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)
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Found 8625 products of "Metabolism"
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FTX-6746
CAS:<p>FTX-6746 is an orally active and selective PPARG reverse inhibitor with anticancer activity. It can be used in research on urothelial carcinoma.</p>Formula:C16H7ClF2N2OPurity:98.68%Color and Shape:SolidMolecular weight:316.69Tilivapram
CAS:<p>Tilivapram is a PDE4 (phosphodiesterase IV) inhibitor that can be used in the study of mental illness.</p>Formula:C16H15Cl2N3O4Purity:99.87%Color and Shape:SolidMolecular weight:384.21Nampt 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:324.37(-)-Ketoconazole
CAS:<p>(-)-Ketoconazole is a potential mitochondrial CYP24A1 inhibitor and has antifungal activity against Aspergillus fumigatus.</p>Formula:C26H28Cl2N4O4Purity:98%Color and Shape:SolidMolecular weight:531.43Fenleuton
CAS:<p>Fenleuton is a 5-lipoxygenase inhibitor.</p>Formula:C17H15FN2O3Purity:98%Color and Shape:SolidMolecular weight:314.31L 656224
CAS:<p>L 656224 is a 5-LO inhibitor.</p>Formula:C20H21ClO3Purity:98%Color and Shape:SolidMolecular weight:344.83Migoprotafib
CAS:<p>Migoprotafib (GDC-1971) is a potent and highly selective SHP2 (Src Homology-2 Domain-Containing Phosphatase 2) inhibitor for advanced solid tumours.</p>Formula:C25H26N8OColor and Shape:SolidMolecular weight:454.53IDO1-IN-2
CAS:<p>IDO1-IN-2 is a potent and selective IDO1 inhibitor with IC50s of 81 nM, 59 nM (mouse), and 28 nM (rat), respectively. It has anti-cancer activity.</p>Formula:C15H17FN6O4Purity:98%Color and Shape:SolidMolecular weight:364.3320(S)-Hydroxycholesterol
CAS:<p>20(S)-Hydroxycholesterol (20α-Hydroxycholesterol) is an allosteric activator of the oncoprotein smoothened (Smo).</p>Formula:C27H46O2Purity:99.25% - 99.79%Color and Shape:SolidMolecular weight:402.6514-dehydro Zymostenol
CAS:<p>14-dehydro Zymostenol, a cholesterol precursor, boosts MBP+ oligodendrocytes from precursors at 5.8-17 μM.</p>Formula:C27H44OColor and Shape:SolidMolecular weight:384.64BN-82685
CAS:<p>BN-82685, a quinone-based CDC25 inhibitor, shows in vitro and in vivo efficacy, suggesting potential as an anticancer therapy.</p>Formula:C12H15N3O2SPurity:98%Color and Shape:SolidMolecular weight:265.33TAK 21d
CAS:<p>Potent FAAH inhibitor</p>Formula:C19H17F2N7OPurity:98%Color and Shape:SolidMolecular weight:397.38PF 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:382.87Win-62005
CAS:<p>Win-62005 is an inhibitor of cyclic AMP phosphodiesterase III (PDE III)(Kis: 25 and 26 nM for rat heart and canine aorta).</p>Formula:C12H10N4OPurity:98%Color and Shape:SolidMolecular weight:226.23hCAI/II-IN-2
CAS:<p>hCAI/II-IN-2 (2b) inhibits hCA I/II (Ki: 40.97 nM, 15.15 nM) and IX (61.88 nM), fights AMS with anti-hypoxic effects, but has low cellular activity.</p>Formula:C12H12N4O5S2Color and Shape:SolidMolecular weight:356.38103D5R
CAS:<p>103D5R selectively inhibits hif-1α, reducing its levels in hypoxia or with cobalt ions, dose- and time-dependently.</p>Formula:C20H21N3O2Color and Shape:SolidMolecular weight:335.4Dacisteine
