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(165 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 8628 productos de "Metabolismo"
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SHP2-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:248.19TDP1 Inhibitor-2
CAS:<p>TDP1 Inhibitor-2 strongly blocks TDP1 (IC50: 99 nM) & treats SCAN1 (IC50: 3.5 μM).</p>Fórmula:C25H14Cl2O5Forma y color:SolidPeso molecular:465.28Semotiadil recemate fumarate
CAS:Semotiadil recemate fumarate is the recemate of Semotiadil fumarate. Semotiadil fumarate is a novel antagonist of vasoselective Ca2+ channel.Fórmula:C33H36N2O10SPureza:98%Forma y color:SolidPeso molecular:652.71JTP 103237
CAS:<p>JTP 103237 is a potent and selective monoacyglycerol acyltransferase 2 (MOGAT2) inhibitor.</p>Fórmula:C24H29F3N6OForma y color:SolidPeso molecular:474.52hACC2-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>Fórmula:C23H32N2O4SForma y color:SolidPeso molecular:432.58S32826 disodium
CAS:autotaxin inhibitorFórmula:C21H36NNa2O4PPureza:98%Forma y color:SolidPeso molecular:443.478-CSC
CAS:<p>8-CSC: hMAO-B inhibitor (Ki: 235 nM, baboon liver) & A2A receptor affinity (Ki: 36 nM, rat brain).</p>Fórmula:C16H15ClN4O2Pureza:98%Forma y color:SolidPeso molecular:330.77Glyoxalase I inhibitor 4
CAS:<p>Glyoxalase I inhibitor 4 is a potent inhibitor of glyoxalase I (GLO1) (Ki: 10 nM).</p>Fórmula:C17H21IN4O8SForma y color:SolidPeso molecular:568.34AZD8329
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>Fórmula:C25H31N3O3Pureza:99.31%Forma y color:SolidPeso molecular:421.53(R)-MLN-4760
CAS:<p>(R)-MLN-4760, the R-enantiomer of MLN-4760, functions as an ACE2 inhibitor and exhibits a half maximal inhibitory concentration (IC50) of 8.4 μM, identifying it</p>Fórmula:C19H23Cl2N3O4Forma y color:SolidPeso molecular:428.31Besigliptin Tosylate
CAS:<p>Besigliptin Tosylate, a DPP-4 inhibitor, is used potentially for the treatment of type 2 diabetes.</p>Fórmula:C25H36FN5O5SForma y color:SolidPeso molecular:537.65FTX-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>Fórmula:C16H7ClF2N2OPureza:98.68%Forma y color:SolidPeso molecular:316.69Tilivapram
CAS:<p>Tilivapram is a PDE4 (phosphodiesterase IV) inhibitor that can be used in the study of mental illness.</p>Fórmula:C16H15Cl2N3O4Pureza:99.87%Forma y color:SolidPeso molecular:384.21SQ28603
CAS:SQ28603 is a potent and selective neutral endopeptidase 3.4.24.11 (NEP) inhibitor.Fórmula:C13H17NO3SPureza:98%Forma y color:SolidPeso molecular:267.34A 924
CAS:<p>A 924 is an amino acid derivative with antineoplastic activity.</p>Fórmula:C30H57N7O11Forma y color:SolidPeso molecular:691.81hCAIX-IN-7
CAS:<p>hCAIX-IN-7 (6c) selectively inhibits tumor-related isoform hCAIX (KI: 410.6 nM) and weakly affects hCAI/II (KI: >10000 nM).</p>Fórmula:C18H12FNO3Forma y color:SolidPeso molecular:309.29Renytoline
CAS:<p>Renytoline is a new anti-inflammatory of arthritis.</p>Fórmula:C21H16N2Pureza:98%Forma y color:SolidPeso molecular:296.37ST-1892
CAS:<p>ST-1892 is a soluble partial FXR agonist.</p>Fórmula:C16H12N2O3Pureza:98%Forma y color:SolidPeso molecular:280.28KB 5666
CAS:<p>KB 5666, a quinazoline derivative, is a lipid peroxidation inhibitor. It protects the brain from both cellular and functional consequences of ischemia.</p>Fórmula:C24H32N4O5Pureza:98%Forma y color:SolidPeso molecular:456.54hCA 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:562.44GNE-3500
