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ZINC09410451
CAS :ZINC09410451 is a potent ebolavirus (EBOV) inhibitor.Formule :C24H27ClN4O3Couleur et forme :SolidMasse moléculaire :454.95TAK-960
CAS :<p>TAK-960 is an orally bioavailable, selective inhibitor of Plks with IC50 values of 0.8, 16.9, and 50.2 nM for Plk1, Plk2, and Plk3, respectively.</p>Formule :C27H34F3N7O3Degré de pureté :97.06%Couleur et forme :SolidMasse moléculaire :561.6N 0840
CAS :N 0840 is a selective, orally active A(1) adenosine receptor antagonist.Formule :C11H15N5Couleur et forme :SolidMasse moléculaire :217.27Carbazomycin C
CAS :Carbazomycin C, from Streptomyces, targets S. aureus, B. anthracis, fungi, P. falciparum, and is cytotoxic to several cancer cells, inhibiting 5-LO.Formule :C16H17NO3Couleur et forme :SolidMasse moléculaire :271.31SKF-104557
CAS :<p>N-Despropyl ropinirole, a ropinirole metabolite, enhances CHO cell acidification via D2/D3/D4 receptors; also a ropinirole impurity. EC50: 0.63-1.23 µM.</p>Formule :C13H18N2OCouleur et forme :SolidMasse moléculaire :218.29Azumolene sodium anhydrous
CAS :Azumolene sodium, a muscle relaxant, blocks calcium release from muscles and halts SOCE linked to RyR1 except when induced by thapsigargin.Formule :C13H8BrN4NaO3Couleur et forme :SolidMasse moléculaire :371.13Betazole
CAS :Betazole, an oral H2 receptor agonist, stimulates gastric acid and raises bile duct pressure, used for gastric secretory testing.Formule :C5H9N3Couleur et forme :SolidMasse moléculaire :111.15DCAI Hydrochloride
CAS :DCAI hydrochloride is an inhibitor of nucleotide exchange and nucleotide release, by binding to the pocket adjacent to the Ras-SOS interface.Formule :C11H13Cl3N2Couleur et forme :SolidMasse moléculaire :279.59COR167
CAS :<p>COR167 is a CB2 agonist with immunomodulatory effects, protective brain properties, and antinociception.</p>Formule :C28H38N2O2Couleur et forme :SolidMasse moléculaire :434.61E09241
CAS :E09241 boosts OPG, doesn't change RANKL, aids osteoblasts, hinders osteoclasts via Wnt/β-catenin pathway.Formule :C11H9ClN2O2Couleur et forme :SolidMasse moléculaire :236.65N-Phenylthiourea
CAS :N-Phenylthiourea (Phenylthiocarbamide) is EC 1.14.18.1 (tyrosinase) inhibitor, a diphenolase inhibitor, and a non-competitive inhibitor of the PvdP tyrosinase.Formule :C7H8N2SDegré de pureté :99.71%Couleur et forme :SolidMasse moléculaire :152.22Nelociguat
CAS :<p>Nelociguat (BAY60-4552) is an sGC stimulator, crucial in NO signal pathways.</p>Formule :C19H17FN8O2Degré de pureté :99.19%Couleur et forme :SolidMasse moléculaire :408.39Dibenzosuberenol
CAS :Dibenzosuberenol is used in oxidations, carboxylic acid/ketone synthesis, NK1 receptor antagonists creation, and catalysis studies.Formule :C15H12OCouleur et forme :SolidMasse moléculaire :208.26CB-892
CAS :<p>CB-892 is a novel inhibitor of hiv-1 gene expression</p>Formule :C15H14N2O4Couleur et forme :SolidMasse moléculaire :286.28HDAC-IN-6
CAS :HDAC-IN-6 is an HDAC inhibitor, targeting HDAC2, HDAC3, HDAC4, HDAC5, HDAC7, HDAC8, and HDAC9.Formule :C28H36F3N5O7Couleur et forme :SolidMasse moléculaire :611.61Epigenetic Multiple Ligand
CAS :Epigenetic Multiple Ligand inhibits many chromatin enzymes like SIRT1/2 and induces apoptosis or differentiation.Formule :C19H12Br4O4Couleur et forme :SolidMasse moléculaire :623.91BZL-HIS-OME 2HCL
