Metabolism
Metabolism inhibitors are compounds that interfere with metabolic pathways, altering the production and utilization of energy within cells. These inhibitors are used to study the regulation of metabolism, the role of metabolic pathways in diseases like cancer and diabetes, and to develop new therapeutic strategies. Metabolism inhibitors can target various enzymes and processes involved in glycolysis, fatty acid oxidation, and other metabolic functions. At CymitQuimica, we offer a wide range of high-quality metabolism inhibitors to support your research in biochemistry, metabolic disorders, and drug development.
Subcategories of "Metabolism"
- AhR(41 products)
- Aminopeptidase(67 products)
- CETP(18 products)
- Carbonic Anhydrase(178 products)
- Casein Kinase(130 products)
- DHFR(33 products)
- Decarboxylase(4 products)
- Dehydrogenase(270 products)
- FAAH(64 products)
- FXR(58 products)
- Factor Xa(80 products)
- Fatty Acid Synthase(33 products)
- Ferroptosis(215 products)
- GR(3 products)
- GSNOR(3 products)
- Glucokinase(54 products)
- HIF/HIF Prolyl-Hydroxylase(142 products)
- HMG-CoA Reductase(33 products)
- Hydroxylase(30 products)
- IDO(82 products)
- LDL(8 products)
- Lipase(97 products)
- Lipid(59 products)
- Lipoxygenase(125 products)
- MAO(87 products)
- MPO(2 products)
- NAMPT(36 products)
- P450(6 products)
- PAI-1(25 products)
- PDE(166 products)
- PED(1 products)
- PKM(15 products)
- PPAR(164 products)
- Phospholipase(82 products)
- ROR(42 products)
- Retinoid Receptor(29 products)
- SGK(11 products)
- Thioredoxin(12 products)
- Transferase(30 products)
- Transporter(42 products)
- UGT(4 products)
- Xanthine Oxidase (XO) Inhibitors(9 products)
Show 34 more subcategories
Found 8625 products of "Metabolism"
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Anserinone B
CAS:<p>Anserinone B: Antifungal, antibacterial; inhibits S.fimicola (50%), A. furfuraceus (37%); cytotoxic to human tumor cells (GI50=4.4 µg/mL).</p>Formula:C11H14O4Color and Shape:SolidMolecular weight:210.23Safrazine Hydrochloride
CAS:<p>Safrazine Hydrochloride is a monoamine oxidase inhibitor (MOI) that is irreversible.</p>Formula:C11H17ClN2O2Color and Shape:SolidMolecular weight:244.718ABT-418
CAS:<p>ABT-418, a nicotinic acetylcholine receptor (nAchR) agonist, is used potentially for the treatment of attention deficit disorder.</p>Formula:C9H14N2OColor and Shape:SolidMolecular weight:166.22ALRT 1550
CAS:<p>ALRT 1550, a retinoic acid agent (RAR) agonist, is used potentially for the treatment of cervical carcinoma.</p>Formula:C23H32O2Color and Shape:SolidMolecular weight:340.5Esuprone
CAS:<p>Esuprone (LU-43839) is a novel reversible and highly selective MAO-A inhibitor with anticonvulsant activity for the treatment of depression.</p>Formula:C13H14O5SPurity:99.45%Color and Shape:SolidMolecular weight:282.31Tigulixostat
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>Formula:C16H14N4O2Purity:98.22% - 99.71%Color and Shape:SolidMolecular weight:294.31Acetyl-L-carnitine
CAS:<p>Acetyl-L-carnitine, an amino-acid supplement, crosses the blood-brain barrier to aid in neuroinflammation and Alzheimer's.</p>Formula:C9H17NO4Purity:>99.99%Color and Shape:SolidMolecular weight:203.24AM 374
CAS:<p>AM 374 (HDSF), a fatty acid amide hydrolase (FAAH) inhibitor, demonstrates the capacity to inhibit amidase activity, boasting an IC50 value of 13 nM.</p>Formula:C16H33FO2SPurity:98.39%Color and Shape:SolidMolecular weight:308.5NG-497
CAS:<p>NG-497, a selective inhibitor of human ATGL, blocks lipolysis in adipocytes and aids cancer research.</p>Formula:C18H21NO4Purity:99.56%Color and Shape:SolidMolecular weight:315.36Troriluzole
