Otros inhibidores
Esta categoría abarca una amplia variedad de inhibidores que no encajan en las clasificaciones estándar, pero que son fundamentales para diversas investigaciones bioquímicas y farmacológicas. Estos inhibidores pueden dirigirse a vías, enzimas e interacciones moleculares únicas o menos estudiadas, proporcionando herramientas valiosas para áreas de investigación especializadas. En CymitQuimica, ofrecemos una selección diversa de inhibidores de alta calidad que abarcan múltiples objetivos biológicos y disciplinas de investigación, lo que le permite explorar nuevas vías terapéuticas y profundizar su comprensión de los procesos biológicos complejos.
Se han encontrado 37902 productos de "Otros inhibidores"
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18:0-LPS
CAS:<p>18:0-LPS (Lysophosphatidylserine C18:0) is an endogenous lipid identified during the oxidation of phospholipids. It holds potential for use in cardiovascular disease research.</p>Fórmula:C24H48NO9PForma y color:SolidPeso molecular:525.613O-Desmethyl Midostaurin
CAS:O-Desmethyl Midostaurin is the active Midostaurin metabolite via cytochrome P450 liver enzyme metabolism.Fórmula:C34H28N4O4Pureza:98%Forma y color:SolidPeso molecular:556.61Namitecan
CAS:<p>Namitecan is an effective inhibitor of topoisomerase I. It has antitumor property.</p>Fórmula:C23H22N4O5Pureza:98%Forma y color:SolidPeso molecular:434.44Antibiotic LL Z1640-2
CAS:<p>Antibiotic LL Z1640-2 is an inhibitor against the TAK1 activity.</p>Fórmula:C19H22O7Forma y color:SolidPeso molecular:362.38Dexnebivolol
CAS:<p>Dexnebivolol (R67138), a ß-adrenergic antagonist, is Nebivolol's enantiomer with β1 blocking and vasodilation properties.</p>Fórmula:C22H25F2NO4Forma y color:SolidPeso molecular:405.43Oncopterin
CAS:<p>Oncopterin is found in urine from patients with solid and blood cancers.</p>Fórmula:C12H18N6O3Forma y color:SolidPeso molecular:294.31(±)-HIP-B
CAS:<p>(±)-HIP-B is an excitatory amino acid transporter blocker.</p>Fórmula:C6H8N2O4Pureza:98%Forma y color:SolidPeso molecular:172.149-Hydroxyoudemansin A
CAS:<p>9-Hydroxyoudemansin A exhibits antifungal activity with a minimum inhibitory concentration (MIC) of 12.5 μg/mL against Saccharomyces cerevisiae. It shows resistance to fungi such as Candida albicans, Rhodotorula, Penicillium, and Streptomyces, with MIC values all exceeding 50 μg/mL. It does not possess antibacterial properties.</p>Fórmula:C16H20O4Forma y color:SolidPeso molecular:276.328Granaticin B
CAS:<p>Granaticin B inhibits the initial phase of RNA biosynthesis and exhibits activity against Gram-positive bacteria, mycobacteria (weak), and Trichomonas vaginalis, along with the ability to suppress tumor cells.</p>Fórmula:C28H30O12Forma y color:SolidPeso molecular:558.531Chlorflavonin
CAS:<p>Chlorflavonin exhibits antifungal activity against several fungi, including Aspergillus, yeast, and Botrytis cinerea, with exceptionally strong activity against Aspergillus nidulans, where the minimum inhibitory concentration is as low as 0.08 μg/mL.</p>Fórmula:C18H15ClO7Forma y color:SolidPeso molecular:378.761FTI-2628
CAS:<p>FTI-2628 is a novel inhibitor of protein farnesyltransferase (FT), inhibiting the growth of P. falciparum in red blood cells and suppressing parasitemia.</p>Fórmula:C31H34N4O3SForma y color:SolidPeso molecular:542.69Unoprostone isopropyl
CAS:<p>Unoprostone isopropyl, a prostanoid and synthetic docosanoid, is approved for the treatment of ocular hypertension and open-angle glaucoma.</p>Fórmula:C25H44O5Pureza:98%Forma y color:SolidPeso molecular:424.61Hetrombopag olamine
CAS:<p>Hetrombopag olamine is a non-peptide thrombopoietin (TPO) receptor agonist with oral activity.</p>Fórmula:C29H36N6O7Pureza:98%Forma y color:SolidPeso molecular:580.63Ep vinyl quinidine
CAS:<p>3-Epiquinine is a Quinidine stereoisomer, used in malaria, antiarrhythmic, inhibits P450db, and blocks K+ channels, IC50: 19.9 μM.</p>Fórmula:C20H24N2O2Forma y color:SolidPeso molecular:324.42GW311616
CAS:<p>GW-311616 is a long duration, orally bioavailable, and selective human neutrophil elastase (HNE) inhibitor (IC50: 22 nM; Ki: 0.31 nM).</p>Fórmula:C19H31N3O4SForma y color:SolidPeso molecular:397.5312(S)-HEPE
CAS:<p>12(S)-HEPE, made from EPA by 12-LO, is an anti-inflammatory ω-3 derivative affecting leukotriene formation.</p>Fórmula:C20H30O3Forma y color:SolidPeso molecular:318.45HbF inducer-1
<p>HbF inducer-1 is a fetal hemoglobin inducer which is orally bioavailable.</p>Fórmula:C18H19N3O3Forma y color:SolidPeso molecular:325.36Leucomycin A7
CAS:<p>Leucomycin A7 is a component of the leucomycin complex, isolated from *Streptomyces kitasatoensis*. It possesses antibacterial activity, effectively inhibiting the growth of gram-positive bacteria, while its inhibitory effect on gram-negative bacteria is comparatively weaker.</p>Fórmula:C38H63NO14Forma y color:SolidPeso molecular:757.905Pyrrolomycin A
CAS:<p>Pyrrolomycin A is a pyrrole antibiotic that exhibits activity against Gram-positive bacteria, Gram-negative bacteria, and fungi.</p>Fórmula:C4H2Cl2N2O2Forma y color:SolidPeso molecular:180.977Pterulinic acid