CAS :<p>BZL-HIS-OME 2HCL is the dihydrochloride salt of BZL-HIS-OME, a sweet almond and yeast β-glucosidase inhibitor.</p>Formule :C14H19Cl2N3O2Couleur et forme :SolidMasse moléculaire :332.22iST2-1
CAS :<p>iST2-1 is a first-in-class ST2 inhibitor active in vivo.</p>Formule :C22H22N2O4Couleur et forme :SolidMasse moléculaire :378.42ST101036
CAS :MC activators have recently been described as safe and effective vaccine adjuvants. ST101036 exhibited high degranulation potency in both human and mouse MCs.Formule :C18H21F3N4Couleur et forme :SolidMasse moléculaire :350.386(5H)-Phenanthridinone
CAS :<p>6(5H)-Phenanthridinone suppresses PARP1/2, reduces RDM4 cell growth, downregulates pro-inflammatory genes, and alleviates EAE symptoms in rats.</p>Formule :C13H9NOCouleur et forme :SolidMasse moléculaire :195.22MAO-B ligand-1
CAS :MAO-B ligand-1 is a selective MAO-B inhibitor.Formule :C19H19N5O4SCouleur et forme :SolidMasse moléculaire :413.45ZINC32540717
CAS :<p>ZINC32540717 is a potent ebolavirus (EBOV) inhibitor.</p>Formule :C23H26N4O3Couleur et forme :SolidMasse moléculaire :406.48ITE
CAS :ITE is a potent endogenous agonist of aryl hydrocarbon receptor (AhR) (Ki : 3 nM), has immunosuppressive activity.Formule :C14H10N2O3SDegré de pureté :97.91% - 99.14%Couleur et forme :SolidMasse moléculaire :286.31AM6701
CAS :<p>AM6701 is a novel highly potent inhibitor of human alpha/beta hydrolase domain 6 (habhd6)</p>Formule :C17H17N5ODegré de pureté :99.25%Couleur et forme :SolidMasse moléculaire :307.357SU 5616
CAS :<p>SU 5616 (WAY-608241) regulates abnormal cell proliferation and modulates tyrosine kinase signaling.</p>Formule :C13H8ClNOSDegré de pureté :98.84%Couleur et forme :SoildMasse moléculaire :261.7311β-HSD1 inibitor 19
CAS :3-chloro-4-sulfonyl-Benzonitrile inhibits hHSD1/mHSD1, IC50: 16nM/10nM.Formule :C19H16ClF4N3O2SDegré de pureté :99.58%Couleur et forme :SoildMasse moléculaire :461.86JB002
CAS :<p>JB002, a myosin II inhibitor, exhibits potent activity with an IC50 of ≤10 μM.</p>Formule :C18H15NO3Degré de pureté :99.74%Couleur et forme :SoildMasse moléculaire :293.32ZIM
CAS :ZIM, from 4-Aminoantipyrine, induces DNA and chromosomal damage, cell death, and phagocytosis, with potential in cancer therapy.Formule :C20H19N3O3Degré de pureté :99.85%Couleur et forme :SolidMasse moléculaire :349.38PCSK9-IN-10
CAS :<p>PCSK9-IN-10: potent oral PCSK9 inhibitor (IC50 = 6.4 µM), upregulates LDLR, curbs atherosclerosis, for hyperlipidemia research.</p>Formule :C18H23N5O4Degré de pureté :99.06%Couleur et forme :SoildMasse moléculaire :373.41p53-MDM2-IN-1
CAS :<p>p53-MDM2-IN-1 (Example 30), an inhibitor targeting the p53-MDM2/X protein interaction, exhibits a K i value of 23.35 µM.</p>Formule :C23H20ClN3O3Degré de pureté :99.98%Couleur et forme :SoildMasse moléculaire :421.886-Methyl-3-pyridinecarboxaldehyde
CAS :<p>6-Methyl-3-pyridinecarboxaldehyde (6-Methoxynicotinaldehyde) has partial antitumor activity.</p>Formule :C7H7NO2Degré de pureté :99.9%Couleur et forme :SolidMasse moléculaire :137.142-Quinolinecarboxaldehyde
CAS :<p>2-Quinolinecarboxaldehyde, a small rigid molecule, used in Henry reaction, inhibits AChE (IC50: 13.48 μM).</p>Formule :C10H7NODegré de pureté :99.5%Couleur et forme :Off-White CrystallineMasse moléculaire :157.17CDK8-IN-13
