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PROTAC STING degrader-4
PROTACSTING degrader-4 is a covalent STINGPROTAC degrader free of nitro groups, exhibiting a DC50 of 3.23 μM. It effectively inhibits STING and its downstream signaling pathways, including p-TBK1 and p-NF-κB (p-P65), as well as immune-inflammatory cytokines. Additionally, PROTACSTING degrader-4 mitigates renal and blood inflammation in mouse models of Cisplatin-induced acute kidney injury (AKI).Fórmula:C39H42Cl2N8O9Cor e Forma:SolidPeso molecular:836.24518RU 59063
CAS:RU 59063 is a prototype of a new class of high-affinity nonsteroidal androgen receptor (AR) ligands.Fórmula:C17H18F3N3O2SPureza:99.09%Cor e Forma:SolidPeso molecular:385.4PPA-037
CAS:<p>PPA-037 is an orally active and highly selective inhibitor of cyclin-dependent kinase 12 (CDK12). It induces the degradation of Cyclin K, thereby enhancing antiproliferative effects on tumor cells. PPA-037 holds potential for use in cancer research.</p>Fórmula:C25H27N7Cor e Forma:SolidPeso molecular:425.53GGACK hydrochloride
<p>GGACK (H-Glu-Gly-Arg-CMK) hydrochloride is an irreversible substrate-like inhibitor of the serine protease urokinase-type plasminogen activator (uPA).</p>Fórmula:C14H26Cl2N6O5Cor e Forma:SolidPeso molecular:428.13417E3 ligase Ligand 66
CAS:<p>E3ligaseLigand 66 is an E3 ligase ligand that facilitates the recruitment of IAP proteins. It can be linked with SARS-CoV-2 Mpro ligand 1 via a linker to form PROTACBP-198.</p>Fórmula:C26H34N4O4SCor e Forma:SolidPeso molecular:498.64Apoptosis inducer 37
Apoptosis inducer37 (Derivative 10) is an agent that induces apoptosis and exhibits anticancer properties by causing cell cycle arrest at the S-G2/M phase and promoting cell apoptosis. It significantly inhibits HCT116, SKOV3, and HepG2 cancer cells with IC50 values of 24.98 μM, 26.15 μM, and 23.09 μM, respectively. Apoptosis inducer37 demonstrates antitumor activity and can be utilized in ovarian cancer research.Fórmula:C27H37BrN2O4SCor e Forma:SolidPeso molecular:564.16574(1S,2R,7S)-Sitafloxacin
CAS:<p>(1S,2R,7S)-Sitafloxacin (DU-6856) is an enantiomer of Sitafloxacin and functions as a topoisomerase inhibitor. As an antibiotic, it demonstrates inhibitory activity against Escherichia coli DNA gyrase (IC50 0.18 μg/mL) and Staphylococcus aureus topoisomerase IV. (1S,2R,7S)-Sitafloxacin exhibits antibacterial properties and is utilized in the study of various bacterial infections.</p>Fórmula:C19H18ClF2N3O3Cor e Forma:SolidPeso molecular:409.81Antibacterial agent 275
<p>Antibacterialagent 275 (Ⅲ1) is an antibacterial compound with a λmax value of 730 nm. It is applicable for research in antimicrobial photodynamic therapy (aPDT).</p>Fórmula:C108H118Br4N8O4Cor e Forma:SolidPeso molecular:1906.60095Sivelestat sodium tetrahydrate
CAS:<p>Sivelestat sodium tetrahydrate (ONO5046 sodium tetrahydrate) is a competitive inhibitor of human neutrophil elastase, with an IC50 of 44 nM and a Ki of 200 nM.</p>Fórmula:C20H29N2NaO11SPureza:99.68%Cor e Forma:SolidPeso molecular:528.51TrxR-IN-8
