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Volumn 9, Issue 20, 1999, Pages 3009-3014

Nonpeptidic SH2 inhibitors of the tyrosine kinase ZAP-70

Author keywords

[No Author keywords available]

Indexed keywords

1,2,4 OXADIAZOLE DERIVATIVE; DRUG ANALOG; FUNCTIONAL GROUP; PEPTIDE; PROTEIN TYROSINE KINASE INHIBITOR; SULFONE DERIVATIVE; TYROSINE; UNCLASSIFIED DRUG; UREA DERIVATIVE; ZAP 70 SULFIDE;

EID: 0033581630     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(99)00524-7     Document Type: Article
Times cited : (23)

References (24)
  • 1
    • 0026484261 scopus 로고
    • For a review on the biological significance of SH2 domains see
    • For a review on the biological significance of SH2 domains see: Pawson, T.; Gish, G. D. Cell 1992, 71, 359.
    • (1992) Cell , vol.71 , pp. 359
    • Pawson, T.1    Gish, G.D.2
  • 8
    • 0032478162 scopus 로고    scopus 로고
    • Nonpeptidic monodentate ZAP-70 SH2 inhibitors have also been reported
    • Nonpeptidic monodentate ZAP-70 SH2 inhibitors have also been reported: Revesz, L.; Bonne, F.; Manning, U.; Zuber, J.-F. Bioorg. Med. Chem. Lett. 1998, 8, 405.
    • (1998) Bioorg. Med. Chem. Lett. , vol.8 , pp. 405
    • Revesz, L.1    Bonne, F.2    Manning, U.3    Zuber, J.-F.4
  • 10
    • 0031796005 scopus 로고    scopus 로고
    • For a review on Src SH2 inhibitors see
    • For a review on Src SH2 inhibitors see: Sawyer, T. K. Biopolymers 1998, 47, 243.
    • (1998) Biopolymers , vol.47 , pp. 243
    • Sawyer, T.K.1
  • 14
    • 0009539801 scopus 로고    scopus 로고
    • 2O that were buffered with 0.1% TFA.
    • 2O that were buffered with 0.1% TFA.
  • 20
    • 0009517354 scopus 로고    scopus 로고
    • 3. The methyl ester group was then hydrolyzed using aqueous NaOH. The resulting acid was converted to the acid chloride using oxalyl chloride
    • 3. The methyl ester group was then hydrolyzed using aqueous NaOH. The resulting acid was converted to the acid chloride using oxalyl chloride.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.