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(67 productos)
- CETP(18 productos)
- Anhídrido carbónico(178 productos)
- Caseína quinasa(130 productos)
- DHFR(33 productos)
- Descarboxilasa(4 productos)
- Deshidrogenasa(271 productos)
- FAAH(64 productos)
- FXR(58 productos)
- Factor Xa(80 productos)
- Ácido graso sintasa(33 productos)
- Ferroptosis(215 productos)
- GR(3 productos)
- GSNOR(3 productos)
- Glucoquinasa(54 productos)
- HIF / HIF Prolilhidroxilasa(142 productos)
- HMG-CoA reductasa(33 productos)
- Hidroxilasa(30 productos)
- IDO(82 productos)
- LDL(8 productos)
- Lipasa(98 productos)
- Lípido(58 productos)
- Lipoxigenasa(124 productos)
- MAO(87 productos)
- MPO(2 productos)
- NAMPT(36 productos)
- P450(6 productos)
- PAI-1(25 productos)
- PDE(166 productos)
- PED(1 productos)
- PKM(15 productos)
- PPAR(164 productos)
- Fosfolipasa(82 productos)
- ROR(42 productos)
- Receptor de retinoides(29 productos)
- SGK(11 productos)
- Tiorredoxina(12 productos)
- Transferasa(30 productos)
- Transportador(42 productos)
- UGT(4 productos)
- Inhibidores de la xantina oxidasa (XO)(9 productos)
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Se han encontrado 8626 productos de "Metabolismo"
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OMS-824
CAS:<p>OMS-824 is a phosphodiesterase-10 inhibitor that slows or stops the hydrolysis of cAMP and cGMP.</p>Fórmula:C21H21BrN4O4Pureza:98%Forma y color:SolidPeso molecular:473.322-Iodoestradiol
CAS:2-Iodoestradiol is an effective human sex hormone-binding globulin (SHBG) ligand.Fórmula:C18H23IO2Pureza:98%Forma y color:SolidPeso molecular:398.28myomiR-IN-1
CAS:<p>myomiR-IN-1 inhibits myoD translation in C2C12 cells, doesn't affect myoD mRNA, and reduces differentiation markers.</p>Fórmula:C33H27NO6Pureza:98%Forma y color:SolidPeso molecular:533.57α-RA-F
CAS:<p>Alpha-RA-F increases collagen, lowers MMPs in human fibroblasts, non-toxic.</p>Fórmula:C16H16N2O4Pureza:98%Forma y color:SolidPeso molecular:300.31ARI-3531
CAS:<p>ARI-3531 is a selective prolyl endopeptidase inhibitor.</p>Fórmula:C15H22BN3O4Forma y color:SolidPeso molecular:319.16Ipenoxazone
CAS:<p>Ipenoxazone is an effective and centrally acting muscle relaxant.</p>Fórmula:C22H34N2O2Pureza:98%Forma y color:SolidPeso molecular:358.52MLS000536924
CAS:<p>MLS000536924 is a potent and selective competitive human epithelial 15-lipoxygenase-2 inhibitor.</p>Fórmula:C16H15N3SForma y color:SolidPeso molecular:281.38MMV-667492
CAS:<p>MMV-667492 is an effective inhibitor of Ezrin.</p>Fórmula:C17H19N3O3Pureza:98%Forma y color:SolidPeso molecular:313.35L-651392
CAS:<p>L-651392 is an inhibitor of leukotriene.</p>Fórmula:C14H10BrNO3SForma y color:SolidPeso molecular:352.2L 30
CAS:<p>L 30 is a blocker of the sodium channel.</p>Fórmula:C15H24N2OPureza:98%Forma y color:SolidPeso molecular:248.364-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:460.6PMPMEase-IN L-28
CAS:<p>PMPMEase-IN L-28 is a novel inhibitor of prenylated methylated protein methylesterase.</p>Fórmula:C17H29FO2S2Pureza:98%Forma y color:SolidPeso molecular:348.54BFE-37
