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Survodutide (10mg)

$230.00

Product Usage DisclaimerΒ 

This material is suppliedΒ exclusively as a laboratory research chemicalΒ forΒ in vitro scientific study. All descriptions and are providedΒ for informational and educational purposes only.

This compound isΒ not approvedΒ for human or animal consumption, injection, ingestion, inhalation, topical use, or any other biological application. It must be handled only by qualified, trained personnel in a properly equipped laboratory.

This product isΒ notΒ a drug, supplement, food, cosmetic, or therapeutic agent, and it may not be rebranded, repackaged, or marketed as any such item.Β Misuse, mislabeling, or unauthorized application is strictly prohibited.

Nothing on this website constitutes medical advice, professional guidance, or a recommendation of use.

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Description

Survodutide – Advanced Biochemical Mechanism Profile

(Dual GLP-1 / Glucagon Receptor Agonist; Peptide Research Compound)

Survodutide is a synthetic peptide designed to act as a co-agonist at both the glucagon receptor (GCGR) and glucagon-like peptide-1 receptor (GLP-1R).
Both receptors are class B GPCRs primarily coupled to Gs, producing adenylyl cyclase activation β†’ cAMP accumulation β†’ PKA signaling, alongside secondary ERK1/2 and PI3K-Akt cascades.


βœ… 1. Primary Molecular Targets

A. GLP-1 Receptor (GLP-1R) – Gs-coupled GPCR

Ligand binding causes:

  1. GsΞ± activation β†’ adenylyl cyclase

  2. ↑ cAMP

  3. PKA activation

  4. CREB phosphorylation

  5. Gene transcription changes in metabolic tissues


B. Glucagon Receptor (GCGR) – Gs-dominant GPCR

Activation leads to:

  • Adenylyl cyclase β†’ cAMP ↑

  • Regulation of glycogen metabolism enzymes

  • Secondary contributions from Gq/PLC/IP₃ in select cell systems


βœ… 2. Intracellular Signaling Pathways

A. cAMP / PKA / CREB (Primary Pathway)

  • cAMP accumulation activates PKA

  • PKA phosphorylates CREB

  • CREB binds cAMP-response elements (CREs) on metabolic and mitochondrial genes

Representative CREB-responsive targets:

  • PPARGC1A (PGC-1Ξ±)

  • NRF1, TFAM (mitochondrial biogenesis)

  • SLC2A4 (GLUT4)

  • PDK4


B. PI3K β†’ Akt Pathway

Triggered downstream of GLP-1R signaling:

  • PI3K activation β†’ Akt phosphorylation

  • Influences transcription of metabolic and stress-response genes

Measured targets in research systems:

  • FOXO1, GSK-3Ξ², SREBP-1c

  • BCL2, MCL1 (mitochondrial survival signaling)


C. MAPK / ERK1/2

Both GCGR and GLP-1R can signal through:

  • Ras β†’ Raf β†’ MEK β†’ ERK1/2

  • ERK nuclear translocation β†’ immediate-early gene expression

ERK-responsive genes:

  • FOS, JUN, EGR1

  • CCND1 (cell-cycle progression)


βœ… 3. Second Messenger Systems

Component Role in Survodutide Signaling
cAMP ↑ Central second messenger for both receptors
PKA Phosphorylates CREB, ion channels, metabolic enzymes
CREB Drives transcription of mitochondrial and metabolic genes
ERK1/2 Mitogenic and transcriptional responses
Ca²⁺ Can be elevated via GCGR-linked PLC/IP₃ pathways

βœ… 4. Enzymatic Targets and Metabolic Regulators

Survodutide signaling influences expression/activity of:

Glycogen metabolism enzymes

  • Glycogen synthase (GYS)

  • Glycogen phosphorylase (PYGL/PYGM)

Mitochondrial regulators

  • CPT1, ACADL, PGC-1Ξ±

Lipid & carbohydrate transport

  • SLC2A4 (GLUT4)

  • CD36

  • FABP family


βœ… 5. Gene Targets Commonly Monitored in Research

Category Example Genes
cAMP/CREB Axis CREB1, NR4A1, PPARGC1A (PGC-1Ξ±)
Mitochondrial Biogenesis NRF1, TFAM, COX genes
Glucose & Lipid Metabolism SLC2A4 (GLUT4), CPT1B, ACADL, PDK4
MAPK-Responsive FOS, JUN, EGR1, CCND1
Cell Survival / Stress BCL2, MCL1, SOD2

βœ… Mechanistic Summary

  • Dual GLP-1R and GCGR agonist

  • Activates Gs β†’ adenylyl cyclase β†’ cAMP β†’ PKA β†’ CREB

  • Secondary activation of ERK1/2 and PI3K/Akt

  • Drives transcription of metabolic, mitochondrial, and immediate-early genes in model systems


Research-Only Classification

Survodutide is supplied exclusively for in-vitro laboratory research.
Not approved for human or animal administration, therapeutic use, or any biological application outside controlled research environments.

Additional information

Weight N/A
Size

10 Mg