推荐产品
质量水平
检测方案
≥99.0% (HPLC)
形式
crystals
旋光性
[α]20/D +57±2°, c = 1% in chloroform
药品控制
USDEA Schedule IIIN; regulated under CDSA - not available from Sigma-Aldrich Canada
SMILES字符串
C[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@H]34)[C@@H]1CC[C@@H]2O
InChI
1S/C18H26O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h10,13-17,20H,2-9H2,1H3/t13-,14+,15+,16-,17-,18-/m0/s1
InChI key
NPAGDVCDWIYMMC-IZPLOLCNSA-N
基因信息
human ... SERPINA6(866) , SHBG(6462)
rat ... Ar(24208) , Nr3c2(25672) , Pgr(25154)
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一般描述
19-Nortestosterone, also known as nandrolone or 17β-hydroxy-19-nor-4-androsten-3-one, is an androgenic anabolic steroid (AAS).
应用
19-Nortestosterone can be used as a reactant to prepare:
- Fluorescent nandrolone-BODIPY conjugates to study intracellular localization and tracking of nandrolone using fluorescence microscope.
- Optically pure hexadecahydrochrysene diastereomers, and chrysene enantiomers.
其他说明
可能实行销售限制
警示用语：
Danger
危险声明
危险分类
Carc. 2 - Repr. 1B
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
The use of symmetry in enantioselective synthesis: Four pairs of chrysene enantiomers prepared from 19-nortestosterone
Stastna E, et al.
Organic & Biomolecular Chemistry, 9(12), 4685-4694 (2011)
Simeon Pierre Fodouop Chegaing et al.
Steroids, 162, 108679-108679 (2020-06-23)
Although the discovery of antibiotics has decreased the spread and severity of infectious diseases, their uncontrolled use has lead to the emergence of bacterial resistance to existing chemotherapeutic agents. Bacterial disease thus remains a challenge for health authorities in worldwide
Synthesis and biological evaluation of nandrolone-bodipy conjugates
J Michal, et al.
Steroids, 97, 62-66 (2015)
V Bricout et al.
European journal of applied physiology, 92(1-2), 1-12 (2004-03-26)
Norsteroids are xenobiotics with androgenic and anabolic properties known since as far back as the 1930s. In doping controls, the use of the banned xenobiotic norsteroids is detected in the competitor's urines by the measurement of norandrosterone (19-NA) and noretiocholanolone
P Kintz et al.
Journal of pharmaceutical and biomedical analysis, 24(5-6), 1125-1130 (2001-03-15)
A sensitive, specific and reproducible method for the quantitative determination of nandrolone in human hair has been developed. The sample preparation involved a decontamination step of the hair with methylene chloride. The hair sample (about 100 mg) was solubilized in
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