Deidrogenasi
Le deidrogenasi sono enzimi coinvolti nelle reazioni di ossidoriduzione delle vie metaboliche, svolgendo un ruolo centrale nella produzione di energia e nella respirazione cellulare. Questi enzimi sono cruciali per processi come il ciclo dell'acido citrico, la glicolisi e l'ossidazione degli acidi grassi. Gli inibitori delle deidrogenasi sono strumenti importanti nello studio delle malattie metaboliche, del cancro e dello stress ossidativo. Presso CymitQuimica, offriamo una selezione completa di inibitori delle deidrogenasi per supportare la tua ricerca in metabolismo, biologia del cancro e biochimica.
Trovati 302 prodotti di "Deidrogenasi"
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Ivosidenib
CAS:Ivosidenib (AG-120) is an oral IDH1 inhibitor targeting mutated IDH1 to reduce 2-hydroxyglutarate and hinder tumor growth.Formula:C28H22ClF3N6O3Purezza:98.71% - 99.98%Colore e forma:SolidPeso molecolare:582.96AGI-5198
CAS:AGI-5198 (IDH-C35) is a highly effective and specific inhibitor of IDH1 R132H/R132C mutants (IC50: 0.07/0.16 μM).Formula:C27H31FN4O2Purezza:97.37% - 99.23%Colore e forma:SolidPeso molecolare:462.56(R)-GNE-140
CAS:(R)-GNE-140 (GNE-140) is an effective LDHA/LDHB inhibitor (IC50s: 3/5 nM) and is 18-fold more potent than S enantiomer.Formula:C25H23ClN2O3S2Purezza:98.25% - 98.91%Colore e forma:SolidPeso molecolare:499.04Nitrofen
CAS:Nitrofen is a selective contact herbicide. Nitrofen is a protoporphyrinogen oxidase and retinal dehydrogenase inhibitor.Formula:C12H7Cl2NO3Purezza:99.92%Colore e forma:Less Crystals Or Black Solid Used As A Pre- Or Post-Emergence HerbicidePeso molecolare:284.09SW033291
CAS:SW033291 is a small-molecule inhibitor of 15-PGDH (Ki=0.1 nM) that increases prostaglandin PGE2 levels in bone marrow and other tissues.Formula:C21H20N2OS3Purezza:97.26% - 99.02%Colore e forma:SolidPeso molecolare:412.59LDHA-IN-4
CAS:LDHA-IN-4 (AZ33) is an LDHA inhibitor. Binding affinity to 6-His-tagged human LDHA expressed in E.coli BL21 (DE3) by SPR analysis with an active value of 93 nM.Formula:C25H27N3O6SPurezza:98.17% - 99.68%Colore e forma:SolidPeso molecolare:497.566PGD-IN-S3
CAS:6PGD-IN-S3 (6PGD Inhibitor S3) is an inhibitor of 6-phosphogluconate dehydrogenase (6PGD).Formula:C15H10O4Purezza:99.12%Colore e forma:SolidPeso molecolare:254.24AZD7545
CAS:AZD7545 is a potent PDHK inhibitor.Formula:C19H18ClF3N2O5SPurezza:99.12% - 99.96%Colore e forma:SolidPeso molecolare:478.87BVT-14225
CAS:BVT-14225 is a selective 11β-Hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitor (IC50=52 nM).Formula:C16H20ClN3O3S2Purezza:97.78%Colore e forma:SolidPeso molecolare:401.93Perfluorooctanoic acid
CAS:Perfluorooctanoic acid (PFOA) (PFOA) is a persistent and widespread industry-made chemical.Formula:C8HF15O2Purezza:99.70%Colore e forma:White To Off-White Powder OthersolidPeso molecolare:414.07PHGDH-inactive
CAS:PHGDH inactive is inactive against PHGDH and serves as a negative control for NCT-502 and NCT-503 [1].Formula:C17H21N5SPurezza:99.83%Colore e forma:SolidPeso molecolare:327.45MK-8245
