Cafedrine

Chemical linkage of norephedrine and theophylline
  • C01CA21 (WHO)
Identifiers
  • (RS)-7-[2-[(1-hydroxy-1-phenylpropan-2-yl)amino]ethyl]-1,3-dimethylpurine-2,6-dione
CAS Number
  • 58166-83-9 checkY
PubChem CID
  • 5489638
ChemSpider
  • 4590188 checkY
UNII
  • 0UYY5V4U2Q
ChEMBL
  • ChEMBL2104207 ☒N
CompTox Dashboard (EPA)
  • DTXSID50866678 Edit this at Wikidata
Chemical and physical dataFormulaC18H23N5O3Molar mass357.414 g·mol−13D model (JSmol)
  • Interactive image
  • O=C2N(c1ncn(c1C(=O)N2C)CCNC(C)C(O)c3ccccc3)C
InChI
  • InChI=1S/C18H23N5O3/c1-12(15(24)13-7-5-4-6-8-13)19-9-10-23-11-20-16-14(23)17(25)22(3)18(26)21(16)2/h4-8,11-12,15,19,24H,9-10H2,1-3H3/t12-,15-/m0/s1 checkY
  • Key:UJSKUDDDPKGBJY-WFASDCNBSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Cafedrine (INN), also known as norephedrinoethyltheophylline, is a chemical linkage of norephedrine and theophylline and is a cardiac stimulant used to increase blood pressure in people with hypotension.[1]

See also

References

  1. ^ Morton IK, Hall JM (1999). "Calcitonin gene-related peptide receptor antagonist". Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Dordrecht: Springer Netherlands. p. 59. ISBN 9789401144391.
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Receptor
(ligands)
P0 (adenine)
P1
(adenosine)
P2
(nucleotide)
P2X
(ATPTooltip Adenosine triphosphate)
P2Y
Transporter
(blockers)
CNTsTooltip Concentrative nucleoside transporters
ENTsTooltip Equilibrative nucleoside transporters
PMATTooltip Plasma membrane monoamine transporter
Enzyme
(inhibitors)
XOTooltip Xanthine oxidase
Others
Others
See also: Receptor/signaling modulators


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