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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/02/26 18:21:48」(JST)

English Journal

Steroid conversion with CYP106A2 - production of pharmaceutically interesting DHEA metabolites.

Schmitz D, Zapp J, Bernhardt R1.
Microbial cell factories.Microb Cell Fact.2014 Jun 5;13:81. doi: 10.1186/1475-2859-13-81.
BACKGROUND: Steroids are lipophilic compounds with a gonane skeleton and play an important role in higher organisms. Due to different functionalizations - mainly hydroxylations - at the steroid molecule, they vary highly in their mode of action. The pharmaceutical industry is, therefore, interested
PMID 24903845

Does hormonal contraception prior to in vitro fertilization (IVF) negatively affect oocyte yields? A pilot study.

Barad DH1, Kim A, Kubba H, Weghofer A, Gleicher N.
Reproductive biology and endocrinology : RB&E.Reprod Biol Endocrinol.2013 Apr 4;11:28. doi: 10.1186/1477-7827-11-28.
BACKGROUND: As oral contraceptives (OCs) suppress anti-Müllerian hormone (AMH), and hormonal contraceptives (HCs), likely, suppress functional ovarian reserve, this study was initiated to determine whether HC affect oocyte yields.METHODS: We investigated in a retrospective cohort study 43 oocyte do
PMID 23557032

Bimodal binding and free energy of the progesterone receptor in the induction of female sexual receptivity by progesterone and synthetic progestins.

Kubli-Garfias C1, González-Flores O, Gómora-Arrati P, González-Mariscal G, Vázquez-Ramírez R, Beyer C.
The Journal of steroid biochemistry and molecular biology.J Steroid Biochem Mol Biol.2013 Jan;133:43-50. doi: 10.1016/j.jsbmb.2012.08.010. Epub 2012 Aug 31.
Synthetic progestins (SPs) are used for regulation of fertility, contraception and hormone replacement therapy. The acetylated medroxyprogesterone (MPA), megestrol (MGA) and chlormadinone (CLA) are related to progesterone (P). Other SPs are 19-nortestosterone derivatives such as: norethisterone (NET
PMID 22960752

Gonane
Names
	Preferred IUPAC name 2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17-Hexadecahydro-1H-cyclopenta[a]phenanthrene; Tetracyclo[8.7.0.02,7.011,15]heptadecane[citation needed]
	Other names 18-Norestrane[citation needed]
Identifiers
CAS Number	4732-76-7 (1R,2S,10S,11R,15S)- heptadecane
ChEBI	CHEBI:35528
ChemSpider	5256859 (1R,2S,10S,11R,15S)- heptadecane ; 5256861 (1R,2S,7R,10S,11R,15S)- heptadecane ; 5256860 (1R,2S,7S,10S,11R,15S)- heptadecane ; 1077
Jmol interactive 3D	Image
KEGG	C19639
PubChem	1108; 6857523 (1R,2S,10S,11R,15S)- heptadecane; 6857525 (1R,2S,7R,10S,11R,15S)- heptadecane; 6857524 (1R,2S,7S,10S,11R,15S)- heptadecane
	InChI InChI=1S/C17H28/c1-2-6-14-12(4-1)8-10-17-15-7-3-5-13(15)9-11-16(14)17/h12-17H,1-11H2/t12?,13-,14-,15+,16+,17-/m0/s1 Key: UACIBCPNAKBWHX-CTBOZYAPSA-N ;
	SMILES C2C1[C@H](CCCC1)[C@H]3CC[C@H]4[C@H]([C@@H]3C2)CCC4 ;
Properties
Chemical formula	C17H28
Molar mass	232.41 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	Infobox references

Names

Preferred IUPAC name 2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17-Hexadecahydro-1H-cyclopenta[a]phenanthrene; Tetracyclo[8.7.0.0^2,7.0^11,15]heptadecane^{[citation needed]}
Other names 18-Norestrane^{[citation needed]}
Identifiers
CAS Number	4732-76-7 (1R,2S,10S,11R,15S)- heptadecane^N
ChEBI	CHEBI:35528^Y
ChemSpider	5256859 (1R,2S,10S,11R,15S)- heptadecane^Y 5256861 (1R,2S,7R,10S,11R,15S)- heptadecane^Y 5256860 (1R,2S,7S,10S,11R,15S)- heptadecane^Y 1077^Y
Jmol interactive 3D	Image
KEGG	C19639^N
PubChem	1108 6857523 (1R,2S,10S,11R,15S)- heptadecane 6857525 (1R,2S,7R,10S,11R,15S)- heptadecane 6857524 (1R,2S,7S,10S,11R,15S)- heptadecane
InChI InChI=1S/C17H28/c1-2-6-14-12(4-1)8-10-17-15-7-3-5-13(15)9-11-16(14)17/h12-17H,1-11H2/t12?,13-,14-,15+,16+,17-/m0/s1^Y Key: UACIBCPNAKBWHX-CTBOZYAPSA-N^Y
SMILES C2C1[C@H](CCCC1)[C@H]3CC[C@H]4[C@H]([C@@H]3C2)CCC4
Properties
Chemical formula	C₁₇H₂₈
Molar mass	232.41 g·mol⁻¹
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
Infobox references