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274925-86-9

274925-86-9 structure
274925-86-9 structure
  • Name: Nebicapone
  • Chemical Name: 1-(3,4-dihydroxy-5-nitrophenyl)-2-phenylethanone
  • CAS Number: 274925-86-9
  • Molecular Formula: C14H11NO5
  • Molecular Weight: 273.24100
  • Catalog: Signaling Pathways Metabolic Enzyme/Protease COMT
  • Create Date: 2016-02-20 07:32:23
  • Modify Date: 2024-01-20 17:48:48
  • Nebicapone (BIA 3-202), a reversible catechol-O-methyltransferase (COMT) inhibitor, is mainly metabolized by glucuronidation. Nebicapone is mainly peripherally acting inhibitor that decreases the biotransformation of L-DOPA to 3-O-methyl-DOPA by inhibition of COMT, and it is potential for the treatment of Parkinson's disease.[1].

Name 1-(3,4-dihydroxy-5-nitrophenyl)-2-phenylethanone
Synonyms 1-(3,4-dihydroxy-5-nitrophenyl)-2-phenyl-ethanone
1-(3,4-dihydroxy-5-nitrophenyl)-2-phenyl-1-ethanone
Nebicapone
UNII-NM2KXJ990T
BIA 3-202
Description Nebicapone (BIA 3-202), a reversible catechol-O-methyltransferase (COMT) inhibitor, is mainly metabolized by glucuronidation. Nebicapone is mainly peripherally acting inhibitor that decreases the biotransformation of L-DOPA to 3-O-methyl-DOPA by inhibition of COMT, and it is potential for the treatment of Parkinson's disease.[1].
Related Catalog
References

[1]. Loureiro AI, et al. Human metabolism of nebicapone (BIA 3-202), a novel catechol-o-methyltransferase inhibitor: characterization of in vitro glucuronidation. Drug Metab Dispos. 2006 Nov;34(11):1856-62.

Molecular Formula C14H11NO5
Molecular Weight 273.24100
Exact Mass 273.06400
PSA 103.35000
LogP 2.95460
Hazard Codes Xi

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274925-86-9 structure

274925-86-9

Literature: Learmonth, David A.; Alves, Paula C. Synthetic Communications, 2002 , vol. 32, # 4 p. 641 - 649

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274925-86-9 structure

274925-86-9

Literature: Learmonth, David A.; Vieira-Coelho, Maria A.; Benes, Jan; Alves, Paula C.; Borges, Nuno; Freitas, Ana P.; Soares-da-Silva, Patricio Journal of Medicinal Chemistry, 2002 , vol. 45, # 3 p. 685 - 695

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274925-86-9 structure

274925-86-9

Literature: Learmonth, David A.; Vieira-Coelho, Maria A.; Benes, Jan; Alves, Paula C.; Borges, Nuno; Freitas, Ana P.; Soares-da-Silva, Patricio Journal of Medicinal Chemistry, 2002 , vol. 45, # 3 p. 685 - 695

~%

274925-86-9 structure

274925-86-9

Literature: Learmonth, David A.; Vieira-Coelho, Maria A.; Benes, Jan; Alves, Paula C.; Borges, Nuno; Freitas, Ana P.; Soares-da-Silva, Patricio Journal of Medicinal Chemistry, 2002 , vol. 45, # 3 p. 685 - 695

~%

274925-86-9 structure

274925-86-9

Literature: Learmonth, David A.; Vieira-Coelho, Maria A.; Benes, Jan; Alves, Paula C.; Borges, Nuno; Freitas, Ana P.; Soares-da-Silva, Patricio Journal of Medicinal Chemistry, 2002 , vol. 45, # 3 p. 685 - 695

~%

274925-86-9 structure

274925-86-9

Literature: Learmonth, David A.; Vieira-Coelho, Maria A.; Benes, Jan; Alves, Paula C.; Borges, Nuno; Freitas, Ana P.; Soares-da-Silva, Patricio Journal of Medicinal Chemistry, 2002 , vol. 45, # 3 p. 685 - 695

~%

274925-86-9 structure

274925-86-9

Literature: Learmonth, David A.; Alves, Paula C. Synthetic Communications, 2002 , vol. 32, # 4 p. 641 - 649