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(269 products)
- FAAH(64 products)
- FXR(58 products)
- Factor Xa(80 products)
- Fatty Acid Synthase(32 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(124 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)
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Found 8626 products of "Metabolism"
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Anticancer agent 70
CAS:<p>Compound 21 is a powerful anticancer agent with cytotoxicity against various cancers, causing cell cycle arrest and affecting p53/p21 levels and mitochondria.</p>Formula:C13H9Cl2N3O2SColor and Shape:SolidMolecular weight:342.2PGMI-004A
CAS:<p>PGMI-004A is an effective inhibitor of phosphoglycerate mutase 1 (IC50: 13.1 μM).</p>Formula:C21H12F3NO6SPurity:98%Color and Shape:SolidMolecular weight:463.38Rev 6207
CAS:<p>Rev 6207 is a non-sulfhydryl ACE-inhibitor.</p>Formula:C21H31N3O5Color and Shape:SolidMolecular weight:405.49PGAM1-IN-1
CAS:<p>PGAM1-IN-1 is an inhibitor of phosphoglycerate mutase 1 ( PGAM1 ) with an IC 50 of 6.4 μM [1].</p>Formula:C19H11ClFNO6SPurity:98%Color and Shape:SolidMolecular weight:435.81MIPS1455
CAS:<p>MIPS1455 is a photoactivatable allosteric M1 muscarinic acetylcholine receptor ligand.</p>Formula:C24H17NO4Purity:98%Color and Shape:SolidMolecular weight:383.4Eprozinol dihydrochloride
CAS:<p>Eprozinol dihydrochloride has anti-bronchoconstrictive activity.</p>Formula:C22H31ClN2O2Color and Shape:SolidMolecular weight:390.95Arabinose 1,5-diphosphate
CAS:<p>Arabinose 1,5-diphosphate is a bisphosphatase inhibitor.</p>Formula:C5H12O11P2Color and Shape:SolidMolecular weight:310.09AJS1669
CAS:<p>AJS1669, an activator of muscle glycogen synthase, improves glucose metabolism and reduces body fat mass in mice.</p>Formula:C26H21F2NO6SColor and Shape:SolidMolecular weight:513.51Cholesteryl Palmitoleate
CAS:<p>Cholesteryl palmitoleate, a cholesterol ester, exhibits elevated plasma levels in ApoE-/- mice following exposure to cigarette smoke and in pediatric patients diagnosed with biliary atresia. It serves as a standard for identifying cholesterol esters in human meibomian gland secretions.</p>Formula:C43H74O2Color and Shape:SolidMolecular weight:623.1Albifylline
CAS:<p>Albifylline: a xanthine derivative, anti-asthmatic, reduces leukocyte adhesion, enhances liver microcirculation post-hemorrhagic shock.</p>Formula:C13H20N4O3Color and Shape:SolidMolecular weight:280.32AHR-activator-1023
CAS:<p>AHR-activator-1023 is the aryl hydrocarbon receptor activator. It is also a specific FGF2-induced branching morphogenesis modulator.</p>Formula:C14H8Cl2N2OColor and Shape:SolidMolecular weight:291.13AHR-15010
CAS:<p>AHR-15010 is a novel anti-arthritic agent.</p>Formula:C10H16N2O8S2Purity:98%Color and Shape:SolidMolecular weight:356.37K103 Hydrochloride
CAS:<p>K103 Hydrochloride, an inhibitor of peptidoglycan synthesis, targets the lipid II precursor.</p>Formula:C19H22Cl2N2SPurity:98%Color and Shape:SolidMolecular weight:381.36MK-0952
CAS:<p>MK-0952 treats memory loss and cognitive issues; it's a potent, selective PDE4 inhibitor with restricted blood activity.</p>Formula:C28H22FN3O4Color and Shape:SolidMolecular weight:483.492-Methyldecanenitrile
CAS:<p>2-Methyldecanenitrile, intense peach scent with lactone notes, stable in all pH, effective at low concentration.</p>Formula:C11H21NPurity:98%Color and Shape:Colourless Liquid LiquidMolecular weight:167.29AZD8329
CAS:<p>AZD8329 is an 11β-HSD1 inhibitor that inhibits 11β-HSD2, 17β-HSD1, 17β-HSD3, and can be used to study allergic reactions in humans.</p>Formula:C25H31N3O3Purity:99.31%Color and Shape:SolidMolecular weight:421.53GSK 264220A
CAS:<p>endothelial lipase and lipoprotein lipase inhibitor</p>Formula:C17H21N3O4SPurity:98%Color and Shape:SolidMolecular weight:363.43Levophencynonate HCl
CAS:<p>Levophencynonate HCl is a muscarinic receptor antagonist.</p>Formula:C22H32ClNO3Purity:98%Color and Shape:SolidMolecular weight:393.95Z-321
CAS:<p>Z-321 is an inhibitor of prolyl endopeptidase.</p>Formula:C19H24N2O2SPurity:98%Color and Shape:SolidMolecular weight:344.47DU717
CAS:<p>DU717 is an antihypertensive agent.</p>Formula:C12H15ClN4O2SPurity:99.64%Color and Shape:SolidMolecular weight:314.793-Oxo-hop-22(29)-ene
CAS:<p>3-Oxo-hop-22(29)-ene inhibits yeast α-glucosidase, moderately affects T. cruzi and L. mexicana, and has slight anti-inflammatory activity.</p>Formula:C30H48OColor and Shape:SolidMolecular weight:424.7LEO 39652
CAS:<p>LEO 39652: Dual-soft PDE4 inhibitor, IC50s: PDE4A/B: 1.2 nM, PDE4C: 3.0 nM, PDE4D: 3.8 nM; TNF-α IC50: 6.0 nM; for Atopic dermatitis research.</p>Formula:C23H23N3O5Color and Shape:SolidMolecular weight:421.45CGP-28014
CAS:<p>CGP-28014 inhibits COMT, boosts renal dopamine & DOPAC excretion, lowers HVA, no effect on renal sodium.</p>Formula:C12H19N3OColor and Shape:SolidMolecular weight:221.3ME-143
CAS:<p>ME-143, a 2nd-gen NADH oxidase inhibitor, blocks WNT/β-catenin pathway, active against various cancers in vitro/vivo.</p>Formula:C21H18O4Color and Shape:SolidMolecular weight:334.37AMPD2 inhibitor 2
