574-93-6
Chemical Structure
Phthalocyanine
- CAS No.: 574-93-6
- Formula:C32H18N8
- Molecular Weight:514.54
IUPAC Name: phthalocyanine
InChIKey: IEQIEDJGQAUEQZ-UHFFFAOYSA-N
SMILES: [H]N1C2=C3C=CC=CC3=C1/N=C4C5=C(C(/N=C6C7=C(/C(N/6[H])=N/C8=N/C(C9=C8C=CC=C9)=N\2)C=CC=C7)=N/4)C=CC=C5
Biological Activity: Phthalocyanine is a type of pigment and Photosensitizer. Upon irradiation, Phthalocyanine generates ROS or converts light energy into heat, inducing oxidative damage, cytotoxicity, and photodynamic killing of bacterial biofilms. Phthalocyanine produces chemiluminescence when oxidized. It can be used in studies related to cancer, bacterial infections, and photodynamic approaches[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Phthalocyanine | 98.0% | Phthalocyanine is a type of pigment and Photosensitizer. Upon irradiation, Phthalocyanine generates ROS or converts light energy into heat, inducing oxidative damage, cytotoxicity, and photodynamic killing of bacterial biofilms. Phthalocyanine produces chemiluminescence when oxidized. It can be used in studies related to cancer, bacterial infections, and photodynamic approaches. | ||||||||||||||||||||
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Similarity Score 0.82
HY-W112972(7E,14E,21E)-6H,29H-Phthalocyanine,sodiumsalt -
Similarity Score 0.81
HY-W112152Dilithium phthalocyanine -
Similarity Score 0.61
HY-W127721Tetrasulfophthalocyanine -
Similarity Score 0.57
HY-W076000Tin(II)phthalocyanine -
Similarity Score 0.56
HY-19204Zinc phthalocyanine -
Similarity Score 0.56
HY-W072992Iron(II) phthalocyanine -
Similarity Score 0.56
HY-W073017Copper(II) Phthalocyanine (purified by sublimation) -
Similarity Score 0.56
HY-18761Cobalt phthalocyanine -
Similarity Score 0.53
HY-W110771Titanyl Phthalocyanine(purifiedbysublimation) -
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References
- [1]. Rennie CC, et al. Targeted cancer phototherapy using phthalocyanine-anticancer drug conjugates. Dalton transactions (Cambridge, England : 2003). 2022 Sep 13;51(35):13157-13175. [Content Brief]
- [2]. Dahlen M A. The phthalocyanines a new class of synthetic pigments and dyes[J]. Industrial & Engineering Chemistry, 1939, 31(7): 839-847.
- [3]. Spesia MB, et al. Evolution of Phthalocyanine Structures as Photodynamic Agents for Bacteria Inactivation. Chem Rec. 2022 Apr;22(4):e202100292. [Content Brief]
- [4]. Jiang Z, et al. Pharmaceutical development, composition and quantitative analysis of phthalocyanine as the photosensitizer for cancer photodynamic therapy. J Pharm Biomed Anal. 2014 Jan;87:98-104. [Content Brief]
