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(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 8626 productos de "Metabolismo"
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RORγt Inverse agonist 8
CAS:<p>RORγt Inverse agonist 8 is a potent, selective, orally bioavailable RORγt inverse agonist(human RORγt-LBD with an IC50 of 19 nM).</p>Fórmula:C26H33N7O2Pureza:98%Forma y color:SolidPeso molecular:475.59IMB-XMA0038
CAS:<p>IMB-XMA0038 is a Mycobacterium tuberculosis aspartate semialdehyde dehydrogenase inhibitor with antimicrobial activity for use in tuberculosis research.</p>Fórmula:C11H10N4O6Pureza:98.94% - 99.96%Forma y color:SolidPeso molecular:294.22MPO-IN-4
CAS:<p>MPO-IN-4, a potent MPO inhibitor (IC50=25 nM), also inhibits TPO (IC50=2.2 μM), but not MGMT.</p>Fórmula:C12H11N5Forma y color:SolidPeso molecular:225.25RG 6866
CAS:RG 6866 is a inhibitor of 5-lipoxygenase.Fórmula:C16H17NO3Pureza:98%Forma y color:SolidPeso molecular:271.31BI 689648
CAS:BI 689648 is a highly selective inhibitor of aldosterone synthase(CYP11B1 and CYP11B2 with IC50s of 310 and 2.1 nM, respectively).Fórmula:C16H18N4O2Forma y color:SolidPeso molecular:298.34SCH 42495 racemate
CAS:<p>SCH 42495 racemate is the racemate of SCH 42495. SCH 42495 is an orally active neutral inhibitor of metalloendopeptidase (NEP), with antihypertensive effect.</p>Fórmula:C20H29NO4S2Pureza:98%Forma y color:SolidPeso molecular:411.58Theodrenaline
CAS:<p>Theodrenaline is a cardiac stimulant, also acts as an agent of anti-hypotensive together with cafedrine.</p>Fórmula:C17H21N5O5Pureza:98%Forma y color:SolidPeso molecular:375.38Fumarate hydratase-IN-1
CAS:Fumarate hydratase-IN-1 is a cell-permeable fumarate hydratase inhibitor with antiproliferative activity and can be used to study cellular activity.Fórmula:C27H30N2O4Pureza:98.96% - 99.49%Forma y color:SolidPeso molecular:446.54Fenoverine
CAS:<p>Fenoverine (Spasmopriv) has antispasmodic activity and can be used to study gastrointestinal spasms.</p>Fórmula:C26H25N3O3SPureza:98.34%Forma y color:SolidPeso molecular:459.56Xanthine oxidoreductase-IN-3
CAS:<p>Xanthine oxidoreductase-IN-3, an oral XOR inhibitor with IC50 of 26.3 nM, is useful for acute hyperuricemia research.</p>Fórmula:C14H10ClN5OPureza:98.1%Forma y color:SolidPeso molecular:299.72Cronidipine
CAS:<p>Cronidipine (LF 20254), a calcium channel antagonist, is used potentially for the treatment of hypertension and myocardia ischemia.</p>Fórmula:C30H32ClN3O8Pureza:99.47%Forma y color:SolidPeso molecular:598.04SERCA2a activator 1
CAS:<p>SERCA2a activator 1 boosts heart function by reducing phospholamban restraint and enhancing cardiac contraction-relaxation cycles.</p>Fórmula:C32H29N3O4SPureza:99.75%Forma y color:SolidPeso molecular:551.66PTP1B-IN-3
CAS:<p>PTP1B-IN-3 是一种具有有选择性和高效性的 PTP1B 抑制剂，具有抗癌活性，抑制 PTP1B 和 TCPTP 。PTP1B-IN-3 可用于研究糖尿病。</p>Fórmula:C12H7BrF2NO3PPureza:99.31% - 99.97%Forma y color:SolidPeso molecular:362.06Tiapamil hydrochloride
CAS:<p>Tiapamil hydrochloride (Ro 11-1781 hydrochloride) is a calcium channel blocker with antihypertensive activity used in the study of angina pectoris.</p>Fórmula:C26H38ClNO8S2Pureza:99.17%Forma y color:SolidPeso molecular:592.16Imanixil
