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RAD140

One of the most popular SARMs known for its "dry" anabolic properties. .

$65.99

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  • Active Ingredient: RAD140
  • Strength: 15mg/ml
  • Each Bottle Contains: 30ml

📄 Short Description

Are you Looking for RAD140 for sale? at our store, you can easily buy RAD140 liquid. RAD140 is considered a very common SARM, which has shown to be a potent anabolic agent in clinical research.

✅ 3rd-Party Lab Tests  

Lab test date: 27/04/2024
Lab: Colmaric Analyticals
Speficiation: >98%
Result: 98%

Data on our Liquid RAD140 for Sale

Synonyms Testolone
Concentration 15mg per ml
Solvent USP Grade Polyethylene Glycol 400
Molar Mass 393.83 g·mol−1
CAS 1182367-47-0
Chemical Formula C20H16ClN5O2

This product is for laboratory research purposes only and is not approved by the FDA for human use. RAD140 is NOT a dietary supplement. Any information about its use in this product description refers to clinical research only. By ordering from this site, you agree to our terms of service.

Additional information about our RAD140

RAD140, also commonly known as Testolone, is one of several novel selective androgen receptor modulators (SARMs) that was initially studied and tested as an alternative to TRT (testosterone replacement therapy). It should not be interchanged with RAD 150, Testolone also known as TLB 150 which is an esterified form of the same compound. As with other SARMs, RAD140 binds directly and selectively to the androgen receptors (AR) thus it does not produce androgenic effects as similar substances like testosterone  DHT or other anabolic compounds do.

A study on male monkeys checked the anabolic effects after 28 days of RAD 140 at three different dosages of 0.01mg/kg, 0.1mg/kg, and 1mg/kg per day. RAD 140 demonstrated an excellent affinity for AR (Ki = 7 nM), higher even than DHT and most anabolic steroids. As general knowledge, the affinity for the androgen receptor (AR) for Testosterone in a recent preclinical model was 29 nM, and 10 nM for DHT. In the same study, an average weight gain of 10% was observed in both the 0.1mg/kg/day group and the 1mg/kg/day group, demonstrating a quantity response curve that has peaked and showed no additional benefit with increased dosages. Also, an effect on body fat mass in either group was not established consistently, nonetheless, it did show muscle mass increased in the 0.1 and 1mg/kg/day groups. No noteworthy increases in liver enzymes or prostate weight were reported in either test group implying a high level of selectivity for androgen receptors (AR) in muscle tissue [1].

Why You Should Buy RAD140 From Our Store?

By choosing to buy SARMs at our store Sarmful.com you are investing in the highest quality ingredients, that means minimum 98% (and often higher) pure compounds tested and certified by accredited US third party labs- visit out tests page for more info.

More benefits:

  • Each Bottle includes a graduated 1mL glass pipette for convenient measurement.
  • SARMS are sold in glass bottles with UV resistance which minimizes degradation and BPA leaching from plastics.
  • Consistent dosing with less than 5% in variance in concentration.
  • We Bottle our SARMS in the US and send them directly from the US.
  • We pack, store and ship them in a securely way to avoid evaporation during storage and transit
  • Each bottle contains a seal for tamper proof avoidance.
  • Our SARMS are suspended in USP grade (the highest grade) PEG400
  • Transparent business methods without dodgy product descriptions and payment methods

The History of RAD140

RAD140 was developed in 2010 as a SARM that selectively targets and blocks DHT without affecting testosterone. Initially, Radius Health developed the compound. Radius Health is a health care company specializing in the development and commercialization of novel therapies in the field of musculoskeletal health.

RAD140 has shown potential as a treatment option for conditions revolving around bone loss and muscle wasting. As a result, in 2020 it was licensed to Ellipses Pharmaceuticals to try and further its development for some of these use cases.

RAD140 Neuro Benefits

In a study conducted in 2014 which investigated the neuroprotective benefits of RAD 140 on cultured neurons and male rats that were lesioned with kainate, divided into two parts (in vitro and another in vivo through animal testing). The in vitro results showed that RAD 140 was able to prevent cell death and restore mitochondrial membrane potential, demonstrating that it may offer neuroprotection benefits much like those of testosterone and other androgens. The in vivo phase of the same study checked the efficacy of RAD 140 on male rats with kainate-induced seizures and showed a significant reduction in seizures. Overall, this study has shown that RAD140 is capable of providing some neuroprotection both in vitro and in vivo [2].

A different study on rats in which a test group was treated with 3 mg/kg RAD140 was able to mimic the same level of muscle tissue growth as the group treated with a 3 times lower dosage of 1 mg/kg Testosterone, with about half of the androgenic activity in the prostate. it also found that RAD140 had neuroprotective effects that may combat Alzheimer’s disease and similar disorders, and may even surprisingly be safer than conventional testosterone therapy [3].

