Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nurufe Kemikli"'
Publikováno v:
Medicinal Chemistry Research. 21:4499-4505
The photoinactivation of three different human cancer cell lines, HeLa, neuroblastoma and U87 and antimicrobial activities against Gram-positive (Bacillus subtilis) and Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa) by protoporphyr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1314498983303b7050e8dda1af163688
https://doi.org/10.1007/s00044-011-9951-3
https://doi.org/10.1007/s00044-011-9951-3
Publikováno v:
Journal of Alloys and Compounds. 502:439-444
Dopamine conjugated protoporphyrin, PPD, was prepared by the coupling reaction of protoporphyrin IX and dopamine in the presence of dicyclohexylcarbodiimide (DCC) and N-hydroxysuccinimide (NHS) in DMF. The crude product was washed with ethanol–cycl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4de230e6859770969fc214d7f631550b
https://doi.org/10.1016/j.jallcom.2010.04.192
https://doi.org/10.1016/j.jallcom.2010.04.192
Publikováno v:
Reactive and Functional Polymers. 69:705-713
Octaarmed star-shaped poly(e-caprolactone) (OSPCL) was successfully synthesized via the ring-opening polymerization (ROP) of e-caprolactone (e-CL) with a magnesium porphyrazine as the multisite initiator and tin(II) 2-ethylhexanoate (Sn(Oct2)) as the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bcfd53b6472d6b4d693a6256e691145
https://doi.org/10.1016/j.reactfunctpolym.2009.05.005
https://doi.org/10.1016/j.reactfunctpolym.2009.05.005
Autor:
Ramazan Ozturk, Nurufe Kemikli
Publikováno v:
Inorganic Chemistry Communications. 11:338-340
Porphyrazines with phosphonic acid groups on the peripheral positions have been prepared by the cyclotetramerization of 1,2-bis{2-(diethyl phosphonate)ethylthio} maleonitrile and followed by the cleavage of the phosphonate esters with TMSBr.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5450c68e88f06e049ab5254a3c360c91
https://doi.org/10.1016/j.inoche.2007.12.020
https://doi.org/10.1016/j.inoche.2007.12.020
Autor:
Batyr Garlyyev, Abdulhadi Baykal, Zehra Durmus, Nurufe Kemikli, Hüseyin Sözeri, Ramazan Ozturk
The coupling of benzyl protected dopamine with meso-tetra(4-carboxyphenyl)porphine (m-TCPP) and a simple deprotection by hydrogenation under catalyst (Pd/C) to remove the benzyl groups afforded the meso-tetra(4-carboxyphenyl)porphine-dopamine conjuga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a3fd89c25078d9ec91daebb9ac0859b
http://hdl.handle.net/20.500.12645/26804
http://hdl.handle.net/20.500.12645/26804
