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(178 productos)
- Caseína quinasa(130 productos)
- DHFR(33 productos)
- Descarboxilasa(4 productos)
- Deshidrogenasa(271 productos)
- FAAH(64 productos)
- FXR(58 productos)
- Factor Xa(80 productos)
- Ácido graso sintasa(33 productos)
- Ferroptosis(215 productos)
- GR(3 productos)
- GSNOR(3 productos)
- Glucoquinasa(54 productos)
- HIF / HIF Prolilhidroxilasa(142 productos)
- HMG-CoA reductasa(33 productos)
- Hidroxilasa(30 productos)
- IDO(82 productos)
- LDL(8 productos)
- Lipasa(98 productos)
- Lípido(58 productos)
- Lipoxigenasa(124 productos)
- MAO(87 productos)
- MPO(2 productos)
- NAMPT(36 productos)
- P450(6 productos)
- PAI-1(25 productos)
- PDE(166 productos)
- PED(1 productos)
- PKM(15 productos)
- PPAR(165 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 8628 productos de "Metabolismo"
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S-NEPC
CAS:<p>Cytochrome P450 derivatives act as vasodilators. Blocking sEH, their inactivator, may treat hypertension. S-NEPC measures sEH activity.</p>Fórmula:C16H13NO6Forma y color:SolidPeso molecular:315.281N-Desmethyl Sildenafil
CAS:<p>N-Desmethyl Sildenafil (UK-103,320) (Desmethylsildenafil) is a prominent metabolite of Sildenafil, a potent inhibitor of phosphodiesterase type 5 (PDE5).</p>Fórmula:C21H28N6O4SPureza:99.35%Forma y color:SolidPeso molecular:460.55Pyrrophenone
CAS:<p>Pyrrophenone selectively and reversibly inhibits cPLA2 (IC50=4.2 nM), blocks AA, PGE2, and LTC4 production in cells, and is less effective on other PLA2s.</p>Fórmula:C49H37F2N3O5S2Forma y color:SolidPeso molecular:849.97DSPE-PEG2000-TAASGVRSMH
<p>DSPE-PEG2000-TAASGVRSMH is a PEG compound composed of DSPE and TAASGVRSMH. This compound exhibits strong affinity for the NG2 proteoglycan on PC membranes. DSPE-PEG2000-TAASGVRSMH can be utilized for drug delivery.</p>Forma y color:Odour Solid16α-hydroxy Dehydroepiandrosterone
CAS:16α-hydroxy Dehydroepiandrosterone (16α-OH-DHEA) is a neurosteroid found in the brain and a precursor in the biosynthesis of placental estriol.Fórmula:C19H28O3Forma y color:SolidPeso molecular:304.42(1R,2R)-MK-8189
CAS:<p>(1R,2R)-MK-8189 is an isomer of MK-8189, a potent and selective pyrimidine PDE10A inhibitor.</p>Fórmula:C19H22N6OSPureza:>99.99% - >99.99%Forma y color:SoildPeso molecular:382.481-O-Hexadecyl-2-O-docosahexaenoyl-sn-glycero-3-phosphorylcholine
CAS:<p>Endogenous metabolite in urine, 1-O-Hexadecyl-2-O-docosahexaenoyl-sn-glycero-3-phosphorylcholine, linked to obesity research.</p>Fórmula:C46H82NO7PForma y color:SolidPeso molecular:792.12Cetirizine 3-chloro impurity
CAS:<p>Cetirizine 3-chloro impurity is an impurity of Cetirizine 3-chloro [1] .</p>Fórmula:C21H25ClN2O3Forma y color:SolidPeso molecular:388.895-(3-Hydroxyphenyl)-5-phenylhydantoin
CAS:<p>5-(3-Hydroxyphenyl)-5-phenylhydantoin is a bioactive chemical.</p>Fórmula:C15H12N2O3Forma y color:SolidPeso molecular:268.27Girentuximab
