Synopsis
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1. (r)-n,n-diisopropyl-3-(2-hydroxy-5-hydroxymethylphenyl)-3-phenylpropanamine
2. 5-hydroxymethyl Tolterodine
3. Pnu 200577
4. Pnu-200577
1. 207679-81-0
2. (r)-5-hydroxymethyl Tolterodine
3. 5-hydroxymethyl Tolterodine
4. (r)-2-(3-(diisopropylamino)-1-phenylpropyl)-4-(hydroxymethyl)phenol
5. Pnu-200577
6. 5-hydroxymethyltolterodine
7. Desfesoterodine [inn]
8. 5-hmt
9. Pnu 200577
10. 3-[(1r)-3-[bis(1-methylethyl)amino]-1-phenylpropyl]-4-hydroxybenzenemethanol
11. 5-hydroxymethyl Tolterodine (pnu 200577, 5-hmt, 5-hm)
12. Spm 7605
13. Yu871o78gr
14. (+)-n,n-diisopropyl-3-(2-hydroxy-5-hydroxymethylphenyl)-3-phenylpropylamine
15. 207679-81-0 (free Base)
16. Benzenemethanol, 3-[(1r)-3-[bis(1-methylethyl)amino]-1-phenylpropyl]-4-hydroxy-
17. Desfesoterodine (inn)
18. (r)-(+)-2-(3-diisopropylamino-1-phenylpropyl)-4-hydroxymethylphenol
19. Benzenemethanol, 3-((1r)-3-(bis(1-methylethyl)amino)-1-phenylpropyl)-4-hydroxy-
20. 2-[(1r)-3-[di(propan-2-yl)amino]-1-phenylpropyl]-4-(hydroxymethyl)phenol
21. Unii-yu871o78gr
22. Desfesoterodin
23. R-5-hydroxymethyl Tolterodine
24. 5-hm
25. (r)-2-[3-(diisopropylamino)-1-phenylpropyl]-4-(hydroxymethyl)phenol
26. 5-hydroxymethyl-tolterodine
27. Intermediate Of Fesoterodine
28. Schembl209062
29. (r)-5-hydroxymethyltolterodine
30. Zinc6047
31. Chembl3348932
32. Desfesoterodine [who-dd]
33. Dtxsid40431319
34. Chebi:177454
35. Dd 01
36. Hms3884p12
37. Bcp02922
38. Spm-7605
39. Mfcd09264524
40. Pnu200577
41. S2659
42. Akos005146249
43. Akos015841720
44. Ccg-267936
45. Cs-0825
46. Db15578
47. Ncgc00346585-01
48. Ac-23943
49. Bs-15813
50. Hy-76569
51. Bcp0726000296
52. 5-hydroxymethyl Tolterodine (pnu 200577)
53. 5-hydroxymethyl Tolterodine - Pnu 200577
54. Sw219846-1
55. D10853
56. F31141
57. 264h524
58. J-013606
59. Q27294711
60. (r)-2-(3-diisopropylamino-1-phenylpropyl)-4-hydroxy Methyl Phenol
61. (r)-2-(3-diisopropylamino-1-phenylpropyl)-4-hydroxy Methylphenol
62. (r)-2-(3-diisopropylamino-1-phenylpropyl)-4-hydroxymethylphenol
63. (r)-4-hydroxymethyl-2-(3-diisopropylamino-1-phenylpropyl)-phenol
| Molecular Weight | 341.5 g/mol |
|---|---|
| Molecular Formula | C22H31NO2 |
| XLogP3 | 4.4 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 8 |
| Exact Mass | 341.235479232 g/mol |
| Monoisotopic Mass | 341.235479232 g/mol |
| Topological Polar Surface Area | 43.7 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 357 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
G - Genito urinary system and sex hormones
G04 - Urologicals
G04B - Urologicals
G04BD - Drugs for urinary frequency and incontinence
G04BD13 - Desfesoterodine
5-Hydroxymethyl tolterodine is a known human metabolite of tolterodine.
S73 | METXBIODB | Metabolite Reaction Database from BioTransformer | DOI:10.5281/zenodo.4056560
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ANALYTICAL
ABOUT THIS PAGE
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PharmaCompass offers a list of Desfesoterodine 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 Desfesoterodine manufacturer or Desfesoterodine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Desfesoterodine manufacturer or Desfesoterodine supplier.
PharmaCompass also assists you with knowing the Desfesoterodine API Price utilized in the formulation of products. Desfesoterodine API Price is not always fixed or binding as the Desfesoterodine Price is obtained through a variety of data sources. The Desfesoterodine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 207679-81-0 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 207679-81-0, including repackagers and relabelers. The FDA regulates 207679-81-0 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 207679-81-0 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 207679-81-0 supplier is an individual or a company that provides 207679-81-0 active pharmaceutical ingredient (API) or 207679-81-0 finished formulations upon request. The 207679-81-0 suppliers may include 207679-81-0 API manufacturers, exporters, distributors and traders.
click here to find a list of 207679-81-0 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 207679-81-0 DMF (Drug Master File) is a document detailing the whole manufacturing process of 207679-81-0 active pharmaceutical ingredient (API) in detail. Different forms of 207679-81-0 DMFs exist exist since differing nations have different regulations, such as 207679-81-0 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 207679-81-0 DMF submitted to regulatory agencies in the US is known as a USDMF. 207679-81-0 USDMF includes data on 207679-81-0's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 207679-81-0 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 207679-81-0 suppliers with USDMF on PharmaCompass.
207679-81-0 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 207679-81-0 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 207679-81-0 GMP manufacturer or 207679-81-0 GMP API supplier for your needs.
A 207679-81-0 CoA (Certificate of Analysis) is a formal document that attests to 207679-81-0's compliance with 207679-81-0 specifications and serves as a tool for batch-level quality control.
207679-81-0 CoA mostly includes findings from lab analyses of a specific batch. For each 207679-81-0 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.
207679-81-0 may be tested according to a variety of international standards, such as European Pharmacopoeia (207679-81-0 EP), 207679-81-0 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (207679-81-0 USP).
