Find Bimiralisib manufacturers, exporters & distributors on PharmaCompass

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Chemistry

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Also known as: 1225037-39-7, Pqr309, Pi3k-in-2, Pqr-309, 5-(4,6-dimorpholino-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-amine, Ncb5
Molecular Formula
C17H20F3N7O2
Molecular Weight
411.4  g/mol
InChI Key
ADGGYDAFIHSYFI-UHFFFAOYSA-N
FDA UNII
6Z3QHB00LB

Bimiralisib
BIMIRALISIB is a small molecule drug with a maximum clinical trial phase of II (across all indications) and has 5 investigational indications.
1 2D Structure

Bimiralisib

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
5-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-amine
2.1.2 InChI
InChI=1S/C17H20F3N7O2/c18-17(19,20)12-9-13(21)22-10-11(12)14-23-15(26-1-5-28-6-2-26)25-16(24-14)27-3-7-29-8-4-27/h9-10H,1-8H2,(H2,21,22)
2.1.3 InChI Key
ADGGYDAFIHSYFI-UHFFFAOYSA-N
2.2 Other Identifiers
2.2.1 UNII
6Z3QHB00LB
2.3 Synonyms
2.3.1 Depositor-Supplied Synonyms

1. 1225037-39-7

2. Pqr309

3. Pi3k-in-2

4. Pqr-309

5. 5-(4,6-dimorpholino-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-amine

6. Ncb5

7. Bimiralisib [inn]

8. Bimiralisib [usan]

9. Bimiralisib [who-dd]

10. Bimiralisib (pqr309)

11. 6z3qhb00lb

12. Nc-b5

13. Chembl4084907

14. 5-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-amine

15. 2-pyridinamine, 5-(4,6-di-4-morpholinyl-1,3,5-triazin-2-yl)-4-(trifluoromethyl)-

16. 5-[bis(morpholin-4-yl)-1,3,5-triazin-2-yl]-4-(trifluoromethyl)pyridin-2-amine

17. Mfcd28902193

18. Pqr309; Bimiralisib

19. Pqr-309(bimiralisib)

20. Bimiralisib (usan/inn)

21. Pqr-309(bimiralisib)?

22. Unii-6z3qhb00lb

23. Gtpl8383

24. Schembl1309049

25. Pqr309; Bimiralisib Free Base

26. Pqr 309

27. Bimiralisib [usan:inn:who-dd]

28. Bcp15887

29. Ex-a2018

30. Bdbm50240975

31. Nsc785117

32. S8738

33. Akos027439949

34. Cs-4672

35. Db14846

36. Nsc-785117

37. Ac-31532

38. As-49856

39. Hy-12868

40. D11440

41. N11425

42. Brd-k62374002-001-01-5

43. Q27088437

44. 5-(4,6-di-4-morpholinyl-1,3,5-triazin-2-yl)-4-(trifluoromethyl)-2-pyridinamine

45. 5-[4,6-bis(morpholin-4-yl)-1,3,5-triazin-2-yl]-4-(trifluoromethyl)pyridin-2-amine

46. A3w

2.4 Create Date
2012-08-19
3 Chemical and Physical Properties
Molecular Weight 411.4 g/mol
Molecular Formula C17H20F3N7O2
XLogP31.3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count12
Rotatable Bond Count3
Exact Mass Da
Monoisotopic Mass Da
Topological Polar Surface Area103
Heavy Atom Count29
Formal Charge0
Complexity506
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1

ABOUT THIS PAGE

Looking for 1225037-39-7 / Bimiralisib API manufacturers, exporters & distributors?

Bimiralisib manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Bimiralisib 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 Bimiralisib manufacturer or Bimiralisib supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bimiralisib manufacturer or Bimiralisib supplier.

PharmaCompass also assists you with knowing the Bimiralisib API Price utilized in the formulation of products. Bimiralisib API Price is not always fixed or binding as the Bimiralisib Price is obtained through a variety of data sources. The Bimiralisib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Bimiralisib

Synonyms

1225037-39-7, Pqr309, Pi3k-in-2, Pqr-309, 5-(4,6-dimorpholino-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-amine, Ncb5

Cas Number

1225037-39-7

Unique Ingredient Identifier (UNII)

6Z3QHB00LB

About Bimiralisib

BIMIRALISIB is a small molecule drug with a maximum clinical trial phase of II (across all indications) and has 5 investigational indications.

Bimiralisib Manufacturers

A Bimiralisib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bimiralisib, including repackagers and relabelers. The FDA regulates Bimiralisib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bimiralisib API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

Bimiralisib Suppliers

A Bimiralisib supplier is an individual or a company that provides Bimiralisib active pharmaceutical ingredient (API) or Bimiralisib finished formulations upon request. The Bimiralisib suppliers may include Bimiralisib API manufacturers, exporters, distributors and traders.

Bimiralisib GMP

Bimiralisib 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 Bimiralisib 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 Bimiralisib GMP manufacturer or Bimiralisib GMP API supplier for your needs.

Bimiralisib CoA

A Bimiralisib CoA (Certificate of Analysis) is a formal document that attests to Bimiralisib's compliance with Bimiralisib specifications and serves as a tool for batch-level quality control.

Bimiralisib CoA mostly includes findings from lab analyses of a specific batch. For each Bimiralisib 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.

Bimiralisib may be tested according to a variety of international standards, such as European Pharmacopoeia (Bimiralisib EP), Bimiralisib JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Bimiralisib USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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