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(74 productos)
- CETP(20 productos)
- Anhídrido carbónico(185 productos)
- Caseína quinasa(137 productos)
- DHFR(34 productos)
- Descarboxilasa(4 productos)
- Deshidrogenasa(289 productos)
- FAAH(65 productos)
- FXR(59 productos)
- Factor Xa(83 productos)
- Ácido graso sintasa(36 productos)
- Ferroptosis(218 productos)
- GR(3 productos)
- GSNOR(4 productos)
- Glucoquinasa(56 productos)
- HIF / HIF Prolilhidroxilasa(145 productos)
- HMG-CoA reductasa(33 productos)
- Hidroxilasa(34 productos)
- IDO(84 productos)
- LDL(8 productos)
- Lipasa(104 productos)
- Lípido(62 productos)
- Lipoxigenasa(132 productos)
- MAO(87 productos)
- MPO(2 productos)
- NAMPT(38 productos)
- P450(6 productos)
- PAI-1(26 productos)
- PDE(166 productos)
- PED(1 productos)
- PKM(15 productos)
- PPAR(168 productos)
- Fosfolipasa(82 productos)
- ROR(43 productos)
- Receptor de retinoides(28 productos)
- SGK(11 productos)
- Tiorredoxina(12 productos)
- Transferasa(29 productos)
- Transportador(43 productos)
- UGT(4 productos)
- Inhibidores de la xantina oxidasa (XO)(9 productos)
Mostrar 34 subcategorías más
Se han encontrado 9054 productos de "Metabolismo"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
LH10
LH10 is an FXR agonist based on fexaramine, with an EC50 of 0.14 μM. It offers hepatoprotective effects, mitigating conditions such as cholestasis induced by alpha naphthylisothiocyanate (ANIT), acute liver injury caused by APAP, and non-alcoholic steatohepatitis (NASH).Fórmula:C34H33N3O2Forma y color:SolidPeso molecular:515.64FXR agonist 11
CAS:FXR agonist11 (Compound 14) is an FXR activator with an EC50 of 1.2 μM and a maximal effect of 73.7%. It significantly increases GSH levels in the liver and is used to study drug-induced liver injury.Fórmula:C18H16N2O5Forma y color:SolidPeso molecular:340.33Cyano-myracrylamide
CAS:<p>Cyano-myracrylamide is an inhibitor of zinc finger DHHC domain-containing palmitoyltransferase 20 (zDHHC20) with an IC50 value of 1.35 µM. It also inhibits the S-palmitoylation of EGFR and CD36. In HEK293T cells expressing recombinant E. coli GobX, recombinant human MyD88, or endogenous Ras, Cyano-myracrylamide inhibits the S-palmitoylation of E. coli E3 ligase GobX, MyD88, and Ras, which are substrates of zDHHC20, zDHHC9, and zDHHC6.</p>Fórmula:C19H34N2OForma y color:SolidPeso molecular:306.49ZG-2033
CAS:ZG-2033 (Compound 26) is an orally active HIF-2α agonist that exhibits nanomolar activity (EC50 = 490 nM) in a luciferase reporter assay. It demonstrates an anti-anemic effect and shows synergistic effects with AKB-6548 in anemia, making it useful for the study of renal anemia.Fórmula:C15H14N2O2SForma y color:SolidPeso molecular:286.35LH1513
LH1513 is a dioxalate salt derivative of l-lysine that inhibits CaOx crystallization more effectively than citrate and pyruvate. It shows potential preventive activity in hyperoxaluria models and effectively prevents urinary CaOx crystal formation in Agxt knockout mice. AGXT-1 is a mitochondrial protein involved in metabolic processes.Fórmula:C10H11N2Na3O8Forma y color:SolidPeso molecular:356.173,4-Dihydroxyamphetamine hydrochloride
