Entre las marcas de nuestros más de 25 colaboradores destaca TargetMol
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Termina el 31 dic( quedan 12 días )
Valproic Acid
CAS:<p>Valproic Acid (2-Propylpentanoic Acid) is a branched chain fatty acid which potentially enhances central GABAergic neurotransmission and inhibits Na+ channels.</p>Fórmula:C8H16O2Pureza:97.78% - 99%Forma y color:Colourless To Pale Yellow Liquid ViscousPeso molecular:144.21SCR1693
CAS:SCR1693 is a dual acetylcholinesterase inhibitor (AChEI) and a calcium channel blocker (CCB).Fórmula:C24H28ClN3O2Forma y color:SolidPeso molecular:425.95Asoxime dimethanesulfonate
CAS:<p>Asoxime dimethanesulfonate is an oxime reactivator that counters nerve agent poisoning, restoring AChE activity inhibited by toxins like sarin.</p>Fórmula:C16H22N4O9S2Forma y color:SolidPeso molecular:478.49Lanopepden camsylate
CAS:<p>Lanopepden, or GSK-1322322, inhibits bacterial peptide deformylase, targets pneumonia/skin infections, and kills key resistant strains.</p>Fórmula:C32H50FN7O8SForma y color:SolidPeso molecular:711.8514GT-0198 HCl
CAS:<p>GT-0198: novel GlyT2 inhibitor with phenoxymethylbenzamide, effective in neuropathic pain without binding major neurotransmitter systems.</p>Fórmula:C21H24ClF3N2O2Forma y color:SolidPeso molecular:428.88HA-23
CAS:<p>HA-23 is a Ca(2+)-channel blocker.</p>Fórmula:C13H12N2O2SForma y color:SolidPeso molecular:260.31HA-22
CAS:<p>HA-22 is a Ca(2+)-channel blocker.</p>Fórmula:C16H16N2O3Forma y color:SolidPeso molecular:284.31Deltarasin HCl
CAS:<p>Deltarasin hinders KRAS-PDEδ, impairs cancer cell growth via a PDEδ pocket, disrupting RAS/RAF signaling and autophagy.</p>Fórmula:C40H37N5O·xHClForma y color:SolidPeso molecular:713.144CD2019
CAS:<p>CD2019: RARbeta agonist, promotes axonal growth, targets PI3K in adult spinal cord repair.</p>Fórmula:C25H26O3Forma y color:SolidPeso molecular:374.47FK-352
CAS:<p>FK-352 is a pyrazolopyridine derivative and adenosine-1 receptor antagonist.</p>Fórmula:C23H23N3O3Forma y color:SolidPeso molecular:389.45TAI-95
CAS:<p>TAI-95 is an inhibitor of highly expressed cancer protein 1 (Hec1).</p>Fórmula:C24H23N5O3S2Forma y color:SolidPeso molecular:493.60Tizanidine
CAS:<p>Tizanidine, an α2-adrenergic receptor agonist, suppresses the release of neurotransmitters from central nervous system (CNS) noradrenergic neurons.</p>Fórmula:C9H8ClN5SPureza:99.11%Forma y color:White SolidPeso molecular:253.71Caspase-6-IN-1
CAS:<p>Caspase-6-IN-1 is a novel Allosteric Inhibitor of Caspase-6 Activation, blocking the interaction between C6 and mHTT1-586.</p>Fórmula:C19H13NO3Forma y color:SolidPeso molecular:303.31Lu 26-046
CAS:<p>Lu 26-046 is a muscarinic receptor agonist.</p>Fórmula:C10H12N2OSForma y color:SolidPeso molecular:208.28SAR-104772
CAS:<p>SAR-104772 is a novel inhibitor of TAFIa (activated thrombin-activatable fibrinolysis inhibitor).</p>Fórmula:C29H34N4O8S2Forma y color:SolidPeso molecular:630.731Cgs 22706
CAS:<p>Cgs 22706 is an adenosine A2 receptor antagonist.</p>Fórmula:C17H22N6O7S2Forma y color:SolidPeso molecular:486.52Ciprokiren
