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
- Apoptosis
- Ciclo celular / Checkpoint
- Cromatina / Epigenética
- Señalización citoesquelética
- Daño al ADN / Reparación del ADN
- Endocrinología / Hormonas
- Enzima
- GPCR / proteína G
- Inmunología e inflamación
- Virus de la gripe
- Señalización JAK / STAT
- Señalización MAPK
- Transportador de membrana / canal de iones
- Metabolismo
- Microbiología / Virología
- Neurociencia
- Otros inhibidores
- Reducción de oxidación
- Señalización PI3K / Akt / mTOR
- Proteasas / Proteasoma
- Células madre y Derivados
- Tirosina quinasa / adaptadores
- Ubiquitinación
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Productos de "Inhibidores"
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Esafosfan trisodium
CAS:Esafosfan trisodium (FDP trisodium) is a cytoprotective natural sugar phosphate for the potential treatment of sickle cell anemia and cardiovascular ischemia.Fórmula:C6H11Na3O12P2Pureza:98.05% - 99.87%Forma y color:SolidPeso molecular:406.06Apramycin (Nebramycin II)
CAS:Apramycin: a veterinary aminoglycoside antibiotic, blocks translocation, binds to eukaryotic/bacterial RNA despite differing key residues.Fórmula:C21H41N5O11Forma y color:SolidPeso molecular:539.58DN-F01
DN-F01 exhibits a potent calcium-dependent inhibitory effect on cardiac myofibrillar ATPase activity, with an IC50 of 11 ± 4 nmol/L.Fórmula:C22H16N2O2Forma y color:SolidPeso molecular:340.37TL13-12
CAS:TL13-12 is a selective degrader of ALK-PROTAC and inhibits ALK activity (IC50: 0.69 nM).Fórmula:C45H53ClN10O10SPureza:98%Forma y color:SolidPeso molecular:961.49UC-1V150
CAS:UC-1V150: TLR7 agonist, triggers immune response, anti-tumor, precursor for ISAC synthesis.Fórmula:C16H17N5O4Forma y color:SolidPeso molecular:343.34Methyl 3,4-dihydroxybenzoate
CAS:Methyl 3,4-dihydroxybenzoate (Protocatechuic acid methyl ester) is a major metabolite of antioxidant polyphenols found in green tea.Fórmula:C8H8O4Pureza:100% - 98.51%Forma y color:White To Off-White Crystalline PowderPeso molecular:168.15LYS006 hydrochloride (1799681-85-8 Free base)
LYS006 hydrochloride, a potent LTA4H inhibitor (IC50 2 nM), is used in research on inflammation and autoimmune diseases.Fórmula:C16H15Cl2FN6O3Pureza:99.67%Forma y color:SoildPeso molecular:429.23Bilobalide
CAS:Bilobalide ((-)-Bilobalide), a bioactive from Gingko Biloba, is active on hypoxia-induced alterations.Fórmula:C15H18O8Pureza:98.27% - 99.91%Forma y color:White SolidPeso molecular:326.33,3'-Diethylthiacyanine iodide
CAS:3,3'-Diethylthiacyanine iodide, a cyanine fluorescent dye, exhibits a significant affinity for bacterial cells [1].Fórmula:C19H19IN2S2Forma y color:SolidPeso molecular:466.4Upadacitinib
CAS:Upadacitinib (ABT-494), a selective JAK1 inhibitor, is researched for autoimmune diseases; IC50: 43 nM.Fórmula:C17H19F3N6OPureza:98.96% - 99.93%Forma y color:SolidPeso molecular:380.37Ref: TM-T7503
1mg47,00€2mg62,00€5mg89,00€10mg130,00€25mg220,00€50mg306,00€100mg434,00€200mg662,00€500mg1.169,00€1mL*10mM (DMSO)48,00€Isopropyl dodec-11-enylfluorophosphonate
CAS:Isopropyl dodec-11-enylfluorophosphonate (IDEFP) is an organophosphorus ester functioning as a central cannabinoid receptor (CB1) antagonist and exhibitsFórmula:C15H30FO2PPureza:98%Forma y color:SolidPeso molecular:292.37RA-9
CAS:RA-9 is a potent and selective proteasome-associated inhibitor of deubiquitinating enzymes (DUBs), with favorable toxicity profile and anticancer activity.Fórmula:C19H15N3O5Pureza:98.15%Forma y color:SolidPeso molecular:365.34BRD7-IN-1
CAS:BRD7-IN-1, a BI7273 derivative, forms PROTAC VZ185, targeting BRD7/9 with DC50s of 4.5/1.8 nM via VHL ligand linkage.Fórmula:C22H28Cl2N4O3Pureza:98.95%Forma y color:SolidPeso molecular:467.39A 410099.1 amide-PEG2-amine-Boc
CAS:A 410099.1 is an IAP ligand for PROTACs with an amide-PEG3 linker and terminal amine, suitable for creating protein conjugates.Fórmula:C38H60N6O8Forma y color:SolidPeso molecular:728.932Acid-C3-SSPy
CAS:Acid-C3-SSPy is a cleavable DBA-DM4 linker used in the synthesis of DBA-DM4 , a drug-linker conjugate for ADC.Fórmula:C9H11NO2S2Forma y color:SolidPeso molecular:229.31Adenostemmoic acid C
CAS:Adenostemmoic acid C is a natural product for research related to life sciences. The catalog number is TN5619 and the CAS number is 130217-18-4.Fórmula:C20H32O6Pureza:98%Forma y color:SolidPeso molecular:368.47Benzene, 1-bromo-3-fluoro-
CAS:Benzene, 1-bromo-3-fluoro- is a bioactive chemical.Fórmula:C6H4BrFForma y color:Clear Colourless Tolight Yellow LiquidPeso molecular:175.003-Hydroxy Midostaurin-D5
3-Hydroxy Midostaurin-D5, a deuterium-labeled metabolite of PKC412, inhibits FLT3 autophosphorylation (IC50: 132 nM in vitro, 9.8 μM in plasma).Fórmula:C35H25D5N4O5Pureza:98%Forma y color:SolidPeso molecular:591.67Benastatin A
CAS:Benastatin A, a polyketide from Streptomyces, inhibits GST (Ki=5 μM), fights MRSA (MIC=3.12 μg/ml), induces apoptosis and G1/G0 arrest in colon cancer cells.Fórmula:C30H28O7Forma y color:SolidPeso molecular:500.54Altromycin F
CAS:Altromycin F is a new pluramycin-like antibiotic.Fórmula:C47H59NO17Forma y color:SolidPeso molecular:909.97
