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 8626 products of "Metabolism"
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KCN1
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:465.56LAZABEMIDE
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:199.64F-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:595.85CYP1B1-IN-3
CAS:<p>CYP1B1-IN-3: strong CYP1B1 inhibitor (IC50: 6.6 nM); weak on CYP1A1/CYP1A2; hinders cell migration, invasion; blocks P-gp, AKT/ERK, FAK/SRC, EMT.</p>Formula:C20H16FN3O2S2Color and Shape:SolidMolecular weight:413.49Acetyltrialanine
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:273.29JBP485
CAS:<p>JBP485 is an inhibitor of renal transporters OAT1 and OAT3. JBP485 is an antihepatitis agent as a substrate for intestinal PEPT1.</p>Formula:C8H12N2O4Color and Shape:SolidMolecular weight:200.19PGAM1-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:435.81hCAIX/XII-IN-3
CAS:<p>Compound 6q inhibits hCAIX/CAXII; K i : hCAI >10000 nM, hCAII >10000 nM, hCAIX 66.2 nM, hCAXII 4.4 nM.</p>Formula:C20H13F3N2O4Color and Shape:SolidMolecular weight:402.32YCT529 free acid
CAS:<p>YCT529 free acid is a potent, selective and orally active RAR-α inhibitor .</p>Formula:C29H25NO3Color and Shape:SolidMolecular weight:435.51hDHODH-IN-9
CAS:<p>hDHODH-IN-9 is a potent hDHODH inhibitor, IC50=0.34 μM, toxic to MCF-7/A375 cells, promising for cancer research.</p>Formula:C21H21NO4Color and Shape:SolidMolecular weight:351.4CM39
CAS:<p>CM39 inhibits ALDH, linked to cancer stem-like cells & chemoresistance.</p>Formula:C19H15FN4OSColor and Shape:SolidMolecular weight:366.41Oxythiamine diphosphate
CAS:<p>Oxythiamine diphosphate is a competitivethiamine pyrophosphate inhibitor(Ki of 30 nM).</p>Formula:C12H17N3O8P2SPurity:98%Color and Shape:SolidMolecular weight:425.29hCAIX/XII-IN-6
<p>hCAIX/XII-IN-6: Oral carbonic anhydrase inhibitor, targets hCA I/II/IV/IX/XII, aids rheumatoid arthritis research. Ki: 6697/2950/4093/4.1/7.7 nM.</p>Formula:C26H23N3O6S4Color and Shape:SolidMolecular weight:601.74hCAI/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:394.47Prolyl Endopeptidase Inhibitor 1
CAS:<p>Prolyl Endopeptidase Inhibitor 1 is a potent inhibitor of prolyl endopeptidase (PEP; PE)(Ki : 15 nM) , has anti-amnesic effect.</p>Formula:C15H24N2O4Purity:98%Color and Shape:SolidMolecular weight:296.36DTP348
CAS:<p>DTP348: Oral carbonic anhydrase IX inhibitor & hypoxic cell radiosensitizer with sulfamide & 5-nitroimidazole components.</p>Formula:C6H11N5O4SColor and Shape:SolidMolecular weight:249.25Sp-cAMPS
CAS:<p>Rp-cAMPS TEA salt is a cAMP-dependent protein kinase (PKA) activator.</p>Formula:C10H12N5O5PSColor and Shape:SolidMolecular weight:345.27Nitrefazole
CAS:<p>Nitrefazole: a 4-nitroimidazole, inhibits ALDH enzyme crucial for alcohol metabolism, has potent, durable effects.</p>Formula:C10H8N4O4Color and Shape:SolidMolecular weight:248.19hCAII-IN-2
CAS:<p>hCAII-IN-2 inhibits human carbonic anhydrases I, II, IX, XII with Ki values of 261.4, 3.8, 19.6, 45.2 nM respectively.</p>Formula:C25H18ClN5O4SColor and Shape:SolidMolecular weight:519.96URB-694
CAS:<p>URB-694 is a fatty acid amide hydrolase (FAAH) inhibitor.</p>Formula:C19H21NO3Color and Shape:SolidMolecular weight:311.37UKI-1
CAS:<p>UKI-1 is a urokinase-type plasminogen activator system synthetic inhibitor.</p>Formula:C32H47N5O5SPurity:98%Color and Shape:SolidMolecular weight:613.8111β-HSD1-IN-6
