en · de · es · fr · pt
sr9009-notes.peptides4088.com › Info › Sr9009 Identity And Mechanism — Questions and Answers

Sr9009 Identity And Mechanism — Questions and Answers

By Editorial Desk · published 2026-01-03 · last reviewed 2026-01-22 · Info

This is a working overview of LC-MS, written for readers who want more than a one-paragraph summary but less than a textbook.

Reviewed 2026-01-22. Anything still debated is marked as such rather than presented as settled.

SR9009 Identity and Mechanism

SR9009 is a synthetic small molecule that acts on the nuclear receptors REV-ERBα and REV-ERBβ. These receptors are part of the circadian clock machinery and normally repress transcription of certain target genes. In laboratory research, SR9009 is used as a chemical tool to study how REV-ERB activity influences metabolism, inflammation, and daily biological rhythms. The compound is not an approved medicine, and its effects in humans remain largely uncharacterized. It is often described as an investigational agent rather than a therapeutic product.

REV-ERB proteins typically suppress gene expression by recruiting corepressor complexes to DNA response elements. SR9009 binds these receptors and strengthens that repressive action in cell-based assays. Studies in rodents have reported changes in lipid handling, mitochondrial function, and exercise capacity after treatment. Such findings are often cited as evidence for metabolic effects, but species differences and limited pharmacokinetic data make direct translation to humans uncertain. Researchers continue to examine which effects are robust and which depend on specific experimental conditions.

SR9009 is frequently discussed alongside other REV-ERB ligands, including synthetic agonists and natural heme-related molecules. Its selectivity for REV-ERB over related nuclear receptors has been measured in binding and reporter assays, though off-target activity at higher concentrations is possible. The compound is prohibited in sport by the World Anti-Doping Agency, and it is not approved for any medical use in major jurisdictions. Products sold online may be labeled as research chemicals, and their identity and purity are not guaranteed by regulatory review.

Identity, Handling, and Regulation

Handling practices for SR9009 focus on minimizing degradation and contamination. The solid is generally stored desiccated at or below -20 °C, protected from light and moisture. Stock solutions are often prepared in dimethyl sulfoxide or ethanol, then aliquoted to avoid repeated freeze–thaw cycles. Aqueous solubility is low, so formulations for animal studies may require cosolvents or suspending agents. Personnel should follow institutional chemical safety procedures, because toxicological data for humans are incomplete.

Regulatory status varies by country and intended use. Major drug agencies have not granted marketing authorization for SR9009 as a medicine, and it is not listed as a controlled substance in many jurisdictions. It is often sold as a research chemical, a category that may fall outside pharmaceutical manufacturing rules. Buyers should verify local laws and supplier documentation, including certificates of analysis. The lack of standardized quality controls raises concerns about identity, purity, and actual content in products marketed online.

Sr9009 at a glance

PropertyValueNotes
Common nameSR9009Also marketed informally as Stenabolic
Chemical classSynthetic REV-ERB agonistBinds REV-ERBα and REV-ERBβ
Molecular formulaC24H30ClN3O4SApproximate molecular weight 492 g/mol
CAS Registry Number1379686-30-2Identifier for the parent compound
Regulatory statusNot approved for human useProhibited in sport by WADA

Background and Mechanism of SR9009

SR9009 is a synthetic small molecule studied as a REV-ERB agonist. REV-ERBα and REV-ERBβ are nuclear receptors that help regulate circadian rhythms and metabolic gene expression. The compound was identified in academic screening efforts to find synthetic ligands for these receptors. In cell and animal studies, SR9009 alters transcription of genes involved in lipid and glucose metabolism, and it can shift circadian behavior. It is not an approved therapeutic agent.

Mechanistically, SR9009 binds the ligand-binding domain of REV-ERBα/β and enhances recruitment of corepressor complexes. This represses target genes rather than activating them. Because REV-ERB proteins normally compete with ROR proteins at shared response elements, the net effect depends on tissue and timing. Researchers use SR9009 to probe how nuclear receptor signaling links the clock to metabolism, inflammation, and muscle biology. Findings are largely preclinical, and the precise contribution of each receptor subtype remains under study.

SR9009 is frequently discussed in fitness and research-chemical contexts, yet it has no approved medical indication. Regulatory agencies have not authorized it for human use, and it is not a standard prescription drug. Some sports organizations list it as a prohibited substance because of its potential performance-enhancing properties. Published human data are sparse, so claims about its effects in people often rely on animal models or anecdotal reports. Quality and identity of online materials can vary widely.

