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5a-androstane-3a,17P-diol

C7H5NO4 499-83-2) see Pyridinol carbamate 2p,16p-diplperidino-5a-androstane-3a,17p diol... [Pg.2370]

Pancuronium bromide (2P,16P-dipiperidino-5a-androstan-3a,17p —diol diacetate... [Pg.502]

Pancuronium bromide (2p,16p-dipiperidino-5a-androstan-3a,17P-diol diacetate dimetho-bromide)... [Pg.853]

Reddy, D.S. Venkatarangan, L. Chien, B. Ramu, K. A high-performance liquid chromatography-tandem mass spectrometry assay of the androgenic neurosteroid 3a-androstanediol (5a-androstane-3a,17p-diol) in plasma. Steroids 2005, 70 (13), 879-885. [Pg.231]

Ryan DE, Dixon R, Evans RH, Ramanathan L, Thomas PE, Wood AW, Levin W (1984) Rat hepatic cytochrome P-450 isozyme specificity for the metabolism of the steroid sulfate, 5a-androstane-3a,17P-diol-3,17-disulfate. Arch Biochem Biophys 233 636-642... [Pg.838]

For a GC-MS assay using benchtop instruments, the method has excellent sensitivity. Sensitivity is lowest for testosterone with a signal-to-noise ratio (S/ N) of 2.4 for 10 pg, and highest for 5a-androstane-3a,17p diol with a S/N of 17 for 10 pg. For the steroids studied, the intra- and interassay coefficients of variation are between 2.7 and 7.6%, respectively. Accuracy was determined by spiking plasma with known amounts of steroids. The agreement between the values found and the amounts added was excellent with relative errors less than 7.5%. Standard curves were prepared by analysis of a selection of reference analyte/internal standard mixtures of known concentrations. All standard plots were linear. [Pg.329]

We are able to determine two steroid conjugates, 5a-androstane-3a,17p diol glucuronide (ADG) and DHEA-S by ID-GC-MS. Cleavage of the conjugate group is required prior to GC [2], The released free steroids are analyzed according to the GC-MS conditions described above. [Pg.335]

Figure 16 Porphyrin/porphyrin exciton coupling and UV-visible and CD spectra in CHjClj (c= 1.0 pM) of 5a-androstane -3a,17P-diol bis[p-(10, 5, 20 -triphenyl-5 -porphyrinyl)benzoate] (solid line) and UV-visible spectrum of 5-(4 -carboxyphenyi)-10,15,20-... Figure 16 Porphyrin/porphyrin exciton coupling and UV-visible and CD spectra in CHjClj (c= 1.0 pM) of 5a-androstane -3a,17P-diol bis[p-(10, 5, 20 -triphenyl-5 -porphyrinyl)benzoate] (solid line) and UV-visible spectrum of 5-(4 -carboxyphenyi)-10,15,20-...
Methyltestosterone 17a-methyl-5a-androstane-3a,17P-diol 17a-methyl-5P-androstane-3a,17P-diol 17P-methyl-androst-4,6-dien-17a-ol-3-one... [Pg.288]

See other pages where 5a-androstane-3a,17P-diol is mentioned: [Pg.555]    [Pg.113]    [Pg.502]    [Pg.125]    [Pg.748]    [Pg.34]    [Pg.555]    [Pg.635]    [Pg.18]    [Pg.23]    [Pg.28]    [Pg.658]    [Pg.165]    [Pg.47]    [Pg.872]    [Pg.326]    [Pg.24]    [Pg.97]    [Pg.287]    [Pg.287]    [Pg.288]    [Pg.288]    [Pg.295]   
See also in sourсe #XX -- [ Pg.295 , Pg.296 , Pg.297 , Pg.298 , Pg.299 , Pg.302 ]



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5a-androstane- 3a,17/3-diol

ANDROSTAN

Androstane

Androstanes

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