CAS :<p>CDK8-IN-13 is a CDK8 inhibitor (IC50: 51.9 nM) with potent, selective and oral activity.</p>Formule :C14H11N3ODegré de pureté :99.28%Couleur et forme :SoildMasse moléculaire :237.26Oglufanide
CAS :<p>Oglufanide (H-Glu-Trp-OH) is a naturally occurring thymic immunomodulator,and inhibits vascular endothelial growth factor (VEGF).</p>Formule :C16H19N3O5Degré de pureté :99.80%Couleur et forme :SolidMasse moléculaire :333.346,6'-Dimethyl-2,2'-dipyridyl
CAS :<p>6,6'-Dimethyl-2,2'-dipyridyl (6,6'-Bi-2-picoline) is a novel time-resolved fluorescent immunoassay (TRFIA) chelate with a good bactericidal effect for the study</p>Formule :C12H12N2Degré de pureté :99.96%Couleur et forme :SolidMasse moléculaire :184.24BI 1015550
CAS :<p>Nerandomilast (BI 1015550) is an orally active PDE4B inhibitor with IC50 of 7.2 nM.Cost-effective and quality-assured.</p>Formule :C20H25ClN6O2SDegré de pureté :98.06% - 99.71%Couleur et forme :SoildMasse moléculaire :448.97PI5P4Ks-IN-2
CAS :<p>PI5P4Ks-IN-2 inhibits PI5P4K isoforms α, β, γ, γ+ with IC50 <4.3, <4.6, 6.2, 0.32 µM, respectively.</p>Formule :C22H23N5Degré de pureté :98.36% - 99.02%Couleur et forme :SoildMasse moléculaire :357.45pCDPK1/TgCDPK1-IN-3
CAS :<p>CpCDPK1/TgCDPK1-IN-3 inhibits Cp/TgCDPK1; IC50: 0.003/0.0036 µM. It's used to research Toxoplasma, Cryptosporidium diseases.</p>Formule :C17H18N6Degré de pureté :99.63%Couleur et forme :SoildMasse moléculaire :306.36LI-2242
CAS :<p>LI-2242: Potent IP6K inhibitor, IC50s - IP6K1: 31nM, IP6K2: 42nM, IP6K3: 8.7nM, IPMK: 1944nM; improves hepatic steatosis and diabetes.</p>Formule :C20H18Cl2N2O3Degré de pureté :98%Couleur et forme :SoildMasse moléculaire :405.27HPK1-IN-36
CAS :<p>HPK1-IN-36 (compound 2) is a potent inhibitor of hematopoietic progenitor kinase 1 (HPK1), demonstrating an inhibitory concentration 50 (IC50) of 0.5 nM [1].</p>Formule :C22H24ClF3N6O2Degré de pureté :98%Couleur et forme :SoildMasse moléculaire :496.91Anti-Influenza agent 4
CAS :<p>Anti-Influenza agent 4 selectively inhibits A/Parma (EC50: 62 nM) and A/Roma (EC50: 150 nM) influenza strains.</p>Formule :C19H18N2O5SDegré de pureté :98.94% - 98.95%Couleur et forme :SolidMasse moléculaire :386.42YM-58790
CAS :YM-58790 is a potent mAChR blocker with Ki values of 28 nM (M1), 260 nM (M2), 15 nM (M3), and reduces bladder contractions in rats.Formule :C27H31N3O2Degré de pureté :99.87%Couleur et forme :SoildMasse moléculaire :429.55CLK1-IN-3
CAS :Clk1-in-3 is a + selective and highly potent sexual Clk1 inhibitor with an IC50 of 5 nM and 300 pairs higher affinity than Dyrk1A.Formule :C24H23FN6ODegré de pureté :98.46% - 99.76%Couleur et forme :SoildMasse moléculaire :430.48PNU-74654
CAS :<p>PNU 74654 blocks β-catenin/Tcf4, disrupting Wnt signaling (Kd = 450 nM).</p>Formule :C19H16N2O3Degré de pureté :97.27%Couleur et forme :SolidMasse moléculaire :320.34c-Myc inhibitor 7
CAS :<p>c-Myc inhibitor 7 degrades c-MYC, CK1α, GSPT1, IKZF1/2/3 proteins in tumors, for research on related diseases.</p>Formule :C35H30N6O5Couleur et forme :SoildMasse moléculaire :614.65Flaviviruses-IN-2
