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99% Purity SARMS MK677 Pure Research Chemicals Ibutamoren MK-677 White Powder CAS 159634-47-6
99% SARMS MK677 Raw Steroids Ibutamoren MK-677 White Powder CAS 159634-47-6
Quick Detail: Product Name:Ibutamoren(MK677) CAS No:159752-10-0 Molecular Formula:C27H36N4O5S.CH4O3S Molecular Weight:624.776 Assay:98% min Quality Standard:USP/ISO9001 Appearance:White Powder Supply Ability:500-800kg/month Storage:Store at 8ºC-20ºC, protect from moisture and light. Related Products:S-23 Powder,SR9009 Powder.
Description: Ibutamoren mesylate (MK-677) is an orally active nonpeptide growth hormone (GH) secretagogue. Nutrobal (Mk-677) was found to be very safe. This is an amazing cutting stack with Cardarine and Andarine, which will help melt off the stubborn fat and increase your muscle mass.
MK-677, acts as a potent, orally active growth hormonesecretagogue, mimicking the GH stimulating action of the endogenous hormone ghrelin. It has been demonstrated to increase the release of, and produces sustained increases in plasma levels of several hormones including growth hormone and IGF-1, but without affecting cortisol levels. It is currently under development as a potential treatment for reduced levels of these hormones, such as in growth hormone deficient children or elderly adults, and human studies have shown it to increase both muscle mass and bone mineral density, making it a promising therapy for the treatment of frailty in the elderly. It also alters metabolism of body fat and so may have application in the treatment of obesity.
Application: An experimental drug meant to control lipids and increase the level of HDL, or good cholesterol, in the bloodstream. A cell-permeable, thiazolyl compound that acts as a potent, high affinity, PPARd agonist.
Usage An experimental drug meant to control lipids and increase the level of HDL, or good cholesterol, in the bloodstream. A cell-permeable, thiazolyl compound that acts as a potent, high affinity, PPARδ agonist. Exhibits selectivity for PPARδ compared to PPARα and PPARγ. Does not exibit any activity against other nuclear or non-nuclear receptors. Reported to increase cholesterol efflux and ABAC1 expression in macrophages, fibroblasts, and intestinal cells.
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