UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
B B B0 B1 B4 B7 B8 BA BB BC BD BE BF BG BH BI BK BL BM BN BO BP BR BS BT BU BV BW BX BY BZ
BE BE+ BEA BEB BEC BED BEE BEF BEG BEH BEI BEK BEL BEM BEN BEP BER BES BET BEU BEV BEX

(11Beta,17beta)-9-fluoro-11,17-dihydroxy-17-methylandrost-4-en-3-one

[A halogenated derivative of 17-alpha-methyltestosterone. Similar to testosterone, fluoxymesterone binds to and activates specific nuclear receptors, resulting in an increase in protein anabolism, a decrease in amino acid catabolism, and retention of nitrogen, potassium, and phosphorus. This agent also may competitively inhibit prolactin receptors and estrogen receptors, thereby inhibiting the growth of hormone-dependent tumor lines. Fluoxymesterone is approximately five times more potent than methyltestosterone. (NCI04) ( NCI )]
UMLS (NCI) C0016366
 
Steroid
Pharmacologic Substance
Hormone
Relation/PAR: Androstenediols
Steroids, Fluorinated
[HS100] ANDROGENS/ANABOLICS
Relation/CHD: FLUOXYMESTERONE 10 MG
FLUOXYMESTERONE 2 MG
FLUOXYMESTERONE 5 MG

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