CAS:<p>Dacisteine (N,S-Diacetyl-L-cysteine) is an inhibitor of New Delhi metallo-beta-lactamase-1 (NDM-1, IC50 = 1000 μM).</p>Formula:C7H11NO4SPurity:99.57%Color and Shape:SolidMolecular weight:205.23Dehydronitrosonisoldipine
CAS:<p>Dehydronitrosonisoldipine blocks SARM1, slows axon decay & cADPR synthesis; useful in neurodegeneration research.</p>Formula:C20H22N2O5Purity:99.68%Color and Shape:SolidMolecular weight:370.4hACC2-IN-1
CAS:<p>hACC2-IN-1 is a potent inhibitor of acetyl coenzyme A carboxylase 2 (ACC2) with an IC50 value of 2.5 μM for hACC2. hACC2-IN-1 has potential for obesity studies.</p>Formula:C23H32N2O4SColor and Shape:SolidMolecular weight:432.58PDE5-IN-5
CAS:<p>PDE5-IN-5 is a selective inhibitor of phosphodiesterase 5 (PDE5) (IC50: 2.0 nM).</p>Formula:C23H20BrN3O4Color and Shape:SolidMolecular weight:482.33D-Erythro-dihydrosphingosine
CAS:<p>D-Erythro-dihydrosphingosine (C18-Dihydrosphingosine) inhibits arachidonic acid release and cPLA2α activity.</p>Formula:C18H39NO2Purity:99.50% - 99.88%Color and Shape:SolidMolecular weight:301.51Tritoqualine
CAS:<p>Tritoqualine is used as an inhibitor of histidine decarboxylase.</p>Formula:C26H32N2O8Purity:98%Color and Shape:SolidMolecular weight:500.54Autotaxin-IN-1
CAS:<p>Autotaxin-IN-1: strong inhibitor for osteoarthritis pain; IC50=2.2 nM; good PK and PK/PD.</p>Formula:C21H23N7O2Purity:98%Color and Shape:SolidMolecular weight:405.45Tralkoxydim
CAS:<p>Tralkoxydim (Tralkoxydime) is an alkyl ketone herbicide. Tralkoxydim works as an ACCase inhibitor.</p>Formula:C20H27NO3Purity:97.44%Color and Shape:SolidMolecular weight:329.43Lirimilast
CAS:<p>Lirimilast: oral PDE4 inhibitor (IC50: 49 nM), anti-inflammatory, treats asthma/COPD.</p>Formula:C17H12Cl2N2O6SPurity:98%Color and Shape:SolidMolecular weight:443.26Palonidipine
CAS:<p>Palonidipine is an antagonist of calcium, is potential for the therapy of angina-pectoris and hypertension.</p>Formula:C29H34FN3O6Purity:98%Color and Shape:SolidMolecular weight:539.6Pparδ agonist 2
CAS:<p>Pparδ agonist 2 is an agonist of PPARδ.</p>Formula:C20H18F3N3O3SPurity:98%Color and Shape:SolidMolecular weight:437.44LGE-899
CAS:<p>LGE-899 (Sonidegib metabolite M48) is a main metabolite of Sonidegib which is an inhibitor of the hedgehog pathway.</p>Formula:C15H11F3O3Purity:99.93%Color and Shape:SolidMolecular weight:296.24IDO-IN-12
CAS:<p>IDO-IN-12 is an inhibitor of indoleamine 2,3-dioxygenase (IDO).</p>Formula:C13H11BrFN5O3SPurity:99.727%Color and Shape:SolidMolecular weight:416.2311β-HSD1-IN-1
CAS:<p>11β-HSD1-IN-1 is an inhibitor of 11β-hydroxydehydrogenase 1 (11β-HSD1, IC50: 52 nM), and used for the treatment of pain.</p>Formula:C18H14ClF4N3OPurity:99.84%Color and Shape:SolidMolecular weight:399.77(R)-Nepicastat HCl
CAS:<p>(R)-Nepicastat HCl (RS-25560-198 HCl), R-enantiomer, inhibits bovine/human dopamine-β-hydroxylase (IC50: 25.1/18.3 nM); not affecting other enzymes/receptors.</p>Formula:C14H15F2N3S·HClPurity:98%Color and Shape:SolidMolecular weight:331.81Seviteronel
