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Chemistry

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Also known as: 1619931-27-9, Gb002, (s)-n-(3-(1-((6-(3,4-dimethoxyphenyl)pyrazin-2-yl)amino)ethyl)phenyl)-5-methylnicotinamide, Pk-10571, Seralutinib [usan], Gb-002
Molecular Formula
C27H27N5O3
Molecular Weight
469.5  g/mol
InChI Key
JHJNPOSPVGRIAN-SFHVURJKSA-N
FDA UNII
3P63ZTE3OY

Seralutinib
1 2D Structure

Seralutinib

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
N-[3-[(1S)-1-[[6-(3,4-dimethoxyphenyl)pyrazin-2-yl]amino]ethyl]phenyl]-5-methylpyridine-3-carboxamide
2.1.2 InChI
InChI=1S/C27H27N5O3/c1-17-10-21(14-28-13-17)27(33)31-22-7-5-6-19(11-22)18(2)30-26-16-29-15-23(32-26)20-8-9-24(34-3)25(12-20)35-4/h5-16,18H,1-4H3,(H,30,32)(H,31,33)/t18-/m0/s1
2.1.3 InChI Key
JHJNPOSPVGRIAN-SFHVURJKSA-N
2.1.4 Canonical SMILES
CC1=CC(=CN=C1)C(=O)NC2=CC=CC(=C2)C(C)NC3=NC(=CN=C3)C4=CC(=C(C=C4)OC)OC
2.1.5 Isomeric SMILES
CC1=CC(=CN=C1)C(=O)NC2=CC=CC(=C2)[C@H](C)NC3=NC(=CN=C3)C4=CC(=C(C=C4)OC)OC
2.2 Other Identifiers
2.2.1 UNII
3P63ZTE3OY
2.3 Synonyms
2.3.1 Depositor-Supplied Synonyms

1. 1619931-27-9

2. Gb002

3. (s)-n-(3-(1-((6-(3,4-dimethoxyphenyl)pyrazin-2-yl)amino)ethyl)phenyl)-5-methylnicotinamide

4. Pk-10571

5. Seralutinib [usan]

6. Gb-002

7. 3p63zte3oy

8. N-[3-[(1s)-1-[[6-(3,4-dimethoxyphenyl)pyrazin-2-yl]amino]ethyl]phenyl]-5-methylpyridine-3-carboxamide

9. 3-pyridinecarboxamide, N-(3-((1s)-1-((6-(3,4-dimethoxyphenyl)-2-pyrazinyl)amino)ethyl)phenyl)-5-methyl-

10. Seralutinib [inn]

11. Unii-3p63zte3oy

12. Seralutinib [who-dd]

13. Chembl4650333

14. Schembl17324860

15. Gtpl10618

16. Ex-a5138

17. Who 11243

18. At11371

19. Pk10571

20. Structure 2a [wo2014110200a1]

21. Hy-109190

22. Cs-0116463

23. N-(3-((1s)-1-((6-(3,4-dimethoxyphenyl)-2-pyrazinyl)amino)ethyl)phenyl)-5-methyl-3-pyridinecarboxamide

2.4 Create Date
2015-03-23
3 Chemical and Physical Properties
Molecular Weight 469.5 g/mol
Molecular Formula C27H27N5O3
XLogP33.7
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count7
Rotatable Bond Count8
Exact Mass469.21138974 g/mol
Monoisotopic Mass469.21138974 g/mol
Topological Polar Surface Area98.3 Ų
Heavy Atom Count35
Formal Charge0
Complexity667
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1

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ABOUT THIS PAGE

Seralutinib Manufacturers

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

Seralutinib Suppliers

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

Seralutinib GMP

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

Seralutinib CoA

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

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

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