![Protoporphyrin IX: the Good, the Bad, and the Ugly | Journal of Pharmacology and Experimental Therapeutics Protoporphyrin IX: the Good, the Bad, and the Ugly | Journal of Pharmacology and Experimental Therapeutics](https://jpet.aspetjournals.org/content/jpet/356/2/267/F2.large.jpg)
Protoporphyrin IX: the Good, the Bad, and the Ugly | Journal of Pharmacology and Experimental Therapeutics
![Molecules | Free Full-Text | Modifications of Porphyrins and Hydroporphyrins for Their Solubilization in Aqueous Media | HTML Molecules | Free Full-Text | Modifications of Porphyrins and Hydroporphyrins for Their Solubilization in Aqueous Media | HTML](https://www.mdpi.com/molecules/molecules-22-00980/article_deploy/html/images/molecules-22-00980-sch016-550.jpg)
Molecules | Free Full-Text | Modifications of Porphyrins and Hydroporphyrins for Their Solubilization in Aqueous Media | HTML
![Protoporphyrin IX–gold nanoparticle conjugates as an efficient photosensitizer in cervical cancer therapy - ScienceDirect Protoporphyrin IX–gold nanoparticle conjugates as an efficient photosensitizer in cervical cancer therapy - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1572100013000148-sc1.jpg)
Protoporphyrin IX–gold nanoparticle conjugates as an efficient photosensitizer in cervical cancer therapy - ScienceDirect
![Facile iodination of the vinyl groups in protoporphyrin IX dimethyl ester and subsequent transformation of the iodinated moieties - Tetrahedron - X-MOL Facile iodination of the vinyl groups in protoporphyrin IX dimethyl ester and subsequent transformation of the iodinated moieties - Tetrahedron - X-MOL](https://xpic.x-mol.com/20180519%2F10.1016_j.tet.2018.05.040.jpg)
Facile iodination of the vinyl groups in protoporphyrin IX dimethyl ester and subsequent transformation of the iodinated moieties - Tetrahedron - X-MOL
![US20080242857A1 - Process For Preparing Porphyrin Derivatives, Such As Protoporphyrin (IX) And Synthesis Intermediates - Google Patents US20080242857A1 - Process For Preparing Porphyrin Derivatives, Such As Protoporphyrin (IX) And Synthesis Intermediates - Google Patents](https://patentimages.storage.googleapis.com/e4/76/04/5ecf3ea981fb07/US20080242857A1-20081002-C00046.png)
US20080242857A1 - Process For Preparing Porphyrin Derivatives, Such As Protoporphyrin (IX) And Synthesis Intermediates - Google Patents
3-[18-(2-Carboxyethyl)-7,12-bis(ethenyl)-3,8,13,17-tetramethylporphyrin-21,23-diid-2-yl]propanoic acid;palladium(2+) | C34H32N4O4Pd - PubChem
![Functionalization of Deutero- and Protoporphyrin IX Dimethyl Esters via Palladium-Catalyzed Coupling Reactions - J. Org. Chem. - X-MOL Functionalization of Deutero- and Protoporphyrin IX Dimethyl Esters via Palladium-Catalyzed Coupling Reactions - J. Org. Chem. - X-MOL](https://xpic.x-mol.com/20190517%2F10.1021_acs.joc.9b00350.jpg)
Functionalization of Deutero- and Protoporphyrin IX Dimethyl Esters via Palladium-Catalyzed Coupling Reactions - J. Org. Chem. - X-MOL
![Carbon monoxide – physiology, detection and controlled release - Chemical Communications (RSC Publishing) DOI:10.1039/C3CC49196J Carbon monoxide – physiology, detection and controlled release - Chemical Communications (RSC Publishing) DOI:10.1039/C3CC49196J](https://pubs.rsc.org/image/article/2014/CC/c3cc49196j/c3cc49196j-f1_hi-res.gif)
Carbon monoxide – physiology, detection and controlled release - Chemical Communications (RSC Publishing) DOI:10.1039/C3CC49196J
![US20080242857A1 - Process For Preparing Porphyrin Derivatives, Such As Protoporphyrin (IX) And Synthesis Intermediates - Google Patents US20080242857A1 - Process For Preparing Porphyrin Derivatives, Such As Protoporphyrin (IX) And Synthesis Intermediates - Google Patents](https://patentimages.storage.googleapis.com/8c/f5/1f/92a35962417bc1/US20080242857A1-20081002-C00001.png)
US20080242857A1 - Process For Preparing Porphyrin Derivatives, Such As Protoporphyrin (IX) And Synthesis Intermediates - Google Patents
![US20080242857A1 - Process For Preparing Porphyrin Derivatives, Such As Protoporphyrin (IX) And Synthesis Intermediates - Google Patents US20080242857A1 - Process For Preparing Porphyrin Derivatives, Such As Protoporphyrin (IX) And Synthesis Intermediates - Google Patents](https://patentimages.storage.googleapis.com/10/50/08/dbf091474d7fb8/US20080242857A1-20081002-C00009.png)
US20080242857A1 - Process For Preparing Porphyrin Derivatives, Such As Protoporphyrin (IX) And Synthesis Intermediates - Google Patents
![Protoporphyrin IX–gold nanoparticle conjugates as an efficient photosensitizer in cervical cancer therapy - ScienceDirect Protoporphyrin IX–gold nanoparticle conjugates as an efficient photosensitizer in cervical cancer therapy - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1572100013000148-gr1.jpg)
Protoporphyrin IX–gold nanoparticle conjugates as an efficient photosensitizer in cervical cancer therapy - ScienceDirect
![WO2019190787A1 - Method for stabilizing hemoglobin and reagents for performing the same - Google Patents WO2019190787A1 - Method for stabilizing hemoglobin and reagents for performing the same - Google Patents](https://patentimages.storage.googleapis.com/26/7d/ec/f5e8733f8e69db/imgf000027_0001.png)
WO2019190787A1 - Method for stabilizing hemoglobin and reagents for performing the same - Google Patents
![PDF) Functionalization of Deutero- and Protoporphyrin IX Dimethyl Esters via Palladium-Catalyzed Coupling Reactions PDF) Functionalization of Deutero- and Protoporphyrin IX Dimethyl Esters via Palladium-Catalyzed Coupling Reactions](https://i1.rgstatic.net/publication/332460548_Functionalization_of_Deutero-_and_Protoporphyrin_IX_Dimethyl_Esters_via_Palladium-Catalyzed_Coupling_Reactions/links/5ce56886458515712ebb648d/largepreview.png)
PDF) Functionalization of Deutero- and Protoporphyrin IX Dimethyl Esters via Palladium-Catalyzed Coupling Reactions
![In vitro antimalarial activity of metalloporphyrins against Plasmodium falciparum | Semantic Scholar In vitro antimalarial activity of metalloporphyrins against Plasmodium falciparum | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/2f46acd693b39e2aa7dcf04186d12a0d9760e8e9/2-Figure1-1.png)