CAS:MK-8245 is a liver-targeting SCD inhibitor for human SCD1 (IC50: 1 nM) and for rat/mouse SCD1 (IC50: 3 nM), with anti-diabetic and anti-dyslipidemic function.Formula:C17H16BrFN6O4Purezza:97.58% - 99%Colore e forma:SolidPeso molecolare:467.25NCT-501
CAS:NCT-501 is a potent and selective inhibitor of Aldehyde Dehydrogenase 1A1 (ALDH1A1) with IC50 of 40 nM.Formula:C21H32N6O3Purezza:99.19%Colore e forma:SolidPeso molecolare:416.52G6PDi-1
CAS:G6PDi-1 is an effective G6PD inhibitor. It depletes NADPH and decreases inflammatory cytokine production.Formula:C14H12N4OSPurezza:98.69%Colore e forma:SolidPeso molecolare:284.34BMS-823778 hydrochloride
CAS:<p>BMS-823778 hydrochloride is a potent, selective, and orally active inhibitor of 11β-HSD1 (11β-Hydroxysteroid Dehydrogenase Type 1), demonstrating an IC50 (half</p>Formula:C18H19Cl2N3OColore e forma:SolidPeso molecolare:364.27Galloflavin
CAS:Galloflavin is a lactate dehydrogenase inhibitor. Galloflavin inhibits both human LDH isoforms (type A and type B).Cost-effective and quality-assured.Formula:C12H6O8Purezza:96.24% - 97.47%Colore e forma:SolidPeso molecolare:278.17BVT 2733
CAS:<p>BVT 2733 is a new, non-steroidal, isoform-specific inhibitor of 11β-HSD1.</p>Formula:C17H21ClN4O3S2Purezza:98% - 99.64%Colore e forma:SolidPeso molecolare:428.96NCT-505
CAS:NCT-505 is a potent and selective inhibitor of aldehyde dehydrogenase (ALDH1A1, IC50 = 7 nM) and a weak inhibitor of hALDH1A2, hALDH1A3, hALDH2, hALDH3A1 withFormula:C27H28FN5O3SPurezza:99.93%Colore e forma:SolidPeso molecolare:521.61PfDHODH-IN-1
CAS:PfDHODH-IN-1 is an inhibitor of Plasmodium falciparum dihydroorotate dehydrogenase(PfDHODH) which catalyzes the rate-limiting step for DNA and RNA biosynthesis.Formula:C14H11F3N2O2Purezza:99.87%Colore e forma:SolidPeso molecolare:296.24CM10
CAS:CM10 is an aldehyde dehydrogenase 1A family(ALDH1A) inhibitor.Formula:C20H23N3OPurezza:99.84%Colore e forma:SolidPeso molecolare:321.42Dihydrouracil
CAS:5,6-Dihydrouracil (5,6-Dihydrouracil) is an intermediate breakdown product of uracil.Formula:C4H6N2O2Purezza:99.75%Colore e forma:SolidPeso molecolare:114.1NCT-501 hydrochloride
CAS:NCT-501 hydrochloride: potent, selective ALDH1A1 inhibitor based on theophylline; IC50 of 40 nM; highly discriminant against other ALDHs.Formula:C21H33ClN6O3Colore e forma:SolidPeso molecolare:452.98BI-187004
CAS:BI-187004 is an 11β-hydroxysteroid dehydrogenase 1 inhibitor.Formula:C21H18N4OPurezza:98.63%Colore e forma:SolidPeso molecolare:342.39L-Allylglycine
CAS:L-Allylglycine is a potent inhibitor of the synthetic enzyme for GABA, glutamic acid decarboxylase.Formula:C5H9NO2Purezza:≥98%Colore e forma:White To Off-White Crystalline PowderPeso molecolare:115.13AKR1C3-IN-4
CAS:AKR1C3-IN-4: potent, selective AKR1C3 inhibitor, IC50 = 0.56 μM, potential for CRPC research.Formula:C14H10F3NO2Purezza:98.59%Colore e forma:SolidPeso molecolare:281.23Vidofludimus