CAS:<p>Seviteronel (VT-464) is a novel CYP17 cleavage enzyme inhibitor and androgen receptor antagonist for the study of breast and prostate cancer.</p>Formula:C18H17F4N3O3Purity:99.67% - 99.98%Color and Shape:SolidMolecular weight:399.34BN82002
CAS:<p>BN82002 (CDC25 Phosphatase Inhibitor I) is a synthetic inhibitor of CDC25 phophatases</p>Formula:C19H25N3O4Purity:98.24%Color and Shape:SolidMolecular weight:359.42RWJ 63556
CAS:<p>RWJ 63556 is an orally active inhibitor of COX-2 selective/5-lipoxygenase, shows anti-inflammatory activities.</p>Formula:C11H10FNO3S2Purity:99.92%Color and Shape:SolidMolecular weight:287.33Endothelial 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:647.25Enazadrem
CAS:<p>Enazadrem is a 5-lipoxygenase inhibitor with antiinflammatory activities.</p>Formula:C18H25N3OPurity:98%Color and Shape:SolidMolecular weight:299.41IQA
CAS:<p>IQA is a casein kinase 2 (CK2) inhibitor.</p>Formula:C17H12N2O3Color and Shape:SolidMolecular weight:292.29CaV1.3 antagonist-1
CAS:<p>CaV1.3 antagonist-1 is a selective CaV1.3L-type calcium channel antagonist useful for researching neurological disorders and cardiovascular diseases.</p>Formula:C17H19ClN2O3Color and Shape:SolidMolecular weight:334.8STL1267
CAS:<p>STL1267 is a REV-ERB agonist that crosses the blood-brain barrier and inhibits BMAL1 gene expression.</p>Formula:C17H11ClN4OPurity:99.19%Color and Shape:SolidMolecular weight:322.75IACS-8968 S-enantiomer
CAS:<p>IACS-8968 S-enantiomer is the S-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).</p>Formula:C17H18F3N5O2Purity:98%Color and Shape:SolidMolecular weight:381.3511β-HSD1-IN-10
CAS:<p>11β-HSD1-IN-10, a potent inhibitor of 11β-HSD1 with an IC50 value of 1.8 µM for humans, is suitable for research into obesity, hyperglycemia, and cognitive</p>Formula:C16H10F3NO2Color and Shape:SolidMolecular weight:305.25UK51656
CAS:<p>UK51656 is an antagonist of calcium (IC50: 4 nM).</p>Formula:C22H28ClN3O6Purity:98%Color and Shape:SolidMolecular weight:465.93AMPD2 inhibitor 1
CAS:<p>AMPD2 inhibitor 1 is an adenosine monophosphate deaminase 2 (AMPD2) inhibitor, useful for studying anorexia in the nervous system.</p>Formula:C25H22N2O2Color and Shape:SolidMolecular weight:382.45Thialysine HCl
CAS:<p>Thialysine HCl is a cytotoxic cysteine derivative that inhibits Escherichia coli, acting as a protein synthesis inhibitor and metabolite.</p>Formula:C5H13ClN2O2SColor and Shape:SolidMolecular weight:200.697-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:390.56GNX-865
CAS:<p>GNX-865 is an inhibitor of mitochondrial permeability transition pore (mtPTP).</p>Formula:C16H14ClNO3Color and Shape:SolidMolecular weight:303.74GT 949
CAS:<p>GT 949 is a selective excitatory positive allosteric modulator of amino acid transporter-2 (EAAT2) (EC50: 0.26 nM).</p>Formula:C30H37N7O2Purity:99.95%Color and Shape:SolidMolecular weight:527.66TM6089
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:306.34SCD1 Inhibitor
CAS:<p>SCD1 Inhibitor is a novel stearoyl-CoA desaturase1 (SCD1) inhibitor.</p>Formula:C21H20F3N3O3Color and Shape:SolidMolecular weight:419.4IMB-XMA0038