<p>AMPD2 inhibitor 2: strong h/mAMPD2 blocker, IC50s: 0.1/0.28μM. Potentially assesses AMPD2's role in high-fat diet mice.</p>Formula:C26H27F2N3O3Color and Shape:SolidMolecular weight:467.5111β-HSD1-IN-9
CAS:<p>11β-HSD1-IN-9 is a potent inhibitor of 11β-HSD1, displaying IC50 values of 0.48 µM for human and 1.3 µM for murine variants, respectively.</p>Formula:C13H9F3N2OColor and Shape:SolidMolecular weight:266.22CL 242817
CAS:<p>CL 242817 is an inhibitor of angiotensin converting enzyme (ACE).</p>Formula:C18H21NO5SColor and Shape:SolidMolecular weight:363.43Nampt-IN-7
CAS:<p>Nampt-IN-7 (GF8) inhibits NAMPT (IC50: 7.31 μM) and kills HepG2 cells (IC50: 24.28 μM).</p>Formula:C20H21N5O3Color and Shape:SolidMolecular weight:379.41DGAT1-IN-3
CAS:<p>DGAT1-IN-3: a potent, selective DGAT-1 inhibitor (IC50: 38 nM human, 120 nM rat), oral, for obesity and dyslipidemia research.</p>Formula:C20H19F3N4O3Color and Shape:SolidMolecular weight:420.3914(S)-HDHA
CAS:<p>DHA is an ω-3 important for development and therapy for inflammation and cancer; its derivative, 14(S)-HDHA, aids in reducing inflammation.</p>Formula:C22H32O3Color and Shape:SolidMolecular weight:344.49Camylofin Hydrochloride
CAS:<p>Camylofin HCl is an antispasmodic used in labor treatment and is also used to deliver drug therapy for ulcerative colinitis.</p>Formula:C19H33ClN2O2Purity:98%Color and Shape:SolidMolecular weight:356.948-CSC
CAS:<p>8-CSC: hMAO-B inhibitor (Ki: 235 nM, baboon liver) & A2A receptor affinity (Ki: 36 nM, rat brain).</p>Formula:C16H15ClN4O2Purity:98%Color and Shape:SolidMolecular weight:330.77Risotilide
CAS:<p>Risotilide is a voltage-dependent potassium channel inhibitor. It can prolong cardiac action potentials and refractory periods.</p>Formula:C15H27N3O4S2Purity:98%Color and Shape:SolidMolecular weight:377.52F-1394
CAS:<p>F-1394 is an ACAT inhibitor that reduces atherosclerosis and neointimal thickening without changing serum cholesterol.</p>Formula:C33H61N3O6Color and Shape:SolidMolecular weight:595.85NC1153
CAS:<p>NC1153 blocks IL-2/JAK3/STAT5a/b, aids allograft survival, reduces toxicities.</p>Formula:C18H38Cl2N2OPurity:98%Color and Shape:SolidMolecular weight:369.42MAO-B Inhibitor 58
CAS:<p>MAO-B inhibitor 58 is an effective, selective, and reversible inhibitor of monoamine oxidase B.</p>Formula:C14H9Cl2N3Color and Shape:SolidMolecular weight:290.15KCN1
CAS:<p>KCN1: a synthetic sulfonamide, nanomolar HIF inhibitor with preclinical anti-glioma and anti-pancreatic cancer effects.</p>Formula:C26H27NO5SColor and Shape:SolidMolecular weight:465.56RORγt modulator 2
CAS:<p>RORγt modulator 2 is a modulator of retinol-related orphan receptor γt (RORyt) (IC50<50 nM) and can be used in the study of RORγt-mediated diseases such as pain</p>Formula:C28H29ClN2O4SColor and Shape:SolidMolecular weight:525.06Muristerone A
CAS:<p>Muristerone A is a phytoecdysteroid analog of ecdysone and a potent ecdysteroid receptor agonist with a K d of 1 nM [1].</p>Formula:C27H44O8Color and Shape:SolidMolecular weight:496.63CK2-IN-6
CAS:<p>CK2-IN-6: Potent CK2 inhibitor for cancer, inflammation, pain, and immune research.</p>Formula:C19H16ClN7O2Color and Shape:SolidMolecular weight:409.83IDO1-IN-17
CAS:<p>IDO1-IN-17 (I-4) is an IDO1 inhibitor, with an IC 50 of 0.44 μM in hela cells .</p>Formula:C28H32BrClFN5O2Color and Shape:SolidMolecular weight:604.94Carbonic anhydrase inhibitor 13
CAS:<p>Carbonic anhydrase inhibitor 13 (compound 7) is a potent inhibitor of carbonic anhydrase (CA).</p>Formula:C17H15N5O3S2Color and Shape:SolidMolecular weight:401.46hCAIX-IN-6
CAS:<p>6B and 14g inhibit tumor-associated HCA IX with low nanomolar potency; 6K targets HCA XII. All are potential cancer drug leads.</p>Formula:C18H12N2O4SColor and Shape:SolidMolecular weight:352.36MSPG
CAS:<p>mGlu receptor antagonist</p>Formula:C9H11NO5SPurity:98%Color and Shape:SolidMolecular weight:245.25α-Glucosidase-IN-10
CAS:<p>α-Glucosidase-IN-10 (compound 13) is a potent inhibitor of α-glucosidase (IC50: 92.7 μM). α-Glucosidase-IN-10 can be used to study type II diabetes.</p>Formula:C21H15BrN4O2SColor and Shape:SolidMolecular weight:467.34S 12340
CAS:<p>S 12340 is a potent inhibitor of the oxidative modification of low-density lipoprotein.</p>Formula:C24H38N2O3SColor and Shape:SolidMolecular weight:434.64UCM 765
CAS:<p>UCM 765 is a partial agonist of melatonin MT(2) receptor.</p>Formula:C17H20N2O2Purity:98%Color and Shape:SolidMolecular weight:284.35TUPS
CAS:<p>TUPS is a selective soluble epoxide hydrolase inhibitor which protects against isoprenaline-induced cardiac hypertrophy.</p>Formula:C14H18F3N3O4SColor and Shape:SolidMolecular weight:381.37AX 048
CAS:<p>Group IVA cPLA2 inhibitor AX 048 halts arachidonic acid release, preventing prostaglandin production, with XI(50) of 0.022 and ED50 of 1.2 mg/kg.</p>Formula:C22H41NO4Color and Shape:SolidMolecular weight:383.57Oxagrelate
