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1. 3-phenyl-1-(pyridin-2-yl)-4-propyl-1h-5-hydroxypyrazole Hcl
2. 3-phenyl-4-propyl-1-(2-pyridinyl)-1h-pyrazol-5-ol
3. 3-phenyl-4-propyl-1-(2-pyridinyl)-1h-pyrazol-5-ol Hydrochloride
4. Apx-115
5. Apx-115 Free Base
6. Ewha-18278
7. Ewha-18278 Free Base
8. Isuzinaxib
1. Apx-115
2. 1395946-75-4
3. Ewha-18278
4. Unii-q99g5ze5u5
5. Q99g5ze5u5
6. 3-phenyl-4-propyl-1-(pyridin-2-yl)-1h-pyrazol-5-ol Hydrochloride
7. 3-phenyl-4-propyl-1-(2-pyridinyl)-1h-pyrazol-5-ol Hydrochloride
8. 5-phenyl-4-propyl-2-pyridin-2-yl-1h-pyrazol-3-one;hydrochloride
9. 1-(pyridin-2-yl)-3-phenyl-4-propyl-1h-pyrazol-5-ol Hydrochloride
10. 1h-pyrazol-5-ol, 3-phenyl-4-propyl-1-(2-pyridinyl)-, Hydrochloride (1:1)
11. Apx115
12. Apx-115 [who-dd]
13. Chembl4650358
14. Schembl15610231
15. Ex-a4040a
16. Vfc94675
17. Hy-120801
18. Cs-0079216
| Molecular Weight | 315.8 g/mol |
|---|---|
| Molecular Formula | C17H18ClN3O |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 4 |
| Exact Mass | 315.1138399 g/mol |
| Monoisotopic Mass | 315.1138399 g/mol |
| Topological Polar Surface Area | 45.2 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 412 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
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PharmaCompass offers a list of APX-115 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 APX-115 manufacturer or APX-115 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred APX-115 manufacturer or APX-115 supplier.
PharmaCompass also assists you with knowing the APX-115 API Price utilized in the formulation of products. APX-115 API Price is not always fixed or binding as the APX-115 Price is obtained through a variety of data sources. The APX-115 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A APX-115 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of APX-115, including repackagers and relabelers. The FDA regulates APX-115 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. APX-115 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 APX-115 supplier is an individual or a company that provides APX-115 active pharmaceutical ingredient (API) or APX-115 finished formulations upon request. The APX-115 suppliers may include APX-115 API manufacturers, exporters, distributors and traders.
APX-115 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 APX-115 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 APX-115 GMP manufacturer or APX-115 GMP API supplier for your needs.
A APX-115 CoA (Certificate of Analysis) is a formal document that attests to APX-115's compliance with APX-115 specifications and serves as a tool for batch-level quality control.
APX-115 CoA mostly includes findings from lab analyses of a specific batch. For each APX-115 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.
APX-115 may be tested according to a variety of international standards, such as European Pharmacopoeia (APX-115 EP), APX-115 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (APX-115 USP).