CAS:<p>Ciprokiren, a renin inhibitor by Roche, halts human renin; IC50: 0.07/0.65 nmol/L. Lowers blood pressure in animals. Preclinical development ceased.</p>Fórmula:C37H55N5O8SForma y color:SolidPeso molecular:729.93Furaprevir
CAS:<p>Furaprevir is an HCV NS3/4A Inhibitor</p>Fórmula:C47H56N6O10SForma y color:SolidPeso molecular:897.05CP 132484
CAS:<p>CP 132484: potent, selective 5-HT₂ agonist; favors 5-HT2A, 5-HT2C over 5-HT2B. Limited 5-HT2A over 5-HT2C selectivity.</p>Fórmula:C14H18N2OForma y color:SolidPeso molecular:230.31Ormosinine
CAS:Ormosinine is an inhibitor of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase.Fórmula:C40H66N6Forma y color:SolidPeso molecular:630.99Ici D8731
CAS:<p>Ici D8731 is a nonpeptide angiotensin II antagonist with potential as a treatment for hypertension and heart failure.</p>Fórmula:C25H21N5OForma y color:SolidPeso molecular:407.47BR103
CAS:<p>BR103 is a C3aR-selective agonist that is metabolically stable.</p>Fórmula:C24H28N6O3Forma y color:SolidPeso molecular:448.52Fosphenytoin disodium
CAS:Fosphenytoin disodium (ACC-9653) is a prodrug of phenytoin that is rapidly converted to phenytoin, a voltage-gated sodium channel blockerFórmula:C16H13N2Na2O6PPureza:99.97%Forma y color:White Crystalline PowderPeso molecular:406.24Azalanstat HCl
CAS:<p>Azalanstat: anti-obesity drug, inhibits cholesterol synthesis by blocking lanosterol 14α-demethylase, reduces LDL cholesterol in hamsters.</p>Fórmula:C22H26Cl3N3O2SForma y color:SolidPeso molecular:502.879Azalanstat mesylate
CAS:<p>Azalanstat, an anti-obesity drug, inhibits cholesterol synthesis by targeting P450 enzyme lanosterol 14α-demethylase; reduces LDL more than HDL in hamsters.</p>Fórmula:C23H28ClN3O5S2Forma y color:SolidPeso molecular:526.063UCSF924NC
CAS:<p>UCSF924NC, a DRD4 antagonist, has 1/2500th affinity of its counterpart, UCSF924.</p>Fórmula:C19H21N3OForma y color:SolidPeso molecular:307.39ND-654
CAS:<p>ND-654 is an acetyl CoA carboxylase inhibitor.</p>Fórmula:C29H33N3O8SForma y color:SolidPeso molecular:583.65TAPI-0
CAS:<p>TAPI-0 is a matrix metalloprotease (MMP) and TACE inhibitor.</p>Fórmula:C24H32N4O5Forma y color:SolidPeso molecular:456.53PF-06284674
CAS:<p>PF-06284674 is a cell permeable, potent and selective M2 isoform of pyruvate kinase (PKM2) activator.</p>Fórmula:C17H14N4OForma y color:SolidPeso molecular:290.32Alnespirone hydrochloride
CAS:<p>Alnespirone hydrochloride is a selective 5-HT1A receptor full agonist of the azapirone chemical class. It has both antidepressant and anxiolytic effects.</p>Fórmula:C26H39ClN2O4Forma y color:SolidPeso molecular:479.06KF 20274
CAS:<p>KF 20274 is an adenosine A1 antagonist; purinergic receptor antagonist.</p>Fórmula:C21H29N5OForma y color:SolidPeso molecular:367.49GNE-431
CAS:<p>GNE-431: potent, selective noncovalent Btk inhibitor, IC50=3.2 nM; effective against C481R, T474I, T474M mutants, may counter ibrutinib resistance.</p>Fórmula:C30H32N10O2Forma y color:SolidPeso molecular:564.64Toborinone
CAS:<p>Toborinone is a phosphodiesterase III inhibitor.</p>Fórmula:C21H24N2O5Forma y color:SolidPeso molecular:384.43TAK-448 TFA
