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"
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CHIC35
CAS:<p>CHIC-35 is a selective deacetylase SIRT1 inhibitor.</p>Fórmula:C14H15ClN2OForma y color:SolidPeso molecular:262.73Fomesafen
CAS:<p>Fomesafen (PP-021) is a diphenyl ether herbicide and an inhibitor of efficient and selective protoporphyrinogen IX oxidase (PPO).</p>Fórmula:C15H10ClF3N2O6SPureza:99.91% - 99.93%Forma y color:White Crystalline Solid Fomesafen Is A White Crystalline Solid Used As An HerbicidePeso molecular:438.76GDC-0834 S-enantiomer
CAS:<p>GDC-0834, the S-enantiomer, is a potent and selective inhibitor of Bruton's tyrosine kinase (BTK).</p>Fórmula:C33H36N6O3SPureza:98%Forma y color:SolidPeso molecular:596.74EphB1-IN-10
CAS:<p>EphB1-IN-10 is a potent and selective covalent inhibitor of receptor tyrosine kinase EphB1.</p>Fórmula:C17H15ClN4O2Forma y color:SolidPeso molecular:342.78Austrocortirubin
CAS:<p>Austrocortirubin is a DNA damage inducer at the G0/G1, S, and G2 cell cycle stages distinct from other DNA damage agents.</p>Fórmula:C16H16O7Forma y color:SolidPeso molecular:320.29EL-102
CAS:<p>EL-102 is a HIF1α inhibitor with anticancer activity that inhibits microtubule protein polymerization and can be used to study prostate cancer.</p>Fórmula:C19H16N2O3S2Pureza:99.34%Forma y color:SolidPeso molecular:384.47PI3Kδ-IN-10
CAS:<p>PI3Kδ-IN-10 is a highly potent and orally active PI3Kδ inhibitor (IC50= 2 nM).</p>Fórmula:C19H16ClN9Forma y color:SolidPeso molecular:405.84Cymserine
CAS:<p>Cymserine: reversible inhibitor of butyrylcholinesterase, less effective on acetylcholinesterase.</p>Fórmula:C23H29N3O2Forma y color:SolidPeso molecular:379.5SCH 57790
CAS:<p>SCH 57790: selective muscarinic M2 blocker, boosts acetylcholine & cognition, may treat Alzheimer's.</p>Fórmula:C25H31N3O2SPureza:99% - 99.12%Forma y color:SolidPeso molecular:437.6Vandetanib Fumarate
CAS:<p>Oral tyrosine kinase inhibitor Vandetanib Fumarate targets RET, VEGFRs, EGFR in thyroid cancer.</p>Fórmula:C26H28BrFN4O6Pureza:98%Forma y color:SolidPeso molecular:591.43DRP1i27
CAS:<p>DRP1i27 inhibits human Drp1 at GTPase site, prevents mitochondrial fission, and shields cells from ischemia-reperfusion damage.</p>Fórmula:C20H26N6OForma y color:SolidPeso molecular:366.46BMS-200
CAS:BMS-200 is a potent PD-1/PD-L1 interaction inhibitor with IC50 of 80 nM.Fórmula:C27H27F2NO6Forma y color:SolidPeso molecular:499.5Ro 41-0960
CAS:<p>Ro 41-0960 is used as a reversible and orally-active COMT-inhibitor.</p>Fórmula:C13H8FNO5Pureza:98%Forma y color:SolidPeso molecular:277.2Tripolin A
CAS:<p>Tripolin A is a specific non-ATP competitive inhibitor of Aurora A kinase(Aurora A and Aurora B with IC50 values of 1.5 μM and 7 μM, respectively)</p>Fórmula:C15H11NO3Pureza:98%Forma y color:SolidPeso molecular:253.25Chlordene
CAS:<p>Chlordene, as a polychlorinated flame retardant, has bioaccumulation and biomagnification potentials.</p>Fórmula:C10H6Cl6Forma y color:SolidPeso molecular:338.87CLK1-IN-1
CAS:<p>CLK1-IN-1 is a potent and selective inhibitor of the Cdc2-like kinase 1 (CLK1; IC50: 2 nM).</p>Fórmula:C24H16FN5OForma y color:SolidPeso molecular:409.42MK6
