Metabolismo
Os inibidores do metabolismo são compostos que interferem nas vias metabólicas, alterando a produção e utilização de energia dentro das células. Esses inibidores são usados para estudar a regulação do metabolismo, o papel das vias metabólicas em doenças como o câncer e o diabetes, e para desenvolver novas estratégias terapêuticas. Os inibidores do metabolismo podem direcionar várias enzimas e processos envolvidos na glicólise, na oxidação de ácidos graxos e em outras funções metabólicas. Na CymitQuimica, oferecemos uma ampla gama de inibidores do metabolismo de alta qualidade para apoiar sua pesquisa em bioquímica, distúrbios metabólicos e desenvolvimento de medicamentos.
Subcategorias de "Metabolismo"
- AhR(41 produtos)
- Aminopeptidase(67 produtos)
- CETP(18 produtos)
- Anidrase carbónica(177 produtos)
- Caseína quinase(130 produtos)
- DHFR(32 produtos)
- Descarboxilase(4 produtos)
- Desidrogenase(267 produtos)
- FAAH(63 produtos)
- FXR(58 produtos)
- Factor Xa(80 produtos)
- Sintase de Ácidos graxos(32 produtos)
- Ferroptose(215 produtos)
- GR(3 produtos)
- GSNOR(3 produtos)
- Glucoquinase(53 produtos)
- HIF/HIF Prolil-Hidroxilase(142 produtos)
- HMG-CoA Reductase(32 produtos)
- Hidroxilase(30 produtos)
- IDO(82 produtos)
- LDL(8 produtos)
- Lipase(96 produtos)
- Lipídio(59 produtos)
- Lipoxigenase(124 produtos)
- MAO(87 produtos)
- MPO(2 produtos)
- NAMPT(36 produtos)
- P450(6 produtos)
- PAI-1(25 produtos)
- PDE(165 produtos)
- PED(1 produtos)
- PKM(15 produtos)
- PPAR(164 produtos)
- Fosfolipase(82 produtos)
- ROR(42 produtos)
- Receptor de Retinóide(29 produtos)
- SGK(11 produtos)
- Tiorredoxina(12 produtos)
- Transferase(30 produtos)
- Tansportador(42 produtos)
- UGT(4 produtos)
- Inibidores de Xantina Oxidase (XO)(9 produtos)
Exibir 34 mais subcategorias
Foram encontrados 8597 produtos de "Metabolismo"
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Impurity of Doxercalciferol
CAS:<p>Doxercalciferol impurity, synthetic ergocalciferol analog, treats secondary hyperparathyroidism, inhibits parathyroid.</p>Fórmula:C28H44O2Pureza:98%Cor e Forma:SolidPeso molecular:412.65α-1,3-N-Acetylgalactosaminyltransferase (Pm1138)
CAS:<p>Alpha-1,3-N-Acetylgalactosaminyltransferase (Pm1138) (EC 2.4.1.40(Pm1138)), also known as the ABO system transferase, exhibits glycosyl transferase activity [1</p>Cor e Forma:SolidA 58365 A
CAS:<p>A 58365 A, an ACE inhibitor from Streptomyces chromofuscus, treats heart failure and hypertension.</p>Fórmula:C12H13NO6Cor e Forma:SolidPeso molecular:267.23Lagunamycin
CAS:<p>Lagunamycin is used as a novel 5-lipoxygenase inhibitor.</p>Fórmula:C19H21N3O4Cor e Forma:SolidPeso molecular:355.39Eurestobart
CAS:<p>Eurestobart is a humanized IgG1κ (IgG1 kappa) monoclonal antibody that specifically targets the enzyme ectonucleoside triphosphate diphosphohydrolase (ENTPDase</p>Pureza:98%Cor e Forma:LiquidPiliformic Acid