CAS:Vidofludimus (SC12267) (4SC-101, SC12267) is a novel small molecule inhibitor of dihydroorotate dehydrogenase (DHODH).Formula:C20H18FNO4Purezza:98.33% - 99.58%Colore e forma:SolidPeso molecolare:355.36VER-246608
CAS:VER-246608 inhibits PDK (IC50: 35-91 nM), boosts PDC, reduces glycolysis, causes cancer cell cytostasis, and enhances doxorubicin effects.Formula:C28H23ClF2N4O4Purezza:98.5%Colore e forma:SolidPeso molecolare:552.96AKR1C3-IN-1
CAS:AKR1C3-IN-1 is a potent and selective inhibitor of AKR1C3(IC50 of 13 nM).Formula:C16H15NO4SPurezza:98.02%Colore e forma:SolidPeso molecolare:317.36NCT-503
CAS:<p>NCT-503 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor with no activity against other dehydrogenases. NCT-503 has antitumor activity. Cost-effective and quality-assured.</p>Formula:C20H23F3N4SPurezza:98.91% - 99.84%Colore e forma:SolidPeso molecolare:408.48Tiazofurin
CAS:Tiazofurin, a synthetic nucleoside, has anti-cancer effects and inhibits IMPDH as TAD after metabolism.Formula:C9H12N2O5SPurezza:99.91%Colore e forma:SolidPeso molecolare:260.27Mutant IDH1-IN-1
CAS:Mutant IDH1-IN-1 is a potent mutant IDH1 R132 h inhibitor with IC50 < 0.1 uM.Formula:C30H31FN4O2Purezza:99.49% - >99.99%Colore e forma:SolidPeso molecolare:498.59Nitrofurazone
CAS:Nitrofurazone (Furacilin) is a topical anti-infective agent effective against gram-negative and gram-positive bacteria.Formula:C6H6N4O4Purezza:99.87%Colore e forma:Pale Yellow Needles Solution) 6 0 - 6 5 Alkaline Solutions Are Dark Orange (Ntp 1992)Peso molecolare:198.14AG-120 (racemic)
CAS:AG-120 (racemic) is an oral IDH1 inhibitor with potential anti-cancer effects.Formula:C28H22ClF3N6O3Purezza:99.56%Colore e forma:SolidPeso molecolare:582.96Vidofludimus hemicalcium
CAS:Vidofludimus hemicalcium: oral DHODH inhibitor, FXR modulator, for autoimmune and fatty liver research.Formula:C20H18FNO4CaColore e forma:SolidPeso molecolare:375.4Imidazole-5-propionic acid
CAS:<p>Imidazole-5-propionic acid (Imidazolylpropionic acid) is a product of histidine metabolism and may involve oxidation or transamination.</p>Formula:C6H8N2O2Purezza:99.62%Colore e forma:SolidPeso molecolare:140.14PfDHODH-IN-2
CAS:PfDHODH-IN-2: powerful antimalarial, blocks PfDHODH (IC50: 1.11 μM), for malaria research.Formula:C13H12ClNO3SPurezza:98.9%Colore e forma:SolidPeso molecolare:297.76AGI-6780
CAS:AGI-6780 is a potent and selective inhibitor of IDH2 R140Q mutant.Formula:C21H18F3N3O3S2Purezza:98.19% - 99.7%Colore e forma:SolidPeso molecolare:481.51Fomepizole
CAS:Fomepizole (4-Methylpyrazole), a competitive inhibitor of alcohol dehydrogenase, is used as an antidote in methanol or ethylene glycol poisoning.Formula:C4H6N2Purezza:98.1% - 99.94%Colore e forma:Yellow <13°C Solid >13°C LiquidPeso molecolare:82.1Brequinar
CAS:Brequinar (NSC-368390) is a potent inhibitor of dihydroorotate dehydrogenase, with potent activities against a broad spectrum of viruses.Formula:C23H15F2NO2Purezza:99.1% - 99.57%Colore e forma:SolidPeso molecolare:375.37AG-636
