86335-11-7 Usage
Uses
Used in Pharmaceutical Industry:
Androstenedione is used as a precursor in the synthesis of other steroid hormones for pharmaceutical applications. Its role in the production of testosterone and estrogen makes it a key component in the development of medications targeting hormonal imbalances and related health issues.
Used in Sports Performance Enhancement:
Androstenedione has been utilized as a dietary supplement and a performance-enhancing drug due to its ability to increase the production of testosterone, which can potentially improve athletic performance. However, its legal status as a performance-enhancing substance varies by country, and its use may be subject to regulation or restriction.
Used in Medical Research:
Androstenedione is used as a subject of research in the development of treatments for various medical conditions, including breast cancer and osteoporosis. Its hormonal properties and precursor role make it a valuable compound for exploring new therapeutic approaches and understanding the underlying mechanisms of these diseases.
Used in Hormone Replacement Therapy:
In some cases, androstenedione may be used as a component in hormone replacement therapy, particularly for conditions where the balance of sex hormones is disrupted. Its ability to be converted into both testosterone and estrogen makes it a versatile option for hormone regulation.
Check Digit Verification of cas no
The CAS Registry Mumber 86335-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,3 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 86335-11:
(7*8)+(6*6)+(5*3)+(4*3)+(3*5)+(2*1)+(1*1)=137
137 % 10 = 7
So 86335-11-7 is a valid CAS Registry Number.
86335-11-7Relevant academic research and scientific papers
Biotransformation of androst-4-ene-3,17-dione by some fungi
Yildirim, Kudret,Kuru, Ali,Keskin, Ece,Salihoglu, Aylin,Bukum, Neslihan
, p. 594 - 597 (2017/11/14)
The incubations of androst-4-ene-3,17-dione with Aspergillus candidus MRC 200634, Aspergillus tamarii MRC 72400, Aspergillus wentii MRC 200316 and Mucor hiemalis MRC 70325 for 5 days are reported. A. candidus MRC 200634 mainly hydroxylated androst-4-ene-3,17-dione at C-11α, C-15α and C-15β whilst A. wentii MRC 200316 hydroxylated it mainly at C-6β. A. tamarii MRC 72400 showed predominately a Baeyer–Villiger monooxygenase activity. M. hiemalis MRC 70325 hydroxylated the substrate at C-14α and reduced most of it at C-17.
A GENERAL METHOD FOR THE SELECTIVE REDUCTION OF KETONES IN THE PRESENCE OF ENONES.
Ward, Dale E.,Rhee, Chung K.,Zoghaib, Wajdi M.
, p. 517 - 520 (2007/10/02)
Ketones can be reduced in the presence of conjugated enones by sodium borohydride in 50percent methanol in dichloromethane at -78 deg C.The selectivity is generally excellent.In favorable cases the reaction can be carried out at room temperature in dichloromethane with acetic acid as catalyst.
