메뉴 건너뛰기




Volumn 13, Issue 8, 2003, Pages 1483-1486

Phenylbutyrates as potent, orally bioavailable vitronectin receptor (integrin αvβ3) antagonists

Author keywords

[No Author keywords available]

Indexed keywords

10,11 DIHYDRO 3 [3 (2 PYRIDINYLAMINO)PROPOXY] 5H DIBENZO[A,D]CYCLOHEPTENE 10 ACETIC ACID; ARYLBUTYRIC ACID DERIVATIVE; UNCLASSIFIED DRUG; VITRONECTIN RECEPTOR;

EID: 0037451878     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(03)00102-1     Document Type: Article
Times cited : (28)

References (23)
  • 1
    • 0036313063 scopus 로고    scopus 로고
    • (a) For recent reviews on integrin αvβ3, see: Coleman P.J., Duong L.T. Exp. Opin. Ther. Patents. 12:2002;1009 (b) Hölzemann G. Idrugs. 4:2001;72 (c) Miller W.H., Keenan R.M., Willette R.N., Lark M.W. Drug Disc. Today. 5:2000;397 (d) Duggan M.E., Hutchinson M.E. Exp. Opin. Ther. Patents. 10:2000;1367 (e) Hartman G.D., Duggan M.E. Exp. Opin. Invest. Drugs. 9:2000;1281.
    • (2002) Exp. Opin. Ther. Patents , vol.12 , pp. 1009
    • Coleman, P.J.1    Duong, L.T.2
  • 2
    • 0001943567 scopus 로고    scopus 로고
    • (a) For recent reviews on integrin αvβ3, see: Coleman P.J., Duong L.T. Exp. Opin. Ther. Patents. 12:2002;1009 (b) Hölzemann G. Idrugs. 4:2001;72 (c) Miller W.H., Keenan R.M., Willette R.N., Lark M.W. Drug Disc. Today. 5:2000;397 (d) Duggan M.E., Hutchinson M.E. Exp. Opin. Ther. Patents. 10:2000;1367 (e) Hartman G.D., Duggan M.E. Exp. Opin. Invest. Drugs. 9:2000;1281.
    • (2001) Idrugs , vol.4 , pp. 72
    • Hölzemann, G.1
  • 3
    • 0034283972 scopus 로고    scopus 로고
    • (a) For recent reviews on integrin αvβ3, see: Coleman P.J., Duong L.T. Exp. Opin. Ther. Patents. 12:2002;1009 (b) Hölzemann G. Idrugs. 4:2001;72 (c) Miller W.H., Keenan R.M., Willette R.N., Lark M.W. Drug Disc. Today. 5:2000;397 (d) Duggan M.E., Hutchinson M.E. Exp. Opin. Ther. Patents. 10:2000;1367 (e) Hartman G.D., Duggan M.E. Exp. Opin. Invest. Drugs. 9:2000;1281.
    • (2000) Drug Disc. Today , vol.5 , pp. 397
    • Miller, W.H.1    Keenan, R.M.2    Willette, R.N.3    Lark, M.W.4
  • 4
    • 0033863801 scopus 로고    scopus 로고
    • (a) For recent reviews on integrin αvβ3, see: Coleman P.J., Duong L.T. Exp. Opin. Ther. Patents. 12:2002;1009 (b) Hölzemann G. Idrugs. 4:2001;72 (c) Miller W.H., Keenan R.M., Willette R.N., Lark M.W. Drug Disc. Today. 5:2000;397 (d) Duggan M.E., Hutchinson M.E. Exp. Opin. Ther. Patents. 10:2000;1367 (e) Hartman G.D., Duggan M.E. Exp. Opin. Invest. Drugs. 9:2000;1281.
    • (2000) Exp. Opin. Ther. Patents , vol.10 , pp. 1367
    • Duggan, M.E.1    Hutchinson, M.E.2
  • 5
    • 0034040525 scopus 로고    scopus 로고
    • (a) For recent reviews on integrin αvβ3, see: Coleman P.J., Duong L.T. Exp. Opin. Ther. Patents. 12:2002;1009 (b) Hölzemann G. Idrugs. 4:2001;72 (c) Miller W.H., Keenan R.M., Willette R.N., Lark M.W. Drug Disc. Today. 5:2000;397 (d) Duggan M.E., Hutchinson M.E. Exp. Opin. Ther. Patents. 10:2000;1367 (e) Hartman G.D., Duggan M.E. Exp. Opin. Invest. Drugs. 9:2000;1281.
    • (2000) Exp. Opin. Invest. Drugs , vol.9 , pp. 1281
    • Hartman, G.D.1    Duggan, M.E.2
  • 11
    • 85031199822 scopus 로고    scopus 로고
    • R for ethyl (R)-(+)-4-(4-hydroxyphenyl)-3-phenylbutyrate=23.0 min.
  • 12
    • 85031193993 scopus 로고    scopus 로고
    • Tables of crystal data, fractional atomic coordinates, anisotropic thermal parameters for non-hydrogen atoms, bond distances and angles have been included with the deposited supplementary material (deposition number CCDC 186477) sent to the Cambridge Crystallographic Data Centre, Lensfield Road, Cambridge CB2 1EW, United Kingdom. Listings of structure factors are available from the authors upon request.
  • 13
    • 85031208805 scopus 로고    scopus 로고
    • 3 (64%).
  • 18
    • 9544258252 scopus 로고    scopus 로고
    • i values represent the means of values determined in two to three separate experiments. See:
    • i values represent the means of values determined in two to three separate experiments. See: Wong A., Hwang S.M., McDevitt P., McNulty D., Stadel J.M., Johanson K. Mol. Pharm. 50:1996;529.
    • (1996) Mol. Pharm. , vol.50 , pp. 529
    • Wong, A.1    Hwang, S.M.2    McDevitt, P.3    McNulty, D.4    Stadel, J.M.5    Johanson, K.6
  • 21
    • 0001075697 scopus 로고
    • Swarbrick, J., Ed.; Marcel Dekker: New York
    • Pharmacokinetic parameters were determined using non-compartmental analysis of plasma concentration of test compound versus time data determined in three rats. Oral bioavailability was calculated from the dose-normalized iv and po. AUC values, where AUC is the area under the plasma concentration versus time curve. See: Gibaldi, M., Perrier, D. In Pharmacokinetics, 2nd ed.; Swarbrick, J., Ed.; Marcel Dekker: New York, 1982; Vol. 15, pp 145-198.
    • (1982) Pharmacokinetics, 2nd Ed. , vol.15 , pp. 145-198
    • Gibaldi, M.1    Perrier, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.