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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/06/21 16:57:06」(JST)

English Journal

Biddle ST, O'Donnell A, Houghton E, Creaser CS.SourceHFL Sport Science, Quotient Bioresearch, Newmarket Road, Fordham, CB7 5WW, UK.
Rapid communications in mass spectrometry : RCM.Rapid Commun Mass Spectrom.2013 Oct 30;27(20):2229-38. doi: 10.1002/rcm.6689.
RATIONALE: Norethisterone has been used as a successful oral contraceptive in humans for many years. It was recently permitted for use as an oestrus suppressant in racing greyhounds. To monitor the use of norethisterone as part of a routine drug surveillance programme, knowledge of its metabolism wa
PMID 24019188

Prometaphase arrest-dependent phosphorylation of Bcl-2 family proteins and activation of mitochondrial apoptotic pathway are associated with 17α-estradiol-induced apoptosis in human Jurkat T cells.

Han CR, Jun do Y, Kim YH, Lee JY, Kim YH.SourceCollege of Natural Sciences, Kyungpook National University, Daegu, Republic of Korea.
Biochimica et biophysica acta.Biochim Biophys Acta.2013 Oct;1833(10):2220-32. doi: 10.1016/j.bbamcr.2013.05.016. Epub 2013 May 23.
In Jurkat T cell clone (JT/Neo), G2/M arrest, apoptotic sub-G1 peak, mitochondrial membrane potential (Δψm) loss, and TUNEL-positive DNA fragmentation were induced following exposure to 17α-estradiol (17α-E2), whereas none of these events (except for G2/M arrest) were induced in Jurkat cells ove
PMID 23707954

Effect of various forms of postmenopausal hormone therapy on the risk of ovarian cancer--a population-based case control study from Finland.

Koskela-Niska V, Pukkala E, Lyytinen H, Ylikorkala O, Dyba T.SourceDepartment of Obstetrics and Gynecology, Helsinki University Central Hospital, HUS, Finland. virpi.koskela-niska@fimnet.fi
International journal of cancer. Journal international du cancer.Int J Cancer.2013 Oct 1;133(7):1680-8. doi: 10.1002/ijc.28167. Epub 2013 Apr 16.
Postmenopausal hormone therapy (HT) associates with an increased risk of ovarian cancer, but its' influence on tumor histology is not as well known. Therefore, we evaluated the effect of various types of HT on the risk of epithelial ovarian cancer by histological subtype. All Finnish women diagnosed
PMID 23526244

Syntheses of Biologically Active Natural Products and Leading Compounds for New Pharmaceuticals Employing Effective Construction of a Polycyclic Skeleton

リンク元

Estrane
	IUPAC name Estrane
	Systematic name 15-Methyltetracyclo[8.7.0.02,7. 011,15] heptadecane[citation needed]
Identifiers
PubChem	12313694, 5460658 (1R,2S,10R,11S,15S)-15-methyl,heptadec, 6857465 (1R,2S,7R,10R,11S,15S)-15-methyl,heptadec, 6857457 (1R,2S,7S,10R,11S,15S)-15-methyl,heptadec
ChemSpider	11179505 , 4574149 (1R,2S,10R,11S,15S)-15-methyl,heptadec , 5256802 (1R,2S,7R,10R,11S,15S)-15-methyl,heptadec , 5256794 (1R,2S,7S,10R,11S,15S)-15-methyl,heptadec
ChEBI	CHEBI:23966
Beilstein Reference	3125721
Jmol-3D images	Image 1
	SMILES CC12CCCC1C1CCC3CCCCC3C1CC2 ;
	InChI InChI=1S/C18H30/c1-18-11-4-7-17(18)16-9-8-13-5-2-3-6-14(13)15(16)10-12-18/h13-17H,2-12H2,1H3 ; Key: GRXPVLPQNMUNNX-UHFFFAOYSA-N ;
Properties
Molecular formula	C18H30
Molar mass	246.43 g mol−1
	Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
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	Infobox references