Entre las marcas de nuestros más de 25 colaboradores destaca TargetMol
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Termina el 31 dic( quedan 8 días )
SMANT hydrochloride
CAS:SMANT hydrochloride (N-(4-bromophenyl)-3-(3,5-dimethylpiperidin-1-yl)propanamide hydrochloride) is an antagonist of Smoothened accumulation.Fórmula:C16H24BrClN2OPureza:99.81%Forma y color:SolidPeso molecular:375.73SMER3
CAS:<p>SMER3 is an inhibitor of the Skp1-Cullin-F-box (SCF)(Met30) ubiquitin ligase, a member of the SCF E3-ligase family, which regulates diverse cellular processes</p>Fórmula:C11H4N4O2Pureza:98.35%Forma y color:SolidPeso molecular:224.18SMIFH2
CAS:<p>SMIFH2 is formin homology 2 (FH2) domains inhibitor.</p>Fórmula:C15H9BrN2O3SPureza:97.41%Forma y color:SolidPeso molecular:377.21SN 003
CAS:SN 003 is a CRF1 antagonist.Fórmula:C19H25N5O2Pureza:98%Forma y color:SolidPeso molecular:355.43SNAP 5089
CAS:α1A-adrenoceptor antagonistFórmula:C36H40N4O5Pureza:98%Forma y color:SolidPeso molecular:608.73SNAP
CAS:NO donorFórmula:C7H12N2O4SPureza:98%Forma y color:Green Crystalline SolidPeso molecular:220.25SNC 162
CAS:SNC 162 is a potent and selective delta-opioid receptor (δ-opioid) agonist with analgesic, antidepressant and antiarrhythmic effects.Fórmula:C27H37N3OPureza:98%Forma y color:SolidPeso molecular:419.6Sodium acetate
CAS:Sodium acetate is Commonly used laboratory reagentFórmula:C2H3NaO2Pureza:≥98% - ≥98%Forma y color:White Solid PowderPeso molecular:82.03Sodium Dihydrogen Phosphate
CAS:Sodium Dihydrogen Phosphate exhibits inhibitory activity against hCA1/2/4/5A/9 and is widely used in biochemical experiments and drug synthesis research.Fórmula:H2NaO4PPureza:98%Forma y color:SolidPeso molecular:119.98Solifenacin hydrochloride
CAS:Solifenacin Hcl is a muscarinic receptor antagonist.Fórmula:C23H27ClN2O2Pureza:98%Forma y color:SolidPeso molecular:398.93JZL195
CAS:<p>JZL195 is a selective and efficacious dual FAAH/MAGL inhibitor.</p>Fórmula:C24H23N3O5Pureza:99.81%Forma y color:SolidPeso molecular:433.46Sonepiprazole
CAS:Sonepiprazole (PNU-101387G) is a chemical compound known for its selective antagonistic properties toward D4 dopamine receptors, exhibiting dissociationFórmula:C21H27N3O3SPureza:99.81%Forma y color:SolidPeso molecular:401.52Spiperone hydrochloride
CAS:5-HT2A serotonin and selective D2-like dopamine receptor antagonistFórmula:C23H27ClFN3O2Pureza:98%Forma y color:SolidPeso molecular:431.93Spiroxatrine
CAS:<p>Spiroxatrine (R 5188) is a 5-HT1α and α2-adrenergic dual antagonist with sedative activity for the study of diseases related to the cardiovascular system.</p>Fórmula:C22H25N3O3Pureza:99.94%Forma y color:SolidPeso molecular:379.45SR11237
CAS:<p>SR11237 is a Pan retinoid X receptor (RXR) agonist.</p>Fórmula:C24H28O4Pureza:98.79%Forma y color:SolidPeso molecular:380.48SR 11302
CAS:SR 11302 is an inhibitor of activator protein-1 (AP-1).Fórmula:C26H32O2Pureza:98.65%Forma y color:SolidPeso molecular:376.53SR 140333