CAS:<p>Imanixil boosts LDLR, cuts cholesterol and VLDL production, reducing atherosclerosis.</p>Fórmula:C17H17F3N6O2Pureza:>99.99% - >99.99%Forma y color:SolidPeso molecular:394.35IQB-782
CAS:<p>IQB-782 is a mucolytic agent with mucolytic expectorant activity for the study of obstructive lung disease.</p>Fórmula:C4H9N3O2SPureza:>99.99%Forma y color:SolidPeso molecular:163.2AChE/BChE/MAO-B-IN-1
CAS:<p>AChE/BChE/MAO-B-IN-1 is a reversible, non-time-dependent inhibitor of AChE, BChE and MAO-B that crosses the blood-brain barrier and exhibits inhibitory effects</p>Fórmula:C20H24N2O2Pureza:98.17%Forma y color:SolidPeso molecular:324.42hCAI/II-IN-6
CAS:<p>hCAI/II-IN-6 is a selective and orally active inhibitor of human carbonic anhydrase (CA).</p>Fórmula:C19H24N4O3SPureza:97.07%Forma y color:SolidPeso molecular:388.48Allopurinol riboside
CAS:<p>Allopurinol riboside, an allopurinol metabolite, inhibits purine nucleoside phosphorylase in parasites with a Ki of 277 μM.</p>Fórmula:C10H12N4O5Pureza:99.46% - 99.73%Forma y color:SolidPeso molecular:268.23BW-1370U87
CAS:BW-1370U87 is an MAO-A inhibitor increasing brain amines, showing promise in depression models.Fórmula:C14H12O3SPureza:99.82% - 99.89%Forma y color:SolidPeso molecular:260.31BPDA2
CAS:BPDA2 selectively inhibits SHP2 (IC50=92nM) over SHP1/1B (33.39/40.71μM), curbs RTKs, and hampers SHP2-driven breast cancer cell traits.Fórmula:C24H30O5Pureza:99.80%Forma y color:SolidPeso molecular:398.49Phosphatase-IN-1
CAS:<p>Phosphatase-IN-1 is a phosphatidic acid phosphatase (Pah) inhibitor with antifungal activity for the study of rice blast and ruderalia.</p>Fórmula:C16H16Cl2FNO2Pureza:99.88%Forma y color:SolidPeso molecular:344.21K-111
CAS:<p>K-111 is a PPAR alpha agonist. K-111 improves insulin resistance, reducing bodyweight, and ameliorating atherogenic dyslipidemia.</p>Fórmula:C18H25Cl3O2Pureza:99.64% - 99.88%Forma y color:SolidPeso molecular:379.75Lidorestat
CAS:<p>Lidorestat (IDD-676) is an aldose reductase inhibitor (IC50: 5 nM) with effective, selective and oral activity.</p>Fórmula:C18H11F3N2O2SPureza:99.98%Forma y color:SolidPeso molecular:376.35SBI-425
CAS:<p>SBI-425: orally available TNAP inhibitor, enhances cardiovascular health & survival, no bone impact.</p>Fórmula:C13H12ClN3O4SPureza:99.88%Forma y color:SolidPeso molecular:341.775-ALA benzyl ester hydrochloride
CAS:<p>5-ALA benzyl ester hydrochloride: a photodetection agent that promotes PPIX in colon cancer cells.</p>Fórmula:C12H16ClNO3Pureza:98.39% - 99.38%Forma y color:SolidPeso molecular:257.71Lifarizine
CAS:<p>Lifarizine (RS-87476), a calcium-sodium channel antagonist, shows neuroprotective activity in a simplified rat survival model of double vessel occlusion.</p>Fórmula:C29H32N4Pureza:99.88%Forma y color:SolidPeso molecular:436.59Qc1
CAS:<p>Qc1 is an inhibitor of threonine dehydrogenase (TDH) inhibitor and can be used in studies about metabolic diseases.</p>Fórmula:C23H16F3N3O2SPureza:99.75%Forma y color:SolidPeso molecular:455.45Farglitazar
