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(2.519 productos)
- Apoptosis(5.786 productos)
- Ciclo celular / Checkpoint(4.444 productos)
- Cromatina / Epigenética(2.235 productos)
- Señalización citoesquelética(1.382 productos)
- Daño al ADN / Reparación del ADN(2.823 productos)
- Endocrinología / Hormonas(3.499 productos)
- Enzima(3.639 productos)
- GPCR / proteína G(8.314 productos)
- Inmunología e inflamación(3.516 productos)
- Virus de la gripe(296 productos)
- Señalización JAK / STAT(404 productos)
- Señalización MAPK(1.199 productos)
- Transportador de membrana / canal de iones(2.786 productos)
- Metabolismo(9.417 productos)
- Microbiología / Virología(6.967 productos)
- Neurociencia(9.920 productos)
- Otros inhibidores(37.931 productos)
- Reducción de oxidación(41 productos)
- Señalización PI3K / Akt / mTOR(1.399 productos)
- Proteasas / Proteasoma(1.596 productos)
- Células madre y Derivados(832 productos)
- Tirosina quinasa / adaptadores(2.015 productos)
- Ubiquitinación(1.646 productos)
Mostrar 16 subcategorías más
Se han encontrado 66627 productos de "Inhibidores"
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Talipexole
CAS:<p>Talipexole (B-HT920) is an agonist of dopamine, and is an antiparkinsonian agent.</p>Fórmula:C10H15N3SPureza:98%Forma y color:SolidPeso molecular:209.31SLM6031434 HCl
CAS:<p>SLM6031434 HCl (SLM-6031434 HCl) is a SphK2 inhibitor that reduces LPS-induced TNF伪 and IL-1尾 production.</p>Fórmula:C22H31ClF3N5O2Pureza:98%Forma y color:SolidPeso molecular:489.96SPRC
CAS:<p>"SPRC, a synthetic antioxidant, boosts H2S production, activates STAT3, and guards against doxorubicin heart damage."</p>Fórmula:C6H9NO2SPureza:98%Forma y color:SolidPeso molecular:159.21VU0359516
CAS:<p>VU0359516 is a mGluR4 positive allosteric modulators.</p>Fórmula:C16H13N3O3Forma y color:SolidPeso molecular:295.29A2AAR/HDAC-IN-2
CAS:<p>A2AAR/HDAC-IN-2: potent dual A2AAR/HDAC inhib., Ki 10.3 nM, IC50 18.5 nM, anti-tumor potential.</p>Fórmula:C23H26N6O4Forma y color:SolidPeso molecular:450.49AMG2504
CAS:<p>AMG2504 is a TRPA1 inhibitor.</p>Fórmula:C15H10Cl4N2O3SForma y color:SolidPeso molecular:440.13SQ-24,798
CAS:<p>SQ-24,798 is an inhibitor of the thrombin-activatable fibrinolysis and carboxypeptidase N (CPN).</p>Fórmula:C7H15N3O2SPureza:98%Forma y color:SolidPeso molecular:205.28ORY-1001 free base
CAS:<p>ORY-1001: potent KDM1A inhibitor (IC50 <20nM), selective, affects THP-1 cell gene regulation and apoptosis, hinders MV(4;11) cell growth (EC50 <1nM).</p>Fórmula:C15H22N2Pureza:98%Forma y color:SolidPeso molecular:230.35Desaspidin
CAS:<p>Desaspidin, an anthelmintic found in Coastal woodfern, inhibits chloroplast phosphorylation since the 1950s.</p>Fórmula:C24H30O8Forma y color:SolidPeso molecular:446.49Mivobulin
CAS:<p>Mivobulin is an inhibitor of tubulin .</p>Fórmula:C17H19N5O2Pureza:98%Forma y color:SolidPeso molecular:325.37Pentisomide
CAS:<p>Pentisomide: class-I antiarrhythmic, affects depolarization & repolarization, inhibits ischemia-reperfusion arrhythmias, in phase II trials.</p>Fórmula:C19H33N3OPureza:98%Forma y color:SolidPeso molecular:319.48PD 122860
CAS:<p>PD 122860 is a dihydropyridine enhancing heart contractility, altering ECG, and relaxing aortic rings.</p>Fórmula:C23H20F3N3O4SPureza:98%Forma y color:SolidPeso molecular:491.48iNOS inhibitor-10
CAS:<p>iNOS Inhibitor-10, with an IC50 of 65 nM, exhibits antiproliferative effects on triple-negative breast cancer cells [1].</p>Fórmula:C22H23N3O2SPureza:98%Forma y color:SolidPeso molecular:393.5NK-1145
