Hematoporphyrin

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Hematoporphyrin
File:Hematoporphyrin.png
Systematic (IUPAC) name
7,12-bis(1-hydroxyethyl)-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropanoic acid
Clinical data
Legal status
  • ℞ (Prescription only)
Routes of
administration
Oral
Identifiers
CAS Number 14459-29-1
ATC code none
PubChem CID: 11103
ChemSpider 10632 YesY
UNII HBT6M5H379 YesY
ChEMBL CHEMBL317840 YesY
Chemical data
Formula C34H38N4O6
Molecular mass 598.69 g/mol
  • O=C(O)CCC=5c2nc(cc4c(c(c(cc1c(c(c(n1)cc/3nc(c2)\C(=C\3C)CCC(=O)O)C(O)C)C)n4)C(O)C)C)C=5C
  • InChI=1S/C34H38N4O6/c1-15-21(7-9-31(41)42)27-14-28-22(8-10-32(43)44)16(2)24(36-28)12-29-34(20(6)40)18(4)26(38-29)13-30-33(19(5)39)17(3)25(37-30)11-23(15)35-27/h11-14,19-20,37-40H,7-10H2,1-6H3,(H,41,42)(H,43,44)/b23-11-,24-12-,25-11-,26-13-,27-14-,28-14-,29-12-,30-13- YesY
  • Key:KFKRXESVMDBTNQ-AMPAVEGJSA-N YesY
  (verify)

Hematoporphyrin (Photodyn, Sensibion) is an endogenous porphyrin formed by the acid hydrolysis of hemoglobin. Nencki and Zaleski determined its chemical structure in 1900.[1]

Hematoporphyrin has been used as an antidepressant and antipsychotic since the 1920s.[2][3]

See also

References

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