CAS :<p>Flaviviruses-IN-2 is a potent flaviviruses inhibitor. Flaviviruses-IN-2 reduces West Nile virus (WNV) protease activity and inhibits WNV by 56%.</p>Formule :C21H20N2O3SDegré de pureté :99.68%Couleur et forme :SoildMasse moléculaire :380.46Acetylsulfamerazine
CAS :<p>Acetylsulfamerazine, a metabolite of sulphamethazine, slightly inhibits cellulose digestion and rumen endocrine, with anti-microbial properties.</p>Formule :C13H14N4O3SDegré de pureté :99.88%Couleur et forme :SolidMasse moléculaire :306.34SCFSkp2-IN-2
CAS :<p>SCFSkp2-IN-2, a Skp2 inhibitor, exhibits a dissociation constant (K_D) of 28.77 μM.</p>Formule :C17H20N4O2Degré de pureté :99.86%Couleur et forme :SolidMasse moléculaire :312.37Fmoc-N-methyl-L-alloisoleucine
CAS :<p>Fmoc-N-methyl-L-alloisoleucine is a biochemical reagent for biosynthesis.</p>Formule :C22H25NO4Degré de pureté :99.41%Couleur et forme :SoildMasse moléculaire :367.44PF-17
CAS :1-[6-(4-methoxysulfonylphenoxy)-4-pyrimidinyl]piperidine-4-carbamic acid tert-butyl ester is a PUF60 inhibitor potentially for ovarian cancer treatment.Formule :C21H28N4O5SDegré de pureté :99.96%Couleur et forme :SoildMasse moléculaire :448.54Antibacterial agent 125
CAS :<p>Antibacterial agent 125 shows strong activity against Gram-positive pathogens; MICs: 0.25-8 μM; used in antimicrobial resistance research.</p>Formule :C15H11ClN2ODegré de pureté :98.45%Couleur et forme :SoildMasse moléculaire :270.71CDK8-IN-12
CAS :<p>CDK8-IN-12: selective CDK8 inhibitor (Ki 14 nM), oral anticancer, blocks GSK-3α/β, PCK-θ, halts MV4-11 cell growth.</p>Formule :C21H20ClN3O2Degré de pureté :99.46% - 99.83%Couleur et forme :SoildMasse moléculaire :381.864-N-Nonyloxyphenol
CAS :<p>4-N-Nonyloxyphenol, kaolinite nanotube photosensitizer, degrades phenolic pesticides, and disrupts endocrine.</p>Formule :C15H24O2Degré de pureté :99.94%Couleur et forme :SoildMasse moléculaire :236.35A-967079
CAS :<p>A 967079 is a potent, selective, and bioavailable inhibitor of the TRPA1 channel, with IC50 values of 67 and 289 nM for the human and rat isoforms, respectively</p>Formule :C12H14FNODegré de pureté :98.34% - 99.75%Couleur et forme :SolidMasse moléculaire :207.244-N-Dodecyloxyphenol
CAS :<p>4-N-Dodecyloxyphenol is an additive for ferroelectric crystals without chiral groups, aiding in the SmC phase display.</p>Formule :C18H30O2Degré de pureté :99.88%Couleur et forme :SolidMasse moléculaire :278.43LabMol-319
CAS :LabMol-319 is a potent Zika virus (ZIKV) NS5 RdRp inhibitor with antiviral activity for the study of ZIKV virus.Formule :C22H16N2O5Degré de pureté :99.92%Couleur et forme :SolidMasse moléculaire :388.37HPK1-IN-34
CAS :HPK1-IN-34 (Compound 143) is an inhibitor of HPK1 (Haematopoietic progenitor kinase 1) with an IC₅₀ < 0.1 μM, suitable for cancer and immunology research.Formule :C25H28N4O2SDegré de pureté :99.39%Couleur et forme :SolidMasse moléculaire :448.58PERK-IN-6
CAS :<p>PERK-IN-6 is a novel and highly potent PERK inhibitor (IC50:2.5 nM).</p>Formule :C23H22N6ODegré de pureté :99.62% - 99.92%Couleur et forme :SolidMasse moléculaire :398.46SLC26A3-IN-1
CAS :<p>"SLC26A3-IN-1 inhibits SLC26A3, an anion transporter linked to diarrhea, with 340 nM IC50."</p>Formule :C23H18O4Degré de pureté :98.96%Couleur et forme :SolidMasse moléculaire :358.39FM04
