Metabolismo
Los inhibidores del metabolismo son compuestos que interfieren con las vías metabólicas, alterando la producción y utilización de energía dentro de las células. Estos inhibidores se utilizan para estudiar la regulación del metabolismo, el papel de las vías metabólicas en enfermedades como el cáncer y la diabetes, y para desarrollar nuevas estrategias terapéuticas. Los inhibidores del metabolismo pueden dirigirse a diversas enzimas y procesos involucrados en la glucólisis, la oxidación de ácidos grasos y otras funciones metabólicas. En CymitQuimica, ofrecemos una amplia gama de inhibidores del metabolismo de alta calidad para apoyar su investigación en bioquímica, trastornos metabólicos y desarrollo de fármacos.
Subcategorías de "Metabolismo"
- AhR(41 productos)
- Aminopeptidasa(67 productos)
- CETP(18 productos)
- Anhídrido carbónico(177 productos)
- Caseína quinasa(130 productos)
- DHFR(32 productos)
- Descarboxilasa(4 productos)
- Deshidrogenasa(267 productos)
- FAAH(63 productos)
- FXR(58 productos)
- Factor Xa(80 productos)
- Ácido graso sintasa(32 productos)
- Ferroptosis(215 productos)
- GR(3 productos)
- GSNOR(3 productos)
- Glucoquinasa(53 productos)
- HIF / HIF Prolilhidroxilasa(142 productos)
- HMG-CoA reductasa(32 productos)
- Hidroxilasa(30 productos)
- IDO(82 productos)
- LDL(8 productos)
- Lipasa(96 productos)
- Lípido(59 productos)
- Lipoxigenasa(124 productos)
- MAO(87 productos)
- MPO(2 productos)
- NAMPT(36 productos)
- P450(6 productos)
- PAI-1(25 productos)
- PDE(165 productos)
- PED(1 productos)
- PKM(15 productos)
- PPAR(164 productos)
- Fosfolipasa(82 productos)
- ROR(42 productos)
- Receptor de retinoides(29 productos)
- SGK(11 productos)
- Tiorredoxina(12 productos)
- Transferasa(30 productos)
- Transportador(42 productos)
- UGT(4 productos)
- Inhibidores de la xantina oxidasa (XO)(9 productos)
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Se han encontrado 8597 productos de "Metabolismo"
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Acetate kinase (ACK)
CAS:<p>ACK, found in bacteria/archaea, phosphorylates acetate with ATP and cations, yielding acetyl-CoA; used in biochemistry.</p>Forma y color:SolidNaphthol AS-GR phosphate disodium
CAS:<p>Naphthol AS-GR phosphate disodium: intense green fluorescent probe for phosphatases in histochemistry.</p>Fórmula:C22H16NNa2O5PForma y color:SolidPeso molecular:451.32Pristanic acid
CAS:<p>Pristanic acid, found in blood, aids in studying Alpha Methylacyl CoA Racemase Deficiency and Zellweger Syndrome.</p>Fórmula:C19H38O2Forma y color:SolidPeso molecular:298.5RMC-4630
CAS:<p>RMC-4630 (SHP2-IN-7) is an inhibitor of SHP2.</p>Fórmula:C20H27ClN6O2SPureza:99.07% - 99.65%Forma y color:SolidPeso molecular:450.99Burnettramic Acid A aglycone
CAS:<p>Burnettramic acid A aglycone, from A. burnettii, has anticancer properties; cytotoxic to NS-1 cells (IC50 = 8.4 μg/ml), not to fibroblasts (>100 μg/ml).</p>Fórmula:C35H61NO7Forma y color:SolidPeso molecular:607.873D-Threonine
CAS:<p>D-Threonine (H-D-Thr-OH) is one of the metabolites of Saccharomyces cerevisiae.</p>Fórmula:C4H9NO3Pureza:≥98%Forma y color:SolidPeso molecular:119.12Folitixorin calcium
CAS:<p>Folitixorin calcium is an antineoplastic enhancing agent.</p>Fórmula:C20H25CaN7O6Forma y color:SolidPeso molecular:499.541FZQ-21