CAS:<p>Piliformic acid: a fungal metabolite, cytotoxic to BC-1 cells (IC50=5μg/ml), fights L. braziliensis (IC50=78.5μM) & C. gloeosporioides (MIC=292μM).</p>Fórmula:C11H18O4Cor e Forma:SolidPeso molecular:214.26tetranor-12(R)-HETE
CAS:<p>Corneal metabolism of 12(R)-HETE yields 8(R)-HHxTrE via β-oxidation, losing four carbons from C-1.</p>Fórmula:C16H26O3Cor e Forma:SolidPeso molecular:266.381MU1742
<p>MU1742 is a probe for CK1δ and CK1ε protein kinases [1] .</p>Fórmula:C22H22F2N6Cor e Forma:SolidPeso molecular:408.45VHL-IN-1
<p>VHL-IN-1 (compound 30), a ubiquitin E3 ligase von Hippel-Lindau (VHL) inhibitor with a dissociation constant (Kd) of 37 nM, potently stabilizes HIF-1α and</p>Fórmula:C28H37FN4O4SPureza:98%Cor e Forma:SolidPeso molecular:544.68α-Glucosidase-IN-36
<p>α-Glucosidase-IN-36 (compound 5g) is a potent inhibitor of α-glucosidase, exhibiting an IC50 value of 6.69 ± 0.18 μM and inhibition constants Ki and Kis of 1.65</p>Fórmula:C26H24BrN5O3SPureza:98%Cor e Forma:SolidPeso molecular:566.47Kyotorphin
CAS:<p>Kyotorphin is a Morphine-like dipeptide.</p>Fórmula:C15H23N5O4Cor e Forma:SolidPeso molecular:337.38Etodolac Acyl Glucuronide
CAS:<p>Etodolac acyl glucuronide is an NSAID metabolite formed by UGT1A9, UGT1A10, and UGT2B7 glucuronidation.</p>Fórmula:C23H29NO9Cor e Forma:SolidPeso molecular:463.483Biotin sodium
CAS:<p>Biotin (Vitamin B7) sodium aids in metabolism, cell growth, fatty acid synthesis, and gluconeogenesis.</p>Fórmula:C10H15N2NaO3SCor e Forma:SolidPeso molecular:266.29hCAI/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%Cor e Forma: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%Cor e Forma:SolidPeso molecular:776.46LDHA-IN-3
CAS:<p>LDHA-IN-3 is a potent selenobenzene-based LDHA inhibitor with a 145.2 nM IC50, useful in cancer research.</p>Fórmula:C13H9F3SePureza:99.71%Cor e Forma:SolidPeso molecular:301.17HIF-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%Cor e Forma: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%Cor e Forma:SolidPeso molecular:382.4Metrizamide
CAS:<p>Metrizamide is a nonionic radiopaque contrast agent.</p>Fórmula:C18H22I3N3O8Cor e Forma:SolidPeso molecular:789.1Sulotroban potassium
<p>Sulotroban potassium is a small molecule thromboxane A2 receptor (TXA2R) antagonist that can be used to study myocardial infarction and thrombosis.</p>Fórmula:C16H16KNO5SPureza:98.02%Cor e Forma:SoildPeso molecular:373.46Coenzyme A
CAS:<p>Coenzyme A is an obligatory cofactor in all living cells synthesized from pantothenate (Vitamin B5), adenosine triphosphate (ATP), and cysteine.</p>Fórmula:C21H36N7O16P3SPureza:93.84%Cor e Forma:SolidPeso molecular:767.53Forrestiacids 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%Cor e Forma:SolidPeso molecular:771.12SGK1-IN-4
CAS:<p>SGK1-IN-4 is a selective inhibitor of SGK1 and can be used in studies about osteoarthritis.</p>Fórmula:C23H21ClFN5O4SPureza:97.03%Cor e Forma:SolidPeso molecular:517.96N-Formyl-2-aminophenol
CAS:<p>N-Formyl-2-aminophenol (N-(2-hydroxyphenyl)methanamide) is a bacterial secondary metabolite found in P. chrysogenum and exhibits antioxidant properties.</p>Fórmula:C7H7NO2Cor e Forma:SolidPeso molecular:137.136Glucocerebrosidase