CAS:<p>Pterulinic acid is an inhibitor of coenzyme I:coenzyme Q oxidoreductase. It demonstrates IC50 values (μg/mL) of 50 for the mammalian cell line L1210, 20 for HL60, 25 for HeLaS3, and 100 for BHK.</p>Fórmula:C15H11ClO4Forma y color:SolidPeso molecular:290.70Memnobotrin A
CAS:<p>Memnobotrin A is an antibiotic with inhibitory effects on the NCI-460, MCF7, and SF-268 cell lines.</p>Fórmula:C25H33NO5Forma y color:SolidPeso molecular:427.53DDCPPB-Glu
CAS:<p>DDCPPB-Glu is a 6-5 fused ring heterocycle antifolate that shows antitumor activity.</p>Fórmula:C22H27N5O5Pureza:98%Forma y color:SolidPeso molecular:441.48Ceclazepide
CAS:<p>Ceclazepide is an antagonist of cholecystokinin receptor.</p>Fórmula:C30H32N6O5Pureza:98%Forma y color:SolidPeso molecular:556.61DMP 728
CAS:<p>DMP 728 is an antagonist of Glycoprotein IIb-IIIa.</p>Fórmula:C26H40N8O10SPureza:98%Forma y color:SolidPeso molecular:656.71NSC 357754
CAS:<p>NSC 357754 is an inhibitor of Claudin. It can enhance transepithelial electrical resistance and reduce specific cation permeability. NSC 357754 is useful for research involving Claudin-2 and/or Claudin-15 mediated intestinal disorders.</p>Fórmula:C26H20N4O2Forma y color:SolidPeso molecular:420.463(rel)-Myrislignan
CAS:<p>(rel)-Myrislignan, a lignan compound with a relative configuration, has been isolated from Myristica fragrans Houtt.</p>Fórmula:C21H26O6Pureza:98%Forma y color:SolidPeso molecular:374.43(R)-FL118
CAS:<p>FL118 inhibits human survivinion expression and activates tumor suppressor p53 as a MOA in p53 wild-type cancer cells.</p>Fórmula:C21H16N2O6Forma y color:SolidPeso molecular:392.36Orvepitant
CAS:<p>Orvepitant is a potent and selective NK1 antagonist, which may be potentially useful for patients with major depressive disorder (MDD), anxiety and insomnia.</p>Fórmula:C31H35F7N4O2Forma y color:SolidPeso molecular:628.62Feudomycin B
CAS:<p>Feudomycin B is a macrolactam antibiotic that exhibits antitumor cell activity.</p>Fórmula:C28H31NO10Forma y color:SolidPeso molecular:541.546SORT1-IN-1
CAS:<p>SORT1-IN-1 (compound 2) is a SORT1 inhibitor.</p>Fórmula:C17H13F3N2O4Forma y color:SolidPeso molecular:366.29PD 113271
CAS:<p>PD 113,271 is an analog of the fermentation products fostriecin with antitumor activity in vitro and in vivo.</p>Fórmula:C19H27O10PPureza:98%Forma y color:SolidPeso molecular:446.39Adecypenol
CAS:<p>Adecypenol is a unique adenosine deaminase inhibitor. It shows effective inhibitory activity against calf intestinal adenosine deaminase.</p>Fórmula:C12H16N4O4Pureza:98%Forma y color:SolidPeso molecular:280.28hCA IX-IN-1
<p>hCA IX-IN-1 inhibits human carbonic anhydrases I, II, IX, and XII with Ki values of 331.4, 28.4, 9.4, 17.8 nM and exhibits anticancer properties.</p>Fórmula:C19H18N2O3SForma y color:SolidPeso molecular:354.42MDK-3298
CAS:<p>MDK-3298 is a reversible covalent inhibitor of Mcl-1, a target of protein-protein interaction (PPI).</p>Fórmula:C35H32BN3O7Pureza:98%Forma y color:SolidPeso molecular:617.46S-1033
CAS:<p>S-1033 is an FP receptor agonist.</p>Fórmula:C20H33NaO4Forma y color:SolidPeso molecular:360.4698Leucomycin U
CAS:<p>Leucomycin U is a macrolide antibiotic. It demonstrates significant activity against Gram-positive bacteria and also exhibits effects on spirochetes, rickettsiae, and chlamydiae.</p>Fórmula:C37H61NO14Forma y color:SolidPeso molecular:743.878SLN124
<p>SLN124, a GalNAc-siRNA targeting TMPRSS6, may normalize iron balance by restoring ferroregulation.</p>Forma y color:SolidMesulergine
CAS:<p>Mesulergine is metabolized into dopaminergic agonists.</p>Fórmula:C18H26N4O2SForma y color:SolidPeso molecular:362.49Asperenone
CAS:<p>Asperenone is a 15-lipoxygenase (15-LOX) inhibitor with an IC50 of 0.3 mM. Additionally, it acts as a platelet aggregation inhibitor with an IC50 of 0.23 mM. Asperenone also exhibits antifungal properties, inhibiting the growth of pathogenic fungi Ophiostoma crassivaginatum and O. piliferum, and may be utilized in research related to cardiovascular diseases and anti-infective treatments.</p>Fórmula:C20H22OForma y color:SolidPeso molecular:278.388C.I. Pigment Red 60
CAS:<p>C.I. Pigment Red 60 is a bright, scarlet, semi-transparent red pigment.</p>Fórmula:C17H9N2Na3O9S2Pureza:98%Forma y color:SolidPeso molecular:518.35Gepotidacin hydrochloride
CAS:<p>Gepotidacin (GSK-2140944) is a potent DNA topoisomerase inhibitor, a novel antibacterial efficacious against various anaerobes.</p>Fórmula:C24H29ClN6O3Forma y color:SolidPeso molecular:484.98YKL-04-085
CAS:<p>YKL-04-085 inhibits viral translation effectively, with strong antiviral action at much lower doses than those affecting host-cell growth.</p>Fórmula:C30H29N5O2Forma y color:SolidPeso molecular:491.6Lycopodine
CAS:<p>Lycopodine, a bioactive compound derived from Lycopodium clavatum spores, effectively inhibits the proliferation of HeLa cells through the induction of</p>Fórmula:C16H25NOPureza:98%Forma y color:SolidPeso molecular:247.38KF-19418
