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Looking for 133514-43-9 / Avexitide API manufacturers, exporters & distributors?

Avexitide manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Avexitide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Avexitide manufacturer or Avexitide supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Avexitide manufacturer or Avexitide supplier.

PharmaCompass also assists you with knowing the Avexitide API Price utilized in the formulation of products. Avexitide API Price is not always fixed or binding as the Avexitide Price is obtained through a variety of data sources. The Avexitide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Avexitide

Synonyms

133514-43-9, Exendin-3 (9-39), Asp-leu-ser-lys-gln-met-glu-glu-glu-ala-val-arg-leu-phe-ile-glu-tr, P, -leu-lys-asn-gly-gly-pro-ser-ser-gly-ala-pro-pro-pro-ser-nh2, Exendin-3 (9-39) amide

Cas Number

133514-43-9

About Avexitide

Avexitide is a truncated form of the glucagon-like peptide 1 receptor (GLP-1R) agonist exendin-4 peptide, with GLP-1 receptor (GLP-1R) antagonistic and GLP-1R-mediated signaling inhibiting activities. Upon administration, avexitide competitively binds to and inhibits the activity of GLP-1R, thereby inhibiting GLP-1/GLP-1R-mediated signaling. This antagonizes the glucagonostatic and the insulinotropic effects of GLP-1. By abrogating GLP-1-mediated simulation of insulin release and reduction of glucagon secretion after food intake, exendin 9-39 may be used to help study the potential effects of overproduction of GLP-1 on food intake, weight loss and glucose levels. GLP-1R, located on pancreatic beta cells, is overexpressed on certain tumor cell types. GLP-1 is a gastrointestinal (GI) and insulinotropic hormone that is released after a meal and plays a key role in the regulation of blood glucose levels.

Avexitide Manufacturers

A Avexitide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Avexitide, including repackagers and relabelers. The FDA regulates Avexitide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Avexitide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

Avexitide Suppliers

A Avexitide supplier is an individual or a company that provides Avexitide active pharmaceutical ingredient (API) or Avexitide finished formulations upon request. The Avexitide suppliers may include Avexitide API manufacturers, exporters, distributors and traders.

Avexitide GMP

Avexitide Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of Avexitide GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Avexitide GMP manufacturer or Avexitide GMP API supplier for your needs.

Avexitide CoA

A Avexitide CoA (Certificate of Analysis) is a formal document that attests to Avexitide's compliance with Avexitide specifications and serves as a tool for batch-level quality control.

Avexitide CoA mostly includes findings from lab analyses of a specific batch. For each Avexitide CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Avexitide may be tested according to a variety of international standards, such as European Pharmacopoeia (Avexitide EP), Avexitide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Avexitide USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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