CAS:3,4-Dihydroxyamphetamine (α-Methyldopamine) (hydrochloride) is a minor metabolite of 3,4-Methylenedioxymethamphetamine (MDMA) and exhibits cytotoxicity in rat hepatocytes. Additionally, 3,4-Dihydroxyamphetamine (hydrochloride) is applicable in hypertension research.Fórmula:C9H14ClNO2Forma y color:SolidPeso molecular:203.67Calcium Channel antagonist 5
CAS:Calcium Channel antagonist5 (compound 32) is a calcium channel antagonist with a pIC50 of 5.50.Fórmula:C17H18N2O6Forma y color:SolidPeso molecular:346.34CCR1/5/8 activator 1
CAS:CCR1/5/8 activator 1 is a cytoplasmic phospholipase A inhibitor with antifungal activity.Fórmula:C10H9NOPureza:99.94%Forma y color:SolidPeso molecular:159.18Oxodipine
CAS:Oxodipine blocks rabbit aortic contraction and weakens rat cardiac force; reduces Ca currents in myocytes; side effects: mouse constipation, dog gum swelling.Fórmula:C19H21NO6Pureza:99.64%Forma y color:SolidPeso molecular:359.37AK-4
AK-4 is an antidiabetic agent that functions as a mitochondrial uncoupler.Fórmula:C21H14Cl2N2O4SForma y color:SolidPeso molecular:461.32LOC1886
CAS:LOC1886 is a covalent inhibitor of GPX4, with slightly lower potency compared to RSL3 and ML162.Fórmula:C13H11N3O2Forma y color:SolidPeso molecular:241.25ASM-IN-3
CAS:ASM-IN-3 (Compound 21b) is a selective acid sphingomyelinase (ASM) inhibitor that can penetrate the blood-brain barrier, with an IC50 of 3.37 μM against purified human ASM. By inhibiting ASM activity in the hippocampus and promoting neurogenesis, ASM-IN-3 alleviates depressive-like behavior in reserpine-induced depressive rats.Fórmula:C17H13ClN2O4Forma y color:SolidPeso molecular:344.75Microcystin YR
CAS:Microcystin YR (Cyanoginosin YR) is a cyclic peptide and acts as an inhibitor of protein phosphatase 2A (PP2A).Fórmula:C52H72N10O13Forma y color:SolidPeso molecular:1045.19Pyruvate carboxylase
CAS:<p>Pyruvate carboxylase, a biotin-containing enzyme, catalyzes the carboxylation of pyruvate to oxaloacetate, a reaction dependent on HCO3− and MgATP.</p>Pureza:98%Forma y color:Solidω-conotoxin MoVIA
<p>ω-Conotoxin MVIIA is a potent, selective inhibitor of Ca_v2.2, exhibiting an IC_50 of 0.33 μM in the SH-SY5Y fluorimetric hCa_v2.2 assay [1].</p>Fórmula:C147H233N45O47S7Pureza:98%Forma y color:SolidPeso molecular:3607.15DDC 3′-O-β-D glucuronide
Compound 5, DDC 3′-O-β-D-glucuronide, is a drug metabolite with properties that inhibit the fibrillization and oligomerization of Aβ42, suggesting its potentialPureza:98%Forma y color:Odour Solidα-Glucosidase-IN-25
<p>α-Glucosidase-IN-25 (Compound (R)-8k) serves as a competitive inhibitor for α-glucosidase, demonstrating an inhibitory concentration 50 (IC50) of 1.19μM, making</p>Fórmula:C29H22N6O3Pureza:98%Forma y color:SolidPeso molecular:502.52MAGL-IN-11
<p>MAGL-IN-11 (compound 29) is a selective, reversible inhibitor of monoacylglycerol lipase (MAGL), with potential in researching inflammation, cancer, and</p>Pureza:98%Forma y color:Odour Solidα-Amylase/α-Glucosidase-IN-5