CAS:<p>KF-19418 is a follicle stimulant that directly activates follicles in vitro and promotes hair growth in vivo.</p>Fórmula:C21H14N4OForma y color:SolidPeso molecular:338.36Anti-Trypanosoma cruzi agent-1
<p>Anti-Trypanosoma cruzi agent-1 (Compd E5) has a potent anti-Toxoplasma effect.</p>Fórmula:C23H29N3O5Forma y color:SolidPeso molecular:427.49Taprostene
CAS:<p>Taprostene (CG-4203), a stable Prostacyclin analogue, protects endothelium and myocardium post-ischemia in cats, with minimal hemodynamic impact.</p>Fórmula:C24H30O5Forma y color:SolidPeso molecular:398.498,9-Epoxyeicosatrienoic acid
CAS:<p>8,9-Epoxyeicosatrienoic acid offers unique protective effects on the glomerulus. It inhibits the increase in glomerular albumin permeability caused by circulating permeability factors (FSPF). Additionally, 8,9-Epoxyeicosatrienoic acid is used in research related to glomerular dysfunction.</p>Fórmula:C20H32O3Forma y color:SolidPeso molecular:320.47Ciprokiren
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:729.93Ornoprostil
CAS:<p>Ornoprostil, a prostaglandin E1 analogue, acts as a mucosal protectant.</p>Fórmula:C23H38O6Pureza:98%Forma y color:SolidPeso molecular:410.54(-)-15-Deoxyspergualin
CAS:<p>(-)-15-Deoxyspergualin is a potent antitumor agent that demonstrates significant inhibition against mouse leukemia L-1210.</p>Fórmula:C17H37N7O3Forma y color:SolidPeso molecular:387.52Butaprost
CAS:<p>Butaprost: EP2 receptor agonist, EC50=33 nM, Ki=2.4 μM (murine), reduces fibrosis via TGF-β/Smad2.</p>Fórmula:C24H40O5Pureza:98%Forma y color:SolidPeso molecular:408.57BE-10988
CAS:<p>BE-10988 is a DNA topoisomerase (DNAtopoisomerase) inhibitor. It suppresses the growth of P388 murine leukemia cell lines that are resistant to Doxorubicin and Vinblastine by promoting the formation of DNA topoisomerase complexes.</p>Fórmula:C13H10N4O3SForma y color:SolidPeso molecular:302.31AMD-7049
CAS:<p>AMD-7049 is a biochemical.</p>Fórmula:C25H39N5Forma y color:SolidPeso molecular:409.61(S)-5-hydroxy-6-methoxy Duloxetine maleate
<p>(S)-5-hydroxy-6-methoxy Duloxetine, an active metabolite of the (S)-duloxetine, functions as a serotonin (5-HT) and norepinephrine reuptake inhibitor.</p>Fórmula:C19H21NO3S·C4H4O4Forma y color:SolidPeso molecular:459.51RS 2135
CAS:<p>RS 2135 is a novel class I antiarrhythmic agent to inhibit ischemia-induced ventricular arrhythmias.</p>Fórmula:C18H21ClN2O2Pureza:98%Forma y color:SolidPeso molecular:332.83Erizepine
CAS:<p>Erizepine, an octopamine receptor 3 (OAR3) antagonist, exhibits a Ki value of 474 nM. This compound is utilized in insect research.</p>Fórmula:C20H22N2Forma y color:SolidPeso molecular:290.4OM-153
CAS:<p>OM-153 blocks tankyrase 1 (IC50: 13 nM) and 2 (IC50: 2 nM), stifling WNT signaling and COLO 320DM cell growth.</p>Fórmula:C28H24FN7O2Forma y color:SolidPeso molecular:509.53SARS-CoV-2-IN-6
<p>SARS-CoV-2-IN-6 is an inhibitor of SARS-CoV-2 3CLpro with the IC 50 value of 73 nM.</p>Fórmula:C17H13ClN2O2Forma y color:SolidPeso molecular:312.75Detajmium
CAS:<p>Detajmium is an anti-arrhythmia compound. It is an Na(+)-channel-blocking drug with an extremely long recovery from use-dependent sodium channel block.</p>Fórmula:C27H42N3O3Pureza:98%Forma y color:SolidPeso molecular:456.64LK-732
CAS:<p>LK-732 is a thrombin inhibitor with antithrombotic activity. It exhibits dose-dependent inhibition in models of hypercoagulability, with an IC50 value of 1.3 mg/kg. LK-732 is used in cardiovascular and cerebrovascular research.</p>Fórmula:C25H29N5O3SForma y color:SolidPeso molecular:479.59THR-β agonist 4
CAS:<p>THR-β agonist 4 is a potent agonist of THR-β.</p>Fórmula:C16H11Cl2F2N5O6SForma y color:SolidPeso molecular:510.26Cedarmycin B
CAS:<p>Cedarmycin B exhibits activity against Candida, Cryptococcus neoformans, and Aspergillus fumigatus, with a minimum inhibitory concentration (MIC) ranging from 12.5 to 50 μg/mL.</p>Fórmula:C12H18O4Forma y color:SolidPeso molecular:226.269(25S)-δ7-Dafachronic acid
CAS:<p>(25S)-delta7-Dafachronic acid, an orphan nuclear receptor DAF-12 ligand, inhibits the dauer-promoting activity of DAF-12.</p>Fórmula:C27H42O3Pureza:98%Forma y color:SolidPeso molecular:414.62nNOS-IN-25
CAS:<p>nNOS-IN-25 is an effective, selective, and cell-permeable inhibitor of neuronal nitric oxide synthase.</p>Fórmula:C21H22N4Pureza:98%Forma y color:SolidPeso molecular:330.43(6S)-CP-470711
CAS:<p>(6S)-CP-470711 (Compound 8) acts as an inhibitor of sorbitol dehydrogenase (SDH) in both humans and rats, exhibiting inhibitory concentrations (IC50) of 19 nM and 27 nM, respectively. Additionally, (6S)-CP-470711 has been shown to ameliorate diabetes in rats induced by Streptozotocin.</p>Fórmula:C18H26N6O2Forma y color:SolidPeso molecular:358.44AT-IAP
CAS:AT-IAP is an effective dual antagonist of XIAP and cIAP1.Fórmula:C29H40FN5O2Pureza:98%Forma y color:SolidPeso molecular:509.66Ici D1542
CAS:<p>Ici D1542: potent TXS inhibitor & TXA2 receptor antagonist, effective thromboxane blocker in vitro.</p>Fórmula:C25H30N2O7Pureza:98%Forma y color:SolidPeso molecular:470.51SSTR5 antagonist 2 TFA
