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1. 2-((4-tert-butylcyclohexyl)methyl)-3-hydroxy-1,4-naphthoquinone
2. Bw 720c
3. Bw-720c
1. 88426-33-9
2. Butalex
3. Bw-720c
4. 3-[(4-tert-butylcyclohexyl)methyl]-4-hydroxynaphthalene-1,2-dione
5. Bw 720c
6. 2-((4-tert-butylcyclohexyl)methyl)-3-hydroxy-1,4-naphthoquinone
7. 2-[[4-(1,1-dimethylethyl)cyclohexyl]methyl]-3-hydroxy-1,4-naphthalenedione
8. Chembl3182074
9. 0354rt7lg4
10. Mmv689480
11. 2-((4-(1,1-dimethylethyl)cyclohexyl)methyl)-3-hydroxy-1,4-naphthalenedione
12. Buparvaquonum [latin]
13. Buparvacuona
14. Buparvacuona [spanish]
15. Buparvaquonum
16. 2-((4-(tert-butyl)cyclohexyl)methyl)-3-hydroxynaphthalene-1,4-dione
17. 1,4-naphthalenedione, 2-((4-(1,1-dimethylethyl)cyclohexyl)methyl)-3-hydroxy-
18. Buparvaquone [inn:ban]
19. Brn 5566006
20. Unii-0354rt7lg4
21. 2-[(4-tert-butylcyclohexyl)methyl]-3-hydroxynaphthalene-1,4-dione
22. 1,4-naphthalenedione, 2-[[4-(1,1-dimethylethyl)cyclohexyl]methyl]-3-hydroxy-
23. 2-((4-tert-butylcyclohexyl)methyl)-3-hydroxy-1,4-naphthochinon
24. Buparvaquone [mi]
25. Buparvaquone [inn]
26. (rs,rs,rs,rs)-2-((4-tert-butylcyclohexyl)methyl)-3-hydroxy-1,4-naphthoquinone
27. Dsstox_cid_31638
28. Dsstox_rid_97522
29. Dsstox_gsid_57849
30. Schembl22978
31. Buparvaquone [mart.]
32. Chembl292009
33. Schembl9598809
34. Zinc1073
35. Dtxsid4057849
36. Schembl11030015
37. Schembl21863689
38. Buparvaquone, >=98% (hplc)
39. Ex-a977
40. Bcp09338
41. Tox21_113753
42. Bdbm50504365
43. Mfcd01712789
44. S4971
45. Akos015899876
46. Zinc100233123
47. Zinc100871160
48. Zinc169287877
49. Zinc584567000
50. Ccg-267769
51. Cs-3254
52. Ncgc00253624-01
53. As-12853
54. Butalex;bw 720c;bw-720c;bw720c
55. Hy-17581
56. Cas-88426-33-9
57. Ft-0663898
58. F17374
59. Buparvaquone, Vetranal(tm), Analytical Standard
60. 426b339
61. Sr-05000022562
62. Q-200767
63. Q4998022
64. Sr-05000022562-1
65. 2-[[4alpha-(1,1-dimethylethyl)cyclohexan-1alpha-yl]methyl]-3-hydroxy-1,4-naphthalenedione
66. 2-hydroxy-3-[[(1alpha)-4beta-tert-butylcyclohexyl]methyl]-1,4-naphthoquinone
| Molecular Weight | 326.4 g/mol |
|---|---|
| Molecular Formula | C21H26O3 |
| XLogP3 | 5.3 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 3 |
| Exact Mass | 326.18819469 g/mol |
| Monoisotopic Mass | 326.18819469 g/mol |
| Topological Polar Surface Area | 54.4 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 544 |
| 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 | 1 |
Antiprotozoal Agents
Substances that are destructive to protozoans. (See all compounds classified as Antiprotozoal Agents.)
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ABOUT THIS PAGE
A Buparvaquone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Buparvaquone, including repackagers and relabelers. The FDA regulates Buparvaquone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Buparvaquone 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 Buparvaquone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Buparvaquone supplier is an individual or a company that provides Buparvaquone active pharmaceutical ingredient (API) or Buparvaquone finished formulations upon request. The Buparvaquone suppliers may include Buparvaquone API manufacturers, exporters, distributors and traders.
click here to find a list of Buparvaquone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Buparvaquone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Buparvaquone API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Buparvaquone as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Buparvaquone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Buparvaquone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Buparvaquone suppliers with NDC on PharmaCompass.
Buparvaquone 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 Buparvaquone 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 Buparvaquone GMP manufacturer or Buparvaquone GMP API supplier for your needs.
A Buparvaquone CoA (Certificate of Analysis) is a formal document that attests to Buparvaquone's compliance with Buparvaquone specifications and serves as a tool for batch-level quality control.
Buparvaquone CoA mostly includes findings from lab analyses of a specific batch. For each Buparvaquone 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.
Buparvaquone may be tested according to a variety of international standards, such as European Pharmacopoeia (Buparvaquone EP), Buparvaquone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Buparvaquone USP).
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