Jump to content

Quinaprilat: Difference between revisions

From Wikipedia, the free encyclopedia
Content deleted Content added
auto mw
 
Line 1: Line 1:
{{Short description|Chemical compound}}
{{Short description|Chemical compound}}
{{Drugbox
{{Drugbox
| IUPAC_name = (3''S'')-2-[(2''S'')-2-<nowiki>[[</nowiki>(1''S'')-1-carboxy-3-phenylpropyl]amino]propanoyl]-3,4-dihydro-1''H''-isoquinoline-3-carboxylic acid
| IUPAC_name = (3''S'')-2-[(2''S'')-2-{{!((}}(1''S'')-1-carboxy-3-phenylpropyl]amino]propanoyl]-3,4-dihydro-1''H''-isoquinoline-3-carboxylic acid
| image = Quinaprilat structure.svg
| image = Quinaprilat structure.svg
| width = 222
| alt =
| alt =
| image2 =
| image2 =
Line 48: Line 47:
| chemical_formula =
| chemical_formula =
| C=23 | H=26 | N=2 | O=5
| C=23 | H=26 | N=2 | O=5
| molecular_weight = 410.46294
| SMILES = C[C@@H](C(=O)N1CC2=CC=CC=C2C[C@H]1C(=O)O)N[C@@H](CCC3=CC=CC=C3)C(=O)O
| SMILES = C[C@@H](C(=O)N1CC2=CC=CC=C2C[C@H]1C(=O)O)N[C@@H](CCC3=CC=CC=C3)C(=O)O
| StdInChI = 1S/C23H26N2O5/c1-15(24-19(22(27)28)12-11-16-7-3-2-4-8-16)21(26)25-14-18-10-6-5-9-17(18)13-20(25)23(29)30/h2-10,15,19-20,24H,11-14H2,1H3,(H,27,28)(H,29,30)/t15-,19-,20-/m0/s1
| StdInChI = 1S/C23H26N2O5/c1-15(24-19(22(27)28)12-11-16-7-3-2-4-8-16)21(26)25-14-18-10-6-5-9-17(18)13-20(25)23(29)30/h2-10,15,19-20,24H,11-14H2,1H3,(H,27,28)(H,29,30)/t15-,19-,20-/m0/s1

Latest revision as of 09:48, 23 March 2024

Quinaprilat
Clinical data
Other namesCI-928
ATC code
  • None
Identifiers
  • (3S)-2-[(2S)-2-[[(1S)-1-carboxy-3-phenylpropyl]amino]propanoyl]-3,4-dihydro-1H-isoquinoline-3-carboxylic acid
CAS Number
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC23H26N2O5
Molar mass410.470 g·mol−1
3D model (JSmol)
  • C[C@@H](C(=O)N1CC2=CC=CC=C2C[C@H]1C(=O)O)N[C@@H](CCC3=CC=CC=C3)C(=O)O
  • InChI=1S/C23H26N2O5/c1-15(24-19(22(27)28)12-11-16-7-3-2-4-8-16)21(26)25-14-18-10-6-5-9-17(18)13-20(25)23(29)30/h2-10,15,19-20,24H,11-14H2,1H3,(H,27,28)(H,29,30)/t15-,19-,20-/m0/s1
  • Key:FLSLEGPOVLMJMN-YSSFQJQWSA-N

Quinaprilat is the active metabolite of quinapril.[1]

References

[edit]
  1. ^ Ferry JJ, Horvath AM, Sedman AJ, Latts JR, Colburn WA (1987). "Influence of food on the pharmacokinetics of quinapril and its active diacid metabolite, CI-928". Journal of Clinical Pharmacology. 27 (5): 397–9. doi:10.1002/j.1552-4604.1987.tb03037.x. PMID 3693584. S2CID 36546103.