The anti-tumor effects of androstene steroids exhibit a strict structure-activity relationship dependent upon the orientation of the hydroxyl group on carbon-17.
Saved in:
| Title: | The anti-tumor effects of androstene steroids exhibit a strict structure-activity relationship dependent upon the orientation of the hydroxyl group on carbon-17. |
|---|---|
| Authors: | Graf MR; Department of Neurosurgery - Harold F. Young Neurosurgical Center and the Massey Cancer Center, Virginia Commonwealth University Medical Center, P.O. Box 980631, 1200 E. Broad Street, Richmond, VA 23298-0631, USA. mgraf@hsc.vcu.edu, Jia W, Lewbart ML, Loria RM |
| Source: | Chemical biology & drug design [Chem Biol Drug Des] 2009 Dec; Vol. 74 (6), pp. 625-9. Date of Electronic Publication: 2009 Oct 12. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101262549 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1747-0285 (Electronic) Linking ISSN: 17470277 NLM ISO Abbreviation: Chem Biol Drug Des Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
|---|---|
| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 19824892 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: The anti-tumor effects of androstene steroids exhibit a strict structure-activity relationship dependent upon the orientation of the hydroxyl group on carbon-17. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Graf+MR%22">Graf MR</searchLink>; Department of Neurosurgery - Harold F. Young Neurosurgical Center and the Massey Cancer Center, Virginia Commonwealth University Medical Center, P.O. Box 980631, 1200 E. Broad Street, Richmond, VA 23298-0631, USA. mgraf@hsc.vcu.edu<br /><searchLink fieldCode="AU" term="%22Jia+W%22">Jia W</searchLink><br /><searchLink fieldCode="AU" term="%22Lewbart+ML%22">Lewbart ML</searchLink><br /><searchLink fieldCode="AU" term="%22Loria+RM%22">Loria RM</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101262549%22">Chemical biology & drug design</searchLink> [Chem Biol Drug Des] 2009 Dec; Vol. 74 (6), pp. 625-9. <i>Date of Electronic Publication: </i>2009 Oct 12. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Blackwell%22">Wiley-Blackwell </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101262549 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1747-0285 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217470277%22">17470277 </searchLink><i>NLM ISO Abbreviation: </i>Chem Biol Drug Des <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=19824892 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/j.1747-0285.2009.00900.x Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 625 Titles: – TitleFull: The anti-tumor effects of androstene steroids exhibit a strict structure-activity relationship dependent upon the orientation of the hydroxyl group on carbon-17. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Graf MR – PersonEntity: Name: NameFull: Jia W – PersonEntity: Name: NameFull: Lewbart ML – PersonEntity: Name: NameFull: Loria RM IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 12 Text: 2009 Dec Type: published Y: 2009 Identifiers: – Type: issn-electronic Value: 1747-0285 Numbering: – Type: volume Value: 74 – Type: issue Value: 6 Titles: – TitleFull: Chemical biology & drug design Type: main |
| ResultId | 1 |