CAS:Girentuximab (G250) is an anti-carbonic anhydrase IX (CAIX) monoclonal antibody with anti-cancer activity for the study of uroepithelial carcinoma PET (ZiPUP).Forma y color:LiquidPeso molecular:145.55 kDaMTHFD2-IN-1
<p>MTHFD2-IN-1 (compound 12) is a potent inhibitor of methylenetetrahydrofolate dehydrogenase (MTHFD2) [1].</p>Fórmula:C24H21NO6Forma y color:SolidPeso molecular:419.43DSPE-PEG1000-PP1
<p>DSPE-PEG1000-PP1 is a PEG compound composed of DSPE and the PP1 peptide. The PP1 peptide targets inflammatory atherosclerotic plaques. DSPE-PEG1000-PP1 is suitable for drug delivery applications.</p>Forma y color:Odour SolidChaetosemin J
CAS:<p>Chaetosemin J, antifungal, inhibits Botrytis, Alternaria, Magnaporthe, Gibberella; MIC 12.5-25 μM.</p>Fórmula:C14H14O4Forma y color:SolidPeso molecular:246.26(1S,2R)-Globalagliatin
CAS:<p>(1S,2R)-Globalagliatin is a highly potent glucokinase (GK) activator for the study of type 2 diabetes.</p>Fórmula:C28H37N3O3S3Pureza:99.09% - >99.99%Forma y color:SoildPeso molecular:559.81ACAT-IN-7
CAS:<p>ACAT-IN-7 inhibits ACAT enzyme; blocks NF-κB mediated transcription.</p>Fórmula:C32H49N3O5SForma y color:SolidPeso molecular:587.82(25R)-12α-Hydroxyspirost-4-en-3-one
CAS:<p>'(25R)-12α-Hydroxyspirost-4-en-3-one is a minor metabolite resulting from Nocardia globerula's metabolization of Hecogenin [1].'</p>Fórmula:C27H40O4Forma y color:SolidPeso molecular:428.6N-Decanoyl p-Nitroaniline
CAS:<p>DepNA, a nitroaniline fatty acid amide, measures FAAH activity by releasing yellow dye p-nitroaniline upon exposure, detectable via spectrophotometer.</p>Fórmula:C16H24N2O3Forma y color:SolidPeso molecular:292.379ACAT-IN-6
CAS:<p>ACAT-IN-6, from EP1236468A1 example 200, is a potent ACAT inhibitor that blocks NF-κB transcription.</p>Fórmula:C31H47N3O5SForma y color:SolidPeso molecular:573.79Transketolase-IN-5
Transketolase-IN-5 (compound 6ba) is an inhibitor of transketolase. It exhibits herbicidal activity against Amaranthus retroflexus, Setaria viridis, and Digitaria sanguinalis.Fórmula:C20H24ClN5OPeso molecular:385.16694FZQ-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:470.23179α-Glucosidase-IN-54
CAS:<p>α-Glucosidase-IN-54 (compound 2) functions as an α-glucosidase inhibitor, exhibiting an IC 50 value of 0.011 mM, and is derived from Syzygium jambos (L.). This compound is employed in diabetes research [1].</p>Fórmula:C24H36O3Forma y color:SolidPeso molecular:372.54D-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:119.12HLF1-11
CAS:<p>HLF1-11: human lactoferrin peptide, antimicrobial, inhibits MPO, steers monocytes to macrophages, boosts immunity.</p>Fórmula:C56H95N25O14SForma y color:SolidPeso molecular:1374.58Fmoc-Gly-Ser(psi(Me,Me)pro)-OH
CAS:<p>Fmoc-Gly-Ser(psi(Me,Me)pro)-OH is a dipeptide.</p>Fórmula:C23H24N2O6Forma y color:SolidPeso molecular:424.45Forrestiacids J
