Survodutide

Survodutide features a designed peptide backbone containing hydrophobic, polar, and charged residues that modulate solubility and folding. Researchers evaluate its structure-activity behavior and conformational preferences. The sequence supports studies of receptor-ligand determinants. Applications include peptide engineering, structural optimization, and binding analysis.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
Survodutide(CAS 2805997-46-8)

CAT No: R2481

CAS No:2805997-46-8

Synonyms/Alias:Survodutide;2805997-46-8;GTPL13383;EX-A7878;BI456906;BI 456906;

Custom Peptide Synthesis
cGMP Peptide
  • Registration of APIs
  • CMC information required for an IND
  • IND and NDA support
  • Drug master files (DMF) filing
M.F/Formula
C192H289N47O61
M.W/Mr.
4232

Survodutide is a synthetic peptide compound designed as a dual agonist for both the glucagon and glucagon-like peptide-1 (GLP-1) receptors, positioning it as a highly valuable tool in metabolic and endocrinological research. As a member of the incretin mimetic class, Survodutide exhibits unique receptor-binding properties that enable the modulation of key metabolic pathways. Its structural design and dual receptor activity make it a significant subject for studies aiming to unravel the complex interplay between glucose homeostasis, energy expenditure, and lipid metabolism. The compound is particularly relevant for academic, pharmaceutical, and industrial laboratories investigating the molecular underpinnings of metabolic regulation and peptide-based signaling mechanisms.

Metabolic pathway elucidation: Survodutide is frequently employed in studies focused on dissecting the molecular mechanisms governing energy balance and glucose metabolism. By acting as a dual agonist at GLP-1 and glucagon receptors, it enables researchers to probe the coordinated effects of these signaling pathways on hepatic glucose production, insulin secretion, and peripheral energy utilization. Its use facilitates a deeper understanding of the crosstalk between pancreatic and hepatic systems, providing a robust platform for investigating the regulation of metabolic homeostasis under various physiological and pathological conditions.

Peptide receptor pharmacology: The compound serves as a sophisticated model for characterizing the pharmacodynamics and pharmacokinetics of dual-acting peptide agonists. Experimental applications include receptor binding assays, second messenger quantification, and downstream signaling analyses in cell-based and tissue systems. Survodutide's distinct profile allows for the comparative evaluation of receptor selectivity, efficacy, and potency, supporting the development of structure-activity relationship (SAR) models and guiding the rational design of next-generation incretin-based peptides.

Obesity and lipid metabolism research: In preclinical metabolic studies, Survodutide is utilized to explore the regulation of adiposity, lipid oxidation, and energy expenditure. Its dual activity enables the investigation of mechanisms underlying weight regulation, fat mobilization, and the browning of adipose tissue. Researchers leverage these properties to examine how simultaneous activation of GLP-1 and glucagon receptors influences lipid profiles, thermogenesis, and overall energy balance, thereby advancing the broader understanding of metabolic adaptation and obesity-related pathways.

Peptide synthesis and analog development: Survodutide is also valuable as a reference molecule in peptide chemistry and analog development. Its well-defined sequence and receptor specificity provide a template for the synthesis of novel peptide analogs with tailored pharmacological properties. Chemists and peptide engineers use it to benchmark synthetic strategies, optimize sequence modifications, and evaluate the impact of structural alterations on biological activity, stability, and receptor engagement.

Analytical method development: The compound is frequently incorporated into analytical workflows for the validation of peptide quantification and detection methods. It serves as a standard in liquid chromatography-mass spectrometry (LC-MS) and immunoassay platforms, aiding in the development and calibration of robust analytical techniques for peptide-based therapeutics. This application supports quality control, bioanalytical research, and the establishment of reproducible protocols for peptide quantification in complex biological matrices.

InChI
InChI=1S/C192H289N47O61/c1-12-103(6)157(186(295)221-122(170(279)227-134(83-113-88-203-119-48-34-33-47-117(113)119)177(286)223-128(77-101(2)3)173(282)219-126(66-70-153(261)262)172(281)232-140(97-242)183(292)210-104(7)160(197)269)51-37-40-75-201-146(252)90-205-147(253)91-206-165(274)138(95-240)215-149(255)93-208-166(275)139(96-241)214-148(254)92-204-144(250)68-64-127(189(298)299)213-145(251)53-31-23-21-19-17-15-13-14-16-18-20-22-24-32-54-151(257)258)237-181(290)132(79-109-43-27-25-28-44-109)226-179(288)136(86-155(265)266)228-168(277)120(49-35-38-73-193)216-162(271)106(9)211-161(270)105(8)212-167(276)123(52-41-76-202-191(198)199)217-171(280)125(65-69-152(259)260)220-178(287)135(85-154(263)264)229-174(283)129(78-102(4)5)222-175(284)130(81-111-55-59-115(247)60-56-111)224-169(278)121(50-36-39-74-194)218-184(293)141(98-243)233-176(285)131(82-112-57-61-116(248)62-58-112)225-180(289)137(87-156(267)268)230-185(294)142(99-244)234-188(297)159(108(11)246)238-182(291)133(80-110-45-29-26-30-46-110)231-187(296)158(107(10)245)236-150(256)94-207-164(273)124(63-67-143(196)249)235-190(300)192(71-42-72-192)239-163(272)118(195)84-114-89-200-100-209-114/h25-30,33-34,43-48,55-62,88-89,100-108,118,120-142,157-159,203,240-248H,12-24,31-32,35-42,49-54,63-87,90-99,193-195H2,1-11H3,(H2,196,249)(H2,197,269)(H,200,209)(H,201,252)(H,204,250)(H,205,253)(H,206,274)(H,207,273)(H,208,275)(H,210,292)(H,211,270)(H,212,276)(H,213,251)(H,214,254)(H,215,255)(H,216,271)(H,217,280)(H,218,293)(H,219,282)(H,220,287)(H,221,295)(H,222,284)(H,223,286)(H,224,278)(H,225,289)(H,226,288)(H,227,279)(H,228,277)(H,229,283)(H,230,294)(H,231,296)(H,232,281)(H,233,285)(H,234,297)(H,235,300)(H,236,256)(H,237,290)(H,238,291)(H,239,272)(H,257,258)(H,259,260)(H,261,262)(H,263,264)(H,265,266)(H,267,268)(H,298,299)(H4,198,199,202)/t103-,104+,105-,106-,107+,108+,118-,120-,121-,122+,123-,124-,125-,126+,127?,128+,129-,130+,131-,132-,133-,134+,135-,136-,137-,138+,139+,140+,141-,142-,157-,158-,159-/m0/s1
InChI Key
MEDXQFAHWBMVIM-YIUAJOCSSA-N

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