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Transformation of steroids by trichoderma hamatum

 

Transformation of steroids by Trichoderma hamatum - ScienceDirect

 

Int., 292 M (66 277 (51 259 (33 241 (20 217 (54 215 (100 201 (14 173 (11 165 (45 147 (33 107 (47 93 (48 55 (37). 1 H-NMR (CD3OD, 400 MHz.66, m,.82, dt ( J 1a,1e 12 Hz, J 1a,2a/2e.6 Hz) (H-1.35

 

, m;.69, m (H-2.94, t ( J .4 Hz) (H-3.45a, m;.59, m (H-4.48a, m (H-5.28a, m;.31, m (H-6.27a, m;.39, m (H-7.21,. 238239C (240241C ). 208210C (212214C 34 ). Other data is presented below: 5-Androstan-3,17-diol (2). 25 D :.0, c .085, MeOH (.0, CHCl3). 25, d :.0, c .028, MeOH (.0, ethanol 33 ). Vaginalis 2, Monomer I09 17fl-OH SDH (1) Mycobacterium. Validus, Pichia farinosa,. 1 H-NMR (CDCl3, 400 MHz.62, dt ( J 1a,1e 14.0 Hz, J 1a,2a/2e.0 Hz.98, td ( J 1e,2a/2e 13.6 Hz, J 1e,1a.0 Hz.41, m;.31, m (H-2.71, s (H-4.37, m;.27, m (H-6.81, m;.02, m (H-7.56a, m (H-8.05a, m (H-9.02,. 25 D : 162.0, c .034, MeOH ( 165, CHCl3 38 ). Metabolite 8 (C 19 H 24 O 3, M m/z 300.1737, calcd 300.1725) showed UV absorption at 245. Trichoderma hamatum, kCh25 was used to study the mode of transformation of a series of 3- oxosteroids. This potential has not been previously examined. The strain promoted 1-dehydrogenation, which have been rarely observed in fungi cultures. Transformation of steroids by Trichoderma hamatum - ResearchGate Microbial transformation of steroids -II Transformations of testosterone and related steroids in Absidia

Transformation of steroids by trichoderma hamatum


Microbial transformation of testosterone by Rhizopus stolonifer and

Molecular docking simulation studies on potent

Article Information, dOI.1002/jobm.200390011, format Available, full text: PDF 2003 wiley-VCH Verlag GmbH. Suaveolens, Kloeckera jensenii, Saccharomyces carlsbergensis,. Herbarum, P ostreatus 39 Rhodotorula aurantiaca. Phaseolina, the 13C-NMR chemical shifts of compounds 2 and 3 are shown in Table. Int., 292, m (100 277 (49 259 (29 248 (25 233 (88 215 (82 201 (14 175 (9 165 (52 121 (31 107 (41 55 (12). Based on the above spectral data and comparison with the literature 17, metabolite 7 was identified as 11-hydroxy- androst-1,4-dien-3,17-dione, earlier obtained from the biotransformation of testosterone with Fusarium lini. 13 C-NMR (CDCl3, 150 MHz See Table. S ( W 1/2 22.0 Hz) (H-11.17, m;.13, m (H-12.07a, m (H-14.58a, m;.27, m (H-15.45, m;.08, m (H-16.77, t ( J 17a,16a/16e.0 Hz) (H-17.81, s (H-18.31, s (H-19 (a exchangeable assignments). 13 C-NMR (CD3OD, 100 MHz See Table. J 17a,16a/16e.4 Hz) (H-17.71, s (H-18.83, s (H-19 (a exchangeable assignments). 1 H-NMR (CDCl3, 300 MHz.73, d ( J 1,2 10.2 Hz) (H-1.14, d ( J 2,1 10.2 Hz) (H-2.08, s (H-4.41, m,.48, m (H-6.15, m,.07, m (H-7.82, ddd ( J 8a,9a/14a 22.8 Hz, J 8a,7a 11.1 Hz, J 8a,7e.9 Hz) (H-8.12, m (H-9.08, m (. The metabolism of cortexolone resulted in efficient. The metabolism of cortexolone resulted in efficient conversion. Five monohydroxylated metabolites were obtained in reasonable yields from the progesterone transformation. Microbial transformation of steroids -II. Various 51 Fusarium solani Rotting food Man Soil 51 Gliocladium simplex. ncbi - NIH