<p>FZQ-21 (Compound 70P) is an inhibitor of the water-soluble epoxide hydrolase (sEH), with an IC50 value of 4 nM. The IC50 for inhibiting human sEH is 1.5 nM, which is comparable to that of EC5026 (1.7 nM). FZQ-21 is utilized in sepsis research.</p>Fórmula:C28H30N4O3Peso molecular:470.23179PTP1B-IN-27
<p>PTP1B-IN-27 (Compound 7i) is an inhibitor of protein tyrosine phosphatase 1-B (PTP-1B) with an IC50 of 8.2 µM. Additionally, it inhibits α-glucosidase with an IC50 of 120 µM and exhibits competitive inhibition characteristics (Ki=118 µM).</p>Fórmula:C26H24FN7O2SPeso molecular:517.16962MPO-IN-7
<p>MPO-IN-7 (compound MDC) is a myeloperoxidase inhibitor with IC50 values of 41 μM for α-glucosidase, 25 μM for dipeptidyl peptidase-4, and 4.5 μM for myeloperoxidase. MPO-IN-7 exhibits antioxidant and anti-inflammatory activities in vitro.</p>Fórmula:C16H14N2O6Peso molecular:330.08519SLC7A11-IN-3
<p>SLC7A11-IN-3 (Compound 42711_11) acts as an inhibitor of SLC7A11.</p>Forma y color:Odour SolidCasuarictin
CAS:<p>Casuarictin, a potent competitive inhibitor of α-glucosidase, exhibits an IC50 of 0.21 μg/mL and functions as a presenilin stabilization factor-like (PSFL)</p>Fórmula:C41H28O26Pureza:98%Forma y color:SolidPeso molecular:936.65Evinacumab
CAS:<p>Evinacumab (REGN1500) is a humanized monoclonal antibody targeting ANGPTL3. It is useful for studying cardiovascular diseases.</p>Pureza:100% (SEC-HPLC) - 99.43% (SEC-HPLC)Forma y color:LiquidPeso molecular:145.5 kDaα-Amylase/α-Glucosidase-IN-12
<p>α-Amylase/α-Glucosidase-IN-12 (compound 10k) is a dual inhibitor targeting α-glucosidase and α-amylase, with IC50 values of 34.52 nM and 24.62 nM, respectively. This inhibitor is designed based on [triazolo[4,3-b][1,2,4]triazine and holds potential for diabetes research.</p>Fórmula:C19H13F3N6OSPeso molecular:430.08236Transketolase-IN-5
<p>Transketolase-IN-5 (compound 6ba) is an inhibitor of transketolase. It exhibits herbicidal activity against Amaranthus retroflexus, Setaria viridis, and Digitaria sanguinalis.</p>Fórmula:C20H24ClN5OPeso molecular:385.16694Carbonic anhydrase inhibitor 18
<p>Carbonic anhydrase inhibitor18 (Compound 9) is an inhibitor of human carbonic anhydrase (hCA) isozymes, with Ki values of 604.8 nM for hCA I, 333.6 nM for hCA II, 1.9 nM for hCA IX, and 6.7 nM for hCA XII. Carbonic anhydrase inhibitor18 is applicable in cancer research.</p>Fórmula:C26H28N4O6S2Peso molecular:556.14503PROTAC NAMPT Degrader-1
<p>PROTACNAMPT Degrader-1 is an effective NAMPT-targeting PROTAC with a DC50 value of 217 nM. It exhibits antiproliferative activity, with an IC50 value of 0.12 μM against A2780 cells.</p>Fórmula:C57H69N13O8S2Peso molecular:1127.48335LYP-IN-1
CAS:<p>LYP-IN-1 is a potent, selective inhibitor of lymphoid-specific tyrosine phosphatase useful for studying autoimmune disorders and immune signaling.</p>Fórmula:C28H20ClNO6Pureza:92.43%Forma y color:SolidPeso molecular:501.92α-Glucosidase-IN-55
<p>α-Glucosidase-IN-55 (Compound 8g) is an orally active, competitive inhibitor of α-glucosidase with an IC50 value of 12.1 µM and a Ki value of 9.66 µM. It is useful for research related to Type 2 Diabetes Mellitus (T2DM), as it can enhance glycemic control and metabolic health.</p>Fórmula:C31H22ClN3SPeso molecular:503.1223Fexarene
CAS:<p>Fexarene is a non-steroidal FXR agonist.</p>Fórmula:C32H33NO3Pureza:98%Forma y color:SolidPeso molecular:479.62