CAS:<p>BFE-37 is a partial agonist of beta-adrenergic.</p>Fórmula:C16H23NO3Pureza:98%Forma y color:SolidPeso molecular:277.36Maxacalcitol
CAS:<p>Maxacalcitol (22-Oxacalcitriol) is a ligand of VDR-like receptors and a non-serum calcium vitamin D3 analogue.</p>Fórmula:C26H42O4Pureza:≥98%Forma y color:SolidPeso molecular:418.616-Hydroxyluteolin
CAS:<p>6-Hydroxyluteolin, a flavonoid compound extracted from Salvia amarissima Ortega, inhibits aldose reductase (AR) and has antimicrobial activity.</p>Fórmula:C15H10O7Pureza:99.69%Forma y color:SolidPeso molecular:302.24Senazodan hydrochloride
CAS:<p>Senazodan hydrochloride (Senazodan HCl) is a Ca2+ sensitizer and phosphodiesterase 3 (PDE3) inhibitor used in the study of cardiovascular diseases.</p>Fórmula:C15H15ClN4OPureza:99.93%Forma y color:SolidPeso molecular:302.76IDO-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:544.4BKIDC-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>Fórmula:C22H23N5O2Forma y color:SolidPeso molecular:389.45(E/Z)-Ensifentrine
CAS:<p>RPL-554 (LS-193,855) is a dual PDE3/4 inhibitor with bronchodilator and anti-inflammatory properties, in trials for asthma and hay fever by Verona Pharma.</p>Fórmula:C26H31N5O4Forma y color:SolidPeso molecular:477.56AMP-Deoxynojirimycin
CAS:<p>AMP-Deoxynojirimycin (AMP-DNM) is a ceramide glucosyltransferase and GCase 2 inhibitor for the study of Parkinson's and diabetes.</p>Fórmula:C22H39NO5Pureza:>99.99%Forma y color:SolidPeso molecular: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>Fórmula:C22H31NO3Pureza:>99.99%Forma y color:SolidPeso molecular:357.49SHP2-IN-5
CAS:<p>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 cell</p>Fórmula:C12H8O6Forma y color:SolidPeso molecular:248.19JTP 103237
CAS:<p>JTP 103237 is a potent and selective monoacyglycerol acyltransferase 2 (MOGAT2) inhibitor.</p>Fórmula:C24H29F3N6OForma y color:SolidPeso molecular:474.52IDO-IN-12
CAS:<p>IDO-IN-12 is an inhibitor of indoleamine 2,3-dioxygenase (IDO).</p>Fórmula:C13H11BrFN5O3SPureza:99.727%Forma y color:SolidPeso molecular:416.23α-Glucosidase-IN-6
CAS:<p>α-Glucosidase-IN-6 is a competitive inhibitor of α-glucosidase (IC50: 5.69 μM) and exhibits potential for anti-diabetic studies.</p>Fórmula:C24H17ClF3NO3SForma y color:SolidPeso molecular:491.91Endothelial lipase inhibitor-1
CAS:<p>Endothelial lipase inhibitor-1 is a potent endothelial lipase inhibitor with an IC50 of 49 nM.</p>Fórmula:C22H22N4O4Pureza:99.59%Forma y color:SolidPeso molecular:406.43Deltasonamide 2
CAS:<p>Deltasonamide 2 is a competitive, high affinity PDEδ inhibitor with a Kd of ~385 pM.</p>Fórmula:C30H39ClN6O4S2Pureza:98%Forma y color:SolidPeso molecular:647.25THPP-4
CAS:<p>THPP-4 inhibits phosphodiesterase 10A (PDE10A).</p>Fórmula:C20H21ClN6O2Forma y color:SolidPeso molecular:412.87hCAI/II-IN-4
CAS:<p>hCAI/II-IN-4 inhibits hCA I & II (Ki: 16.95 & 15.22 nM), hCA IX (Ki: 27.04 nM), has anti-hypoxia benefits and is low-toxic for AMS research.</p>Fórmula:C15H15N3O5S2Forma y color:SolidPeso molecular:381.43CaV1.3 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>Fórmula:C17H19ClN2O3Forma y color:SolidPeso molecular:334.8STL1267