CAS:<p>Potent, oral SSTR5 antagonist 2 TFA may treat type 2 diabetes.</p>Fórmula:C34H36F4N2O7Pureza:98%Forma y color:SolidPeso molecular:660.65L 671776
CAS:<p>L 671776 is an inositol monophosphatase inhibitor.</p>Fórmula:C23H32O5Pureza:98%Forma y color:SolidPeso molecular:388.5SARS-CoV-2 nsp3-IN-1
<p>Compound 15c selectively inhibits SARS-CoV-2 nsp3 Mac1 with IC50 of 6.1 μM.</p>Fórmula:C17H15N5O2Forma y color:SolidPeso molecular:321.33Rafutrombopag
CAS:<p>Rafutrombopag is a thrombopoietin (TPO) agonist.</p>Fórmula:C25H22N4O5Forma y color:SolidPeso molecular:458.47SB 204070 hydrochloride
CAS:<p>SB 204070 hydrochloride is an inhibitor of beta-lactamase, it is isolated from Spondias mombin.</p>Fórmula:C19H27ClN2O4Pureza:98%Forma y color:SolidPeso molecular:382.88ONO-DI-004
CAS:<p>ONO-DI-004 is a selective EP1 Prostanoid receptor agonist.</p>Fórmula:C24H38O6Forma y color:SolidPeso molecular:422.55Ro-51
CAS:<p>dual P2X3 and P2X2/3 antagonist</p>Fórmula:C17H23IN4O4Pureza:98%Forma y color:SolidPeso molecular:474.29Chloroquinocin
CAS:<p>Chloroquinocin exhibits moderate activity against Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA).</p>Fórmula:C17H15ClO5Forma y color:SolidPeso molecular:334.751AM-3189
CAS:<p>AM-3189: potent, selective GPR40 agonist with low CNS penetration, good pharmacokinetics, and efficacy mirroring AMG 837.</p>Fórmula:C27H25ClN2O3Forma y color:SolidPeso molecular:460.95AGN-795
CAS:<p>AGN-795 is a biochemical.</p>Fórmula:C14H20N2Forma y color:SolidPeso molecular:216.328SARS-CoV-2 nsp14-IN-2
<p>SARS-CoV-2 nsp14-IN-2: Strong Nsp14 methyltransferase inhibitor (IC50: 0.09 μM), potential for COVID-19 research.</p>Fórmula:C21H21N5O5SForma y color:SolidPeso molecular:455.49Cofpropamine
CAS:<p>Cofpropamine, a caffeine derivative that inhibits polyadenylation, enhances the suppressive effects of Cyclophosphamide in animal models of rat adjuvant arthritis and mouse collagen-induced arthritis.</p>Fórmula:C13H21N5O3Forma y color:SolidPeso molecular:295.34FW 34569
CAS:<p>FW 34569, an enkephalin analog, boosts growth hormones and prolactin, reduces cortisol and LH; FSH stable.</p>Fórmula:C30H43N5O7SPureza:98%Forma y color:SolidPeso molecular:617.7616(S)-Iloprost
CAS:<p>Iloprost, a potent prostacyclin analog, binds to human IP & EP1 receptors with high affinity; inhibits platelet aggregation effectively.</p>Fórmula:C22H32O4Forma y color:SolidPeso molecular:360.49Aspochalasin M
CAS:<p>Aspochalasin M shows moderate activity on HL-60 cells (IC50=20.0 μ M). Aspochalasin M has research potential in leukemia diseases.</p>Fórmula:C24H35NO4Forma y color:SolidPeso molecular:401.54RORγt Inverse agonist 2
CAS:<p>RORγt Inverse agonist 2 is a selective, orally active inverse agonist of RORγt(EC50 of 119 nM).</p>Fórmula:C27H25F8NO5SPureza:98%Forma y color:SolidPeso molecular:627.54IMR687
CAS:<p>IMR687: a PDE9 inhibitor that could improve memory in Alzheimer's by slowing cGMP hydrolysis.</p>Fórmula:C21H26N6O2Pureza:98%Forma y color:SolidPeso molecular:394.47IMP-321
CAS:IMP-321 is a soluble dimeric recombinant form of LAG-3 and first-in-class antigen presenting cell activator.Fórmula:C56H78N18O14SForma y color:SolidPeso molecular:1259.4DGY-08-097
CAS:<p>DGY-08-097: potent HCV NS3 degrader, low resistance risk, strong inhibition in cells, DC50 of 50nM at 4h.</p>Fórmula:C60H76N10O14Forma y color:SolidPeso molecular:1161.3BILA 1906 BS
CAS:BILA 1906 BS is an inhibitor of substrate analog protease.Fórmula:C41H52N6O4SPureza:98%Forma y color:SolidPeso molecular:724.95NUCC-555
CAS:<p>NUCC-555 is a first-in-class antagonist of activin. It opens a completely new approach to inhibiting the activity of TGF-beta receptor superfamily members.</p>Fórmula:C25H25N5O3Pureza:98%Forma y color:SolidPeso molecular:443.5BSc5367
CAS:<p>BSc5367 inhibits Nek1 kinase (IC50: 11.5 nM), key in cell cycle, DNA repair, impacting ALS, PKD, cancer.</p>Fórmula:C20H15N3O2Forma y color:SoildPeso molecular:329.35Fonsartan free acid
CAS:<p>Fonsartan: Angiotensin receptor blocker, halts angiotensin II effects on rat vascular cells.</p>Fórmula:C26H32N4O5S2Pureza:98%Forma y color:SolidPeso molecular:544.69SARS-CoV-2-IN-22
CAS:<p>SARS-CoV-2-IN-22 is a SARS-CoV-2 pseudovirus inhibitor (IC50: 16.96 μM).</p>Fórmula:C27H24N2O3SForma y color:SolidPeso molecular:456.56T-3861174
CAS:<p>T-3861174 is a prolyl tRNA synthetase (PRS) inhibitor, exhibiting significant in vitro anti-tumor activity with GCN2-ATF4 pathway activation.</p>Fórmula:C26H25FN6O2Forma y color:SolidPeso molecular:472.51CEP-2563
CAS:<p>CEP-2563 is a prodrug of CEP-751. It also used as an antitumor agent, inhibiting protein kinases.</p>Fórmula:C36H41ClN6O6Pureza:98%Forma y color:SolidPeso molecular:689.20ZL-Pin13
CAS:<p>ZL-Pin13: potent Pin1 inhibitor (IC50: 67 nM), halts MDA-MB-231 cell growth, reduces Pin1 substrates.</p>Fórmula:C24H23ClN2O3SForma y color:SoildPeso molecular:454.97TLR7/8 antagonist 2
