Metabolismo
Los inhibidores del metabolismo son compuestos que interfieren con las vías metabólicas, alterando la producción y utilización de energía dentro de las células. Estos inhibidores se utilizan para estudiar la regulación del metabolismo, el papel de las vías metabólicas en enfermedades como el cáncer y la diabetes, y para desarrollar nuevas estrategias terapéuticas. Los inhibidores del metabolismo pueden dirigirse a diversas enzimas y procesos involucrados en la glucólisis, la oxidación de ácidos grasos y otras funciones metabólicas. En CymitQuimica, ofrecemos una amplia gama de inhibidores del metabolismo de alta calidad para apoyar su investigación en bioquímica, trastornos metabólicos y desarrollo de fármacos.
Subcategorías de "Metabolismo"
- AhR(41 productos)
- Aminopeptidasa(74 productos)
- CETP(20 productos)
- Anhídrido carbónico(185 productos)
- Caseína quinasa(137 productos)
- DHFR(34 productos)
- Descarboxilasa(4 productos)
- Deshidrogenasa(289 productos)
- FAAH(65 productos)
- FXR(59 productos)
- Factor Xa(83 productos)
- Ácido graso sintasa(36 productos)
- Ferroptosis(218 productos)
- GR(3 productos)
- GSNOR(4 productos)
- Glucoquinasa(56 productos)
- HIF / HIF Prolilhidroxilasa(145 productos)
- HMG-CoA reductasa(33 productos)
- Hidroxilasa(34 productos)
- IDO(84 productos)
- LDL(8 productos)
- Lipasa(104 productos)
- Lípido(62 productos)
- Lipoxigenasa(132 productos)
- MAO(87 productos)
- MPO(2 productos)
- NAMPT(38 productos)
- P450(6 productos)
- PAI-1(26 productos)
- PDE(166 productos)
- PED(1 productos)
- PKM(15 productos)
- PPAR(168 productos)
- Fosfolipasa(82 productos)
- ROR(43 productos)
- Receptor de retinoides(28 productos)
- SGK(11 productos)
- Tiorredoxina(12 productos)
- Transferasa(29 productos)
- Transportador(43 productos)
- UGT(4 productos)
- Inhibidores de la xantina oxidasa (XO)(9 productos)
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Se han encontrado 9054 productos de "Metabolismo"
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AMG-221
CAS:AMG-221: potent 11β-HSD1 inhibitor, lowers glucose & insulin, reduces obesity in mice.Fórmula:C14H22N2OSPureza:98%Forma y color:SolidPeso molecular:266.4JTP-4819
CAS:<p>JTP-4819: potent PEP inhibitor, may treat Alzheimer's, boosts brain peptides and acetylcholine, aiding memory.</p>Fórmula:C19H25N3O4Forma y color:SolidPeso molecular:359.42MitoTEMPO hydrate
CAS:MitoTEMPO, a mitochondria-targeted antioxidant, scavenges superoxide and alkyl radicals supporting potential therapy for mitochondrial dysfunction.Fórmula:C29H35N2O2P·Cl·H2OForma y color:SolidPeso molecular:528.04Enpp-1-IN-5
CAS:<p>Enpp-1-IN-5 is a potent enpp-1 inhibitor with potential in cancer and infectious disease research.</p>Fórmula:C17H26N6O4SForma y color:SolidPeso molecular:410.49mIDH1-IN-1
CAS:mIDH1-IN-1 is a selective mIDH1 inhibitor (IC50: 961.5 nM), blocks 2-HG production, and hinders IDH1 mutant cell growth (IC50: 41.8 nM).Fórmula:C25H27N3O5Forma y color:SolidPeso molecular:449.5UK-414,495
CAS:<p>UK-414,495 is a potent, selective inhibitor of the neutral endopeptidase, the enzyme normally serves to break down the neuropeptide VIP.</p>Fórmula:C16H25N3O3SForma y color:SolidPeso molecular:339.45Xanthine oxidoreductase-IN-2
