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	<title>Transdermals &#8211; BEHEMOTH LABZ</title>
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		<title>SR-9009 Stenabolic Liquid</title>
		<link>https://behemothlabz.com/product/sr-9009-stenabolic-liquid/</link>
					<comments>https://behemothlabz.com/product/sr-9009-stenabolic-liquid/#comments</comments>
		
		<dc:creator><![CDATA[uanwar016]]></dc:creator>
		<pubDate>Thu, 03 Sep 2026 07:43:56 +0000</pubDate>
				<guid isPermaLink="false">https://behemothlabz.com/?post_type=product&#038;p=82214</guid>

					<description><![CDATA[Buy SR-9009 Stenabolic Liquid Online SR-9009 Stenabolic is a synthetic REV-ERB agonist investigated primarily in laboratory and animal research. It is studied for its effects on circadian signaling, metabolic regulation, inflammation, and exercise-related biology. Product Information SR-9009 interacts with REV-ERB nuclear receptors that regulate genes involved in the body's molecular clock. The liquid format represents [...]]]></description>
										<content:encoded><![CDATA[<h2><b>Buy SR-9009 Stenabolic Liquid Online</b></h2>
<p><span style="font-weight: 400;">SR-9009 Stenabolic is a synthetic REV-ERB agonist investigated primarily in laboratory and animal research. It is studied for its effects on circadian signaling, metabolic regulation, inflammation, and exercise-related biology.</span></p>
<h2><b>Product Information</b></h2>
<p><span style="font-weight: 400;">SR-9009 interacts with REV-ERB nuclear receptors that regulate genes involved in the body's molecular clock. The liquid format represents the formulation of the compound; available research concerns SR-9009 itself rather than a clinically established liquid formulation. SR-9009, also known as Stenabolic, is studied primarily as a REV-ERB agonist in preclinical research.</span></p>
<h2><b>How It Works</b></h2>
<p><span style="font-weight: 400;">SR-9009 activates REV-ERB receptors and changes transcription of genes involved in circadian and metabolic regulation. These effects can influence energy metabolism and inflammatory signaling in experimental models.</span></p>
<h2><b>POTENTIAL BENEFITS</b></h2>
<h3><b>1. Circadian Biology Research</b></h3>
<p><span style="font-weight: 400;">REV-ERB activation provides researchers with a way to examine the molecular clock and its relationship with sleep-wake and metabolic processes.</span></p>
<h3><b>2. Metabolic Pathway Research</b></h3>
<p><span style="font-weight: 400;">SR-9009 has been investigated for effects on lipid and glucose metabolism in animal models, making it relevant to metabolic-signaling research.</span></p>
<h3><b>3. Exercise &amp; Muscle Research</b></h3>
<p><span style="font-weight: 400;">Preclinical work has examined SR-9009 in relation to exercise tolerance and skeletal-muscle metabolic pathways.</span></p>
<h3><b>4. Inflammation Research</b></h3>
<p><span style="font-weight: 400;">Research has demonstrated effects on inflammatory signaling, including NLRP3 and cytokine-related pathways in experimental models.</span></p>
<h2><b>Dosage</b></h2>
<p><span style="font-weight: 400;">There is <b>no established human dosage for SR-9009</b>. Published research uses animal doses under controlled experimental conditions and does not establish an appropriate dose for humans. Formulation into a liquid does not create a validated clinical dosage.</span></p>
<h2><b>Side Effects</b></h2>
<p><span style="font-weight: 400;">Because human safety data are limited, the full adverse-effect profile is unknown. Altering REV-ERB signaling could potentially affect circadian, metabolic, cardiovascular, and inflammatory systems.</span></p>
<h3><b>References</b></h3>
<ol>
<li style="font-weight: 400;"><a href="https://pubmed.ncbi.nlm.nih.gov/27603791/" target="_blank" rel="nofollow noopener"><span style="font-weight: 400;">PubMed — Pharmacological targeting of REV-ERBs</span></a></li>
<li style="font-weight: 400;"><a href="https://pubmed.ncbi.nlm.nih.gov/39059249/" target="_blank" rel="nofollow noopener"><span style="font-weight: 400;">PubMed — SR9009 and exercise/metabolic research</span></a></li>
<li style="font-weight: 400;"><a href="https://pubmed.ncbi.nlm.nih.gov/34324866/" target="_blank" rel="nofollow noopener"><span style="font-weight: 400;">PubMed — SR9009 and inflammation</span></a></li>
<li style="font-weight: 400;"><a href="https://pubmed.ncbi.nlm.nih.gov/37161366/" target="_blank" rel="nofollow noopener"><span style="font-weight: 400;">PubMed — SR9009 and NASH/metabolism</span></a></li>
</ol>
<p><b>Note:</b><span style="font-weight: 400;"> BehemothLabz does not sell this product. Purchase links on this page may direct you to third-party suppliers through affiliate links.</span></p>
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			<slash:comments>61885</slash:comments>
		