CAS:<p>STL1267 is a REV-ERB agonist that crosses the blood-brain barrier and inhibits BMAL1 gene expression.</p>Fórmula:C17H11ClN4OPureza:99.19%Forma y color:SolidPeso molecular:322.75PF-04279405
CAS:<p>PF-04279405 is a potent and selective glucokinase activator.</p>Fórmula:C25H25FN4O4Forma y color:SolidPeso molecular:464.49AMPD2 inhibitor 1
CAS:AMPD2 inhibitor 1 is an adenosine monophosphate deaminase 2 (AMPD2) inhibitor, useful for studying anorexia in the nervous system.Fórmula:C25H22N2O2Forma y color:SolidPeso molecular: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>Fórmula:C5H13ClN2O2SForma y color:SolidPeso molecular:200.69BI-L 357
CAS:<p>BI-L 357, a prodrug of BL-L 226, is a selective, orally active inhibitor of 5-lipoxygenase.</p>Fórmula:C18H18O4SForma y color:SolidPeso molecular:330.4TM6089
CAS:<p>TM6089 is an inhibitor of Prolyl Hydroxylase that stimulates HIF activity without iron chelation, induces angiogenesis, and protects organ against ischemia.</p>Fórmula:C13H14N4O3SPureza:99.70%Forma y color:SolidPeso molecular:306.34SGK1-IN-1
CAS:<p>SGK1-IN-1 (compound 14n) is a highly potent SGK1 (Serum/Glucocorticoid Regulated Kinase 1) inhibitor</p>Fórmula:C17H12ClFN6O2SPureza:98%Forma y color:SolidPeso molecular:418.83SSI-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>Fórmula:C19H21ClN4O3Pureza:98%Forma y color:SolidPeso molecular:388.85Erythronic acid
CAS:<p>Erythronic acid, an endogenous carbohydrate metabolite, is instrumental for research into metabolism-associated disorders.</p>Fórmula:C4H8O5Pureza:98%Forma y color:SolidPeso molecular:136.1hCA I-IN-2
CAS:<p>hCA I-IN-2 (6d) inhibits hCA I (Ki: 18.8 nM) more selectively over II, IX, XII (Ki: 375.1, 1721, 283.9 nM).</p>Fórmula:C26H20BrN5O3SForma y color:SolidPeso molecular:562.44IACS-8968
CAS:<p>IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).</p>Fórmula:C17H18F3N5O2Pureza:98%Forma y color:SolidPeso molecular:381.35PGMI-004A
CAS:<p>PGMI-004A is an effective inhibitor of phosphoglycerate mutase 1 (IC50: 13.1 μM).</p>Fórmula:C21H12F3NO6SPureza:98%Forma y color:SolidPeso molecular:463.38Kojibiose
CAS:<p>Kojibiose (Kojibiose) is a disaccharide in honey. Kojibiose is a product of the caramelization of glucose.</p>Fórmula:C12H22O11Pureza:99.933%Forma y color:SolidPeso molecular:342.3IDO-IN-3
CAS:<p>IDO-IN-3 is a potent indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 290 nM).</p>Fórmula:C11H12BrFN6O2Forma y color:SolidPeso molecular:359.15Mufemilast
CAS:<p>Mufemilast is an inhibitor of phosphodiesterase 4 (PDE4).</p>Fórmula:C20H22N2O7S2Forma y color:SolidPeso molecular:466.53Dacisteine
CAS:<p>Dacisteine (N,S-Diacetyl-L-cysteine) is an inhibitor of New Delhi metallo-beta-lactamase-1 (NDM-1, IC50 = 1000 μM).</p>Fórmula:C7H11NO4SPureza:99.57%Forma y color:SolidPeso molecular:205.23(R)-Irsenontrine
CAS:<p>(R)-Irsenontrine (R-E2027), R-enantiomer, is a potent PDE9 inhibitor, IC50 = 0.041 μM, for neurological disease research.</p>Fórmula:C22H22N4O3Forma y color:SolidPeso molecular:390.44L-Xylulose