CAS:<p>Troriluzole is a glutamate modulator with anticancer activity and is used in the study of spinocerebellar ataxia.</p>Formula:C15H16F3N5O4SPurity:97.14%Color and Shape:SolidMolecular weight:419.38S-2474
CAS:<p>S-2474, an inhibitor of COX-2 and 5-lipoxygenase, has anti-inflammatory and neuroprotective activities, and inhibits cell death.</p>Formula:C20H31NO3SPurity:99.03%Color and Shape:SolidMolecular weight:365.53IGP-1
CAS:<p>iGP-1 is a cell-permeable mitochondrial sn-Glycerol 3-phosphate dehydrogenase (mGPDH) inhibitor.</p>Formula:C17H15N3O3Purity:99.12% - 99.15%Color and Shape:SolidMolecular weight:309.32Sultiame
CAS:<p>Sultiame is an inhibitor of carbonic anhydrase. Sultiame can be used in antiepileptic research.</p>Formula:C10H14N2O4S2Purity:99.91%Color and Shape:SolidMolecular weight:290.36MFI8
CAS:<p>MFI8 is a compound that regulates mitochondrial fission and can be used to study aging.</p>Formula:C16H18ClNOPurity:99.08% - 99.78%Color and Shape:SolidMolecular weight:275.77GAC0003A4
CAS:<p>GAC0003A4 is an LXR inverse agonist with antitumor activity for the study of advanced pancreatic cancer and other recalcitrant malignancies.</p>Formula:C20H24N2O3Purity:98.41%Color and Shape:SolidMolecular weight:340.42Isomazole
CAS:<p>Isomazole is a novel orally available phosphodiesterase (PDE) inhibitor with calcium-sensitizing properties that inhibits PDE3 and PDE4.</p>Formula:C14H13N3O2SPurity:98.66%Color and Shape:SolidMolecular weight:287.34Malic enzyme inhibitor ME1
CAS:<p>Malic enzyme inhibitor ME1 (ME1) is a specific inhibitor of Malic enzyme (IC50 = 0.15 μM). Malic enzyme inhibitor ME1 reduces cell viability/metabolic activity.</p>Formula:C20H21N3O3Purity:99.84%Color and Shape:SolidMolecular weight:351.4Autotaxin-IN-3
CAS:<p>Autotaxin-IN-3 is an inhibitor of Autotaxin (IC50 = 2.4 nM) which is responsible for the increase in lysophosphatidic acid in ascites and plasma.</p>Formula:C22H21N9O2Purity:99.54% - 99.79%Color and Shape:SolidMolecular weight:443.46BPDA2
CAS:<p>BPDA2 selectively inhibits SHP2 (IC50=92nM) over SHP1/1B (33.39/40.71μM), curbs RTKs, and hampers SHP2-driven breast cancer cell traits.</p>Formula:C24H30O5Purity:99.80%Color and Shape:SolidMolecular weight:398.49Lonapalene
CAS:<p>Lonapalene is a topically effective inhibitor of 5-lipoxygenase.</p>Formula:C16H15ClO6Purity:98.67% - 99.33%Color and Shape:SolidMolecular weight:338.74ALDH1A3-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>Formula:C13H17NOPurity:99.84%Color and Shape:SolidMolecular weight:203.28Luciferase-IN-1
CAS:<p>Luciferase-IN-1 is a luciferase inhibitor that can be used to study bacterial and fungal infections.</p>Formula:C15H14N2SPurity:97.84%Color and Shape:SolidMolecular weight:254.35YM 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>Formula:C16H12BrN5Purity:99.965%Color and Shape:SolidMolecular weight:354.2Bupicomide
CAS:<p>Bupicomide is a dopamine β-hydroxylase inhibitor with antihypertensive and vasodilatory activity and may be used in the study of hypertension.</p>Formula:C10H14N2OPurity:99.84% - >99.99%Color and Shape:SolidMolecular weight:178.23Clopimozide
CAS:<p>Clopimozide (R-29764), a long-acting oral antischizophrenic, blocks calcium channels and [3H] nilandipine binding.</p>Formula:C28H28ClF2N3OPurity:98.19% - >99.99%Color and Shape:SolidMolecular weight:495.99Crobenetine
CAS:<p>Crobenetine (BIII 890 CL) Free Base is a selective NaV channel blocker that eliminates VTD-induced [Ca2+] elevation.</p>Formula:C25H33NO2Purity:98.99%Color and Shape:SolidMolecular weight:379.54RPR107393 free base
