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1. Tiaprost
2. Tiaprost, (1r-(1alpha(z),2beta(1e,3r*),3alpha,5alpha))-isomer
3. Tiaprost, (1r-(1alpha(z),2beta(1e,3s*),3alpha,5alpha))-isomer
1. Tiaprost
2. 71116-82-0
3. (e)-7-[3,5-dihydroxy-2-[(e)-3-hydroxy-4-thiophen-3-yloxybut-1-enyl]cyclopentyl]hept-5-enoic Acid
4. 5-heptenoic Acid,7-[3,5-dihydroxy-2-[3-hydroxy-4-(3-thienyloxy)-1-butenyl]cyclopentyl]-
5. 7-[3,5-dihydroxy-2-[3-hydroxy-4-(3-thienyloxy)-1-butenyl]cyclopentyl]-5-heptenoic Acid
6. Schembl12495592
7. Schembl12495595
8. Dtxsid901021711
9. Bcp30311
10. Akos015896642
11. Hy-111478
12. Cs-0041593
13. A850966
| Molecular Weight | 396.5 g/mol |
|---|---|
| Molecular Formula | C20H28O6S |
| XLogP3 | 1.7 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 11 |
| Exact Mass | 396.16065978 g/mol |
| Monoisotopic Mass | 396.16065978 g/mol |
| Topological Polar Surface Area | 136 Ų |
| Heavy Atom Count | 27 |
| Formal Charge | 0 |
| Complexity | 509 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 5 |
| Defined Bond Stereocenter Count | 2 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Tiaprost 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 Tiaprost manufacturer or Tiaprost supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tiaprost manufacturer or Tiaprost supplier.
PharmaCompass also assists you with knowing the Tiaprost API Price utilized in the formulation of products. Tiaprost API Price is not always fixed or binding as the Tiaprost Price is obtained through a variety of data sources. The Tiaprost Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Iliren manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iliren, including repackagers and relabelers. The FDA regulates Iliren manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iliren API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Iliren manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Iliren supplier is an individual or a company that provides Iliren active pharmaceutical ingredient (API) or Iliren finished formulations upon request. The Iliren suppliers may include Iliren API manufacturers, exporters, distributors and traders.
click here to find a list of Iliren suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Iliren 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 Iliren 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 Iliren GMP manufacturer or Iliren GMP API supplier for your needs.
A Iliren CoA (Certificate of Analysis) is a formal document that attests to Iliren's compliance with Iliren specifications and serves as a tool for batch-level quality control.
Iliren CoA mostly includes findings from lab analyses of a specific batch. For each Iliren 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.
Iliren may be tested according to a variety of international standards, such as European Pharmacopoeia (Iliren EP), Iliren JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Iliren USP).
