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Looking for 2097416-76-5 / ATG-017 API manufacturers, exporters & distributors?

ATG-017 manufacturers, exporters & distributors 1

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PharmaCompass offers a list of ATG-017 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 ATG-017 manufacturer or ATG-017 supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred ATG-017 manufacturer or ATG-017 supplier.

PharmaCompass also assists you with knowing the ATG-017 API Price utilized in the formulation of products. ATG-017 API Price is not always fixed or binding as the ATG-017 Price is obtained through a variety of data sources. The ATG-017 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

ATG-017

Synonyms

Azd-0364, Azd0364, 2097416-76-5, Vo9kx45qiq, Chembl4482864, (6r)-7-[(3,4-difluorophenyl)methyl]-6-(methoxymethyl)-2-[5-methyl-2-[(2-methylpyrazol-3-yl)amino]pyrimidin-4-yl]-5,6-dihydroimidazo[1,2-a]pyrazin-8-one

Cas Number

2097416-76-5

Unique Ingredient Identifier (UNII)

VO9KX45QIQ

About ATG-017

Tizaterkib is an orally bioavailable inhibitor of the extracellular signal-regulated kinases 1 (ERK1) and 2 (ERK2), with potential antineoplastic activity. Upon oral administration, tizaterkib specifically targets, binds to and inhibits the activity of the serine/threonine-protein kinases ERK1 and ERK2, thereby preventing the phosphorylation of ERK1/2 substrates and the activation of mitogen-activated protein kinase (MAPK)/ERK-mediated signal transduction pathways. This results in the inhibition of ERK-dependent proliferation and survival of tumor cells. The MAPK/ERK pathway, also known as the RAS/RAF/MEK/ERK pathway, is hyperactivated in a variety of tumor cell types due to mutations in upstream targets. It plays a key role in the proliferation, differentiation and survival of tumor cells.

ATG-017 Manufacturers

A ATG-017 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ATG-017, including repackagers and relabelers. The FDA regulates ATG-017 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ATG-017 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

ATG-017 Suppliers

A ATG-017 supplier is an individual or a company that provides ATG-017 active pharmaceutical ingredient (API) or ATG-017 finished formulations upon request. The ATG-017 suppliers may include ATG-017 API manufacturers, exporters, distributors and traders.

ATG-017 GMP

ATG-017 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 ATG-017 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 ATG-017 GMP manufacturer or ATG-017 GMP API supplier for your needs.

ATG-017 CoA

A ATG-017 CoA (Certificate of Analysis) is a formal document that attests to ATG-017's compliance with ATG-017 specifications and serves as a tool for batch-level quality control.

ATG-017 CoA mostly includes findings from lab analyses of a specific batch. For each ATG-017 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.

ATG-017 may be tested according to a variety of international standards, such as European Pharmacopoeia (ATG-017 EP), ATG-017 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (ATG-017 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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