| Weight | 680.764 g/mol |
|---|---|
| Formula | C44H32N4O4 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 6 |
| Aromatic Rings | 8 |
| Rotatable Bonds | 4 |
TEMOPORFIN (122341-38-2)
Score:
#1661 in Physics
,
#1894 in Biochemistry
,
#5107 in Chemistry
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- Temoporfin (Foscan, 5,10,15,20Tetra(mhydroxyphenyl)chlorin)A Secondgeneration Photosensitizer (Photochemistry and Photobiology, 2011)
- Temoporfin-loaded invasomes : Development, characterization and in vitro skin penetration studies (Journal of Controlled Release, 2008)
- Cellular uptake, subcellular localization and photodamaging effect of Temoporfin (mTHPC) in nasopharyngeal carcinoma cells: comparison with hematoporphyrin derivative (Cancer Letters, 2000)
- Lead structures for applications in photodynamic therapy. Part 1: Synthesis and variation of m-THPC (Temoporfin) related amphiphilic A2BC-type porphyrins (Tetrahedron, 2005)
- Development of different temoporfin-loaded invasomesnovel nanocarriers of temoporfin: Characterization, stability and in vitro skin penetration studies (Colloids and Surfaces B: Biointerfaces, 2009)
- Surface charged temoporfin-loaded flexible vesicles: in vitro skin penetration studies and stability. (International Journal of Pharmaceutics, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CC2=NC1=C(C3=CC=C(N3)C(=C4C=CC(=N4)C(=C5C=CC(=C2C6=CC(=CC=C6)O)N5)C7=CC(=CC=C7)O)C8=CC(=CC=C8)O)C9=CC(=CC=C9)O
-
InChIKeyLYPFDBRUNKHDGX-UHFFFAOYSA-N
- Pubchem - TEMOPORFIN
- Wikipedia - Temoporfin
Temoporfin (INN) is a photosensitizer (based on chlorin) used in photodynamic therapy for the treatment of squamous cell carcinoma of the head and neck . It is marketed in the European Union under the brand name Foscan. The U.S.
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