CAS:<p>Xanthine oxidoreductase-IN-2 inhibits XOR with 7.2 nM IC50 and shows hypouricemic effects in mice.</p>Fórmula:C21H19N3O2Forma y color:SolidPeso molecular:345.39α-Glucosidase-IN-8
CAS: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].Fórmula:C19H20FN3O2Forma y color:SolidPeso molecular:341.38Eggmanone
CAS:EGM1: potent PDE4D3 inhibitor, IC50=72 nM, 40-50x selectivity over other PDEs, activates PKA, blocks Hh.Fórmula:C20H20N2O2S3Forma y color:SolidPeso molecular:416.58hCAIX-IN-6
CAS:6B and 14g inhibit tumor-associated HCA IX with low nanomolar potency; 6K targets HCA XII. All are potential cancer drug leads.Fórmula:C18H12N2O4SForma y color:SolidPeso molecular:352.36Carbonic anhydrase inhibitor 13
CAS:Carbonic anhydrase inhibitor 13 (compound 7) is a potent inhibitor of carbonic anhydrase (CA).Fórmula:C17H15N5O3S2Forma y color:SolidPeso molecular:401.46IDO1-IN-17
CAS:IDO1-IN-17 (I-4) is an IDO1 inhibitor, with an IC 50 of 0.44 μM in hela cells .Fórmula:C28H32BrClFN5O2Forma y color:SolidPeso molecular:604.94FAAH-IN-5
CAS:FAAH-IN-5 (Compound 7) selectively, irreversibly inhibits FAAH (IC50: 10.5 nM) with low PAMPA permeability.Fórmula:C21H19N3O6SForma y color:SolidPeso molecular: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>Fórmula:C22H20F6N6Forma y color:SolidPeso molecular:482.42PKR activator 2
CAS:PKR activator 2 is a potent activator of pyruvate kinase-R (PKR).Fórmula:C18H16N8OSPureza:98%Forma y color:SolidPeso molecular:392.44FXR agonist 4
FXR agonist 4: EC50 of 1.05μM, treats hyperlipidemia, steatosis, insulin resistance, inflammation in DIO mice, for NAFLD research.Fórmula:C21H28ClN3OForma y color:SolidPeso molecular:373.92Protizinic acid
CAS:Protizinic acid is an oral NSAID with anti-inflammatory and antipyretic properties, inhibiting PLA2 at IC50 of 210μM.Fórmula:C17H17NO3SForma y color:SolidPeso molecular:315.39ACC1/2-IN-2
CAS:PF-3: potent ACC1/2 inhibitor; IC50: 22 nM (ACC1), 48 nM (ACC2); anti-cancer research potential.Fórmula:C24H25N3O3Forma y color:SolidPeso molecular:403.47SCH-42354
CAS:SCH-42354: potent oral NEP inhibitor, activates ANP & leu-enkephalin, has anti-hypertensive properties, IC50s of 8.3 & 10.0 nM.Fórmula:C16H23NO3S2Forma y color:SolidPeso molecular:341.49ICI 211965
CAS:ICI 211965 is a selective and orally potent of 5-Lipoxygenase (5-LPO).Fórmula:C24H23NO2SPureza:98%Forma y color:SolidPeso molecular:389.51(S)-Bromoenol lactone
CAS:(S)-BEL, a chiral inhibitor of iPLA2β, blocks vasopressin-induced arachidonate release in A10 cells; IC50 = 2μM.Fórmula:C16H13BrO2Forma y color:SolidPeso molecular:317.18PTP1B-IN-15
CAS:PTP1B-IN-15 is a potent and selective protein tyrosine phosphatase 1B (PTP1B) inhibitor that has shown research potential in type II diabetes and obesity.Fórmula:C19H17Br2NO5SForma y color:SolidPeso molecular:531.22Carbonic anhydrase inhibitor 11
CAS:Potent carbonic anhydrase inhibitor VI targets CA II, IX, XII with Ki: 40, 39, 900 nM respectively.Fórmula:C19H15F3N4O3S2Forma y color:SolidPeso molecular:468.47hCAIX/XII-IN-4
CAS:hCAIX/XII-IN-4 inhibits CAIX/XII with Ki: 4.5 nM (CAXII), 23.6 nM (CAIX), and >10000 nM (CAI/CAII).Fórmula:C20H16N2O5Forma y color:SolidPeso molecular:364.3511β-HSD1-IN-6