Related pages on this site

Detection, Regulation, and Misconceptions

Regulatory agencies have not approved SR9009 for human therapeutic use. It is typically sold as a research chemical with labels stating that it is not for human consumption. The World Anti-Doping Agency prohibits the substance in sport, generally under the category of non-approved substances. Customs and national laws may restrict importation, sale, or possession. Product quality and legal status can vary by country and vendor, and therapeutic claims are not permitted in regulated advertising because the compound lacks approval.

Several misconceptions surround SR9009. It is often described as a SARM, a steroid, or an exercise pill, but its known target is the REV-ERB receptor family. Rodent studies have examined exercise capacity and metabolic markers, yet human outcomes remain unproven. Oral bioavailability appears low in animals, and human pharmacokinetics are not well characterized. Online products may contain impurities or different compounds, so identity and purity testing are important for research use.

Analytical chemists detect SR9009 with liquid chromatography-tandem mass spectrometry, commonly abbreviated LC-MS/MS. Sample preparation may involve protein precipitation, liquid-liquid extraction, or solid-phase extraction before analysis. Laboratories can target the parent compound or its metabolites, depending on the matrix and the purpose of testing. Anti-doping methods require sensitive and specific assays because concentrations in biological samples can be low. Reference standards and validated methods are essential for reliable identification and quantification.

Background and Receptor Pharmacology

Regulatory and sporting contexts treat SR9009 as a prohibited substance in many elite competitions. Its presence on banned lists reflects concerns about performance enhancement and unknown long-term safety. Analytical chemists have developed methods to detect the parent compound and its metabolites in urine and blood. Literature discussions distinguish between in vitro potency, animal pharmacology, and anecdotal human reports. The latter are difficult to verify because products sold online may lack purity or contain different compounds.

SR9009 is a synthetic small molecule studied as an agonist of the nuclear receptors REV-ERBα and REV-ERBβ. These receptors help regulate circadian rhythms, lipid metabolism, and inflammatory gene expression. In cell and animal experiments, SR9009 alters transcription of clock-controlled genes and metabolic pathways. The compound is not a hormone and does not resemble classical steroid structures. Its activity depends on binding to the ligand-binding domain of REV-ERB, where it can modify corepressor recruitment.

Research interest in SR9009 grew from studies of circadian biology and metabolic disease. Preclinical reports describe effects on exercise capacity, muscle metabolism, and blood lipid levels in rodents, but these findings come from controlled laboratory settings. The compound has low oral bioavailability in animals, which limits systemic exposure after swallowing. Investigators often use injected routes in experiments to achieve measurable plasma concentrations. Human clinical data are sparse, no approved therapeutic product exists, and whether animal effects translate to humans remains an open question.

Background from the literature

Wood is a hygroscopic substance. It has the ability to take in or give off moisture in the form of vapour. Water contained in wood exerts vapour pressure of its own, which is determined by the maximum size of the capillaries filled with water at any time. If water vapour pressure in the ambient space is lower than vapour pressure within wood, desorption takes place. The largest-sized capillaries, which are full of water at the time, empty first. Vapour pressure within the wood falls as water is successively contained in smaller capillaries. A stage is eventually reached when vapour pressure within the wood equals vapour pressure in the ambient space above the wood, and further desorption ceases. The amount of moisture that remains in the wood at this stage is in equilibrium with water vapour pressure in the ambient space, and is termed the equilibrium moisture content or EMC (Siau, 1984). Because of its hygroscopicity, wood tends to reach a moisture content that is in equilibrium with the relative humidity and temperature of the surrounding air.

This time, South African ground forces struck three hundred kilometres north of the border to eliminate PLAN training camps at Bambi and Cheraquera. On that occasion, the SADF killed 70 PLAN insurgents and destroyed several small caches of arms. PLAN learned of the attack in advance and had nearly completed its withdrawal when the SADF arrived; the insurgents fought a brief delaying action rather than attempt to defend their bases. The air war over Angola expanded with the ground fighting. FAPLA's modest air force, consisting of a handful of transports and a few MiG-21s, maintained a large base at Menongue. During Protea and Daisy the SADF scrambled its own fighters to overfly the base during ground operations and prevent the FAPLA aircraft from taking off. The Soviets had begun training Angolan MiG pilots, but in the meantime Cubans shouldered the burden of the air war in Angola, flying in support of both FAPLA and PLAN. In November 1981 a MiG-21MF with a Cuban pilot was shot down by South African Mirage F1CZs over the Cunene River. The Mirages reportedly downed a second MiG in October 1982, however this second shootdown has been disputed by Cuban sources. The expulsion of FAPLA from most of Cunene Province marked a revival of fortunes for Jonas Savimbi and his rump UNITA movement, which was able to seize undefended towns and settlements abandoned in the wake of Operations Protea and Daisy. Savimbi focused on rebuilding his power base throughout southeastern Angola while FAPLA and its Cuban allies were otherwise preoccupied fighting the SADF.

multicellular Composed of more than one cell. The term is used especially to describe organisms or tissues consisting of many cells descendant from the same original parent cell which work together in an organized way, but may also describe groups of nominally single-celled organisms such as protists and bacteria which live symbiotically with each other in large colonies. Contrast unicellular.

