Page last updated: 2024-12-06

mesoporphyrin ix

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Mesoporphyrin IX is a porphyrin compound that is structurally similar to protoporphyrin IX, a key component of heme. It differs from protoporphyrin IX by the presence of two ethyl groups instead of two vinyl groups at positions 2 and 4. Mesoporphyrin IX can be synthesized through chemical reduction of protoporphyrin IX. It exhibits fluorescence properties and has been investigated for its potential applications in photodynamic therapy, a cancer treatment modality. The compound's fluorescence allows for targeted delivery and activation of cytotoxic reactive oxygen species upon excitation with light. This makes it a promising candidate for the development of novel cancer therapies. Research on mesoporphyrin IX also focuses on its ability to interact with various biological targets, including proteins and nucleic acids, which could lead to further therapeutic applications.'

mesoporphyrin IX: RN given refers to parent cpd; mesoheme is the iron salt of mesoporphyrin IX [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

mesoporphyrin IX : A member of the class of mesoporphyrins obtained by formal hydrogenation of the two vinyl groups in protoporphyrin. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID72422
CHEMBL ID276179
CHEBI ID133626
SCHEMBL ID314687
SCHEMBL ID5447002
SCHEMBL ID18428593
MeSH IDM0098853

Synonyms (27)

Synonym
nsc-19665
nsc19665
7,12-diethyl-3,8,13,17-tetramethyl-21h,23h-porphine-2,18-dipropanoic acid
3-[(1z,4z,9z,15z)-18-(2-carboxyethyl)-8,13-diethyl-3,7,12,17-tetramethyl-21,23-dihydroporphyrin-2-yl]propanoic acid
mpix
mesoporphyrin ix
493-90-3
nsc-409898
nsc409898
mesoporphyrin
3-[(1z,4z,9z,15z)-18-(2-carboxyethyl)-7,12-diethyl-3,8,13,17-tetramethyl-21,23-dihydroporphyrin-2-yl]propanoic acid
3,3'-(7,12-diethyl-3,8,13,17-tetramethylporphyrin-2,18-diyl)dipropanoic acid
CHEBI:133626
7,12-diethyl-3,8,13,17-tetramethyl-2,18-porphinedipropionic acid
CHEMBL276179
3-[18-(2-carboxyethyl)-8,13-diethyl-3,7,12,17-tetramethyl-22,23-dihydroporphyrin-2-yl]propanoic acid
einecs 207-782-4
SCHEMBL314687
SCHEMBL5447002
UQVVDGKMSUMXBI-UJJXFSCMSA-N
21h,23h-porphine-2,18-dipropanoic acid, 7,12-diethyl-3,8,13,17-tetramethyl-
7,12-diethyl-3,8,13,17-tetramethyl-21h,23h-porphine-2,18-dipropanoate
SCHEMBL18428593
mesoprotoporphyrin
mesoporphyrin ix - reference standard
NCAJWYASAWUEBY-UHFFFAOYSA-N
DTXSID10862030

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" The photodynamic effects mediated by mesoporphyrin caused a delayed toxic reaction, the presence of a "shoulder" on the dose-response curve, indicating the capacity for limited repair of photodamage."( Modes of photodynamic vs. sonodynamic cytotoxicity.
Cain, C; Fowlkes, JB; Jeffers, R; Kessel, D; Lo, J, 1995
)
0.29

Dosage Studied

ExcerptRelevanceReference
" The photodynamic effects mediated by mesoporphyrin caused a delayed toxic reaction, the presence of a "shoulder" on the dose-response curve, indicating the capacity for limited repair of photodamage."( Modes of photodynamic vs. sonodynamic cytotoxicity.
Cain, C; Fowlkes, JB; Jeffers, R; Kessel, D; Lo, J, 1995
)
0.29
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Pathways (1)

PathwayProteinsCompounds
3,8-divinyl-chlorophyllide a biosynthesis I (aerobic, light-dependent)1221

Bioassays (2)

Assay IDTitleYearJournalArticle
AID106898Inhibition of HIV-1 P24 production.1994Journal of medicinal chemistry, Apr-15, Volume: 37, Issue:8
Three-dimensional structure-activity analysis of a series of porphyrin derivatives with anti-HIV-1 activity targeted to the V3 loop of the gp120 envelope glycoprotein of the human immunodeficiency virus type 1.
AID104239Inhibition of HIV-1 P24 production.1994Journal of medicinal chemistry, Apr-15, Volume: 37, Issue:8
Three-dimensional structure-activity analysis of a series of porphyrin derivatives with anti-HIV-1 activity targeted to the V3 loop of the gp120 envelope glycoprotein of the human immunodeficiency virus type 1.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (126)

TimeframeStudies, This Drug (%)All Drugs %
pre-199019 (15.08)18.7374
1990's36 (28.57)18.2507
2000's36 (28.57)29.6817
2010's26 (20.63)24.3611
2020's9 (7.14)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 27.51

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index27.51 (24.57)
Research Supply Index4.86 (2.92)
Research Growth Index4.66 (4.65)
Search Engine Demand Index29.12 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (27.51)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews2 (1.56%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other126 (98.44%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]