CAS:11β-HSD1-IN-6 is a potent inhibitor of 11β hydroxysteroid dehydrogenase enzymes (11β-HSDs).Fórmula:C21H19ClN4OForma y color:SolidPeso molecular:378.86Tyrphostin 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>Fórmula:C15H10N6Forma y color:SolidPeso molecular:274.28Glucocerebrosidase-IN-1
CAS:Glucocerebrosidase-IN-1 inhibits GCase with IC50 of 29.3 μM, Ki 18.5 μM, useful for Gaucher's and Parkinson's research.Fórmula:C13H27NO3Forma y color:SolidPeso molecular:245.36MDPD
CAS:MDPD boosts AtFAAH, the enzyme degrading NAEs in Arabidopsis, reducing NAE 12:0's growth inhibition.Fórmula:C21H19N3O3Forma y color:SolidPeso molecular:361.39Vorozole
CAS:<p>Vorozole (R83842) is an orally active, potent, and selective nonsteroidal aromatase inhibitor.Vorozole exhibits antitumor activity in vivo and may be used in</p>Fórmula:C16H13ClN6Pureza:99.65% - 99.94%Forma y color:SolidPeso molecular:324.77Lombricine
CAS:Lombricine, as a phosphodiester of 2-guanidinoethanol and D-serine in structure, is a phosphagen that is unique to earthworms.Fórmula:C6H15N4O6PForma y color:SolidPeso molecular:270.18LY 113174
CAS:LY 113174, a novel nonsteroidal aromatase inhibitor, may prove useful in the treatment of estrogen-dependent diseases.Fórmula:C17H10Cl2N2Forma y color:SolidPeso molecular:313.18FC11409B
CAS:FC11409B is a CAIX inhibitor, inhibiting breast cancer invasion and metastasis.Fórmula:C29H23BF4N2O3SForma y color:SolidPeso molecular:566.38RORγt modulator 3
CAS:RORγt modulator 3 is a modulator of retinol-related orphan receptor γt (RORγt) and can be used to study RORγt-mediated diseases such as pain, COPD, inflammationFórmula:C25H25ClFN3O4SForma y color:SolidPeso molecular:518Zidovudine glucuronide
CAS:Zidovudine glucuronide: an NRTI antiretroviral for HIV/AIDS treatment; blocks HIV reverse transcriptase, stops viral DNA formation.Fórmula:C16H21N5O10Forma y color:SolidPeso molecular:443.37Lp-PLA2-IN-4
CAS:Lp-PLA2-IN-4, a potent inhibitor of Lp-PLA2/PAF-AH, may target Alzheimer's, atherosclerosis. (WO2021228159A1, Compound 38)Fórmula:C23H18F5N3O4Forma y color:SolidPeso molecular:495.4Flutolanil
CAS:Flutolanil: a fungicide targeting R. solani in rice, toxic to zebrafish.Fórmula:C17H16F3NO2Forma y color:SolidPeso molecular:323.31JZP-MA-13
JZP-MA-13: selective α/β-hydrolase domain 6 inhibitor, IC 50 392 nM, doesn't inhibit MAGL/ABHD12/FAAH, used in PET imaging.Fórmula:C14H15FN4O3SForma y color:SolidPeso molecular:338.36BRD9500
CAS:BRD9500 is an oral PDE3 inhibitor, IC50: 10 nM (PDE3A), 27 nM (PDE3B); effective in SK-MEL-3 cancer model.Fórmula:C15H18FN3O2Forma y color:SolidPeso molecular:291.32α-Glucosidase-IN-6
CAS:α-Glucosidase-IN-6 is a competitive inhibitor of α-glucosidase (IC50: 5.69 μM) and exhibits potential for anti-diabetic studies.Fórmula:C24H17ClF3NO3SForma y color:SolidPeso molecular:491.91JTP 103237
CAS:<p>JTP 103237 is a potent and selective monoacyglycerol acyltransferase 2 (MOGAT2) inhibitor.</p>Fórmula:C24H29F3N6OForma y color:SolidPeso molecular:474.52SHP2-IN-5
CAS:SHP2-IN-5 (compound 1) is a non-receptor protein tyrosine phosphatase inhibitor targeting SHP2 with an IC50 value of 97 nM, associated with regulating cellFórmula:C12H8O6Forma y color:SolidPeso molecular:248.19Methazolamide-d6
