[go: up one dir, main page]

Yildirim et al., 2018 - Google Patents

Biotransformation of testosterone by Ulocladium chartarum MRC 72584

Yildirim et al., 2018

View PDF
Document ID
14961351950770279817
Author
Yildirim K
Kuru A
Yılmaz Å
Publication year
Publication venue
Journal of Chemical Research

External Links

Snippet

Biotransformation of testosterone by Ulocladium chartarum MRC 72584 Page 1 JOURNAL OF CHEMICAL RESEARCH 2018 444 RESEARCH PAPER VOL. 42 AUGUST, 444–446 Steroids are biologically and pharmaceutically important substances that possess many physiological …
Continue reading at journals.sagepub.com (PDF) (other versions)

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/02—Oxygen as only ring hetero atom
    • C12P17/06—Oxygen as only ring hetero atom containing a six-membered hetero ring, e.g. fluorescein
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12R—PROCESSES USING MICRO-ORGANISMS
    • C12R1/00—Processes using micro-organisms
    • C12R1/645—Processes using micro-organisms using fungi
    • C12R1/80—Pencillium
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/16—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D309/28—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D309/30—Oxygen atoms, e.g. delta-lactones
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07J—STEROIDS
    • C07J63/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by expansion of only one ring by one or two atoms
    • C07J63/008—Expansion of ring D by one atom, e.g. D homo steroids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07J—STEROIDS
    • C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane

Similar Documents

Publication Publication Date Title
Hawas et al. Bioactive anthraquinones from endophytic fungus Aspergillus versicolor isolated from red sea algae
Keller-Juslen et al. Tetronomycin, a novel polyether of unusual structure
Evidente et al. Ophiobolin E and 8-epi-ophiobolin J produced by Drechslera gigantea, a potential mycoherbicide of weedy grasses
Chen et al. The betulinic acid production from betulin through biotransformation by fungi
Yildirim et al. Biotransformation of testosterone by Ulocladium chartarum MRC 72584
Gallo et al. Endophytic fungi found in association with Smallanthus sonchifolius (Asteraceae) as resourceful producers of cytotoxic bioactive natural products
Huang et al. Biotransformation of dehydroepiandrosterone (DHEA) with Penicillium griseopurpureum Smith and Penicillium glabrum (Wehmer) Westling
Fu et al. Biotransformation of ursolic acid by an endophytic fungus from medicinal plant Huperzia serrata
Choudhary et al. Biotransformation of adrenosterone by filamentous fungus, Cunninghamella elegans
Liu et al. Synthesis of steroidal lactone by penicillium citreo-viride
Javid et al. Baeyer-Villiger oxidation of progesterone by Aspergillus sojae PTCC 5196
Yildirim et al. Baeyer–Villiger oxidation of some steroids by Aspergillus tamarii MRC 72400
Harinantenaina et al. Chemical constituents of Malagasy liverworts, Part II: Mastigophoric acid methyl ester of biogenetic interest from Mastigophora diclados (Lepicoleaceae subf. Mastigophoroideae)
Bedir et al. Microbial transformation of Astragalus sapogenins using Cunninghamella blakesleeana NRRL 1369 and Glomerella fusarioides ATCC 9552
Yildirim et al. Microbial transformation of some steroids by Cladosporium cladosporioides MRC 70282
Wang et al. Metabolites from the co-culture of nigranoic acid and Umbelopsis dimorpha SWUKD3. 1410, an endophytic fungus from Kadsura angustifolia
Yildirim et al. Biotransformation of some steroids by Mucor hiemalis MRC 70325
Yildirim et al. Biotransformation of androst-4-ene-3, 17-dione by some fungi
Yildirim et al. Biotransformation of some steroids by Aspergillus candidus
Qin et al. Cembranoid, steroid, and sesquiterpenoid derivatives from the South China Sea soft coral Sinularia numerosa
Uchida et al. New sesquicillins, insecticidal antibiotics produced by Albophoma sp. FKI-1778
Daoubi et al. Hemisynthesis and absolute configuration of novel 6-pentyl-2H-pyran-2-one derivatives from Trichoderma spp.
Yildirim et al. The biotransformation of some steroids by Aspergillus sydowii MRC 200653
Xie et al. Two triterpenoids and other constituents from Petasites tricholobus
Inacio et al. Microbial transformation of some triterpenoids of Guayule resin by Chaetomium sp.