CAS:<p>IMB-XMA0038 is a Mycobacterium tuberculosis aspartate semialdehyde dehydrogenase inhibitor with antimicrobial activity for use in tuberculosis research.</p>Formula:C11H10N4O6Purity:98.94% - 99.96%Color and Shape:SolidMolecular weight:294.22LYS006
CAS:<p>LYS006 is a highly efficient and selective LTA4H (leukotriene A4 hydrolase) inhibitor,for neutrophil-driven inflammatory diseases ulcerative colitis.</p>Formula:C16H14ClFN6O3Purity:99.33%Color and Shape:SoildMolecular weight:392.77THR-0921
CAS:<p>THR-0921 (CLX-0921) is a peroxisome proliferator-activated receptor (PPAR) agonist that can be used to study cardiovascular and metabolic diseases.</p>Formula:C28H25NO7SPurity:100% - 99.83%Color and Shape:SolidMolecular weight:519.57SGK1-IN-1
CAS:<p>SGK1-IN-1 (compound 14n) is a highly potent SGK1 (Serum/Glucocorticoid Regulated Kinase 1) inhibitor</p>Formula:C17H12ClFN6O2SPurity:98%Color and Shape:SolidMolecular weight:418.83(-)-L-threo-PDMP (hydrochloride)
CAS:<p>(-)-L-threo-PDMP boosts ganglioside production, enhances neurite and synapse growth, and aids memory post-ischemia at 40 mg/kg/day.</p>Formula:C23H39ClN2O3Color and Shape:SolidMolecular weight:427.03PTP1B-IN-4
CAS:<p>PTP1B-IN-4 (NUN-17724) is an allosteric PTP1B inhibitor with an IC50 of 8 μM. PTP1B-IN-4 can be used in studies about obesity and diabetes.</p>Formula:C26H19Br2N3O7S3Purity:98.19%Color and Shape:SolidMolecular weight:741.45XY101
CAS:<p>XY101 is a selective, metabolically stable and orally available agonist of RORγ inverse(IC50 of 30 nM and a Kd of 380 nM).</p>Formula:C25H20F7NO4SPurity:99.83%Color and Shape:SolidMolecular weight:563.48PF-07208254
CAS:<p>PF-07208254, a potent BDK inhibitor, enhances cardiometabolic endpoints in mice [1].</p>Formula:C7H2ClFO2S2Purity:98%Color and Shape:SolidMolecular weight:236.67PDE9-IN-1
CAS:<p>PDE9-IN-1 is a selective and orally bioavailable Inhibitor of PDE9A(IC50 of 8.7 nM).</p>Formula:C17H23FN6O2Purity:99.86%Color and Shape:SolidMolecular weight:362.4MB05032
CAS:<p>MB05032 is a fructose-,-bisphosphatase inhibitor that inhibits gluconeogenesis and may reduce d-lactate-triggered ETosis.</p>Formula:C11H15N2O4PSPurity:99.66%Color and Shape:SolidMolecular weight:302.29SSI-4
CAS:<p>SSI-4 is a Stearoyl CoA desaturase 1 (SCD1) inhibitor that can be labeled with carbon-11 (11C) for use as a ligand in small animal in vivo PET/CT imaging</p>Formula:C19H21ClN4O3Purity:98%Color and Shape:SolidMolecular weight:388.85Angiogenesis 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:376.4IDO1-IN-21
CAS:<p>IDO1-IN-21 (compound 10m), with an IC50 of 0.64 μM, acts as an IDO1 inhibitor and has demonstrated efficacy in suppressing tumor growth in murine models [1].</p>Formula:C21H19F2N3O6SPurity:98%Color and Shape:SolidMolecular weight:479.45WES-1
CAS:<p>WES-1 (Compound 8g), a carbonic anhydrase IX inhibitor (Ki: 55.9 μM), exhibits broad-spectrum antiproliferative activity against various cancer cell lines,</p>Formula:C20H20N4O3SPurity:98%Color and Shape:SolidMolecular weight:396.46PGAM1-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:435.81RORγt inverse agonist 28
CAS:<p>RORγt inverse agonist 28 is a potent RORγt inverse agonist.</p>Formula:C23H18Cl2F3NO5SColor and Shape:SolidMolecular weight:548.36Erythronic acid
