Redetermination of 5α-androstane-3,17-dione

被引:2
|
作者
Jasinski, Jerry P. [1 ]
Butcher, Ray J. [2 ]
Al-arique, Q. N. M. Hakim [3 ]
Yathirajan, H. S. [3 ]
Narayana, B. [4 ]
机构
[1] Keene State Coll, Dept Chem, Keene, NH 03435 USA
[2] Howard Univ, Dept Chem, Washington, DC 20059 USA
[3] Univ Mysore, Dept Studies Chem, Mysore 570006, Karnataka, India
[4] Mangalore Univ, Dept Studies Chem, Mangalagangothri 574199, Karnataka, India
关键词
CRYSTAL; ANDROSTANES; BOND;
D O I
10.1107/S1600536810019720
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
The structure of the title compound, C(19)H(28)O(2), has been redermined at 295 (2) K, with much improved precision. The structure and molecular packing of the title compound was first reported by Coiro et al. [Acta Cryst. (1973). B29, 1404-1409] by means of potential-energy calculations. The cell parameters in this study differ considerably in space group C2. It is a derivative of testosterone and consists of a cyclopentanone ring (A) fused to to successive cyclohexane (B and C) and cyclohexanone (D) rings. The three cyclohexanone rings are in slightly distorted boat configurations and the cyclopentanone ring is a distorted half-chair. The crystal packing is stabilized by weak intermolecular C-H center dot center dot center dot O interactions involving O atoms from each of the cyclohexanone and cyclopentanone rings and H atoms from each of their respective rings.
引用
收藏
页码:O1517 / U2348
页数:12
相关论文
共 50 条
  • [21] 3α-Hydroxy-5α-androstane-4,17-dione
    Departamento de Física, Faculdade de Cie. e Tecnologia, Universidade de Coimbra, P-3000 Coimbra, Portugal
    不详
    Acta Crystallogr Sect C Cryst Struct Commun, 12 (2149-2151):
  • [22] 3α-Hydroxy-5α-androstane-4,17-dione
    Andrade, LCR
    Paixao, JA
    de Almeida, MJ
    da Silva, EJT
    Melo, MLSE
    Neves, ASC
    ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY, 1999, 55 : 2149 - 2151
  • [23] REDUCTION OF GRAFT VERSUS HOST REACTIVITY OF MOUSE AND RAT SPLEEN-CELLS BY 5ALPHA-ANDROSTANE-3,17-DIONE
    SKOWRONCENDRZAK, A
    PLONKA, I
    BUBAK, M
    REMBIESA, R
    FOLIA BIOLOGICA, 1976, 22 (03) : 190 - 195
  • [24] 5,19-cyclo-9β,10ξ-androstane-3,17-dione promotes neurotrophic factor biosynthesis in 1321N1 human astrocytorna cells and improves passive avoidance learning impairment
    Obara, Yutaro
    Haganuma, Asami
    Murakami, Shinsuke
    Chiba, Toshiki
    Mori, Koichiro
    Nakagawasai, Osamu
    Tadano, Takeshi
    Kikuchi, Haruhisa
    Oshima, Yoshiteru
    Nakahata, Norimichi
    BRAIN RESEARCH, 2007, 1184 : 57 - 64
  • [25] MICROBIOLOGICAL HYDROXYLATION OF ANDROST-4-ENE-3,17-DIONE AND ANDROST-1,4-DIENE-3,17-DIONE
    KOLYVANOVA, TS
    BAYUNOVA, VI
    GABINSKAYA, KN
    KOROBOVA, YN
    GRINENKO, GS
    KHIMIKO-FARMATSEVTICHESKII ZHURNAL, 1989, 23 (05): : 635 - 637
  • [26] A REINVESTIGATION OF THE REACTION OF BROMINE WITH 5BETA-ESTRANE-3,17-DIONE
    ABULHAJJ, YJ
    JOURNAL OF ORGANIC CHEMISTRY, 1986, 51 (15): : 3059 - 3061
  • [27] REACTION OF DELTA5-ANDROSTENE-3,17-DIONE WITH CUPRIC ION
    KOERNER, DR
    BIOCHIMICA ET BIOPHYSICA ACTA, 1969, 176 (04) : 880 - &
  • [28] SEXUAL SPECIFIC C-4 HYDROXYLATION OF 5 ALPHA-ANDROSTANE-3,17-DIONE IN RATS AND INFLUENCE OF ANTIANDROGEN CYPROTERON ACETATE
    WENZEL, M
    BOLLERT, B
    PITZEL, L
    HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1972, 353 (06): : 861 - &
  • [29] An efficient synthesis of 5α-androst-1-ene-3,17-dione
    Zhang, Huyue
    Qiu, Zhuibai
    STEROIDS, 2006, 71 (13-14) : 1088 - 1090
  • [30] Conversion of etioallocholan-3,17-dione into androsterone
    Dorfman, RI
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1940, 132 (01) : 457 - 458