CAS:<p>TAK-448: investigational kisspeptin analog, GPR54 agonist, alters LH/FSH, T levels, and shows anti-prostate cancer potential.</p>Fórmula:C60H81F3N16O16Forma y color:SolidPeso molecular:1339.4IC2418
CAS:<p>IC2418 is an MmpL3 inhibitor, being active against drug-resistant Mycobacterium tuberculosis.</p>Fórmula:C18H24N2OForma y color:SolidPeso molecular:284.4Dexefaroxan
CAS:<p>Dexefaroxan is an alpha(2)-adrenoceptor antagonist.</p>Fórmula:C13H16N2OForma y color:SolidPeso molecular:216.28NEU617
CAS:<p>NEU617 is an inhibitor of the growth of protozoan parasites, against T. brucei bloodstream proliferation.</p>Fórmula:C31H26ClFN4O2Forma y color:SolidPeso molecular:541.02(S)-Azelastine
CAS:<p>(S)-Azelastine is an antihistamine reducing receptors H1R, M1R, M3R, and inhibiting HNEpC cell growth.</p>Fórmula:C22H24ClN3OForma y color:SolidPeso molecular:381.9(R)-Azelastine
CAS:<p>(R)-Azelastine, an antihistamine, reduces H1R, M1R, M3R levels and inhibits HNEpC growth.</p>Fórmula:C22H24ClN3OForma y color:SolidPeso molecular:381.9S 4404
CAS:<p>S 4404 is a fluorescent peptide inhibitor of prolyl-4-hydroxylase.</p>Fórmula:C28H33N7O9Forma y color:SolidPeso molecular:611.6Rwj 29009
CAS:<p>Rwj 29009 is a potassium channel activator with prominent coronary and peripheral vasodilating actions.</p>Fórmula:C14H18N2O5SForma y color:SolidPeso molecular:326.37Spr 210
CAS:<p>Spr 210 is an aldose reductase (AR) inhibitor with potential uses as a therapeutic agent for preventing and improving some diabetic complications.</p>Fórmula:C18H11F3N2O3S2Forma y color:SolidPeso molecular:424.42Eicosapentaenoic acid ethyl ester
CAS:<p>Eicosapentaenoic acid ethyl ester (Ethyl eicosapentaenoate) is an omega-3 fatty acid.</p>Fórmula:C22H34O2Pureza:95% - 98.13%Forma y color:SolidPeso molecular:330.50BMS-961955
CAS:<p>BMS-961955 is an allosteric inhibitor of the hepatitis C virus NS5B polymerase.</p>Fórmula:C37H43FN4O4SForma y color:SolidPeso molecular:658.83G-4120
CAS:<p>G-4120 is a biochemical that has been shown to have a dose-dependent complete inhibition of arterial and venous thrombosis.</p>Fórmula:C26H36N8O11SForma y color:SolidPeso molecular:668.68AJ-3941
CAS:<p>AJ-3941: Selective calcium channel blocker, prevents lipid peroxidation, potential for treating brain vessel disorders.</p>Fórmula:C35H35FN2O9Forma y color:SolidPeso molecular:646.67NA 382
CAS:<p>NA 382 is a staurosporine derivative that inhibits multidrug resistance.</p>Fórmula:C31H28N4O6Forma y color:SolidPeso molecular:552.58DHPM-93
CAS:<p>DHPM-93 is a the most potent inhibitor of sodium iodide symporter (nis) reported to date</p>Fórmula:C18H18N2O5Forma y color:SolidPeso molecular:342.35CCG-203586
CAS:<p>CCG-203586 is a novel potent glucosylceramide synthase (GCS) inhibitor.</p>Fórmula:C26H32N2O4Forma y color:SolidPeso molecular:436.54HJC-0123
CAS:<p>HJC-0123: inhibits STAT3, boosts cleaved caspase-3, hinders cell growth, triggers apoptosis, effective in ER-negative breast/pancreatic cancer.</p>Fórmula:C24H16N2O3SForma y color:SolidPeso molecular:412.46UNC1666
