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1. Magnesium Uridine Triphosphate
2. Magnesium Utp
3. Mg Utp
4. Mg-utp
5. Triphosphate, Magnesium Uridine
6. Triphosphate, Uridine
7. Uridine Triphosphate
8. Utp
9. Utp, Magnesium
1. Uridine Triphosphate
2. 63-39-8
3. Uridine 5'-(tetrahydrogen Triphosphate)
4. Utp
5. Uteplex
6. 5'-utp
7. Uridine 5'-triphosphoric Acid
8. Ins316
9. Uridine-5'-triphosphate
10. H4utp
11. Brn 0071520
12. Chembl336296
13. Chebi:15713
14. Ins-316
15. Ut0s826z60
16. (((2r,3s,4r,5r)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2h)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)triphosphoric Acid
17. Uridine5'-triphosphate
18. Einecs 200-558-7
19. Unii-ut0s826z60
20. Uridintriphosphat
21. [[(2r,3s,4r,5r)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] Phosphono Hydrogen Phosphate
22. 3h-uridine Triphosphate
23. Spectrum_001697
24. Uridine 5_-triphosphate
25. 108321-53-5
26. Spectrum2_000525
27. Spectrum3_001596
28. Spectrum4_000851
29. Spectrum5_001167
30. Bmse000295
31. Schembl76682
32. Bspbio_003192
33. Kbiogr_001481
34. Kbioss_002177
35. 4-24-00-01222 (beilstein Handbook Reference)
36. Divk1c_000269
37. Spbio_000509
38. Gtpl1734
39. Uridine 5''-triphosphoric Acid
40. Dtxsid0041147
41. Kbio1_000269
42. Kbio2_002177
43. Kbio2_004745
44. Kbio2_007313
45. Kbio3_002692
46. 5''-utp
47. 5'-uridylate Triphosphate
48. Ninds_000269
49. Zinc3861755
50. Bdbm50118213
51. Uridine Triphosphate [who-dd]
52. Akos016011172
53. Uridine 5'-triphosphate [mi]
54. Cs-7777
55. Db04005
56. Idi1_000269
57. Uridine Mono(tetrahydrogen Triphosphate)
58. Ncgc00163323-01
59. [[(2r,3s,4r,5r)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-hydroxy-phosphoryl] Phosphono Hydrogen Phosphate
60. Uridine 5''-(tetrahydrogen Triphosphate)
61. Hy-107372
62. C00075
63. Uridine 5'-triphosphate Sodium Salt, Aldrichcpr
64. 063u398
65. Uridine, Mono(tetrahydrogen Triphosphate) (ester)
66. Uridine 5'-(tetrahydrogen Triphosphate) (8ci,9ci)
67. Dc99d596-4755-4e87-b3aa-f1d6cfedce9a
68. Q32904692
69. ((2r,3s,4r,5r)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2h)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl Tetrahydrogen Triphosphate
70. [(2r,3s,4r,5r)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl (hydroxy-phosphonooxyphosphoryl) Hydrogen Phosphate
71. [[[5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxyphosphonic Acid
72. 2,4(1h,3h)-pyrimidinedione, 1-[5-o-[hydroxy[[hydroxy(phosphonooxy)phosphinyl]oxy]phosphinyl]-.beta.-d-ribofuranosyl]-
| Molecular Weight | 484.14 g/mol |
|---|---|
| Molecular Formula | C9H15N2O15P3 |
| XLogP3 | -5.8 |
| Hydrogen Bond Donor Count | 7 |
| Hydrogen Bond Acceptor Count | 15 |
| Rotatable Bond Count | 8 |
| Exact Mass | 483.96852877 g/mol |
| Monoisotopic Mass | 483.96852877 g/mol |
| Topological Polar Surface Area | 259 Ų |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 839 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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A Uridine Triphosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Uridine Triphosphate, including repackagers and relabelers. The FDA regulates Uridine Triphosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Uridine Triphosphate 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 Uridine Triphosphate supplier is an individual or a company that provides Uridine Triphosphate active pharmaceutical ingredient (API) or Uridine Triphosphate finished formulations upon request. The Uridine Triphosphate suppliers may include Uridine Triphosphate API manufacturers, exporters, distributors and traders.
click here to find a list of Uridine Triphosphate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Uridine Triphosphate DMF (Drug Master File) is a document detailing the whole manufacturing process of Uridine Triphosphate active pharmaceutical ingredient (API) in detail. Different forms of Uridine Triphosphate DMFs exist exist since differing nations have different regulations, such as Uridine Triphosphate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Uridine Triphosphate DMF submitted to regulatory agencies in the US is known as a USDMF. Uridine Triphosphate USDMF includes data on Uridine Triphosphate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Uridine Triphosphate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Uridine Triphosphate suppliers with USDMF on PharmaCompass.
Uridine Triphosphate 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 Uridine Triphosphate 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 Uridine Triphosphate GMP manufacturer or Uridine Triphosphate GMP API supplier for your needs.
A Uridine Triphosphate CoA (Certificate of Analysis) is a formal document that attests to Uridine Triphosphate's compliance with Uridine Triphosphate specifications and serves as a tool for batch-level quality control.
Uridine Triphosphate CoA mostly includes findings from lab analyses of a specific batch. For each Uridine Triphosphate 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.
Uridine Triphosphate may be tested according to a variety of international standards, such as European Pharmacopoeia (Uridine Triphosphate EP), Uridine Triphosphate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Uridine Triphosphate USP).
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