CAS:<p>Oxagrelate inhibits cAMP phosphodiesterase and reduces platelet aggregation by collagen and ADP.</p>Formula:C14H16N2O4Color and Shape:SolidMolecular weight:276.29PDE5-IN-4
CAS:<p>PDE5-IN-4, a phosphodiesterase 5 (PDE5) inhibitor, is utilized in research concerning acute myocardial infarction and reperfusion-related damage,</p>Formula:C21H27N5O5SColor and Shape:SolidMolecular weight:461.53Boc-Glu(OBzl)-OSu
CAS:<p>Boc-Glu(OBzl)-OSu can be used for the synthesis of solid phase peptides containing benzyl glutamate residues.</p>Formula:C21H26N2O8Color and Shape:SolidMolecular weight:434.44α-Amylase/α-Glucosidase-IN-2
CAS:<p>α-Amylase/α-Glucosidase-IN-2 (compound 5) exhibits strong inhibition activity towards both α-amylase and α-glucosidase enzymes, with IC 50 values of 13.02 μM</p>Formula:C22H16ClN5Color and Shape:SolidMolecular weight:385.85IDO1-IN-15
CAS:<p>IDO1-IN-15 is an effective IDO1 inhibitor with IC50 of 127 nM. The potency of IDO1-IN-15 against IDO1 enzyme is comparable with Epacadostat in vitro.</p>Formula:C13H14BrFN6O3Color and Shape:SolidMolecular weight:401.19CL67
CAS:<p>CL67 is a hypoxia-inducible factor pathway inhibitor. It acts by binding to a G-quadruplex higher-order structure in the HIF promoter sequence in vitro.</p>Formula:C38H42N10O2Color and Shape:SolidMolecular weight:670.81hCAIX-IN-14
CAS:<p>hCAIX-IN-14 is a potent inhibitor of human CA IX with a K i value of 134.8 nM .</p>Formula:C11H17ClN6O2SColor and Shape:SolidMolecular weight:332.81ATX inhibitor 8
CAS:<p>ATX inhibitor 8 is an inhibitor of the autocrine motor factor Autotaxin (ATX).</p>Formula:C28H26N10OColor and Shape:SolidMolecular weight:518.57FAAH-IN-7
<p>FAAH-IN-7: Reversible FAAH inhibitor, IC50=8.29 nM, reduces oxidative stress, neuroprotective in neuroinflammation.</p>Formula:C26H29N3O4Color and Shape:SolidMolecular weight:447.53Enpp-1-IN-8
CAS:<p>Enpp-1-IN-8: potent inhibitor of enpp-1, an enzyme breaking down various nucleotide bonds; potential in cancer/infectious disease research.</p>Formula:C19H26N6O4SColor and Shape:SolidMolecular weight:434.51Risarestat
CAS:<p>Risarestat (CT-112) is a potent aldose reductase inhibitor and thyroid hormone receptor (TR) antagonist for the treatment of hypoglycemia.</p>Formula:C16H21NO4SPurity:98.39%Color and Shape:SolidMolecular weight:323.41Rentiapril racemate
CAS:<p>Rentiapril racemate (SA-446 racemate) is the racemate of Rentiapril.Rentiapril racemate has anti-inflammatory activity and may be used in glaucoma research.</p>Formula:C13H15NO4S2Purity:98.96% - >99.99%Color and Shape:SolidMolecular weight:313.39MDK-4823
CAS:<p>MDK-4823 (LMPTP inhibitor1) blocks LMPTP, fighting insulin resistance and diabetes in obesity.</p>Formula:C28H36N4OColor and Shape:SolidMolecular weight:444.61NBD-125
CAS:<p>NBD-125 (B-12) is a berberine analogue. NBD-125 is an RXRα activator. The IC50 value of NBD-125 in KM12C cell is 31.10 μM [1].</p>Formula:C19H18ClNO2Color and Shape:SolidMolecular weight:327.81p-Synephrine
CAS:<p>p-Synephrine is a natural product for research related to life sciences. The catalog number is T8265 and the CAS number is 614-35-7.</p>Formula:C9H13NO2Purity:98%Color and Shape:SolidMolecular weight:167.21Nampt-IN-9
CAS:<p>Nampt-IN-9 (Compound 8) is a potent inhibitor of NAMPT with anticancer properties.Nampt-IN-9 can be used to study ductal adenocarcinoma of the pancreas.</p>Formula:C26H33N3O4Color and Shape:SolidMolecular weight:451.56Delapril
CAS:<p>Delapril is an ACE inhibitor. It blocks the conversion of angiotensin I to angiotensin II.</p>Formula:C26H32N2O5Purity:98%Color and Shape:SolidMolecular weight:452.54Metyltetraprole
CAS:<p>Metyltetraprole: potent fungicide, effective against Zymoseptoria, low EC50 (0.002 ppm), inhibits respiratory chain.</p>Formula:C19H17ClN6O2Color and Shape:SolidMolecular weight:396.83α-Glucosidase-IN-9
CAS:<p>α-Glucosidase-IN-9 (compound 7) is a highly potent α-glucosidase inhibitor with an IC50 of 55.6 μM, making it suitable for type II diabetes research [1].</p>Formula:C19H12N4OSColor and Shape:SolidMolecular weight:344.39GNX-865
CAS:<p>GNX-865 is an inhibitor of mitochondrial permeability transition pore (mtPTP).</p>Formula:C16H14ClNO3Color and Shape:SolidMolecular weight:303.74TM6008
CAS:<p>TM6008 is an inhibitor of prolyl hydroxylase that protects against cell death after hypoxia.</p>Formula:C21H17N5O3Purity:98%Color and Shape:SolidMolecular weight:387.39(Rac)-3′-Hydroxy simvastatin
CAS:<p>(Rac)-3′-Hydroxy Simvastatin, a metabolite of Simvastatin, acts as a competitive inhibitor of HMG-CoA reductase, demonstrating a K i value of 0.2 nM.</p>Formula:C25H38O6Color and Shape:SolidMolecular weight:434.57YM-75466
CAS:<p>YM-75466 is a factor Xa inhibitor reducing TAT in plasma dose-dependently without prolonging coagulation.</p>Formula:C28H35N5O8S2Color and Shape:SolidMolecular weight:633.74LTV-1
CAS:<p>LTV-1 has the potential for autoimmunity treatment. LTV-1 is a potent lymphoid tyrosine phosphatase (LYP) inhibitor in T cells with an IC50 of 508 nM.</p>Formula:C26H20N2O5SColor and Shape:SolidMolecular weight:472.51GNE-3500