CAS:<p>Erythronic acid, an endogenous carbohydrate metabolite, is instrumental for research into metabolism-associated disorders.</p>Formula:C4H8O5Purity:98%Color and Shape:SolidMolecular weight:136.117β-HSD10-IN-2
CAS:<p>17β-HSD10-IN-2 (compound 11), a benzothiazolylurea-based inhibitor, specifically targets 17β-hydroxysteroid dehydrogenase type 10 (17β-HSD10), avoiding</p>Formula:C15H10ClN3O4SPurity:98%Color and Shape:SolidMolecular weight:363.78ASM-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:390.19LZWL02003
CAS:<p>LZWL02003, an anti-neuroinflammatory agent, demonstrates a protective effect on MPP+-induced neuronal damage and reduces ROS expression.</p>Formula:C18H18N2O2Purity:98%Color and Shape:SolidMolecular weight:294.35LP-533401
CAS:<p>LP-533401 is an inhibitor of Tryptophan hydroxylase 1. It is used for regulates serotonin production in the gut.</p>Formula:C27H22F4N4O3Purity:98%Color and Shape:SolidMolecular weight:526.48SHP844
CAS:<p>SHP844: SHP2 inhibitor, IC50 18.9 µM, affects cell growth/survival by regulating tyrosine phosphorylation.</p>Formula:C29H24ClN5O6Color and Shape:SolidMolecular weight:573.98hCAIX-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:479.55FR-221647
CAS:<p>FR-221647: non-nucleoside adenosine deaminase blocker, moderate efficacy, better pharmacokinetics than EHNA/Pentostatin.</p>Formula:C14H17N3O2Color and Shape:SolidMolecular weight:259.3Manitimus
CAS:<p>Manitimus is a potent immunosuppressive drug, and is an inhibitor of dehydroorotate dehydrogenase,.</p>Formula:C15H11F3N2O2Purity:99.75% - 99.75%Color and Shape:SolidMolecular weight:308.26CAY10761
CAS:<p>CAY10761 inhibits ENPP1 (IC50: 467 μM human, 429 μM snake), mushroom tyrosinase (Ki: 1.9 μM), and urease from different sources (IC50: 0.093-<0.125 mM).</p>Formula:C7H8N4O2S2Color and Shape:SolidMolecular weight:244.29Acetyltrialanine
CAS:<p>Acetyltrialanine is a dipeptide compound that binds at two sites on the Tb+3-pancreatic elastase complex and can be used as a nitrogen source.</p>Formula:C11H19N3O5Purity:99.53%Color and Shape:White PowderMolecular weight:273.29Ebaresdax hydrochloride
CAS:<p>Ebaresdax hydrochloride has analgesic activity and is used in the study of painful diabetic neuropathy caused by type I or type II diabetes.</p>Formula:C12H15ClN2O3SPurity:99.11% - 99.77%Color and Shape:SolidMolecular weight:302.78IACS-8968
CAS:<p>IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).</p>Formula:C17H18F3N5O2Purity:98%Color and Shape:SolidMolecular weight:381.35WAY-213613
CAS:<p>WAY-213613: Potent GLT-1/EAAT2 inhibitor (IC50: 85 nM), selective over EAAT1/EAAT3; inactive at glutamate receptors.</p>Formula:C16H13BrF2N2O4Purity:98%Color and Shape:SolidMolecular weight:415.19Reglitazar
CAS:<p>Reglitazar, a dual PPARα/γ agonist, enhances insulin signaling, reduces insulin resistance, and lowers hypertriglyceridemia in obese rats.</p>Formula:C22H20N2O5Purity:97.07% - 98.72%Color and Shape:SolidMolecular weight:392.4Calcium glycerophosphate