In some other studies, different androgens have demonstrated clinical significance in preventing neuronal death and improving cognitive function in Alzheimer’s Disease (AD), mainly by a nongenomic mechanism of the AR.  Rapid phosphoinositide 3-kinase/Akt signaling, which is activated by androgens, regulates the expression of proteins closely linked to the death of cells such as bax, seladin 1, survivin, XIAP, and bcl-xl [8]. Interestingly enough, these androgens can also maintain the health and wholeness of neurons thus improving boost function [9]. This same study also demonstrated that Aβ impairs synaptic structure and function of hippocampal neurons which can be reversed by androgen administration resulting in improved cognitive function in animal models with Alzheimer’s Disease. Sadly though, the exact mechanisms are not yet fully understood, but androgen’s action of inhibiting Aβ-induced apoptosis appears to play a significant role [9].

RAD140 and Breast Cancer

A study conducted not too long ago in 2017 investigated the effects of RAD 140 on active cells of breast cancer. This study checked the efficacy of RAD140 in stopping the growth of breast cancer cells that were positive for both androgen receptors (ARs) and estrogen receptors (ERs). The study results demonstrated that in both in vivo and in vitro models of AR/ER  breast cancer, RAD140 was able to significantly diminish the growth and spread of metastases of active breast cancer cells without disrupting their regular cell cycle, indicating it may be a promising therapy for treating such cancers types in the future [4]. Furthermore, the same study also demonstrated that RAD140 had specific different mechanisms of action from those of anti-estrogens and aromatase inhibitors, which implies that it could provide an additional therapeutic approach to treating hormone-sensitive breast cancers. All in all, this study has shown that RAD140 could be a potential option for AR/ER-positive breast cancer but more data is needed to determine its safety relative to other methods utilized at this time.

RAD140 Side Effects

RAD 140 does not have the same side effect profile as some comparable products. However, it has been known to cause a few side effects in some subjects. These can include increased aggression, hormonal disorders, nausea, headache, acne, and hair loss.

One study from 2010 found that after 28 days of testing RAD140, testosterone levels in all three test groups was suppressed to approximately 200−300 ng/dL, with similar suppression outcomes in all groups. Although testosterone levels were significantly different for only the 0.01 mg/kg group (p < 0.05) [6].

Another study conducted on a single case only indicated drug-induced liver injury following after 11 months of the use of an anti-depressant, as well as intermittent use of RAD 140 and LGD-4033. The problems of this study however are the fact that it includes only one test subject (no control group), 11 months of consistent antidepressant use, the quality and quantity of SARMs used were not monitored, and additional comorbidities were not investigated [7]. Several other case studies exist indicating the potential for selective androgen receptor modulators to contribute to liver injury but none involve a significant group sample size or test controls to date, thuss hard to draw any meaningful conclusion.

In rat studies, there were some slight changes in liver enzymes that were not considered to be clinically significant. Overall, studies in rats have shown that RAD 140 appears to be safer than testosterone replacement therapy.

 

The Half-Life of RAD140

The half-life of RAD 140 is about  44.7 hours [5], meaning that a single test keeps its effects going the entire day-2 days. This makes it one of the longer-lasting SARMs out there.

Where Can You Find RAD140 For Sale

RAD 140 is available for sale as a medical research compound at specialty retailers that sell other types of SARMs.

RAD140 Chemical Structure and Chemical Properties

RAD140 Chemical Structure

RAD140 Chemical Structure

  • Synonyms: 2-chloro-4-({(1R,2S)-1-[5-(4-cyanophenyl)-1,3,4-oxadiazol-2-yl]-2-hydroxypropyl}amino)-3-methylbenzonitrile
  • Empirical Formula: C20H16ClN5O2
  • SMILES: ClC1=C(C#N)C=CC(=C1C)N[C@H]([C@H](C)O)C2=NN=C(O2)C3=CC=C(C=C3)C#N
  • International Chemical Identifier: InChI=1S/C20H16ClN5O2/c1-11-16(8-7-15(10-23)17(11)21)24-18(12(2)27)20-26-25-19(28-20)14-5-3-13(9-22)4-6-14/h3-8,12,18,24,27H,1-2H3/t12-,18+/m0/s1Key:XMBUPPIEVAFYHO-KPZWWZAWSA-N
  • CAS: 1182367-47-0

RAD140 Solubility

  • Water Solubility: RAD140 is not soluble in water.
  • DMSO: soluble.
  • Ethanol: soluble
  • Propylene glycol: soluble

Other properties

  • RAD140 smell: Pure RAD140 has a mild odor.
  • Appearance (raw powder): Off-white fine powder.