CAS:<p>Farglitazar (GI-262570) is a PPAR-γ agonist and insulin sensitizer used in the study of diabetes.</p>Fórmula:C34H30N2O5Pureza:99.4% - 99.52%Forma y color:SolidPeso molecular:546.61alphaSYN-IN-NAB2
CAS:<p>alphaSYN-IN-NAB2: a NAB2 gene protein guarding neurons against alpha-SYN harm; aids endosomal transport, cell processes, and can study various diseases.</p>Fórmula:C23H20ClN3OPureza:98.49%Forma y color:SolidPeso molecular:389.88Izonsteride
CAS:<p>Izonsteride (LY320236) is a selective and potent 5alpha reductase inhibitor with dual action on the type I and type II isoforms of the enzyme.Izonsteride is</p>Fórmula:C24H26N2OS2Pureza:99.55%Forma y color:SolidPeso molecular:422.61BMS-823778
CAS:<p>BMS-823778 is a potent inhibitor of 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD-1) for the study of type 2 diabetes.</p>Fórmula:C18H18ClN3OPureza:99.39% - 99.75%Forma y color:SolidPeso molecular:327.81OSMI-4
CAS:<p>OSMI-4 is a low nanomolar O-GlcNAc transferase (OGT) inhibitor that can be used to study OGT inhibition in different human cell lines.Cost-effective and quality-assured.</p>Fórmula:C27H26ClN3O7S2Pureza:99.68%Forma y color:SolidPeso molecular:604.09HTS07545
CAS:<p>HTS07545, an SQOR inhibitor (IC50: 30nM), slows H2S breakdown, researched for heart failure.</p>Fórmula:C22H18N2O3Pureza:99.71%Forma y color:SolidPeso molecular:358.39MFI8
CAS:MFI8 is a compound that regulates mitochondrial fission and can be used to study aging.Fórmula:C16H18ClNOPureza:99.08% - 99.78%Forma y color:SolidPeso molecular:275.77Zifaxaban
CAS:<p>Zifaxaban (TY-602) is an oral selective factor Xa inhibitor with an IC50 of 11.1 nM, highly specific over other serine proteases, used in thrombosis studies.</p>Fórmula:C20H16ClN3O4SPureza:97.46% - 99.82%Forma y color:SolidPeso molecular:429.88CM037
CAS:<p>CM037 (A-37) is a selective ALDH1A1 (acetaldehyde dehydrogenase 1A1) inhibitor (IC50; 4.6 µM) with antitumor activity and may be used in studies to eliminate</p>Fórmula:C21H25N3O3S2Pureza:99.34%Forma y color:SolidPeso molecular:431.57Dalvastatin
CAS:<p>Dalvastatin (RG-12561) is an orally available inhibitor of HMG-CoA reductase and cholesterol-lowering synthesis.Dalvastatin competitively inhibits rat hepatic</p>Fórmula:C24H31FO3Pureza:98.80%Forma y color:SolidPeso molecular:386.5IGP-1
CAS:<p>iGP-1 is a cell-permeable mitochondrial sn-Glycerol 3-phosphate dehydrogenase (mGPDH) inhibitor.</p>Fórmula:C17H15N3O3Pureza:99.12% - 99.15%Forma y color:SolidPeso molecular:309.32AICAR monophosphate
CAS:<p>AICAR monophosphate (Aica ribonucleotide) is a purine precursor with antineoplastic activity and can be used in studies about type 2 diabetes.</p>Fórmula:C9H15N4O8PPureza:99.8%Forma y color:SolidPeso molecular:338.21AZ3976
CAS:<p>AZ3976 is an inhibitor of PAI-1 with an IC50 of 16 μM in a plasma clot lysis assay. AZ3976 displays profibrinolytic activities.</p>Fórmula:C15H19N5O3Pureza:98.14%Forma y color:SolidPeso molecular:317.34Vatanidipine
CAS:<p>Vatanidipine (AE0047) is a novel dihydropyridine (DHP)-type calcium channel blocker with slow-onset pharmacological actions.A slow-onset and long-lasting</p>Fórmula:C41H42N4O6Pureza:99.95%Forma y color:SolidPeso molecular:686.8ALDH1A3-IN-2
