D5768
Deuteroporphyrin IX dihydrochloride
from bovine blood
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About This Item
Empirical Formula (Hill Notation):
C30H30N4O4 · 2HCl
CAS Number:
Molecular Weight:
583.51
EC Number:
MDL number:
UNSPSC Code:
12171500
biological source
bovine blood
absorption
6,500-7,500 at 398 nm in 0.1 M HCl at 1% (actual value given on label.)
storage temp.
−20°C
SMILES string
Cl.Cl.Cc1cc2cc3[nH]c(cc3C)cc4nc(cc5[nH]c(cc1n2)c(C)c5CCC(O)=O)c(CCC(O)=O)c4C
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K Kuzelová et al.
Biochemistry, 34(35), 11245-11255 (1995-09-05)
The effect of pH on the transfer of deuteroporphyrin from dimyristoylphosphatidylcholine (DMPC) unilamellar vesicles to human serum albumin is investigated using a stopped-flow with fluorescence detection. The kinetics of this process allows for the determination of the rate constants for
Y Nitzan et al.
Journal of photochemistry and photobiology. B, Biology, 42(3), 211-218 (1998-05-22)
The photodynamic effects of photosensitizers on Acinetobacter baumannii were studied. These Gram negative bacteria have recently been implicated in various infections, mainly acquired in hospitals. They have outstanding characteristics of multidrug high resistance to antimicrobial agents. The best photodynamic effect
Irena Bronshtein et al.
Photochemistry and photobiology, 81(2), 446-451 (2004-12-08)
The effect of the acidity of the environment on the topography and photophysics of sensitizer molecules in homogeneous solutions, and when embedded in a lipid microenvironment, was studied. Four hematoporphyrin (HP) analogs were studied, which have chemical "spacers" of varying
Bingcheng Hu et al.
Ultrasonics sonochemistry, 17(2), 288-291 (2009-10-20)
A facile, efficient and general method for preparing deuteroporphyrin derivatives by using concentrated H(2)SO(4) and alcohol under ultrasound irradiation has been developed. A series of new deuteroporphyrin derivatives bearing different propionic ester groups have been synthesized in good yields starting
F E Dayan et al.
Archives of biochemistry and biophysics, 351(1), 27-34 (1998-03-17)
Chlorins are cyclic tetrapyrrole derivatives of great interest for use in photodynamic therapy. We have found that horseradish peroxidase (EC 1.11.1.7) (HRP) can convert deuteroporphyrin IX (Deutero) into chlorins. Some characteristics of this enzymatic transformation were investigated. The formation of
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