CAS:<p>GNE-3500: potent, selective RORc inverse agonist; orally bioavailable; promising for treating inflammatory diseases.</p>Fórmula:C24H30FN3O3SForma y color:SolidPeso molecular:459.58YM-75466
CAS:<p>YM-75466 is a factor Xa inhibitor reducing TAT in plasma dose-dependently without prolonging coagulation.</p>Fórmula:C28H35N5O8S2Forma y color:SolidPeso molecular:633.74TPN729
CAS:<p>TPN729, a PDE5 inhibitor, has an IC50 of 2.28 nM, used to research erectile dysfunction.</p>Fórmula:C25H36N6O4SForma y color:SolidPeso molecular:516.66PF04471141 HCl
CAS:<p>PF-04471141 is an effective and selective inhibitor of the calcium-activated phosphodiesterase PDE1 (IC50 = 35 nM).</p>Fórmula:C16H24ClN3O3Pureza:98%Forma y color:SolidPeso molecular:341.83Antiproliferative agent-10
<p>Antiproliferative agent-10: Ruthenium(II) complex that blocks cancer cell growth by halting mitochondrial calcium uptake.</p>Fórmula:C35H36Cl2N7PRuForma y color:SolidPeso molecular:757.663-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:424.7Lirimilast
CAS:Lirimilast: oral PDE4 inhibitor (IC50: 49 nM), anti-inflammatory, treats asthma/COPD.Fórmula:C17H12Cl2N2O6SPureza:98%Forma y color:SolidPeso molecular:443.26DU717
CAS:<p>DU717 is an antihypertensive agent.</p>Fórmula:C12H15ClN4O2SPureza:99.64%Forma y color:SolidPeso molecular:314.79GlcN-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:391.49LEO 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:421.45(Rac)-3′-Hydroxy simvastatin
CAS:<p>(Rac)-3′-Hydroxy Simvastatin, a metabolite of Simvastatin, acts as a competitive inhibitor of HMG-CoA reductase, demonstrating a K i value of 0.2 nM.</p>Fórmula:C25H38O6Forma y color:SolidPeso molecular:434.57Tyrphostin 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:274.28α-Glucosidase-IN-20
CAS:<p>α-Glucosidase-IN-20 (Compound 3B) is a highly effective and orally active inhibitor of α-glucosidase.</p>Fórmula:C23H21NOSForma y color:SolidPeso molecular:359.48hCAIX/XII-IN-4
CAS:<p>hCAIX/XII-IN-4 inhibits CAIX/XII with Ki: 4.5 nM (CAXII), 23.6 nM (CAIX), and >10000 nM (CAI/CAII).</p>Fórmula:C20H16N2O5Forma y color:SolidPeso molecular:364.35Carbonic anhydrase inhibitor 11
CAS:<p>Potent carbonic anhydrase inhibitor VI targets CA II, IX, XII with Ki: 40, 39, 900 nM respectively.</p>Fórmula:C19H15F3N4O3S2Forma y color:SolidPeso molecular:468.47PTP1B-IN-15
CAS:<p>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.</p>Fórmula:C19H17Br2NO5SForma y color:SolidPeso molecular:531.22HIF-PHD-IN-2
CAS:<p>HIF-PHD-IN-2 (compound 25) is a highly effective PHD inhibitor, displaying IC50 values below 100 nM for PHD1, PHD2, and PHD3 [1].</p>Fórmula:C17H15N5O3SForma y color:SolidPeso molecular:369.4α-Amylase-IN-2
CAS:α-Glucosidase-IN-3, an oxime ester derivative of oleanolic acid (OA), exhibits inhibitory activity against α-glucosidase (IC50 = 1.28 µM) and α-amylase (IC50 =Fórmula:C39H52BrNO4Forma y color:SolidPeso molecular:678.74α-Glucosidase-IN-9
CAS:<p>α-Glucosidase-IN-9 (compound 7) is a highly potent α-glucosidase inhibitor with an IC50 of 55.6 μM, making it suitable for type II diabetes research [1].</p>Fórmula:C19H12N4OSForma y color:SolidPeso molecular:344.39(S)-Bromoenol lactone
CAS:<p>(S)-BEL, a chiral inhibitor of iPLA2β, blocks vasopressin-induced arachidonate release in A10 cells; IC50 = 2μM.</p>Fórmula:C16H13BrO2Forma y color:SolidPeso molecular:317.18TAK 21d