CAS:<p>L-Xylulose: a rare sugar, key in metabolism, α-glucosidase inhibitor, lowers glucose, precursor to antiviral drug components.</p>Fórmula:C5H10O5Forma y color:SolidPeso molecular:150.13IDO1/TDO-IN-2
CAS:<p>IDO1/TDO-IN-2: IDO1/TDO inhibitor; IC50s: IDO1, 0.1μM; TDO, 0.07μM; potential for cancer research.</p>Fórmula:C16H9N3O2Forma y color:SolidPeso molecular:275.26ML299
CAS:<p>ML299 (VU0463568) is a dual PLD1/2 inhibitor (PLD1 and PLD2, IC50 of 6 nM, 20 nM, respectively).</p>Fórmula:C23H26BrFN4O2Pureza:98%Forma y color:SolidPeso molecular:489.38NCT-506
CAS:<p>NCT-506 is an orally bioavailable inhibitors of aldehyde dehydrogenase 1A1 (ALDH1A1) (IC50 of 7 nM).</p>Fórmula:C25H23FN4O3SPureza:98%Forma y color:SolidPeso molecular:478.542'-O-Methyladenosine
CAS:<p>2'-O-Methyladenosine, a methylated adenine residue is found in the urine of normals and adenosine deaminase deficient patients.</p>Fórmula:C11H15N5O4Pureza:99.89%Forma y color:White SolidPeso molecular:281.27Spiraprilat
CAS:<p>Spiraprilat is an ACE inhibitor. It also is an active metabolite of spirapril.</p>Fórmula:C20H26N2O5S2Pureza:98%Forma y color:SolidPeso molecular:438.56ML218
CAS:ML218 is an inhibitor of T-type Ca2+ channels (Cav3.1, Cav3.2, Cav3.3).ML218 inhibits the synaptic activity of subthalamic nucleus (STN) neurons.Fórmula:C19H26Cl2N2OPureza:99.2% - 99.45%Forma y color:SolidPeso molecular:369.33MK-4409
CAS:MK-4409, a potent and selective fatty acid amide hydrolase (FAAH) inhibitor, is being investigated for the treatment of inflammatory and neuropathic pain.Fórmula:C22H17ClFN3O2SPureza:99.80% - 99.87%Forma y color:SolidPeso molecular:441.91S07-2010
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>Fórmula:C19H21N3O3SPureza:98.13%Forma y color:SolidPeso molecular:371.45Imazodan
CAS:<p>Imazodan is a compound with positive inotropic activity and is a type III phosphodiesterase inhibitor that can be used to study heart failure.</p>Fórmula:C13H12N4OPureza:98% - 98.31%Forma y color:SolidPeso molecular:240.26Valibose
CAS:<p>Valibose, α-glucosidase inhibitor, improves glucose/lipid metabolism, lowers serum BUN/NAG, reduces kidney weight index.</p>Fórmula:C10H21NO6Forma y color:SolidPeso molecular:251.28CAY10486
CAS:<p>CAY10486 blocks ACAT-1/2, which form cholesterol esters, potentially reducing atherosclerosis; inhibits LDL oxidation. IC50 ~60μM; 28% effect at 3μM.</p>Fórmula:C19H19NO4Forma y color:SolidPeso molecular:325.36SCH-351591
CAS:<p>SCH-351591 is an orally active inhibitor of phosphodiesterase 4.</p>Fórmula:C17H10Cl2F3N3O3Pureza:98%Forma y color:SolidPeso molecular:432.18ASP3662
CAS:<p>ASP3662/SPI-62: Potent, selective CNS-penetrable 11β-HSD1 inhibitor; potential neuropathic pain treatment.</p>Fórmula:C19H16ClF3N4O2Forma y color:SolidPeso molecular:424.8Trandolaprilate hydrate
CAS:<p>Trandolaprilate hydrate, a powerful ACE inhibitor and Trandolapril's main metabolite, is lipophilic with partial c-fos blocking.</p>Fórmula:C22H32N2O6Forma y color:SolidPeso molecular:420.5YCT529 free acid
CAS:<p>YCT529 free acid is a potent, selective and orally active RAR-α inhibitor .</p>Fórmula:C29H25NO3Forma y color:SolidPeso molecular:435.51SCD1 Inhibitor
