BonesLabsBlog

BonesLabs Blog

Research Articles & Lab Insights

Updates on our supply, methodology references, and notes from the bench — written by the BonesLabs team for the research community.

Showing 37-54 of 95 posts | page 3/6

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Research Article

9-ME-BC

9-Me-BC (9-Methyl-β-carboline): A β-Carboline Research Compound in Dopaminergic and Neuroprotection Studies Research summary. 9-Me-BC (9-methyl-β-carboline) is a small-molecule research compound from the β-carboline alkaloid family. It is not a peptide but is included alongside peptides in research-supplier catalogues for its preclinical activity in dopaminergic neuroscience research. The β-carboline family is biologically heterogeneous — some members […]

BonesLabs
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Research Article

N-Acetyl-Semax-Amidate

N-Acetyl Semax Amidate: A Stabilised ACTH(4-10)-Derived Heptapeptide Research summary. N-Acetyl Semax Amidate is a chemically protected analogue of Semax, a synthetic heptapeptide originally developed in Russia as an analogue of adrenocorticotropic hormone (ACTH) fragment 4-10. The N-acetyl C-amide modifications cap both peptide termini, extending stability against aminopeptidase and carboxypeptidase clearance and producing an analogue with […]

BonesLabs
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Research Article

N-Acetyl-Selank-Amidate

N-Acetyl Selank Amidate: A Stabilised Analogue of the Tuftsin-Derived Russian Anxiolytic Peptide Research summary. N-Acetyl Selank Amidate is a chemically protected analogue of Selank, a heptapeptide developed at the Russian Academy of Medical Sciences as a synthetic analogue of the immunomodulatory peptide tuftsin. The N-acetyl C-amidate modifications cap both peptide termini, blocking aminopeptidase and carboxypeptidase […]

BonesLabs
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Research Article

N-Acetyl-Epithalon-Amidate

N-Acetyl Epithalon Amidate: A Stabilised N-Terminal-Acetylated Analogue of the AEDG Tetrapeptide Research summary. N-Acetyl Epithalon Amidate is a chemically modified analogue of the Khavinson tetrapeptide Epithalon (Ala-Glu-Asp-Gly, AEDG). It is generated by N-terminal acetylation and C-terminal amidation of the parent sequence — modifications intended to extend metabolic stability and reduce exopeptidase clearance compared with the […]

BonesLabs
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Research Article

Mezdutide

Mezdutide (Mazdutide, IBI362): A GLP-1/Glucagon Dual Receptor Agonist in Late-Stage Metabolic Research Research summary. Mezdutide (also written mazdutide; development codes IBI362, OXM3) is an investigational dual agonist peptide that activates both the glucagon-like peptide-1 (GLP-1) receptor and the glucagon receptor. It is being developed by Innovent Biologics, originally licensed from Eli Lilly's oxyntomodulin-analogue programme. Within […]

BonesLabs
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Research Article

Melanotan-2

Melanotan 2 (MT-II): A Cyclic Melanocortin Receptor Agonist Studied in Pigmentation, Appetite, and Sexual-Behaviour Models Research summary. Melanotan 2 (MT-II) is a synthetic cyclic heptapeptide analogue of α-melanocyte-stimulating hormone (α-MSH). It was developed in the 1980s at the University of Arizona during a research programme exploring melanocortin receptor pharmacology and photoprotective pigmentation. Compared with native […]

BonesLabs
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Research Article

Lemon-Bottle

Lemon Bottle: An Injectable Lipolytic Formulation in the Aesthetic-Research Landscape Research summary. Lemon Bottle is a marketed injectable lipolytic formulation positioned for localised subcutaneous adipose contour refinement. Promotional materials describe a multi-component blend of riboflavin (vitamin B2), lecithin (a phospholipid fraction), and bromelain (a proteolytic enzyme complex), and the product is typically framed as a […]

BonesLabs
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Research Article

KPV-Alpha-MSH

KPV: The C-Terminal Tripeptide of α-MSH as a Research Anti-Inflammatory Research summary. KPV (lysine-proline-valine) is the C-terminal tripeptide fragment of α-melanocyte-stimulating hormone (α-MSH) and corresponds to ACTH(11–13). Despite its minimal three-residue size, KPV retains a substantial portion of the anti-inflammatory activity of the parent α-MSH while lacking the pigment-inducing activity of the larger peptide. The […]

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