CAS :FM04 is a potent oral P-gp inhibitor (EC50: 83 nM), disrupting human P-gp NBD2 to enhance cancer treatment.Formule :C26H25NO4Degré de pureté :99.87%Couleur et forme :SolidMasse moléculaire :415.48KYN-101
CAS :<p>KYN-101 is an and aryl hydrocarbon receptor (AHR) inhibitor with anticancer activity. KYN-101 is used for the study of breast cancer and acute myeloid leukemia.</p>Formule :C22H19FN6Degré de pureté :98.35%Couleur et forme :SolidMasse moléculaire :386.43H1k
<p>H1k is an eudistomin Y fluorescent derivative and lysosome-targeted antiproliferative agent that downregulates the expression of cell cycle protein B1.</p>Formule :C27H22N2ODegré de pureté :98.13%Couleur et forme :SoildMasse moléculaire :390.48CDD-1102 HCl
CDD-1102 HCl is a novel BRDT-BD4 / BRD2-BD1302 selective inhibitor that shows non-hormonal contraceptive potential in ex vivo experiments.Formule :C32H31ClN6O3Degré de pureté :98.30%Couleur et forme :SoildMasse moléculaire :583.08S1R agonist 2
CAS :<p>S1R agonist 2 is a selective S1R agonist with a Ki of 88 nM for S2R and 1.1 nM for S1R and is protective against ROS and NMDA-induced neurotoxicity.</p>Formule :C21H27NODegré de pureté :98.85%Couleur et forme :SolidMasse moléculaire :309.452-Iminobiotin
CAS :2-Iminobiotin inhibits iNOS/nNOS; Ki: 21.8 μM (mouse iNOS), 37.5 μM (rat nNOS).Formule :C10H17N3O2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :243.33Myosin V-IN-1
CAS :<p>Myosin V-IN-1: potent, selective Myosin V inhibitor, Ki of 6 μM; hinders actin-activated ATPase by blocking ADP release.</p>Formule :C29H26N6O3SDegré de pureté :98.64% - 98.64%Couleur et forme :SolidMasse moléculaire :538.62BI-2493
CAS :BI-2493 is a highly selective pan-KRAS inhibitor and structural analog of BI-2865.BI-2493 exhibits antitumor activity and inhibits tumor cell growth.Cost-effective and quality-assured.Formule :C24H27N7OSDegré de pureté :97.74% - 99.88%Couleur et forme :SoildMasse moléculaire :461.58BI-2865
CAS :BI-2865 is a non-covalent pan-KRAS inhibitor.Cost-effective and quality-assured.Formule :C23H27N7O2SDegré de pureté :99.29% - 99.39%Couleur et forme :SoildMasse moléculaire :465.57PDCD4-IN-1
CAS :<p>PDCD4-IN-1, a PDCD4 inhibitor (Kd : 350 nM), promotes BDNF expression in hippocampal neuronal cells HT-22.</p>Formule :C12H9BrClN3ODegré de pureté :99.21%Couleur et forme :SoildMasse moléculaire :326.58TASK-1-IN-1
CAS :<p>TASK-1-IN-1: Potent, selective TASK-1 blocker (IC50: 148 nM), weaker on TASK-3 (IC50: 1750 nM), anticancer properties.</p>Formule :C22H20N2O2Degré de pureté :99.57%Couleur et forme :SoildMasse moléculaire :344.41CHET3
CAS :CHET3 is a highly selective allosteric activator for TASK-3-containing K2P channels. CHET3 has shown potent in vivo analgesic effects. Cost-effective and quality-assured.Formule :C21H21N5O3SDegré de pureté :98.28% - 99.92%Couleur et forme :SoildMasse moléculaire :423.49DPTN dihydrochloride
CAS :DPTN dihydrochloride is a potent and selective A3AR antagonist with Ki values of 1.65, 9.61 and 8.53 nM in human, mouse and rat, respectively.Formule :C22H20Cl2N4OSDegré de pureté :99.95%Couleur et forme :SoildMasse moléculaire :459.39SFI003
CAS :SFI003 is a novel SRSF3 inhibitor that exerts anticancer activity against colorectal cancer by modulating the SRSF3 / DHCR24 / ROS axis and driving apoptosis inFormule :C19H17N5OSDegré de pureté :99.44%Couleur et forme :SoildMasse moléculaire :363.44MMP-9-IN-7