<p>TLR7/8 antagonist 2: potent, orally active, IC50: 4.9 nM (TLR7), 0.6 nM (TLR8); potential for lupus therapy research.</p>Fórmula:C22H26FN5Forma y color:SolidPeso molecular:379.47PZ-3022
CAS:<p>PZ-3022 is an orally active, conformational PanK activator that counteracts C3-CoA inhibition. In a mouse model of propionic acidemia, it elevates hepatic CoASH and C2-CoA levels while reducing C3-CoA, making it useful for studying mitochondrial defects in propionic acidemia.</p>Fórmula:C20H21N5OForma y color:SolidPeso molecular:347.41Cbl-b-IN-1
CAS:<p>Cbl-b-IN-1 is a potent Cbl-b inhibitor (IC50 <100 nM) with potential anticancer activity for the study of intestinal inflammation.</p>Fórmula:C29H34N6O2Pureza:99.68%Forma y color:SolidPeso molecular:498.631L-739750
CAS:<p>L-739,750 is an inhibitor (FTI) of peptidomimetic farnesyltransferase.</p>Fórmula:C23H39N3O6S2Pureza:98%Forma y color:SolidPeso molecular:517.7Antitumor agent-47
<p>Antitumor agent-47, a silibinin derivative, shows cytotoxicity in NCI-H1299 (IC50: 8.07µM) and HT29 (IC50: 6.27µM) cells.</p>Fórmula:C30H27NO11Forma y color:SolidPeso molecular:577.54MSK-195
CAS:<p>MSK-195 is an effective TRPV1 agonist.</p>Fórmula:C28H40N2O5Pureza:98%Forma y color:SolidPeso molecular:484.63Chitinase-IN-4
<p>Chitinase-IN-4 (compound 8f) is a potent and selective inhibitor of OfChi-h with an IC50 value of 0.1 μM and good insecticidal activity.</p>Fórmula:C21H24ClN7Forma y color:SolidPeso molecular:409.92L-Tyrosyl-L-glutamic acid
CAS:<p>L-Tyrosyl-L-glutamic acid acts as an inhibitor of the amino acid permease GAP1.</p>Fórmula:C14H18N2O6Forma y color:SolidPeso molecular:310.3Kaitocephalin
CAS:<p>Kaitocephalin: naturally occurring, non-selective antagonist blocking glutamate receptors, made by Eupenicillium shearii fungus.</p>Fórmula:C18H21Cl2N3O9Forma y color:SolidPeso molecular:494.284-Chloropyridine
CAS:<p>4-Chloropyridine acts as an inhibitor of Nicotinamide N-methyltransferase (NNMT). Serving as a substrate for NNMT, this compound enhances the electrophilicity at the C4 position through methylation of the pyridine nitrogen. This modification facilitates an aromatic nucleophilic substitution reaction with the non-catalytic cysteine (C159) in NNMT, ultimately leading to suicidal activity inhibition of the enzyme. 4-Chloropyridine is a promising candidate for the development of activity-based probes targeting NNMT functions.</p>Fórmula:C5H4ClNForma y color:SolidPeso molecular:113.55Pim-1 kinase inhibitor 3
CAS:<p>Pim-1 kinase inhibitor 3 (Compound H5) is a potent inhibitor of Pim-1 kinase, demonstrating an inhibitory concentration (IC50) of 35.13 nM [1].</p>Fórmula:C20H25N3O2Forma y color:SolidPeso molecular:339.43ASB14780
<p>ASB14780 is a 4-phenoxy derivative and an inhibitor of cytoplasmic phospholipase cPLA2α (IC50: 20 nM).</p>Forma y color:SolidPyrisulfoxin B
CAS:<p>Pyrisulfoxin B is an antibiotic produced by the bacterium Streptomyces (BS-75).</p>Fórmula:C13H11N3O2SForma y color:SolidPeso molecular:273.31BRD-9526
CAS:<p>BRD-9526 is a potent and selective inhibitor of Sonic Hedgehog (Shh).</p>Fórmula:C26H31Cl2N3O6SPureza:98%Forma y color:SolidPeso molecular:584.51L 767679
CAS:<p>L 767679 is an antagonist of the fibrinogen receptors.</p>Fórmula:C20H24N4O4Pureza:98%Forma y color:SolidPeso molecular:384.43Pateamine A
CAS:<p>Pateamine A: marine-sourced macrolide from Mycale hentscheli; anticancer, antiviral, and translation inhibitor.</p>Fórmula:C31H45N3O4SForma y color:SolidPeso molecular:555.77SSR-182289A (Free)
CAS:<p>SSR-182289A (Free) is a thrombin inhibitor.</p>Fórmula:C30H33F2N5O4SPureza:98%Forma y color:SolidPeso molecular:597.68Dinordrin
CAS:<p>Dinordrin is an implantation inhibitor and hormone.</p>Fórmula:C27H36O4Pureza:98%Forma y color:SolidPeso molecular:424.57U 75875
CAS:<p>U 75875 is a protease inhibitor.</p>Fórmula:C45H61N7O7Forma y color:SolidPeso molecular:812.01L 365209
CAS:<p>L 365209 is an oxytocin antagonist.</p>Fórmula:C40H50N8O6Pureza:98%Forma y color:SolidPeso molecular:738.88MEIS-IN-1
CAS:<p>MEIS-IN-1 is a potent MEIS inhibitor that induces the expansion of hematopoietic stem cells in mice and humans.</p>Fórmula:C24H21F3N2O4Forma y color:SolidPeso molecular:458.43SX 3202
CAS:<p>SX 3202 is an aldose reductase inhibitor being developed for the treatment of diabetic neuropathy.</p>Fórmula:C17H11BrFN3O4Forma y color:SolidPeso molecular:420.1914,15-dehydro Leukotriene B4
CAS:<p>LTB4 is a leukocyte-activating fatty acid via 5-lipoxygenase. Two receptors, BLT1 and BLT2, bind it. 14,15-dehydro LTB4 is a stronger BLT1 antagonist.</p>Fórmula:C20H30O4Forma y color:SolidPeso molecular:334.45Rpi 856 C
CAS:<p>Rpi 856 C is a retrovirus protease inhibitor from Streptomyces that is effective against HIV-1 and HTLV-1 proteases.</p>Fórmula:C39H56N6O10Pureza:98%Forma y color:SolidPeso molecular:768.90Anticancer agent 79
<p>Anticancer agent 79 (3d) has potent activity against breast cancer, with cytotoxic effects on T47-D, IC50=13.64±0.26μM.</p>Fórmula:C20H12F3NO5Forma y color:SolidPeso molecular:403.31Gypsetin
