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Megestrol acetate-d3-1
Biological Activity：Megestrol acetate-d3-1 is deuterium labeled Megestrol acetate. Megestrol acetate is a synthetic and orally active progesteronal agent. Megestrol acetate is effective as an appetite stimulant for wasting syndromes such as cachexia. Megestrol acetate decreases nuclear and cytosol androgen receptors human BPH tissue. Megestrol acetate has the potential for HIV study and downregulates autophagic catabolic pathway[2][3][4][5].
Research Area：Endocrinology|Cancer
Targets：Autophagy|Progesterone Receptor|HIV
Related Small Molecules:HIV-1 TAT (48-60);Gestonorone Capronate;Seletracetam lithium;HIV-IN-2;Triptonine B;FC131;Peritassine A;Flavopiridol;TAT (48-57);Chlormadinone acetate-d6-1;FGI-106 tetrahydrochloride;(Z)-9-Propenyladenine;Apabetalone;Decanoyl-RVKR-CMK TFA;ONX-0914 TFA;17α-Hydroxyprogesterone;Apelin-36(rat, mouse);Ulonivirine
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