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Equilin Glucoronide D4

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SZ目录编号 SZ-E035D04
CAS 号 NA
分子式 C24H24D4O8
分子量 448.5
投资状态 Custom Synthesis


Disclaimer

SynZeal product information given on this website is as per the existing understanding while publishing the details on website. The customer is responsible for assessing the accuracy of the information at the time of actual purchase.

SynZeal will update these details as per new development or finding in product specification without further noticed.

化学名称: (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(((9S,13S,14S)-13-methyl-17-oxo-9,11,12,13,14,15,16,17-octahydro-6H-cyclopenta[a]phenanthren-3-yl-2,4,16,16-d4)oxy)tetrahydro-2H-pyran-2-carboxylic acid

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

微笑: C[C@@]1(C2=O)[C@](CC2([2H])[2H])([H])C3=CCC4=C(C=C([2H])C(O[C@@H]([C@@H]([C@@H](O)[C@@H]5O)O)O[C@@H]5C(O)=O)=C4[2H])[C@@]3([H])CC1

Equilin Glucoronide D4 is chemically (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(((9S,13S,14S)-13-methyl-17-oxo-9,11,12,13,14,15,16,17-octahydro-6H-cyclopenta[a]phenanthren-3-yl-2,4,16,16-d4)oxy)tetrahydro-2H-pyran-2-carboxylic acid. Equilin Glucoronide D4 is supplied with detailed characterization data compliant with regulatory guideline. Equilin Glucoronide D4 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Equilin.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.

The Major Metabolite of Equilin, 4-Hydroxyequilin, Autoxidizes to an o-Quinone Which Isomerizes to the Potent Cytotoxin 4-Hydroxyequilenin-o-quinone
Fagen Zhang, Yumei Chen, Emily Pisha, Li Shen, Yansan Xiong, Richard B. van Breemen, and Judy L. Bolton
Chem. Res. Toxicol. 1999, 12, 204-213
 
HPLC-¯uorescence determination of equilin and equilenin in postmenopausal women's urine
Rita Gatti1 *, Michele Franchina2 , Maria Grazia Gioia1 and Vanni Cavrini1
BIOMEDICAL CHROMATOGRAPHY Biomed. Chromatogr. 14: 82–88 (2000)
 
Quantitative Separation of Free Estrogens by Liquid Partition Chromatography
G. j. krol, R. p. masserano, J. f. carney, and B. t. kho
The United States Pharmacopeia Volume59, Issue10 October 1970 Pages 1483-1487

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