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1. Htl22562
2. Htl-22562
3. Htl0022562
4. Htl-0022562
5. 2097085-63-5
6. N-((r)-3-(7-methyl-1h-indazol-5-yl)-1-oxo-1-(((s)-1-oxo-3-(piperidin-4-yl)-1-(4-(pyridin-4-yl)piperazin-1-yl)propan-2-yl)amino)propan-2-yl)-2'-oxo-1',2'-dihydrospiro(piperidine-4,4'-pyrido(2,3-d)(1,3)oxazine)-1-carboxamide
7. Unii-qp50eso5ra
8. Chembl4635331
9. Schembl18788046
10. Gtpl11113
11. Compound 8 [pmid: 32558564]
12. Hy-145353
13. Cs-0371795
14. Qlq
| Molecular Weight | 763.9 g/mol |
|---|---|
| Molecular Formula | C40H49N11O5 |
| XLogP3 | 2.1 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 9 |
| Exact Mass | 763.39181371 g/mol |
| Monoisotopic Mass | 763.39181371 g/mol |
| Topological Polar Surface Area | 190 Ų |
| Heavy Atom Count | 56 |
| Formal Charge | 0 |
| Complexity | 1380 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of HTL0022562 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 HTL0022562 manufacturer or HTL0022562 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred HTL0022562 manufacturer or HTL0022562 supplier.
PharmaCompass also assists you with knowing the HTL0022562 API Price utilized in the formulation of products. HTL0022562 API Price is not always fixed or binding as the HTL0022562 Price is obtained through a variety of data sources. The HTL0022562 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A QP50ESO5RA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of QP50ESO5RA, including repackagers and relabelers. The FDA regulates QP50ESO5RA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. QP50ESO5RA 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 QP50ESO5RA supplier is an individual or a company that provides QP50ESO5RA active pharmaceutical ingredient (API) or QP50ESO5RA finished formulations upon request. The QP50ESO5RA suppliers may include QP50ESO5RA API manufacturers, exporters, distributors and traders.
QP50ESO5RA 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 QP50ESO5RA 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 QP50ESO5RA GMP manufacturer or QP50ESO5RA GMP API supplier for your needs.
A QP50ESO5RA CoA (Certificate of Analysis) is a formal document that attests to QP50ESO5RA's compliance with QP50ESO5RA specifications and serves as a tool for batch-level quality control.
QP50ESO5RA CoA mostly includes findings from lab analyses of a specific batch. For each QP50ESO5RA 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.
QP50ESO5RA may be tested according to a variety of international standards, such as European Pharmacopoeia (QP50ESO5RA EP), QP50ESO5RA JP (Japanese Pharmacopeia) and the US Pharmacopoeia (QP50ESO5RA USP).
