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Volumn 3, Issue 4, 2004, Pages 295-296

Tadalafil and vardenafil

Author keywords

[No Author keywords available]

Indexed keywords

APOMORPHINE; PHOSPHODIESTERASE V INHIBITOR; PLACEBO; PROSTAGLANDIN E1; SILDENAFIL; TADALAFIL; VARDENAFIL;

EID: 16544391738     PISSN: 14741776     EISSN: None     Source Type: Journal    
DOI: 10.1038/nrd1362     Document Type: Note
Times cited : (13)

References (10)
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    • Lue, T. F. Erectile dysfunction. N. Engl. J. Med. 342, 1802-1813 (2000).
    • (2000) N. Engl. J. Med. , vol.342 , pp. 1802-1813
    • Lue, T.F.1
  • 2
    • 84942949401 scopus 로고
    • Impotence. NIH Consensus Development Panel on Impotence
    • NIH Consensus Conference
    • NIH Consensus Conference. Impotence. NIH Consensus Development Panel on Impotence. JAMA 270, 83-90 (1993).
    • (1993) JAMA , vol.270 , pp. 83-90
  • 3
    • 0036717930 scopus 로고    scopus 로고
    • Phosphodiesterase 5 inhibitors: Current status and potential applications
    • Rotella, D. P. Phosphodiesterase 5 inhibitors: current status and potential applications. Nature Rev. Drug Disc. 1, 674-682 (2002).
    • (2002) Nature Rev. Drug Disc. , vol.1 , pp. 674-682
    • Rotella, D.P.1
  • 4
    • 0030572496 scopus 로고    scopus 로고
    • Sildenafil (Viagra), a potent and selective inhibitor of type 5 cGMP phosphodiesterase with utility for the treatment of male erectile dysfunction
    • Terrett, N. K. et al. Sildenafil (Viagra), a potent and selective inhibitor of type 5 cGMP phosphodiesterase with utility for the treatment of male erectile dysfunction. Bioorg. Med. Chem. Lett. 6, 1819-1824 (1996).
    • (1996) Bioorg. Med. Chem. Lett. , vol.6 , pp. 1819-1824
    • Terrett, N.K.1
  • 5
    • 0141992797 scopus 로고    scopus 로고
    • The discovery of tadalafil: A novel and highly selective PDE5 inhibitor. 1:5,6,11,11a-tetrahydro-1H-imidazo[1′,5′ :1,6]pyrido[3,4- b]indole-1,3(2H)-dione analogues
    • Daugan, A. et al. The discovery of tadalafil: a novel and highly selective PDE5 inhibitor. 1:5,6,11,11a-tetrahydro-1H-imidazo[1′,5′:1,6]pyrido[3,4- b]indole-1,3(2H)-dione analogues. J. Med. Chem. 46, 4525-4532 (2003).
    • (2003) J. Med. Chem. , vol.46 , pp. 4525-4532
    • Daugan, A.1
  • 6
    • 0141992796 scopus 로고    scopus 로고
    • The discovery of tadalafil: A novel and highly selective PDE5 inhibitor. 2: 2,3,6,7,12,12a-hexahydropyrazino[1′,2′ :1,6]pyrido[3,4-b]indole-1,4-dione analogues
    • Daugan, A. et al. The discovery of tadalafil: a novel and highly selective PDE5 inhibitor. 2: 2,3,6,7,12,12a-hexahydropyrazino[1′,2′ :1,6]pyrido[3,4-b]indole-1,4-dione analogues. J. Med. Chem. 46, 4533-4542 (2003).
    • (2003) J. Med. Chem. , vol.46 , pp. 4533-4542
    • Daugan, A.1
  • 7
    • 0037170832 scopus 로고    scopus 로고
    • Imidazo[5,1-f][1,2,4]triazin-4(3H)-ones, a new class of potent PDE 5 inhibitors
    • Haning, H. et al. Imidazo[5,1-f][1,2,4]triazin-4(3H)-ones, a new class of potent PDE 5 inhibitors. Bioorg. Med. Chem. Lett. 12, 865-868 (2002).
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 865-868
    • Haning, H.1
  • 8
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    • FDA Drug Approvals List [online], (cited 10 Feb 2004)
    • FDA Drug Approvals List [online], (cited 10 Feb 2004), (2003).
    • (2003)
  • 9
    • 85039538791 scopus 로고    scopus 로고
    • FDA Drug Approvals List [online], (cited 10 Feb 2004)
    • FDA Drug Approvals List [online], (cited 10 Feb 2004), (2003).
    • (2003)
  • 10
    • 0026353632 scopus 로고
    • Nitric oxide as a mediator of relaxation of the corpus cavernosum in response to nonadrenergic, noncholinergic neurotransmission
    • Rajfer, J. et al. Nitric oxide as a mediator of relaxation of the corpus cavernosum in response to nonadrenergic, noncholinergic neurotransmission. N. Engl. J. Med. 326, 90-94 (1992).
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    • Rajfer, J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.