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7584630 |
Photochromic ocular devices
Described are photochromic ocular devices such as contact lenses and intraocular lenses made of an organic polymeric material and at least one photochromic material capable upon exposure to actinic...
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7329687 |
Flavanoid compounds as chemotherapeutic, chemopreventive, and antiangiogenic agents
Compounds useful as chemotherapeutic, chemopreventive, and antiangiogenic agents are provided. The compounds are flavanoids, including flavanones, flavanols, and chalcones. The compounds have the...
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7253207 |
Quinones as disease therapies
Novel quinones are provided, as well as compositions comprising these novel quinones. Methods of using the novel quinones in treatment of various indications including cancer are also provided.
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7250120 |
Benzo-, naphtho- and phenanthrochromene substituted by carbamated or ureated phenyls, preparation thereof and compositions and articles containing them
Disclosed are novel benzo-, naphtho- and phenanthrochromenes substituted by carbamated or ureated phenyls having the following general formula (I):
wherein R 1 represents a group
their...
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7105685 |
Cannabinol derivatives
The invention provides cannabinol derivatives and pharmaceutical preparations thereof.
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6967249 |
Photochromic 3H-naphtho[2,1-b]-pyran compounds and photochromic articles produced therewith
Specific photochromic 3H-naphtho[2,1-b]-pyran compounds useful with various types of synthetic resin materials to form photochromic articles, especially ophthalmic lenses, and photochromic articles...
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6939007 |
Photochromic bis-naphthopyran compounds and methods for their manufacture
The invention provides photochromic bis-naphthopyran compounds as well as methods for their manufacture and their use. The bis-naphthopyran compounds of the invention exhibit a wide range of color,...
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6890950 |
Lapachone delivery systems, compositions and uses related thereto
In part, the present invention is directed to a system comprising a lapachone or a prodrug thereof and a polymer, such as a biocompatible and optionally biodegradable polymer, methods for treatment...
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6887533 |
Fluorinated oxaanthracenes and their use in liquid-crystal mixtures
Compounds of the formula (I)
where:
X 1 is H or F G 1 -G 2 is —CH 2 —CH— or CH═C— R 1 , R 2 are a) H b) the M 2 -A 2 -R 5 moiety c) for example, a straight-chain or...
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6863843 |
Naphthopyran compounds, photoresponsive compositions and lenses
A photochromic [1,2-b] naphthopyran having a fluoro substituent in at least one of the 7-position or the 9-position of the naphthopyran provides a stable photochromic compound with a narrow range...
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6700001 |
Process for stereoselective synthesis of 2-hydroxymethyl chromans
A process for the stereoselective synthesis of 2-hydroxymethyl-chromans of formula (II) is provided where R, R 1 , R 2 and R 3 are as defined herein. The compound of formula (II) is prepared...
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6630597 |
Photochromic 6-aryl substituted 3H-naphtho(2,1-b)pyrans
Described are novel photochromic 6-aryl substituted 3H-naphtho[2,1-b]pyran compounds, examples of which are naphthopyran compounds having a substituted aryl group at the number 6 carbon atom and...
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6627121 |
Photochromic naphthopyran compounds
A photochromic naphthopyran of formula (I) wherein R 1 through R 15 , which may be the same or different, are independently selected from the group consisting of hydrogen, C 1 -C 4 alkyl, C 1 -C...
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6602903 |
Substituted heterocyclic compounds
The invention relates to compounds of formula (I): and medicinal products containing the same are useful in treating or in preventing melatoninergic disorders.
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6555028 |
Polymeric matrix compatibilized naphthopyrans
Described are polymeric matrix compatibilized naphthopyran compounds, examples of which are certain 2H-naphtho[1,2-b]pyrans, 3H-naphtho[2,1-b]pyrans and indeno[2,1-f]naphtho[1,2-b]pyrans each...
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6478989 |
Aromatic substituted naphthopyrans
Described are photochromic 2H-naphtho[1,2-b]pyrans characterized by having an aromatic substituent in the 5 position. The aromatic group at 5-position of the naphthopyran is a substituted or...
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6478988 |
Photochromic substituted naphthopyran compounds
The present invention relates to naphthopyrans, particularly 3,3-[substituted]-naphtho[2,1-b]pyrans and 2,2-[substituted]-naphtho[1,2-b]pyrans and particularly to novel substitution on the...
