Temocene: the porphycene analogue of temoporfin (Foscan®)

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Temocene: the porphycene analogue of temoporfin (Foscan®). / Garcia-Diaz, Maria; Sanchez-Garcia, David; Nonell, Santi; Soriano, Jorge; Villanueva, Angeles; Stockert, Juan Carlos; Canete, Magdalena; Sagrista, Maria Lluisa; Mora, Margarita.

In: MedChemComm, Vol. 2, No. 7, 01.07.2011, p. 616-619.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Garcia-Diaz, M, Sanchez-Garcia, D, Nonell, S, Soriano, J, Villanueva, A, Stockert, JC, Canete, M, Sagrista, ML & Mora, M 2011, 'Temocene: the porphycene analogue of temoporfin (Foscan®)', MedChemComm, vol. 2, no. 7, pp. 616-619. https://doi.org/10.1039/c1md00065a

APA

Garcia-Diaz, M., Sanchez-Garcia, D., Nonell, S., Soriano, J., Villanueva, A., Stockert, J. C., ... Mora, M. (2011). Temocene: the porphycene analogue of temoporfin (Foscan®). MedChemComm, 2(7), 616-619. https://doi.org/10.1039/c1md00065a

Vancouver

Garcia-Diaz M, Sanchez-Garcia D, Nonell S, Soriano J, Villanueva A, Stockert JC et al. Temocene: the porphycene analogue of temoporfin (Foscan®). MedChemComm. 2011 Jul 1;2(7):616-619. https://doi.org/10.1039/c1md00065a

Author

Garcia-Diaz, Maria ; Sanchez-Garcia, David ; Nonell, Santi ; Soriano, Jorge ; Villanueva, Angeles ; Stockert, Juan Carlos ; Canete, Magdalena ; Sagrista, Maria Lluisa ; Mora, Margarita. / Temocene: the porphycene analogue of temoporfin (Foscan®). In: MedChemComm. 2011 ; Vol. 2, No. 7. pp. 616-619.

Bibtex

@article{04c9def588a24da9afbdcbb876723b19,
title = "Temocene: the porphycene analogue of temoporfin (Foscan{\circledR})",
abstract = "Temocene, a porphycene analogue of temoporfin, has been synthesized. Compared to temoporfin, temocene is endowed with 2.5-fold larger absorption coefficients in the red part of the spectrum while keeping its excellent photophysical and singlet oxygen photosensitization ability. While its photodynamic activity towards HeLa cells is lower than that of temoporfin, its higher photostability, lower dark toxicity and mitochondrial localisation make temocene a promising candidate for photodynamic therapy applications.",
keywords = "Former Faculty of Pharmaceutical Sciences",
author = "Maria Garcia-Diaz and David Sanchez-Garcia and Santi Nonell and Jorge Soriano and Angeles Villanueva and Stockert, {Juan Carlos} and Magdalena Canete and Sagrista, {Maria Lluisa} and Margarita Mora",
year = "2011",
month = "7",
day = "1",
doi = "10.1039/c1md00065a",
language = "English",
volume = "2",
pages = "616--619",
journal = "MedChemComm",
issn = "2040-2503",
publisher = "Royal Society of Chemistry",
number = "7",

}

RIS

TY - JOUR

T1 - Temocene: the porphycene analogue of temoporfin (Foscan®)

AU - Garcia-Diaz, Maria

AU - Sanchez-Garcia, David

AU - Nonell, Santi

AU - Soriano, Jorge

AU - Villanueva, Angeles

AU - Stockert, Juan Carlos

AU - Canete, Magdalena

AU - Sagrista, Maria Lluisa

AU - Mora, Margarita

PY - 2011/7/1

Y1 - 2011/7/1

N2 - Temocene, a porphycene analogue of temoporfin, has been synthesized. Compared to temoporfin, temocene is endowed with 2.5-fold larger absorption coefficients in the red part of the spectrum while keeping its excellent photophysical and singlet oxygen photosensitization ability. While its photodynamic activity towards HeLa cells is lower than that of temoporfin, its higher photostability, lower dark toxicity and mitochondrial localisation make temocene a promising candidate for photodynamic therapy applications.

AB - Temocene, a porphycene analogue of temoporfin, has been synthesized. Compared to temoporfin, temocene is endowed with 2.5-fold larger absorption coefficients in the red part of the spectrum while keeping its excellent photophysical and singlet oxygen photosensitization ability. While its photodynamic activity towards HeLa cells is lower than that of temoporfin, its higher photostability, lower dark toxicity and mitochondrial localisation make temocene a promising candidate for photodynamic therapy applications.

KW - Former Faculty of Pharmaceutical Sciences

UR - http://www.scopus.com/inward/record.url?scp=79960157980&partnerID=8YFLogxK

U2 - 10.1039/c1md00065a

DO - 10.1039/c1md00065a

M3 - Journal article

AN - SCOPUS:79960157980

VL - 2

SP - 616

EP - 619

JO - MedChemComm

JF - MedChemComm

SN - 2040-2503

IS - 7

ER -

ID: 46457104