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Merck
CN

74640

Sigma-Aldrich

19-去甲睾酮

≥99.0% (HPLC)

别名:

17β-羟基-19-去甲雄甾-4-烯-3-酮, 17β-羟基-4-雌烯-3-酮, 19-去甲雄甾烯醇酮, 4-雌烯-17β-醇-3-酮, Nadrolone, 诺龙

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关于此项目

经验公式（希尔记法）:
C18H26O2
化学文摘社编号:
434-22-0
分子量:
274.40
Beilstein:
2055849
EC 号:
207-101-0
MDL编号:
MFCD00003664
UNSPSC代码:
51111800
PubChem化学物质编号:
57652521
NACRES:
NA.22

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质量水平

200

方案

≥99.0% (HPLC)

表单

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

官能团

hydroxyl
ketone

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

象形图

Health hazard
GHS08

警示用语：

Danger

危险声明

H351,H360FD

危险分类

Carc. 2 - Repr. 1B

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

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
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCN2901
BCCF3920
BCBP2063V
BCBJ1311V
BCBB6343V

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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)
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)
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
Pieter Van Renterghem et al.
Analytica chimica acta, 768, 41-48 (2013-03-12)
Due to their performance enhancing properties, use of anabolic steroids (e.g. testosterone, nandrolone, etc.) is banned in elite sports. Therefore, doping control laboratories accredited by the World Anti-Doping Agency (WADA) screen among others for these prohibited substances in urine. It
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