The Summary of RAD 140

RAD 140 has been shown in studies to build muscle mass in primates with less of a side effect profile than most other SARMs. It is still a relatively new compound and more research is needed. Its research for use as an androgen replacement therapeutic could produce some interesting breakthroughs in upcoming animal lab experiments.

Abuse Warning

SARMs should only be used under the direct supervision and direction of a trained and licensed medical doctor or a designated research authority. Sarmful strongly discourages the use of SARMs for performance enhancement in fields of various sports such as bodybuilding and achievement sports, etc.

S4 is an investigational compound still undergoing research and NOT yet FDA approved, nor it is a dietary supplement. Sarmful is solely a research chemical supplier specializing in sourcing and quality control. We are not medical doctors. Sarmful discourages strongly against “bro science” and peer consensus when making decisions about human health.

We do not encourage or condone consumer use of SARMs products, they are for research purposes only.

References and Further Read

  1. Miller, C. P., Shomali, M., Lyttle, C. R., O’Dea, L. S., Herendeen, H., Gallacher, K., Paquin, D., Compton, D. R., Sahoo, B., Kerrigan, S. A., Burge, M. S., Nickels, M., Green, J. L., Katzenellenbogen, J. A., Tchesnokov, A., & Hattersley, G. (2010). Design, Synthesis, and Preclinical Characterization of the Selective AR Modulator (SARM) RAD140. ACS medicinal chemistry letters2(2), 124–129. GW 501516 https://pubs.acs.org/doi/10.1021/ml1002508
  2. Jayaraman, A., Christensen, A., Moser, V. A., Vest, R. S., Miller, C. P., Hattersley, G., & Pike, C. J. (2014). Selective AR modulator RAD140 is neuroprotective in cultured neurons and kinate-lesioned male rats. Endocrinology155(4), 1398–1406. https://doi.org/10.1210/en.2013-1725
  3. D. K. Hamson, S. R. Wainwright, J. R. Taylor, B. A. Jones, N. V. Watson, L. A. M. Galea, Androgens Increase Survival of Adult-Born Neurons in the Dentate Gyrus by an Androgen Receptor-Dependent Mechanism in Male Rats, Endocrinology, Volume 154, Issue 9, 1 September 2013, Pages 3294–3304, https://doi.org/10.1210/en.2013-1129
  4. Yu, Ziyang et al. “Selective Androgen Receptor Modulator RAD140 Inhibits the Growth of Androgen/Estrogen Receptor–Positive BC Models with a Distinct Mechanism of Action.” MK 677 Clinical Cancer Research 23 (2017): 7608 – 7620.
  5. LoRusso P, Hamilton E, Ma C, Vidula N, Bagley RG, Troy S, Annett M, Yu Z, Conlan MG, Weise A. A First-in-Human Phase 1 Study of a Novel Selective AR Modulator (SARM), RAD140, in ER+/HER2- Metastatic BC. Clin Br Cancer. 2022 Jan;22(1):67-77. doi: 10.1016/j.clbc.2021.08.003. Epub 2021 Aug 20. PMID: 34565686.
  6. Miller, C. P., Shomali, M., Lyttle, C. R., O’Dea, L. S., Herendeen, H., Gallacher, K., Paquin, D., Compton, D. R., Sahoo, B., Kerrigan, S. A., Burge, M. S., Nickels, M., Green, J. L., Katzenellenbogen, J. A., Tchesnokov, A., & Hattersley, G. (2010). Design, Synthesis, and Preclinical Characterization of the Selective AR Modulator (SARM) RAD140. ACS medicinal chemistry letters2(2), 124–129 https://doi.org/10.1021/ml1002508
  7. Flores JE, Chitturi S, Walker S. Drug-Induced Liver Injury by Selective Androgenic Receptor Modulators. Hepatol Commun. 2020 Jan 3;4(3):450-452. doi: 10.1002/hep4.1456. PMID: 32140660; PMCID: PMC7049679.
  8. Bing L, Wu J, Zhang J, Chen Y, Hong Z, Zu H. DHT inhibits the Aβ25-35-induced apoptosis by regulation of seladin-1, survivin, XIAP, bax, and bcl-xl expression through a rapid PI3-K/Akt signaling in C6 glial cell lines. Neurochem Res. 2014;40(1):41–48.
  9. Huo DS, Sun JF, Zhang B, Yan XS, Wang H, Jia JX, Yang ZJ. Protective effects of testosterone on cognitive dysfunction in Alzheimer’s disease model rats induced by oligomeric beta amyloid peptide 1–42. J Toxicol Environ Health A. 2016;79(19):856–863.
RAD140

$65.99

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