CAS:<p>MK6 is a novel potent and highly selective MAO-B inhibitor</p>Fórmula:C17H13BrOForma y color:SolidPeso molecular:313.19(R)-(+)-Blebbistatin O-Benzoate
CAS:<p>(R)-(+)-Blebbistatin O-Benzoate, a non-muscle myosin II inhibitor, halts cell blebbing and migration; used for (S)-(-)-Blebblastatin control.</p>Fórmula:C25H20N2O3Forma y color:SolidPeso molecular:396.44XMD-12
CAS:<p>XMD-12, also known as DUN57447, Aurora inhibitor (compound 1) or Aurora-IN-1, is an Auroro inhibitor, which targets Aurora A/B/C. (5.6/18.4/24.6 nM).</p>Fórmula:C24H26N6O2Forma y color:SolidPeso molecular:430.5L-erythro-Chloramphenicol
CAS:<p>L-erythro-Chloramphenicol functions as a potent inhibitor of electron transport.</p>Fórmula:C11H12Cl2N2O5Pureza:98%Forma y color:SolidPeso molecular:323.13KBP-7018
CAS:<p>KBP-7018: potent tyrosine kinase inhibitor targeting c-KIT, RET, PDGFR with IC50s of 10, 7.6, 25nM.</p>Fórmula:C31H30N4O5Forma y color:SolidPeso molecular:538.59Kijimicin Na
CAS:<p>Kijimicin Na: sodium salt of a polyether antibiotic, fights HIV in acute/chronic infections.</p>Fórmula:C36H61NaO11Forma y color:SolidPeso molecular:692.86WAY 163909
CAS:WAY 163909 is an effective and selective agonist of the 5-HT(2C) receptor (Ki: 10.5±1.1 nM).Fórmula:C14H18N2Pureza:98%Forma y color:SolidPeso molecular:214.31N-Salicyloyltryptamine
CAS:<p>N-Salicyloyltryptamine (STP): a tryptamine with anticonvulsant, anti-inflammatory, analgesic effects; inhibits Na+, Ca2+, K+ channels (IC50 34.6 μM).</p>Fórmula:C17H16N2O2Forma y color:SolidPeso molecular:280.32Aldose reductase-IN-2
CAS:<p>Aldose reductase-IN-2 (5f) inhibits AR with antioxidant effects; potential anti-diabetic drug.</p>Fórmula:C25H28N4O5Forma y color:SolidPeso molecular:464.51THR-18
CAS:<p>THR-18, an 18-mer peptide from PAI-1, binds tPA away from its active site, separating clot-busting benefits from harmful effects.</p>Fórmula:C105H167F3N28O28S2Forma y color:SolidPeso molecular:2390.7742ML218 hydrochloride
CAS:<p>ML218 hydrochloride inhibits T-type Ca2+ channels Cav3.1-3.3; most effective on Cav3.2 and Cav3.3 (IC50s: 310 nM, 270 nM).</p>Fórmula:C19H27Cl3N2OPureza:98%Forma y color:SolidPeso molecular:405.79AND-302
CAS:<p>AND-302 is a potent agent of anticonvulsant. It also has in vitro neuroprotection.</p>Fórmula:C8H9F3N2O2SPureza:98%Forma y color:SolidPeso molecular:254.23ELN318463
CAS:<p>ELN 318463 selectively inhibits γ-secretase; EC50: 12 nM (PS1), 656 nM (PS2); 51x more selective for PS1; targets APP.</p>Fórmula:C19H20BrClN2O3SPureza:98%Forma y color:SolidPeso molecular:471.8COX-2-IN-21
CAS:<p>COX-2-IN-21 (Compound 5c) is an orally active, selective COX-2 inhibitor (IC50: 0.039 μM). COX-2-IN-21 has good anti-inflammatory potential.</p>Fórmula:C21H22N6O4Forma y color:SolidPeso molecular:422.44Avitriptan HCl
CAS:<p>Avitriptan (BMS-180048), a 5-HT1 receptor agonist, treats migraines and induces CYP1A1 in hepatic/intestinal cells.</p>Fórmula:C22H32Cl2N6O3SForma y color:SolidPeso molecular:531.497AUY954 HCl
CAS:<p>AUY-954 is a potent and selective S1P(1) modulator. AUY-954 prevents experimental autoimmune neuritis in rats.</p>Fórmula:C25H21ClF3NO2SForma y color:SolidPeso molecular:491.95JNJ-42314415