CAS:<p>Glucocerebrosidase (Glucosylceramidase; GBA), a lysosomal enzyme, catalyzes the hydrolysis of the β-glucosidic linkage in glucocerebroside (GC) to yield glucose</p>Pureza:98%Cor e Forma:Solidisomer-GAT 107
CAS:<p>isomer-GAT 107 ((-)GAT 107) is an inactive isomer of (+)GAT 107.</p>Fórmula:C18H17BrN2O2SPureza:99.33%Cor e Forma:SoildPeso molecular:405.31PF-07238025
<p>PF-07238025, a potent branched-chain ketoacid dehydrogenase kinase (BDK) inhibitor with an EC50 of 19 nM, enhances the stability of the BDK-BCKDH core E2</p>Fórmula:C19H18N2O3SPureza:98%Cor e Forma:SolidPeso molecular:354.425,7-Dichloropyrazolo[1,5-a]pyrimidine
CAS:<p>5,7-Dichloropyrazolo[1,5-a]pyrimidine (fragment 5) is an inhibitor of the enzyme phosphodiesterase 10A (PDE10A) with a Ki value of 24 μM. This compound can be employed in research related to schizophrenia.</p>Fórmula:C6H3Cl2N3Cor e Forma:SolidPeso molecular:188.01CAY10677
CAS:<p>CAY10677 has a wide range of applications in life science related research.</p>Fórmula:C25H37N5Cor e Forma:SolidPeso molecular:407.59Dihydrozeatin riboside
CAS:<p>Dihydrozeatin riboside is a cytokinin that can be isolated from Phaseolus vulgaris L.</p>Fórmula:C15H23N5O5Cor e Forma:SolidPeso molecular:353.37(±)14-HDHA
CAS:<p>(±)14-HDHA is an oxidized metabolite of DHA and can be further oxidized to the 14-oxoDHA, 14-HDoHE inhibits LPS-induced IL-6 mRNA expression.</p>Fórmula:C22H32O3Cor e Forma:SolidPeso molecular:344.49Anirolac
CAS:<p>Anirolac is a nonsteroidal anti-inflammatory agent.</p>Fórmula:C16H15NO4Pureza:98%Cor e Forma:SolidPeso molecular:285.29Ilexsaponin B2
CAS:<p>Ilexsaponin B2 is a natural product for research related to life sciences. The catalog number is TJS0502 and the CAS number is 108906-69-0.</p>Fórmula:C47H76O17Pureza:99.72%Cor e Forma:SolidPeso molecular:913.1Ninopterin
CAS:<p>Ninopterin is an experimental antineoplastic and folic acid analog.</p>Fórmula:C20H21N7O6Pureza:98%Cor e Forma:SolidPeso molecular:455.42Casein Kinase 2 Substrate Peptide
CAS:<p>CK2 Substrate Peptide, C-terminus linked to EDANS, used for CK2 activity assays.</p>Fórmula:C45H73N19O24Cor e Forma:SolidPeso molecular:1264.17PDE4-IN-4
CAS:<p>PDE4-IN-4 is a compound acting as both a potent M3 antagonist (p IC 50 = 10.2) and a PDE4 inhibitor (p IC 50 = 8.8), designed for inhalation-based treatment of</p>Fórmula:C36H37Cl2N3O7SCor e Forma:SolidPeso molecular:726.675-Cholestene-26-oic acid-3β-ol
CAS:<p>5-Cholestene-26-oic acid-3β-ol is a cholesterol catabolite [1] .</p>Fórmula:C27H44O3Cor e Forma:SolidPeso molecular:416.64Valienamine
CAS:<p>Valienamine: an alpha-glucosidase inhibitor found in validamycin A and antidiabetic acarbose.</p>Fórmula:C7H13NO4Cor e Forma:SolidPeso molecular:175.18TEI-9648
CAS:<p>TEI-9648: Potent, specific VDR antagonist, blocks 1α,25(OH)2D3 effects, may aid bone metabolism study.</p>Fórmula:C27H38O4Cor e Forma:SolidPeso molecular:426.597DSPE-PEG1000-K237