CAS:<p>NVP-BAG956 (BAG956) is a PI3K/PDK inhibitor that inhibits PI3Kδ, and can be used to study melanoma.</p>Formula:C22H22N2OPurity:99.13% - 99.57%Color and Shape:SolidMolecular weight:330.42IDH2R140Q-IN-2
CAS:<p>IDH2R140Q-IN-2 is an IDH2R140Q inhibitor indicated for the study of acute myeloid leukaemia (AML).</p>Formula:C21H18F6N6OPurity:99.92%Color and Shape:SolidMolecular weight:484.4KT182
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>Formula:C27H26N4O2Purity:99.66%Color and Shape:SolidMolecular weight:438.52AZ3976
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>Formula:C15H19N5O3Purity:98.14%Color and Shape:SolidMolecular weight:317.34uk-50001
CAS:<p>UK-50001 is a PDE4 inhibitor for treating inflammation, allergies, respiratory issues, and wounds.</p>Formula:C26H24F3N3O4Purity:99.90%Color and Shape:SolidMolecular weight:499.48Salnacedin
CAS:<p>Salnacedin (G-201) treats immune, skin, and musculoskeletal issues, suitable for acne, dermatitis, and psoriasis research.</p>Formula:C12H13NO5SPurity:99.13%Color and Shape:SolidMolecular weight:283.3Lecimibide
CAS:<p>Lecimibide (DuP 128) is a potent and selective inhibitor of acyl coenzyme A: cholesterol acyltransferase (ACAT), which can be used to study diseases due to high</p>Formula:C34H40F2N4OSPurity:99.44% - 99.87%Color and Shape:SolidMolecular weight:590.77CERM-11956
CAS:<p>Pelretin (BASF 43915) is a potential protein inhibitor for the study of dermatologic diseases.</p>Formula:C29H38N2O7Purity:99.38%Color and Shape:SolidMolecular weight:526.62Vatanidipine
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>Formula:C41H42N4O6Purity:99.95%Color and Shape:SolidMolecular weight:686.8Zifaxaban
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>Formula:C20H16ClN3O4SPurity:97.46% - 99.82%Color and Shape:SolidMolecular weight:429.88IHVR-17028
CAS:<p>IHVR-17028 is a potent broad-spectrum ERα-glucosidase I (α-glucosidase? I) inhibitor with IC50 of 0.24 μM and antiviral activity.</p>Formula:C23H44N2O5Purity:97.90%Color and Shape:SolidMolecular weight:428.61UCM05
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>Formula:C24H16O10Purity:99.25%Color and Shape:SolidMolecular weight:464.38HTS07545
CAS:<p>HTS07545, an SQOR inhibitor (IC50: 30nM), slows H2S breakdown, researched for heart failure.</p>Formula:C22H18N2O3Purity:99.71%Color and Shape:SolidMolecular weight:358.39PBRM
CAS:<p>PBRM (17β-HSD1-IN-2) is a selective covalent inhibitor of 17β-HSD1, used in breast cancer and endometriosis research.</p>Formula:C28H34BrNO2Purity:99.56% - 99.59%Color and Shape:SolidMolecular weight:496.48Verofylline
CAS:<p>Verofylline (Verofyllinum) is an orally available, long-acting, multiacting, methylxanthine-substituted bronchodilator with inhibitory effects on PDE4 for the</p>Formula:C12H18N4O2Purity:98.33% - 98.83%Color and Shape:SolidMolecular weight:250.3KLH45
CAS:<p>KLH45 is an effective and selective inhibitor of Spastic Paraplegia-Related Triglyceride Hydrolase DDHD2(IC50 = 1.3 nM).</p>Formula:C24H25F3N4O2Purity:99.61%Color and Shape:SolidMolecular weight:458.48VU0155069
CAS:<p>VU0155069, a selective PLD1 inhibitor (IC50: 46 nM), halts cancer cell migration in transwell assays.</p>Formula:C26H27ClN4O2Purity:99.5%Color and Shape:SolidMolecular weight:462.97NCGC 607
CAS:<p>NCGC 607 is a a noninhibitory chaperone of glucocerebrosidase (GCase).</p>Formula:C24H22IN3O4Purity:99.69%Color and Shape:SolidMolecular weight:543.35PD173212