CAS:<p>GNE-3500: potent, selective RORc inverse agonist; orally bioavailable; promising for treating inflammatory diseases.</p>Formula:C24H30FN3O3SColor and Shape:SolidMolecular weight:459.58hCAIX-IN-7
CAS:<p>hCAIX-IN-7 (6c) selectively inhibits tumor-related isoform hCAIX (KI: 410.6 nM) and weakly affects hCAI/II (KI: >10000 nM).</p>Formula:C18H12FNO3Color and Shape:SolidMolecular weight:309.29DMPAC-Chol
CAS:<p>DMPAC-Chol, a cationic cholesterol, aids gene transfection, DNA protection, binds DNA, and lowers HepG2 viability at 37.5 μg/ml.</p>Formula:C33H58N2O2Color and Shape:SolidMolecular weight:514.83Glyoxalase I inhibitor 2
CAS:<p>Glyoxalase I inhibitor 2 (compound 26) blocks GLO1 effectively (IC50: 0.5 μM), promising for depression and anxiety research.</p>Formula:C24H23N3O4SColor and Shape:SolidMolecular weight:449.52Fluindione
CAS:<p>Fluindione is a hematologic drug.</p>Formula:C15H9FO2Color and Shape:SolidMolecular weight:240.23Senazodan
CAS:<p>Senazodan is a sensitiser of Ca2+, and shows inhibition effect on PDE III.</p>Formula:C15H14N4OPurity:98%Color and Shape:SolidMolecular weight:266.3URB532
CAS:<p>URB532 is an irreversible fatty acid amide hydrolase (FAAH) inhibitor.</p>Formula:C18H21NO3Purity:98%Color and Shape:SolidMolecular weight:299.36AN3199
CAS:<p>AN3199 is a selective inhibitor of PDE4 with an IC50 of 94.5 nM.</p>Formula:C17H18BNO5Purity:99.45%Color and Shape:SolidMolecular weight:327.14SCD1 inhibitor-1
CAS:SCD1 inhibitor-1 is a potent and liver-selective inhibitor of stearoyl-CoA desaturase-1 (SCD1).Formula:C21H23N3NaO3S2Purity:98%Color and Shape:SolidMolecular weight:452.54Inolitazone dihydrochloride
CAS:<p>Inolitazone dihydrochloride is an effective, high-affinity PPARγ agonist; its biological activity is dependent on PPARγ (IC50:0.8 nM) to inhibit cell growth.</p>Formula:C27H28Cl2N4O4SColor and Shape:SolidMolecular weight:575.51Kojibiose
CAS:<p>Kojibiose (Kojibiose) is a disaccharide in honey. Kojibiose is a product of the caramelization of glucose.</p>Formula:C12H22O11Purity:99.933%Color and Shape:SolidMolecular weight:342.3sEH inhibitor-6
CAS:<p>sEH inhibitor-6 (Compound 3g) is a highly potent soluble epoxide hydrolase (sEH) inhibitor, exhibiting an IC 50 value of 0.5 nM [1].</p>Formula:C21H14ClN3O2Color and Shape:SolidMolecular weight:375.81Cholesteryl behenate
CAS:<p>Cholesteryl behenate is a standard in electrospray ionization tandem mass spectrometry for the analysis of cholesteryl esters and cholesterol.</p>Formula:C49H88O2Purity:98%Color and Shape:SolidMolecular weight:709.22PSB-1410
CAS:<p>PSB-1410 is a selective and highly efficient monoamine oxidase B (MAO-B) inhibitor, which can be used in research on neurological diseases.</p>Formula:C15H10Cl2N2OPurity:98.69%Color and Shape:SolidMolecular weight:305.16CYP3A4-IN-3
CAS:<p>CYP3A4-IN-3, a ritonavir analogue, is a potent CYP3A4 inhibitor with an IC50 of 0.075 μM, used as an antiviral and immunosuppressant.</p>Formula:C34H39N3O3SColor and Shape:SolidMolecular weight:569.76α-Glucosidase-IN-4
CAS:<p>α-Glucosidase-IN-4 is a potent α-glucosidase inhibitor with antihypertensive and hypoglycemic activity.</p>Formula:C19H14O4Purity:99.69%Color and Shape:SolidMolecular weight:306.31BI 689648
CAS:<p>BI 689648 is a highly selective inhibitor of aldosterone synthase(CYP11B1 and CYP11B2 with IC50s of 310 and 2.1 nM, respectively).</p>Formula:C16H18N4O2Color and Shape:SolidMolecular weight:298.34Quazodine
CAS:<p>Quazodine is a phosphodiesterase inhibitor.</p>Formula:C12H14N2O2Color and Shape:SolidMolecular weight:218.25EP6
CAS:<p>EP6 blocks 5-LO, key in the AA cascade, reducing leukotrienes to curb inflammation and allergies.</p>Formula:C24H30N4OPurity:98%Color and Shape:SolidMolecular weight:390.52Abiraterone metabolite 1
CAS:<p>Abiraterone metabolite 1, a derivative of abiraterone, inhibits CYP17A1, halts androgen formation, aiding in prostate cancer treatment.</p>Formula:C24H33NOPurity:98%Color and Shape:SolidMolecular weight:351.52hCAII-IN-1
CAS:<p>hCAII-IN-1 (7f) inhibits CA II/IX with Kis 1.2 nM/113.6 nM, potential for cancer treatment.</p>Formula:C21H21BrN6O4SColor and Shape:SolidMolecular weight:533.4ALRT 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:340.5Endothelial lipase inhibitor-1
CAS:<p>Endothelial lipase inhibitor-1 is a potent endothelial lipase inhibitor with an IC50 of 49 nM.</p>Formula:C22H22N4O4Purity:99.59%Color and Shape:SolidMolecular weight:406.43Deltasonamide 2
CAS:<p>Deltasonamide 2 is a competitive, high affinity PDEδ inhibitor with a Kd of ~385 pM.</p>Formula:C30H39ClN6O4S2Purity:98%Color and Shape:SolidMolecular weight:647.257-Ketolithocholic acid
CAS:<p>7-Ketolithocholic acid absorbs and reduces endogenous bile acid and cholesterol secretion.</p>Formula:C24H38O4Purity:98.68% - 99.9%Color and Shape:White - Almost White Solid PowderMolecular weight:390.56TM6089
CAS:<p>TM6089 is an inhibitor of Prolyl Hydroxylase that stimulates HIF activity without iron chelation, induces angiogenesis, and protects organ against ischemia.</p>Formula:C13H14N4O3SPurity:99.70%Color and Shape:SolidMolecular weight:306.34hCAIX-IN-10
