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Looking for 2098884-52-5 / PAT-1251 API manufacturers, exporters & distributors?

PAT-1251 manufacturers, exporters & distributors 1

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PharmaCompass offers a list of PAT-1251 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 PAT-1251 manufacturer or PAT-1251 supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred PAT-1251 manufacturer or PAT-1251 supplier.

PharmaCompass also assists you with knowing the PAT-1251 API Price utilized in the formulation of products. PAT-1251 API Price is not always fixed or binding as the PAT-1251 Price is obtained through a variety of data sources. The PAT-1251 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

PAT-1251

Synonyms

2007885-39-2, Y3hmf6g24b, [3-[4-(aminomethyl)-6-(trifluoromethyl)pyridin-2-yl]oxyphenyl]-[(3r,4r)-3-fluoro-4-hydroxypyrrolidin-1-yl]methanone, (3-((4-(aminomethyl)-6-(trifluoromethyl)-2-pyridinyl)oxy)phenyl)((3r,4r)-3-fluoro-4-hydroxy-1-pyrrolidinyl)methanone, 2098884-52-5, Methanone, (3-((4-(aminomethyl)-6-(trifluoromethyl)-2-pyridinyl)oxy)phenyl)((3r,4r)-3-fluoro-4-hydroxy-1-pyrrolidinyl)-

Cas Number

2098884-52-5

Unique Ingredient Identifier (UNII)

Y3HMF6G24B

About PAT-1251

LOXL2 Inhibitor GB2064 is an orally available, small-molecule, irreversible inhibitor of lysyl oxidase homolog 2 (lysyl oxidase-like protein 2; LOXL2) with potential antifibrotic activity. Upon oral administration, the aminomethyl pyridine moiety of LOXL2 inhibitor GB2064 interacts with the active site of LOXL2 to form a pseudo-irreversible inhibitory complex, thereby inhibiting the catalytic activity of LOXL2. LOXL2, a secreted glycoprotein, catalyzes the post-translational oxidative deamination of lysine residues on target proteins, including collagen and elastin, leading to the formation of deaminated lysine (allysine). Condensation with other allysines or lysines drives the formation of inter- and intramolecular cross-linkages that impact remodeling of the extracellular matrix (ECM), potentially leading to fibrosis. Inhibition of LOXL2, which is often upregulated in fibrotic tissue, may reduce fibrosis in certain chronic fibrotic diseases.

PAT-1251 Manufacturers

A PAT-1251 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PAT-1251, including repackagers and relabelers. The FDA regulates PAT-1251 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PAT-1251 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

PAT-1251 Suppliers

A PAT-1251 supplier is an individual or a company that provides PAT-1251 active pharmaceutical ingredient (API) or PAT-1251 finished formulations upon request. The PAT-1251 suppliers may include PAT-1251 API manufacturers, exporters, distributors and traders.

PAT-1251 GMP

PAT-1251 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 PAT-1251 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 PAT-1251 GMP manufacturer or PAT-1251 GMP API supplier for your needs.

PAT-1251 CoA

A PAT-1251 CoA (Certificate of Analysis) is a formal document that attests to PAT-1251's compliance with PAT-1251 specifications and serves as a tool for batch-level quality control.

PAT-1251 CoA mostly includes findings from lab analyses of a specific batch. For each PAT-1251 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.

PAT-1251 may be tested according to a variety of international standards, such as European Pharmacopoeia (PAT-1251 EP), PAT-1251 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (PAT-1251 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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