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09626

Sigma-Aldrich

Protoporphyrin IX dimethyl ester

~90% (HPLC)

Sinonimo/i:

Dimethyl 8,13-divinyl-3,7,12,17-tetramethyl-21H,23H-porphine-2,18-dipropionate, Ooporpyhrin dimethyl ester

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About This Item

Formula empirica (notazione di Hill):
C36H38N4O4
Numero CAS:
5522-66-7
Peso molecolare:
590.71
Beilstein:
381574
Numero CE:
226-870-3
Numero MDL:
MFCD00064531
Codice UNSPSC:
12171500
ID PubChem:
329748780
NACRES:
NA.32

Saggio

~90% (HPLC)

Forma fisica

powder

Punto di fusione

225-228 °C (lit.)

Solubilità

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

Stringa SMILE

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-
XNCGCBXDDMJCKW-MFBGAUBSSA-N

Informazioni sul gene

human ... TERT(7015)

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Applicazioni

Protoporphyrin IX dimethyl ester has been demonstrated to a potent photosensitizer of human nasopharyngeal carcinoma.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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P P Tamburini et al.
Archives of biochemistry and biophysics, 245(2), 512-522 (1986-03-01)
The role of cytochrome b5 heme propionate groups in the functional interactions between cytochromes P-450 RLM5 and b5 has been investigated by comparing the capacity of RLM5 to interact with both native b5 and a b5 derivative in which the
S Adak et al.
The Biochemical journal, 334 ( Pt 1), 51-56 (1998-08-07)
The role of haem propionates in oxidative and reductive reactions catalysed by horseradish peroxidase (HRP) was studied after successful reconstitution of ferric protoporphyrin IX dimethyl ester (PPDME) into the apoperoxidase. The reconstituted enzyme oxidizes neither guaiacol (aromatic electron donor) nor
Application of time-resolved fluorometry to the resolution of porphyrin-photoproduct mixtures.
P Valat et al.
Photochemistry and photobiology, 47(6), 787-790 (1988-06-01)
Vanaja Manivasager et al.
International journal of oncology, 29(4), 997-1002 (2006-09-12)
5-Aminolevulinic acid (5-ALA) and its esters have been under intense investigation to enhance the endogenous production of protoporphyrin IX (PpIX) in tumour cells for the purpose of photodynamic diagnosis. In this study we have investigated the use of exogenous PpIX
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
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