CAS:<p>UNC1666 is a dual ATP-competitive small molecule tyrosine kinase inhibitor, which potently diminishes Mer and Flt3 phosphorylation in AML.</p>Fórmula:C26H35N5O4SForma y color:SolidPeso molecular:513.65S 0960
CAS:<p>S 0960 is a dimeric bile acid analogue, a specific inhibitor of the sodium-dependent bile salt transporter in the ileum, used in metabolic disease research.</p>Fórmula:C48H79NO8Pureza:99.32% - >99.99%Forma y color:SolidPeso molecular:798.14MEN-10354
CAS:<p>MEN-10354 is a less potent and less selective NK-2 tachykinin receptor antagonist compared to the linear analog, R 396.</p>Fórmula:C37H46N8O9Forma y color:SolidPeso molecular:746.81UAWJ246
CAS:<p>UAWJ246 is a SARS-CoV-2 Protease inhibitor (IC50 = 45 nM). UAWJ246 provides new directions for the development of Mpro inhibitors as SARS-CoV-2 antivirals.</p>Fórmula:C25H34N4O6Forma y color:SolidPeso molecular:486.56ITP-2
CAS:<p>ITP-2 activates hERG channels, shifts inactivation midpoint depolarization, and activation voltage hyperpolarization.</p>Fórmula:C19H14F3N5O2Forma y color:SolidPeso molecular:401.34ST7612AA1
CAS:<p>ST7612AA1: potent, oral HDAC inhibitor; reactivates HIV-1 latency; shows antitumor effects; may study malaria.</p>Fórmula:C20H27N3O4SPureza:99.71%Forma y color:SolidPeso molecular:405.51MRT-92 HCl salt
CAS:<p>MRT-92 is a potent Smoothened receptor inhibitor with an IC50 of 0.4 nM, affecting Hh pathway and cancer drug target.</p>Fórmula:C33H35ClN4O5Forma y color:SolidPeso molecular:603.12HA-29
CAS:<p>HA-29 is an inhibitor of thromboxane A2 and prostaglandin endoperoxide receptors.</p>Fórmula:C16H16N2O3Forma y color:SolidPeso molecular:284.31CP 100356
CAS:<p>CP 100356: Specific MDR1 (P-Gp) inhibitor with low uM/nM potency against MDR-1 substrates in MDCKII cells.</p>Fórmula:C31H36N4O6Forma y color:SolidPeso molecular:560.64Erythromycin hydrochloride
CAS:<p>Erythromycin hydrochloride is an inhibitor of protein translation and mammalian mRNA splicing. It inhibits growth of gram negative and gram positiove bacteria.</p>Fórmula:C37H68ClNO13Forma y color:SolidPeso molecular:770.39(+)-Donepezil
CAS:<p>(+)-Donepezil is an isomer of Donepezil -- a nootropic acting as an inhibitor of acetylcholinesterase.</p>Fórmula:C24H29NO3Forma y color:SolidPeso molecular:379.49MDL-100173
CAS:<p>MDL-100173 is a dual angiotensin-converting enzyme (ACE)/neutral endopeptidase (NEP) inhibitor.</p>Fórmula:C24H26N2O4SForma y color:SolidPeso molecular:438.54SAR296968
CAS:<p>SAR296968 is a novel selective NCX inhibitor, improving cardiac function and restoring sympathovagal balance in heart failure.</p>Fórmula:C22H22N2O4SForma y color:SolidPeso molecular:410.49Nomifensine maleate
CAS:<p>Nomifensine maleate (Nomifensine (maleate)) is a selective inhibitor of dopamine uptake. Nomifensine maleate is used in adult attention deficit disorder.</p>Fórmula:C20H22N2O4Pureza:98.46%Forma y color:SolidPeso molecular:354.4Calanolide B
CAS:<p>Calanolide B is one of a novel class of HIV-inhibiting coumarins from the tropical rainforest tree, Calophyllum lanigerum.</p>Fórmula:C22H26O5Forma y color:SolidPeso molecular:370.44CHDI340246
