11.2
[1]. Bryant C Hollins, et al. Enriching carbonylated proteins inside a microchip through the use of oxalyldihydrazide as a crosslinker. Lab Chip. 212 Jul 21;12(1):2526-32.
[2]. D P Singh, et al. Antibacterial activity and spectral studies of trivalent chromium, manganese, iron macrocyclic complexes derived from oxalyldihydrazide and glyoxal. J Enzyme Inhib Med Chem. 29 Jun;2(3):883-9.
[3]. D P Singh, et al. Synthesis and spectroscopic studies of biologically active compounds derived from oxalyldihydrazide and benzil, and their Cr(III), Fe(III) and Mn(III) complexes. Eur J Med Chem. 29 Apr;():1731-6.
[]. Huanan Li, et al. Efficient Delivery of DOX to Nuclei of Hepatic Carcinoma Cells in the Subcutaneous Tumor Model Using pH-Sensitive Pullulan-DOX Conjugates. ACS Appl Mater Interfaces. 215 Jul 29;7(29):15855-65.
[5]. Khlood Abou Melha, et al. Antimicrobial, spectral, magnetic and thermal studies of Cu(II), Ni(II), Co(II), UO(2)(VI) and Fe(III) complexes of the Schiff base derived from oxalylhydrazide. J Enzyme Inhib Med Chem. 28 Apr;23(2):285-95.
H228-H32-H315-H319-H335
P21-P2-P261-P26-P27-P271-P28-P32+P352-P3+P3-P33-P362-P37+P378-P51
GHS2
.1