CAS:SR 140333 is a NK1 receptor antagonist.Fórmula:C37H45Cl3N2O2Pureza:98%Forma y color:SolidPeso molecular:656.12SR 142948
CAS:<p>SR 142948 is a neurotensin (NT) receptor antagonist.</p>Fórmula:C39H51N5O6Pureza:98%Forma y color:SolidPeso molecular:685.85SR 1555 (hydrochloride) (1386439-51-5 free base)
SR 1555 is a novel RORγ-specific synthetic ligand.Fórmula:C22H22F6N2O2·HClPureza:98%Forma y color:SolidPeso molecular:496.9SR 16584
CAS:α3β4 nAChR antagonistFórmula:C17H22N2OPureza:99.84%Forma y color:SolidPeso molecular:270.37SR1664
CAS:<p>SR1664 is a potent and selective PPARγ inhibitor with potential antidiabetic activity.</p>Fórmula:C33H29N3O5Pureza:98.02%Forma y color:SolidPeso molecular:547.6Apalutamide
CAS:<p>Apalutamide (ARN-509) is a small molecule and androgen receptor (AR) antagonist with potential antineoplastic activity.</p>Fórmula:C21H15F4N5O2SPureza:99.03% - 99.91%Forma y color:SolidPeso molecular:477.43SR 2640 hydrochloride
CAS:SR 2640 hydrochloride is a competitive antagonist of leukotriene D4 and E4 and can be used in studies about leukotrienes in human asthma.Fórmula:C23H19ClN2O3Pureza:98.04%Forma y color:SolidPeso molecular:406.86SR 33805 oxalate
CAS:Ca2+ channel antagonistFórmula:C34H42N2O9SPureza:98%Forma y color:SolidPeso molecular:654.77SR 3576
CAS:JNK3 inhibitor, potent and selectiveFórmula:C27H27N5O5Pureza:98%Forma y color:SolidPeso molecular:501.53SR 49059
CAS:vasopressin V1A receptor antagonistFórmula:C28H27Cl2N3O7SPureza:98%Forma y color:SolidPeso molecular:620.5SR 57227 hydrochloride
CAS:<p>SR 57227A (SR 57227 hydrochloride) is a potent, orally active and selective 5-HT3 receptor agonist. It with ability to cross the blood brain barrier.</p>Fórmula:C10H14ClN3·HClPureza:99.89%Forma y color:SolidPeso molecular:248.15SSR 146977
CAS:NK3 receptor antagonistFórmula:C35H42Cl2N4O2Pureza:98%Forma y color:SolidPeso molecular:621.64ST1936
CAS:ST1936 (ST 1936 oxalate) is a 5-HT6 receptor agonist that stimulates cAMP, Ca2+, ERK1/2, and Fyn kinases by fully activating cloned human 5-HT6 receptors.Fórmula:C13H17ClN2Pureza:98%Forma y color:SolidPeso molecular:236.74ST 91
CAS:<p>ST-91 is an agonist of α2-adrenoceptor with a mixed α-adrenergic receptor type/subtype selection profile.</p>Fórmula:C13H20ClN3Pureza:99.83%Forma y color:SolidPeso molecular:253.77STEARDA
CAS:STEARDA potentiates TRPV1-mediated effects of NADA.Fórmula:C26H45NO3Pureza:98%Forma y color:SolidPeso molecular:419.64AC1NS4RE
CAS:<p>It is a tyrosine kinase inhibitor.</p>Fórmula:C15H13ClN2OPureza:99.53%Forma y color:SolidPeso molecular:272.73StemRegenin 1 Hydrochloride
CAS:StemRegenin 1 Hydrochloride is an AhR antagonist (IC₅₀ = 127 nM) that inhibits RANKL-induced osteoclast generation and differentiation.Fórmula:C24H24ClN5OSPureza:99.94%Forma y color:SolidPeso molecular:466Strontium chloride
CAS:Strontium chloride is an agonist of Calcium sensing receptor (CaSR) and directly affects C-type nerve fibers.Fórmula:Cl2SrPureza:98%Forma y color:White Solid CrystallinePeso molecular:158.52Sulfathiazole sodium