		
			</item>
		<item>
		<title>7-Keto DHEA Transdermal</title>
		<link>https://behemothlabz.com/product/7-keto-dhea-transdermal/</link>
		
		<dc:creator><![CDATA[James Damo]]></dc:creator>
		<pubDate>Thu, 03 Sep 2026 07:23:44 +0000</pubDate>
				<guid isPermaLink="false">https://behemothlabz.com/?post_type=product&#038;p=68946</guid>

					<description><![CDATA[Product Details 7-Keto DHEA is a metabolite structurally derived from dehydroepiandrosterone (DHEA), an endogenous steroid synthesized within adrenal cortical tissue. Unlike its parent compound, 7-Keto DHEA is characterized by structural modifications that prevent conversion into androgenic or estrogenic metabolites. In research environments, this compound is examined for its involvement in metabolic pathway regulation, particularly those [...]]]></description>
										<content:encoded><![CDATA[<h2><b>Product Details</b></h2>
<p><span style="font-weight: 400;">7-Keto DHEA is a metabolite structurally derived from dehydroepiandrosterone (DHEA), an endogenous steroid synthesized within adrenal cortical tissue. Unlike its parent compound, 7-Keto DHEA is characterized by structural modifications that prevent conversion into androgenic or estrogenic metabolites.</span></p>
<p><span style="font-weight: 400;">In research environments, this compound is examined for its involvement in metabolic pathway regulation, particularly those associated with mitochondrial activity and enzymatic processes. Investigations focus on how its structure influences biochemical signaling without conversion into downstream steroid hormones.</span></p>
<p><span style="font-weight: 400;">The compound is provided in a controlled format designed to preserve stability and maintain consistency for laboratory-based applications.</span></p>
<h2><b>Mechanism of Action</b></h2>
<p><span style="font-weight: 400;">7-Keto DHEA is studied for its interaction with enzymatic systems involved in mitochondrial lipid β-oxidation. These pathways are associated with substrate metabolism at the cellular level, particularly within mitochondrial compartments responsible for energy-related biochemical processes.</span></p>
<p><span style="font-weight: 400;">Additionally, it has been examined in relation to thermogenesis-associated pathways, where research focuses on molecular signaling linked to heat production and substrate utilization. Rather than describing outcomes, studies emphasize how enzymatic modulation may influence intracellular metabolic activity.</span></p>
<p><span style="font-weight: 400;">The compound is also analyzed for its interaction with thyroid-related signaling pathways, including those involving triiodothyronine (T3). These pathways are associated with transcriptional regulation and metabolic signaling at the cellular level.</span></p>
<p><span style="font-weight: 400;">Furthermore, ongoing investigations explore its role in immune-related signaling environments, particularly in relation to biomarker expression and regulatory pathways involved in cellular communication.</span></p>
<h2><b>Chemical Properties</b></h2>
<table>
<tbody>
<tr>
<td><b>Property</b></td>
<td><b>7-Keto DHEA</b></td>
</tr>
<tr>
<td><span style="font-weight: 400;">Molecular Formula</span></td>
<td><span style="font-weight: 400;">C19H28O2</span></td>
</tr>
<tr>
<td><span style="font-weight: 400;">IUPAC Name</span></td>
<td><span style="font-weight: 400;">(3S,8R,9S,10R,13S,14S)-3-hydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-one</span></td>
</tr>
<tr>
<td><span style="font-weight: 400;">Molar Mass</span></td>
<td><span style="font-weight: 400;">288.424 g/mol</span></td>
</tr>
<tr>
<td><span style="font-weight: 400;">CAS Number</span></td>
<td><span style="font-weight: 400;">53-43-0</span></td>