CAS:<p>Gypsetin inhibits the activity of acyl-CoA:cholesterol acyltransferase (ACAT), showing inhibitory effects on rat liver microsomal ACAT with an IC50 of 18 μM, and competes with oleoyl-CoA substrate, possessing a Ki value of 5.5 μM. Additionally, Gypsetin prevents the formation of cholesterol esters from oleic acid with an IC50 of 0.65 μM.</p>Fórmula:C32H36N4O4Forma y color:SolidPeso molecular:540.653AVE 0991
CAS:<p>AVE 0991 is a nonpeptide analog of angiotensin-(1-7), a Mas agonist with inhibitory effects on [125I]-Ang-(1-7) and on neuroinflammation in Alzheimer's disease.</p>Fórmula:C29H32N4O5S2Pureza:98.69%Forma y color:SolidPeso molecular:580.72Leucomycin V
CAS:<p>Leucomycin V is a macrolide antibiotic. Leucomycin A9 exhibits strong activity against Gram-positive bacteria and also affects spirochetes, rickettsiae, and chlamydiae.</p>Fórmula:C35H59NO13Forma y color:SolidPeso molecular:701.842MDL-28050
CAS:<p>MDL-28050 is a synthetic analog of hirudin 55-65 C-terminal fragment and a peptide inhibitor.</p>Fórmula:C61H88N10O23Forma y color:SolidPeso molecular:1329.4SORT1-IN-3
CAS:<p>SORT1-IN-3 (compound 5) is a SORT1 inhibitor characterized by its ability to permeate the blood-brain barrier.</p>Fórmula:C16H26ClNO3Forma y color:SolidPeso molecular:315.84Dinalbuphine sebacate
CAS:<p>Dinalbuphine sebacate: long-acting nalbuphine prodrug, μ-opioid partial agonist/antagonist, κ-opioid high-efficacy agonist.</p>Fórmula:C52H68N2O10Forma y color:SolidPeso molecular:881.1Flusoxolol
CAS:<p>Flusoxolol is a beta-adrenoceptor partial agonist.</p>Fórmula:C22H30FNO4Forma y color:SolidPeso molecular:391.48Iroxanadine hydrobromide
CAS:<p>Iroxanadine hydrobromide is a MAPK p38 inhibitor potentially for the treatment of atherosclerosis.</p>Fórmula:C14H21BrN4OForma y color:SolidPeso molecular:341.25CE-2072
CAS:<p>CE-2072 is a synthetic host serine proteases inhibitor.</p>Fórmula:C33H41N5O6Pureza:98%Forma y color:SolidPeso molecular:603.71NRX-2663
CAS:<p>NRX-2663 boosts β-catenin binding to E3 ligase SCFβ-TrCP (Kd: 54.8 nM, EC50: 22.9 nM).</p>Fórmula:C20H13F3N2O5Forma y color:SolidPeso molecular:418.32DS69910557
<p>DS69910557: potent hPTHR1 antagonist, IC50 0.08 μM, oral, for hyperparathyroidism & osteoporosis research.</p>Fórmula:C32H33Cl2FN4O3Forma y color:SolidPeso molecular:611.53P7170
CAS:<p>P7170 is an anti-cancer agent active as an mTORC1/C2 and activin receptor-like kinase 1 (ALK1) inhibitor.</p>Fórmula:C21H16F3N9Forma y color:SolidPeso molecular:451.42LPA5 antagonist 1
<p>LPA5 antagonist 1: selective, potent (IC50=32 nM), high brain permeability, studies inflammatory/neuropathic pain.</p>Fórmula:C28H26N2O4SForma y color:SolidPeso molecular:486.58KCa2 channel modulator 2
Compound 2q is a potent, subtype-selective K/Ca 2 modulator, effective on human K Ca 2.3 and rat K Ca 2.2a with EC50s of 0.60 μM and 0.64 μM.Fórmula:C16H15ClFN5Forma y color:SolidPeso molecular:331.78PCSK9-IN-17
CAS:<p>PCSK9-IN-17 is a PCSK9 inhibitor utilized in the research of cholesterol metabolism.</p>Fórmula:C16H19N5OSForma y color:SolidPeso molecular:329.42Ro 31-8472
CAS:<p>Ro 31-8472 is an angiotensin-converting enzyme (ACE) inhibitor and an analog of cilazaprilat.</p>Fórmula:C20H27N3O6Pureza:98%Forma y color:SolidPeso molecular:405.44BMS-748730
CAS:<p>BMS-748730, also known as 4′-Hydroxy Dasatinib, is a Dasatinib metabolite.</p>Fórmula:C22H26ClN7O3SForma y color:SolidPeso molecular:504.01ChemR23-IN-3
<p>ChemR23-IN-3 is a potent thiazole-based ChemR23 inhibitor with an IC 80 value of 12 nM.</p>Fórmula:C31H33N5O5S2Forma y color:SolidPeso molecular:619.75METTL3-IN-3
CAS:METTL3-IN-3 is a polyheterocyclic compound, acts as METTL3 inhibitor .Fórmula:C26H28BrFN6O2Forma y color:SolidPeso molecular:555.44A 70450
CAS:<p>A 70450, an inhibitor of aspartyl proteinase, can be used as an antifungal agent and may have a role in HIV protease inhibition therapy.</p>Fórmula:C42H71ClN6O5Pureza:98%Forma y color:SolidPeso molecular:775.50Alkannin
CAS:<p>Alkannin: potent, tumor-specific PKM2 inhibitor; non-inhibitory to PKM1/PKL; potential anticancer agent.</p>Fórmula:C16H16O5Forma y color:SolidPeso molecular:288.3Agosterol A
CAS:<p>Agosterol A is isolated from marine sponge Spongia.</p>Fórmula:C33H52O8Forma y color:SolidPeso molecular:576.76mPGES-1-IN-1
<p>MPGES-1, potential anti-inflammatory drug target, has IC50 of 0.03 μM with mPGES-1-IN-1.</p>Fórmula:C21H14N4O2SForma y color:SolidPeso molecular:386.43Pulvomycin
CAS:<p>Pulvomycin is a protein biosynthesis inhibitor preventing ternary complex formation between elongation factor Tu, GTP, and aminoacyl-tRNA.</p>Fórmula:C47H66O13Pureza:98%Forma y color:SolidPeso molecular:839.032Mimocine
CAS:<p>Mimosine, a plant amino acid, is known to act as a normoxic inducer of hypoxia-inducible factor (HIF).</p>Fórmula:C15H14N2O5Forma y color:SolidPeso molecular:302.28LA-810
CAS:<p>LA-810 is a nitrous oxide donor.</p>Fórmula:C15H25N5O7SForma y color:SolidPeso molecular:419.45MSX-3 free acid
CAS:<p>MSX-3 free acid is an A2A adenosine receptor antagonist and a prodrug of MSX-2.</p>Fórmula:C21H23N4O7PForma y color:SolidPeso molecular:474.40ZD6021