CAS:<p>11β-HSD1-IN-6 is a potent inhibitor of 11β hydroxysteroid dehydrogenase enzymes (11β-HSDs).</p>Formula:C21H19ClN4OColor and Shape:SolidMolecular weight:378.86CAY10761
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:244.29FR-221647
CAS:<p>FR-221647: non-nucleoside adenosine deaminase blocker, moderate efficacy, better pharmacokinetics than EHNA/Pentostatin.</p>Formula:C14H17N3O2Color and Shape:SolidMolecular weight:259.3JMS-053
CAS:<p>JMS-053 is a phosphatase DUSP3 inhibitor that inhibits CDC25B and prevents VEGF from disrupting the microvascular endothelial barrier.</p>Formula:C13H8N2O2SPurity:≥98.0%Color and Shape:SolidMolecular weight:256.28Genz-669178
CAS:<p>Genz-669178 is a wild-type inhibitor of Plasmodium falciparum dihydroorotate dehydrogenase (PfDHODH).</p>Formula:C17H14N4OSPurity:98%Color and Shape:SolidMolecular weight:322.3811β-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:305.25Indolapril hydrochloride
CAS:<p>Indolapril hydrochloride is a nonsulfhydryl angiotensin converting enzyme (ACE) inhibitor with antihypertensive activity.</p>Formula:C24H35ClN2O5Color and Shape:SolidMolecular weight:467(±)-γ-Tocopherol
CAS:<p>(±)-γ-Tocopherol is a form of vitamin E with antioxidant and anti-inflammatory properties.</p>Formula:C28H48O2Color and Shape:SolidMolecular weight:416.68CD 1530
CAS:<p>CD 1530 is an ARγ agonist (Kd:150 nM) with potential anticancer activity for the study of oral carcinogenesis.</p>Formula:C27H26O3Purity:98.13%Color and Shape:SolidMolecular weight:398.49IQA
CAS:<p>IQA is a casein kinase 2 (CK2) inhibitor.</p>Formula:C17H12N2O3Color and Shape:SolidMolecular weight:292.29Factor VII-IN-1
CAS:<p>Factor VII-IN-1 (example 43) is an effective Factor VII (FVII) inhibitor (IC50=1.1 μM) with anticoagulant properties.</p>Formula:C15H10BrNO3Purity:99.19%Color and Shape:SolidMolecular weight:332.15Dacisteine
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:205.23Tyrphostin AG 1112
CAS:<p>Tyrphostin AG 1112 is a Bcr-Abl kinase blocker. It can activate the terminal differentiation of K562 cells and the purging of Ph+ cells.</p>Formula:C15H10N6Color and Shape:SolidMolecular weight:274.28Win-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:226.23103D5R
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:335.4BN-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:265.33hCAI/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:356.38IM176OUT05
CAS:<p>IM176OUT05 activates stem cell metabolism with hair regrowth-promoting effects.</p>Formula:C11H17N5Color and Shape:SolidMolecular weight:219.29FASN-IN-4
CAS:<p>FAS-IN-1 is a potent inhibitor of Fatty acid synthase (FAS) wtih IC50 of 10 nM.</p>Formula:C26H27N3O4SPurity:98%Color and Shape:SolidMolecular weight:477.58L 656224
CAS:<p>L 656224 is a 5-LO inhibitor.</p>Formula:C20H21ClO3Purity:98%Color and Shape:SolidMolecular weight:344.83Methyl-3β-hydroxycholenate
CAS:<p>Methyl-3β-hydroxycholenate (Methyl 3beta-hydroxychol-5-enoate) is a modulator of RORγ.</p>Formula:C25H40O3Purity:98.78%Color and Shape:SolidMolecular weight:388.58K134
CAS:<p>K134 is an inhibitor of phosphodiesterase 3. The IC50s of K134 for PDE3A, PDE3B, PDE5, PDE2 and PDE4 are 0.1, 0.28, 12.1, >300 and >300 μM, respectively.</p>Formula:C22H29N3O4Purity:98%Color and Shape:SolidMolecular weight:399.482-Hydroxy atorvastatin calcium salt