CAS:<p>SCD1 Inhibitor is a novel stearoyl-CoA desaturase1 (SCD1) inhibitor.</p>Fórmula:C21H20F3N3O3Forma y color:SolidPeso molecular:419.414-dehydro Zymostenol
CAS:<p>14-dehydro Zymostenol, a cholesterol precursor, boosts MBP+ oligodendrocytes from precursors at 5.8-17 μM.</p>Fórmula:C27H44OForma y color:SolidPeso molecular:384.64GlcN-6-P Synthase-IN-1
CAS:<p>'GlcN-6-P Synthase-IN-1, IC50 3.47 μM, inhibits GlcN-6-P synthase & CYP3A4. Has antimicrobial activity and CNS penetration.'</p>Fórmula:C20H21N7SForma y color:SolidPeso molecular:391.49DNJNAc
CAS:<p>DNJNAc (2-Acetamido-1,2-dideoxynojirimycin) is a potent β-hexosaminidase inhibitor, reducing cartilage matrix degradation, relevant in glycoconjugate studies.</p>Fórmula:C8H16N2O4Pureza:98.65% - 99.37%Forma y color:SolidPeso molecular:204.221-Methyluric acid
CAS:<p>1-Methyluric acid (1-Methylurate) acts on the bladder mucosa and increases the levels of insulin, triglycerides, cholesterol, and blood glucose.</p>Fórmula:C6H6N4O3Pureza:98.05%Forma y color:SolidPeso molecular:182.14MK-0952
CAS:<p>MK-0952 treats memory loss and cognitive issues; it's a potent, selective PDE4 inhibitor with restricted blood activity.</p>Fórmula:C28H22FN3O4Forma y color:SolidPeso molecular:483.493-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>Fórmula:C30H48OForma y color:SolidPeso molecular: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>Fórmula:C23H23N3O5Forma y color:SolidPeso molecular:421.45Tyrphostin 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:274.28URB-694
CAS:<p>URB-694 is a fatty acid amide hydrolase (FAAH) inhibitor.</p>Fórmula:C19H21NO3Forma y color:SolidPeso molecular:311.37Nitrefazole
CAS:<p>Nitrefazole: a 4-nitroimidazole, inhibits ALDH enzyme crucial for alcohol metabolism, has potent, durable effects.</p>Fórmula:C10H8N4O4Forma y color:SolidPeso molecular:248.19DTP348
CAS:<p>DTP348: Oral carbonic anhydrase IX inhibitor & hypoxic cell radiosensitizer with sulfamide & 5-nitroimidazole components.</p>Fórmula:C6H11N5O4SForma y color:SolidPeso molecular:249.25Oxythiamine diphosphate
CAS:<p>Oxythiamine diphosphate is a competitivethiamine pyrophosphate inhibitor(Ki of 30 nM).</p>Fórmula:C12H17N3O8P2SPureza:98%Forma y color:SolidPeso molecular:425.29CM39
CAS:<p>CM39 inhibits ALDH, linked to cancer stem-like cells & chemoresistance.</p>Fórmula:C19H15FN4OSForma y color:SolidPeso molecular:366.41IDO1-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>Fórmula:C28H32BrClFN5O2Forma y color:SolidPeso molecular:604.94Carbonic anhydrase inhibitor 13
CAS:<p>Carbonic anhydrase inhibitor 13 (compound 7) is a potent inhibitor of carbonic anhydrase (CA).</p>Fórmula:C17H15N5O3S2Forma y color:SolidPeso molecular: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>Fórmula:C18H12N2O4SForma y color:SolidPeso molecular:352.36UK-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:339.45mIDH1-IN-1
CAS:<p>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).</p>Fórmula:C25H27N3O5Forma y color:SolidPeso molecular:449.5Enpp-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:410.49Oxagrelate
