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EPG Steel 75 Testosterone Boost

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EPG Steel 75 Testosterone Boost

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Product description

Acacetin (5,7-Dihydroxy-4-methoxyflavone) is an anti-aromatase and estrogenic activity blocker that is derived from the Damiana Plant. Aromotase is the essential part to estrogen synthesis in the human body and Acacetin has been shown by researchers to be the most effective natural substance to block the synthesis. Also by boosting testosterone and decreasing estrogen levels at the same time. It elevates the users natural myotropic state that helps you: Build Lean Muscle Mass - Burn and Reduce Fat Storage Leading to More Muscle Mass - Better Recovery and Increased Libido!...Fenugreek extract improves the testosterone levels by partially blocking the enzymes responsible for breakdown of testosterone. Users observed increase in testosterone levels. A reduction in body fat was observed that is directly linked to improved androgenic activity…Tongkat ali (botanical name – Eurycoma longifolia) extract enhances testosterone levels and improves sexual performance Tongkat Ali is a medicinal plant from Malaysia and Thailand used extensively for its aphrodisiac properties…Mucuna pruriens / 3,4-dihydroxyphenylalanine is a rich source of L-dopa metabolites including epinephrine and norepinephrine metabolites. These metabolites raise dopamine levels in the brain leading to the activation of sexual behavior, as well as an increase in the plasma testosterone levels…Epimedium or Horny goat weed has long been considered as an extremely potent aphrodisiac. The compound icariin that is found in epimedium works by relaxing muscles by increasing the nitric oxide levels and increasing the blood flow to the sexual organs, thereby increasing libido and desire…Tribulus Terrestris: A Herculean testosterone enhancer that stimulates the body's production of the luteinizing hormone, which promotes the production of testosterone… L –Citrulline: Is clinically proven to increase hardness and sexual activity. L-arginine: Supplementation improves nitric oxide-mediated vasodilation; however, it’s ha

EPG Steel 75 Testosterone Boost

Since Jan 2010, Selleckchem products have been cited in 415 studies from top scientific journals.

Thirteen Nobel Prize winners have published 44 articles with Selleck products.

THE NOBEL PRIZE

Michael Houghton

Won the Nobel Prize in Physiology or Medicine in 2020

Charles M. Rice

Won the Nobel Prize in Physiology or Medicine in 2020

  • Nat Commun, 2020, 11(1):1677
  • bioRxiv, 2020, 2020.10.09.334128
  • bioRxiv, 2020, 2020.01.20.910927
  • Viruses, 2019, 11(11)E1039
  • Cell Rep, 2018, 25(4):833-840.e3
  • Cell, 2018, 172(3):423-438.e25
  • Gastroenterology, 2017, 153(2):566-578.e5
  • Gastroenterology, 2016, 150(1):82-85.e4
  • Antimicrob, 2016, 60(6):3786-93
  • Nature, 2015, 524(7566):471-5
  • Antimicrob, 2015, 59(6):3482-92
  • J Virol, 2014, 88(20):12098-111

    PubMed: 25122776

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  • Antimicrob, 2014, 58(9):5386-94
  • J Virol, 2013, 87(13):7593-607
  • Nature, 2013, 501(7466):237-41
  • Nature, 2013, 99(1):6-11
  • Antimicrob, 2012, 56(10):5365-73

James P. Allison

Won the Nobel Prize in Physiology or Medicine in 2018

Michael Rosbash

Won the Nobel Prize in Physiology or Medicine in 2017

Eric Richard Kandel

Won the Nobel Prize in Physiology or Medicine in 2000

Brian K. Kobilka

Won the Nobel Prize in Chemistry in 2012

Robert Lefkowitz

Won the Nobel Prize in Chemistry in 2012

Aaron Ciechanover

Won the Nobel Prize in Chemistry in 2004

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Catalog No. Product Name Target Pathway Information
S8944 G150 Others Others G150 is a potent and highly selective human cyclic GMP-AMP synthase (h-cGAS) inhibitor with IC50 of 10.2 nM.
S8913 TH5487 Others Others TH5487 is a selective active-site inhibitor of 8-oxoguanine DNA glycosylase 1 (OGG1) with IC50 of 342 nM.
S8938 KGA-2727 SGLT GPCR & G Protein KGA-2727 is a potent, selective, high-affinity inhibitor of sodium glucose cotransporter 1 (SGLT1) with Ki of 97.4 nM and 43.5 nM for human SGLT1 and rat SGLT1, respectively. The selectivity ratios (Ki for SGLT2/Ki for SGLT1) of KGA-2727 are 140 (human) and 390 (rat). KGA-2727 exhibits antidiabetic efficacy in rodent models.
S8939 Mizagliflozin SGLT GPCR & G Protein Mizagliflozin is a novel, potent, selective sodium glucose co-transporter 1 (SGLT1) inhibitor with Ki of 27 nM for human SGLT1. The selectivity ratio (Ki value for human SGLT2/Ki value for human SGLT1) of mizagliflozin is 303. Mizagliflozin shows the potential use for the amelioration of chronic constipation.
S7013 Guadecitabine (SGI-110) Others Others Guadecitabine (SGI-110) is a next-generation hypomethylating agent whose active metabolite decitabine has a longer in-vivo exposure time than intravenous decitabine.
S8812 CM272 DNA Methyltransferase Epigenetics CM-272 is a novel first-in-class dual reversible inhibitor of G9a (GLP) and DNMTs with IC50 of 8 nM, 382 nM, 85 nM, 1200 nM, 2 nM for G9a, DNMT1, DNMT3A, DNMT3B, GLP, respectively. CM-272 prolongs survival in in vivo models of haematological malignancies by at least in part inducing immunogenic cell death.
S9729 Visomitin (SKQ1) Others Others INT-777 (S-EMCA) is a novel potent and selective TGR5 agonist with EC50 values of 0.18 μM, 3.9 μM and 1.45 μM for WT TGR5, TGR5(N76A) and TGR5(Y89F) respectively.
S8500 BAY1125976 Akt PI3K/Akt/mTOR BAY 1125976 is a selective allosteric AKT1/2 inhibitor,exhibits high efficacy on AKT signaling-dependent tumor growth in mouse models. BAY1125976 inhibits the activity of AKT1 (IC50 = 5.2 nM at 10 µM ATP and 44 nM at 2 mM ATP) and AKT2 (IC50 = 18 nM at 10 µM ATP and 36 nM at 2 mM ATP) very potently.Whereas BAY1125976 is almost inactive on AKT3 (IC50 = 427 nM at 10 µM ATP).
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Tags: kinase inhibitors, tyrosine kinase inhibitors, enzyme inhibitors, protein inhibitors, proteins kinase inhibitors, small molecules, phosphatase inhibitors