CAS:<p>2-Hydroxy atorvastatin calcium salt is a hydroxy metabolite of Atorvastatin calcium salt which is a potent HMG-CoA reductase inhibitor (IC50 = 8 nM).</p>Formula:C33H34FN2O60·5CaPurity:97.06%Color and Shape:SolidMolecular weight:593.68CL67
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:670.81(RS)-Eflucimibe
CAS:<p>Eflucimibe is an ACAT inhibitor.</p>Formula:C29H43NO2SPurity:98%Color and Shape:SolidMolecular weight:469.72SK-216
CAS:<p>SK-216,PAI-1 inhibitor. Reduces tumor angiogenesis. Inhibits VEGF-induced endothelial cell migration. Alleviates pulmonary fibrosis.</p>Formula:C29H29NNa2O6Purity:98.29%Color and Shape:SolidMolecular weight:533.52(-)-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:531.43SRPKIN-1
CAS:<p>SRPKIN-1 is a covalent and irreversible inhibitor of SRPK1/2 (IC50s: 35.6 and 98 nM, respectively).</p>Formula:C27H21FN2O3SPurity:98%Color and Shape:SolidMolecular weight:472.53PKM2 activator 5
CAS:<p>PKM2 activator 5 is a novel and potent PKM2 activator (AC50: 0.316 µM) with potential anticancer activity for the study of cancer metabolism-related diseases.</p>Formula:C18H19FN2O6S2Purity:98%Color and Shape:SolidMolecular weight:442.48CS-722 Free base
CAS:<p>CS-722 Free base: synthetic muscle relaxant; inhibits spinal reflex and sodium/calcium currents affecting synaptic activity.</p>Formula:C16H19ClN2O4Purity:99.52%Color and Shape:SolidMolecular weight:338.79IDO-IN-3
CAS:<p>IDO-IN-3 is a potent indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 290 nM).</p>Formula:C11H12BrFN6O2Color and Shape:SolidMolecular weight:359.15Rovazolac
CAS:<p>Rovazolac (ALX-101) is a liver x receptor (LXR) modulator used in the study of immune system disorders and atopic dermatitis.</p>Formula:C21H19F3N2O4SPurity:99.35%Color and Shape:SolidMolecular weight:452.45ALDH1A1-IN-2
CAS:<p>ALDH1A1-IN-2 is an aldehyde dehydrogenase 1a1 inhibitor with anticancer activity.ALDH1A1-IN-2 may be used in the study of breast cancer, inflammation or obesity</p>Formula:C25H23ClN4O3SPurity:99.48%Color and Shape:SolidMolecular weight:494.99BAY 73-6691
CAS:<p>BAY 73-6691 is an inhibitor of brain penetrant PDE9A.</p>Formula:C15H12ClF3N4OColor and Shape:SolidMolecular weight:356.73GSK2945
CAS:<p>GSK2945, a specific Rev-erbα antagonist, boosts CYP7A1 and cholesterol metabolism. EC50: 21.5 μM (mouse), 20.8 μM (human).</p>Formula:C20H18Cl2N2O2SPurity:98%Color and Shape:SolidMolecular weight:421.348-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:330.77TP-004
CAS:<p>TP-004 is a potent and reversible methionine aminopeptidase 2 (MetAP2) inhibitor (IC50: 6 nM).</p>Formula:C17H16F3N5OPurity:98%Color and Shape:SolidMolecular weight:363.34Succinyladenosine
CAS:<p>Succinyladenosine, a marker for ASL deficiency, is made by dephosphorylating S-AMP with 5-nucleotidase.</p>Formula:C14H17N5O8Color and Shape:SolidMolecular weight:383.317SCH-351591
CAS:<p>SCH-351591 is an orally active inhibitor of phosphodiesterase 4.</p>Formula:C17H10Cl2F3N3O3Purity:98%Color and Shape:SolidMolecular weight:432.18Gcase 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:384.43PDE9-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:362.4HSL-IN-1
CAS:<p>HSL-IN-1 is an HSL inhibitor that significantly reduces the reactive metabolite load and reduces the release of free fatty acids from stored fat.</p>Formula:C19H13BClF3N2O4Purity:>99.99%Color and Shape:SolidMolecular weight:436.58Nebicapone