<p>α-Amylase/α-Glucosidase-IN-5 (compound 4l) functions as a dual inhibitor, effectively inhibiting both α-glucosidase (Glucosidase) and α-amylase (Amylases) with</p>Fórmula:C30H27BrN3O3PPureza:98%Forma y color:SolidPeso molecular:588.43Mortatarin F
<p>Mortatarin F (Compound 1), a renyleted flavonoid derived from mulberry leaves, functions as an α-glucosidase inhibitor with an IC50 value of 8.7 μM, making it</p>Fórmula:C25H30O7Pureza:98%Forma y color:SolidPeso molecular:442.5Ovalbumin (154-159)
CAS:<p>Ovalbumin (154-159), a peptide fragment derived from ovalbumin, acts as a potent inhibitor of the angiotensin-converting enzyme (ACE) and is utilized in</p>Fórmula:C28H52N10O9Pureza:98%Forma y color:SolidPeso molecular:672.77CA inhibitor 2
<p>Compound 4H is a potent carbonic anhydrase inhibitor with an IC50 value of 0.033 μM [1].</p>Fórmula:C7H9N7O3S3Pureza:98%Forma y color:SolidPeso molecular:335.39Denecimig
CAS:<p>Denecimig (Mim8) is a bispecific and humanized IgG4κ antibody, hemophilia A, activated coagulation factors IXa (FIXa) and X (FX) arresting bleeding.</p>Pureza:95%Forma y color:LiquidCarbonic anhydrase inhibitor 15
<p>Carbonic Anhydrase Inhibitor 15 (Compound 8), with an inhibitory constant (K_i) of 8.5 nM for hCA II, exhibits analgesic effects [1].</p>Fórmula:C27H33N5O2S2Pureza:98%Forma y color:SolidPeso molecular:523.71IHMT-IDH1-053
IHMT-IDH1-053 (compound 16) is an irreversible inhibitor exhibiting high selectivity for the IDH1 R132H mutant, achieving an IC50 of 4.7 nM.Fórmula:C25H33FN6O4SPureza:98%Forma y color:SolidPeso molecular:532.63Ledelabricin alfa
<p>Ledelabricin alfa, an isoform A variant of human proteoglycan 4 (PRG4), functions as a lubricant for joints and boundaries.</p>Pureza:98%Forma y color:Odour LiquidnSMase2-IN-1
nSMase2-IN-1 is an orally active inhibitor of Neutral sphingomyelinase 2 (nSMase2) with a potent IC50 value of 0.13 ± 0.06 μM.Fórmula:C12H17N5OPureza:98%Forma y color:SolidPeso molecular:247.3hCAXII-IN-7
hCAXII-IN-7 (compound 6e) functions as an inhibitor of human carbonic anhydrase XII (hCA XII) and possesses blood-brain barrier (BBB) permeability.Fórmula:C26H25N5O6S2Pureza:98%Forma y color:SolidPeso molecular:567.645-LOX-IN-5
<p>Compound 29, also known as 5-LOX-IN-5, is a 5-lipoxygenase (5-LOX) inhibitor with an inhibitory concentration 50 (IC50) of 56 nM, utilized in research</p>Fórmula:C19H18BrN3O2SPureza:98%Forma y color:SolidPeso molecular:432.33RPR132595A hydrochloride
<p>RPR132595A (NPC) hydrochloride, an active metabolite of CPT-11, is produced via cytochrome P-450 3A4 (CYP3A4) metabolism and is ultimately eliminated via</p>Fórmula:C28H31ClN4O6Pureza:98%Forma y color:SolidPeso molecular:555.02KR-27425
<p>Compound 13, an AChE activator 1, is a non-pyridinium oxime that reactivates paraoxon-inhibited acetylcholinesterase (AChE) [1].</p>Pureza:98%Forma y color:Odour SolidNAMPT degrader-3
NAMPT Degrader-3 (compound C5) is a NAMPT degrader that functions through a VHL- and proteasome-dependent mechanism.Fórmula:C56H74N8O7SPureza:98%Forma y color:SolidPeso molecular:1003.3A3373
