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Looking for 915019-65-7 / Dactolisib API manufacturers, exporters & distributors?

Dactolisib manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Dactolisib

Synonyms

915019-65-7, Nvp-bez235, Bez235, Nvp-bez 235, Bez-235, 2-methyl-2-(4-(3-methyl-2-oxo-8-(quinolin-3-yl)-2,3-dihydro-1h-imidazo[4,5-c]quinolin-1-yl)phenyl)propanenitrile

Cas Number

915019-65-7

Unique Ingredient Identifier (UNII)

RUJ6Z9Y0DT

About Dactolisib

Dactolisib is an orally bioavailable imidazoquinoline targeting the phosphatidylinositol 3 kinase (PI3K) and the mammalian target of rapamycin (mTOR), with potential antineoplastic activity. Dactolisib inhibits PI3K kinase and mTOR kinase in the PI3K/AKT/mTOR kinase signaling pathway, which may result in tumor cell apoptosis and growth inhibition in PI3K/mTOR-overexpressing tumor cells. Activation of the PI3K/mTOR pathway promotes cell growth, survival, and resistance to chemotherapy and radiotherapy; mTOR, a serine/threonine kinase downstream of PI3K, may also be activated independent of PI3K.

Dactolisib Manufacturers

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

Dactolisib Suppliers

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

Dactolisib GMP

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

Dactolisib CoA

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

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

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