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(2.542 productos)
- Apoptosis(5.816 productos)
- Ciclo celular / Checkpoint(4.466 productos)
- Cromatina / Epigenética(2.252 productos)
- Señalización citoesquelética(1.381 productos)
- Daño al ADN / Reparación del ADN(2.830 productos)
- Endocrinología / Hormonas(3.518 productos)
- Enzima(3.640 productos)
- GPCR / proteína G(8.362 productos)
- Inmunología e inflamación(3.540 productos)
- Virus de la gripe(296 productos)
- Señalización JAK / STAT(405 productos)
- Señalización MAPK(1.201 productos)
- Transportador de membrana / canal de iones(2.809 productos)
- Metabolismo(9.462 productos)
- Microbiología / Virología(7.003 productos)
- Neurociencia(9.942 productos)
- Otros inhibidores(37.827 productos)
- Reducción de oxidación(40 productos)
- Señalización PI3K / Akt / mTOR(1.399 productos)
- Proteasas / Proteasoma(1.598 productos)
- Células madre y Derivados(830 productos)
- Tirosina quinasa / adaptadores(2.012 productos)
- Ubiquitinación(1.651 productos)
Mostrar 16 subcategorías más
Se han encontrado 66618 productos de "Inhibidores"
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GCN2-IN-7
CAS:<p>GCN2-IN-7 is an inhibitor of the environmental sensing protein GCN2 with antitumor activity for the study of melanoma.</p>Fórmula:C22H23BrN8OSPureza:99.12%Forma y color:SolidPeso molecular:527.44AMPA receptor antagonist-3
CAS:<p>AMPA receptor antagonist-3 is an AMPA receptor antagonist.</p>Fórmula:C20H19N5O2SPureza:99.79%Forma y color:SolidPeso molecular:393.46Filibuvir
CAS:<p>Filibuvir (PF-00868554) inhibits HCV polymerase genotypes 1a/1b, EC50s 59 nM.</p>Fórmula:C29H37N5O3Pureza:99.28% - >99.99%Forma y color:SolidPeso molecular:503.64WAY-639889
CAS:<p>WAY-639889 is a small molecule compound with selective and potent inhibitory effects on neuropeptide Y-5 receptors.</p>Fórmula:C25H27N5OPureza:99.73%Forma y color:SolidPeso molecular:413.51Adomeglivant
CAS:<p>Adomeglivant (LY2409021) is a potent and selective glucagon receptor antagonist. Which is used in clinical trial for type 2 diabetes mellitus.</p>Fórmula:C32H36F3NO4Pureza:99.91%Forma y color:SolidPeso molecular:555.63Didesmethyl cariprazine
CAS:<p>Didesmethyl cariprazine, Cariprazine's active metabolite, treats schizophrenia/bipolar with D3/D2 affinity; half-life 1-3 weeks.</p>Fórmula:C19H28Cl2N4OPureza:99.52%Forma y color:SolidPeso molecular:399.36Dalzanemdor
CAS:<p>Dalzanemdor (SAGE-718) is an NMDA receptor-positive modulator of metabolism that can be used to study Huntington's chorea, Alzheimer's disease, and cognitive</p>Fórmula:C27H43F3O2Pureza:98.2% - >99.99%Forma y color:SolidPeso molecular:456.62Phos-tag Acrylamide AAL-107
CAS:<p>Phos-tag Acrylamide AAL-107 is a polyacrylamide-conjugated phosphate-binding tag,visualizing phosphorylated proteins. High-Quality, Low-Cost!</p>Fórmula:C33H38N8O3Pureza:99.86% - >99.99%Forma y color:SoildPeso molecular:594.71Anti-inflammatory agent 49
