Molecular structure of Deuteroporphyrin IX dihydrochloride, CAS Number: 68929-05-5
Deuteroporphyrin IX dihydrochloride (CAS 68929-05-5)
CAS Number:
68929-05-5
Molecular Weight:
583.51
Molecular Formula:
C30H32Cl2N4O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Deuteroporphyrin IX dihydrochloride serves as a key subject in the field of biochemical research due to its role in heme synthesis studies. Researchers leverage this compound to probe the mechanisms of porphyrin metabolism and its interactions with various enzymes, such as heme oxygenase, which is for understanding heme catabolism. Its photodynamic properties are also exploited in research focused on photosensitization processes, particularly those that pertain to energy transfer at the molecular level. Moreover, the use of deuteroporphyrin IX dihydrochloride in spectroscopic studies allows for the examination of porphyrin structure-function relationships, aiding in the elucidation of molecular behavior under different conditions.
Deuteroporphyrin IX dihydrochloride (CAS 68929-05-5) References
- Photodynamic effect of deuteroporphyrin IX and hematoporphyrin derivatives on single neuron. | Uzdensky, AB., et al. 2001. Biochem Biophys Res Commun. 281: 1194-9. PMID: 11243861
- Do liposome-binding constants of porphyrins correlate with their measured and predicted partitioning between octanol and water? | Kepczyński, M., et al. 2002. Photochem Photobiol. 76: 127-34. PMID: 12194207
- Porphyrin-mediated cell surface heme capture from hemoglobin by Porphyromonas gingivalis. | Paramaesvaran, M., et al. 2003. J Bacteriol. 185: 2528-37. PMID: 12670977
- Porphyrins and porphines inhibit the ribonuclease P reaction in vitro. | Hori, Y., et al. 2002. Nucleic Acids Res Suppl. 111-2. PMID: 12903130
- Regulatory elements in the KlHEM1 promoter. | Núñez, L., et al. 2008. Biochim Biophys Acta. 1779: 128-33. PMID: 18073144
- The bactericidal activity of a deuteroporphyrin-hemin mixture on gram-positive bacteria. A microbiological and spectroscopic study. | Malik, Z., et al. 1990. J Photochem Photobiol B. 6: 419-30. PMID: 2120409
- Iron(III) mesoporphyrin IX and iron(III) deuteroporphyrin IX bind to the Porphyromonas gingivalis HmuY hemophore. | Wojaczyński, J., et al. 2011. Biochem Biophys Res Commun. 411: 299-304. PMID: 21740890
- Mechanistic aspects of photoinactivation of Candida albicans by exogenous porphyrins. | Oriel, S. and Nitzan, Y. 2012. Photochem Photobiol. 88: 604-12. PMID: 22220682
- The effect of lipid composition on the permeability of fluorescent markers from photosensitized membranes. | Ytzhak, S., et al. 2013. Photochem Photobiol. 89: 619-24. PMID: 23278678
- Coproporphyrins I and III as Functional Markers of OATP1B Activity: In Vitro and In Vivo Evaluation in Preclinical Species. | Shen, H., et al. 2016. J Pharmacol Exp Ther. 357: 382-93. PMID: 26907622
- Structure-activity relationship of porphyrin-induced photoinactivation with membrane function in bacteria and erythrocytes. | Kato, H., et al. 2018. Photochem Photobiol Sci. 17: 954-963. PMID: 29892767
- Type-I Hemins and Free Porphyrins from a Western Australian Sponge Isabela sp. | Sala, S., et al. 2023. Mar Drugs. 21: PMID: 36662214
- Horseradish peroxidase-dependent oxidation of deuteroporphyrin IX into chlorins. | Dayan, FE., et al. 1998. Arch Biochem Biophys. 351: 27-34. PMID: 9500844
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Deuteroporphyrin IX dihydrochloride, 50 mg | sc-263087 | 50 mg | $247.00 | |||
Deuteroporphyrin IX dihydrochloride, 100 mg | sc-263087A | 100 mg | $409.00 |