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filingDate 1992-10-27^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0d61a931abe8466e1643630d8337ccff
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a05aa04201bfb9bb1758129f876d87c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cf482d11c4276f68e54ad3f21dcdf455
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e37b7eb02f20818506d1cd0868c7fc80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_830d78b2fb3668c283f3e5ee17f3a942
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b64ee263b00f82978448b18ab5fa6929
publicationDate 1994-03-01^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0656724-A
titleOfInvention Method for producing new alkene derivative
abstract (57) [Summary] (Modified) [Structure] Formula (II): (In the formula, n is 0 or 1 to 4; R 1 and R 2 are H, O H, an alkoxy group having 1 to 4 carbon atoms, a benzyloxy group or a methoxymethoxy group; R 3 is H, OH, a halogen atom, an alkoxy group having 1 to 4 carbon atoms, a benzyloxy group, A compound of formula (I) obtained by dehydrating a compound of (methoxymethoxy group, etc.): And a compound of formula (I). [Effect] The compound of formula (I) and its non-toxic pharmacologically acceptable salt or ester exhibit useful pharmacological actions such as estrogen activity, anti-estrogen activity, progesterone activity and anti-tumor activity.
priorityDate 1982-05-27^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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