CAS:AG-636 is a potent, reversible, selective and orally active DHODH inhibitor(IC50 of 17 nM). It has strong anticancer effects.Formula:C21H17N3O2Purezza:99.19%Colore e forma:SolidPeso molecolare:343.38Brequinar sodium
CAS:Bipenquinate is a potent and selective inhibitor of dihydroorotate dehydrogenase (DHODH) with IC50 of 20 nM, blocking de novo pyrimidine biosynthesis.Formula:C23H14F2NNaO2Purezza:98.16%Colore e forma:SolidPeso molecolare:397.36WIN 18446
CAS:inhibitor of aldehyde dehydrogenase 1a2 (ALDH1a2)Formula:C12H20Cl4N2O2Purezza:99.69%Colore e forma:SolidPeso molecolare:366.11DS-1001b
CAS:DS-1001b is an inhibitor of mutant IDH-1 (Isocitrate Dehydrogenase-1)Formula:C29H29Cl3FN3O4Purezza:99.81%Colore e forma:SolidPeso molecolare:608.92BAY-1436032
CAS:BAY-1436032 is a novel, selective and orally available inhibitor of pan-mutant isocitrate dehydrogenase 1 (IDH1).Formula:C26H30F3N3O3Purezza:99.65% - 99.71%Colore e forma:SolidPeso molecolare:489.53DS44960156
CAS:DS44960156 is an inhibitor of methylenetetrahydrofolate dehydrogenase 2 (MTHFD2) that inhibits both MTHFD2 and MTHFD1 and can be used in cancer research.Formula:C20H15NO5Purezza:99.13%Colore e forma:SolidPeso molecolare:349.34Enasidenib mesylate
CAS:Enasidenib mesylate (AG-221 mesylate) is a IDH2 inhibitor that promotes differentiation of leukemia myeloid cells for the treatment of acute myeloid leukemia.Formula:C20H21F6N7O4SPurezza:99.85%Colore e forma:SolidPeso molecolare:569.48GSK1940029
CAS:GSK1940029 (SCD inhibitor 1) is a stearoyl-coa desaturase (SCD) inhibitor.Formula:C18H16Cl2N4O2Purezza:99.48% - 99.49%Colore e forma:SolidPeso molecolare:391.25Nedosiran
CAS:Nedosiran, a GalNAc-dsRNA conjugate for RNAi, targets LDH to treat primary hyperoxaluria and ESRD.Colore e forma:SolidTriflupromazine
CAS:Triflupromazine is a dopamine receptor D1/D2 antagonist and LHDA inhibitor that suppresses dopamine activity in (CNS)mental disorders, sedation, and antiemesis.Formula:C18H19F3N2SColore e forma:SolidPeso molecolare:352.42Nitrophenide
CAS:Nitrophenide, a 3,3'-Dinitrodiphenyl disulfide, blocks M1PDH in the mannitol cycle, serving as an anticoccidial.Formula:C12H8N2O4S2Purezza:99.78%Colore e forma:SolidPeso molecolare:308.33hDHODH-IN-2
CAS:hDHODH-IN-2: Leflunomide metabolite analog, inhibits human dihydroorotate dehydrogenase, anti-inflammatory.Formula:C19H16N2O2Purezza:98%Colore e forma:SolidPeso molecolare:304.349SCH-451659
CAS:SCH-451659 is an 17β-hydroxysteroid dehydrogenases (17β-HSDs) inhibitor.Formula:C30H39Cl2N3O2Purezza:98%Colore e forma:SolidPeso molecolare:544.56673-A
CAS:673-A inhibits ALDH1A, depletes ovarian CSCs, induces necroptosis, and reverses chemo resistance.Formula:C15H13NOColore e forma:SolidPeso molecolare:223.27DHODH-IN-12
CAS:DHODH-IN-12 is a leflunomide derivative and a weak dihydrorotate dehydrogenase (DHODH) inhibitor with a pKa of 5.07.Formula:C10H9N3O2Purezza:99.53%Colore e forma:SolidPeso molecolare:203.2CM39