CAS:<p>Methazolamide-d6 is a GC/LC-MS standard for measuring methazolamide, a glaucoma drug that lowers eye pressure and fluid, reduces seizures, and combats ROS.</p>Fórmula:C5H2D6N4O3S2Forma y color:SolidPeso molecular:242.31Riboflavine phosphate
CAS:<p>Riboflavine phosphate (Flavin mononucleotide) is a derivative of Riboflavin.</p>Fórmula:C17H21N4O9PPureza:98%Forma y color:SolidPeso molecular:456.34TK-642
CAS:TK-642 is a potent and selective SHP2 inhibitor with oral activity, based on pyrazole and pyrazine structures (IC50 = 2.7 nmol/L). It effectively inhibits the proliferation of esophageal carcinoma cells and induces apoptosis, making it useful for studying esophageal cancer.Fórmula:C17H20ClN7SForma y color:SolidPeso molecular:389.912-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>Fórmula:C16H13NO4SPureza:99.75%Forma y color:SolidPeso molecular:315.34Clethodim
CAS:Clethodim is a selective herbicide inhibiting acetyl-CoA carboxylase, effective on grasses with low environmental persistence and moderate toxicity to wildlife.Fórmula:C17H26ClNO3SPureza:99.99%Forma y color:Light Yellow LiquidPeso molecular:359.91IDO-IN-11
CAS:<p>IDO-IN-11 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50s of 0.18 μM (Kinase) and 0.014 μM (Hela Cell).</p>Fórmula:C19H23BrFN7O4SPureza:98%Forma y color:SolidPeso molecular:544.4Senazodan hydrochloride
CAS:Senazodan hydrochloride (Senazodan HCl) is a Ca2+ sensitizer and phosphodiesterase 3 (PDE3) inhibitor used in the study of cardiovascular diseases.Fórmula:C15H15ClN4OPureza:99.93%Forma y color:SolidPeso molecular:302.76Maxacalcitol
CAS:Maxacalcitol (22-Oxacalcitriol) is a ligand of VDR-like receptors and a non-serum calcium vitamin D3 analogue.Fórmula:C26H42O4Pureza:≥98%Forma y color:SolidPeso molecular:418.61ML404
CAS:ML404 is the mitochondrial permeability transition pore inhibitor.Fórmula:C17H13ClN2O3Pureza:98%Forma y color:SolidPeso molecular:328.75MR 16728 hydrochloride
CAS:stimulates the release of acetylcholine from synaptosomesFórmula:C23H37ClN2OPureza:98%Forma y color:SolidPeso molecular:393.01ML387
CAS:ML387 is an inhibitor of human NAD(+)- dependent 15- hydroxyprostaglandin dehydrogenase.Fórmula:C20H21N3O2Pureza:98%Forma y color:SolidPeso molecular:335.4L 662583
CAS:L 662583 is a topical inhibitor of carbonic anhydrase.Fórmula:C13H17ClN2O5S3Pureza:98%Forma y color:SolidPeso molecular:412.93Cedefingol
CAS:<p>Cedefingol is an antineoplastic agent.</p>Fórmula:C20H41NO3Pureza:98%Forma y color:SolidPeso molecular:343.544-Acetylsimvastatin
CAS:<p>4-Acetylsimvastatin is acetylated simvastatin. Simvastatin is a competitive inhibitor of HMG-CoA reductase (Ki: 0.2 nM).</p>Fórmula:C27H40O6Pureza:98%Forma y color:SolidPeso molecular:460.6L 30
CAS:L 30 is a blocker of the sodium channel.Fórmula:C15H24N2OPureza:98%Forma y color:SolidPeso molecular:248.36LP8
CAS:LP8 is a novel inhibitor of Trypanosoma cruzi CYP51.Fórmula:C16H19N3O4SPureza:98%Forma y color:SolidPeso molecular:349.4KC-12615
CAS:KC-12615 is an inhibitior of endopeptidase.Fórmula:C29H34N2O6Forma y color:SolidPeso molecular:506.59Leucinal
CAS:Leucinal inhibits the activity of brain aminopeptidase and potentiates analgesia induced by leu-enkephalen.Fórmula:C6H13NOForma y color:SolidPeso molecular:115.17Texasin