CAS :N-[2-[(5-Cl-2-methoxyphenyl)amino]-4'-methyl[4,5'-bithiazol]-2'-yl]acetamide inhibits pro-MMP activation, treats MMP9/MMP13 syndromes.Formule :C16H15ClN4O2S2Degré de pureté :97.65%Couleur et forme :SolidMasse moléculaire :394.92-Iminobiotin hydrobromide
CAS :<p>2-Iminobiotin hydrobromide (Guanidinobiotin) is a cyclic guanidino analog of biotin that acts as a reversible inhibitor of inducible nitric oxide synthase (iNOS</p>Formule :C10H18BrN3O2SDegré de pureté :98.13%Couleur et forme :SolidMasse moléculaire :324.24FK 3311
CAS :<p>FK 3311 (COX-2 Inhibitor V) is a cell permeable and orally available sulfonanilide that acts as a COX-2 inhibitor and non-steroidal anti-inflammatory drug (</p>Formule :C15H13F2NO4SDegré de pureté :97.98%Couleur et forme :SolidMasse moléculaire :341.33B-Raf IN 14
CAS :B-Raf IN 14 is a BRAF inhibitor.Formule :C15H14BrN5O3SDegré de pureté :98.38%Couleur et forme :SolidMasse moléculaire :424.27WAY-299017
CAS :WAY-299017 is a potent and selective UPPS inhibitor for the treatment of bacterial infections.Formule :C17H14N2O3Degré de pureté :97.01%Couleur et forme :SolidMasse moléculaire :294.32-benzylsulfanyl-6-methoxy-4-methylquinazoline
CAS :<p>2-benzylsulfanyl-6-methoxy-4-methylquinazoline: a TRPML modulator for lysosomal and ROS-related ailments.</p>Formule :C17H16N2OSDegré de pureté :99.49%Couleur et forme :SolidMasse moléculaire :296.39AKOS037652256
CAS :<p>AKOS037652256 modulates TRPML, treating TRPML-linked diseases like lysosomal disorders, muscular dystrophy, neurodegeneration, and oxidative stress.</p>Formule :C24H26ClFN4O4S2Degré de pureté :98.81%Couleur et forme :SolidMasse moléculaire :553.07BTA-EG4 hydrate
CAS :<p>BTA-EG4 hydrate aids in diagnosing and mitigating Alzheimer's, enhancing cognitive abilities.</p>Formule :C22H28N2O4SCouleur et forme :SolidMasse moléculaire :416.53HyT36
CAS :<p>HyT36: hydrophobic tag that destabilizes fusion proteins & Her3 pseudokinase; treats cells with acute erht.</p>Formule :C25H44ClNO3Degré de pureté :99.86%Couleur et forme :SolidMasse moléculaire :442.07H2-Gamendazole
CAS :<p>H2-Gamendazole: inhibits spermatogenesis, cancer therapy, targets heat shock proteins & EF1α, regulates Hsp90.</p>Formule :C18H13Cl2F3N2O2Degré de pureté :97.36%Couleur et forme :SolidMasse moléculaire :417.21Imidacloprid-urea
CAS :<p>Imidacloprid-urea, a byproduct of imidacloprid, may alter its environmental behavior by competing for soil binding sites.</p>Formule :C9H10ClN3ODegré de pureté :99.89%Couleur et forme :SolidMasse moléculaire :211.65Xanthine oxidoreductase-IN-4
CAS :<p>Xanthine oxidoreductase-IN-4: oral XOR inhibitor, IC50 of 29.3 nM, potential for hyperuricemia research.</p>Formule :C16H15N5O2Degré de pureté :98.25%Couleur et forme :SoildMasse moléculaire :309.32Biotin-aniline
CAS :<p>Biotin-aniline is a probe that reacts strongly to RNA and DNA.</p>Formule :C18H26N4O2SDegré de pureté :99.23%Couleur et forme :SolidMasse moléculaire :362.49AMD 3465 hexahydrobromide
CAS :AMD 3465 hexahydrobromide (GENZ-644494 (hexahydrobromide)) is a CXCR4 receptor antagonist with potential anticancer and anti-HIV activity.Formule :C24H44Br6N6Degré de pureté :99.39%Couleur et forme :SolidMasse moléculaire :896.07CpCDPK1/TgCDPK1-IN-2