CAS:<p>Potent FAAH inhibitor</p>Fórmula:C19H17F2N7OPureza:98%Forma y color:SolidPeso molecular:397.38CaV1.3 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:322.75Metyltetraprole
CAS:<p>Metyltetraprole: potent fungicide, effective against Zymoseptoria, low EC50 (0.002 ppm), inhibits respiratory chain.</p>Fórmula:C19H17ClN6O2Forma y color:SolidPeso molecular:396.83CYP1B1-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>Fórmula:C20H16FN3O2S2Forma y color:SolidPeso molecular:413.49PDE5-IN-6c
CAS:<p>PDE5-IN-6c is a potent and selective inhibitor of PDE5A1.</p>Fórmula:C23H21ClN4O2Pureza:98%Forma y color:SolidPeso molecular:420.89AHR-activator-1023
CAS:<p>AHR-activator-1023 is the aryl hydrocarbon receptor activator. It is also a specific FGF2-induced branching morphogenesis modulator.</p>Fórmula:C14H8Cl2N2OForma y color:SolidPeso molecular:291.13Tenuazonic acid
CAS:<p>Tenuazonic acid, a nonhost-selective mycotoxin from Alternaria alternate, inhibits PSII by blocking electron transport at D1 protein.</p>Fórmula:C10H15NO3Pureza:98%Forma y color:SolidPeso molecular:197.23Albifylline
CAS:<p>Albifylline: a xanthine derivative, anti-asthmatic, reduces leukocyte adhesion, enhances liver microcirculation post-hemorrhagic shock.</p>Fórmula:C13H20N4O3Forma y color:SolidPeso molecular:280.32Kurasoin B
CAS:<p>Kurasoin B is an inhibitor of protein farnesyltransferase.</p>Fórmula:C18H17NO2Forma y color:SolidPeso molecular:279.33PD-34799-SA
CAS:<p>PD-34799-SA is an effective inhibitor of vasoconstrictor responses to sympathetic nerve stimulation.</p>Fórmula:C10H16N4O4Pureza:98%Forma y color:SolidPeso molecular:256.262NPD7155
CAS:<p>NPD7155 is a competitive inhibitor of MTH1.</p>Fórmula:C15H21N5Pureza:98%Forma y color:SolidPeso molecular:271.36Jesaconitine
CAS:<p>Jesaconitine is an Aconitine analog.</p>Fórmula:C35H49NO12Pureza:98%Forma y color:SolidPeso molecular:675.76UCM 765
CAS:<p>UCM 765 is a partial agonist of melatonin MT(2) receptor.</p>Fórmula:C17H20N2O2Pureza:98%Forma y color:SolidPeso molecular:284.35Izumerogant
CAS:<p>Izumerogant is an inverse agonist of the retinoid-related orphan receptor-gamma (RORγ).</p>Fórmula:C22H18ClF4N5O2Forma y color:SolidPeso molecular:495.86Brocresine
CAS:<p>Brocresine is an aromatic L-amino acid decarboxylase inhibitor. It has both a peripheral and central action.</p>Fórmula:C7H8BrNO2Pureza:98%Forma y color:SolidPeso molecular:218.05LYPLAL1-IN-1
CAS:LYPLAL1-IN-1 is a selective covalent small-molecule inhibitor of Lysophospholipase-like 1 (IC50: 0.006 μM). LYPLAL1-IN-1 also enhances glucose production.Fórmula:C29H29N7O4Pureza:98%Forma y color:SolidPeso molecular:539.59MP-10 succinate
CAS:<p>MP-10 succinate is a potent and specific inhibitor of PDE10A.</p>Fórmula:C29H26N4O5Pureza:98%Forma y color:SolidPeso molecular:510.54CYP3A4-IN-3
CAS:<p>CYP3A4-IN-3, a ritonavir analogue, is a potent CYP3A4 inhibitor with an IC50 of 0.075 μM, used as an antiviral and immunosuppressant.</p>Fórmula:C34H39N3O3SForma y color:SolidPeso molecular:569.76Ocaphane Hydrochloride
CAS:Ocaphane Hydrochloride is a strong antitumor agent used on a number of animal tumors.Fórmula:C14H22Cl4N2O2Pureza:98%Forma y color:SolidPeso molecular:392.14Roflurane
CAS:Roflurane is a halocarbon drug. It has been investigated as an inhalational anesthetic.Fórmula:C3H4BrF3OPureza:98%Forma y color:SolidPeso molecular:192.96Cholesteryl behenate