CAS:<p>Nk-1145 is a parasympathetic drug of the autonomic nervous system, which can cause behavioral stimulation and excitement.</p>Fórmula:C14H19NOForma y color:SolidPeso molecular:217.31VUF16839
CAS:<p>VUF16839 is a high-affinity non-imidazole histamine H3 receptor agonist.</p>Fórmula:C10H17N5Forma y color:SolidPeso molecular:207.28AMP-PCP
CAS:<p>AMP-PCP is an ATP analog and can bind to the Hsp90 N-terminal domain (Kd: 3.8 μM). AMP-PCP binding favors the formation of the active homodimer of Hsp90.</p>Fórmula:C11H18N5O12P3Pureza:98%Forma y color:SolidPeso molecular:505.21Salicylglutamic acid
CAS:<p>Salicylglutamic acid, as a conjugate of salicylic acid and glutamic acid, can be used to prolong the blood concentration of salicylic acid.</p>Fórmula:C12H13NO6Forma y color:SolidPeso molecular:267.23K-Ras G12C-IN-3
CAS:<p>K-Ras G12C-IN-3: novel, irreversible inhibitor of K-Ras G12C mutant protein for cancer treatment.</p>Fórmula:C21H19Cl3N2O3Forma y color:SolidPeso molecular:453.75TRPC6-IN-2
CAS:<p>TRPC6-IN-2 is a TRPC protein inhibitor, specifically inhibiting TRPC6 protein.</p>Fórmula:C19H17Cl2FN6Forma y color:SolidPeso molecular:419.28YM 114
CAS:<p>YM 114 is an anatagonist of 5-HT(3) receptor.</p>Fórmula:C16H18ClN3OPureza:98%Forma y color:SolidPeso molecular:303.79CP-100356 hydrochloride
CAS:<p>CP-100356 hydrochloride is an MDR1 (P-gp) and BCRP inhibitor, a nucleotide-derived substrate analog that induces stomatal opening in the dark.</p>Fórmula:C31H37ClN4O6Pureza:99.19%Forma y color:SolidPeso molecular:597.1DF-1012
CAS:<p>DF-1012 is a 5-HT3 receptor antagonist and is also an orally-available antitussive, antiasthmatic and anti-inflammatory drug.</p>Fórmula:C16H20N4OPureza:98%Forma y color:SolidPeso molecular:284.36KP-23172
CAS:<p>KP-23172 is a inhibitor of PI3-K/Akt pathway.</p>Fórmula:C10H4N6OPureza:98%Forma y color:SolidPeso molecular:224.18L 648051
CAS:<p>L 648051 is a leukotriene D4 receptor antagonist.</p>Fórmula:C24H28O8SPureza:98%Forma y color:SolidPeso molecular:476.54ICA
CAS:<p>ICA (N-[4-(2-Pyridinyl)-2-thiazolyl]-2-pyridinamine) is a SK channel inhibitor and exhibits antileishmanial activity (IC50: 2.1 µM).</p>Fórmula:C13H10N4SPureza:99.68%Forma y color:SolidPeso molecular:254.31SK&F-95601
CAS:<p>F-95601 is a proton pump inhibitor.</p>Fórmula:C18H19ClN4O3SForma y color:SolidPeso molecular:406.89XL-188
CAS:<p>XL-188: Potent, selective USP7 inhibitor, IC50 = 193 nM (domain), 90 nM (full). Boosts p53, p21; degrades HDM2. Unique among DUB inhibitors.</p>Fórmula:C32H42N6O4Forma y color:SolidPeso molecular:574.71HN 11500
CAS:<p>HN 11500 is an antithrombotic agent and thromboxane A2 receptor antagonist.</p>Fórmula:C14H15NO5S2Forma y color:SolidPeso molecular:341.39HDAC6-IN-5
CAS:<p>HDAC6-IN-5 (11b), potent HDAC6 blocker, crosses BBB, IC50: 0.025μM, hinders Aβ1-42/AChE aggregation, boosts neurites, low toxicity.</p>Fórmula:C20H14BrN3O2Forma y color:SolidPeso molecular:408.25Clovoxamine
CAS:<p>Clovoxamine fumarate (DU 23811 fumarate) is a 5-HT reuptake, serotonin and norepinephrine inhibitor with antidepressant and anticonvulsant activity.</p>Fórmula:C14H21ClN2O2Pureza:99.44% - 99.75%Forma y color:SolidPeso molecular:284.78UCB 35625
CAS:<p>chemokine CCR1 and CCR3 receptor antagonist</p>Fórmula:C29H37Cl2IN2O2Pureza:98%Forma y color:SolidPeso molecular:643.43CID-2858522
CAS:<p>CID-2858522 is an effective and specific antigen receptor-mediated NF-κB activation inhibitor (IC50: 70 nM).</p>Fórmula:C28H39N3O3Pureza:96.12%Forma y color:SolidPeso molecular:465.63Ono-3307 mesylate