CAS:<p>Compound SC9, an anti-inflammatory agent, serves as a potent and selective inhibitor of the Drp1-Fis1 interaction, mitigating FIS1-mediated mitochondrial</p>Fórmula:C21H22N8O3SPureza:99.56% - 99.74%Forma y color:SolidPeso molecular:466.52WAY-639228
CAS:<p>WAY-639228-A has potential antithrombotic and anticoagulant activity for the study of cerebral thrombosis.</p>Fórmula:C22H24N2O2SPureza:99.75%Forma y color:SolidPeso molecular:380.5Ropsacitinib
CAS:<p>Ropsacitinib (PF-06826647) is a selective TYK2 inhibitor, which binds to TYK2 catalytically active JH1 domain (IC50: 17 nM).</p>Fórmula:C20H17N9Pureza:99.87%Forma y color:SolidPeso molecular:383.41h-NTPDase-IN-2
CAS:h-NTPDase-IN-2 is a broad-spectrum NTPDase inhibitor that inhibits multiple h-NTPDas isoforms.Fórmula:C19H16N4SPureza:99.58%Forma y color:SolidPeso molecular:332.42JWG-071
CAS:JWG-071: First ERK5 kinase probe, BET inhibitor, 1 μM BRD4 IC, boosts ERK5 function and BRD4 selectivity.Fórmula:C34H44N8O3Pureza:99.83%Forma y color:SolidPeso molecular:612.77hRIO2 kinase ligand-1
CAS:hRIO2 kinase ligand-1 is a potent ligand for hRIO2 kinase (Kd: 520 nM).Fórmula:C17H14N2OPureza:99.89%Forma y color:SolidPeso molecular:262.31RO5263397
CAS:<p>RO5263397: TAAR1 agonist, orally active, studied as antidepressant, COX-2 inhibitor.</p>Fórmula:C10H11FN2OPureza:98.58%Forma y color:SolidPeso molecular:194.21Aucuparin
CAS:<p>Aucuparin (2,6-dimethoxy-4-phenylphenol) is a plant antibiotic with anti-inflammatory activity.</p>Fórmula:C14H14O3Pureza:99.98%Forma y color:SolidPeso molecular:230.26A7132
CAS:<p>A7132 is an antibacterial agent and possesses broad and potent antibacterial activity.</p>Fórmula:C19H16F2N4O3Pureza:95.49%Forma y color:SolidPeso molecular:386.35Supercinnamaldehyde
CAS:<p>Supercinnamaldehyde is a potent activator of transient receptor potential ankyrin 1 (TRPA1), exhibiting an EC50 of 0.8 μM, and induces activation of TRPA1 ion</p>Fórmula:C12H11NO2Pureza:98.89%Forma y color:SolidPeso molecular:201.22Oditrasertib
CAS:<p>Oditrasertib, a RIPK1 inhibitor characterized by an IC50 value below 100 nM, is employed in inflammation research.</p>Fórmula:C14H15F2N3O2Pureza:98.65% - 99.65%Forma y color:SolidPeso molecular:295.28α-(difluoromethyl)-DL-Arginine
CAS:<p>α-(difluoromethyl)-DL-Arginine (RMI 71897) is an enzyma-activated, irreversible inhibitor of arginine decarboxylase for E.</p>Fórmula:C7H14F2N4O2Pureza:99.77% - 99.78%Forma y color:SolidPeso molecular:224.21Iptacopan
CAS:<p>Iptacopan (LNP023) is an inhibitor with high affinity to factor B, with a KD value of 7.9 nM and an IC50 value of 10 nM. Cost-effective and quality-assured.</p>Fórmula:C25H30N2O4Pureza:99.07% - >99.99%Forma y color:SolidPeso molecular:422.52Selvigaltin
CAS:<p>Selvigaltin (GB1211) is a Gal-3 inhibitor with potential anticancer activity. Selvigaltin is used in the study of cirrhosis and cancer.</p>Fórmula:C19H16BrF3N4O4SPureza:99.49%Forma y color:SolidPeso molecular:533.32Nothofagin
