Cosyntropin acetate

Cosyntropin acetate is a peptide fragment enriched in aromatic, acidic, and basic residues that stabilize helical motifs. The sequence supports examination of folding transitions, peptide-receptor interfaces, and enzymatic processing. Researchers apply it to structural mapping and conformational exploration. Its acetate form improves handling consistency.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
Cosyntropin acetate(CAS 60189-34-6)

CAT No: R2217

CAS No:60189-34-6

Synonyms/Alias:Tetracosactrin acetate;60189-34-6;Tetracosactide acetate;Cosyntropin acetate;SCHEMBL563374;EX-A8106;FT35466;H-Ser-Tyr-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH;

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M.F/Formula
C138H214N40O33S
M.W/Mr.
2993.5
Sequence
One Letter Code:SYSMEHFRWGKPVGKKRRPVKVYP
Three Letter Code:H-Ser-Tyr-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH.CH3CO2H

Cosyntropin acetate, a synthetic polypeptide that mimics the biological activity of adrenocorticotropic hormone (ACTH), is widely recognized for its role in stimulating the adrenal cortex. As a derivative of the first 24 amino acids of natural ACTH, cosyntropin acetate exhibits high specificity for melanocortin 2 receptors, triggering the biosynthesis and release of glucocorticoids, mineralocorticoids, and androgenic steroids. Its stability and reproducibility make it a valuable tool in experimental protocols where endogenous ACTH may introduce variability. The compound is supplied as an acetate salt, enhancing its solubility and facilitating its use in a variety of in vitro and in vivo research applications. With its well-characterized mechanism of action and reliable performance, cosyntropin acetate is an essential reagent for researchers investigating endocrine function, adrenal physiology, and the broader field of peptide signaling.

Endocrine Research: Cosyntropin acetate is extensively utilized in studies exploring the regulation and function of the hypothalamic-pituitary-adrenal (HPA) axis. By providing a controlled stimulus for adrenal steroidogenesis, it enables researchers to dissect the feedback mechanisms and regulatory pathways that govern cortisol and aldosterone production. This application is particularly valuable in elucidating the molecular and cellular responses of adrenal cortical cells to trophic stimulation, supporting detailed investigations into hormonal signaling and adrenal gland physiology.

Adrenal Function Testing: In experimental models, cosyntropin or its acetate salt is frequently employed to assess adrenal responsiveness and steroidogenic capacity. By administering the compound and quantifying subsequent steroid hormone levels, scientists can evaluate the functional integrity of the adrenal cortex under various experimental conditions. This approach is instrumental in studies examining the impact of genetic modifications, environmental stressors, or pharmacological interventions on adrenal output, providing a robust and reproducible method for functional assessment.

Peptide Receptor Studies: The high receptor selectivity of cosyntropin acetate makes it an ideal probe for research into melanocortin receptor signaling. Investigators leverage its ability to activate specific receptor subtypes to map downstream signaling cascades, characterize receptor pharmacodynamics, and investigate receptor-ligand interactions. These studies contribute to a deeper understanding of the structure-function relationships within the melanocortin receptor family and inform the development of novel peptide-based therapeutics.

Steroidogenesis Mechanisms: Cosyntropin acetate serves as a potent inducer of steroid biosynthesis in cultured adrenal cells, enabling detailed analysis of the enzymes and regulatory factors involved in this complex process. Researchers use it to stimulate steroidogenic pathways, monitor gene expression changes, and identify key modulators of hormone synthesis. This application is central to advancing knowledge of adrenal biochemistry and the intricate control of steroid hormone production at the molecular level.

Pharmacological Research: The acetate salt of cosyntropin is employed in preclinical studies to investigate the effects of candidate drugs on adrenal gland function and peptide hormone signaling. By serving as a standardized stimulant, it allows for the evaluation of drug interactions with the HPA axis and the identification of compounds that modulate steroidogenic responses. This application supports drug discovery efforts targeting endocrine pathways and peptide hormone receptors.

Comparative Endocrinology: In addition to its use in mammalian systems, cosyntropin acetate is applied in comparative studies involving non-mammalian species to explore the conservation and divergence of ACTH-mediated signaling across taxa. Researchers utilize it to probe adrenal-like tissues, characterize evolutionary adaptations in steroidogenic mechanisms, and expand the understanding of peptide hormone function in diverse biological contexts. Through these varied applications, cosyntropin acetate continues to be an indispensable tool in advancing endocrine research, peptide pharmacology, and the molecular dissection of adrenal physiology.

InChI
InChI=1S/C136H210N40O31S.C2H4O2/c1-75(2)109(127(200)154-71-106(181)156-88(31-13-17-52-137)114(187)158-89(32-14-18-53-138)115(188)159-91(35-21-56-149-134(142)143)116(189)164-96(37-23-58-151-136(146)147)131(204)175-60-25-39-104(175)126(199)173-111(77(5)6)128(201)163-90(33-15-19-54-139)120(193)171-110(76(3)4)129(202)169-101(65-80-43-47-84(180)48-44-80)132(205)176-61-26-40-105(176)133(206)207)172-125(198)103-38-24-59-174(103)130(203)95(34-16-20-55-140)157-107(182)70-153-113(186)99(66-81-68-152-87-30-12-11-29-85(81)87)167-117(190)92(36-22-57-150-135(144)145)160-121(194)98(63-78-27-9-8-10-28-78)166-123(196)100(67-82-69-148-74-155-82)168-118(191)93(49-50-108(183)184)161-119(192)94(51-62-208-7)162-124(197)102(73-178)170-122(195)97(165-112(185)86(141)72-177)64-79-41-45-83(179)46-42-79;1-2(3)4/h8-12,27-30,41-48,68-69,74-77,86,88-105,109-111,152,177-180H,13-26,31-40,49-67,70-73,137-141H2,1-7H3,(H,148,155)(H,153,186)(H,154,200)(H,156,181)(H,157,182)(H,158,187)(H,159,188)(H,160,194)(H,161,192)(H,162,197)(H,163,201)(H,164,189)(H,165,185)(H,166,196)(H,167,190)(H,168,191)(H,169,202)(H,170,195)(H,171,193)(H,172,198)(H,173,199)(H,183,184)(H,206,207)(H4,142,143,149)(H4,144,145,150)(H4,146,147,151);1H3,(H,3,4)/t86-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,109-,110-,111-;/m0./s1
InChI Key
XDSGCNRPXJYVQS-GLMYKROOSA-N

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