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Volumn 3, Issue 4, 2006, Pages 403-437

Syntheses of peptidomimetics based on pyranose and polyhydroxylated piperidine scaffolds

Author keywords

Carbohydrate based peptidomimetics; D allopyranose; Fibrinogen receptor antagonist; Lipidic peptidomimetics; Nojirimycin; Somatostatin antagonist

Indexed keywords


EID: 33750709250     PISSN: 15701794     EISSN: None     Source Type: Journal    
DOI: 10.2174/157017906778699530     Document Type: Review
Times cited : (29)

References (138)
  • 17
    • 0001019227 scopus 로고
    • The first non-peptidal peptidomimetic was reported in 1986 by Belanger and Dufresne, which recognized the opiate receptor for which it was designed. See
    • The first non-peptidal peptidomimetic was reported in 1986 by Belanger and Dufresne, which recognized the opiate receptor for which it was designed. See Belanger, P. C.; Dufresne, C. Can. J. Chem. 1986, 64, 1514.
    • (1986) Can. J. Chem. , vol.64 , pp. 1514
    • Belanger, P.C.1    Dufresne, C.2
  • 19
    • 0008555933 scopus 로고    scopus 로고
    • Peptidomimetics Protocols. Edited by W. M. Kazmierski. Humana Press Inc. Totowa, NJ
    • Le Merrer, Y.; Poitout, L.; Depezay, J.-C. Methods in Molecular Medicine, Vol. 23: Peptidomimetics Protocols. Edited by W. M. Kazmierski. Humana Press Inc. Totowa, NJ.
    • Methods in Molecular Medicine , vol.23
    • Le Merrer, Y.1    Poitout, L.2    Depezay, J.-C.3
  • 40
    • 0025997018 scopus 로고
    • Molecular structures which can bind to more than one type of receptor are known as "privileged structures". Classical examples in medicinal chemistry include benzodiazepine and steroid systems. See
    • Molecular structures which can bind to more than one type of receptor are known as "privileged structures". Classical examples in medicinal chemistry include benzodiazepine and steroid systems. See Hirschmann, R. Angew. Chem. Int. Ed. Engl. 1991, 30, 1278.
    • (1991) Angew. Chem. Int. Ed. Engl. , vol.30 , pp. 1278
    • Hirschmann, R.1
  • 41
    • 0022636075 scopus 로고
    • For selected reviews on glycoside synthesis see (a)
    • For selected reviews on glycoside synthesis see (a) Schmidt, R. R. Angew. Chem. Int. Ed. 1986, 25, 212.
    • (1986) Angew. Chem. Int. Ed. , vol.25 , pp. 212
    • Schmidt, R.R.1
  • 63
    • 0031189711 scopus 로고    scopus 로고
    • For a review on aspartic acid proteases and their inhibition see
    • For a review on aspartic acid proteases and their inhibition see Babine, R. E.; Bender, S. L. Chem. Rev. 1997, 97, 1359.
    • (1997) Chem. Rev. , vol.97 , pp. 1359
    • Babine, R.E.1    Bender, S.L.2
  • 89
    • 0041906181 scopus 로고    scopus 로고
    • Synthesis of Peptides with Sugar Amino Acids
    • In Goodman, M., Ed. Thieme: Stuggart
    • Graf von Roedern, E.; Born, M. A.; Stöckle, M.; Kessler, H. Synthesis of Peptides with Sugar Amino Acids. In Houben-Weyl; Goodman, M., Ed. Thieme: Stuggart, 2003, Vol. E22c, pp. 807.
    • (2003) Houben-Weyl , vol.E22c , pp. 807
    • Graf von Roedern, E.1    Born, M.A.2    Stöckle, M.3    Kessler, H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.