CAS:Nothofagin: Antioxidant, anti-inflammatory, prevents clotting, inhibits leukocyte activity, may treat vascular inflammation.Fórmula:C21H24O10Pureza:98.51%Forma y color:SolidPeso molecular:436.41Cudetaxestat
CAS:<p>Cudetaxestat (BLD-0409) is a potent inhibitor of orally active autotaxin.</p>Fórmula:C21H15Cl2F2N3O2SPureza:99.9%Forma y color:SolidPeso molecular:482.33JAK-IN-3
CAS:<p>JAK-IN-3 is a potent JAK inhibitor that inhibits JAK3, JAK1, TYK2, and JAK2, and can be used for the study of immune system disorders.</p>Fórmula:C18H20N4O3Pureza:98.04% - 98.19%Forma y color:SolidPeso molecular:340.38CWHM-1552
CAS:<p>CWHM-1552 is an effective Plasmodium falciparum inhibitor. For the 3D7 and Dd2 strains, the IC50s are 51 nM and 53 nM.</p>Fórmula:C22H27F2N3OPureza:99.56%Forma y color:SolidPeso molecular:387.47Ranirestat
CAS:Ranirestat (AS-3201) is an AR inhibitor with neuroprotective properties that improves peripheral nerve dysfunction in rats with advanced diabetic polyneuropathyFórmula:C17H11BrFN3O4Pureza:96.10% - 99.44%Forma y color:SolidPeso molecular:420.19FIIN-1
CAS:<p>FIIN-1 (FGFR irreversible inhibitor-1) is an irreversible and selective FGFR inhibitor with Kd of 2.8, 6.9, 5.4, 120, 32 and 120 nM for FGFR1, FGFR2, FGFR3,</p>Fórmula:C32H39Cl2N7O4Pureza:98.75%Forma y color:SolidPeso molecular:656.6SB 216641 hydrochloride
CAS:<p>SB 216641 hydrochloride (SB-216641A) is a 5-HT1B/D receptor antagonist with anxiolytic properties.</p>Fórmula:C28H31ClN4O4Pureza:98.06% - 99.23%Forma y color:SolidPeso molecular:523.02ALDH2 modulator 1
CAS:<p>ALDH2 modulator 1 is a potent and orally active modulator of acetaldehyde dehydrogenase-2 (ALDH2), which reduces blood alcohol levels in mice.</p>Fórmula:C18H18ClFN2O3Pureza:99.68%Forma y color:SoildPeso molecular:364.8OPC-28326
CAS:<p>OPC-28326: an α2-adrenergic blocker; dilates blood vessels; inhibits α2A/B/C receptors with Ki 2040/285/55 nM.</p>Fórmula:C26H35N3O2Pureza:99.79%Forma y color:SolidPeso molecular:421.58CMP-Sialic acid sodium salt
CAS:CMP-Sialic acid, a sodium salt, inhibits UDP-GlcNAc 2-epimerase allosterically and serves as a sialyltransferase substrate.Fórmula:C20H30N4NaO16PPureza:98.32%Forma y color:SolidPeso molecular:636.43SAG 21k
CAS:<p>SAG 21k is an orally bioactive and potent Hedgehog signaling activator that crosses the blood-brain barrier for the study of cartilage regeneration.</p>Fórmula:C29H28ClF2N3O2SPureza:99.51%Forma y color:SolidPeso molecular:556.07Soraprazan
CAS:BS3 Crosslinker (Bis(sulfosuccinimidyl)suberate) is an ADC linker that can be used to synthesize antibody-coupled active molecules.Fórmula:C21H25N3O3Pureza:97.69% - 99.84%Forma y color:SolidPeso molecular:367.44Piflufolastat
CAS:<p>Piflufolastat (DCFPYL) is a PET imaging agent for prostate cancer PSMA.</p>Fórmula:C18H23FN4O8Pureza:98.98%Forma y color:SolidPeso molecular:442.40990CL
CAS:0990CL is an effective heterotrimer Gαi subunit specific inhibitor, which can interact with purified Go± in GDP-bound state, and can block α2AR mediated cAMPFórmula:C21H21N5Pureza:98.99%Forma y color:SolidPeso molecular:343.42ER 50891