CAS:<p>Nebicapone, a reversible COMT inhibitor, reduces L-DOPA breakdown, aiding Parkinson's treatment.</p>Formula:C14H11NO5Purity:98%Color and Shape:SolidMolecular weight:273.24CAY10487
CAS:<p>CAY10487 reduces aortic fatty streaks in high-cholesterol rabbits by 37.4% and inhibits LDL oxidation by 75% at 2μM, without altering lipids or ACAT activity.</p>Formula:C13H15NO5Color and Shape:SolidMolecular weight:265.26Camylofin 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:356.94PGAM1-IN-2
CAS:<p>PGAM1-IN-2 is an inhibitor of phosphoglycerate mutase 1 ( PGAM1 ) with an IC 50 of 2.1 μM [1].</p>Formula:C25H16N2O7SPurity:98%Color and Shape:SolidMolecular weight:488.47Otamixaban
CAS:<p>Otamixaban (FXV673) is a selective and highly effective Xa inhibitor that inhibits the generation of thrombin and can be used to study acute coronary syndrome.</p>Formula:C25H26N4O4Purity:98.08%Color and Shape:SolidMolecular weight:446.5OMDM-2
CAS:<p>OMDM-2 is a metabolically stable and selective inhibitor of anandamide cellular uptake (ACU), exhibiting a Ki value of 3.0 μM in RBL-2H3 cells.</p>Formula:C27H45NO3Purity:98%Color and Shape:SolidMolecular weight:431.65ML-262
CAS:<p>ML-262 is an effective inhibitor of hepatic lipid droplet formation and is used in studies of non-alcoholic fatty liver disease.</p>Formula:C27H32N2O4SColor and Shape:SolidMolecular weight:480.62Epiroprim
CAS:<p>Epiroprim (Ro11-8958) is a selective dihydrofolate reductase (DHFR) inhibitor with antibacterial activity, inhibiting Staphylococcus and Streptococcus.</p>Formula:C19H23N5O2Purity:99.68% - >99.99%Color and Shape:SolidMolecular weight:353.42Enpp-1-IN-13
CAS:<p>Enpp-1-IN-13 inhibits ENPP1 (IC50: 1.29 μM) & ENPP3 (IC50: 20.2 μM) with anticancer properties.</p>Formula:C28H22ClN5OSColor and Shape:SolidMolecular weight:512.03Spiraprilat
CAS:<p>Spiraprilat is an ACE inhibitor. It also is an active metabolite of spirapril.</p>Formula:C20H26N2O5S2Purity:98%Color and Shape:SolidMolecular weight:438.56sPLA2-X Inhibitor 31
CAS:<p>sPLA2-X Inhibitor 31 targets sPLA2-X with IC50: 26 nM; less effective on sPLA2-IIa (310 nM), sPLA2-V (2230 nM).</p>Formula:C19H15F3N2O4Purity:98%Color and Shape:SolidMolecular weight:392.33MRL-871
CAS:<p>MRL-871 is a selective RORγt allosteric inhibitor, reducing IL-17a mRNA production in EL4 cells, interacting with PPARgamma in partial agonistic binding modes.</p>Formula:C22H12ClF3N2O3Purity:99.66%Color and Shape:SolidMolecular weight:444.79S07-2010
CAS:<p>S07-2010 is a pan-Aldo-Keto Reductase 1C3 (AKR1C3) inhibitor with potential anti-cancer activity, inducing apoptosis in A549/DDP cells.</p>Formula:C19H21N3O3SPurity:98.13%Color and Shape:SolidMolecular weight:371.45AGN 191701
CAS:<p>AGN 191701 is an agonist of the Retinoid X receptor.</p>Formula:C23H28O2SPurity:98%Color and Shape:SolidMolecular weight:368.53AHR-15010
CAS:<p>AHR-15010 is a novel anti-arthritic agent.</p>Formula:C10H16N2O8S2Purity:98%Color and Shape:SolidMolecular weight:356.372'-O-Methyladenosine
CAS:<p>2'-O-Methyladenosine, a methylated adenine residue is found in the urine of normals and adenosine deaminase deficient patients.</p>Formula:C11H15N5O4Purity:99.89%Color and Shape:White SolidMolecular weight:281.27IMB-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:294.22THR-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:519.57BI-135585