CAS:Sulfathiazole Sodium is an organosulfur compound. It also has been used as a short-acting sulfa drug.Fórmula:C9H9N3NaO2S2Pureza:98%Forma y color:SolidPeso molecular:278.31Sulindac sulfone
CAS:Sulindac sulfone is a metabolite of the nonsteroidal anti-inflammatory drug sulindac. Sulindac sulfone is an inhibitor of aldose reductase (IC50 =367 nM).Fórmula:C20H17FO4SPureza:98.2% - 98.83%Forma y color:SolidPeso molecular:372.41Sulprostone
CAS:EP3 and EP1 receptor agonistFórmula:C23H31NO7SPureza:98%Forma y color:White To Off-White SolidPeso molecular:465.56Sumatriptan
CAS:Sumatriptan (GR 43175 free base) is a 5-HT1 receptor agonist with anti-inflammatory activity used in acute migraine and acute myocardial infarction.Fórmula:C14H21N3O2SPureza:99.93%Forma y color:White To Off-White Crystalline PowderPeso molecular:295.4SUN B8155
CAS:SUN B8155 is a CT receptor agonist that induces cAMP formation in cells expressing recombinant human CT receptor.Fórmula:C14H15N3O3Pureza:99.38% - 99.38%Forma y color:SolidPeso molecular:273.29surface antigen (208-215) [Hepatitis B Virus]
HBV's nucleocapsid is enveloped by HBsAg with determinant "a". Subtypes adw, adr, ayw, ayr reflect four genotypes, have distinct geographic distributions.Fórmula:C46H74N8O10Pureza:98%Forma y color:SolidPeso molecular:899.13SX 011
CAS:<p>SX 011 is a p38α inhibitor.</p>Fórmula:C26H27ClFN3O3Pureza:98%Forma y color:SolidPeso molecular:483.96FM4-64
CAS:<p>FM4-64 (SynaptoRedTM C2) is a stylenoid dye. FM4-64 can be used to study endocytosis exocytosis and vesicle trafficking. High-Quality, Low-Cost!</p>Fórmula:C30H45Br2N3Pureza:99.41% - 99.411%Forma y color:SolidPeso molecular:607.51KW-2449
CAS:<p>KW-2449 is a multiple-targeted inhibitor, mostly for Flt3, modestly effective to Bcr-Abl, FGFR1, and Aurora A; little inhibitory on PDGFRβ, IGF-1R, EGFR.</p>Fórmula:C20H20N4OPureza:98.43% - 99.69%Forma y color:SolidPeso molecular:332.4Synthalin sulfate
CAS:Synthalin sulfate is a NMDA receptor antagonist.Fórmula:C12H30N6O4SPureza:98%Forma y color:SolidPeso molecular:354.47T-0156 hydrochloride
CAS:<p>inhibitor of phosphodiesterase type 5 (PDE5)</p>Fórmula:C31H30ClN5O7Pureza:98%Forma y color:SolidPeso molecular:620.05T-0156
CAS:T-0156 is a PEG5 inhibitor that inhibits the hydrolysis of cyclic guanosine monophosphate (cGMP) with low affinity for PDE6, PDE1, PDE2, PDE3 and PDE4.Fórmula:C31H29N5O7Pureza:98.53% - 98.76%Forma y color:SoildPeso molecular:583.59T 98475
CAS:gonadotropin-releasing hormone (GnRH, LHRH) receptor antagonist,orally activeFórmula:C37H37F2N3O4SPureza:98%Forma y color:SolidPeso molecular:657.77Tabimorelin hemifumarate
CAS:orally active ghrelin receptor (GHS-R1a) agonistFórmula:C32H40N403C4H404Pureza:98%Forma y color:SolidPeso molecular:586.72TAK 21d
CAS:Potent FAAH inhibitorFórmula:C19H17F2N7OPureza:98%Forma y color:SolidPeso molecular:397.38
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