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6458974 |
Synthesis of β-lapachone and its intermediates
A novel process for synthesizing β-lapachone (beta-lapachone), an agent that has demonstrated significant antineoplastic activity against human cancer lines. The process comprises the conversion...
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6403347 |
HIV integrase inhibitors
Natural products such as certain chaetochromins are described. These compounds are useful in the inhibition of HIV integrase, the prevention or treatment of infection by HIV and the treatment of...
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6399791 |
Naphthopyran derivatives, compositions and (co) polymer matrices containing same
For subject, the present invention has novel naphthopyran derivatives of formula: optionally substituted in position(s) 2, 3, 4, 6, 7, 8, 9 or/and 10; the substituent Z in position 5 being of...
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6398987 |
Naphthopyrans having a perfluoroalkyl substituent in position 5, preparation and compositions and matrices containing them
The present invention relates to novel compounds of the naphthopyran type which have a perfluoroalkyl group (X) in position 5. These compounds are of formula (I) given below: These compounds (I)...
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6353102 |
Photochromic naphthopyrans
Described are novel photochromic naphtho[1,2-b]pyran compounds having certain substituents at the 2 position of the pyran ring, certain substituents at the 5 and 6 positions and optionally at the...
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6348604 |
Photochromic naphthopyrans
Described are novel photochromic 2H-naphtho[1,2-b]pyran compounds essentially characterized by having two adjacent moderate to strong electron donor substituents at the 8 and 9 positions or a fused...
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6340766 |
Substituted napthopyrans
Described are novel reversible photochromic naphthopyran compounds, examples of which are compounds having a cycloalkyl ester substituent at the number 5 carbon atom and optionally certain...
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6337409 |
Photochromic naphthopyran compounds
A naphthopyran compound represented by the formula: wherein R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , and R 11 are each selected from the group consisting essentially of hydrogen, a first...
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6281366 |
Photochromic [3H]naphtho[2,1-b]pyran compounds containing an acetylenic substituent, process for their manufacture, and photochromic materials and articles obtained
The present invention relates to photochromic [3H]naphtho[2,1-b]pyran compounds containing an acetylenic substituent, process for their manufacture, and photochromic materials and articles obtained...
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6248264 |
Neutral coloring photochromic 2H-naphtho[1,2-b] pyrans and heterocyclic pyrans
Compositions comprising a naphtho [1,2-b]pyran of formula (I): ##STR1## wherein R 7 and/or R 9 is hydrogen or an amino group provided that R 7 and R 9 are not both hydrogen, and the other...
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6211374 |
Water soluble, pyran-based photochromic compounds having carboxylate functionality
The present invention provides water-soluble, pyran-based photochromic compounds characterized by improved stability when in an open, excited configuration. The advantages of the present invention...
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6197225 |
Chromene compound
A photochromic compound featuring a large fading rate to prevent a change in the color tone at the time of fading, exhibiting little color after aged, and exhibiting good durability in the...
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6190580 |
Diaryl-2H-naphthopyrans
Photochromic diaryl-2H-naphthopyran structures, which dye photochromically well at room temperature, lighten up quickly when incorporated into ophthalmic lenses, possess longevity, and due to their...
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6146554 |
Photochromic naphtopyrane colorants, method for the production and use thereof, photochromic object
What is described here are photochromic naphthopyrane dyes with different substituents whose properties can be set by controlled selection of the substituents. In this manner it is possible to take...
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6113814 |
Polymerizable polyalkoxylated naphthopyrans
Described are novel photochromic polymerizable polyalkoxylated naphthopyran compounds, examples of which are certain 2H-naphtho[1,2-b]pyrans, 3H-naphtho[2,1-b]pyrans and...
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6096246 |
Photochromic naphthopyrans, compositions and articles containing them
The invention relates to photochromic compounds of general formula (I), in which: R3 and R5 are C1-C6 alkoxy groups and the rest of the R groups represent various substituents. ##STR1##
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6080338 |
Water soluble photochromic compounds, compositions and optical elements comprising the compounds
Described are novel water soluble photochromic naphthopyran and benzopyran compounds having an alkylaminoalkylamino group on the pyran portion or on the pyran portion and the naphtho- or...