CAS:<p>PD 173212 is a blocker that blocks N-type voltage sensitive calcium channel (Cav2.2).</p>Formula:C38H53N3O3Purity:99.84%Color and Shape:SolidMolecular weight:599.85LDL-IN-3
CAS:<p>LDL-IN-3 shows anti-atherosclerotic and antioxidant activities.</p>Formula:C24H36O3SiPurity:99.75%Color and Shape:SolidMolecular weight:400.63Rbin-2
CAS:<p>Rbin-2: Potent, selective Midasin inhibitor; reversible, cell-permeable; halts eukaryotic ribosome assembly.</p>Formula:C13H11BrN4SPurity:98.75%Color and Shape:SolidMolecular weight:335.22Edoxaban
CAS:<p>Edoxaban: potent, selective FXa inhibitor; Ki 0.561 nM. Used as an oral anticoagulant for stroke prevention, also inhibits thrombin and FIXa.</p>Formula:C24H30ClN7O4SPurity:97.67% - 99.71%Color and Shape:SolidMolecular weight:548.06Izonsteride
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>Formula:C24H26N2OS2Purity:99.55%Color and Shape:SolidMolecular weight:422.61Xanthine oxidoreductase-IN-5
CAS:<p>Xanthine oxidoreductase-IN-5: oral XOR inhibitor; IC50 55 nM; for acute hyperuricemia research.</p>Formula:C17H17N5O2Purity:99.21%Color and Shape:SolidMolecular weight:323.35alphaSYN-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>Formula:C23H20ClN3OPurity:98.49%Color and Shape:SolidMolecular weight:389.88NAAD 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>Formula:C21H25N6NaO15P2Purity:98.6% - 99.87%Color and Shape:SolidMolecular weight:686.4BAY-0069
CAS:<p>BAY-0069 is a potent and selective PPARγ transactivator that inhibits human PPARγ and murine PPARγ with IC50s of 6.3 nM and 24 nM, respectively.BAY-0069 can be</p>Formula:C22H16BrN3O4Purity:99.41%Color and Shape:SoildMolecular weight:466.28Nanterinone
CAS:<p>Nanterinone: oral phosphodiesterase inhibitor, improves acute heart failure hemodynamics.</p>Formula:C15H15N3OPurity:99.53%Color and Shape:SolidMolecular weight:253.3NNC 05-2090 hydrochloride
CAS:<p>NNC 05-2090 HCl: BGT-1 inhibitor, IC50 = 10.6 μM, potential for epilepsy, neurological research.</p>Formula:C27H31ClN2O2Purity:99.05%Color and Shape:SolidMolecular weight:451AChE/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>Formula:C20H24N2O2Purity:98.17%Color and Shape:SolidMolecular weight:324.42Lifarizine
CAS:<p>Lifarizine (RS-87476), a calcium-sodium channel antagonist, shows neuroprotective activity in a simplified rat survival model of double vessel occlusion.</p>Formula:C29H32N4Purity:99.88%Color and Shape:SolidMolecular weight:436.59PDE 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>Formula:C20H23ClN4O2Purity:99.79%Color and Shape:SolidMolecular weight:386.88PC945
CAS:<p>PC945 (Opelconazole) is an antifungal compound that inhibits CYP51A/CYP51B and can be used to study fungal infections of the lungs.</p>Formula:C38H37F3N6O3Purity:98.89% - 99.37%Color and Shape:SolidMolecular weight:682.73PTP1B-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>Formula:C12H7BrF2NO3PPurity:99.31% - 99.97%Color and Shape:SolidMolecular weight:362.06IPN60090
CAS:<p>IPN60090: potent oral GLS1 inhibitor, IC50 of 31 nM, potential for anticancer and immunomodulation.</p>Formula:C24H27F3N8O3Purity:99.76%Color and Shape:SolidMolecular weight:532.52GSK205
CAS:<p>GSK205 is a selective TRPV4 antagonist (IC50: 4.19 μM) for inhibiting TRPV4-mediated Ca2+ influx.</p>Formula:C24H25BrN4SPurity:99.46%Color and Shape:SolidMolecular weight:481.45SBI-425
CAS:<p>SBI-425: orally available TNAP inhibitor, enhances cardiovascular health & survival, no bone impact.</p>Formula:C13H12ClN3O4SPurity:99.88%Color and Shape:SolidMolecular weight:341.77Phosphatase-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>Formula:C16H16Cl2FNO2Purity:99.88%Color and Shape:SolidMolecular weight:344.21Tiapamil 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>Formula:C26H38ClNO8S2Purity:99.17%Color and Shape:SolidMolecular weight:592.16SERCA2a activator 1
