Carbon-13 magnetic resonance. XVII. Pyrimidine and purine nucleosides.
about
Hydrogen bonding of adenine derivatives to tyrosine side chainNew manzamine alkaloids with activity against infectious and tropical parasitic diseases from an Indonesian sponge.A pyrrole derivative from Paeonia suffruticosa.Chemical constituents of the rhizomes of Coeloglossum viride var. bracteatum.Pyramidamycins A-D and 3-hydroxyquinoline-2-carboxamide; cytotoxic benzamides from Streptomyces sp. DGC1.Guanosine 5'-diphosphate, 3'-diphosphate: assignment of structure by 13C nuclear magnetic resonance spectroscopy.Expression of mammalian glutathione S-transferase 5-5 in Salmonella typhimurium TA1535 leads to base-pair mutations upon exposure to dihalomethanes.Isolation and characterization of a new product produced by ionizing irradiation and type I photosensitization of 2'-deoxyguanosine in oxygen-saturated aqueous solution: (2S)-2,5'-ANHYDRO-1-(2'-deoxy-beta-D-erythro-pentofuranosyl)-5-guanidin ylideneSteric and electrostatic effects at the C2 atom substituent influence replication and miscoding of the DNA deamination product deoxyxanthosine and analogs by DNA polymerases.Assignments in the carbon-13 nuclear magnetic resonance spectra of vitamin B12' coenzyme B12' and other corrinoids: application of partially-relaxed fourier transform spectroscopy.Applications of 13 C nuclear magnetic resonance in biochemistry.Nucleoside conformation is determined by the electronegativity of the sugar substituent.A new lignan from the seeds of Sphaerophysa salsula.Fructose-amino acid conjugate and other constituents from Cyperus rotundus L.New alkaloids from the seeds of Notopterygium incisum.Isolation and structural elucidation of novel antimicrobial compounds from maggots of Chrysomyis megacephala Fabricius.
P2860
Q28330898-2606493C-0C43-460E-956B-948405957F6DQ30953370-4CB1222A-7BBC-4028-9137-CDA6A599F7BDQ33393263-F3009918-C116-41CA-A3F5-CEDFFA2BB1B1Q34301799-AD56C215-406C-4241-BBF1-7250D3A070F9Q34304774-087B5CEB-C4DC-4E41-B71D-526F8F83F8F1Q34733028-EFC6E1AD-08EE-44BC-B32F-EE34CE57E048Q36540151-2A6B6C76-4680-4BC9-9C70-798D01CD9B4DQ36741532-61E6BB75-A683-4D28-ACFC-6DE7527218A9Q37371343-8B62EEF4-11F2-4E1A-874E-0C1DE0958A54Q37476278-E7108729-F2C7-4D38-BD0C-171EB8BE5642Q39948293-2A80A090-D868-4803-8428-BC1D484F5F8DQ40480998-61EFFF89-1C6F-45F6-B0C7-8F8FD679A5F8Q45203866-F316A648-CCA6-4412-A182-4BF25298580FQ46234934-96117825-1A16-412E-A8B2-A4830D9A3117Q51577171-75F579CF-9397-4751-96B9-88DE2D0B06E4Q52777790-40CE9A5A-A767-47EA-9465-2C59860124B9
P2860
Carbon-13 magnetic resonance. XVII. Pyrimidine and purine nucleosides.
description
1970 nî lūn-bûn
@nan
1970年の論文
@ja
1970年学术文章
@wuu
1970年学术文章
@zh
1970年学术文章
@zh-cn
1970年学术文章
@zh-hans
1970年学术文章
@zh-my
1970年学术文章
@zh-sg
1970年學術文章
@yue
1970年學術文章
@zh-hant
name
Carbon-13 magnetic resonance. XVII. Pyrimidine and purine nucleosides.
@en
Carbon-13 magnetic resonance. XVII. Pyrimidine and purine nucleosides.
@nl
type
label
Carbon-13 magnetic resonance. XVII. Pyrimidine and purine nucleosides.
@en
Carbon-13 magnetic resonance. XVII. Pyrimidine and purine nucleosides.
@nl
prefLabel
Carbon-13 magnetic resonance. XVII. Pyrimidine and purine nucleosides.
@en
Carbon-13 magnetic resonance. XVII. Pyrimidine and purine nucleosides.
@nl
P2093
P356
P1476
Carbon-13 magnetic resonance. XVII. Pyrimidine and purine nucleosides.
@en
P2093
P304
P356
10.1021/JA00716A042
P407
P577
1970-07-01T00:00:00Z