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6043269 |
cis-3,4-chroman derivatives useful in the prevention or treatment of estrogen related diseases or syndromes
The present invention relates to therapeutically active compounds of formula I ##STR1## a method of preparing the same and to pharmaceutical compositions comprising the compounds. The novel...
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5990305 |
Photochromic diaryl-3H-naphthopyrane
Disclosed is a photochromic compound having a diaryl-3H-napthopyran structure, which has at the 8-position a nitrogen atom-linked hetercyclus, in which the heterocylcus can also have a HALS...
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5969163 |
Ortho-quinone derivatives, novel synthesis therefor, and their use in the inhibition of neoplastic cell growth
A process for the preparation of β-lapachone and dunnione derivatives of formulae I and II ##STR1## wherein, the a solution of lawsone in dimethylsufoxide at a temperature of -78° C. or less is...
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5961892 |
Polyalkoxylated naphthopyrans
Described are novel photochromic polyalkoxylated naphthopyran compounds, examples of which are certain 2H-naphtho 1,2-b!pyrans, 3H-naphtho 2,1-b!pyrans and indeno 2,1-f!naphtho 1,2-b!pyrans, each...
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5952515 |
Diaryl-2h-napthopyrans
The description concerns a photochromicsubstance, with a diaryl-2H-naphthopyrane having a link in the form Y--Ar, Z--Ar, Y--Ar--Y, Y--Ar--Y', Y--Ar--Z, Z--Ar--Z or Z--Ar--Z', in which Y, Y', Z and...
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5912362 |
Process for preparing isochroman compounds
High-purity isochroman compounds can be obtained in high yields according to a simple and economical process for preparing isochroman compounds, comprising the step of adding an aquesous solution...
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5843989 |
C.sub.4 -amide substituted compounds and their use as therapeutic agents
The invention provides certain 5 and/or 8 substituted benzopyran, pyranopyridine or tetrahydroquinaline compounds having C 4 -amide substituent and processes for making them. The compounds...
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5808100 |
Chromene compounds and photochromic materials
A photochromic compound which is initially colored less, exhibits excellent durability and features high color density and high color fading rate, and a photochromic material thereof. The...
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5783598 |
Antiretroviral naphthoquinone compounds compositions and uses thereof
The present invention provides novel antiviral naphthoquinone compounds, which may be isolated from plants of the genus Conospermum or synthesized chemically, in accordance with the present...
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5744070 |
Photochromic substituted naphthopyran compounds
Described are novel reversible photochromic naphthopyran compounds, examples of which are 3H-naphtho 2,1-b!pyrans having an acyl or aroyl oxy-bearing substituent at the number 6 carbon atom and...
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5707557 |
Photochromic 3H-naphthopyrans
Photochromic compounds with a 3H-naphthopyran structure having at least one pyrene moiety in the 3-position, a method for preparing such compounds, and the use of such compounds for producing...
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5705102 |
Photochromic spironaphthopyran compounds
A naphthopyran compound represented by the formula: ##STR1## wherein R 1 , R 2 , R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 are each selected from the group consisting essentially of hydrogen, a...
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5686586 |
Polycyclic aromatic derivatives, process for preparing the same and pharmaceutical and cosmetic compositions containing the same
A polycyclic aromatic compound having the formula ##STR1## and its salts have useful therapeutic and cosmetic action particularly in psoriasis. In the formula, X represents --CHCH--, O or S, ...
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5663375 |
Pharmaceutical compounds
Pharmaceutical compounds of the formula ##STR1## in which n is 0, 1 or 2 and R 1 is attached at any of the positions 7, 8, 9 or 10, and each R 1 is halo, carboxy, trifluoromethyl, hydroxy, C 1 -4...
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5658501 |
Substituted naphthopyrans
Described are novel reversible photochromic 2H-naphtho[1,2-b] pyran compounds, examples of which are compounds having certain substituents at the number 5 carbon atom of the naphtho-portion of the...
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5656206 |
Substituted naphthopyrans
Described are novel reversible photochromic 2H-naphtho[1,2-b]pyran compounds, examples of which are compounds having certain substituents at the number 5 carbon atom of the naphtho portion of the...
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