CAS:CM39 inhibits ALDH, linked to cancer stem-like cells & chemoresistance.Formula:C19H15FN4OSColore e forma:SolidPeso molecolare:366.41Nitrefazole
CAS:Nitrefazole: a 4-nitroimidazole, inhibits ALDH enzyme crucial for alcohol metabolism, has potent, durable effects.Formula:C10H8N4O4Colore e forma:SolidPeso molecolare:248.1911β-HSD1-IN-6
CAS:11β-HSD1-IN-6 is a potent inhibitor of 11β hydroxysteroid dehydrogenase enzymes (11β-HSDs).Formula:C21H19ClN4OColore e forma:SolidPeso molecolare:378.86MEDS433
CAS:MEDS433 inhibits dihydroorotate dehydrogenase (IC50 1.2 nM) and blocks replication of hCoV-OC43, hCoV-229E, SARS-CoV-2 at nanomolar levels.Formula:C20H11F4N3O2Colore e forma:SolidPeso molecolare:401.31hDHODH-IN-11
CAS:hDHODH-IN-11: potent hDHODH inhibitor, IC50 7.2 nM, low cytotoxicity, for AML research.Formula:C24H23N3O3Colore e forma:SolidPeso molecolare:401.46RS6212
CAS:<p>RS6212 is a specific lactate dehydrogenase (LDH) inhibitor (IC50=12.03 μ M）。 RS6212 shows strong anticancer activity in a variety of cancer cell lines.</p>Formula:C20H22N4O3SColore e forma:SolidPeso molecolare:398.48AMG-221
CAS:AMG-221: potent 11β-HSD1 inhibitor, lowers glucose & insulin, reduces obesity in mice.Formula:C14H22N2OSPurezza:98%Colore e forma:SolidPeso molecolare:266.411β-HSD1-IN-10
CAS: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 cognitiveFormula:C16H10F3NO2Colore e forma:SolidPeso molecolare:305.25RORγt/DHODH-IN-2
CAS:RORγt/DHODH-IN-2 (compound 1) is a potent dual RORγt/DHODH inhibitor that can be used in the study of inflammatory bowel disease (IBD).Formula:C25H30N4OSColore e forma:SolidPeso molecolare:434.6DHODH-IN-19
CAS:DHODH-IN-19, a strong DHODH blocker, may help treat cancer and inflammation. (Patent WO2021238881A1)Formula:C22H18ClF6N3O3Colore e forma:SolidPeso molecolare:521.84ASP3662
CAS:ASP3662/SPI-62: Potent, selective CNS-penetrable 11β-HSD1 inhibitor; potential neuropathic pain treatment.Formula:C19H16ClF3N4O2Colore e forma:SolidPeso molecolare:424.8TM-1
CAS:TM-1: PDHK inhibitor, IC50 - PDHK1: 2.97μM, PDHK2: 5.2μM, prevents PDHC phosphorylation, inhibits cancer cell growth.Formula:C26H32N2O6Colore e forma:SolidPeso molecolare:468.54DHODH-IN-3
CAS:DHODH-IN-3: Human DHODH inhibitor with IC50 of 261 nM, Kiapp 32 nM, potential anti-malaria drug.Formula:C17H13ClN2O2Purezza:98%Colore e forma:SolidPeso molecolare:312.75ALDH3A1-IN-2
CAS:ALDH3A1-IN-2 is a potent inhibitor targeting ALDH3A1 (IC50=1.29µM), potentially useful in cancer research.Formula:C11H14N2O3Colore e forma:SolidPeso molecolare:222.2411β-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:C13H9F3N2OColore e forma:SolidPeso molecolare:266.22DHODH-IN-21
CAS:DHODH-IN-21, orally active DHODH blocker with 1.1 nM IC50, shows anticancer activity, potential for AML research.Formula:C20H19ClF4N6O4Colore e forma:SolidPeso molecolare:518.85P1788
CAS:P1788 is a dihydroorotate dehydrogenase (DHODH) inhibitor that can induce DNA damage [1].Formula:C15H17NO3Colore e forma:SolidPeso molecolare:259.3Epostane
