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1. 17 Hydroxy 3 Oxo 17alpha Pregna 4,6 Diene 21 Carboxylic Acid
2. 17-hydroxy-3-oxo-17alpha-pregna-4,6-diene-21-carboxylic Acid
3. Acid, 17-hydroxy-3-oxo-17alpha-pregna-4,6-diene-21-carboxylic
4. Acid, Canrenoic
5. Canrenoate Potassium
6. Canrenoate, Potassium
7. Canrenoic Acid
8. Kalium Can. Ratiopharm
9. Kalium-can.-ratiopharm
10. Sc 14266
11. Sc-14266
12. Sc14266
13. Soldactone
14. Soludactone
15. Spiroctan
1. Canrenoic Acid Potassium Salt
2. Canrenoate Potassium
3. Soldactone
4. 2181-04-6
5. Kanrenol
6. Canrenoate (potassium)
7. Canrenoic Acid Potassium
8. Potassium Aldadiene
9. Potassium Canrenoate [inn]
10. M671f9nlea
11. Canrenoate Potassium [usan]
12. Sc-14266
13. Mls002154212
14. Canrenone Free Acid Potassium Salt
15. Nsc-757789
16. Canrenoate Potassium (usan)
17. Soludactone
18. Apiroctan
19. Venactone
20. Kalii Canrenoas
21. Aldadiene-kalium
22. Kalium Canrenoat
23. Soldactone (tn)
24. Aldadiene-potassium
25. Canrenoato Potasico
26. Ncgc00017146-01
27. Prestwick_910
28. Canrenoate De Potassium
29. Aldadiene Potassium Salt
30. Aldadiene-kalium [german]
31. Unii-m671f9nlea
32. Dsstox_cid_25602
33. Dsstox_rid_80995
34. Dsstox_gsid_45602
35. Schembl49729
36. Kalii Canrenoas [inn-latin]
37. Potassium Canrenoate (jp17)
38. Mf 465a
39. Ccris 9164
40. Chembl1371200
41. Dtxsid2045602
42. Hy-b1582a
43. Canrenoato Potasico [inn-spanish]
44. Hms1568m18
45. Hms2095m18
46. Hms2235n14
47. Hms3712m18
48. Potassium Canrenoate [jan]
49. Einecs 218-554-9
50. Tox21_110800
51. Potassium Canrenoate [mart.]
52. Canrenoate De Potassium [inn-french]
53. Potassium Canrenoate [who-dd]
54. Akos025402245
55. Ac-6875
56. Cb 8109
57. Ccg-220148
58. Nsc 757789
59. Sc 14266
60. Smr001233495
61. Cas-2181-04-6
62. Cs-0013479
63. Canrenone Free Acid Potassium Salt [mi]
64. D01943
65. Q3655600
66. W-107518
67. Potassium 17-hydroxy-3-oxo-17-alpha-pregna-4,6-diene-21-carboxylate
68. Potassium 17-hydroxy-3-oxo-17alpha-pregna-4,6-diene-21-carboxylate
69. Potassium 3-(17-beta-hydroxy-3-oxoandrosta-4,6-dien-17-yl)propionate
70. 17-alpha-pregna-4,6-diene-21-carboxylic Acid, 17-hydroxy-3-oxo-, Monopotassium Salt
71. Potassium 17-hydroxy-3-oxo-17.alpha.-pregna-4,6-diene-21-carboxylate
72. Potassium 3-(3-oxo-17-beta-hydroxy-4,6-androstadien-17-alpha-yl)propanoate
73. Pregna-4,6-diene-21-carboxylic Acid, 17-hydroxy-3-oxo-, Monopotassium Salt (17alpha)-
74. Pregna-4,6-diene-21-carboxylic Acid, 17-hydroxy-3-oxo-, Monopotassium Salt (17.alpha.)-
| Molecular Weight | 396.6 g/mol |
|---|---|
| Molecular Formula | C22H29KO4 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 3 |
| Exact Mass | 396.17029089 g/mol |
| Monoisotopic Mass | 396.17029089 g/mol |
| Topological Polar Surface Area | 77.4 Ų |
| Heavy Atom Count | 27 |
| Formal Charge | 0 |
| Complexity | 713 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 6 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
Mineralocorticoid Receptor Antagonists
Drugs that bind to and block the activation of MINERALOCORTICOID RECEPTORS by MINERALOCORTICOIDS such as ALDOSTERONE. (See all compounds classified as Mineralocorticoid Receptor Antagonists.)
C - Cardiovascular system
C03 - Diuretics
C03D - Aldosterone antagonists and other potassium-sparing agents
C03DA - Aldosterone antagonists
C03DA02 - Potassium canrenoate
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PharmaCompass offers a list of Canrenoate Potassium 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 Canrenoate Potassium manufacturer or Canrenoate Potassium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Canrenoate Potassium manufacturer or Canrenoate Potassium supplier.
PharmaCompass also assists you with knowing the Canrenoate Potassium API Price utilized in the formulation of products. Canrenoate Potassium API Price is not always fixed or binding as the Canrenoate Potassium Price is obtained through a variety of data sources. The Canrenoate Potassium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Soludactone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Soludactone, including repackagers and relabelers. The FDA regulates Soludactone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Soludactone 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 Soludactone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Soludactone supplier is an individual or a company that provides Soludactone active pharmaceutical ingredient (API) or Soludactone finished formulations upon request. The Soludactone suppliers may include Soludactone API manufacturers, exporters, distributors and traders.
click here to find a list of Soludactone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Soludactone Drug Master File in Japan (Soludactone JDMF) empowers Soludactone API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Soludactone JDMF during the approval evaluation for pharmaceutical products. At the time of Soludactone JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Soludactone suppliers with JDMF 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 Soludactone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Soludactone 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 Soludactone 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 Soludactone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Soludactone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Soludactone suppliers with NDC on PharmaCompass.
Soludactone 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 Soludactone 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 Soludactone GMP manufacturer or Soludactone GMP API supplier for your needs.
A Soludactone CoA (Certificate of Analysis) is a formal document that attests to Soludactone's compliance with Soludactone specifications and serves as a tool for batch-level quality control.
Soludactone CoA mostly includes findings from lab analyses of a specific batch. For each Soludactone 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.
Soludactone may be tested according to a variety of international standards, such as European Pharmacopoeia (Soludactone EP), Soludactone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Soludactone USP).