CAS:<p>ALDH1A3-IN-2 is a potent ALDH1A3 inhibitor with an IC50 of 0.30 μM.ALDH1A3-IN-2 has potential for cancer disease research.</p>Fórmula:C13H17NOPureza:99.84%Forma y color:SolidPeso molecular:203.28CYP1B1-IN-4
CAS:<p>CYP1B1-IN-4: 2,4-diarylthiazole, selective CYP1B1 inhibitor (IC50=0.2 nM), low cytotoxicity, stable in liver microsomes.</p>Fórmula:C18H14N2O2SPureza:98.74%Forma y color:SolidPeso molecular:322.38S19-1035
<p>S19-1035: potent AKR1C3 inhibitor with 3.04 nM IC50, useful for tumor research.</p>Fórmula:C19H17ClN2O3Pureza:99.98%Forma y color:SoildPeso molecular:356.80Verofylline
CAS:<p>Verofylline (Verofyllinum) is an orally available, long-acting, multiacting, methylxanthine-substituted bronchodilator with inhibitory effects on PDE4 for the</p>Fórmula:C12H18N4O2Pureza:98.33% - 98.83%Forma y color:SolidPeso molecular:250.3Troriluzole
CAS:<p>Troriluzole is a glutamate modulator with anticancer activity and is used in the study of spinocerebellar ataxia.</p>Fórmula:C15H16F3N5O4SPureza:97.14%Forma y color:SolidPeso molecular:419.38Bupicomide
CAS:<p>Bupicomide is a dopamine β-hydroxylase inhibitor with antihypertensive and vasodilatory activity and may be used in the study of hypertension.</p>Fórmula:C10H14N2OPureza:99.84% - >99.99%Forma y color:SolidPeso molecular:178.23UCM05
CAS:<p>UCM05 is a potent FASN and FtsZ inhibitor active against HER2+ breast cancer and B. subtilis (MIC 100 μM), but not E. coli.</p>Fórmula:C24H16O10Pureza:99.25%Forma y color:SolidPeso molecular:464.38IDH2R140Q-IN-2
CAS:IDH2R140Q-IN-2 is an IDH2R140Q inhibitor indicated for the study of acute myeloid leukaemia (AML).Fórmula:C21H18F6N6OPureza:99.92%Forma y color:SolidPeso molecular:484.4Orellanine
CAS:<p>Orellanine, from Cortinarius orellanus, is nephrotoxic and hinders macromolecule synthesis in kidney cells and liver mitochondria.</p>Fórmula:C10H8N2O6Pureza:99.66%Forma y color:SolidPeso molecular:252.18sEH inhibitor-7
CAS:<p>sEH inhibitor-7 is a soluble epoxide hydrolase (sEH) inhibitor that inhibits sEH in human and mouse with IC 50 s of 6.2 μM and 0.15 μM, respectively.</p>Fórmula:C15H21NO2Pureza:99.56%Forma y color:SolidPeso molecular:247.33RPR107393 free base
CAS:<p>NVP-BAG956 (BAG956) is a PI3K/PDK inhibitor that inhibits PI3Kδ, and can be used to study melanoma.</p>Fórmula:C22H22N2OPureza:99.13% - 99.57%Forma y color:SolidPeso molecular:330.42Atibeprone
CAS:Atibeprone is a MAO-B inhibitor with antidepressant activity for the study of Parkinson's disease.Fórmula:C17H18N2O3SPureza:99.18% - 99.86%Forma y color:SolidPeso molecular:330.4PHGDH-IN-3
CAS:<p>PHGDH-IN-3, an oral PHGDH blocker with 2.8 μM IC50, may help in cancer research.</p>Fórmula:C24H18FN3O4S2Pureza:97.24% - 98.55%Forma y color:SolidPeso molecular:495.55EWP 815
CAS:<p>EWP 815, a disulfiram analog, inhibits Ins(1,4)P2, Ins(1,4,5)P3 phosphatases, and dopamine β-hydroxylase.</p>Fórmula:C12H22N4S4Pureza:98%Forma y color:SolidPeso molecular:350.59AGN 196996
CAS:<p>AGN 196996: strong RARα inhibitor (Ki: 2 nM), weak for RARβ/γ (Ki: 1087/8523 nM).</p>Fórmula:C24H20BrNO5Pureza:98.74%Forma y color:SolidPeso molecular:482.32MK-0873