CAS:Epostane is a 3β-hydroxysteroid dehydrogenase inhibitor that blocks the biosynthesis of progesterone and pregnenolone.Cost-effective and quality-assured.Formula:C22H31NO3Purezza:>99.99%Colore e forma:SolidPeso molecolare:357.49DHODH-IN-20
CAS:Dhodh-in-20 (Compound 133), a potent DHODH inhibitor, may help study acute myeloid leukemia and inhibit tumor growth.Formula:C24H25F4N3O3Colore e forma:SolidPeso molecolare:479.47ALDH1A1-IN-3
CAS:ALDH1A1-IN-3 selectively inhibits ALDH1A1, enhances HepG2 glucose consumption for metabolic research.Formula:C31H36F3N5O4Colore e forma:SolidPeso molecolare:599.64DHODH-IN-24
CAS:DHODH-IN-24 (compound 16) serves as a powerful inhibitor of human dihydroorotate dehydrogenase (DHODH), exhibiting an IC50 value of 91 nM [1].Formula:C26H26N4Colore e forma:SolidPeso molecolare:394.51BI-4924
CAS:BI-4924 is a PHGDH inhibitor that disrupts serine biosynthesis by intracellular trapping and can be used to study metabolic disorders.Formula:C21H20Cl2N2O6SPurezza:99.55%Colore e forma:SolidPeso molecolare:499.36KM04416
CAS:KM04416 is a GPD2 inhibitor that inhibits LUAD progression by modulating immune cell infiltration.Formula:C12H11NO3SPurezza:99.88%Colore e forma:SolidPeso molecolare:249.29BI-135585
CAS:BI-135585 is an orally active, selective and potent inhibitor of human 11β-hydroxysteroid dehydrogenase-1 (HSD1) for the study of type 2 diabetes.Formula:C28H32N2O4Purezza:99.45% - 99.57%Colore e forma:SolidPeso molecolare:460.57hDHODH-IN-9
CAS:hDHODH-IN-9 is a potent hDHODH inhibitor, IC50=0.34 μM, toxic to MCF-7/A375 cells, promising for cancer research.Formula:C21H21NO4Colore e forma:SolidPeso molecolare:351.4CM026
CAS:CM026 inhibits ALDH1A1 selectively, binds to its aldehyde pocket uncompetitively.Formula:C22H30N6O4Colore e forma:SolidPeso molecolare:442.51ML387
CAS:ML387 is an inhibitor of human NAD(+)- dependent 15- hydroxyprostaglandin dehydrogenase.Formula:C20H21N3O2Purezza:98%Colore e forma:SolidPeso molecolare:335.4Oxycinchophen
CAS:Oxycinchophen: Quinoline-based anti-rheumatic with P-selectin inhibition, DHOD blockade, and anti-inflammatory impacts on vascular muscle.Formula:C16H11NO3Purezza:98%Colore e forma:SolidPeso molecolare:265.26GW648495
CAS:GW648495 is a PfDHODH inhibitor that shows greater than 4,000-fold selectivity for the malarial enzyme.Formula:C16H13N5Purezza:98%Colore e forma:SolidPeso molecolare:275.31BVT-116429
CAS:BVT-116429 is an inhibitor of 11β-HSD1.Formula:C13H12F4N2OSPurezza:98%Colore e forma:SolidPeso molecolare:320.31Genz-669178
CAS:Genz-669178 is a wild-type inhibitor of Plasmodium falciparum dihydroorotate dehydrogenase (PfDHODH).Formula:C17H14N4OSPurezza:98%Colore e forma:SolidPeso molecolare:322.38GA11
CAS:<p>GA11is an inhibitor of ALDH1. It also displays anti-GBM effects in vitro and in vivo.</p>Formula:C19H14N2Purezza:98%Colore e forma:SolidPeso molecolare:270.33EN40