CAS:<p>A3373 is a novel inhibitor targeting both Phospholipase D1 (PLD1) and Phospholipase D2 (PLD2), demonstrating half maximal inhibitory concentrations (IC50) of</p>Fórmula:C17H9F7N2OPureza:98%Forma y color:SoildPeso molecular:390.26α-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%Forma y color:SolidPeso molecular:290.36RORγt inverse agonist 31
RORγt inverse agonist 31 (14g) is a potent antagonist of the retinoic acid receptor-related orphan receptor γt (RORγt), exhibiting an inhibitory concentration (Fórmula:C23H15Cl2F3N4O3SPureza:98%Forma y color:SolidPeso molecular:555.36Eurestobart
CAS:<p>Eurestobart is a humanized IgG1κ (IgG1 kappa) monoclonal antibody that specifically targets the enzyme ectonucleoside triphosphate diphosphohydrolase (ENTPDase</p>Pureza:98%Forma y color:Liquidα-Glucosidase-IN-38
α-Glucosidase-IN-38 (Compound 11j) is a potent α-glucosidase inhibitor, demonstrating an IC50 of 12.44±0.38 μM, and is significant in the context of DiabetesPureza:98%Forma y color:Odour SolidAlternaphenol B2
<p>Alternaphenol B2, a selective inhibitor of mutant isocitrate dehydrogenase 1 (IDH1m), is sourced from the coral-derived fungus Parengyodontium album SCSIO</p>Pureza:98%Forma y color:Odour SolidVHL-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%Forma y color:SolidPeso molecular:544.68Myoregulin TFA
Myoregulin (MLN peptide) TFA, belonging to the regulin family, is a regulator of muscle performance through modulation of intracellular calcium dynamics.Fórmula:C239H391N53O67S3·xC2HF3O2Pureza:98%Forma y color:SolidPeso molecular:5175.17 (free base)α-Glucosidase-IN-36
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 1.65Fórmula:C26H24BrN5O3SPureza:98%Forma y color:SolidPeso molecular:566.47Ovotransferrin (328-332)
CAS:<p>Ovotransferrin (328-332), with an IC50 of 20 μM, exhibits protective activity against hypertension by inhibiting the Angiotensin-Converting Enzyme (ACE) and</p>Fórmula:C25H46N8O7Pureza:98%Forma y color:SolidPeso molecular:570.68ω-Conotoxin CnVIIA
CAS:<p>ω-Conotoxin CnVIIA, a 27-amino-acid neuropeptide toxin, serves as an N-type calcium current blocker [1].</p>Fórmula:C110H179N39O36S7Pureza:98%Forma y color:SolidPeso molecular:2848.29UDP-3-O-acyl-GlcNAc diammonium
<p>UDP-3-O-acyl-GlcNAc diammonium serves as a metabolite in E. coli, playing a critical role in the biosynthesis pathway of 3-deoxy-D-manno-octulosonate (KDO) [1].</p>Fórmula:C31H59N5O19P2Pureza:98%Forma y color:SolidPeso molecular:867.77α-Glucosidase-IN-30
<p>α-Glucosidase-IN-30 (compound 8c) is a potent, orally active competitive inhibitor of α-glucosidase, exhibiting a K i of 40.0 µM and an IC50 of 49.0 µM.</p>Fórmula:C20H19N7O2Pureza:98%Forma y color:SolidPeso molecular:389.41Hepcidin-25 (human) (acetate)
CAS:<p>Hepcidin-25 (human) acetate is a modulator of iron metabolism that demonstrates anti-inflammatory and antibacterial effects through the modulation of iron-</p>Fórmula:C113H170N34O31S9·xC2H4O2Pureza:98%Forma y color:Solidω-Conotoxin MVIID
