1
Peter Loeliger: Stilbene derivatives. Hoffmann La Roche, Jon S Saxe, George M Gould, William H Epstein, April 20, 1982: US04326055 (177 worldwide citation)

This invention is directed to 5,6,7,8-tetrahydro-naphthyl or indanyl stilbene derivatives which are useful as tumor inhibiting agents, in the treatment of neoplasms, dermatological conditions and rheumatic illnesses.


2
Koichi Shudo: Stilbene derivatives. Gordon W Hueschen, February 2, 1988: US04723028 (111 worldwide citation)

The application discloses certain stilbene compounds, pharmaceutical compositions thereof, method of treating thereof, method of diagnosis therewith, and method for the preparation thereof. The compounds and compositions are useful for diagnosis of leukemia types, the treatment of dermatological dis ...


3
Mark S Cushman, Ernest Hamel: Stilbene derivatives as anticancer agents. Research Corporation Technologies, Scully Scott Murphy & Presser, July 4, 1995: US05430062 (59 worldwide citation)

The present invention relates to stilbene derivatives which possess utility as anti-cancer agents. The compounds can be used to treat cancers which are susceptible to treatment therewith, and can be utilized in a method of treating such cancers. Pharmaceutical compositions containing the compounds a ...


4
Phillip D Montgomery, Richard N Moore, Walter R Knox: Production of stilbene and styrene. Monsanto Company, Elizabeth F Sporar, Paul L Passley, June 22, 1976: US03965206 (33 worldwide citation)

Toluene and toluene derivatives are dehydrocoupled to stilbene and stilbene derivatives in a vapor phase reaction in the presence of a metal oxide. The stilbene products are purified of by-product polar impurities. The purified stilbene can be catalytically reacted in the vapor phase with ethylene t ...


5
Sharon R Isaac, Kevin M Harris: Golf ball clear coating with optical brighteners. Acushnet Company, Lucas & Just, May 28, 1991: US05018742 (32 worldwide citation)

An improvement in the appearance of golf balls is disclosed. The "clear coat," i.e. the transparent coat which is the last put on the outer surface of the golf ball, has included in it an optical brightener, preferably one selected from the group consisting of stilbene derivatives, styryl derivative ...


6
Sharon R Isaac, Kevin M Harris: Optical brightners in golf ball clear coatings. Acushnet Company, Lucas & Just, September 12, 1989: US04865326 (31 worldwide citation)

An improvement in the appearance of golf balls is disclosed. The "clear coat," i.e. the transparent coat which is the last put on to the outer surface of the golf ball, has included in it an optical brightener, preferably one selected from the group consisting of stilbene derivatives, styryl derivat ...


7
Koji Obsumi, Takashi Tsuji, Yoshihiro Morinaga, Kazuo Ohishi: Stilbene derivatives and pharmaceutical compositions containing them. Ajinomoto, Sughrue Mion Zinn Macpeak & Seas, June 11, 1996: US05525632 (31 worldwide citation)

A stilbene derivative of the following general formula (I) or a pharmaceutically acceptable acid addition salt thereof have low toxicity, but are water soluble and effective as carcinostatics: ##STR1## wherein R.sup.1, R.sup.2 and R.sup.3, which may be the same or different, each represent an alkyl ...


8
Masaomi Sasaki: Stilbene derivatives. Ricoh Company, Flynn Thiel Boutell & Tanis, January 9, 1990: US04892949 (30 worldwide citation)

An electrophotograhic photoconductor is disclosed which comprises an electroconductive support material and a photosensitive layer comprising at least one of the stilbene compounds of the formula ##STR1## wherein R.sup.1 represents hydrogen or ##STR2## R.sup.2 represents hydrogen, an alkyl group or ...


9
Ulrich Schirmer, Stefan Karbach, Ernst Heinrich Pommer, Eberhard Ammermann, Wolfgang Steglich, Barbara A M Schwalge, Timm Anke: Stilbene derivatives, and fungicides which contain these compounds. BASF Aktiengesellschaft, Keil & Weinkauf, February 2, 1988: US04723034 (28 worldwide citation)

Stilbene derivatives of the formula ##STR1## where R.sup.1 and R.sup.2 independently of one another are each C.sub.1 -C.sub.8 -alkyl, X is hydrogen, halogen, C.sub.1 -C.sub.4 -alkoxy, trifluoromethyl, cyano or nitro, Y is hydrogen, alkyl, haloalkyl, alkoxyalkyl, cycloalkyl, aralkyl, aryl, aryloxy, h ...


10
Koji Ohsumi, Takashi Tsuji, Yoshihiro Morinaga, Kazuo Ohishi: Stilbene derivatives and pharmaceutical compositions containing them. Ajinomoto Co, Sughrue Mion Zinn Macpeak & Seas PLLC, March 24, 1998: US05731353 (27 worldwide citation)

A stilbene derivative of the following general formula (I) or a pharmaceutically acceptable acid addition salt thereof have low toxicity, but are water soluble and effective as carcinostatics: ##STR1## wherein R.sup.1, R.sup.2 and R.sup.3, which may be the same or different, each represent an alkyl ...