</tr>
</tbody>
</table>
<h2><b>Research Applications</b></h2>
<h3><b>Mitochondrial Pathway Analysis</b></h3>
<p><span style="font-weight: 400;">7-Keto DHEA is frequently examined in studies involving mitochondrial function, particularly those focused on lipid β-oxidation and intracellular energy-related processes.</span></p>
<h3><b>Thermogenesis-Associated Signaling Studies</b></h3>
<p><span style="font-weight: 400;">Research involving this compound often explores biochemical pathways associated with thermogenic signaling. These investigations focus on enzymatic interactions and molecular regulation rather than physiological outcomes.</span></p>
<h3><b>Thyroid Hormone Signaling Research</b></h3>
<p><span style="font-weight: 400;">The compound is also utilized in studies examining thyroid-related signaling pathways, including those involving triiodothyronine (T3) and transcriptional regulation mechanisms.</span></p>
<h3><b>Cellular Metabolism and Bioenergetics</b></h3>
<p><span style="font-weight: 400;">Additional research explores how 7-Keto DHEA interacts with pathways related to cellular metabolism, including energy balance, substrate utilization, and regulatory signaling networks.</span></p>
<h2><b>Why Choose BehemothLabz to Buy 7-Keto DHEA for Research</b></h2>
<p><span style="font-weight: 400;">BehemothLabz provides research-grade 7-Keto DHEA manufactured under controlled laboratory conditions with strict quality assurance protocols. Each batch undergoes analytical verification to ensure consistency in molecular composition and purity.</span></p>
<p><span style="font-weight: 400;">Comprehensive documentation, including laboratory testing reports and sourcing transparency, supports reproducibility in experimental settings. BehemothLabz maintains a compliance-focused approach, supplying compounds intended strictly for laboratory-based investigation and analytical research</span></p>
<h2><b>Disclaimer</b></h2>
<p><span style="font-weight: 400;">7-Keto DHEA is intended strictly for laboratory research and analytical purposes only. It is not intended for use in diagnostic procedures, therapeutic applications, or in vivo studies of any kind.</span></p>
<p><span style="font-weight: 400;">Any references to biochemical pathways, receptor interactions, or enzymatic processes are provided solely for informational and research-context purposes. This compound must be handled exclusively by qualified professionals in controlled laboratory environments in accordance with applicable regulations and safety guidelines.</span></p>
<p><span style="font-weight: 400;">Improper handling or use outside of controlled research settings is strictly prohibited.</span></p>
<h2><b>References</b></h2>
<ul>
<li style="font-weight: 400;" aria-level="1"><span style="font-weight: 400;">Martinez-Brito, D., de la Torre, X., Colamonici, C., Curcio, D., &amp; Botrè, F. (2019). 7-keto-DHEAmetabolism in humans. Pitfalls in interpreting the analytical results in the antidoping field. Drug testing and analysis, 11(11-12), 1629–1643. </span><a href="https://doi.org/10.1002/dta.2734" target="_blank" rel="noopener"><span style="font-weight: 400;">https://doi.org/10.1002/dta.2734</span></a></li>
<li style="font-weight: 400;" aria-level="1"><span style="font-weight: 400;">Jeyaprakash, N., Maeder, S., Janka, H., &amp; Stute, P. (2023). A systematic review of the impact of 7-keto-DHEA on body weight. Archives of gynecology and obstetrics, 308(3), 777–785. </span><a href="https://doi.org/10.1007/s00404-022-06884-8" target="_blank" rel="noopener"><span style="font-weight: 400;">https://doi.org/10.1007/s00404-022-06884-8</span></a><span style="font-weight: 400;"> </span></li>
</ul>
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