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09626

Sigma-Aldrich

Protoporphyrin IX Dimethylester

~90% (HPLC)

Synonym(e):

Dimethyl-8,13-divinyl-3,7,12,17-tetramethyl-21H,23H-porphin-2,18-dipropionat, Ooporphyrin-dimethylester

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About This Item

Empirische Formel (Hill-System):
C36H38N4O4
CAS-Nummer:
5522-66-7
Molekulargewicht:
590.71
Beilstein:
381574
EG-Nummer:
226-870-3
MDL-Nummer:
MFCD00064531
UNSPSC-Code:
12171500
PubChem Substanz-ID:
329748780
NACRES:
NA.32

Assay

~90% (HPLC)

Form

powder

mp (Schmelzpunkt)

225-228 °C (lit.)

Löslichkeit

DMSO: soluble
THF: soluble
acetone: soluble
chloroform: soluble
diethyl ether: soluble
ethyl acetate: soluble
methanol: soluble

SMILES String

COC(=O)CCc1c(C)c2cc3[nH]c(cc4nc(cc5[nH]c(cc1n2)c(CCC(=O)OC)c5C)c(C)c4C=C)c(C)c3C=C

InChI

1S/C36H38N4O4/c1-9-23-19(3)27-15-28-21(5)25(11-13-35(41)43-7)33(39-28)18-34-26(12-14-36(42)44-8)22(6)30(40-34)17-32-24(10-2)20(4)29(38-32)16-31(23)37-27/h9-10,15-18,38-39H,1-2,11-14H2,3-8H3/b27-15-,28-15-,29-16-,30-17-,31-16-,32-17-,33-18-,34-18-

InChIKey

XNCGCBXDDMJCKW-MFBGAUBSSA-N

Angaben zum Gen

human ... TERT(7015)

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Anwendung

Protoporphyrin IX-dimethylester wurde als potenter Photosensibilisator menschlicher Nasen-Rachen-Karzinome nachgewiesen.

Verpackung

Bottomless glass bottle. Contents are inside inserted fused cone.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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Dániel Veres et al.
The journal of physical chemistry. B, 116(32), 9644-9652 (2012-07-11)
Application of porphyrins as photosensitizers is based on their light-triggered generation of reactive oxygen species (ROS) that may cause oxidative tissue damage and ultimately kill cells. Cellular membranes are the action grounds of many sensitizers due to their hydrophobic or
C J Walker et al.
The Biochemical journal, 276 ( Pt 3), 691-697 (1991-06-15)
The resolution and reconstitution of the Mg-protoporphyrin IX monomethyl ester oxidative cyclase system into a supernatant and a pellet fraction was accomplished by a procedure involving salt treatment followed by osmotic shock. Recombination of pellet and supernatant fractions was required
S Ookubo et al.
Journal of inorganic biochemistry, 35(4), 305-317 (1989-04-01)
Magnetic circular dichroism (MCD) spectra were observed to characterize the nature of the visible bands for high-spin Fe(III) protoheme derivatives with p-nitrothiophenolate, p-nitrophenolate, and methoxy anion as the fifth ligands in several solvents. The visible MCD bands for p-nitrophenolate heme
T Yoshimura et al.
Archives of biochemistry and biophysics, 230(2), 466-482 (1984-05-01)
The EPR and electronic spectral changes upon titration of systems consisting of (protoporphyrin IX)iron(III) chloride (Fe(PPIX)Cl) or its dimethyl ester (Fe-(PPIXDME)Cl) and imidazole derivatives with tetrabutylammonium hydroxide solution have been measured at 77 and 298 degrees K in various solvents.
Arindam Sen et al.
Journal of controlled release : official journal of the Controlled Release Society, 82(2-3), 399-405 (2002-08-15)
Transdermal drug delivery is an attractive approach for either local or systemic treatment in medicine. In the last decade, different active transdermal delivery methods have been further investigated such as cationic liposomal delivery and electroporation-enhanced delivery. In light of gaining
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