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Nitrogenous bases covalently linked to a sugar with and without phosphate groups; used for synthesis, cell signaling, and as cofactors in enzymatic reactions; includes pyrimidine, purine, pyridine, flavin, pyrrolopyrimidine, and triazole varieties.
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D-Glucosamine 6-phosphate (sodium) (GlcN6P-Na) is a class of biochemical reagents used in glycobiology research Glycobiology studies the structure synthesis biology and evolution of sugars It involves carbohydrate chemistry enzymology of glycan formation and degradation protein-glycan recognition and the role of glycans in biological systems This field is closely related to basic research biomedicine and biotechnology[1]
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Anti-AA2AR/Adenosine A2aR Antibody (3F6-9G5) is a humanized antibody expressed in CHO cells targeting AA2AR/Adenosine A2aR Anti-AA2AR/Adenosine A2aR Antibody (3F6-9G5) contains huIgG1 heavy chain and hu light chain with a predicted molecular weight (MW) of 146 66 kDa The isotype control for Anti-AA2AR/Adenosine A2aR Antibody (3F6-9G5) can be referenced as Human IgG1 kappa Isotype Control (HY-P99001)
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Lamivudine is a nucleoside analog that acts primarily as a reverse transcriptase inhibitor disrupting viral replication by interfering with RNA-dependent DNA polymerase activity It inhibits human immunodeficiency virus type 1 (HIV-1) reverse transcriptase with an IC50 value of approximately 0 316 M Lamivudine also suppresses replication of simian retrovirus (SRV-1 and SRV-2) while exhibiting negligible activity on foamy viruses and amphotropic murine leukemia virus (MLV-A) Due to its antiviral mechanism and dual inhibitory effect against both HIV-1 and hepatitis B virus (HBV) lamivudine is frequently utilized in research involving retroviral infection models particularly HIV-1 and HBV coinfection studies to evaluate viral dynamics antiviral efficacy and biochemical responses
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Mtb ATP synthase-IN-1 is a potent Mycobacterium tuberculosis ATP synthase inhibitor (compound 6ab) for anti-mycobacterial research. It exhibits MIC 0.452-0.499 μg/mL against M. tuberculosis, demonstrates good metabolic stability and acceptable oral bioavailability, and shows low cytotoxicity in Vero cells.
Potent inhibition of M. tuberculosis ATP synthase
MIC 0.452-0.499 μg/mL against M. tuberculosis
Good metabolic stability
Low cytotoxicity (Vero IC50 > 64 μg/mL)
High purity (~98.6%)
Available in multiple solid and solution pack sizes
Stable storage recommendations for powder and solutions
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