<p>ω-Conotoxin MVIID (SNX-238) is a peptide from the Conus genus that inhibits the ω-Conotoxin-GVIA-sensitive, high-threshold calcium (Ca 2+) current in fish</p>Fórmula:C99H164N42O33S7Pureza:98%Forma y color:SolidPeso molecular:2695.08ω-Conotoxin CVIA
CAS:<p>ω-Conotoxin CVIA, a 27-amino acid neuropeptide, functions as a blocker of voltage-sensitive calcium channels (VSCCs) [1].</p>Fórmula:C97H161N39O36S6Pureza:98%Forma y color:SolidPeso molecular:2641.95Casuarictin
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:936.65Flaccidoside III
CAS:<p>Flaccidoside III, a flavonoid and triterpenoid compound extracted from the aerial parts of N.</p>Fórmula:C59H96O26Pureza:98%Forma y color:SolidPeso molecular:1221.38SP4f
<p>SP4f, an activator of PPAR-γ, exhibits an EC50 value of 826 nM in HK-2 cells.</p>Pureza:98%Forma y color:Odour SolidGlutathione Peroxidase
CAS:Glutathione Peroxidase (GSH-Px; EC 1.11.1.9), a member of the peroxidase family, catalyzes the oxidation of reduced glutathione (GSH) to oxidized glutathione (Pureza:98%Forma y color:SolidIsocrenatoside
CAS:Isocrenatoside (compound 6), a cyclic octapeptide derived from the ethanolic extract of Microtoena prainiana stems, functions as an angiotensin-convertingFórmula:C29H34O15Pureza:98%Forma y color:SolidPeso molecular:622.57α-Amylase/α-Glucosidase-IN-3
<p>α-Amylase/α-Glucosidase-IN-3 (Compound 17) serves as a dual inhibitor targeting both α-Amylase and α-Glucosidase, exhibiting IC50 values of 0.70 μM and 1.10 μM</p>Fórmula:C23H14Cl4N6O2SPureza:98%Forma y color:SolidPeso molecular:580.27Complement factor I
CAS:<p>Complement factor I, a serine protease, attenuates complement activity both in the fluid phase and on cell surfaces, working alongside cofactors such as factor</p>Pureza:98%Forma y color:Solidω-Tbo-IT1
<p>ω-Tbo-IT1, a peptide toxin extracted from the venom of Tibellus oblongus, functions as an inhibitor of insect calcium channels [1].</p>Fórmula:C171H285N61O53S9Pureza:98%Forma y color:SolidPeso molecular:4332.05α-Glucosidase-IN-39
<p>α-Glucosidase-IN-39 is a potent α-glucosidase enzyme inhibitor, exhibiting an IC50 value of 869.06 ppm. It is applicable for use in antidiabetic studies [1].</p>Pureza:98%Forma y color:Odour SolidZLY28
ZLY28 is a novel, first-in-class compound with specific intestinal restriction and oral activity, serving as a dual modulator of FXR and FABP1.Fórmula:C29H23Cl2NO4Pureza:98%Forma y color:SolidPeso molecular:520.4α-Glucosidase-IN-34
<p>α-Glucosidase-IN-34 (compound 7f) is a potent inhibitor of α-glucosidase, exhibiting an IC50 of 2.90 μM, and is applicable in research related to type 2</p>Fórmula:C28H20N2O4Pureza:98%Forma y color:SolidPeso molecular:448.47PROTAC PTPN2 degrader-2
CAS:<p>PROTAC PTPN2 degrader-2 (example 187B) is a potent agent capable of degrading PTPN2, which holds potential for research in cancer and metabolic diseases [1].</p>Fórmula:C49H49ClN6O11S2Pureza:98%Forma y color:SolidPeso molecular:997.53Endo-1,3-β-glucanase
CAS:Endo-1,3-β-glucanase (Lyticase) is a glucanase from fungi and Chlamydomonas reinhardtii that displays lytic activity on fungal cells.Forma y color:SolidPROTAC SGK3 degrader-1