CAS:<p>Forrestiacid J is an inhibitor of ATP-citrate lyase (ACL), exhibiting an IC50 value of 2.6 μM [1].</p>Fórmula:C50H74O6Pureza:98%Forma y color:SolidPeso molecular:771.12Forrestiacids K
CAS:<p>Forrestiacid K, a terpenoid derived from Pseudotsuga forrestii, functions as an inhibitor of ATP-citrate lyase (ACL) [1].</p>Fórmula:C50H74O6Pureza:98%Forma y color:SolidPeso molecular:771.123-Oxocholic acid
CAS:<p>3-Oxocholic acid(3-Ketocholic acid) is the metabolite of bile acid and the main product of bile degradation by Clostridium perfringens in the intestine.3-</p>Fórmula:C24H38O5Pureza:99.63%Forma y color:SolidPeso molecular:406.56KT-362 free base
CAS:<p>KT-362 is a calcium channel blocker with antihypertensive properties that can be used in the study of cardiovascular disease.</p>Fórmula:C22H28N2O3SPureza:99.76%Forma y color:SoildPeso molecular:400.5311β-HSD1 inibitor 17
CAS:<p>11β-HSD1 inibitor 17 is an inhibitor of 11β-hydroxysteroid dehydrogenase (11β-HSD1).</p>Fórmula:C22H20F3N3O2SPureza:99.26% - 99.72%Forma y color:SoildPeso molecular:447.47Dimethylaminomicheliolide HCl
CAS:<p>Dimethylaminomicheliolide HCl has potential anti-inflammatory and anti-tumor activity and inhibits the proliferation of glioblastoma cells by targeting pyruvate</p>Fórmula:C17H28ClNO3Pureza:99.55%Forma y color:SoildPeso molecular:329.86HIF-1α-IN-2 hydrochloride
<p>HIF-1α-IN-2 hydrochloride is a potent HIF-1α inhibitor exhibiting anticancer activity, demonstrated by IC50 values of 28 nM in MDA-MB-231 cells and 15 nM in</p>Fórmula:C21H20ClN3OSPureza:98%Forma y color:SolidPeso molecular:397.92hCAIX/XII-IN-7
<p>Compound 3e (hCAIX/XII-IN-7) is a potent inhibitor of human carbonic anhydrase (hCA) isozymes IX and XII, displaying inhibitory constants (Kis) of 503.7 nM for</p>Fórmula:C17H14N6O3SPureza:98%Forma y color:SolidPeso molecular:382.4N-Fmoc-D-glutamine
CAS:N-Fmoc-D-glutamine is Fmoc-protected alpha-glutamine. Alpha-glutamine is an α-amino acid and the most abundant free amino acid in human blood.Fórmula:C20H20N2O5Pureza:99.14%Peso molecular:368.38Prolylglutamic acid
CAS:<p>Prolylglutamic acid (H-Pro-Glu-OH) is a proline-glutamic acid dipeptide and endogenous metabolite, targeting the LipY lipase of pathogenic mycobacteria.</p>Fórmula:C10H16N2O5Forma y color:SolidPeso molecular:244.24Cidofovir diphosphate tri(triethylamine)
<p>Cidofovir diphosphate triethylamine: active metabolite inhibiting HCMV, HSV-1, HSV-2 DNA polymerases with K i values 6.6, 0.86, 1.4 μM.</p>Fórmula:C26H61N6O12P3Forma y color:SolidPeso molecular:742.72ω-Hexatoxin-Hv1a
CAS:<p>ω-Hexatoxin-Hv1a, a neurotoxin extracted from the venom of the spider Hadronyche versuta, inhibits voltage-gated calcium channels [1] [2].</p>Fórmula:C162H247N49O61S6Pureza:98%Forma y color:SolidPeso molecular:4049.38(-)-Jasmonoyl-L-isoleucine
