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Merck

258385

Protoporphyrin IX disodium salt

≥90% (HPLC)

Synonym(s):

3,7,12,17-Tetramethyl-8,13-divinyl-2,18-porphinedipropionic acid disodium salt, Depocolin-S, Ooporphyrin disodium salt

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About This Item

Empirical Formula (Hill Notation):
C34H32N4Na2O4
CAS Number:
50865-01-5
Molecular Weight:
606.62
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
24855640
EC Number:
256-815-9
Beilstein/REAXYS Number:
5227034
MDL number:
MFCD00151108

Key Documents

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InChI key

JZRNDUPVNXWZDY-HXFTUNQESA-L

InChI

1S/C34H34N4O4.2Na/c1-7-21-17(3)25-13-26-19(5)23(9-11-33(39)40)31(37-26)16-32-24(10-12-34(41)42)20(6)28(38-32)15-30-22(8-2)18(4)27(36-30)14-29(21)35-25;;/h7-8,13-16,36-37H,1-2,9-12H2,3-6H3,(H,39,40)(H,41,42);;/q;2*+1/p-2/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16-;;

SMILES string

[Na+].[Na+].Cc1c(CCC([O-])=O)c2cc3[nH]c(cc4nc(cc5[nH]c(cc1n2)c(C=C)c5C)c(C=C)c4C)c(C)c3CCC([O-])=O

assay

≥90% (HPLC)

form

powder

λmax

406 nm

storage temp.

2-8°C

Quality Level

200

Related Categories

Application

Protoporphyrin disodium salt (PpIX) was used as a dye content for fluorescence spectroscopic characterization in a study. The cytotoxic effect of PpIX on sarcoma 180 solid tumors cells was reported in a study.

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

258385-BULK: + 258385-250MG: + 258385-VAR: + 258385-5G: + 258385-1G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKDB3203
MKDB2887
MKCX9723
MKCX7527
MKCV9066

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Hirotsugu Kobuchi et al.
PloS one, 7(11), e50082-e50082 (2012-11-29)
Accumulation of protoporphyrin IX (PpIX) in malignant cells is the basis of 5-aminolevulinic acid (ALA)-mediated photodynamic therapy. We studied the expression of proteins that possibly affect ALA-mediated PpIX accumulation, namely oligopeptide transporter-1 and -2, ferrochelatase and ATP-binding cassette transporter G2
Leng-Yin Wang et al.
Nanoscale, 5(1), 416-421 (2012-11-29)
Various nanocarriers for photosensitizers have been developed to solve the problems of limiting the clinical utility of photodynamic therapy (PDT); however, to date, no carriers capable of supplying oxygen have been reported. We reported the development of a novel system
Agata Nowak-Stępniowska et al.
Acta biochimica Polonica, 59(4), 603-611 (2012-11-29)
Mitochondria are cell energetic centers where ATP is produced. They also play a very important role in the PDT as intracellular sites of photosensitizer localization. Photosensitizers gathering in mitochondria (like porphyrin derivatives used in this work) are more effective in
Woo Hyung Lee et al.
Chemico-biological interactions, 204(1), 49-57 (2013-04-30)
Porphyrins are used for photodynamic therapy for their light-absorbing properties, and some of them were approved for the treatment of certain types of cancers. Porphyrins prevent activation of hypoxia inducible factor-1α (HIF-1α) by inhibiting heat shock protein 90 (HSP90). This
Sonodynamic antitumor effect of protoporphyrin IX disodium salt on S180 solid tumor
Liu Q, et al.
Chemotherapy, 53(6), 429-436 (2007)
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