydroxylase.</p>Fórmula:C8H8N2O5Forma y color:SolidPeso molecular:212.16SHP2-IN-5
CAS:<p>SHP2-IN-5 (compound 1) is a non-receptor protein tyrosine phosphatase inhibitor targeting SHP2 with an IC50 value of 97 nM, associated with regulating cell</p>Fórmula:C12H8O6Forma y color:SolidPeso molecular:248.19IND31119
CAS:<p>IND31119 is a novel selective inhibitor of PfHsp90, bypassing its highly similar human orthologs.</p>Fórmula:C25H38N4O4Forma y color:SolidPeso molecular:458.59LUF5831
CAS:<p>LUF5831 is an agonist of adenosine A1 receptor.</p>Fórmula:C15H12N4O2SForma y color:SolidPeso molecular:312.35Hexoprenaline Sulfate
CAS:<p>Hexoprenaline Sulfate: selective β2 agonist, treats bronchospasm in asthma, bronchitis, emphysema; oral/IV/inhalation.</p>Fórmula:C22H34N2O10SForma y color:SolidPeso molecular:518.58BRN-103
CAS:<p>BRN-103 inhibits VEGF signaling, blocking VEGR2, AKT, and eNOS activation in human cells.</p>Fórmula:C24H25ClN4OForma y color:SolidPeso molecular:420.93ITP-2
CAS:<p>ITP-2 activates hERG channels, shifts inactivation midpoint depolarization, and activation voltage hyperpolarization.</p>Fórmula:C19H14F3N5O2Forma y color:SolidPeso molecular:401.343-Tyr-octreotide
CAS:<p>3-Tyr-octreotide is a biochemical that has been evaluated for tumor inhibition.</p>Fórmula:C49H66N10O11S2Forma y color:SolidPeso molecular:1035.24Antifungal agent 69
CAS:<p>Antifungal agent 69 (compound 13), a eugenol-imidazole derivative, demonstrates targeted activity against Candida albicans with a minimum inhibitory</p>Fórmula:C23H23ClN2O4Forma y color:SolidPeso molecular:426.89LSP1-2111
CAS:<p>LSP1-2111 is a mGlu4 receptor subtype agonist.</p>Fórmula:C12H17N2O9PForma y color:SolidPeso molecular:364.25Fasobegron
CAS:<p>Fasobegron is a agonist of β3-adrenoreceptor .</p>Fórmula:C24H24ClNO4Forma y color:SolidPeso molecular:425.91Pca 4233
CAS:<p>Pca 4233 belongs to a class of selective PAF-receptor antagonists.</p>Fórmula:C20H25NO4SForma y color:SolidPeso molecular:375.48Noremopamil
CAS:<p>Noremopamil is a calcium entry blocker, also being used as the precursor for radiolabelling emopamil.</p>Fórmula:C22H28N2Forma y color:SolidPeso molecular:320.47CAY10485
CAS:<p>CAY10485 blocks human ACAT-1 & ACAT-2 (IC50: 95 & 81 μM) and hinders oxidation of LDL by 91% at 2 μM, possibly impacting atherosclerosis development.</p>Fórmula:C27H27NO7Forma y color:SolidPeso molecular:477.51Penclomedine
CAS:<p>Penclomedine is an antineoplastic agent which alkylates and crosslinks DNA, resulting in DNA strand breaks and inhibition of DNA and RNA synthesis.</p>Fórmula:C8H6Cl5NO2Forma y color:SolidPeso molecular:325.4Lergotrile mesylate
CAS:<p>Lergotrile mesylate, an ergoline derivative, suppresses prolactin in vivo and in vitro.</p>Fórmula:C18H22ClN3O3SForma y color:SolidPeso molecular:395.9UCCF-029
CAS:<p>UCCF-029 is an activator of cystic fibrosis transmembrane conductance regulator (CFTR).</p>Fórmula:C18H11NO2Forma y color:SolidPeso molecular:273.29EGFR/BRAFV600E-IN-1
CAS:<p>EGFR/BRAFV600E-IN-1 inhibits EGFR (0.08 μM) & BRAFV600E (0.15 μM), affects A-549, MCF-7, Panc-1 & HT-29 (IC50: 0.79-1.3 μM).</p>Fórmula:C24H24ClN3O3Forma y color:SolidPeso molecular:437.92Dihydronarwedine
CAS:<p>Dihydronarwedine is a metabolite of Galanthamine, an inhibitor of glycogen synthase kinase 3β (GSK3β)</p>Fórmula:C17H21NO3Forma y color:SolidPeso molecular:287.35Pemrametostat succinate
CAS:<p>Pemrametostat succinate, an oral PRMT5 inhibitor, strongly curbs tumor growth in vitro and animal studies.</p>Fórmula:C28H38N6O7Forma y color:SolidPeso molecular:570.654-Chlorokynurenine
CAS:<p>4-Chlorokynurenine is a prodrug of 7-Cl-kynurenic acid (7-Cl-KYNA), a potent, selective antagonist of the NMDA/glycine receptor.</p>Fórmula:C10H11ClN2O3Forma y color:SolidPeso molecular:242.66P-4010
CAS:<p>P-4010 is effective against herpes simplex.</p>Fórmula:C26H43N5O4Forma y color:SolidPeso molecular:489.65Seliforant
CAS:<p>Seliforant is a histamine H4 receptor antagonist.</p>Fórmula:C12H21N5Pureza:98%Forma y color:SolidPeso molecular:235.33Desmethylene Tadalafil
CAS:<p>Desmethylene Tadalafil is a phosphodiesterase 5 inhibitor.</p>Fórmula:C21H19N3O4Forma y color:SolidPeso molecular:377.39GR-203040 HCl
CAS:<p>GR203040 inhibits cyclophosphamide-induced damage in the rat and ferret bladder. GR-203040 is a selective NK1 receptor antagonist.</p>Fórmula:C20H26Cl2N6OForma y color:SolidPeso molecular:437.37Ophthalmic acid
CAS:<p>Ophthalmic acid is a glutathione analog in which cysteine is substituted by L-aminobutyrate.</p>Fórmula:C11H19N3O6Forma y color:SolidPeso molecular:289.29OT-551
CAS:<p>OT-551, a NF-κB inhibitor, is used potentially for the treatment of cataracts and age-related macular degeneration.</p>Fórmula:C13H23NO3Pureza:98%Forma y color:SolidPeso molecular:241.33hCAIX/XII-IN-2
CAS:<p>Compound 6a: Selective hCAIX/XII inhibitor; Ki: 30 nM (hCAIX), 3.6 nM (hCAXII); >10,000 nM (hCAI/II).</p>Fórmula:C19H14N2O4Forma y color:SolidPeso molecular:334.33GSK-3008348
CAS:<p>GSK-3008348 is an antagonist of integrin alpha(v)beta6.</p>Fórmula:C29H37N5O2Pureza:99.547%Forma y color:SolidPeso molecular:487.64Fexaramate
CAS:<p>Fexaramate is a potent, selective agonist of farnesoid X receptor.</p>Fórmula:C31H37NO5Forma y color:SolidPeso molecular:503.63