CAS:<p>"hCAIX-IN-10 (6i) selectively inhibits carbonic anhydrase IX/XII (Ki: 61.5/586.8 nM), markers in tumor cells, affecting acid-base balance."</p>Formula:C28H21N3O3SColor and Shape:SolidMolecular weight:479.55SHP844
CAS:<p>SHP844: SHP2 inhibitor, IC50 18.9 µM, affects cell growth/survival by regulating tyrosine phosphorylation.</p>Formula:C29H24ClN5O6Color and Shape:SolidMolecular weight:573.98Angiogenesis agent 1
CAS:<p>Compound C-31, a salidroside-based glycoside, activates HIF-1α and may aid in diabetic limb ischemia studies.</p>Formula:C20H24O7Purity:98%Color and Shape:SolidMolecular weight:376.4RORγt inverse agonist 28
CAS:<p>RORγt inverse agonist 28 is a potent RORγt inverse agonist.</p>Formula:C23H18Cl2F3NO5SColor and Shape:SolidMolecular weight:548.36ASM-IN-1
CAS:<p>ASM-IN-1: Oral acid sphingomyelinase inhibitor, IC50 = 1.5 µM; reduces lipid plaques, plasma ceramide, Ox-LDL.</p>Formula:C16H12BrN3O4Purity:98%Color and Shape:SolidMolecular weight:390.19HZ52
CAS:<p>HZ52: Potent reversible 5-LO inhibitor; IC50 0.7 μM; blocks LTs in human leukocytes.</p>Formula:C24H26ClN3O2SColor and Shape:SolidMolecular weight:456ATX inhibitor 20
CAS:<p>ATX inhibitor 20 is a potent inhibitor of ATX (IC50: 2.3 nM).</p>Formula:C31H34FN5O3Color and Shape:SolidMolecular weight:543.63Endothall
CAS:<p>Endothall is an effective protein phosphatase 2A (PP2A) inhibitor, exerting inhibitory effects on both PP2A and PP1, with IC50 values of 90 nM and 5 µM,</p>Formula:C8H10O5Purity:98.92% - ≥98%Color and Shape:Cyrstalline White Solid The Monohydrate Is In The Form Of Colorless Crystals Non Corrosive Used As A Selective HerbicideMolecular weight:186.16AVE5688
CAS:<p>AVE5688 is an inhibitor of glycogen phosphorylase (GP, IC50s: 430 nM and 915 nM; Kds: 170 nM and 530 nM for rmGPb and rmGPa).</p>Formula:C16H8ClF5N2O5Purity:99.65%Color and Shape:SolidMolecular weight:438.69GK187
CAS:<p>GK187 is a selective and potent Group VIA calcium-independent phospholipase A2 (GVIA iPLA2) inhibitor, used in the study of neurological disorders.</p>Formula:C14H15F5O2Color and Shape:SolidMolecular weight:310.26Leniquinsin
CAS:<p>Leniquinsin is an antihypertensive compound. It is a phosphodiesterase inhibitor and a potent vasodilator.</p>Formula:C20H20N2O4Purity:98%Color and Shape:SolidMolecular weight:352.381E7-03
CAS:<p>1E7-03 is an inhibitor of HIV-1 transcription, by targeting host Protein Phosphatase-1 (PP1).</p>Formula:C28H29N3O6Color and Shape:SolidMolecular weight:503.55Oosponol
CAS:<p>Oosponol is a dopamine beta-hydroxylase inhibitor exhibiting hypotensive effects.</p>Formula:C11H8O5Purity:98%Color and Shape:SolidMolecular weight:220.18Lucerastat
CAS:<p>Lucerastat（NBDGJ） is an orally available inhibitor of GCS for Fabry disease by reducing harmful substrates.. GCS is a key enzyme in sphingolipid synthesiss.</p>Formula:C10H21NO4Purity:98%Color and Shape:SolidMolecular weight:219.282-TEDC
CAS:<p>2-TEDC: Potent LOX inhibitor, blocks 5-LOX, 12-LOX, 15-LOX (IC50: 0.09, 0.013, 0.5 μM); aids atherosclerosis research.</p>Formula:C16H13NO4SPurity:99.75%Color and Shape:SolidMolecular weight:315.34Clethodim
CAS:<p>Clethodim is a selective herbicide inhibiting acetyl-CoA carboxylase, effective on grasses with low environmental persistence and moderate toxicity to wildlife.</p>Formula:C17H26ClNO3SPurity:99.99%Color and Shape:Light Yellow LiquidMolecular weight:359.91Oleyl Anilide
CAS:<p>"Oleyl analide (OA) inhibits ACAT (IC50 26 μM), linked to toxic oil syndrome (TOS) with eosinophilia, T-cell activation, and high IL-4, IL-2R, IL-5."</p>Formula:C24H39NOColor and Shape:SolidMolecular weight:357.57GGsTop
CAS:<p>GGsTop (Nahlsgen) is a GGT inhibitor with anti-aging activity.</p>Formula:C13H18NO7PPurity:98.96%Color and Shape:SolidMolecular weight:331.26Senazodan hydrochloride
CAS:<p>Senazodan hydrochloride (Senazodan HCl) is a Ca2+ sensitizer and phosphodiesterase 3 (PDE3) inhibitor used in the study of cardiovascular diseases.</p>Formula:C15H15ClN4OPurity:99.93%Color and Shape:SolidMolecular weight:302.76BKIDC-1553
CAS:<p>BKIDC-1553, an orally active antiglycolytic agent and bumped kinase inhibitor-derived compound, has a predicted half-life of approximately 17 hours in humans. It inhibits CYP2C8 and Angiotensin Converting Enzyme, making it suitable for cancer research [1].</p>Formula:C22H23N5O2Color and Shape:SolidMolecular weight:389.45GSK376501A
CAS:<p>GSK376501A is a selective and effective modulator of peroxisome proliferator-activated receptor γ (PPARγ) for the study of type 2 diabetes.</p>Formula:C32H37NO6Purity:>99.99%Color and Shape:SolidMolecular weight:531.64AMP-Deoxynojirimycin
CAS:<p>AMP-Deoxynojirimycin (AMP-DNM) is a ceramide glucosyltransferase and GCase 2 inhibitor for the study of Parkinson's and diabetes.</p>Formula:C22H39NO5Purity:>99.99%Color and Shape:SolidMolecular weight:397.55Epostane