CAS:<p>Cholesteryl behenate is a standard in electrospray ionization tandem mass spectrometry for the analysis of cholesteryl esters and cholesterol.</p>Fórmula:C49H88O2Pureza:98%Forma y color:SolidPeso molecular:709.22GK470
CAS:<p>GK470 is a group IVA cytosolic phospholipase A2 inhibitor.</p>Fórmula:C21H27NO4SForma y color:SolidPeso molecular:389.51(Z)-Pitavastatin calcium
CAS:(Z)-Pitavastatin calcium is the Z-Isomer of Pitavastatin hemicacium. Pitavastatin calcium is a potent of hydroxymethylglutaryl-CoA (HMG-CoA) reductase.Fórmula:C50H50CaF2N2O8Pureza:98%Forma y color:SolidPeso molecular:885.031Safrazine Hydrochloride
CAS:<p>Safrazine Hydrochloride is a monoamine oxidase inhibitor (MOI) that is irreversible.</p>Fórmula:C11H17ClN2O2Forma y color:SolidPeso molecular:244.718ABT-418
CAS:<p>ABT-418, a nicotinic acetylcholine receptor (nAchR) agonist, is used potentially for the treatment of attention deficit disorder.</p>Fórmula:C9H14N2OForma y color:SolidPeso molecular:166.22Hydroxythiohomosildenafil
CAS:<p>Hydroxythiohomosildenafil, an analogue of sildenafil, is a phosphodiesterase-5 (PDE-5) inhibitor.</p>Fórmula:C23H32N6O4S2Pureza:99.45%Forma y color:SolidPeso molecular:520.67CM026
CAS:<p>CM026 inhibits ALDH1A1 selectively, binds to its aldehyde pocket uncompetitively.</p>Fórmula:C22H30N6O4Forma y color:SolidPeso molecular:442.51Nafenopin
CAS:<p>Nafenopin is a peroxisome proliferator, it is used to promote liver tumors and has been used as an antihyperlipoproteinemic agent.</p>Fórmula:C20H22O3Pureza:98%Forma y color:SolidPeso molecular:310.39JNJ-DGAT1-A
CAS:<p>JNJ-DGAT1-A is a DGAT1-selective inhibitor.</p>Fórmula:C31H35Cl2N5O3Forma y color:SolidPeso molecular:596.55TRC210258
CAS:<p>TRC210258 is a TGR5 agonist that acts by decreasing glycemic and dyslipidemic cardiovascular risk in animal models of diabesity.</p>Fórmula:C20H14ClFN4O2Pureza:98%Forma y color:SolidPeso molecular:396.8Statine
CAS:<p>Statine is a protease inhibitor that is active against pepsin and other acid proteases.</p>Fórmula:C8H17NO3Pureza:98%Forma y color:SolidPeso molecular:175.23sEH inhibitor-6
CAS:<p>sEH inhibitor-6 (Compound 3g) is a highly potent soluble epoxide hydrolase (sEH) inhibitor, exhibiting an IC 50 value of 0.5 nM [1].</p>Fórmula:C21H14ClN3O2Forma y color:SolidPeso molecular:375.81Mixanpril
CAS:Mixanpril is an RB 105 lipophilic prodrug.Fórmula:C21H23NO4SPureza:98%Forma y color:SolidPeso molecular:385.48BAY 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:266.34DBC
CAS:<p>DBC is a halogenated hydrocarbon, widely used in biochemical experiments and drug synthesis research.</p>Fórmula:C20H13NPureza:99.76%Forma y color:Needles From Ethanol 7H-Dibenzo(C G)Carbazole Is A Crystalline SolidPeso molecular:267.32AChE/hCA I/II-IN-1
CAS:<p>Compound 6: Potent inhibitor for AChE, Hca I & II with IC50s of 22.21, 60.79, 66.64 nM, useful in glaucoma, Alzheimer's, diabetes research.</p>Fórmula:C15H13N3SForma y color:SolidPeso molecular:267.354,6-O-Ethylidene-α-D-glucose
CAS:<p>4,6-O-Ethylidene-α-D-glucose (Ethylidene-glucose), a derivative of glucose, serves as a competitive inhibitor for the exofacial binding site of glucose</p>Fórmula:C8H14O6Forma y color:SolidPeso molecular:206.19Noreximide