CAS:<p>CaGP inhibits intestinal alkaline phosphatase F3; used for calcium and phosphorus in parenteral nutrition.</p>Formula:C3H7CaO6PPurity:99.84%Color and Shape:SolidMolecular weight:210.14AVE5688
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:438.69Gcase 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:384.43GK187
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:310.26SC-22716
CAS:<p>SC-22716 is a LTA4 hydrolase inhibitor.SC-22716 has anti-inflammatory activity and may be used in the study of inflammatory bowel disease and psoriasis.</p>Formula:C18H21NOPurity:99.91%Color and Shape:SolidMolecular weight:267.37Eribaxaban
CAS:<p>Eribaxaban (PD348292) is an orally available factor Xa inhibitor for the prevention and treatment of venous thromboembolism.</p>Formula:C24H22ClFN4O4Purity:98.99% - 99.13%Color and Shape:SolidMolecular weight:484.91LAZABEMIDE
CAS:<p>Lazabemide (Ro 19-6327) is selective, reversible monoamine oxidase B (MAO-B) inhibitor (IC50 values are 0.03 and > 100 μM for MAO-B and MAO-A respectively).</p>Formula:C8H10ClN3OPurity:98%Color and Shape:SolidMolecular weight:199.64Abiraterone decanoate
CAS:<p>Abiraterone decanoate is a prodrug of Abiraterone that provides controlled release and prolonged inhibition of the enzyme CYP17 through intramuscular.</p>Formula:C34H49NO2Purity:99.69%Color and Shape:SolidMolecular weight:503.76YZ9
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:234.2PD0176078
CAS:<p>PD0176078 () is a newly blocker of N-type Calcium channel.</p>Formula:C23H30F2N2OPurity:99.72%Color and Shape:SolidMolecular weight:388.49CDC25B-IN-1
CAS:<p>CDC25B-IN-1 is an inhibitor of CDC25B with a Ki of 8.5 μM. CDC25B-IN-1 increases the G2/M phase by inhibiting cell proliferation and colony formation.</p>Formula:C20H19NO3Purity:97.05%Color and Shape:SolidMolecular weight:321.37(R)-Lercanidipine hydrochloride
CAS:<p>(R)-Lercanidipine hydrochloride is the R-enantiomer of Lercanidipine. (R)-lercanidipine hydrochloride is a blocker of calcium channel.</p>Formula:C36H42ClN3O6Purity:98%Color and Shape:SolidMolecular weight:648.2PPARα-MO-1
CAS:<p>PPARα-MO-1 is a potent modulator of PPARα.</p>Formula:C27H37NO5Purity:98%Color and Shape:SolidMolecular weight:455.59NF-1819
CAS:<p>NF-1819: strong, selective MGL inhibitor; eases MS symptoms; analgesic; penetrates brain with high permeability.</p>Formula:C24H22FN5O4Purity:99.55%Color and Shape:SolidMolecular weight:463.46Sp-cAMPS
CAS:<p>Rp-cAMPS TEA salt is a cAMP-dependent protein kinase (PKA) activator.</p>Formula:C10H12N5O5PSColor and Shape:SolidMolecular weight:345.27L-Xylulose
CAS:<p>L-Xylulose: a rare sugar, key in metabolism, α-glucosidase inhibitor, lowers glucose, precursor to antiviral drug components.</p>Formula:C5H10O5Color and Shape:SolidMolecular weight:150.13AZD8329
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:421.53Brofaromine
CAS:Brofaromine (CGP 11305A) is an MAO inhibitor (IC50: 0.2 μM for MAO-A).Formula:C14H16BrNO2Color and Shape:SolidMolecular weight:310.19hCAI/II-IN-3
CAS:<p>"hCAI/II-IN-3 (compound 5b) is a potent dual hCA I/II inhibitor with Ki: 51.25nM (I), 13.15nM (II), helps treat AMS."</p>Formula:C16H18N4O4S2Color and Shape:SolidMolecular weight:394.47