CAS:<p>JNJ-42314415 is a potent, specific, and centrally active inhibitor of PDE10A.</p>Fórmula:C19H23N5O2Pureza:98%Forma y color:SolidPeso molecular:353.42IC2418
CAS:<p>IC2418 is an MmpL3 inhibitor, being active against drug-resistant Mycobacterium tuberculosis.</p>Fórmula:C18H24N2OForma y color:SolidPeso molecular:284.4Jmv 390-1
CAS:<p>Jmv 390-1 is an inhibitor of metallopeptidase.</p>Fórmula:C23H35N3O6Pureza:98%Forma y color:SolidPeso molecular:449.54GS 389
CAS:<p>GS 389, a tetrahydroisoquinoline, relaxes blood vessels by inhibiting brain PDE and raising aorta cGMP.</p>Fórmula:C19H23NO3Pureza:98%Forma y color:SolidPeso molecular:313.39Ro 31-4639
CAS:<p>Ro 31-4639 is a phospholipase A2 inhibitor in vitro.</p>Fórmula:C21H46BrNOForma y color:SolidPeso molecular:408.5Thurfyl Salicylate
CAS:<p>Thurfyl Salicylate treats joint, muscle, and soft tissue pain, reducing redness.</p>Fórmula:C12H14O4Forma y color:SolidPeso molecular:222.24BBR 2160
CAS:<p>BBR 2160: a calcium-antagonist dihydropyridine derivative, reduces heart tissue contractility and shortens action potentials.</p>Fórmula:C21H25N3O7SForma y color:SolidPeso molecular:463.5Chymase-IN-1
CAS:<p>Chymase-IN-1 is a selective, orally active inhibitor of human mast cell chymase (IC50: 29 nM).</p>Fórmula:C20H15ClNO4PSPureza:99.17%Forma y color:SolidPeso molecular:431.83K-7174 dihydrochloride
CAS:<p>K-7174 dihydrochloride is a novel cell adhesion inhibitor; inhibits the expression of vascular cell adhesion molecule-1 (VCAM-1) induced by either IL-1β or TNF-</p>Fórmula:C33H50Cl2N2O6Pureza:99.15%Forma y color:SolidPeso molecular:641.67COX-2-IN-2
CAS:<p>COX-2-IN-2 selectively inhibits COX2 (IC50: 0.24 μM); COX-2-IN-1 offers anti-inflammatory and pain relief.</p>Fórmula:C17H12FN3O2SPureza:97.62%Forma y color:SolidPeso molecular:341.36Cgs 15696
CAS:<p>Cgs 15696 is an adenosine antagonist.</p>Fórmula:C13H7ClN4O2Forma y color:SolidPeso molecular:286.67ARN 14494
CAS:<p>ARN 14494, a potent SPT inhibitor (IC50=27.3 nM), reduces ceramide synthesis and neuroinflammation, and protects against β-amyloid toxicity.</p>Fórmula:C24H32N4O3Forma y color:SolidPeso molecular:424.54CP-654577
CAS:<p>CP-654577 inhibits p185(ErBB2) kinase, lowering activated mitogen-activated protein kinase in SKBR3 breast cancer cells.</p>Fórmula:C34H32N4O3Forma y color:SolidPeso molecular:544.64Rwj 29009
CAS:<p>Rwj 29009 is a potassium channel activator with prominent coronary and peripheral vasodilating actions.</p>Fórmula:C14H18N2O5SForma y color:SolidPeso molecular:326.37AL 4114
CAS:AL 4114 is used as an aldose reductase inhibitor.Fórmula:C17H12F2N2O4Pureza:98%Forma y color:SolidPeso molecular:346.29L 669083
CAS:<p>L 669083 is two classes of potent leukotriene biosynthesis inhibitors photoaffinity analogue.</p>Fórmula:C29H29IN4O5SPureza:98%Forma y color:SolidPeso molecular:672.54Carisbamate
CAS:<p>CarisbAMate (JNJ-10234094, RWJ 333369, YKP-509) is an antiepileptic drug candidate.</p>Fórmula:C9H10ClNO3Forma y color:SolidPeso molecular:215.63SGM8
CAS:<p>SGM8 is a covalent allosteric inhibitor of human cytomegalovirus DNA polymerase subunit Interactions.</p>Fórmula:C12H15NOS2Pureza:98%Forma y color:SolidPeso molecular:253.38