CAS:<p>Noreximide is an agent of sedative.</p>Fórmula:C9H9NO2Pureza:98%Forma y color:SolidPeso molecular:163.17Benzpiperylone
CAS:<p>Benzpiperylone is a synthetic anti-inflammatory drug. It also has anti-inflammatory activity.</p>Fórmula:C22H25N3OPureza:98%Forma y color:SolidPeso molecular:347.45Deltasonamide 2 (TFA)
CAS:<p>Deltasonamide 2 TFA is competitive, high affinity PDEδ inhibitor with a Kd of ~385 pM.</p>Fórmula:C32H40ClF3N6O6S2Pureza:98%Forma y color:SolidPeso molecular:761.28ONO-1603
CAS:<p>ONO-1603, a prolyl endopeptidase inhibitor, is used potentially for the treatment of Alzheimer's disease.</p>Fórmula:C16H19ClN2O3Pureza:98%Forma y color:SolidPeso molecular:322.79Transketolase-IN-4
CAS:<p>Transketolase-IN-4: IC50 3.9 μM; targets M. tuberculosis DXS (IC50 114.1 μM) & hinders SW620, LS174T, MIA PaCa-2 tumor cell growth.</p>Fórmula:C19H14ClN3OPureza:99.07%Forma y color:SolidPeso molecular:335.79Levophencynonate
CAS:<p>Levophencynonate is a muscarinic receptor antagonist.</p>Fórmula:C22H31NO3Pureza:98%Forma y color:SolidPeso molecular:357.49PG-9 maleate
CAS:<p>Increases release of acetylcholine</p>Fórmula:C21H26BrNO6Pureza:98%Forma y color:SolidPeso molecular:468.34CD 2314
CAS:<p>CD2314 is a potent and subtype-selective RARβ receptor agonist with a Kd of 195 nM in S91 melanoma cells [1].</p>Fórmula:C23H24O2SForma y color:SolidPeso molecular:364.5SB 210661
CAS:SB 210661 is a potent and selective 5-lipoxygenase inhibitor.Fórmula:C16H14F2N2O4Pureza:98%Forma y color:SolidPeso molecular:336.29TFB-TBOA
CAS:<p>glial glutamate transporter EAAT1 and EAAT2 inhibitor</p>Fórmula:C19H17F3N2O6Pureza:98%Forma y color:SolidPeso molecular:426.34PKM2 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>Fórmula:C18H19FN2O6S2Pureza:98%Forma y color:SolidPeso molecular:442.48Lysine Orotate
CAS:<p>Lysine Orotate blocks Herpes virus replication, effective against HSV-1, HSV-2, CMV, EBV, and Varicella.</p>Fórmula:C11H18N4O6Pureza:98%Forma y color:SolidPeso molecular:302.28FASN-IN-5
CAS:<p>FASN-IN-5 is a FASN inhibitor, useful for studying cancer and metabolic diseases.</p>Fórmula:C29H26N4O2Pureza:99.88%Forma y color:SolidPeso molecular:462.54Ciraparantag TFA
CAS:<p>Ciraparantag TFA reverses anticoagulants by inhibiting thrombin and factor Xa.</p>Fórmula:C26H50F6N12O6Pureza:98%Forma y color:SolidPeso molecular:740.74Teludipine hydrochloride
CAS:Teludipine hydrochloride is a blocker of lipophilic calcium channel.Fórmula:C28H39ClN2O6Pureza:98%Forma y color:SolidPeso molecular:535.07Otamixaban
CAS: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.Fórmula:C25H26N4O4Pureza:98.08%Forma y color:SolidPeso molecular:446.5Sermetacin
CAS:<p>Sermetacin is an anti-inflammatory agent.</p>Fórmula:C22H21ClN2O6Pureza:98%Forma y color:SolidPeso molecular:444.86Pitstop1
CAS:<p>Clathrin-IN-1 selectively inhibits clathrin, potentially blocking virus entry and modulating cell signals.</p>Fórmula:C19H14N2NaO5SPureza:98%Forma y color:SolidPeso molecular:405.38Manninotrionate
CAS:<p>Manninotrionate, an antitumor agent, linked to BSA; rabbit antiserum made, doesn't agglutinate Ehrlich tumor cells with alpha-D-galactosyl groups.</p>Fórmula:C18H32KO17Pureza:98%Forma y color:SolidPeso molecular:559.535PMPMEase-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:277.36TA-7552
CAS:<p>TA-7552 is a potent agent of cholesterol-lowering.</p>Fórmula:C25H26O10Pureza:98%Forma y color:SolidPeso molecular:486.47