CAS:<p>ER-50891 is a potent RARα antagonist, countering retinoic acid inhibition and aiding BMP2-induced osteoblast differentiation.</p>Fórmula:C29H24N2O2Pureza:>99.99%Forma y color:SolidPeso molecular:432.51Vidupiprant
CAS:<p>Vidupiprant (AMG 853) is an effective dual antagonist of CRTH2 and prostanoid D receptor with IC50s of 8 nM and 35 nM in human plasma.</p>Fórmula:C28H27Cl2FN2O6SPureza:98.88%Forma y color:SolidPeso molecular:609.49PHY34
CAS:<p>PHY34 inhibits autophagy at nanomolar potency, with anti-tumor effects on HGSOC in vivo.</p>Fórmula:C30H30O12Pureza:98.71%Forma y color:SolidPeso molecular:582.55A2B receptor antagonist 1
CAS:<p>A2B receptor antagonist 1 (EXAMPLE 9B) is a potent A2B adenosine receptor antagonist.</p>Fórmula:C21H24N6O2Pureza:99.53%Forma y color:SolidPeso molecular:392.45BI-3231
CAS:<p>BI-3231 is a hydroxysteroid 17ß-dehydrogenase 13 HSD17B13 inhibitor that inhibits hHSD17B13 .BI-3231 can be used to study cirrhosis.</p>Fórmula:C16H14F2N4O3SPureza:98.2%Forma y color:SolidPeso molecular:380.37γ-Glu-Tyr
CAS:<p>gamma-Glu-Tyr (gamma-Glutamyltyrosine) is a kokumi peptide against dipeptidyl peptidase-IV (DPP-IV) and is used in the study of diabetes mellitus.</p>Fórmula:C14H18N2O6Pureza:98.92%Forma y color:SolidPeso molecular:310.3OGT 2115
CAS:<p>OGT 2115 blocks heparanase (IC50=0.4µM), cleaving heparan sulfate; antiangiogenic (IC50=1µM).</p>Fórmula:C24H16BrFN2O4Pureza:97.17%Forma y color:SolidPeso molecular:495.3PDE9-IN-(S)-C33
CAS:<p>PDE9-IN-(S)-C33: potent PDE9 inhibitor with 11 nM IC50, for CNS diseases and diabetes study.</p>Fórmula:C18H20ClN5OPureza:98.75%Forma y color:SolidPeso molecular:357.84NEP-IN-1
CAS:<p>NEP-IN-1 is an inhibitor of neutral endopeptidase (NEP, IC50 = 2 nM) and can be used in studies about female sexual arousal disorders.</p>Fórmula:C21H30ClNO4Pureza:99.69%Forma y color:SolidPeso molecular:395.92Linvencorvir
CAS:<p>Linvencorvir is a hepatitis B virus (HBV) core protein variant modifier used to treat chronic HBV infection.</p>Fórmula:C29H35FN6O5SPureza:99.9% - 99.9%Forma y color:SolidPeso molecular:598.69MCT1-IN-3
CAS:<p>MCT1-IN-3 is a monocarboxylate transporter 1 (MCT1) inhibitor.</p>Fórmula:C22H19N3O4Pureza:99.35%Forma y color:SoildPeso molecular:389.4UC-764864
CAS:<p>UC-764864, a UBE2N inhibitor, impedes the enzymatic activity of UBE2N and exhibits cytotoxic effects through the disruption of UBE2N-dependent signaling in</p>Fórmula:C19H18N2OSPureza:99.3%Forma y color:SolidPeso molecular:322.42Xinidamine
CAS:<p>Xinidamine: antitumor agent for prostate hyperplasia, macular degeneration; inhibits PWR-1E cell growth, IC50=4μM.</p>Fórmula:C17H16N2O2Pureza:98.57%Forma y color:SolidPeso molecular:280.32Azelaprag
CAS:<p>Azelaprag (Example 263.0) is a candidate active molecule (EC50= 0.32 nM) for an apelin receptor agonist. treat nervous system diseases. High-Quality, Low-Cost!</p>Fórmula:C25H29N7O4SPureza:98.04% - >99.99%Forma y color:SolidPeso molecular:523.61