CAS:<p>no-3307 mesylate is a protease inhibitor that inhibits a variety of proteases and may be used to study pancreatitis.</p>Fórmula:C15H18N4O7S2Pureza:97.60% - 98.16%Forma y color:SolidPeso molecular:430.46Sulfo-ara-F-NMN
CAS:<p>Sulfo-ara-F-NMN: cell-permeable, NMN analogue, activates SARM1, inhibits CD38 (IC50 ~10μM), induces cADPR, NAD loss, non-apoptotic death.</p>Fórmula:C11H14FN2O6PSPureza:98%Forma y color:SolidPeso molecular:352.28Alvameline Tartrate
CAS:<p>Alvameline Tartrate, a muscarinic M1 receptor agonist and M2/M3 receptor antagonist, is used potentially for treatment of urinary incontinence.</p>Fórmula:C13H21N5O6Forma y color:SolidPeso molecular:343.34FTR-1335
CAS:<p>FTR1335: CaNMT inhibitor with 0.49 nM IC50. Targets fungi, effective on fluconazole-resistant Candida. Blocks protein myristoylation, crucial for selectivity.</p>Fórmula:C31H34N4O2SForma y color:SolidPeso molecular:526.69Edunol
CAS:<p>Edunol is a pterocarpan isolated from Harpalyce brasiliana. It has shown antimyotoxic, antiproteolytic and PLA2 inhibitor properties.</p>Fórmula:C21H20O5Forma y color:SolidPeso molecular:352.38MAT2A-IN-1
CAS:<p>MAT2A-IN-1 suppresses MAT2A, key for MTAP-deficient cancer cell growth; studied for gastric, colon, liver, pancreatic cancers.</p>Fórmula:C29H28F2N6O4Forma y color:SolidPeso molecular:562.57α-Synuclein inhibitor 5
CAS:<p>α-Synuclein inhibitor 5 is a potent inhibitor of α-Synuclein (α-Syn) aggregation across the blood-brain barrier (IC50: 1.22 μM), with 94.3% inhibition at 30 μM.</p>Fórmula:C20H18N2O6SForma y color:SolidPeso molecular:414.43EP009
CAS:<p>EP009, a novel, selective, and orally active inhibitor of JAK3, induces therapeutic response in T-cell malignancies.</p>Fórmula:C14H24O2Forma y color:SolidPeso molecular:224.34APX2014
CAS:<p>APX2014 is a novel potent and specific Ref-1 inhibitor, blocking in vitro cell proliferation and activating apoptosis via PARP cleavage.</p>Fórmula:C18H19NO5Forma y color:SolidPeso molecular:329.35WEN05-03
CAS:<p>WEN05-03 is a novel inhibitor of type III secretion system ATPase EscN from enteropathogenic Eecherichia coli.</p>Fórmula:C17H14N4O4SForma y color:SolidPeso molecular:370.38J1037
CAS:<p>J1037 is a novel Histone Deacetylase 8 (HDAC8) inhibitor .</p>Fórmula:C10H10N2O3SPureza:98%Forma y color:SolidPeso molecular:238.26Isobutyl decanoate
CAS:<p>A decanoate ester obtained by the formal condensation of the carboxy group of decanoc acid (capric acid) with the alcoholic hydroxy group of isobutanol.</p>Fórmula:C14H28O2Pureza:98.99%Forma y color:SolidPeso molecular:228.37LY288513
CAS:<p>Selective CCK2 receptor antagonist</p>Fórmula:C22H18BrN3O2Pureza:98%Forma y color:SolidPeso molecular:436.3GLPG-3221
CAS:<p>GLPG-3221, a potent oral CFTR corrector for cystic fibrosis treatment, has an EC50 of 105 nM.</p>Fórmula:C30H37F3N2O6Pureza:98%Forma y color:SolidPeso molecular:578.62Methylisothiazolinone
CAS:<p>Methylisothiazolinone (MI) is a powerful synthetic biocide and preservative within the group of isothiazolinones.</p>Fórmula:C4H5NOSPureza:99.78%Forma y color:Colorless Prisms LiquidPeso molecular:115.15Benzofurodil
CAS:<p>Benzofurodil is cardiotonic used for the chronic treatment of congestive heart failure.</p>Fórmula:C19H18O7Pureza:98%Forma y color:SolidPeso molecular:358.34Revenast
CAS:<p>Revenast is a potent new anti-allergic compound. The substance is rapidly and extensively metabolized in the body, resulting in an anti-allergic effect.</p>Fórmula:C27H29N5OForma y color:SolidPeso molecular:439.55LY367385
CAS:<p>LY367385 is a highly effective and selective mGluR1a antagonist.</p>Fórmula:C10H11NO4Pureza:98%Forma y color:SolidPeso molecular:209.2
