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5 Amino 1MQ 10MG $180.00Add to cart5 Amino 1MQ 10MG is a 10 milligram format of 5 amino 1 methylquinolinium, commonly referenced in research as a small molecule NNMT inhibitor. Researchers study it in the context of nicotinamide N methyltransferase activity, methylation related pathways, and cellular metabolism. Studies have examined NNMT inhibition in preclinical systems involving energy balance, adipocyte biology, and NAD related chemistry.
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5 Amino 1MQ 50MG $400.00Add to cart5 Amino 1MQ 50MG is a 50-milligram format of 5-amino-1-methylquinolinium (5-amino-1MQ), a small-molecule compound studied as an NNMT inhibitor in laboratory research. Studies have examined NNMT inhibition in relation to cellular methylation balance, NAD metabolism, and broader metabolic signaling pathways.
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5-Amino-1MQ 5MG $120.00Add to cart5-Amino-1MQ 5MG is a 5-milligram format of 5-Amino-1MQ, a small molecule commonly used in research as an NNMT inhibitor. Researchers study NNMT inhibition in the context of cellular NAD metabolism, methylation pathways, and metabolic regulation. Studies have examined 5-Amino-1MQ in preclinical systems focused on adipose biology and energy balance.
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Aod9604 5MG $119.00Add to cartAod9604 5MG is a 5-milligram format of AOD9604, a synthetic peptide analogue based on the human growth hormone fragment 176 191. Researchers study it for its potential role in metabolism and lipolysis related pathways in preclinical models. Studies have also examined AOD9604 in the context of adipose tissue signaling and body composition research.
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Cagrilintide + Semaglutide 10MG $220.00Add to cartCagrilintide + Semaglutide 10MG is a 10-milligram peptide pair combining cagrilintide, an amylin analogue, with semaglutide, a GLP-1 receptor agonist peptide. Researchers study these peptides in metabolic research, including appetite signaling and glucose regulation pathways. This paired format is used in experimental designs that examine co-agonism and complementary endocrine signaling.
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Cagrilintide + Semaglutide 5MG $125.00Add to cartCagrilintide + Semaglutide 5MG is a 5-milligram combined format of two peptide research compounds: cagrilintide (an amylin analogue) and semaglutide (a GLP 1 receptor agonist peptide analogue). Researchers study this pairing in preclinical and clinical research settings focused on appetite regulation and metabolic signaling. Studies have examined how amylin and GLP 1 pathways may interact when investigated together.
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Cagrilintide 10MG $198.00Add to cartCagrilintide 10MG is a 10-milligram format of cagrilintide, a long acting amylin analogue peptide designed to engage amylin receptor pathways. Researchers study cagrilintide in preclinical and translational settings involving appetite signalling, gastric emptying models, and metabolic regulation.
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Cagrilintide 5MG $125.00Add to cartCagrilintide 5MG is a 5-milligram format of cagrilintide, a long acting amylin analogue peptide engineered for extended receptor activity. Researchers study amylin analogues in the context of metabolic signaling, appetite regulation pathways, and gastric emptying models.
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Mazdutide 10MG $218.00Add to cartMazdutide 10MG is a 10-milligram format of mazdutide, a synthetic peptide investigated as a dual agonist at the GLP-1 receptor and glucagon receptor. Researchers study Mazdutide 10MG in metabolic research, including models examining energy balance, glucose regulation, and body weight pathways.
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Mazdutide 5MG $115.00Add to cartMazdutide 5MG is a 5-milligram format of mazdutide, a synthetic peptide studied as a dual GLP 1 and glucagon receptor agonist. Researchers have investigated it in preclinical and early clinical research related to metabolic regulation, energy balance, and glucose homeostasis. Its dual receptor profile makes it a common comparison point in incretin and glucagon pathway studies.
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Survodutide 10MG $99.00Add to cartSurvodutide 10MG is a 10-milligram format of survodutide, a synthetic dual agonist peptide designed to interact with GLP 1 and glucagon receptors. Researchers study it in preclinical and translational settings related to metabolic signaling, energy balance, and hepatic lipid pathways. Its dual receptor profile makes it a common comparator in incretin and glucagon axis research.
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