Synthesis and configurational analysis of a dinucleoside phosphate isotopically ... HUMAN PROSTATIC ACID PHOSPHATASE: A HISTIDINE PHOSPHATASE.
Oct 8, 1980 - HUMAN PROSTATIC ACID PHOSPHATASE: A HISTIDINE PHOSPHATASE. Robert L. Van Etten. Annals of the New York Academy of Sciences ...
independent fractionation processes. It was observed that all product species were mass-independently fractionated (MIF). Kinetic analysis suggests that MIF ...
Aug 28, 2017 - The accurate determination of absolute configuration (AC) of TPE core compounds is complicated and difficult, especially when there is no heavy atoms exist in their structures. Herein, we demonstrate a powerful and convenient method to
Aug 28, 2017 - Block diagram of CD spectrometer; powder X-ray diffraction patterns of TPE, BETPE, and TETPE; excitation parameters and involved transitions for the main excited states of TPE, BETPE, and TETPE (PDF). X-ray crystallographic data for TE
Nov 29, 2017 - Accordingly, the configurations of C-6, C-8, and C-10 were assigned as 6S, 8R, and 10R, respectively. Similarly, the ÎδSR .... In addition, apoptosis induced by ostreol B at the concentrations of 10 and 20 μM was examined using the
Nov 29, 2017 - Following isolation of the polyhydroxy compound, ostreol B, from cultivated cells of the toxic dinoflagellate Ostreopsis cf. ovata collected in South Korea, 1D and 2D NMR spectroscopy were employed to determine the planar chemical stru
Nov 29, 2017 - Environment and Resource Convergence Center, Advanced Institutes of Convergence Technology, Suwon 16229, Republic of Korea.
Nov 29, 2017 - Article Options. ACS ActiveView PDF. Hi-Res Print, Annotate, Reference QuickView. PDF (3302 KB) · PDF w/ Links (716 KB) · Full Text HTML.
Dimeric stilbene glucosides 1â3 [two diastereomers of (â)-gnemonoside A (1a and 1b), (â)-gnemonoside C (2), and (â)-gnemonoside D (3)] as well as a mixture ...
6601
J. Am. Chem. SOC.1980,102, 6601-6602 and NADPH. While the results of others cited above indicate that one pathway for the enzymatic removal of carbon atom 32 of l4a-alkyl and l4a-hydroxymethyl sterols requires molecular oxygen, our results clearly demonstrate that the enzymatic removal of a steroidal 14a-hydroxymethyl group can also proceed via H3GH0";
