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1. R 1507
2. R-1507
3. R-1507 Monoclonal Antibody
4. R1507
5. Ro-4858696
6. Ro-4858696-000
7. Ro-4858696000
8. Ro4858696
9. Ro4858696-000
10. Rv-001
11. Rv001
12. Tepezza
13. Teprotumumab
14. Teprotumumab-trbw
1. Onilcamotide [inn]
2. Unii-uqe6kp7t0d
3. Uqe6kp7t0d
4. Rhoc Peptide Vaccine Rv001v
5. Rv001
6. Rv-001
7. Ala-thr-arg-ala-gly-leu-gln-val-arg-lys-asn-lys-arg-arg-arg-gly-cys-pro-ile-leu
8. 1164096-85-8
9. L-alanyl-l-threonyl-l-arginyl-l-alanylglycyl-l-leucyl-l-glutaminyl-l-valyl-l-arginyl-l-lysyl-l-asparaginyl-l-lysyl-l-arginyl-l-arginyl-l-arginylglycyl-l-cysteinyl-l-prolyl-l-isoleucyl-l-leucine
10. L-leucine, L-alanyl-l-threonyl-l-arginyl-l-alanylglycyl-l-leucyl-l-glutaminyl-l-valyl-l-arginyl-l-lysyl-l-asparaginyl-l-lysyl-l-arginyl-l-arginyl-l-arginylglycyl-l-cysteinyl-l-prolyl-l-isoleucyl-
| Molecular Weight | 2293.7 g/mol |
|---|---|
| Molecular Formula | C96H177N39O24S |
| XLogP3 | -11.3 |
| Hydrogen Bond Donor Count | 41 |
| Hydrogen Bond Acceptor Count | 33 |
| Rotatable Bond Count | 85 |
| Exact Mass | 2293.3582937 g/mol |
| Monoisotopic Mass | 2292.3549388 g/mol |
| Topological Polar Surface Area | 1080 Ų |
| Heavy Atom Count | 160 |
| Formal Charge | 0 |
| Complexity | 4890 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 20 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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ABOUT THIS PAGE
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PharmaCompass offers a list of RV001 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 RV001 manufacturer or RV001 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred RV001 manufacturer or RV001 supplier.
PharmaCompass also assists you with knowing the RV001 API Price utilized in the formulation of products. RV001 API Price is not always fixed or binding as the RV001 Price is obtained through a variety of data sources. The RV001 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A teprotumumab-trbw manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of teprotumumab-trbw, including repackagers and relabelers. The FDA regulates teprotumumab-trbw manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. teprotumumab-trbw 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 teprotumumab-trbw supplier is an individual or a company that provides teprotumumab-trbw active pharmaceutical ingredient (API) or teprotumumab-trbw finished formulations upon request. The teprotumumab-trbw suppliers may include teprotumumab-trbw API manufacturers, exporters, distributors and traders.
teprotumumab-trbw 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 teprotumumab-trbw 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 teprotumumab-trbw GMP manufacturer or teprotumumab-trbw GMP API supplier for your needs.
A teprotumumab-trbw CoA (Certificate of Analysis) is a formal document that attests to teprotumumab-trbw's compliance with teprotumumab-trbw specifications and serves as a tool for batch-level quality control.
teprotumumab-trbw CoA mostly includes findings from lab analyses of a specific batch. For each teprotumumab-trbw 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.
teprotumumab-trbw may be tested according to a variety of international standards, such as European Pharmacopoeia (teprotumumab-trbw EP), teprotumumab-trbw JP (Japanese Pharmacopeia) and the US Pharmacopoeia (teprotumumab-trbw USP).