CAS:<p>BI-135585 is an orally active, selective and potent inhibitor of human 11β-hydroxysteroid dehydrogenase-1 (HSD1) for the study of type 2 diabetes.</p>Formula:C28H32N2O4Purity:99.45% - 99.57%Color and Shape:SolidMolecular weight:460.57sEH inhibitor-3
CAS:<p>sEH inhibitor-3 is an orally available, selective and potent inhibitor of sEH for cancer research.</p>Formula:C19H23F4N3O4Purity:98%Color and Shape:SolidMolecular weight:433.4Glycogen phosphorylase-IN-1
CAS:<p>Glycogen phosphorylase-IN-1 is an hlGPa inhibitor that can be used in the study of type 2 diabetes and canine lupus.</p>Formula:C17H15ClF2N4O4Purity:97.98% - 98.15%Color and Shape:SolidMolecular weight:412.78MDK-4823
CAS:<p>MDK-4823 (LMPTP inhibitor1) blocks LMPTP, fighting insulin resistance and diabetes in obesity.</p>Formula:C28H36N4OColor and Shape:SolidMolecular weight:444.61Enpp-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:434.51FAAH-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:447.53Delapril
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:452.54Isospaglumate sodium
CAS:<p>Isospaglumate sodium is the sodium salt of isospaglumate which is an antiallergic agent.</p>Formula:C11H16N2NaO8Color and Shape:SolidMolecular weight:327.245OSMI-3
CAS:<p>OSMI-3 is a potent and cell-permeable inhibitor of O-GlcNAc transferase (OGT) for the study of cancer and cardiovascular disease.</p>Formula:C32H35N3O9S2Purity:99.03% - 99.08%Color and Shape:SolidMolecular weight:669.77HIF-1α-IN-3
CAS:<p>HIF-1α-IN-3, also known as Compound (S)-3f, is a hypoxia-selective inhibitor of HIF-1α. It exhibits potent antiestrogenic activity [1].</p>Formula:C19H17N5O2Color and Shape:SolidMolecular weight:347.37Agn 190727
CAS:<p>Agn 190727 is a retonoic acid receptor that can induce retinoid-induced hypertriglyceridemia.</p>Formula:C20H22O2Color and Shape:SolidMolecular weight:294.39α-Glucosidase-IN-2
CAS:<p>α-Glucosidase-IN-2 (compound 5d) is a potent inhibitor of α-Glucosidase, exhibiting an inhibitory concentration (IC50) of 9.48 μM, and functions as an</p>Formula:C17H11N3O2S2Color and Shape:SolidMolecular weight:353.42JNJ-42314415
CAS:<p>JNJ-42314415 is a potent, specific, and centrally active inhibitor of PDE10A.</p>Formula:C19H23N5O2Purity:98%Color and Shape:SolidMolecular weight:353.42hCAIX-IN-3
CAS:<p>hCAII-IN-3 (7e) selectively inhibits CA II/IX with Kis of 124.2/30.5 nM, showing promise for cancer treatment.</p>Formula:C21H21BrN6O4SColor and Shape:SolidMolecular weight:533.4α-Glycosidase-IN-1
CAS:<p>α-Glycosidase-IN-1 (compound MZ7) is a potent inhibitor of α-GLY (α-glycosidase) (IC50: 44.72 nM, Ki: 44.74 nM).</p>Formula:C21H19N9O6S2Color and Shape:SolidMolecular weight:557.56Glucosylceramide synthase-IN-1
CAS:<p>Potent oral GCS inhibitor T-036, crosses BBB, targets human (IC50: 31 nM) and mouse GCS (IC50: 51 nM), for Gaucher disease research.</p>Formula:C24H20F4N2O3Color and Shape:SolidMolecular weight:460.429(R)-HODE
CAS:<p>9(R)-HODE, a linoleic acid product, is made by some human/bovine endothelial cells, but its function and forming enzyme are unknown.</p>Formula:C18H32O3Color and Shape:SolidMolecular weight:296.44ATX inhibitor 8
CAS:<p>ATX inhibitor 8 is an inhibitor of the autocrine motor factor Autotaxin (ATX).</p>Formula:C28H26N10OColor and Shape:SolidMolecular weight:518.57FTase-IN-1
CAS:<p>FTase-IN-1, a potent FTase inhibitor, has an IC50 of 0.35 μM with strong antitumor activity and cytotoxicity.</p>Formula:C23H16N2O2SColor and Shape:SolidMolecular weight:384.45