CAS:<p>Epostane is a 3β-hydroxysteroid dehydrogenase inhibitor that blocks the biosynthesis of progesterone and pregnenolone.Cost-effective and quality-assured.</p>Formula:C22H31NO3Purity:>99.99%Color and Shape:SolidMolecular weight:357.49ATX inhibitor 5
CAS:<p>ATX inhibitor 5: potent, oral autotaxin blocker, IC50 15.3 nM, curbs CCl4 liver fibrosis.</p>Formula:C22H18ClF3N6OPurity:98.77%Color and Shape:SolidMolecular weight:474.87Quinapril-d5
CAS:<p>Quinapril-d5: An internal standard for quinapril quantification via GC/LC-MS; a prodrug ACE inhibitor for hypertension and heart failure.</p>Formula:C25H25D5N2O5Color and Shape:SolidMolecular weight:443.55TF-S14
CAS:<p>TF-S14 is an inverse agonist of RORγt. It functions by binding to RORγt and inhibiting its activity, leading to a reduction in Th17 cell-associated cytokine production, including IL-17A, IL-21, and IL-22. TF-S14 is applicable in research related to autoimmune diseases and allogeneic transplant rejection.</p>Formula:C22H27N3O2SColor and Shape:SolidMolecular weight:397.53SAHO
CAS:<p>SAHO is a methyl donor cleaved by SAM enzymes into adenosylhomocysteine and thioadenosine derivatives.</p>Formula:C14H20N6O6SColor and Shape:SolidMolecular weight:400.41JNJ-42314415
CAS:<p>JNJ-42314415 is a potent, specific, and centrally active inhibitor of PDE10A.</p>Formula:C19H23N5O2Purity:98%Color and Shape:SolidMolecular weight:353.42TA-7552
CAS:<p>TA-7552 is a potent agent of cholesterol-lowering.</p>Formula:C25H26O10Purity:98%Color and Shape:SolidMolecular weight:486.47BMP-22
CAS:<p>BMP-22 selectively inhibits autotaxin (IC50=170 nM), blocks LPA production and MM1 cell invasion, and reduces lung metastases in mice at 0.5 mg/kg/day.</p>Formula:C22H39O3PColor and Shape:SolidMolecular weight:382.52BFE-37
CAS:<p>BFE-37 is a partial agonist of beta-adrenergic.</p>Formula:C16H23NO3Purity:98%Color and Shape:SolidMolecular weight:277.36PMPMEase-IN L-28
CAS:<p>PMPMEase-IN L-28 is a novel inhibitor of prenylated methylated protein methylesterase.</p>Formula:C17H29FO2S2Purity:98%Color and Shape:SolidMolecular weight:348.54L 662583
CAS:<p>L 662583 is a topical inhibitor of carbonic anhydrase.</p>Formula:C13H17ClN2O5S3Purity:98%Color and Shape:SolidMolecular weight:412.93Cedefingol
CAS:<p>Cedefingol is an antineoplastic agent.</p>Formula:C20H41NO3Purity:98%Color and Shape:SolidMolecular weight:343.54Pirbuterol hydrochloride
CAS:<p>Pirbuterol hydrochloride is a bronchodilator.</p>Formula:C12H21ClN2O3Color and Shape:SolidMolecular weight:276.76Pegnivacogin
CAS:<p>Pegnivacogin is a coagulation factor IXa RNA aptamer inhibitor.</p>Formula:C20H40N3O11PPurity:98%Color and Shape:SolidMolecular weight:529.52D-4418
CAS:<p>D-4418, a PDE4 inhibitor in development, targets asthma and COPD as an anti-inflammatory treatment.</p>Formula:C16H11Cl2N3O2Purity:98%Color and Shape:SolidMolecular weight:348.18L-651392
CAS:<p>L-651392 is an inhibitor of leukotriene.</p>Formula:C14H10BrNO3SColor and Shape:SolidMolecular weight:352.2MMV-667492
CAS:<p>MMV-667492 is an effective inhibitor of Ezrin.</p>Formula:C17H19N3O3Purity:98%Color and Shape:SolidMolecular weight:313.35MLS000536924
CAS:<p>MLS000536924 is a potent and selective competitive human epithelial 15-lipoxygenase-2 inhibitor.</p>Formula:C16H15N3SColor and Shape:SolidMolecular weight:281.38Lysine Orotate
CAS:<p>Lysine Orotate blocks Herpes virus replication, effective against HSV-1, HSV-2, CMV, EBV, and Varicella.</p>Formula:C11H18N4O6Purity:98%Color and Shape:SolidMolecular weight:302.28PG-9 maleate
CAS:<p>Increases release of acetylcholine</p>Formula:C21H26BrNO6Purity:98%Color and Shape:SolidMolecular weight:468.34OH-Ubenimex
CAS:<p>OH-Ubenimex is an orally active aminopeptidase inhibitor that has an immunomodulating action.</p>Formula:C16H24N2O5Purity:98%Color and Shape:SolidMolecular weight:324.37α-RA-F
CAS:<p>Alpha-RA-F increases collagen, lowers MMPs in human fibroblasts, non-toxic.</p>Formula:C16H16N2O4Purity:98%Color and Shape:SolidMolecular weight:300.31myomiR-IN-1
CAS:<p>myomiR-IN-1 inhibits myoD translation in C2C12 cells, doesn't affect myoD mRNA, and reduces differentiation markers.</p>Formula:C33H27NO6Purity:98%Color and Shape:SolidMolecular weight:533.572-Iodoestradiol
CAS:<p>2-Iodoestradiol is an effective human sex hormone-binding globulin (SHBG) ligand.</p>Formula:C18H23IO2Purity:98%Color and Shape:SolidMolecular weight:398.28OMS-824
CAS:<p>OMS-824 is a phosphodiesterase-10 inhibitor that slows or stops the hydrolysis of cAMP and cGMP.</p>Formula:C21H21BrN4O4Purity:98%Color and Shape:SolidMolecular weight:473.32PF-05387252
CAS:<p>PF-05387252 is an effective and selective inhibitor of the IRAK4.</p>Formula:C25H27N5O2Purity:98%Color and Shape:SolidMolecular weight:429.51Mixanpril
CAS:<p>Mixanpril is an RB 105 lipophilic prodrug.</p>Formula:C21H23NO4SPurity:98%Color and Shape:SolidMolecular weight:385.48Statine
CAS:<p>Statine is a protease inhibitor that is active against pepsin and other acid proteases.</p>Formula:C8H17NO3Purity:98%Color and Shape:SolidMolecular weight:175.23TRC210258