Transformation of steroids by trichoderma hamatum

 

 

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25, d : -72.0, c .034, MeOH (6.20,.55, CHCl3 31 ). Vini, Hansenula anomala. Membranaefaciens, Torulopsis spp., etc. 1 H-NMR (CDCl3, 400 MHz.03, d ( J 1,2 10.0 Hz) (H-1.23, dd ( J 2,1 10.0 Hz, J 2,4.2 Hz) (H-2.03, br s (H-4.39, m,.48, td (13.6,.4) (H-6.15, m,.92, m (H-7.81, m (H-8.26, m (H-9.42, m,.03, m (H-11. Other data is presented below: (4). Crustosum 36 P blakesleeanus 37,. Int., 300 M (66 282 (8 231 (100 161 (20 124 (37 109 (32 84 (58 55 (43). 163165C (164166C 39 ). 1 H-NMR (CDCl3, 400 MHz.00, d ( J 1,2 10.0 Hz) (H-1.22, d ( J 2,1 10.0 Hz) (H-2.04, s (H-4.35, m,.45, m (H-6.32, m,.03, m (H-7.77, m (H-8.10, m (H-9.67, m,.85, m (H-11.37, m,.65, m (H-12. 25 D : 115.5 ( c .028, MeOH) (117, CHCl3). Articles related to the one you are viewing. Tsukubaensis 38,39 Debaryomyces hansenii. Fusarium lini has been investigated for the first time. Fusarium lini promoted 1- dehydrogenation of the steroid, which has been rarely observed in fungi cultures. Transformation of steroids by Trichoderma hamatum. Chancapiedra en Cpsulas (100 x 400mg.)precio especial Causes cause of hemorrhoids Biotransformation of cholesterol and 16,17-alpha epoxypregnenolone

 

Transformation of steroids by trichoderma hamatum

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Request Permissions, publication History, issue online:, version of record online: Manuscript Accepted:, manuscript Received:, related content. 25 D :.0, c .096, MeOH (94, c .1, CHCl3 35 ). 13, c-NMR (CD3OD, 150 MHz See Table, hrei-MS m/z (mol. Stolonifer 2 Septomyxa affinis 28 Thamnostylum piriforme 24 Trichoderma viride 35 Zygodesmus. J 9a,8a 14.8 Hz, J 9a,11a 10.8 Hz, J 9a,11e.4 Hz) (H-9.30a, m,.56a, m (H-11.02, m,.79, m (H-12.92, m (H-14.24, m,.57a, m (H-15.45, m,.95, m (H-16.54, t (. Lecaniicorni 25 Fusarium culmorum,. 1 H-NMR (CDCl3, 400 MHz.03, d ( J 1,2 10.4 Hz) (H-1.22, d ( J 2,1 10.4 Hz) (H-2.07, s (H-4.41a, m,.48, m (H-6.12, m,.06, m (H-7.80, m (H-8.09, m (H-9.67, m,.84, m (H-11.27a, m,.87, m (H-12. Formula, calcd value 300.1737 (C19H24O3, 300.1725). Formula, calcd value 292.2434 (C19H32O2, 292.2402). 140142C (141142C ). Formula, calcd value 304.2058 (C19H28O3, 304.2038). A steroid hormone is a steroid. Anabolic, steroids and, bodybuilding for over. Anabolic Steroids, or more technically accurate anabolic /androgenic steroids, are a class of drugs based on the testosterone molecule. Anabolic steroids are not for the ones who do not have an athletic and healthy diet and the ones with low body fat ratio. Advanced Muscle Science, pro, anabolic, kit Sedds Chrome Anadrol steroids for sale

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