CAS:<p>SERCA2a activator 1 boosts heart function by reducing phospholamban restraint and enhancing cardiac contraction-relaxation cycles.</p>Formula:C32H29N3O4SPurity:99.75%Color and Shape:SolidMolecular weight:551.66AZD-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>Formula:C21H18F6N2O5SPurity:99.82%Color and Shape:SolidMolecular weight:524.43CM037
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>Formula:C21H25N3O3S2Purity:99.34%Color and Shape:SolidMolecular weight:431.574-Hydroxymephenytoin
CAS:<p>4-Hydroxymephenytoin ((+/-)-4'-Hydroxymephenytoin) is the metabolism of an antiepileptic drug mephenytoin. Mephenytoin is used as a CYP2C19 substrate.</p>Formula:C12H14N2O3Purity:99.78%Color and Shape:SolidMolecular weight:234.25MLS000544460
CAS:<p>MLS000544460 is a highly selective and reversible Eya2 phosphatase inhibitor (Kd: 2.0 μM, IC50: 4 μM).MLS000544460 exhibits inhibitory effects on Eya2</p>Formula:C17H12FN3O2SPurity:99.72%Color and Shape:SolidMolecular weight:341.36Fenoverine
CAS:<p>Fenoverine (Spasmopriv) has antispasmodic activity and can be used to study gastrointestinal spasms.</p>Formula:C26H25N3O3SPurity:98.34%Color and Shape:SolidMolecular weight:459.56PDE4B-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>Formula:C19H18ClN3O2SPurity:99.32%Color and Shape:SolidMolecular weight:387.88Clozic
CAS:<p>Clozic (ICI 55897) exhibits reversible anti-proliferative effects and can be used in studies about serving as a potential anti-arthritic agent.</p>Formula:C17H17ClO3Purity:99.95%Color and Shape:SolidMolecular weight:304.77Xanthine 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>Formula:C14H10ClN5OPurity:98.1%Color and Shape:SolidMolecular weight:299.72CYP1B1-IN-4
CAS:<p>CYP1B1-IN-4: 2,4-diarylthiazole, selective CYP1B1 inhibitor (IC50=0.2 nM), low cytotoxicity, stable in liver microsomes.</p>Formula:C18H14N2O2SPurity:98.74%Color and Shape:SolidMolecular weight:322.38CYP1B1-IN-5
CAS:<p>CYP1B1-IN-5: selective CYP1B1 inhibitor, IC50 = 4.7 nM, useful for metabolism disease research.</p>Formula:C14H8INO2Purity:98.61%Color and Shape:SolidMolecular weight:349.12Atibeprone
CAS:<p>Atibeprone is a MAO-B inhibitor with antidepressant activity for the study of Parkinson's disease.</p>Formula:C17H18N2O3SPurity:99.18% - 99.86%Color and Shape:SolidMolecular weight:330.4PHGDH-IN-3
CAS:<p>PHGDH-IN-3, an oral PHGDH blocker with 2.8 μM IC50, may help in cancer research.</p>Formula:C24H18FN3O4S2Purity:97.24% - 98.55%Color and Shape:SolidMolecular weight: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>Formula:C12H22N4S4Purity:98%Color and Shape:SolidMolecular weight:350.59PKUMDL-WQ-2101
CAS:<p>PKUMDL-WQ-2101 is a selective allosteric inhibitor of phosphoglycerate dehydrogenase with anti-tumor activity.</p>Formula:C14H11N3O6Purity:99.57%Color and Shape:SolidMolecular weight:317.25MK-0873
CAS:<p>MK-0873 is a novel and potent selective phosphodiesterase 4 (PDE4) inhibitor.</p>Formula:C25H18N4O3Purity:98.40%Color and Shape:SolidMolecular weight:422.44Tamolarizine
CAS:<p>Tamolarizine (Tamolarizine free base) free base is a novel calcium antagonist.</p>Formula:C27H32N2O3Purity:98.17%Color and Shape:SoildMolecular weight:432.55MM 11253
CAS:<p>MM 11253 is a RARγ antagonist with IC50 of 44nM.</p>Formula:C28H30O2S2Purity:99.41%Color and Shape:SolidMolecular weight:462.67ML 209
