Product fluorescent-dyes-No-ROS-Rox-derivatives

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Catalog	name	Description	price
R-XASYS-00556	GAK inhibitor 49,cas:319492-82-5	GAK inhibitor 49(C20H22N2O5,370.40) is a potent, ATP-competitive and highly selective cyclin G associated kinase (GAK) inhibitor with a Ki of 0.54 nM and a cell IC50 of 56 nM. GAK inhibitor 49 also shows binding to RIPK2.	price>
R-XASYS-00557	6-Hydroxybentazon,cas:60374-42-7	6-Hydroxybentazon(C10H12N2O4S,256.28) is a phase I metabolite of bentazone, and bentazone is a chemical for use in herbicides.	price>
R-XASYS-00558	6-Methyl-5-azacytidine,cas:105330-94-7	6-Methyl-5-azacytidine(C9H14N4O5,258.23) is a potent DNMT inhibitor.	price>
R-XASYS-00559	6-O-Methyl Guanosine,cas:7803-88-5	6-O-Methyl Guanosine(C11H15N5O5,297.27) is a modified nucleoside. 6-O-Methyl Guanosine (6-methylguanosine) inhibit colony-forming ability in a malignant xeroderma pigmentosum cell line.	price>
R-XASYS-00560	NITD-916,cas:1614262-83-7	NITD-916(C20H25NO2,311.42), a 4-hydroxy-2-pyridone derivative, is an orally active and highly lipophilic mycobacterial enoyl reductase InhA inhibitor with an IC50 of 570 nM. NITD-916 forms a ternary complex with InhA and NADH to block access to the fatty acyl substrate binding pocket. NITD-916 has potent anti-tuberculosis effects.	price>
R-XASYS-00561	7-BIA,cas:1313403-49-4	7-BIA(C15H18O6,294.30) is a receptor-type protein tyrosine phosphatase D (PTPRD) inhibitor with an IC50 of ~1-3 μM.7-BIA (7-butoxy illudalic acid analog) inhibits recombinant human PTPRD and recombinant human PTPRS with IC50 values of ~1-3μM and 40μM, respectively.	price>
R-XASYS-00562	7-Chlorokynurenic acid sodium salt,cas:1263094-00-3	7-Chlorokynurenic acid sodium salt(C10H5ClNNaO3,245.59) (7-CKNa) is a synthetic compound that has been used in scientific research since the 1980s. It is a potent, selective antagonist of the kynurenic acid (KYNA) receptor, which is a member of the family of G-protein coupled receptors (GPCRs).	price>
R-XASYS-00563	7DG,cas:26927-01-5	7DG(C26H30O5,422.51) is a selective inhibitor of protein kinase R (PKR). 7DG appears to directly interact with the C-terminal half of PKR, and unlike C16, does not bind the ATP catalytic pocket.	price>
R-XASYS-00564	7-Epi-10-oxo-docetaxel,cas:162784-72-7	7-Epi-10-oxo-docetaxel (Docetaxel Impurity 2)(C43H51NO14,805.86) is a impurity of docetaxel detected by high performance liquid chromatography (HPLC).	price>
R-XASYS-00565	7-Epi-docetaxel,cas:153381-68-1	7-Epi-10-oxo-docetaxel(C43H53NO14,807.88) (Docetaxel Impurity C; 7-Epitaxotere) is a impurity of docetaxel.	price>

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