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Volumn 131, Issue 47, 2009, Pages 17260-17269

17α-estradiol·1/2 H2O: Super-structural ordering, electronic properties, chemical bonding, and biological activity in comparison with other estrogens

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL ACTIVITIES; BIOLOGICAL FUNCTIONS; CHEMICAL BONDINGS; CURVED IMAGES; ELECTRON DENSITIES; ELECTROSTATIC POTENTIALS; EXPERIMENTAL CHARGE DENSITY; HANSEN-COPPENS MULTIPOLE MODEL; HYDROGEN ATOMS; MOLECULAR PROPERTIES; RELATIVE BINDING AFFINITY; SPACE GROUPS; STEROIDAL ESTROGENS; STRUCTURAL ORDERING; TOPOLOGICAL ANALYSIS; X RAY DATA;

EID: 72249095826     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja906057z     Document Type: Article
Times cited : (29)

References (62)
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    • note
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    • (2002)
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    • (2002) Foye's Principles of Medicinal Chemistry , pp. 685-717
    • Brueggemeier, R.W.1    Miller, D.D.2    Dalton, J.T.3
  • 41
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    • note
    • After the multipole refinement.
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  • 52
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    • note
    • DES and DNS molecules have zero dipole moment due to the presence of the center of symmetry.
  • 54
    • 72249121636 scopus 로고    scopus 로고
    • note
    • Calculated in this work using data from refs 17-20.
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    • Gaussian, Inc.: Pittsburgh, PA
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.