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Looking for 1443547-43-0 / Fimaporfin API manufacturers, exporters & distributors?

Fimaporfin manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Fimaporfin

Synonyms

1443547-43-0, 4-[10,15-diphenyl-20-(4-sulfophenyl)-2,3,22,24-tetrahydroporphyrin-5-yl]benzenesulfonic acid;4-[10,15-diphenyl-20-(4-sulfophenyl)-12,13,22,24-tetrahydroporphyrin-5-yl]benzenesulfonic acid;4-[15,20-diphenyl-10-(4-sulfophenyl)-2,3,21,23-tetrahydroporphyrin-5-yl]benzenesulfonic acid, Fimaporfin [inn], Unii-3uvt27c76j, 3uvt27c76j, 4,4'-(15,20-diphenyl-7,8(or 12,13 or 17,18)-dihydro-21h,23h-porphine-5,10-diyl)bisbenzenesulfonic acid, mixture of three isomers a, b and c (25%,50%,25%)

Cas Number

1443547-43-0

About Fimaporfin

Fimaporfin is a synthetic light-activated compound composed of three benzenesulfonic acid isomers: fimaporfin A (TPCS2a; tetraphenyl chlorin disulfonate), fimaporfin B, and fimaporfin C, with potential photosensitizing activity upon photodynamic therapy (PDT). Upon intradermal administration, fimaporfin is incorporated into the tumor cells' endosome and lysosome membranes. Subsequently, cytotoxic agents are administered and accumulate in the endosomal and lysosomal compartments; upon local activation by light, fimaporfin produces reactive oxygen species (ROS), such as singlet oxygen, damaging endo/lysosomal membranes and accumulated cytotoxic agents are released into the tumor cell cytosol. This photochemical internalization (PCI) method can enhance the efficacy and selectivity of cytotoxic agents.

Fimaporfin Manufacturers

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

Fimaporfin Suppliers

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

Fimaporfin GMP

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

Fimaporfin CoA

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

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

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