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Patent

Polyaryl antitumor agents

TLDR
A compound of the formula: Ar.sub.1 -B--Ar.sub-2 where Ar 1 is unsubstituted or substituted phenyl, thienyl, furanyl, or pyrrolyl, in which each substituent of the substituted persons, such as phenyl and pyrronyl, independently, is aldehyde, acyl, ester, carboxyl, amido, nitrile, nitro, cyano, acetal, oxoalkyl, aminoalkyl and oxo-alkyl as discussed by the authors.
Abstract
A compound of the formula: Ar.sub.1 --B--Ar.sub.2 wherein Ar 1 is unsubstituted or substituted phenyl, thienyl, furanyl, or pyrrolyl, in which each substituent of the substituted phenyl, substituted thienyl, substituted furanyl, and substituted pyrrolyl, independently, is aldehyde, acyl, ester, carboxyl, amido, nitrile, nitro, cyano, acetal, ketal, oxoalkyl, aminoalkyl, hydroxyalkyl, haloalkyl, iminoalkyl, acid halide, aminoalkylaminoalkyl, aminoalkylaminoalkylamino, hydroxyalkylaminoalkyl, or hydroxyalkylaminoalkylaminoalkyl; B is, --CH═CH--, or --C C--, in which R is H, alkyl, hydroxyl, alkoxy, ester, aldehyde, hydroxyalkyl, aminoalkyl, carboxyl, --CH(OR 1 ) 2 , or NR 2 R 3 , where each R 1 , independently, is H, alkyl, or acyl; and each of R 2 and R 3 , independently, is H, alkyl, hydroxyalkyl, or aminoalkyl; and Ar 2 is substituted phenyl, substituted thienyl, substituted furanyl, or substituted pyrrolyl, in which each substituent of the substituted phenyl, substituted thienyl, substituted furanyl, and substituted pyrrolyl, independently, is amido, nitrile, nitro, cyano, acetal, ketal, oxoalkyl, aminoalkyl, haloalkyl, iminoalkyl, acid halide, aminoalkylaminoalkyl, aminoalkylaminoalkylamino, hydroxyalkylaminoalkyl, or hydroxyalkylaminoalkylaminoalkyl; or a salt thereof. Also disclosed is a composition which contains a pharmaceutical acceptable carrier and an effective amount of a compound of the above formula.

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Citations
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Novel thiophene derivatives, preparation method thereof and pharmaceutical compositions containing same

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References
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Journal ArticleDOI

Model reactions on roast aroma formation. XIII. The formation of some uncommon N-heterocyclic compounds and furans after roasting of tryptophan with reducing sugars and sugar degradation products

TL;DR: In this paper, after treatment of d -glucose and d -xylose with tryptophan under the conditions of coffee roasting, 311 volatile compounds were identified.
Journal ArticleDOI

Electrochemical synthesis and optical analysis of poly[(2,2′-dithienyl)-5,5′-diylvinylene]

TL;DR: The electrochemical synthesis of poly[2,2′-dithienyl)-5,5′-diylvinylene tetrafluoroborate] (PDTE/BF4) has been accomplished and provides coppery-black free-standing films with a room-temperature four-probe conductivity as high as 15 (Ω cm)−1.
Journal ArticleDOI

Electrochemical preparation of poly(di(2-thienyl) benzene)s and poly(4,4'-di(2-thienyl) biphenyl)

TL;DR: In this article, the infrared spectra of the films indicated oxidative coupling to occur at the 5 and 5′ positions of the thiophene rings in T13B, T14B and TBP.
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Medicinal thiophene compounds

TL;DR: A method of treating inflammation including administering to a subject an effective amount of a compound of the following formula: ##STR1## wherein m is 1-4; and each of A and B, independently, is H, C 1-7 alkyl, C 2-7 alkynyl, (CH 2 ) n CHO, CH 2 ) o COOH, c 1- 7 alkoxy, c 2 -7 alkoxyalkyl, CN, NO 2, halogen, CH(OR 1 ) 2, CO.CR 4, CR 1 =CR 5 R