CAS:<p>ML-209 is an antagonist of retinoic acid receptor-related orphan receptor γt (RORγt; IC50= 1.1 μM in a reporter assay).1It inhibits RORγt-induced transcription</p>Formula:C25H31NO6Purity:99.87%Color and Shape:SolidMolecular weight:441.52NecroX-5
CAS:<p>NecroX-5, a derivative of NecroX, exhibits anti-inflammatory and anti-cancer activities. NecroX-5 reduces intracellular calcium concentration.</p>Formula:C27H39N3O9S3Purity:99.944%Color and Shape:SolidMolecular weight:645.81PF-04447943
CAS:<p>PF-04447943, a selective PDE9A inhibitor (IC50=12nM), may aid sickle cell anemia research with its anti-inflammatory properties.</p>Formula:C20H25N7O2Purity:99.36% - 99.59%Color and Shape:SolidMolecular weight:395.46KRH102140
CAS:<p>KRH102140 is a PHD2 activator that reduces angiogenesis by inhibiting HIF-1alpha, used in cardiovascular disease research.</p>Formula:C25H24FNOPurity:98.31% - 99.61%Color and Shape:SolidMolecular weight:373.46Isolithocholic Acid
CAS:<p>Isolithocholic Acid, a bile acid isomer, forms through microbial metabolism of Lithocholic acid or its 3α-sulfate.</p>Formula:C24H40O3Purity:99.56% - 99.84%Color and Shape:SolidMolecular weight:376.57Cholesterol 24-hydroxylase-IN-1
CAS:<p>Cholesterol 24-hydroxylase-IN-1 is a cholesterol 24-hydroxylase (CH24H or CYP46A1) inhibitor used in the study of neurological disorders such as epilepsy.</p>Formula:C17H23N5OPurity:98.42%Color and Shape:SolidMolecular weight:313.40AMG-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>Formula:C23H30F3N3O4S2Purity:98.37%Color and Shape:SolidMolecular weight:533.63JNJ-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>Formula:C26H24FN5O2SPurity:99.62%Color and Shape:SolidMolecular weight:489.56AC-261066
CAS:<p>AC-261066 is an orally available and isoform-selective agonist of RARβ2 with a pEC50 of 8.0.</p>Formula:C17H20FNO4SPurity:99.64%Color and Shape:SolidMolecular weight:353.41Chloramphenicol 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>Formula:C15H16Cl2N2O8Purity:95.32%Color and Shape:Physical Description White Powder (Ntp 1992)Molecular weight:423.2Dasantafil
CAS:<p>Dasantafil (SCH446132) is a small molecule phosphodiesterase-5A (PDE5A) inhibitor used to treat genitourinary disorders and study erectile dysfunction.</p>Formula:C22H28BrN5O5Purity:99.4% - 99.50%Color and Shape:SolidMolecular weight:522.39Pradefovir
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>Formula:C17H19ClN5O4PPurity:97.50%Color and Shape:SolidMolecular weight:423.79Lifibrol
CAS:<p>Lifibrol (U-83860) is an inhibitor of cholesterol synthesis.Lifibrol has anticholesterol and hypolipidemic properties and promotes the conversion of LDL Apo B-</p>Formula:C21H26O4Purity:99.96%Color and Shape:SolidMolecular weight:342.43Diproteverine HCl
CAS:<p>Diproteverine HCl is a novel calcium antagonist with antianginal properties, antispasmodic and vasoactive.</p>Formula:C26H36ClNO4Purity:98.55% - 99.84%Color and Shape:SolidMolecular weight:462.02Orellanine
CAS:<p>Orellanine, from Cortinarius orellanus, is nephrotoxic and hinders macromolecule synthesis in kidney cells and liver mitochondria.</p>Formula:C10H8N2O6Purity:99.66%Color and Shape:SolidMolecular weight:252.18PKUMDL-LC-101-D04
CAS:<p>PKUMDL-LC-101-D04 enhances GPX4, curbs iron death, boosts enzyme activity 150% at 20 μM, effective in wild-type MEF, reduces lipid peroxide toxicity.</p>Formula:C14H23ClN4O2S2Purity:98.71%Color and Shape:SolidMolecular weight:378.94AWD 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>Formula:C22H14Cl2FN3O3Purity:99.25% - 99.85%Color and Shape:SolidMolecular weight:458.27
