
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(2.764 productos)
- Apoptosis(6.204 productos)
- Ciclo celular / Checkpoint(4.811 productos)
- Cromatina / Epigenética(2.553 productos)
- Señalización citoesquelética(1.519 productos)
- Daño al ADN / Reparación del ADN(2.906 productos)
- Endocrinología / Hormonas(3.703 productos)
- Enzima(3.671 productos)
- GPCR / proteína G(8.966 productos)
- Inmunología e inflamación(3.748 productos)
- Virus de la gripe(297 productos)
- Señalización JAK / STAT(414 productos)
- Señalización MAPK(1.244 productos)
- Transportador de membrana / canal de iones(3.119 productos)
- Metabolismo(10.122 productos)
- Microbiología / Virología(7.569 productos)
- Neurociencia(10.314 productos)
- Otros inhibidores(35.802 productos)
- Reducción de oxidación(40 productos)
- Señalización PI3K / Akt / mTOR(1.411 productos)
- Proteasas / Proteasoma(1.681 productos)
- Células madre y Derivados(752 productos)
- Tirosina quinasa / adaptadores(1.947 productos)
- Ubiquitinación(1.716 productos)
Mostrar 16 subcategorías más
Se han encontrado 66604 productos de "Inhibidores"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Tetrazine-SS-Biotin
CAS:Tetrazine-SS-Biotin, a cleavable ADC linker, finds utility in ADC (antibody-drug conjugate) synthesis [1].Fórmula:C24H32N8O3S3Pureza:98%Forma y color:SolidPeso molecular:576.76Eltanexor
CAS:Eltanexor, an oral XPO1 inhibitor, induces apoptosis in leukemia cells; EC50=60.9 nM.Fórmula:C17H10F6N6OPureza:99.68% - ≥98%Forma y color:SolidPeso molecular:428.29Ref: TM-T11766L
1mg63,00€5mg213,00€10mg250,00€25mg404,00€50mg595,00€100mg863,00€200mg1.161,00€1mL*10mM (DMSO)200,00€Hexapeptide-11
CAS:Hexapeptide-11 is a novel proteostasis network modulator in human diploid fibroblasts.Fórmula:C36H48N6O7Pureza:98%Forma y color:SolidPeso molecular:676.8DBCO-PEG9-amine
CAS:DBCO-PEG9-amine is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules.Fórmula:C39H57N3O11Pureza:98%Forma y color:SolidPeso molecular:743.88Cenupatide acetate
Cenupatide acetate is an urokinase plasminogen activator receptor (uPAR) inhibitor for treating disorders associated altered cell migration, such as cancer.
Fórmula:C30H51N11O7Pureza:97.62%Forma y color:SolidPeso molecular:677.8Ref: TM-TP2338L
1mg74,00€2mg96,00€5mg135,00€10mg215,00€25mg396,00€50mg588,00€100mg835,00€500mg1.700,00€Creoside III
CAS:Creoside III is a natural product for research related to life sciences. The catalog number is TN5837 and the CAS number is 1038602-12-8.Fórmula:C18H24O9Pureza:98%Forma y color:SolidPeso molecular:384.38Cyclo(Phe-Pro) acetate(14705-60-3 free base)
Cyclo(Phe-Pro) acetate(14705-60-3 free base), known as a secondary metabolite of some bacteria and fungi, is also produced by Vibrio vulnificus.Fórmula:C16H20N2O4Pureza:98%Forma y color:SolidPeso molecular:304.35COX-2-IN-35
COX-2-IN-35 (compound 7) is a selective inhibitor of COX-2, demonstrating anti-inflammatory activity, with an inhibitory concentration (IC 50) of 4.37 nM [1].Fórmula:C22H19NO2S2Pureza:98%Forma y color:SolidPeso molecular:393.52WBC100
CAS:WBC100 (14-D-Valine-TPL) is a potent, selective, and orally active c-Myc glue degrader that targets the ubiquitin E3 ligase CHIP-mediated 26S proteasome pathwayFórmula:C25H33NO7Pureza:98%Forma y color:SolidPeso molecular:459.53Sulfo-Cy3 ethylenediamine
Sulfo-Cyanine 3 is an alternative dye primarily used for labeling peptides and oligos in replacing Cy3 that was originally developed by GE Healthcare.Fórmula:C33H44ClKN4O7S2Pureza:98%Forma y color:SolidPeso molecular:747.41t-Boc-Aminooxy-PEG8-alcohol
CAS:t-Boc-Aminooxy-PEG8-alcohol is a PEGylated PROTAC linker suitable for synthesizing PROTACs[1].Fórmula:C21H43NO11Pureza:98%Forma y color:SolidPeso molecular:485.57GLUT inhibitor-1
CAS:GLUT inhibitor-1: oral, targets GLUT1/3 (IC50: 242/179 nM), for cancer/autoimmune research.Fórmula:C32H35N7O2Pureza:98.12%Forma y color:SolidPeso molecular:549.67PEN(mouse) acetate
PEN(mouse) acetate (proSAAS(221-242) Acetate) (1236955-25-1 Free base) is a polypeptide derivative.Fórmula:C104H173N27O36Pureza:99.64%Forma y color:SoildPeso molecular:2377.65IVHD-valtrate
CAS:VHD-valtrate has anticancer effects against human ovarian cancer cells in vitro and in vivo, it is a potential therapeutic agent for ovarian cancer, providing aFórmula:C27H40O11Pureza:98%Forma y color:SolidPeso molecular:540.6α-Conotoxin GI acetate
α-Conotoxin GI acetate is a competitive antagonist of the muscle-type nicotinic acetylcholine receptors (nAChR).Fórmula:C57H84N20O20S4Pureza:96.49%Forma y color:SolidPeso molecular:1497.66Ref: TM-T35325L
1mg177,00€5mg358,00€10mg530,00€25mg850,00€50mg1.153,00€100mg1.558,00€1mL*10mM (DMSO)863,00€22-Hydroxycyclolaudenol
CAS:22-Hydroxycyclolaudenol is a natural product for research related to life sciences. The catalog number is TN6181 and the CAS number is 2077090-18-5.Fórmula:C31H52O2Pureza:98%Forma y color:SolidPeso molecular:456.755Bis-Mal-PEG6
Bis-Mal-PEG6 is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules.Fórmula:C28H42N4O12Pureza:98%Forma y color:SolidPeso molecular:626.651-Hydroxy-9-medroxycanthin-6-one
CAS:1-Hydroxy-9-medroxycanthin-6-one is a natural product for research related to life sciences. The catalog number is TN2537 and the CAS number is 622408-85-9.Fórmula:C15H10N2O3Pureza:98%Forma y color:SolidPeso molecular:266.25tri-GalNAc-COOH (acetylation)
Tri-GalNAc-COOH acetylation represents the acetylated derivative of tri-galactosamine (tri-GalNAc-COOH), utilized in the synthesis of lysosome targeting
Pureza:98%Forma y color:Odour SolidOxmetidine FA
Oxmetidine FA is an orally available specific histamine H2 receptor antagonist with antiulcerogenic properties.Fórmula:C20H23N5O5SPureza:97.34%Forma y color:SoildPeso molecular:445.49

