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Volumn 40, Issue 18, 1999, Pages 3621-3624

An Fmoc solid-phase approach to linear polypyrrole-peptide conjugates

Author keywords

bZIP proteins; Distamycin; Oligopyrrole; Solid phase peptide synthesis

Indexed keywords

CARBONYL DERIVATIVE; DISTAMYCIN A; PEPTIDE; POLYPYRROLE; PYRROLE DERIVATIVE;

EID: 0033617259     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00490-6     Document Type: Article
Times cited : (16)

References (33)
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    • 2 and dried under vacuum
    • 2 and dried under vacuum.
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    • 2O), from 5% to 95% over 15 min, with UV detection at 303 nm
    • 2O), from 5% to 95% over 15 min, with UV detection at 303 nm.
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    • These studies are being carried out using circular dichroism techniques and will be reported in due course
    • [17] These studies are being carried out using circular dichroism techniques and will be reported in due course.
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    • The Fmoc-aminoacids had the following protecting groups: Arg(Pmc), Asp(OtBu), Cys(Trt), Glu(OtBu), Lys(t-Boc), Ser(tBu), Thr(tBu)
    • [20] The Fmoc-aminoacids had the following protecting groups: Arg(Pmc), Asp(OtBu), Cys(Trt), Glu(OtBu), Lys(t-Boc), Ser(tBu), Thr(tBu).
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    • +] m/z = 3100.18
    • +] m/z = 3100.18.
  • 33
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    • Preliminary circular dichroism studies of binding to the DNA fragment ds-(5'-AGGATTTTATGACGTTCG-3') suggest that compound 9 binds only through the minor groove counterpart
    • [22] Preliminary circular dichroism studies of binding to the DNA fragment ds-(5'-AGGATTTTATGACGTTCG-3') suggest that compound 9 binds only through the minor groove counterpart.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.