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(+)-202-791

(+)-202-791 structure

(+)-202-791 

structure
  • CAS No:

    97217-83-9

  • Formula:

    C17H18N4O5

  • Chemical Name:

    (+)-202-791

  • Synonyms:

    3-Pyridinecarboxylic acid,4-(2,1,3-benzoxadiazol-4-yl)-1,4-dihydro-2,6-dimethyl-5-nitro-,1-methylethyl ester,(4S)-;3-Pyridinecarboxylic acid,4-(4-benzofurazanyl)-1,4-dihydro-2,6-dimethyl-5-nitro-,1-methylethyl ester,(S)-;2,1,3-Benzoxadiazole,3-pyridinecarboxylic acid deriv.;(+)-PN 202-791;(S)-(+)-Sandoz 202-791;(+)-202-791;(+)-(S)-202-791;(+)-Sandoz 202-791;(+)-(S)-PN 202-791;(S)-Sandoz 202-791;(+)-SDZ 202-791;3-Pyridinecarboxylic acid,4-(2,1,3-benzoxadiazol-4-yl)-1,4-dihydro-2,6-dimethyl-5-nitro-,1-methylethyl ester,(S)-;101342-80-7;111002-27-8

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

Description

202-791 is a benzoxadiazole and an isopropyl ester.

(+)-202-791 Basic Attributes

358.3 g/mol

358.35

Characteristics

123 Ų

Drug Information

Agents that increase calcium influx into calcium channels of excitable tissues. This causes vasoconstriction in VASCULAR SMOOTH MUSCLE and/or CARDIAC MUSCLE cells as well as stimulation of insulin release from pancreatic islets. Therefore, tissue-selective calcium agonists have the potential to combat cardiac failure and endocrinological disorders. They have been used primarily in experimental studies in cell and tissue culture. (See all compounds classified as Calcium Channel Agonists.)|A class of drugs that act by selective inhibition of calcium influx through cellular membranes. (See all compounds classified as Calcium Channel Blockers.)

202-791

Computed Properties

Molecular Weight:358.3
XLogP3:4.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:4
Exact Mass:358.12771969
Monoisotopic Mass:358.12771969
Topological Polar Surface Area:123
Heavy Atom Count:26
Complexity:667
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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