CAS :<p>CpCDPK1/TgCDPK1-IN-2 is a dual inhibitor of CpCDPK1 and TgCDPK1 with IC50 values of 12 and 5 nM for CpCDPK1 and TgCDPK1, respectively.CpCDPK1/TgCDPK1-IN-2 can</p>Formule :C20H21N5ODegré de pureté :99.12%Couleur et forme :SoildMasse moléculaire :347.41ROS-IN-1
CAS :<p>ROS-IN-1 is a mitochondrial ROS inhibitor that can be used to reduce oxidative stress or inhibit reactive oxygen species (ROS) production.</p>Formule :C13H17NO3SDegré de pureté :97.53%Couleur et forme :SolidMasse moléculaire :267.34Octadecyl Rhodamine B chloride
CAS :<p>Octadecyl Rhodamine B chloride, also known as RBOE, is a polarity-sensitive dye that is often used as a chromophore with other compounds to stain cell membranes</p>Formule :C46H67ClN2O3Degré de pureté :95%Couleur et forme :SoildMasse moléculaire :731.49(R)-BI-2852
CAS :(R)-5-hydroxy isoindolin-1-one is an RAS protein inhibitor with antiproliferative and antitumor properties.Formule :C31H28N6O2Degré de pureté :97.78%Couleur et forme :SoildMasse moléculaire :516.59Maropitant
CAS :<p>Maropitant is a selective neurokinin (NK1) receptor antagonist.</p>Formule :C32H40N2ODegré de pureté :97.35% - 99.75%Couleur et forme :SolidMasse moléculaire :468.67ADRA1D receptor antagonist 1 free base
CAS :ADRA1D antagonist blocks bladder contractions; Ki=1.6 nM, IC30=15 nM, useful in overactive bladder research.Formule :C15H13ClN4OCouleur et forme :SolidMasse moléculaire :300.742-Deoxy-D-glucose 6-phosphate disodium
CAS :2-Deoxy-D-glucose 6-phosphate disodium is a glucose analog that inhibits glycolysis and inhibits the function of hexokinase and glucose-6-phosphate isomerase.Formule :C6H11Na2O8PDegré de pureté :99.88%Couleur et forme :SolidMasse moléculaire :288.1Thiamphenicol glycinate hydrochloride
CAS :Thiamphenicol glycinate hydrochloride is a broad-spectrum antibacterial agent utilized in research on respiratory tract infections.Formule :C14H19Cl3N2O6SCouleur et forme :SolidMasse moléculaire :449.73Eleven-Nineteen-Leukemia Protein IN-1
CAS :<p>ENL-IN-1: Potent ENL YEATS domain inhibitor with 14.5 nM IC50, enhances thermal stability in vitro.</p>Formule :C27H33N7O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :487.6Eleven-Nineteen-Leukemia Protein IN-2
CAS :Eleven-Nineteen-Leukemia Protein IN-2 (compound 23), an ENL inhibitor, exhibits an IC50 of 10.7 nM and is utilized for leukemia research [1].Formule :C22H23N5O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :389.45Eleven-Nineteen-Leukemia Protein IN-3
CAS :<p>ENL YEATS inhibitor Eleven-Nineteen-Leukemia Protein IN-3, IC50 15.4 nM, orally active, suppresses MYC, stabilizes ENL in vitro.</p>Formule :C28H27N5O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :465.55Guanosine 5'-diphosphate
CAS :<p>Guanosine 5'-diphosphate (GDP) as Potential Iron Mobilizer, Preventing the Hepcidin-Ferroportin Interaction and Modulating the Interleukin-6/Stat-3 Pathway.</p>Formule :C10H15N5O11P2Degré de pureté :98.46% - 99.52%Couleur et forme :SolidMasse moléculaire :443.2D-erythro-Sphingosine hydrochloride
CAS :D-erythro-Sphingosine HCl activates TRPM3 and dephosphorylates retinoblastoma protein.Formule :C18H38ClNO2Couleur et forme :SolidMasse moléculaire :335.95