Greek colonies established on the Black Sea coast in the 7th century BC became important centres of commerce with the local tribes. Among the native peoples, Herodotus listed the Getae of the Lower Danube region, the Agathyrsi of Transylvania and the Syginnae of the plains along the river Tisza at the beginning of the 5th century BC. Centuries later, Strabo associated the Getae with the Dacians who dominated the lands along the southern Carpathian Mountains in the 1st century BC. Burebista was the first Dacian ruler to unite the local tribes. He also conquered the Greek colonies in Dobruja and the neighbouring peoples as far as the Middle Danube and the Balkan Mountains between around 55 and 44 BC. After Burebista was murdered in 44 BC, his kingdom collapsed. The Romans reached Dacia during Burebista's reign and conquered Dobruja in 46 AD. Dacia was again united under Decebalus around 85 AD. He resisted the Romans for decades, but the Roman army defeated his troops in 106 AD. Emperor Trajan transformed Banat, Oltenia and the greater part of Transylvania into a new province called Roman Dacia, but Dacian, Germanic and Sarmatian tribes continued to dominate the lands along the Roman frontiers. The Romans pursued an organised colonisation policy, and the provincials enjoyed a long period of peace and prosperity in the 2nd century. Scholars accepting the Daco-Roman continuity theory—one of the main theories about the origin of the Romanians—say that the cohabitation of the native Dacians and the Roman colonists in Roman Dacia was the first phase of the Romanians' ethnogenesis.

Sources: en.wikipedia.org

Further detail

Pseudohypertrophy, or false enlargement, is an increase in the size of an organ due to infiltration of a tissue not normally found in that organ. It is commonly applied to enlargement of a muscle due to infiltration of fat or connective tissue, famously in Duchenne muscular dystrophy. This is in contrast with typical muscle hypertrophy, in which the muscle tissue itself increases in size. Because pseudohypertrophy is not a result of increased muscle tissue, the muscles look bigger but are actually atrophied and thus weaker. Pseudohypertrophy is typically the result of a disease, which can be a disease of muscle or a disease of the nerve supplying the muscle. Causes of pseudohypertrophy include muscle diseases: dystrophinopathies, limb-girdle muscular dystrophies, metabolic myopathy, Dystrophic myotonias, Non-dystrophic myotonias, endocrine disorders, parasitic muscle conditions, amyloid and sarcoid myopathy, and granulomatous myositis. Neurological causes include radiculopathy, poliomyelitis, Charcot-Marie-Tooth disease, spinal muscular atrophy. In pseudohypertrophy where the atrophied muscle tissue has been infiltrated by fat tissue, upon palpitation the seemingly large muscles feel doughy. Not all muscles infiltrated by fat or other tissue are pseudohypertrophic. In muscular steatosis, sometimes the muscles may appear a normal or a slender size, even though the atrophied muscle has been infiltrated with fat tissue, such as the calf muscles in Bethlem myopathy 1.

Sedimentation is one of the most important main wastewater treatment procedures. Gravity settling is a method of separating particles from a fluid. The particle in suspension remains stable in quiescent conditions due to the decrease in water velocity throughout the water treatment process, following which the particles settle by gravitational force. For solids separation that is the removal of suspended solids trapped in the floc. Filtration is the technique of removing pollutants based on their particle size. Pollutant removal from waste water permits water to be reused for a variety of purposes. The types of filters used in the procedure differ depending on the contaminants present in the water. Particle filtration and Membrane filtration are the two main forms of waste water filtration. Dissolved air flotation (Degasification) is the process of removing dissolved gases from a solution. Henry's law states that the amount of dissolved gas in a liquid is proportionate to the partial pressure of the gas. Degasification is a low-cost method of removing carbon dioxide gas from waste water that raises the pH of the water by removing the gas. Deaerator is used to reduce oxygen and nitrogen in boiler feed water applications.

=== Supplementation === Patients are recommended to take folic acid and vitamin B12 supplement even if levels are normal when they are on pemetrexed therapy. (In clinical trials for mesothelioma, folic acid and B12 supplementation reduced the frequency of adverse events.) It is also recommended for patients to be on a glucocorticoid (e.g. dexamethasone) on the day prior, day of, and day after pemetrexed infusion to avoid skin rashes.