CAS:<p>TRC210258 is a TGR5 agonist that acts by decreasing glycemic and dyslipidemic cardiovascular risk in animal models of diabesity.</p>Formula:C20H14ClFN4O2Purity:98%Color and Shape:SolidMolecular weight:396.8JNJ-DGAT1-A
CAS:<p>JNJ-DGAT1-A is a DGAT1-selective inhibitor.</p>Formula:C31H35Cl2N5O3Color and Shape:SolidMolecular weight:596.55WAY127093B racemate
CAS:<p>WAY127093B racemate is the racemate of WAY127093B. WAY127093B is a phosphodiesterase IV inhibitor with oral activity in rats and guinea pigs.</p>Formula:C23H28N4O4Purity:99.67%Color and Shape:SolidMolecular weight:424.49IDO inhibitor 1
CAS:<p>IDO inhibitor 1 is an potent inhibitor of indoleamine-2,3 dioxygenase (IDO) ( IC50 <100 nM).with potential immunomodulating and antineoplastic activities.</p>Formula:C11H13BrFN7O4SPurity:99.805%Color and Shape:SolidMolecular weight:438.23PF 04671536 hydrochloride
CAS:<p>Potent PDE8B/8A inhibitor; IC50: PDE8B-1.3nM, PDE8A-1.9nM; selective over other PDEs; enhances insulin secretion; orally bioavailable.</p>Formula:C14H19ClN8OSColor and Shape:SolidMolecular weight:382.87Imazodan hydrochloride
CAS:<p>Imazodan hydrochloride (CI-914 HCl) is a potent and selective type III phosphodiesterase inhibitor used in the treatment of chronic congestive heart failure.</p>Formula:C13H13ClN4OPurity:98.97%Color and Shape:SolidMolecular weight:276.72Mesopram
CAS:<p>PDE4 inhibitor, orally active</p>Formula:C14H19NO4Purity:98%Color and Shape:SolidMolecular weight:265.3TAK 21d
CAS:<p>Potent FAAH inhibitor</p>Formula:C19H17F2N7OPurity:98%Color and Shape:SolidMolecular weight:397.38Nafenopin
CAS:<p>Nafenopin is a peroxisome proliferator, it is used to promote liver tumors and has been used as an antihyperlipoproteinemic agent.</p>Formula:C20H22O3Purity:98%Color and Shape:SolidMolecular weight:310.39PF-05388169
CAS:<p>PF-05388169 is an effective and selective inhibitor of IRAK4.</p>Formula:C22H21N3O4Purity:98%Color and Shape:SolidMolecular weight:391.42Glyoxalase I inhibitor 4
CAS:<p>Glyoxalase I inhibitor 4 is a potent inhibitor of glyoxalase I (GLO1) (Ki: 10 nM).</p>Formula:C17H21IN4O8SColor and Shape:SolidMolecular weight:568.34CM026
CAS:<p>CM026 inhibits ALDH1A1 selectively, binds to its aldehyde pocket uncompetitively.</p>Formula:C22H30N6O4Color and Shape:SolidMolecular weight:442.51ABT-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:166.22Nampt activator-3
CAS:<p>NAMPT activator-3: a NAT derivative, EC50 of 2.6 μM, KD 132 nM, protects cells, prevents FK866 toxicity, and is neuroprotective in CIPN mice.</p>Formula:C19H20N2O3Color and Shape:SolidMolecular weight:324.37hDHODH-IN-11
CAS:<p>hDHODH-IN-11: potent hDHODH inhibitor, IC50 7.2 nM, low cytotoxicity, for AML research.</p>Formula:C24H23N3O3Color and Shape:SolidMolecular weight:401.46Safrazine Hydrochloride
CAS:<p>Safrazine Hydrochloride is a monoamine oxidase inhibitor (MOI) that is irreversible.</p>Formula:C11H17ClN2O2Color and Shape:SolidMolecular weight:244.718PF 4800567 hydrochloride
CAS:<p>casein kinase 1ε inhibitor</p>Formula:C17H19Cl2N5O2Purity:98%Color and Shape:SolidMolecular weight:396.27TPN729
CAS:<p>TPN729, a PDE5 inhibitor, has an IC50 of 2.28 nM, used to research erectile dysfunction.</p>Formula:C25H36N6O4SColor and Shape:SolidMolecular weight:516.66(R)-MLN-4760
CAS:<p>(R)-MLN-4760, the R-enantiomer of MLN-4760, functions as an ACE2 inhibitor and exhibits a half maximal inhibitory concentration (IC50) of 8.4 μM, identifying it</p>Formula:C19H23Cl2N3O4Color and Shape:SolidMolecular weight:428.31MDK-0738
CAS:<p>MDK-0738 is a potent and selective aldo-keto reductase 1C3 inhibitor.</p>Formula:C15H16O3Purity:98%Color and Shape:SolidMolecular weight:244.29hCAI/II-IN-1
CAS:<p>hCAI/II-IN-1 (Compound 3h) is a human carbonic anhydrase I and II (hCA I/II) inhibitor that acts on hCA I (IC50: 0.047 μM) and hCA II (IC50: 0.024 μM).</p>Formula:C18H29N5O3S3Color and Shape:SolidMolecular weight:459.65hCAI/II-IN-5
CAS:<p>hCAI/II-IN-5 inhibits human carbonic anhydrase I & II, α-Glycosidase, and AChE, for diabetes, heart failure, Alzheimer's, ulcers, epilepsy research.</p>Formula:C21H18Cl2N8O4S2Color and Shape:SolidMolecular weight:581.45Carbazomycin B
CAS:<p>Carbazomycin B, a Streptomyces metabolite, combats fungi, bacteria, P. falciparum, C. albicans, and some cancer cells; inhibits 5-LO (IC50=1.5µM).</p>Formula:C15H15NO2Color and Shape:SolidMolecular weight:241.29Fodipir
CAS:<p>Fodipir, the active metabolite of mangafodipir, plays a crucial role in the mechanism of mangafodipir-mediated cytoprotection, specifically mitigating cell</p>Formula:C22H32N4O14P2Purity:98%Color and Shape:SolidMolecular weight:638.46ML-148
CAS:<p>ML-148 is a selective inhibitor of 15-hydroxy prostaglandin dehydrogenase (15-PGDH, IC50 = 56 nM).</p>Formula:C20H21N3OPurity:99.88%Color and Shape:SolidMolecular weight:319.44′-Deoxyphlorizin
CAS:<p>4'-Deoxyphlorizin inhibits glucose transport; Km 0.59 nM, Ki 0.33 nM for phlorizin hydrolase.</p>Formula:C21H24O9Color and Shape:SolidMolecular weight:420.41Pemetrexed tromethamine
