1983
DOI: 10.1246/nikkashi.1983.214
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Cited by 8 publications
(2 citation statements)
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“…The I-phcnetyl-2-methylimidazolc is complexed by a-CD, and this complcx forms a stable pentacoordinated complcx with iron(I1)-protoporphyrin IX. This double complex formcd a stable oxygen acfduct in aqueous D M F solution at -30°C [33]. The a-CD capped by protoporphyrin IX Fe(I1) is less toxic than the hemin, the i. v. administered CD-protoporphyrin resulted in an LDSo valuc of more than 450 mg/kg, while the LDjo of i. v. administered hcmin is YO mg/kg in rats 1341.…”
Section: Pharmaceutical Applicationsmentioning
confidence: 96%
“…The I-phcnetyl-2-methylimidazolc is complexed by a-CD, and this complcx forms a stable pentacoordinated complcx with iron(I1)-protoporphyrin IX. This double complex formcd a stable oxygen acfduct in aqueous D M F solution at -30°C [33]. The a-CD capped by protoporphyrin IX Fe(I1) is less toxic than the hemin, the i. v. administered CD-protoporphyrin resulted in an LDSo valuc of more than 450 mg/kg, while the LDjo of i. v. administered hcmin is YO mg/kg in rats 1341.…”
Section: Pharmaceutical Applicationsmentioning
confidence: 96%
“…The first trace of non-covalent interactions involving CDs and porphyrins dates back to the early 80s and the work of Tsuchida. 21 In this seminal work, a series of N-substituted 2methylimidazoles, which are both good axial ligands for metalloporphyrins and good guests for α-CDs, were used to form ternary complexes of imidazole, CD and protoporphyrin IX (heme), as shown in Figure 6. The association constants for the binding of the encapsulated imidazole to the iron porphyrin are 15 to 30 times higher than for the same imidazoles in the absence of the CD.…”
Section: Non-covalent Porphyrin(s)-cd(s) Scaffoldsmentioning
confidence: 99%