CAS:<p>ZD6021 is an antagonist of neurokinin 1 receptor.</p>Fórmula:C35H35Cl2N3O2SPureza:98%Forma y color:SolidPeso molecular:632.64Anticancer agent 80
<p>Anticancer agent 80 (Compound 3c) is an anticancer agent that exhibits a significant dark toxic effect on T47-D (IC50: 10.14 μM).</p>Fórmula:C19H12BrNO5Forma y color:SolidPeso molecular:414.21PAD2-IN-1 hydrochloride
<p>PAD2-IN-1 hydrochloride: potent, selective PAD2 inhibitor; 95x less on PAD4, 79x less on PAD3; benzimidazole derivative.</p>Fórmula:C25H30ClFN6O3Forma y color:SolidPeso molecular:517NB-533
CAS:<p>NB-533 is a macrocyclic peptidic BACE-1 inhibitor.</p>Fórmula:C33H55N3O4Forma y color:SolidPeso molecular:557.81HOE-288
CAS:<p>HOE-288 is a converting enzyme (CE) inhibitor.</p>Fórmula:C27H38N2O5Forma y color:SolidPeso molecular:470.60Org-31710
CAS:<p>Org-31710 is a progesterone receptor antagonist potentially for contraception.</p>Fórmula:C30H39NO2Pureza:98%Forma y color:SolidPeso molecular:445.64SSM3 TFA
CAS:<p>SSM3 TFA is a potent furin inhibitor, blocking furin-dependent cell surface processing of anthrax protective antigen-83 in vitro..</p>Fórmula:C22H32N12O2Forma y color:SolidPeso molecular:496.57EP-7041 HCl
CAS:<p>EP-7041 is a novel, potent, and selective Factor XIa inhibitor.</p>Fórmula:C19H27ClN4O4Forma y color:SolidPeso molecular:410.89Cortistatin A
CAS:<p>Cortistatin A is a potent and selective mediator-associated kinase CDK8 and its paralogue CDK19 inhibitor.</p>Fórmula:C30H36N2O3Pureza:98%Forma y color:SolidPeso molecular:472.62GSK3527497
CAS:<p>GSK3527497 is a novel potent and selective inhibitor of transient receptor potential vanilloid-4 (TRPV4).</p>Fórmula:C17H16ClFN4O4SForma y color:SolidPeso molecular:426.85VU6028418
<p>VU6028418 is a highly selective, potent, orally active M4mAChR antagonist that acts on hM4 (IC50: 4.1 nM).</p>Forma y color:LiquidOlanzapine/Samidorphan
CAS:<p>Olanzapine/Samidorphan, a tablet blending olanzapine and samidorphan, targets schizophrenia and bipolar I, curbing weight gain.</p>Fórmula:C38H46N6O4SForma y color:SolidPeso molecular:682.88Miyakamide A2
CAS:<p>Miyakamide A2 is an antibiotic with insecticidal properties. It inhibits the growth of brine shrimp and exhibits weak activity against Xanthomonas species. The IC50 for inhibiting P388 cells is 12.2 μg/mL.</p>Fórmula:C31H32N4O3Forma y color:SolidPeso molecular:508.611Carazostatin
CAS:<p>Carazostatin is an antioxidant, free radical scavenger, and potent lipid peroxidation inhibitor.</p>Fórmula:C20H25NOPureza:98%Forma y color:Pale Yellow SolidPeso molecular:295.42Antiangiogenic agent 3
<p>Antiangiogenic agent 3 blocks HUVEC cell migration, chemotaxis, and lowers Src, cdc42, MAPK gene expression.</p>Fórmula:C19H20O7Forma y color:SolidPeso molecular:360.36Revamilast sodium
CAS:<p>Revamilast sodium, also known as GRC4039 sodium, is a phosphodiesterase IV inhibitor for potentially treating of asthma and rheumatoid arthritis</p>Fórmula:C18H8Cl2F2N3NaO4Forma y color:SolidPeso molecular:462.17Freselestat
CAS:<p>Freselestat (ONO-6818) inhibits neutrophil elastase, reduces interleukin 8, C5B-9, and inflammation in cardiopulmonary bypass.</p>Fórmula:C23H28N6O4Forma y color:SolidPeso molecular:452.51GDC-6036-NH
CAS:<p>GDC-6036-NH is a precursor of compound 17a /b, which is a RAS inhibitor that can be used in cancer research.</p>Fórmula:C26H30ClF4N7OPureza:99.84%Forma y color:SolidPeso molecular:568.01U 80215
CAS:<p>U 80215 is an enzyme-competitive inhibitor.</p>Fórmula:C42H60N8O6SForma y color:SolidPeso molecular:805.04PKG1α activator 3
<p>PKG1α activator 3 is a PKG1α activator (EC50basal/partial=13/0.52 μM).</p>Fórmula:C27H26Cl2N2O6Forma y color:SolidPeso molecular:545.41GNE-203
CAS:<p>GNE-203 is a Met inhibitor.</p>Fórmula:C30H29Cl2F3N8O3Forma y color:SolidPeso molecular:677.50Fusarochromanone
CAS:<p>Fusarochromanone (FC-101) is a mycotoxin produced by Fusarium oxysporum with potent antiangiogenic, anticancer and antimalarial activities.</p>Fórmula:C15H20N2O4Pureza:95.31% - 96%Forma y color:SolidPeso molecular:292.33DSP-6952
CAS:<p>DSP-6952 is a 5-HT4 receptor partial agonist, inhibiting visceral hypersensitivity and ameliorating gastrointestinal dysfunction.</p>Fórmula:C21H32BrClN4O5Forma y color:SolidPeso molecular:535.86ONO-8809
CAS:<p>ONO-8809: Thromboxane A2 antagonist, reduces airway hyperresponse, macrophage accumulation, and MMP-9 in SHRSP brains.</p>Fórmula:C30H46BrNO4SPureza:98%Forma y color:SolidPeso molecular:596.66Antiallergic agent-1
<p>Antiallergic agent-1, an Src family kinase inhibitor, is a new and valuable lead compound with potential as an anti-allergic agent.</p>Fórmula:C27H19F6N5OForma y color:SolidPeso molecular:543.46Methyl Streptonigrin
CAS:<p>Methyl Streptonigrin is an ABCG2 transporter function inhibitor.</p>Fórmula:C26H24N4O8Pureza:98%Forma y color:SolidPeso molecular:520.49GR-71251
CAS:<p>GR-71251 is a Tachykinin receptor antagonist.</p>Fórmula:C74H105N19O13Forma y color:SolidPeso molecular:1468.74MtDTBS-IN-1