CAS:Texasin is a selective inhibitor of human leukocyte 5-lipoxygenase.Fórmula:C16H12O5Pureza:98%Forma y color:SolidPeso molecular:284.26AZD-3289
CAS:AZD-3289, a potent BACE1 inhibitor, is used potentially for the treatment of Alzheimer's disease.Fórmula:C24H14F5N5Forma y color:SolidPeso molecular:467.39tHGA
CAS:tHGA is a potent inhibitor of lipoxygenase.Fórmula:C18H24O4Pureza:98%Forma y color:SolidPeso molecular:304.38Lysine Orotate
CAS:Lysine Orotate blocks Herpes virus replication, effective against HSV-1, HSV-2, CMV, EBV, and Varicella.Fórmula:C11H18N4O6Pureza:98%Forma y color:SolidPeso molecular:302.28PG-9 maleate
CAS:Increases release of acetylcholineFórmula:C21H26BrNO6Pureza:98%Forma y color:SolidPeso molecular:468.34Ipenoxazone
CAS:Ipenoxazone is an effective and centrally acting muscle relaxant.Fórmula:C22H34N2O2Pureza:98%Forma y color:SolidPeso molecular:358.52ARI-3531
CAS:ARI-3531 is a selective prolyl endopeptidase inhibitor.Fórmula:C15H22BN3O4Forma y color:SolidPeso molecular:319.16Oncrasin-72
CAS:Oncrasin-72 is an analog of oncrasin-1. It has antitumor activity mediated by JNK activation and STAT3 inhibition.Fórmula:C16H14ClNOPureza:98%Forma y color:SolidPeso molecular:271.74iGP-5
CAS:iGP-5 is a cell-permeable mitochondrial sn-Glycerol 3-phosphate dehydrogenase (mGPDH) inhibitor.Fórmula:C21H17N3O3Forma y color:SolidPeso molecular:359.38Benzpiperylone
CAS:Benzpiperylone is a synthetic anti-inflammatory drug. It also has anti-inflammatory activity.Fórmula:C22H25N3OPureza:98%Forma y color:SolidPeso molecular:347.45Noreximide
CAS:Noreximide is an agent of sedative.Fórmula:C9H9NO2Pureza:98%Forma y color:SolidPeso molecular:163.17DBC
CAS:DBC is a halogenated hydrocarbon, widely used in biochemical experiments and drug synthesis research.Fórmula:C20H13NPureza:99.76%Forma y color:Needles From Ethanol 7H-Dibenzo(C G)Carbazole Is A Crystalline SolidPeso molecular:267.32BAY 59-9435
CAS:<p>HSL-IN-2 is a selective inhibitor of Hormone Sensitive Lipase (HSL; IC50: 0.023 μM).</p>Fórmula:C14H22N2O3Pureza:98%Forma y color:SolidPeso molecular:266.34Pteropterin monohydrate
CAS:Pteropterin monohydrate is an antineoplastic agent.Fórmula:C29H35N9O13Pureza:98%Forma y color:SolidPeso molecular:717.64DY3002
CAS:DY3002 is a novel, selective and potent EGFR Inhibitor, it overcomes T790M-Mediated Resistance in Non-Small Cell Lung Cancer.Fórmula:C24H25ClN6O2Pureza:98%Forma y color:SolidPeso molecular:464.95Pinoxepin HCl
CAS:Pinoxepin HCl is an antipsychotic.Fórmula:C23H29Cl3N2O2Pureza:98.05%Forma y color:SolidPeso molecular:471.85VU0415374
CAS:VU0415374 is a positive allosteric modulator of mGlu4.Fórmula:C20H16ClN3O3Pureza:98%Forma y color:SolidPeso molecular:381.81Isobutamben
CAS:Isobutamben is an agent of Anesthetic.Fórmula:C11H15NO2Forma y color:SolidPeso molecular:193.24TES-991
CAS:TES-991 is a potent and selective inhibitor of human α Amino-β-carboxymuconate-ε-semialdehyde Decarboxylase (ACMSD)(IC50 of 3 nM).Fórmula:C17H11N7OS2Pureza:98%Forma y color:SolidPeso molecular:393.45N-Monoacetylcystine
CAS:N-Monoacetylcystine is a paracetamol poisoning antidote. It is used in the treatment of influenza A virus pandemic.Fórmula:C8H14N2O5S2Pureza:98%Forma y color:SolidPeso molecular:282.34HIF-IN-33