CAS:<p>MK-0873 is a novel and potent selective phosphodiesterase 4 (PDE4) inhibitor.</p>Fórmula:C25H18N4O3Pureza:98.40%Forma y color:SolidPeso molecular:422.44NecroX-5
CAS:<p>NecroX-5, a derivative of NecroX, exhibits anti-inflammatory and anti-cancer activities. NecroX-5 reduces intracellular calcium concentration.</p>Fórmula:C27H39N3O9S3Pureza:99.944%Forma y color:SolidPeso molecular:645.81PDE IV-IN-1
CAS:<p>PDE IV-IN-1 is a potent phosphodiesterase 4 (PDE4) inhibitor with anti-inflammatory activity for the treatment of asthma, chronic obstructive pulmonary disease</p>Fórmula:C20H23ClN4O2Pureza:99.79%Forma y color:SolidPeso molecular:386.88uk-50001
CAS:<p>UK-50001 is a PDE4 inhibitor for treating inflammation, allergies, respiratory issues, and wounds.</p>Fórmula:C26H24F3N3O4Pureza:99.90%Forma y color:SolidPeso molecular:499.48NAAD sodium salt
CAS:<p>NAAD sodium salt (NAAD Na salt) is a substrate of nicotinamide adenine dinucleotide synthase and can be used in studies about the specificity and kinetics of</p>Fórmula:C21H25N6NaO15P2Pureza:98.6% - 99.87%Forma y color:SolidPeso molecular:686.4DS16570511
CAS:<p>DS16570511 is a novel, cell-permeable inhibitor targeting the mitochondrial calcium uniporter.</p>Fórmula:C30H25Cl2N3O4Pureza:98.34% - 98.45%Forma y color:SolidPeso molecular:562.44Tofimilast
CAS:<p>Tofimilast (CP-325366), a PDE4 inhibitor, is used potentially for the treatment of asthma and chronic obstructive pulmonary disease.</p>Fórmula:C18H21N5SPureza:99.55%Forma y color:SolidPeso molecular:339.46Tigulixostat
CAS:<p>Tigulixostat (LC350189) is a novel xanthine oxidase inhibitor (XOI) that reduces uric acid production and may be used to study gout-related diseases.</p>Fórmula:C16H14N4O2Pureza:98.22% - 99.71%Forma y color:SolidPeso molecular:294.31LY 517717
CAS:<p>LY 517717 is an orally active inhibitor of coagulation factor Xa with antithrombotic activity for the study of venous thromboembolism (VTE).</p>Fórmula:C27H33N5O2Pureza:99.77% - 99.88%Forma y color:SolidPeso molecular:459.58Isolithocholic Acid
CAS:<p>Isolithocholic Acid, a bile acid isomer, forms through microbial metabolism of Lithocholic acid or its 3α-sulfate.</p>Fórmula:C24H40O3Pureza:99.56% - 99.84%Forma y color:SolidPeso molecular:376.57MAO-B-IN-8
CAS:<p>MAO-B-IN-8 is a highly potent and reversible inhibitor of monoamine oxidase-B (MAO-B), which also exhibits inhibitory effects on the microglial production of</p>Fórmula:C18H16O6Pureza:99.62%Forma y color:SolidPeso molecular:328.32BMS 753
CAS:<p>BMS 753 is an agonist of isotype-selective retinoic acid receptor α (RARα, Ki= 2 nM).</p>Fórmula:C21H21NO4Pureza:98.55%Forma y color:SolidPeso molecular:351.4KLH45
CAS:<p>KLH45 is an effective and selective inhibitor of Spastic Paraplegia-Related Triglyceride Hydrolase DDHD2(IC50 = 1.3 nM).</p>Fórmula:C24H25F3N4O2Pureza:99.61%Forma y color:SolidPeso molecular:458.48AMG-1694
CAS:<p>AMG-1694 disrupts GK-GKRP complex, enhancing GK activity with 7 nM IC50; normalizes glucose in diabetic rodents without affecting normoglycemic animals.</p>Fórmula:C23H30F3N3O4S2Pureza:98.37%Forma y color:SolidPeso molecular:533.63PDE4B-IN-2