<p>MtDTBS-IN-1 is a notably potent binder (K_D = 57 nM) and inhibitor (K_i = 5 μM) of MtDTBS.</p>Fórmula:C16H16N4O5Forma y color:SolidPeso molecular:344.32SphK2-IN-2
<p>SphK2-IN-2 (21g) is a potent and selective inhibitor of SphK2 (IC50: 0.23 μM).</p>Fórmula:C21H25ClN10OForma y color:SolidPeso molecular:468.94PARP1-IN-5
<p>PARP1-IN-5 is a potent, selective, orally active, low-toxicity PARP-1 inhibitor with an IC50 value of 14.7 nM. PARP1-IN-5 can be used in cancer research.</p>Fórmula:C25H24N2O5SForma y color:SolidPeso molecular:464.53Anti-TSWV agent 1
<p>Anti-TSWV agent 1 is a highly effective inactivator (EC50:144 μg/mL) of tomato spotted wilt virus (TSWV).</p>Fórmula:C22H27ClN4OS3Forma y color:SolidPeso molecular:495.12GSK579289A
CAS:<p>GSK579289A is an inhibitor of benzimidazole thiophene.</p>Fórmula:C26H27ClN4O3SPureza:98%Forma y color:SolidPeso molecular:511.04Ekatetrone
CAS:<p>Ekatetrone displays activity against both Gram-positive and Gram-negative bacteria, with particularly strong inhibitory effects on Mycobacterium tuberculosis.</p>Fórmula:C19H13NO7Forma y color:SolidPeso molecular:367.309Gilvusmycin
CAS:<p>Gilvusmycin is an antibiotic with potent antitumor properties. It effectively inhibits the proliferation of P388, K562, A431, and MKN28 cells, with IC50 values (ng/mL) of 0.08, 0.86, 0.72, and 0.75, respectively.</p>Fórmula:C38H34N6O8Forma y color:SolidPeso molecular:702.712Anti-inflammatory agent 16
<p>Compound 14 is a peptidomimetic that significantly lowers TNFα, NO, CD40, and CD86, showcasing strong anti-inflammatory effects.</p>Fórmula:C21H23N5O3Forma y color:SolidPeso molecular:393.44Retelliptine
CAS:Retelliptine, a DNA topoisomerase II inhibitor, is used potentially for the treatment of cancer.Fórmula:C25H32N4OPureza:98%Forma y color:SolidPeso molecular:404.55LASSBio-1632
<p>LASSBio-1632: Novel anti-asthmatic, blocks PDE4A/D, reduces AHR & lung TNF-α, crosses BBB.</p>Fórmula:C18H20N2O6SForma y color:SolidPeso molecular:392.43L 739749
CAS:<p>L 739749 is a CAAX peptidomimetic. It is also an inhibitor of farnesyl-protein transferase.</p>Fórmula:C24H41N3O6S2Pureza:98%Forma y color:SolidPeso molecular:531.73Naltalimide
CAS:<p>Naltalimide: µ-opioid receptor partial agonist, improves bladder storage by affecting spinal cord reflex.</p>Fórmula:C28H28N2O5Pureza:98%Forma y color:SolidPeso molecular:472.53Pamiparib maleate
CAS:<p>Pamiparib (BGB-290) is a selective PARP inhibitor that blocks DNA repair and promotes apoptosis.</p>Fórmula:C44H42F2N8O14Pureza:98%Forma y color:SolidPeso molecular:944.859Piperazinomycin
CAS:<p>Piperazinomycin is an antifungal antibiotic, showing inhibitory activity against fungi and yeasts, especially against Trichophyton.</p>Fórmula:C18H20N2O2Forma y color:SolidPeso molecular:296.36Basroparib
CAS:<p>Basroparib is an inhibitor of ribose polymerase (PARP) and has shown antitumour effects.</p>Fórmula:C18H21F2N7O3Forma y color:SolidPeso molecular:421.4KF 20274
CAS:<p>KF 20274 is an adenosine A1 antagonist; purinergic receptor antagonist.</p>Fórmula:C21H29N5OForma y color:SolidPeso molecular:367.49PARP10/15-IN-1
<p>PARP10/15-IN-1 (compound 8l) is a dual PARP10 and PARP15 inhibitor with IC50s of 160 nM and 370 nM, respectively. It can be used in cancer research[1].</p>Fórmula:C13H10N2O3SForma y color:SolidPeso molecular:274.3Ambelline
CAS:<p>Ambelline has antitumor activity.</p>Fórmula:C18H21NO5Pureza:98%Forma y color:SolidPeso molecular:331.36PKCiota-IN-1
CAS:<p>PKCiota-IN-1: Strong PKC-ι inhibitor (IC50=2.7 nM); also blocks PKC-α/ε (IC50s=45/450 nM).</p>Fórmula:C25H22FN5OForma y color:SolidPeso molecular:427.47CYP2C1/CYP2C19-IN-2
<p>CYP2C1/CYP2C19-IN-2 is a potent inhibitor of CYP2C9/CYP2C19 without liver toxicity or genotoxicity and can be used to study Zika virus (ZIKV) infection.</p>Fórmula:C27H28N2O6SForma y color:SolidPeso molecular:508.59GSK945237
CAS:<p>GSK945237 is a type IIA topoisomerase inhibitor, effective on Gram-positive and negative bacteria, with favorable pharmacokinetics and in vivo efficacy.</p>Fórmula:C24H26FN5O3Forma y color:SolidPeso molecular:451.49Tuvatidine
CAS:<p>Tuvatidine is a histamine 2 receptor antagonist.</p>Fórmula:C10H17N9O2S3Forma y color:SolidPeso molecular:391.5Keap1-Nrf2-IN-1 TFA
<p>Keap1-Nrf2-IN-1 TFA (compound35) is a potent inhibitor (IC50: 43 nM) protecting against acetaminophen liver damage.</p>Fórmula:C26H25F3N2O9SForma y color:SolidPeso molecular:598.54(±)-ANAP hydrochloride (1185251-08-4 free base)
<p>(±)-ANAP hydrochloride is the amino acid analog of prodan. It can be used as a fluorescent probes and enhance environmental sensitivity.</p>Fórmula:C15H17ClN2O3Pureza:98%Forma y color:SolidPeso molecular:308.767-Hydroxyguanine
CAS:<p>7-Hydroxyguanine is an antibiotic that inhibits the growth of L1210 leukemia cells.</p>Fórmula:C5H5N5O2Forma y color:SolidPeso molecular:167.126Leustroducsin B
CAS:<p>Leustroducsin B is a novel colony-stimulating factor (CSF) inducer extracted from Streptomyces platensis SANK 60191.</p>Fórmula:C34H56NO10PForma y color:SolidPeso molecular:669.78