CAS:HIF-IN-33 is an inhibitor of HIF pathway.Fórmula:C21H17F3N4O2Pureza:98%Forma y color:SolidPeso molecular:414.38Rociverine
CAS:Rociverine is an anticholinergic compound used as a smooth muscle relaxant.Fórmula:C20H37NO3Forma y color:SolidPeso molecular:339.51MDK-0738
CAS:<p>MDK-0738 is a potent and selective aldo-keto reductase 1C3 inhibitor.</p>Fórmula:C15H16O3Pureza:98%Forma y color:SolidPeso molecular:244.294′-Deoxyphlorizin
CAS:4'-Deoxyphlorizin inhibits glucose transport; Km 0.59 nM, Ki 0.33 nM for phlorizin hydrolase.Fórmula:C21H24O9Forma y color:SolidPeso molecular:420.41VDM 11
CAS:anandamide transport inhibitorFórmula:C27H39NO2Pureza:98%Forma y color:SolidPeso molecular:409.6CP-319340(free base)
CAS:CP-319340 free base is a inhibitor of microsomal triglyceride transfer protein (MTP) .Fórmula:C27H23F3N4OPureza:98%Forma y color:SolidPeso molecular:476.49Diniprofylline
CAS:<p>Diniprofylline, a phosphodiesterase inhibitor, has been used as a peripheral nervous system agent, a bronchodilator agent, and an anti-asthamtic agent.</p>Fórmula:C22H20N6O6Forma y color:SolidPeso molecular:464.43PF-05388169
CAS:PF-05388169 is an effective and selective inhibitor of IRAK4.Fórmula:C22H21N3O4Pureza:98%Forma y color:SolidPeso molecular:391.42Eprozinol dihydrochloride
CAS:Eprozinol dihydrochloride has anti-bronchoconstrictive activity.Fórmula:C22H31ClN2O2Forma y color:SolidPeso molecular:390.95Renytoline
CAS:<p>Renytoline is a new anti-inflammatory of arthritis.</p>Fórmula:C21H16N2Pureza:98%Forma y color:SolidPeso molecular:296.37A 924
CAS:A 924 is an amino acid derivative with antineoplastic activity.Fórmula:C30H57N7O11Forma y color:SolidPeso molecular:691.81Besigliptin Tosylate
CAS:Besigliptin Tosylate, a DPP-4 inhibitor, is used potentially for the treatment of type 2 diabetes.Fórmula:C25H36FN5O5SForma y color:SolidPeso molecular:537.65SMP-028
CAS:SMP-028 is a neutral cholesterol esterase (CEase) inhibitor(IC50 : 1.01 μM).Fórmula:C23H26FN5O2SPureza:98%Forma y color:SolidPeso molecular:455.55GV2-20
CAS:GV2-20 is an effective carbonic anhydrase 2 inhibitors.Fórmula:C15H13N3O6Pureza:98%Forma y color:SolidPeso molecular:331.28L-693612
CAS:L-693612 is an inhibitor of carbonic anhydrase.Fórmula:C14H24N2O5S3Pureza:98%Forma y color:SolidPeso molecular:396.55HT-0712
CAS:HT-0712 is a phosphodiesterase 4 (PDE4) inhibitor.Fórmula:C25H31NO3Pureza:98%Forma y color:SolidPeso molecular:393.52GA11
CAS:<p>GA11is an inhibitor of ALDH1. It also displays anti-GBM effects in vitro and in vivo.</p>Fórmula:C19H14N2Pureza:98%Forma y color:SolidPeso molecular:270.33Chlorambucyl-proline
CAS:<p>Chlorambucyl-proline is a chlorambucil derivative of L-proline. It is an inhibitor of bovine lung angiotensin I-converting enzyme.</p>Fórmula:C19H26Cl2N2O3Pureza:98%Forma y color:SolidPeso molecular:401.33CP 99994 dihydrochloride
CAS:High affinity NK1 antagonistFórmula:C19H26Cl2N2OPureza:98%Forma y color:SolidPeso molecular:369.33Lauroyl glutamic acid
CAS:Lauroyl glutamic acid (N-Lauroyl-L-glutamic acid) exhibits antiasthmatic effects.Fórmula:C17H31NO5Pureza:98.94%Forma y color:SolidPeso molecular:329.43Z-321
CAS:Z-321 is an inhibitor of prolyl endopeptidase.Fórmula:C19H24N2O2SPureza:98%Forma y color:SolidPeso molecular:344.47