CAS:<p>CHDI-340246 is a potent and selective kynurenine mono-oxygenase (KMO) inhibitor.</p>Fórmula:C14H11ClN2O3Forma y color:SolidPeso molecular:290.7JQ1-Acid HCl
CAS:<p>(+)-JQ-1 carboxylic acid: potent BET inhibitor, precursor for PROTACs synthesis.</p>Fórmula:C19H18Cl2N4O2SForma y color:SolidPeso molecular:437.339DK-139
CAS:<p>DK-139 is an inhibitor of NF-kappaB-mediated GROalpha expression, suppressing the TNFalpha-induced invasive capability of MDA-MB-231 human breast cancer cells.</p>Fórmula:C18H18O5Forma y color:SolidPeso molecular:314.33RB-005
CAS:<p>RB-005 is a potent SK1 inhibitor with IC(50) of 3.6 μM, potentially treating proliferative diseases like hypertension and degrades SK1 in human cells.</p>Fórmula:C21H35NOForma y color:SolidPeso molecular:317.51SA 152
CAS:<p>SA 152 is an organophosphoric inhibitor.</p>Fórmula:C19H12F12NO2PForma y color:SolidPeso molecular:545.26APTO-253 isomer
CAS:<p>APTO-253 isomer, a variant with a Fluoro-atom at the 6-position, inhibits MTF-1, inducing KLF4 and blocking cell cycle progression.</p>Fórmula:C22H14FN5Forma y color:SolidPeso molecular:367.38Paullone
CAS:<p>Paullone is an inhibitor of cyclin-dependent kinases (CDKs). The CDKs are a family of protein kinases that are involved in regulation of the cell cycle.</p>Fórmula:C16H12N2OForma y color:SolidPeso molecular:248.28U 92032
CAS:<p>U 92032 is a T-channel antagonist and antioxidant that inhibits lipid peroxidation.</p>Fórmula:C30H35F2N3O2Forma y color:SolidPeso molecular:507.61FCE-27262
CAS:<p>FCE-27262 is a prostaglandin H2/thromboxane A2 receptor antagonist.</p>Fórmula:C23H31N3O3Forma y color:SolidPeso molecular:397.51Oxyphenisatine
CAS:<p>Oxyphenisatine, a laxative with anticancer properties, may cause liver damage over time.</p>Fórmula:C20H15NO3Pureza:97.35%Forma y color:SolidPeso molecular:317.34M2WJ332
CAS:<p>M2WJ332 is a novel M2-S31N inhibitor, showing antiviral activity against Influenza A virus.</p>Fórmula:C18H22N2OSForma y color:SolidPeso molecular:314.45AZD-3839 hemifumarate
CAS:<p>AZD-3839 hemifumarate is a potent and selective BACE1 inhibitor and clinical candidate for the treatment of Alzheimer's disease.</p>Fórmula:C52H36F6N10O4Forma y color:SolidPeso molecular:978.92PF-06412154 HCl
CAS:<p>PF-06412154 HCl is a glucagon receptor antagonist.</p>Fórmula:C24H28ClN3O3Forma y color:SolidPeso molecular:441.96BW-10
CAS:<p>BW-10 potently inhibits bombesin evoked release of gastrointestinal hormones in vitro and in vivo.</p>Fórmula:C57H72N14O8Forma y color:SolidPeso molecular:1081.27(-)-Donepezil
CAS:<p>(-)-Donepezil is an isomer of Donepezil -- a nootropic acting as an inhibitor of acetylcholinesterase.</p>Fórmula:C24H29NO3Forma y color:SolidPeso molecular:379.49AQW-051 fumarate
CAS:<p>AQW-051 fumarate is an α7 nicotinic ACh receptor partial agonist that may act as a cognitive-enhancing agent.</p>Fórmula:C23H26N2O5Forma y color:SolidPeso molecular:410.47ArgTX-48 TFA
CAS:<p>ArgTX-48 is a highly potent and subfamily selective antagonist of the NMDARs and AMPARs.</p>Fórmula:C40H62F9N11O14Forma y color:SolidPeso molecular:1091.9846KNI 174
