Hematoporphyrin

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Hematoporphyrin
Hematoporphyrin.png
Clinical data
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • In general: ℞ (Prescription only)
Identifiers
  • 7,12-bis(1-hydroxyethyl)-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropanoic acid
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
ECHA InfoCard 100.034.939 OOjs UI icon edit-ltr-progressive.svg
Chemical and physical data
Formula C34H38N4O6
Molar mass 598.700 g·mol−1
3D model (JSmol)
Melting point 172.5 °C (342.5 °F)
  • CC1=C(C2=CC3=NC(=CC4=NC(=CC5=C(C(=C(N5)C=C1N2)C(C)O)C)C(=C4CCC(=O)O)C)C(=C3C)CCC(=O)O)C(C)O
  • 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- Yes check.svgY
  • Key:KFKRXESVMDBTNQ-AMPAVEGJSA-N Yes check.svgY
   (verify)

Hematoporphyrin (Photodyn, Sensibion) is a porphyrin prepared from hemin. It is a derivative of protoporphyrin IX, where the two vinyl groups have been hydrated (converted to alcohols). It is a deeply colored solid that is usually encountered as a solution. Its chemical structure was determined in 1900. [1]

It is used as a photosensitizer in photodynamic therapy. Acetylation of hematoporphyrin followed by hydrolysis of the product of that reaction affords a mixture called hematoporphyrin derivative (HPD), which is also used in photodynamic therapy. [2]

Hematoporphyrin has also been used as an antidepressant and antipsychotic since the 1920s. [3] [4]

Related Research Articles

<span class="mw-page-title-main">Porphyrin</span> Heterocyclic organic compound with four modified pyrrole subunits

Porphyrins are a group of heterocyclic macrocycle organic compounds, composed of four modified pyrrole subunits interconnected at their α carbon atoms via methine bridges (=CH−). The parent of porphyrin is porphine, a rare chemical compound of exclusively theoretical interest. Substituted porphines are called porphyrins. With a total of 26 π-electrons, of which 18 π-electrons form a planar, continuous cycle, the porphyrin ring structure is often described as aromatic. One result of the large conjugated system is that porphyrins typically absorb strongly in the visible region of the electromagnetic spectrum, i.e. they are deeply colored. The name "porphyrin" derives from the Greek word πορφύρα (porphyra), meaning purple.

<span class="mw-page-title-main">Chlorin</span> Chemical compound

In organic chemistry, chlorins are tetrapyrrole pigments that are partially hydrogenated porphyrins. The parent chlorin is an unstable compound which undergoes air oxidation to porphine. The name chlorin derives from chlorophyll. Chlorophylls are magnesium-containing chlorins and occur as photosynthetic pigments in chloroplasts. The reduced chlorin variants are present in bacteriochlorophylls and are named ‘bacteriochlorins’ and ‘isobacteriochlorins’.

<span class="mw-page-title-main">Photochemistry</span> Sub-discipline of chemistry

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<span class="mw-page-title-main">Aminolevulinic acid</span> Endogenous non-proteinogenic amino acid

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<span class="mw-page-title-main">Phthalocyanine</span> Chemical compound

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<span class="mw-page-title-main">Chalcone</span> Chemical compound

Chalcone is the organic compound C6H5C(O)CH=CHC6H5. It is an α,β-unsaturated ketone. A variety of important biological compounds are known collectively as chalcones or chalconoids. As bioactive substances, fluorescent materials, and chemical intermediates, they are widely known. Chalcones have been used in medicinal chemistry as antioxidants, anticancer agents, diabetes medications, antiviral agents, antimalarial agents, and more. Aside from being utilized as medicines, they may also be employed as liquid crystals, fluorescent scaffolds, metal sensors, corrosion inhibitors, and plant growth promoters.

<span class="mw-page-title-main">Photosensitizer</span> Type of molecule reacting to light

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<span class="mw-page-title-main">Porphine</span> Chemical compound

Porphine or porphin is an organic chemical compound with formula C20H14N4. The molecule, which is flat, consists of four pyrrole-like rings joined by four methine (=CH−) groups to form a larger macrocycle ring, which makes it the simplest of the tetrapyrroles. It is classified as an aromatic and heterocyclic compound.

<span class="mw-page-title-main">Rose bengal</span> Chemical compound

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<span class="mw-page-title-main">Methyl aminolevulinate</span> Chemical compound

Methyl aminolevulinate (MAL) is a drug used as a sensitizer in photodynamic therapy. It is a prodrug that is metabolized to protoporphyrin IX. It is marketed as Metvix.

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<span class="mw-page-title-main">BODIPY</span> Parent chemical compound of the BODYPY fluorescent dyes

BODIPY is the technical common name of a chemical compound with formula C
9
H
7
BN
2
F
2
, whose molecule consists of a boron difluoride group BF
2
joined to a dipyrromethene group C
9
H
7
N
2
; specifically, the compound 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene in the IUPAC nomenclature. The common name is an abbreviation for "boron-dipyrromethene". It is a red crystalline solid, stable at ambient temperature, soluble in methanol.

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<span class="mw-page-title-main">Pheophorbide</span> Chemical compound

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<span class="mw-page-title-main">Sonodynamic therapy</span>

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References

  1. Luzgina VN, Filippovich EI, Evstigneeva RP (May 1977). "Hematoporphyrin IX". Pharmaceutical Chemistry Journal. 11 (5): 613–20. doi:10.1007/BF00780815. S2CID   44554826.
  2. Kessel D (June 1984). "Hematoporphyrin and HPD: photophysics, photochemistry and phototherapy". Photochemistry and Photobiology. 39 (6): 851–9. doi: 10.1111/j.1751-1097.1984.tb08871.x . PMID   6235529. S2CID   20172683.
  3. O'Neil MJ (2001). The Merck index: an encyclopedia of chemicals, drugs, and biologicals . Rahway, NJ: Merck Research Laboratories. ISBN   0-911910-13-1.
  4. Strecker EA, Palmer HP, Braceland FJ (May 1934). "Hematoporphyrin as a Therapeutic Agent in the Psychoses". American Journal of Psychiatry. 90 (6): 1157–1173. doi:10.1176/ajp.90.6.1157.