Oestrogen synthetase

KAO Y c, ZHOU c, SHERMAN M, LAUGHTON 0 A, CHEN s (1998) Molecular basis of the inhibition of human aromatase (oestrogen synthetase) by flavone and isoflavone phytoestrogens a site-directed mutagenesis study. Environ Health Perspect. 106 85-92. 

Exelderm sulconazole. exemestane [inn] (FCE 24304) is a steroid, with AROMATASE INHIBITOR (oestrogen synthetase inhibitor) activity. It is under investigation for use in certain anticancer treatments. 

Mithramycin ) is an (anthracycline group) antibiotic isolated from Streptomyces sp. It has cytotoxic properties and clinically may be used as an oral and parenteral anticancer agent, particularly for testicular cancer, plomestane (inn, usan] (MDL 18962) is a steroid with AROMATASE inhibitor (oestrogen synthetase inhibitor) activity. It is under investigation for some anticancer applications, e.g. for treatment of breast cancer. 

Flavovirus membrane and capsid proteins Oestrogen synthetase Sendai virus detergent extract Nucleoproteins Nucleoproteins Calmodulin... 

The concept that oestrogens stimulate cell proliferation directly arises mainly from the observation that physiological concentrations of oestrogens stimulate both the de novo and salvage pathways of DNA synthesis as well as inducing a number of enzymes intimately involved in DNA synthesis and including DNA polymerase, thymidine and uridine kinases, thymidilate synthetase and dihydrofolate reductase. There is evidence that some of these enzymes may be regulated at the transcrip-... 

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