CAS:<p>KNI 174 is a new type of anti‐AIDS drug used as an HIV‐1 protease inhibitor</p>Fórmula:C36H45N5O7SForma y color:SolidPeso molecular:691.84CR-6086
CAS:<p>CR6086: potent EP4 antagonist with DMARD effects, low Ki (16.6 nM), and specific anti-inflammatory action.</p>Fórmula:C26H27F3N2O3Forma y color:SolidPeso molecular:472.5MLAF50
CAS:<p>MLAF50 is an inhibitor of the REV1 UBM2-Ubiquitin interaction.</p>Fórmula:C15H12I2O4Forma y color:SolidPeso molecular:510.06Pitavastatin
CAS:<p>Pitavastatin (NK-104) is an HMG-CoA reductase inhibitor with hypocholesterolemic and neuroprotective activities.</p>Fórmula:C25H24FNO4Pureza:97.17%Forma y color:SolidPeso molecular:421.46CD08108
CAS:<p>CD08108 is a MC1R agonist.</p>Fórmula:C31H38N4O4Forma y color:SolidPeso molecular:530.66UU-T01
CAS:<p>UU-T01 inhibits β-catenin/Tcf4 with Ki of 3.14 µM, binds β-catenin directly with KD of 0.531 µM.</p>Fórmula:C10H10N6OForma y color:SolidPeso molecular:230.23N 0861
CAS:<p>N 0861 is a selective adenosine A1 receptor antagonist that attenuates renal insufficiency during adenosine-controlled hypotension in rats.</p>Fórmula:C13H17N5Pureza:98.78%Forma y color:SolidPeso molecular:243.31NNC 0772
CAS:<p>NNC 0772 is a dopamine D-1 receptor antagonist</p>Fórmula:C19H21Cl2NO2Forma y color:SolidPeso molecular:366.28GSK-2256098 HCl
CAS:<p>GSK-2256098 HCl is a focal adhesion kinase-1 (FAK) inhibitor with potential antiangiogenic and antineoplastic activities.</p>Fórmula:C20H24Cl2N6O2Forma y color:SolidPeso molecular:451.35Motuporin
CAS:<p>Motuporin is an inhibitor of type-1 and type-2A protein phosphatase catalytic subunits (PP-1c and PP-2Ac).</p>Fórmula:C40H57N5O10Forma y color:SolidPeso molecular:767.91RO2443
CAS:<p>RO2443 is a dual inhibitor of the MDM2-p53 or MDMX-p53 protein-protein interaction, inducung MDM2 and MDMX dimerization and activating the p53 pathway.</p>Fórmula:C20H14ClF2N3O2Forma y color:SolidPeso molecular:401.79BQ-610
CAS:<p>BQ-610 is an Endothelin A receptor antagonist.</p>Fórmula:C36H44N6O6Forma y color:SolidPeso molecular:656.77Vadaclidine
CAS:<p>Vadaclidine is an orally acting antinociceptive muscarinic agonist.</p>Fórmula:C13H21N3S2Forma y color:SolidPeso molecular:283.46Milnacipran
CAS:<p>Milnacipran, an SNRI with 85% bioavailability, treats fibromyalgia and is well absorbed orally.</p>Fórmula:C15H22N2OForma y color:SolidPeso molecular:246.35Oxycodegol phosphate
CAS:<p>Oxycodegol phosphate is a mu-opioid agonist used in the treatment of Moderate to Severe Chronic Low Back Pain</p>Fórmula:C31H50NO13PForma y color:SolidPeso molecular:675.71Odalasvir
CAS:<p>Odalasvir is a novel NS5A inhibitor for the treatment of hepatitis C.</p>Fórmula:C60H72N8O6Forma y color:SolidPeso molecular:1001.26APX2014
CAS:<p>APX2014 is a novel potent and specific Ref-1 inhibitor, blocking in vitro cell proliferation and activating apoptosis via PARP cleavage.</p>Fórmula:C18H19NO5Forma y color:SolidPeso molecular:329.35APX2009
CAS:<p>APX2009, a 2nd-gen APE1/Ref-1 inhibitor, curbs NFkB activity, survivin, and prostate cancer cell growth; induces cell cycle arrest.</p>Fórmula:C21H25NO4Forma y color:SolidPeso molecular:355.43
