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Looking for 465-16-7 / Oleandrin API manufacturers, exporters & distributors?

Oleandrin manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Oleandrin 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 Oleandrin manufacturer or Oleandrin supplier for your needs.

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

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

API | Excipient name

Oleandrin

Synonyms

Foliandrin, Folinerin, Neriolin, Neriostene, 465-16-7, Corrigen

Cas Number

465-16-7

Unique Ingredient Identifier (UNII)

II95UDU7I4

About Oleandrin

Oleandrin is a lipid soluble cardiac glycoside with potential antineoplastic activity. Upon administration, oleandrin specifically binds to and inhibits the alpha3 subunit of the Na/K-ATPase pump in human cancer cells. This may inhibit the phosphorylation of Akt, upregulate MAPK, inhibit NF-kb activation and inhibit FGF-2 export and may downregulate mTOR thereby inhibiting p70S6K and S6 protein expression. All of this may lead to an induction of apoptosis. As cancer cells with relatively higher expression of the alpha3 subunit and with limited expression of the alpha1 subunit are more sensitive to oleandrin, one may predict the tumor response to treatment with lipid-soluble cardiac glycosides such as oleandrin based on the tumors Na/K-ATPase pump protein subunit expression. Overexpression of the alpha3 subunit in tumor cells correlates with tumor proliferation.

Oleandrin Manufacturers

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

Oleandrin Suppliers

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

Oleandrin GMP

Oleandrin 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 Oleandrin 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 Oleandrin GMP manufacturer or Oleandrin GMP API supplier for your needs.

Oleandrin CoA

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

Oleandrin CoA mostly includes findings from lab analyses of a specific batch. For each Oleandrin 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.

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