CAS:<p>PDE4B-IN-2 (A 33), an oral PDE4B inhibitor, IC50: 15 nM; less potent on PDE4D (IC50: 1.7 µM), has anti-inflammatory properties.</p>Fórmula:C19H18ClN3O2SPureza:99.32%Forma y color:SolidPeso molecular:387.88MM-433593
CAS:<p>MM-433593 is a selective fatty acid amide hydrolase (FAAH-1) inhibitor for the treatment of pain, inflammation, and other disorders.</p>Fórmula:C25H22ClN3O3Pureza:>99.99%Forma y color:SolidPeso molecular:447.91MY10
CAS:<p>MY10, a potent and orally active inhibitor of the receptor protein tyrosine phosphatase (RPTPβ/ζ), effectively reduces binge-like ethanol consumption and</p>Fórmula:C15H10F6OS2Pureza:98.64%Forma y color:SolidPeso molecular:384.36Ladostigil
CAS:<p>Ladostigil is an oral cholinesterase & MAO-B inhibitor used for depression and Alzheimer's studies.</p>Fórmula:C16H20N2O2Pureza:97.48%Forma y color:SolidPeso molecular:272.34Dovramilast
CAS:<p>Dovramilast (CC-11050) is a PDE4 inhibitor that reduces the production of pro-inflammatory mediators in lupus erythematosus.</p>Fórmula:C24H28N2O6SPureza:98.75% - 99.62%Forma y color:SolidPeso molecular:472.55Chloramphenicol succinate
CAS:<p>Chloramphenicol succinate is a bacteriostatic antibiotic. CPSA is a competitive substrate and inhibitor of succinate dehydrogenase (SDH),can be oxidized by.</p>Fórmula:C15H16Cl2N2O8Pureza:95.32%Forma y color:Physical Description White Powder (Ntp 1992)Peso molecular:423.2Pradefovir
CAS:<p>Pradefovir (Remofovir) is a prodrug for chronic HBV, converting to PMEA in the liver with a Km of 60 μM and clearance of 359 ml/min.</p>Fórmula:C17H19ClN5O4PPureza:97.50%Forma y color:SolidPeso molecular:423.79Aleplasinin
CAS:<p>Aleplasinin (PAZ 417) is a selective and orally active inhibitor of Plasminogen activator inhibitor-1(PAI-1) and a key negative regulator of the fibrinolytic</p>Fórmula:C28H27NO3Pureza:99.21%Forma y color:SolidPeso molecular:425.52Diproteverine HCl
CAS:<p>Diproteverine HCl is a novel calcium antagonist with antianginal properties, antispasmodic and vasoactive.</p>Fórmula:C26H36ClNO4Pureza:98.55% - 99.84%Forma y color:SolidPeso molecular:462.02Nampt activator-2
CAS:<p>Nampt activator-2: Potent NAMPT activator (EC50: 0.023 μM), binds CYP2C9 (0.060 μM), 2D6 (0.41 μM), 2C19 (0.59 μM); useful in metabolic disease research.</p>Fórmula:C17H15ClN4O3SPureza:98.30% - 98.33%Forma y color:SolidPeso molecular:390.84JNJ-42226314
CAS:<p>JNJ-42226314 is a MAGL inhibitor with anti-injury effects and has shown efficacy in neuropathic pain and inflammatory pain models.</p>Fórmula:C26H24FN5O2SPureza:99.62%Forma y color:SolidPeso molecular:489.56PKM2 activator 2
CAS:<p>PKM2 activator 2 is a pyruvate kinase M2 (PKM2) activator with an AC 50 value of 66 nM.PKM2 activator 2 has anti-tumor proliferative properties and attenuates</p>Fórmula:C20H18F2N2O4S2Pureza:99.92%Forma y color:SolidPeso molecular:452.495-LOX-IN-1
CAS:<p>5-LOX-IN-1 is a 5-Lipoxygenase (5-LOX) inhibitor (IC50: 2.3 μM).5-LOX-IN-1 can be used for cancer research.</p>Fórmula:C20H18N2O2SPureza:97.45%Forma y color:SolidPeso molecular:350.43Xanthine oxidoreductase-IN-5
CAS:<p>Xanthine oxidoreductase-IN-5: oral XOR inhibitor; IC50 55 nM; for acute hyperuricemia research.</p>Fórmula:C17H17N5O2Pureza:99.21%Forma y color:SolidPeso molecular:323.35Libenzapril