CAS:<p>Pemetrexed tromethamine is a chemotherapy drug used for pleural mesothelioma and non-small cell lung cancer.</p>Formula:C20H21N5O6·2C4H11NO3·2H2OPurity:98%Color and Shape:SolidMolecular weight:705.72Arfolitixorin
CAS:<p>Arfolitixorin is an antifolate modulator.</p>Formula:C20H23N7O6Color and Shape:SolidMolecular weight:457.44Diniprofylline
CAS:<p>Diniprofylline, a phosphodiesterase inhibitor, has been used as a peripheral nervous system agent, a bronchodilator agent, and an anti-asthamtic agent.</p>Formula:C22H20N6O6Color and Shape:SolidMolecular weight:464.43Gcase activator 3
CAS:<p>Gcase activator 3 is a glucocerebrosidase (GCase) activator that enhances GBA1 mutant fibroblast lysosomal GCase activity.</p>Formula:C23H20N4O2Purity:99.08%Color and Shape:SolidMolecular weight:384.43NPD-001
CAS:<p>NPD-001 is an effective inhibitor of TbrPDEB1. NPD-001 is 10-fold more potent on hPDE4 (hPDE4B1 IC50 = 0.6 nM) than on TbrPDEB1 (IC50 = 4 nM).</p>Formula:C33H40N6O4Purity:98%Color and Shape:SolidMolecular weight:584.71CD 2314
CAS:<p>CD2314 is a potent and subtype-selective RARβ receptor agonist with a Kd of 195 nM in S91 melanoma cells [1].</p>Formula:C23H24O2SColor and Shape:SolidMolecular weight:364.5Darexaban glucuronide
CAS:<p>Darexaban glucuronide is the major component in plasma after oral administration of darexaban to humans. Darexaban (YM150) is a direct inhibitor of factor Xa.</p>Formula:C33H38N4O10Color and Shape:SolidMolecular weight:650.68ZSET-845
CAS:<p>ZSET-845 is an enhancer of cognitive which enhances choline acetyltransferase activity in the hippocampus in the rat.</p>Formula:C21H18N2OPurity:98%Color and Shape:SolidMolecular weight:314.38Dibefurin
CAS:<p>Dibefurin blocks calcineurin, a calcium-dependent enzyme, reducing T lymphocyte activation.</p>Formula:C18H16O8Color and Shape:SolidMolecular weight:360.31YZ9
CAS:<p>Y29 is a potent PFKFB3 inhibitor with an IC50 of 0.183 µM, and acts as a competitive inhibitor against Fru-6-P with a Ki of 0.094 µM[1].</p>Formula:C12H10O5Purity:99.59%Color and Shape:SolidMolecular weight:234.2Enpp-1-IN-9
CAS:<p>Enpp-1-IN-9 inhibits ENPP1, cleaves numerous bonds in nucleotides/sugars; may advance cancer/infectious disease research.</p>Formula:C17H24N4O5SColor and Shape:SolidMolecular weight:396.46PD0176078
CAS:<p>PD0176078 () is a newly blocker of N-type Calcium channel.</p>Formula:C23H30F2N2OPurity:99.72%Color and Shape:SolidMolecular weight:388.49PPARα-MO-1
CAS:<p>PPARα-MO-1 is a potent modulator of PPARα.</p>Formula:C27H37NO5Purity:98%Color and Shape:SolidMolecular weight:455.59Glucokinase activator 3
CAS:<p>Glucokinase activator 3: potent GK activator, AC50=38 nM, potential for type 2 diabetes research.</p>Formula:C26H33N2O9PS2Color and Shape:SolidMolecular weight:612.65α-Glucosidase-IN-8
CAS:<p>α-Glucosidase-IN-8 (Compound 4k) is a potent, competitive inhibitor of α-glucosidase. It displays an impressive IC50 value of 0.18 μg/mL [1].</p>Formula:C19H20FN3O2Color and Shape:SolidMolecular weight:341.38Riboflavine phosphate
CAS:<p>Riboflavine phosphate (Flavin mononucleotide) is a derivative of Riboflavin.</p>Formula:C17H21N4O9PPurity:98%Color and Shape:SolidMolecular weight:456.34ML368
CAS:<p>ML368 is a selective inhibitor of CYP3A4.</p>Formula:C26H18N6OPurity:98%Color and Shape:SolidMolecular weight:430.46ACC1/2-IN-1
CAS:<p>ACC1/2-IN-1 is a potent inhibitor of ACC1/2 and acts on ACC1 (IC50: 98.06 nM) and ACC2 (IC50: 29.43 nM). ACC1/2-IN-1 can be used in cancer research.</p>Formula:C34H32N4O4Color and Shape:SolidMolecular weight:560.647β,27-dihydroxy Cholesterol
CAS:<p>7β,27-dihydroxy Cholesterol is an oxysterol and agonist of retinoic acid receptor-related orphan receptor γ (RORγ) and RORγt.</p>Formula:C27H46O3Color and Shape:SolidMolecular weight:418.65N-(α-Linolenoyl) Tyrosine
CAS:<p>Certain chronic neurologic disorders, such as Parkinson's disease, are caused by an insufficiency of the neurotransmitter dopamine secondary to the degeneration</p>Formula:C27H39NO4Color and Shape:SolidMolecular weight:441.6FAAH-IN-5
CAS:<p>FAAH-IN-5 (Compound 7) selectively, irreversibly inhibits FAAH (IC50: 10.5 nM) with low PAMPA permeability.</p>Formula:C21H19N3O6SColor and Shape:SolidMolecular weight:441.46IDH2R140Q-IN-1
CAS:<p>IDH2R140Q-IN-1 is a potent inhibitor of IDH2R140Q (IC50: 6.1 nM) and can be used in studies of acute myeloid leukemia.</p>Formula:C22H20F6N6Color and Shape:SolidMolecular weight:482.42Indolapril hydrochloride
CAS:<p>Indolapril hydrochloride is a nonsulfhydryl angiotensin converting enzyme (ACE) inhibitor with antihypertensive activity.</p>Formula:C24H35ClN2O5Color and Shape:SolidMolecular weight:467HIF-1/2α-IN-2
CAS:<p>HIF-1/2α-IN-2 is a potent inhibitor of HIF-1/2α, which effectively reduces the levels of HIF-1/2α.</p>Formula:C16H11FN4O2SColor and Shape:SolidMolecular weight:342.35OMDM-3
CAS:<p>OMDM-3 is a selective and metabolically stable anandamide cellular uptake (ACU)inhibitor(Ki of 16.6 μM).</p>Formula:C29H43NO3Purity:98%Color and Shape:SolidMolecular weight:453.66