CAS:TrxR-IN-8 (Compound 6f) is a selective inhibitor of TrxR with an IC50 of 10.2 μM. It induces apoptosis through oxidative stress by stimulating the production of reactive oxygen species, reducing intracellular thiols, and lowering the glutathione/glutathione disulfide ratio. TrxR-IN-8 exhibits significant cytotoxicity against non-small cell lung cancer (NSCLC) cells.Fórmula:C16H16INO2Cor e Forma:SolidPeso molecular:381.21BAY 74-4113
CAS:BAY 74-4113 is a DGAT1 inhibitor with an IC50 of 72 nM. It is utilized in research related to obesity.Fórmula:C26H20F2N2O3SCor e Forma:SolidPeso molecular:478.51IRE1-IN-2
<p>IRE1-IN-2 (compound G15) functions as a potent inhibitor of IRE1. It effectively suppresses lipid accumulation induced by FFA, exhibiting an IC50 value of 2.06 μM.</p>Fórmula:C16H20O6Cor e Forma:SolidPeso molecular:308.12599CDK9 degrader-1
CDK9degrader-1 is a selective CDK9 degrader (DC50: 0.4073 µM). It recruits ATG101 to initiate the autophagy-lysosome pathway and forms autophagosomes by recruiting LC3, which then fuse with lysosomes to degrade CDK9 and its partner protein, Cyclin T1 (DC50: 1.215 µM). CDK9degrader-1 induces caspase 3-mediated apoptosis and exhibits antitumor activity in a mouse HCT116 xenograft model.Fórmula:C32H34Cl2N6O4Cor e Forma:SolidPeso molecular:637.56Betamethasone disodium phosphate
CAS:<p>Betamethasone disodium phosphate (Betamethasone 21-phosphate disodium salt) has anti-inflammatory activity and may be used in the study of rheumatoid arthritis.</p>Fórmula:C22H28FNa2O8PPureza:99.37%Cor e Forma:White PowderPeso molecular:516.41TYK2 activator-1
<p>TYK2activator-1 (16b) is a TYK2 activator with an EC50 value of 1.78 μM. It inhibits JAK2 and JAK3 with IC50 values of 6.8 μM and 6.3 μM, respectively.</p>Fórmula:C23H21FN4O2Cor e Forma:SolidPeso molecular:404.16485Dienestrol diacetate
CAS:Dienestrol diacetate, a derivative of the synthetic non-steroid phenolic compound, DIENESTROL, exhibits estrogenic activities.Fórmula:C22H22O4Pureza:98%Cor e Forma:SolidPeso molecular:350.41PLK1-IN-15
CAS:<p>PLK1-IN-15 is a PLK1 inhibitor with an IC50 of 38.5 nM. It exhibits antiproliferative effects on HepG2, Huh7, H1299, and A549 cells, with IC50 values of 2.03, 2.08, 4.79, and 17.11 μM, respectively. Additionally, PLK1-IN-15 can induce cell cycle arrest in the G2/M phase and trigger apoptosis (Apoptosis), demonstrating anticancer activity.</p>Fórmula:C25H29N7O4SCor e Forma:SolidPeso molecular:523.613-Deazaguanosine
CAS:3-Deazaguanosine (C3Guo) exhibits potent antiviral activity against SARS-CoV-2 with an EC50 of 1.14 μM and a CC50 greater than 200 μM in Vero E6 cells. It has the potential to prevent COVID-19.Fórmula:C11H14N4O5Cor e Forma:SolidPeso molecular:282.252'-(2-Nitrobenzyl)-ATP
CAS:<p>2'-(2-Nitrobenzyl)-ATP is an analog of rATP. It acts as a transcription terminator by inhibiting the elongation of RNA chains by T7 RNA polymerase.</p>Fórmula:C17H21N6O15P3Cor e Forma:SolidPeso molecular:642.30Cortodoxone-d7
Cortodoxone-d7 (11-Deoxycortisol-d7) is a deuterium-labeled form of Cortodoxone. Cortodoxone (11-Deoxycortisol; cortexolone) is both a glucocorticoid steroid hormone and a glucocorticoid antagonist. It enhances tryptophan oxygenase (TO) activity and stimulates the secretion of corticosterone. Additionally, Cortodoxone regulates the proliferation and activation of T cells.Fórmula:C21H23D7O4Peso molecular:353.50
