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Volumn 14, Issue 10, 2004, Pages 2463-2467

Identification and synthesis of [1,2,4]triazolo[3,4-a]phthalazine derivatives as high-affinity ligands to the α2δ -1 subunit of voltage gated calcium channel

Author keywords

[No Author keywords available]

Indexed keywords

GABAPENTIN; TRIAZOLE DERIVATIVE; VOLTAGE GATED CALCIUM CHANNEL;

EID: 11144356505     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2004.03.008     Document Type: Article
Times cited : (51)

References (24)
  • 1
    • 0002211644 scopus 로고
    • The Role of Gabapentin
    • D. Chadwick. London: Royal Society of Medicine Services Ltd
    • Taylor C.P. The Role of Gabapentin. Chadwick D. New Trends in Epilepsy Management. 1993;13-40 Royal Society of Medicine Services Ltd, London.
    • (1993) New Trends in Epilepsy Management , pp. 13-40
    • Taylor, C.P.1
  • 8
    • 1942459946 scopus 로고    scopus 로고
    • note
    • 3H]-(S)-22 using protocols similar to those described in Ref. 3 (above). Physiological saline containing 50 mM Tris pH 7.5 was used as the assay buffer and membranes were incubated for 1-2 h at rt.
  • 11
    • 84981836368 scopus 로고
    • 1,2,4-Triazolo[3,4,a]phthalazines 2-4 and 6-12 presented in Table 1 were synthesized by way of the 1-chloro-4-hydrazinophthalazine hydrochloride followed by treatment of triethylamine, appropriate acid chloride, and dioxane at reflux for 12 h. The resulting products were elaborated using the general scheme illustrated in Scheme 1. For references, see:
    • 1,2,4-Triazolo[3,4,a]phthalazines 2-4 and 6-12 presented in Table 1 were synthesized by way of the 1-chloro-4-hydrazinophthalazine hydrochloride followed by treatment of triethylamine, appropriate acid chloride, and dioxane at reflux for 12 h. The resulting products were elaborated using the general scheme illustrated in Scheme 1. For references, see: Druey J., Ringier B.H. Helv. Chim. Acta. 34:1951;195.
    • (1951) Helv. Chim. Acta , vol.34 , pp. 195
    • Druey, J.1    Ringier, B.H.2
  • 15
    • 1942524367 scopus 로고    scopus 로고
    • PCT Int. Appl. WO 0242305 A1, 2001.
    • Chambers, M. S. PCT Int. Appl. WO 0242305 A1, 2001.
    • Chambers, M.S.1
  • 21
    • 0000506063 scopus 로고    scopus 로고
    • Enantioenriched pyridines such as (R)-42 may also be accessed by lipase-catalyzed enantioselective acetylations, see:
    • Enantioenriched pyridines such as (R)-42 may also be accessed by lipase-catalyzed enantioselective acetylations, see: Uenishi J., Hiraoka T., Hata S., Nishiwaki K., Yonemitsu O., Nakamura K., Tsukube K. J. Org. Chem. 63:1998;2481.
    • (1998) J. Org. Chem. , vol.63 , pp. 2481
    • Uenishi, J.1    Hiraoka, T.2    Hata, S.3    Nishiwaki, K.4    Yonemitsu, O.5    Nakamura, K.6    Tsukube, K.7
  • 23
    • 1942524365 scopus 로고    scopus 로고
    • note
    • Enantioenrichment of (S)-46 was determined by analytical chiral HPLC (Regis Whelk O Column 98.9:1:0.1 hexanes-2-propanol-triethylamine, 1 mL/min, UV detection 254 nm).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.