CAS:EN40, as a covalent ligand, is a selective inhibitor of aldehyde dehydrogenase 3A1 (IC50: 2 uM).Formula:C13H15NO2Colore e forma:SolidPeso molecolare:217.26p-Valerylphenol
CAS:p-Valerylphenol (NSC-49186) can be used to synthesize acylphenoxyacetic acid compounds.Formula:C11H14O2Purezza:99.87%Colore e forma:White To Light Beige PowderPeso molecolare:178.23UCK2 Inhibitor-2
CAS:UCK2 Inhibitor-2 is a non-competitive inhibitor of uridine-cytidine kinase 2 (UCK2) with IC50=3.8 µM that inhibits UCK2-mediated nucleoside recycling in cells.Formula:C28H23N3O4SPurezza:98.76% - 99.25%Colore e forma:SolidPeso molecolare:497.57M77976
CAS:M77976 inhibits PDK4 with an IC50 of 648 μM, targeting obesity and diabetes research.Formula:C17H16N2O3Purezza:99.92%Colore e forma:SolidPeso molecolare:296.32Chlorisondamine diiodide
CAS:Chlorisondamine diiodide is a selective nAChR antagonist and ganglionic blocker that persistently antagonizes partial central effects of nicotine.Formula:C14H20Cl4I2N2Purezza:99.97%Colore e forma:SolidPeso molecolare:611.94INCB13739
CAS:INCB13739 is an 11β-HSD1 inhibitor that can be used in the study of hyperlipidemia and hypertriglyceridemia.Formula:C28H25N3O4Purezza:99.32%Colore e forma:SoildPeso molecolare:467.52IMB-XMA0038
CAS:IMB-XMA0038 is a Mycobacterium tuberculosis aspartate semialdehyde dehydrogenase inhibitor with antimicrobial activity for use in tuberculosis research.Formula:C11H10N4O6Purezza:98.94% - 99.96%Colore e forma:SolidPeso molecolare:294.22MDH1-IN-2
CAS:MDH1-IN-2 is a potent MDH1 inhibitor with potential anticancer activity for the study of diseases related to the immune system.Formula:C25H33NO5Purezza:99.21%Colore e forma:SolidPeso molecolare:427.5311β-HSD1-IN-12
CAS:11β-HSD1-IN-12 is an 11β-HSD1 inhibitor.11β-HSD1-IN-12 is implicated in the conversion of glucocorticoids in vivo and can be used to study metabolic syndromeFormula:C19H27ClN2O3SPurezza:99.89%Colore e forma:SolidPeso molecolare:398.95S07-2005 (racemic)
CAS:S07-2005 is a selective AKR1C3 inhibitor with IC50 of 0.13 μM, potential in enhancing cancer chemotherapy.Formula:C20H23NO6Colore e forma:SolidPeso molecolare:373.4AGI-14100
CAS:<p>AGI-14100 is a novel and orally available mIDH1 inhibitor.AGI-14100 is used for the treatment of primary human myeloid leukemia.</p>Formula:C29H22ClF4N5O3Purezza:99.91%Colore e forma:SolidPeso molecolare:599.96RV01
CAS:RV01, a resveratrol-like quinoline, inhibits DNA damage, ALDH2 expression, and has antioxidant and anti-inflammatory properties.Formula:C17H13NO2Purezza:99.93%Colore e forma:SolidPeso molecolare:263.29hDHODH-IN-3
CAS:hDHODH-IN-3 is an inhibitor of human dihydroorotate dehydrogenase with a pMIC50 value of 8.6. hDHODH-IN-3 can inhibit measles virus replication.Formula:C18H19BrN4O2Purezza:99.871%Colore e forma:SolidPeso molecolare:403.27Laflunimus
CAS:Laflunimus (HR325) is a DHODH inhibitor that inhibits immunoglobulin secretion in vitro and in vivo,by interfering with pyrimidine metabolism,neuralgia.Formula:C15H13F3N2O2Purezza:99.86%Colore e forma:SolidPeso molecolare:310.27