CAS:PROTAC SGK3 degrader-1 (SGK3-PROTAC1) is a PROTAC coupler that targets SGK3 and binds ligands to VH032 VHL to induce endogenous SGK3 degradation.Fórmula:C57H73FN10O11S2Pureza:98%Forma y color:SolidPeso molecular:1157.38Daprodustat
CAS:Daprodustat (GSK1278863) is a HIF-prolyl hydroxylase inhibitor.Fórmula:C19H27N3O6Pureza:97% - 99.82%Forma y color:SolidPeso molecular:393.43IFB-088 acetate
CAS:<p>IFB-088 acetate targets PPP1R15A-related diseases, including cancers and protein misfolding disorders.</p>Fórmula:C10H13ClN4O2Pureza:90%Forma y color:SolidPeso molecular:256.69SB-435495
CAS:SB-435495 is a compound characterized by its potent, selective, reversible, and non-covalent inhibition of Lp-PLA2, demonstrating an IC50 value of 0.06 nM.Fórmula:C38H40F4N6O2SPureza:99.07%Forma y color:SolidPeso molecular:720.82Carbonic anhydrase
CAS:<p>Carbonic anhydrase, a zinc enzyme in all life forms, converts CO2 to bicarbonate; studied for cancer, glaucoma, obesity, epilepsy.</p>Forma y color:Solid2-Bromoacetamide
CAS:<p>2-Bromoacetamide (α-Bromoacetamide) is a class of disinfection by-products that exhibit developmental toxicity in animals.</p>Fórmula:C2H4BrNOPureza:99.83%Forma y color:SolidPeso molecular:137.96Clopidogrel Carboxylic Acid hydrochloride
CAS:Clopidogrel Carboxylic Acid hydrochloride (SR 26334) is a major inactive metabolite of clopidogrel, commonly used as a reference standard for metabolic analysi.Fórmula:C15H15Cl2NO2SPureza:99.32%Forma y color:SolidPeso molecular:344.26Sch 32615
CAS:Sch 32615 is an enkephalinase inhibitor with inhibitory action on D-1 and D-2 dopamine receptor-mediated behaviors.Fórmula:C21H24N2O5Pureza:98%Forma y color:SolidPeso molecular:384.43Fludarabine-Cl
CAS:Fludarabine-Cl inhibits ADAR1, potentially preventing/treating cancer-related diseases.Fórmula:C10H11ClFN5O3Forma y color:SolidPeso molecular:303.68Pre-vitamin D3 decanoate
CAS:<p>Pre-vitamin D3 decanoate, a derivative of vitamin D3, can be transformed into the active form of vitamin D in the body. Initially, it is converted to 25-hydroxyvitamin D3 in the liver and then to 1,25-dihydroxyvitamin D3 in the kidneys. During preparation, vitamin D3 might react with triglycerides in the formulation, forming ester compounds that impact the stability and bioavailability of vitamin D3. This compound is utilized in the study of diseases related to vitamin D, including osteoporosis, autoimmune diseases, and certain cancers.</p>Fórmula:C37H62O2Forma y color:SolidPeso molecular:538.89Fmoc-Dab(Boc)-OH
CAS:<p>Fmoc-Dab(Boc)-OH is a chemical intermediate used for chemical synthesis.</p>Fórmula:C24H28N2O6Forma y color:SolidPeso molecular:440.49SDH-IN-1
CAS:SDH-IN-1 (compound 4i) is an SDH (succinate dehydrogenase) inhibitor (IC50 = 4.53 μM) with antifungal activity against S. sclerotiorum fungicidal purposes.Fórmula:C14H9Cl2N3O2SPureza:99.82%Forma y color:SolidPeso molecular:354.21Fmoc-L-aspartic acid
CAS:Fmoc-L-aspartic acid (Fmoc-Asp-OH) is an aspartic acid derivative.Fórmula:C19H17NO6Pureza:99.12% - 99.83%Forma y color:SoildPeso molecular:355.34ADDA 5 hydrochloride
