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1. C Type Natriuretic Peptide
2. C Type Natriuretic Peptide 22
3. C Type Natriuretic Peptide 53
4. C-type Natriuretic Peptide
5. C-type Natriuretic Peptide-22
6. C-type Natriuretic Peptide-53
7. Cnp-22
8. Cnp-53
9. Natriuretic Peptide, C Type
10. Natriuretic Peptide-22, C-type
11. Natriuretic Peptide-53, C-type
12. Peptide, C-type Natriuretic
13. Peptide-22, C-type Natriuretic
14. Peptide-53, C-type Natriuretic
1. 127869-51-6
2. C-type Natriuretic Peptide (32-53) (human, Porcine, Rat)
3. C-type Natriuretic Peptide (cnp) (1-22), Human
4. Atriopeptin C (pig)
5. Natriuretic Peptide,c-type
6. Cnp (1-22), Human
7. Unii-3vcd78874l
8. Cnp-53
9. Dtxsid60155686
10. 3vcd78874l
11. Bdbm287915
12. Us10087144, Compound Cnp
13. Akos024457659
14. Natriuretic Peptide, C-type, >=95% (hplc)
15. C-type Natriuretic Peptide (1-22) (human, Rat, Swine)
16. C-type Natriuretic Peptide (32-53) (human, Porcine, Rat) Acetate Salt
17. Natriuretic Peptide, C-type, Human And Porcine - Cas 127869-51-6
18. C-type Natriuretic Peptide (cnp) (1-22), Humanc-type Natriuretic Peptide (cnp) (1-22), Human
19. H-gly-leu-ser-lys-gly-cys-phe-gly-leu-lys-leu-asp-arg-ile-gly-ser-met-ser-gly-leu-gly-cys-oh
| Molecular Weight | 2197.6 g/mol |
|---|---|
| Molecular Formula | C93H157N27O28S3 |
| XLogP3 | -8.7 |
| Hydrogen Bond Donor Count | 32 |
| Hydrogen Bond Acceptor Count | 35 |
| Rotatable Bond Count | 44 |
| Exact Mass | 2196.0853510 g/mol |
| Monoisotopic Mass | 2196.0853510 g/mol |
| Topological Polar Surface Area | 962 Ų |
| Heavy Atom Count | 151 |
| Formal Charge | 0 |
| Complexity | 4490 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 17 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Natriuretic Agents
Endogenous or exogenous chemicals that regulate the WATER-ELECTROLYTE BALANCE in the body. They consist of peptides and non-peptide compounds. (See all compounds classified as Natriuretic Agents.)
Drugs in Development
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ABOUT THIS PAGE
A TransCon CNP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TransCon CNP, including repackagers and relabelers. The FDA regulates TransCon CNP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TransCon CNP API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A TransCon CNP supplier is an individual or a company that provides TransCon CNP active pharmaceutical ingredient (API) or TransCon CNP finished formulations upon request. The TransCon CNP suppliers may include TransCon CNP API manufacturers, exporters, distributors and traders.
TransCon CNP 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 TransCon CNP 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 TransCon CNP GMP manufacturer or TransCon CNP GMP API supplier for your needs.
A TransCon CNP CoA (Certificate of Analysis) is a formal document that attests to TransCon CNP's compliance with TransCon CNP specifications and serves as a tool for batch-level quality control.
TransCon CNP CoA mostly includes findings from lab analyses of a specific batch. For each TransCon CNP 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.
TransCon CNP may be tested according to a variety of international standards, such as European Pharmacopoeia (TransCon CNP EP), TransCon CNP JP (Japanese Pharmacopeia) and the US Pharmacopoeia (TransCon CNP USP).
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