17-Alpha-Oxo-Nolone, anyone ever hear of this before.
Safety and Information
By: Dr. Jim Kimbrell
Ph.D. Biochemistry & Molecular Microbiology
The purpose of this review is to focus on the explanations for the activity of the compounds (25R)-5alpha-spirostan-2alpha, 3beta, 5alpha-triol-6-OH, NeoHecogenin-3-O-Beta-D-Glucopyranoside, Desoxydiosgenin from Safed Musli and Sophora flavescens (Oxymatrine and Matrine) supplementation, Understanding the physiological role of each compound through limited information on pharmacokinetics.
Musli is known to be a natural steroidal saponagin which is a pharmacological active metabolite with similar mechanisms as phytosterols. Hecogenin is also listed as a steroidal intermediate, which means it has many roles as a precursor to several different hormone metabolic pathways.
One of the metabolic roles of hecogenin is that of a 6-Ketoderivative. It is shown that 6-Ketoderivatives of natural sapogenins via NeoHecogenin, display anabolic activity and do not manifest androgenic properties. This compound produces an accelerated gain of weight and also an increase in weight of the liver, kidneys, musculus tibiliasis anterior and augments the total amount of protein therein.
Metabolic role as a multi analogue pregnene, as shown in the appendix A the common metabolic pathway from (25)-D-Spirosta-3,5-Diene or 3beta* hydroxy-5alpha, 22alpha-spirostan-12-one through intermediate reactions to 3beta-acetoxy-5alpha-pregna-9, (11), 16-diene-20-one, where this compound takes on different types of biological roles. One of these types of biological roles is the manufacture of certain Oxa hormones. In some cases (15%) the synthesis of Oxa hormone analogues from Desoxydiosgenin begins at 17-ethyal-1 I-oxatesterone, form 11-oxa-5alpha-pregnane-3, 20* dione via 3, 17-dioxygenated-9-oxo-9, 12-seco-l l-nor-5alpha-androstan-12* oic ester, from 3 beta-acetoxy-17-hydroxy-5 alpha-pregnan-12-one two products all from NeoHecogenin.
A metabolite 17alpha-hydroxy-4-pregnene-3, 20-dione effecting HCG levels caused decrease in estradiol-17beta levels within days but levels do return after discontinuing supplement possibly caused by an intermediate of 11* oxaprogesterone, 11-oxa-5alpha-pregnane-3, 20-dione which becomes the point of 17-hydroxy functioning by metabolic modified oxidation in sex organs resulting in low progestional activity.
Androgenic/ Anabolic Activity 1:3 ratio:
In humans males 25% females 5% testis or ovary/ adrenal microsomes convert pregnenolone to testosterone via the 4-ene-3oxo pathway, with the major metabolites being progesterone, 17-hydroxypregesterone, 4* androstenedione and testosterone; also some 17-hydroxypregnenolone very little less than 1 % DHEA and 5-androstenedione which does not alter the metabolic profile of pregnenolone metabolism. The synthesis of 11* oxatestosterone from l I-oxa-5alpha-androstane-3, 17-dioneshows in comparison with natural hormone, and a diminished androgenic/anabolic endogenous enzymatic activity however, normal rates return after supplementation is discontinued.
The primary action taken by the compound is the effect the compound has on the liver in which the liver causes the brain to release luteinizing hormone. According to early stages of in-vitro and clinical and preclinical in-vivo medical studies this pharmacologically active compound is reported to enhance testosterone levels by increasing luteinizing hormone. This hormone released by the brain turns on the natural testosterone production, primarily because of this hormone influencing property accompanied by the high anabolic ratio.
Safety Issues on This Compound:
17-Alpha's main ingredients have no reported cases of adverse reactions or over dose. However, this compound should be intended for healthy individuals over the age of seventeen. It is also not recommended to women who are pregnant, nursing or plan to become pregnant.
Oxymatrine (Sophora flavescens):
This ancient herbal extract has been used for years for many different ailments such as: Asthma, reproductive disorders, intestinal infection, allergic reactions, and viral hepatitis. The most interesting aspect of research on this herbal compound is its use as a PDE- 5 inhibitor.
How this works: Nitric oxide reduces pulmonary hypertension by activating soluble guanylate cyclase, which converts GTP to cGMP in vascular smooth muscle. Oxymatrine decreases the hydrolysis of cGMP thus enhancing pulmonary vasodilatation. One study of this compound was done on 3 week old lambs with hypoxia-induced pulmonary hypertension. Where 27% decrease in PVR that lasted for at least 90 minutes. This was similar to the 32% decrease on PVR observed with 1 hour of iNO.
Safety Issues on This Compound:
Their have been 2 reports of this compound causing stomach upset in the liquid tincture form. No cases of overdose have been reported with this compound.
From what I can tell the compound is structured diff. from both bam and mass fx, but I'm sure that they are all very similiar in function and purpose, just my opinion.