CAS:ADDA 5 hydrochloride is a specific and non-competitive inhibitor of CcO (cytochrome c oxidase) that inhibits the proliferation of glioma cellsFórmula:C24H36ClNO2Forma y color:SolidPeso molecular:406Z-Asn-OH
CAS:<p>Z-Asn-OH (N-Cbz-L-asparagine) is a glycine derivative mainly used in peptide synthesis.Cbz-Asn-OH prevents unwanted reactions.</p>Fórmula:C12H14N2O5Pureza:98.21%Forma y color:SolidPeso molecular:266.25Alitame hydrate (Standard)
CAS:Alitame (hydrate) (Standard) is the standard substance of Alitame (hydrate), and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Alitame hydrate is a non-nutritive sweetener that is 2000 times sweeter than sucrose. It is formed from aspartic acid, alanine & an amide.Fórmula:C14H25N3O4SH2OPeso molecular:376.47Myristoyl Ethanolamide
CAS:Myristoyl Ethanolamide is an endogenous cannabinoid analog belonging to the fatty acyl ethanolamine famil，has physiological activity in the nervous system.Fórmula:C16H33NO2Pureza:99.62%Forma y color:SolidPeso molecular:271.44Cinnamyl-3,4-dihydroxy-α-cyanocinnamate
CAS:Cinnamyl-3,4-dihydroxy-α-cyanocinnamate (CDC), 12/15-LO inhibitor for diabetes. Affordable Excellence: Reliable Quality You Can TrustFórmula:C19H15NO4Forma y color:SolidPeso molecular:321.33N-benzoyl-L-aspartic acid
CAS:N-benzoyl-L-aspartic acid, a metabolite, inhibits rice seed germination and is commonly used in organic synthesis and biochemical experiments.Fórmula:C11H11NO5Pureza:99.87%Forma y color:SolidPeso molecular:237.21APL180 TFA
<p>APL180 TFA (L-4F) is an apolipoprotein A-I mimetic peptide that enhances the anti-inflammatory properties of high-density lipoprotein (HDL). APL180 is applicable for cardiovascular disease research.</p>Fórmula:C114H156N24O28·xC2HF3O2Forma y color:SolidPeso molecular:2310.60 (free base)Phenol, 3-iodo-
CAS:Phenol, 3-iodo- is a bioactive chemical.Fórmula:C6H5IOPureza:98%Forma y color:SolidPeso molecular:220.011,3,4,6-Tetrachloro-3α,6α-diphenylglycouril
CAS:1,3,4,6-Tetrachloro-3α,6α-diphenylglycouril is recognized for its enzyme inhibitory properties within biological organisms. It is employed as a potential anti-cancer agent in compound development. Additionally, it plays a role in the modulation of cellular signaling pathways, making it useful for cellular biology research. This compound is considered effective in exerting biological activity under specific conditions.Fórmula:C16H10Cl4N4O2Forma y color:SolidPeso molecular:432.09Quizalofop-p-ethyl
CAS:<p>Quizalofop-p-ethyl ((R)-Quizalofop ethyl) is a selective post-emergent herbicide for annual and perennial weeds, acetyl-CoA carboxylase (ACCase) inhibitor.</p>Fórmula:C19H17ClN2O4Pureza:97.87%Forma y color:White Powder CrystalPeso molecular:372.80Fmoc-D-Met-OH
CAS:<p>Fmoc-D-Met-OH is a useful organic compound for research related to life sciences. The catalog number is T67557 and the CAS number is 112883-40-6.</p>Fórmula:C20H21NO4SForma y color:SolidPeso molecular:371.45Hydroxylamine hydrochloride