CAS:<p>Libenzapril (CGS 16617) is a potent angiotensin-converting enzyme inhibitor used to study myocardial injury.</p>Fórmula:C18H25N3O5Pureza:99.78%Forma y color:SolidPeso molecular:363.41Ch55
CAS:<p>Ch55, a potent HL60 cell differentiator (EC50=200nM), binds well to RAR-α/β, useful for cancer research.</p>Fórmula:C24H28O3Pureza:99.55%Forma y color:SolidPeso molecular:364.48JJKK 048
CAS:<p>JJKK 048 is a potent and selective MAGL inhibitor.</p>Fórmula:C23H22N4O5Pureza:99.77%Forma y color:SolidPeso molecular:434.44PKUMDL-WQ-2101
CAS:<p>PKUMDL-WQ-2101 is a selective allosteric inhibitor of phosphoglycerate dehydrogenase with anti-tumor activity.</p>Fórmula:C14H11N3O6Pureza:99.57%Forma y color:SolidPeso molecular:317.25CYP1B1-IN-5
CAS:<p>CYP1B1-IN-5: selective CYP1B1 inhibitor, IC50 = 4.7 nM, useful for metabolism disease research.</p>Fórmula:C14H8INO2Pureza:98.61%Forma y color:SolidPeso molecular:349.12hCAII-IN-9
CAS:<p>hCAII-IN-9 inhibits hCA II/IX/XII with IC50s of 1.18, 0.17, 2.99 μM; not BBB permeable.</p>Fórmula:C15H16ClN3O5S2Pureza:98.63%Forma y color:SolidPeso molecular:417.89JNJ-DGAT2-A
CAS:<p>JNJ-DGAT2-A, a specific inhibitor of DGAT2(IC50 = 0.14 μM), can be used in studies about the synthesis of triglycerides.</p>Fórmula:C24H16BrFN4O2SPureza:98.3%Forma y color:SolidPeso molecular:523.38AZD-0284
CAS:<p>AZD-0284 is an inverse agonist of the nuclear receptor RORγ. In development for the treatment of plaque psoriasis vulgaris and respiratory tract disorders[1].</p>Fórmula:C21H18F6N2O5SPureza:99.82%Forma y color:SolidPeso molecular:524.43YM 511
CAS:<p>YM 511 is a specific non-steroidal aromatase inhibitor with IC50s of 0.4 and 0.12 nM, minimally affecting other steroids.</p>Fórmula:C16H12BrN5Pureza:99.965%Forma y color:SolidPeso molecular:354.2KT182
CAS:<p>KT182 is a selective and potent inhibitor of α/β-hydrolase domain containing 6 (ABHD6), with an IC50 of 0.24 nM in Neuro2A cells.</p>Fórmula:C27H26N4O2Pureza:99.66%Forma y color:SolidPeso molecular:438.52PF-04447943
CAS:<p>PF-04447943, a selective PDE9A inhibitor (IC50=12nM), may aid sickle cell anemia research with its anti-inflammatory properties.</p>Fórmula:C20H25N7O2Pureza:99.36% - 99.59%Forma y color:SolidPeso molecular:395.46AWD 12-281
CAS:<p>AWD 12-281 is a PDE4 inhibitor with anti-inflammatory activity and bronchodilator activity for the study of chronic obstructive pulmonary disease (COPD).</p>Fórmula:C22H14Cl2FN3O3Pureza:99.25% - 99.85%Forma y color:SolidPeso molecular:458.27G6PD activator AG1
CAS:<p>G6PD activator AG1 is a G6PD agonist that promotes G6PD oligomerization to a catalytically competent form.</p>Fórmula:C24H30N4S2Pureza:98.38% - 99.51%Forma y color:SolidPeso molecular:438.65IMPDH2-IN-2
CAS:<p>IMPDH2-IN-2 is an IMPDH inhibitor with antimicrobial activity and potential anti-tuberculosis activity for the study of inflammation and immune dysfunction.</p>Fórmula:C21H15Cl2N3O3Pureza:99.02%Forma y color:SolidPeso molecular:428.27Rbin-2
CAS:Rbin-2: Potent, selective Midasin inhibitor; reversible, cell-permeable; halts eukaryotic ribosome assembly.Fórmula:C13H11BrN4SPureza:98.65%Forma y color:SolidPeso molecular:335.22