<p>DSPE-PEG1000-K237 is a PEG compound composed of DSPE and the KDR-targeting peptide (K237). K237 functionally disrupts the interaction between VEGF and KDR receptors, producing significant biological effects such as inhibiting angiogenesis and tumor growth. DSPE-PEG1000-K237 is applicable for drug delivery.</p>Cor e Forma:Odour SolidAnti-osteoporosis agent-10
<p>Anti-osteoporosis agent-10 is an inhibitor of osteoporosis that suppresses the formation of osteoclasts with an IC50 of 0.042 μM. It also exhibits antagonistic activity towards PPARγ, with an EC50 value of 0.75 μM.</p>Cor e Forma:Odour SolidWH-15
CAS:<p>WH-15: fluorogenic reporter for PLC-γ1, PLC-δ1, PLC-β2 with Km values of 49; 30, 86.1 µM. Cleaves to fluorescent 6-aminoquinoline for live cell imaging.</p>Fórmula:C31H43N2O18P3Cor e Forma:SolidPeso molecular:824.6α-Glucosidase-IN-31
<p>α-Glucosidase-IN-31 (compound R1) is a potent oral α-Glucosidase inhibitor with an IC50 of 10.1 μM, demonstrating significant blood glucose reduction and</p>Fórmula:C18H18N4Pureza:98%Cor e Forma:SolidPeso molecular:290.36Osmanthuside H
CAS:<p>Osmanthuside H is a useful organic compound for research related to life sciences. The catalog number is T125796 and the CAS number is 149155-70-4.</p>Fórmula:C19H28O11Cor e Forma:SolidPeso molecular:432.422Enpp-1-IN-21
CAS:<p>Enpp-1-IN-21 (compound 4g) is an inhibitor of ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1), with IC50 values of 0.45 μM for ENPP1 and 0.19 μM for ENPP3.</p>Fórmula:C21H16F3NO5SCor e Forma:SolidPeso molecular:451.42CIGB-300
CAS:<p>CIGB-300 (P15-Tat) is an anti-casein kinase 2 (CK2) peptide that exhibits anticancer properties by disrupting the phosphorylation activity of protein kinase CK2. The compound induces apoptosis in various tumor cell lines, making it valuable for research in cancer therapy.</p>Fórmula:C127H215N53O30S3Cor e Forma:SolidPeso molecular:3060.6Daclatasvir Impurity B
CAS:<p>Daclatasvir Impurity B, a noted impurity of the antiviral agent Daclatasvir, acts as a potent inhibitor of the HCV NS5A protein [1].</p>Fórmula:C35H41N7O4Cor e Forma:SolidPeso molecular:623.741,1,3-Tribromoacetone
CAS:<p>1,1,3-Tribromoacetone (1,1,3-tribromo-2-propanone) is an impurity of methotrexate.</p>Fórmula:C3H3Br3OPureza:98%Cor e Forma:SolidPeso molecular:294.77trans-2-Hexadecenoyl-L-carnitine
CAS:<p>trans-2-Hexadecenoyl-L-carnitine is an endogenous metabolite in urine[1].</p>Fórmula:C23H43NO4Cor e Forma:SolidPeso molecular:397.59BVT-2733 hydrochloride
CAS:<p>BVT-2733 hydrochloride is a potent, selective, and orally active non-steroidal 11β-HSD1 inhibitor. It exhibits stronger inhibition on mouse 11β-HSD1 enzyme (IC50=96 nM) compared to the human 11β-HSD1 enzyme (IC50=3341 nM). BVT-2733 hydrochloride shows potential for research in arthritis and obesity-related diseases.</p>Fórmula:C17H22Cl2N4O3S2Cor e Forma:SolidPeso molecular:465.42
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