CAS:Hydroxylamine hydrochloride(Hydroxylammonium chloride) is a selective and potent monoamine oxidase (MAO) inhibitor with inhibitory effects on platelet aggregation.Fórmula:ClH4NOPureza:98%Forma y color:White Solid CrystallinePeso molecular:69.49Chenodeoxycholic Acid-d4
CAS:Chenodeoxycholic Acid-d4 is a deuterium-labelled compound of Chenodeoxycholic Acid, which can be used for isotopic tracing. CDCA is a bile acid.Fórmula:C24H36D4O4Peso molecular:396.6Vitamin K1-d4
CAS:Vitamin K1-d4 is a deuterated compound of Vitamin K1. Vitamin K1 has a CAS number of 84-80-0. Vitamin K1 (Phylloquinone) is a naturally-occurring vitamin. Vitamin K1 is essential for blood clotting, bone and vascular metabolism.Fórmula:C31H42D4O2Peso molecular:454.7204TPC2-A1-N
CAS:TPC2-A1-N is a TPC2 small molecule agonist that can be used to detect different functions of TPC2 channels in intact cells.Fórmula:C17H9Cl2F3N2O2Pureza:99.86%Forma y color:SolidPeso molecular:401.17Fmoc-Lys(Z)-OH
CAS:<p>Fmoc-Lys(Z)-OH is a lysine derivative with an Fmoc protecting group, widely used in biochemical experiments and drug synthesis research.</p>Fórmula:C29H30N2O6Pureza:98.20%Peso molecular:502.56Fmoc-Gln(Trt)-Thr(psi(Me,Me)pro)-OH
CAS:<p>Fmoc-Gln(Trt)-Thr(psi(Me,Me)pro)-OH is a dipeptide.</p>Fórmula:C46H45N3O7Forma y color:SolidPeso molecular:751.87Vitamin D3-d3
CAS:<p>Vitamin D3-d3 is a deuterated compound of Vitamin D3.</p>Fórmula:C27H41D3OForma y color:SolidPeso molecular:387.66Metoprolol acid
CAS:Metoprolol acid is a urinary metoprolol metabolite and doesn't work pharmacologically.Fórmula:C14H21NO4Pureza:98%Forma y color:SolidPeso molecular:267.33Ternidazole hydrochloride
CAS:<p>Ternidazole hydrochloride (Ternidazole HCl) is a 5-nitroimidazole antibiotic with antimicrobial antioxidant and antiprotozoal activity.</p>Fórmula:C7H12ClN3O3Pureza:99.70%Forma y color:SolidPeso molecular:221.64Fmoc-β-HoGlu(OtBu)-OH
CAS:<p>Fmoc-β-HoGlu(OtBu)-OH is an amino acid derivative and has a wide range of applications in life science related research.</p>Fórmula:C25H28NO6Forma y color:SolidPeso molecular:438.501Hippuryl-His-Leu-OH
CAS:<p>Hippuryl-His-Leu-OH tests for angiotensin I enzyme activity, allowing His-Leu detection by fluorescence.</p>Fórmula:C21H27N5O5Forma y color:SolidPeso molecular:429.47Lomitapide Mesylate
CAS:Lomitapide Mesylate (BMS-201038 mesylate) is a methanesulfonic acid form of lomitapide, a small molecule inhibitor of microsomal triglyceride transfer protein.Fórmula:C40H41F6N3O5SPureza:99.92%Forma y color:SolidPeso molecular:789.83Gefitinib impurity 1
CAS:<p>Gefitinib Impurity 1: EGFR inhibitor, oral, targets EGF-stimulated tumor growth (IC50=54 nM), induces autophagy & antitumor effects.</p>Fórmula:C15H19N3O5Forma y color:SolidPeso molecular:321.332,6-Dimethylaniline Hydrochloride
CAS:<p>2,6-Dimethylaniline Hydrochloride is a useful organic compound for research related to life sciences.The CAS number is 21436-98-6.</p>Fórmula:C8H12ClNPureza:99.80%Forma y color:SolidPeso molecular:157.64Desvaleryl Valsartan
CAS:Desvaleryl valsartan is a degradation impurity of valsartan, formed in acidic conditions.Fórmula:C19H21N5O2Forma y color:SolidPeso molecular:351.4