CAS:<p>(-)-Jasmonoyl-L-isoleucine ((-)-JA-L-Ile), an enantiomer of (+)-JA-L-Ile [1], is an inactive endogenous hormone.</p>Fórmula:C18H29NO4Forma y color:SolidPeso molecular:323.43Efmoroctocog alfa
CAS:<p>Efmoroctocog alfa, a recombinant human coagulation factor VIII-Fc fusion protein (rFVIIIFc), serves as a therapeutic agent for Hemophilia A research [1].</p>Forma y color:Solid(S)-O-Desmethyl Venlafaxine N-Oxide
CAS:<p>(S)-O-Desmethyl Venlafaxine N-Oxide is the N-oxide metabolite of Venlafaxine, an SNRI antidepressant.</p>Fórmula:C16H25NO3Forma y color:SolidPeso molecular:279.37(±)-Equol 4'-sulfate (sodium salt)
CAS:(±)-Equol 4’-sulfate is a gut-mediated phase II metabolite of the isoflavonoid phytoestrogen (±)-equol .[1] It has been used as a standard for theFórmula:C15H13NaO6SForma y color:SolidPeso molecular:344.32Rostratin C
CAS:<p>Rostratin C, a cytotoxic disulfide, exhibits in vitro cytotoxicity against human colon carcinoma (HCT-116), demonstrating an IC50 value of 0.76 μg/mL.</p>Fórmula:C20H24N2O8S2Forma y color:SolidPeso molecular:484.54FXR antagonist 2
CAS:<p>Compound A-26, a diarylamide FXR blocker, may aid hyperlipidemia and diabetes type 2 research.</p>Fórmula:C22H26Cl2N2O2Forma y color:SolidPeso molecular:421.36hCAI/II/IV-IN-28
CAS:<p>hCAI/II/IV-IN-28(WAY-638358) is a potent carbonic anhydrase inhibitor with potential anticonvulsant activity.</p>Fórmula:C14H15N3O3SPureza:96.48%Forma y color:SolidPeso molecular:305.35ROS-IN-2
<p>ROS-IN-2 (compound 85), a seco-lupane triterpenoid derivative, inhibits reactive oxygen species (ROS) production and shields mitochondria from oxidative damage</p>Fórmula:C42H62ClNO8SPureza:98%Forma y color:SolidPeso molecular:776.46PROTAC PTPN2 degrader-2 TFA
CAS:<p>PROTAC PTPN2 degrader-2 (example 187B) TFA is a potent degrader of Protein Tyrosine Phosphatase Non-receptor Type 2 (PTPN2), with potential applications in</p>Fórmula:C51H50ClF3N6O13S2Pureza:98%Forma y color:SolidPeso molecular:1111.55MAGL-IN-10
<p>MAGL-IN-10, a reversible monoacylglycerol lipase (MAGL) inhibitor, exhibits favorable ADME properties and low in vivo toxicity.</p>Pureza:98%Forma y color:Odour SolidPurine nucleoside phosphorylase
CAS:Purine nucleoside phosphorylase deficiency impairs T cells; it breaks bonds in DNA components, releasing bases and ribose phosphate.Forma y color:SolidXanthine oxidase-IN-11
<p>Xanthine Oxidase-IN-11, an analog of XO8, is an inhibitor of xanthine oxidase (XO) [1].</p>Fórmula:C10H8N2OSPureza:98%Forma y color:SolidPeso molecular:204.25α-Glucosidase-IN-84
<p>α-Glucosidase-IN-84 (Compound 7j) is a competitive inhibitor of α-glucosidase, exhibiting an IC50 of 50 μM and a Ki of 32 μM. It shows potential for application in metabolic disease research, particularly in studies related to type 2 diabetes.</p>Fórmula:C25H29N7O3SForma y color:SolidPeso molecular:507.608Vitamin D4
CAS:<p>Vitamin D4 is the active Vitamin D analog.</p>Fórmula:C28H46OPureza:98%Forma y color:SolidPeso molecular:398.66