CAS:<p>Oxagrelate inhibits cAMP phosphodiesterase and reduces platelet aggregation by collagen and ADP.</p>Fórmula:C14H16N2O4Forma y color:SolidPeso molecular: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>Fórmula:C21H27N5O5SForma y color:SolidPeso molecular: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>Fórmula:C21H26N2O8Forma y color:SolidPeso molecular:434.44α-Amylase/α-Glucosidase-IN-2
CAS: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 μMFórmula:C22H16ClN5Forma y color:SolidPeso molecular:385.85ML-148
CAS:<p>ML-148 is a selective inhibitor of 15-hydroxy prostaglandin dehydrogenase (15-PGDH, IC50 = 56 nM).</p>Fórmula:C20H21N3OPureza:99.88%Forma y color:SolidPeso molecular:319.4Spirapril
CAS:<p>Spiropril is an ACE inhibitor antihypertensive drug, which belongs to the bicarboxyl group of ACE inhibitors and is used in the treatment of hypertension.</p>Fórmula:C22H30N2O5S2Forma y color:SolidPeso molecular:466.61Enpp-1-IN-6
CAS:<p>Enpp-1-IN-6, a potent enpp-1 inhibitor, may aid cancer and infectious disease studies (WO2021203772A1, compound 51).</p>Fórmula:C22H28N4O5SForma y color:SolidPeso molecular:460.55Teglarinad chloride
CAS:<p>Teglarinad chloride (GMX-1777 chloride) is an inhibitor of NAMPT with antitumor activity that acts by interfering with DNA repair and inhibiting angiogenesis.</p>Fórmula:C30H43Cl2N5O8Pureza:98.09%Forma y color:SolidPeso molecular:672.6mEH-IN-1
CAS:<p>mEH-IN-1 (Compound 62) is a potent mEH enzyme inhibitor with an IC50 of 2.2 nM, relevant in preeclampsia, hypercholanemia, and cancer research.</p>Fórmula:C16H17F6NOSForma y color:SolidPeso molecular:385.37SYN20028567
CAS:<p>SYN20028567, an aromatase (CYP19) inhibitor, exhibits an IC50 value of 9.4 nM. It has potential applications in breast cancer research [1].</p>Fórmula:C20H29N3O3SForma y color:SolidPeso molecular:391.53Agn 190727
CAS:<p>Agn 190727 is a retonoic acid receptor that can induce retinoid-induced hypertriglyceridemia.</p>Fórmula:C20H22O2Forma y color:SolidPeso molecular:294.39α-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>Fórmula:C21H19N9O6S2Forma y color:SolidPeso molecular: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>Fórmula:C24H20F4N2O3Forma y color:SolidPeso molecular:460.42DHODH-IN-21
CAS:<p>DHODH-IN-21, orally active DHODH blocker with 1.1 nM IC50, shows anticancer activity, potential for AML research.</p>Fórmula:C20H19ClF4N6O4Forma y color:SolidPeso molecular:518.85SQ 28853
CAS:<p>SQ 28853 is an inhibitor of ACE with diuretic properties.</p>Fórmula:C19H25ClN4NaO6S3Forma y color:SolidPeso molecular:560.05Y-29794
CAS:<p>Y-29794, a covalent POP inhibitor with a Ki of 0.95 nM, holds research potential for neurodegenerative diseases and cancer.</p>Fórmula:C22H32N2OS2Forma y color:SolidPeso molecular:404.63Allopurinol riboside
CAS:<p>Allopurinol riboside, an allopurinol metabolite, inhibits purine nucleoside phosphorylase in parasites with a Ki of 277 μM.</p>Fórmula:C10H12N4O5Pureza:99.46% - 99.73%Forma y color:SolidPeso molecular:268.23