Sources: en.wikipedia.org

Supporting material

Ordinance No. 46 (full title: Abolition of the Provinces in the British Zone of the Former State of Prussia and Reconstitution thereof as Separate Länder), effective 23 August 1946, was an ordinance issued by the British Military Government (CCG/BE) in the British Zone of Allied-occupied Germany by which, among others, the Prussian Province of Schleswig-Holstein became the State of Schleswig-Holstein, and the Province of Hanover turned into the State of Hanover.

In 1936, Florey received a letter from Hilda stating that their mother Bertha had terminal cancer, so he arranged to travel to Australia with Ethel, Paquita and Charles during the summer break. They travelled on the SS Orsova to Melbourne, where they were met by Bertha, Charlotte, Hilda, Valetta and Hilda's daughter Joan Gardner. In addition to spending time with his family, he visited Peter MacCallum at his laboratory. MacCallum introduced Florey to Roy Douglas (Pansy) Wright, an experimental physiologist, and they arranged for Wright to come to Oxford the following year to assist Florey and Jennings with their work on mucus secretion. Florey then joined Ethel and the children in Adelaide. The family returned to Oxford in October. Bertha died on 27 November. Henceforth, Florey would lead an interdisciplinary team in an attack on a particular problem. Each member of the team tackled a particular aspect in their own way, with simultaneous research along different lines building up a complete picture. This was a manner of collaboration that was practically unknown in the UK at the time. However, the team members, including Florey, all worked on multiple projects at the same time. Florey was strict with his own collaborators, but gave considerable latitude to those working on other aspects of a project. He did not hold team meetings, although he encouraged team members to discuss issues with himself and each other, and he dropped by each laboratory nearly every day to view progress and provide suggestions. The first such project was an investigation of lymphocytes.

Altria, like other tobacco companies, has invested in science and medical companies which develop and produce medical products for conditions caused or aggravated by smoking. As of 2024, Altria's three medical subsidiaries included the following: Cronos group (maker of recreational cannabis), Lexaria Bioscience (Developer of proprietary drug delivery technology, DehydraTECH, to improve active pharmaceutical ingredients entrance into the bloodstream) and Micreos (biotech company focused on discovering and developing recombinant proteins for chronic dermatology and oncology conditions). It has also designed and marketed electronic cigarettes. Altria launched the MarkTen and Green Smoke brands. Both of these were discontinued in December 2018. The company returned to this market through the acquisition of NJOY.

In the early years of using the technique, it was understood that it depended on the atmospheric 14C/12C ratio having remained the same over the preceding few thousand years. To verify the accuracy of the method, several artefacts that were datable by other techniques were tested; the results of the testing were in reasonable agreement with the true ages of the objects. Over time, however, discrepancies began to appear between the known chronology for the oldest Egyptian dynasties and the radiocarbon dates of Egyptian artefacts. Neither the pre-existing Egyptian chronology nor the new radiocarbon dating method could be assumed to be accurate, but a third possibility was that the 14C/12C ratio had changed over time. The question was resolved by the study of tree rings: comparison of overlapping series of tree rings allowed the construction of a continuous sequence of tree-ring data that spanned 8,000 years. (Since that time the tree-ring data series has been extended to 13,900 years.) In the 1960s, Hans Suess was able to use the tree-ring sequence to show that the dates derived from radiocarbon were consistent with the dates assigned by Egyptologists. This was possible because although annual plants, such as corn, have a 14C/12C ratio that reflects the atmospheric ratio at the time they were growing, trees only add material to their outermost tree ring in any given year, while the inner tree rings don't get their 14C replenished and instead start losing 14C through decay. Hence each ring preserves a record of the atmospheric 14C/12C ratio of the year it grew in.

Sources: en.wikipedia.org

Frequently asked questions

What is SR9009?

SR9009 is a synthetic research compound that binds and modulates the nuclear receptors REV-ERBα and REV-ERBβ. It is used in laboratory studies of circadian biology and metabolism, not as an approved medicine. It is also known by the informal name Stenabolic.

Is SR9009 approved for human use?

No. SR9009 has not been approved as a therapeutic drug in the United States, European Union, or other major markets. Human safety and efficacy data are very limited. Its presence in consumer products does not imply regulatory approval.

Why is SR9009 banned in sport?

The World Anti-Doping Agency lists SR9009 as a prohibited substance because it can alter gene expression and metabolic pathways relevant to performance. The ban applies at all times, not only during competition. Detection relies on laboratory methods such as mass spectrometry.

How is SR9009 usually analyzed?

Liquid chromatography–mass spectrometry is common for identity and purity checks. High-performance liquid chromatography with ultraviolet detection can also be used. Both methods require a suitable reference standard.

Network