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US5338854A Expired / Lapsed US ⏱️ 0.0 years remaining

Fluorescent fatty acids derived from dipyrrometheneboron difluoride dyes

Assignee: Molecular Probes Inc
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Filing: 1991-02-13
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Granted: 1994-08-16
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Expires: 2011-02-13
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Abstract

Abstract This invention relates to improved fluorescent fatty acid analogs derived from dipyrrometheneboron difluoride ("BDY") dyes that absorb light at wavelengths longer than 480 nm. The BDY fluorophore or a derivative thereof is incorporated at various locations along the alkyl portion of the fatty acid ("BDY fatty acid"). The general formula of a BDY fatty acid is as follows: ##STR1## wherein at least one of the substituents R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 is a carboxylic acid terminated alkyl residue containing 5 to 22 carbon atoms. The remaining substituents, singly or in any combination, are: additional alkyl or arylalkyl residues containing 1 to 16 aliphatic carbon atoms, or aryl or heteroaryl residues, or hydrogen. Symmetrically substituted BDY fluorophores are conveniently synthesized from a single pyrrole precursor in a "one-pot" reaction. Alternatively, BDY fatty acids are synthesized from two different pyrrole precursors. The combination of fatty acids with these electrically neutral, photostable, strongly colored, and mostly highly fluorescent BDY dyes having relatively narrow absorption and emission spectra results in an improved fluorescent probe particularly useful for studying natural and synthetic lipid membranes and related areas.

Inventors

  • 👤 Hee C. Kang
  • 👤 Richard P. Haugland

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 04:35
CPC Classifications
C; C07; C07D; C07D207/00; C07D207/02; C07D207/44; C07F; C07F5/00; C07F5/02; C07F5/022; H; H01; H01S; H01S3/00; H01S3/14; H01S3/20; H01S3/213

Claims Analysis

Total Claims: 21
Claim 1
Independent Claim 229 words
A compound of the formula: ##STR6## wherein at least one of substituents R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 is a carboxylic acid terminated residue, wherein said residue is a linear hydrocarbon chain that is fully saturated or unsaturated, or contains one or more branches, again being saturated or unsaturated, said substituent containing 5 to 22 carbon atoms; wherein at least one of substituents R 1 , R 2 , R 3 , R 5 , R 6 and R 7 is an aryl or heteroaryl residue, where said aryl residue is unsubstituted phenyl, unsubstituted naphthyl, lower alkyl- or alkoxy-substituted phenyl, or lower alkyl- or alkoxy-substituted naphthyl, and where said heteroaryl residue is pyrrole, thiophene, furan, oxazole, isoxazole, oxadiazole, imidazole, benzoxazole, benzothiazole, benzimidazole, benzofuran, or indole; and the remaining substituents R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 , which may be the same or different, are alkyl or arylalkyl residues containing 1 to 16 aliphatic carbon atoms, or aryl or heteroaryl residues, where said aryl residue is unsubstituted phenyl, unsubstituted naphthyl, lower alkyl- or alkoxy-substituted phenyl, or lower alkyl- or alkoxy-substituted naphthyl, and where said heteroaryl residue is pyrrole, thiophene, furan, oxazole, isoxazole, oxadiazole, imidazole, benzoxazole, benzothizole, benzimidazole, benzofuran, or indole, or H.
Claim 2
Dependent Claim 229 words
A compound of the formula: ##STR6## wherein at least one of substituents R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 is a carboxylic acid terminated residue, wherein said residue is a linear hydrocarbon chain that is fully saturated or unsaturated, or contains one or more branches, again being saturated or unsaturated, said substituent containing 5 to 22 carbon atoms; wherein at least one of substituents R 1 , R 2 , R 3 , R 5 , R 6 and R 7 is an aryl or heteroaryl residue, where said aryl residue is unsubstituted phenyl, unsubstituted naphthyl, lower alkyl- or alkoxy-substituted phenyl, or lower alkyl- or alkoxy-substituted naphthyl, and where said heteroaryl residue is pyrrole, thiophene, furan, oxazole, isoxazole, oxadiazole, imidazole, benzoxazole, benzothiazole, benzimidazole, benzofuran, or indole; and the remaining substituents R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 , which may be the same or different, are alkyl or arylalkyl residues containing 1 to 16 aliphatic carbon atoms, or aryl or heteroaryl residues, where said aryl residue is unsubstituted phenyl, unsubstituted naphthyl, lower alkyl- or alkoxy-substituted phenyl, or lower alkyl- or alkoxy-substituted naphthyl, and where said heteroaryl residue is pyrrole, thiophene, furan, oxazole, isoxazole, oxadiazole, imidazole, benzoxazole, benzothizole, benzimidazole, benzofuran, or indole, or H.
Claim 3
Dependent Claim 40 words
A compound, as claimed in claim 1, wherein no more than two of the substituents R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are carboxylic acid terminated residues.
Claim 4
Dependent Claim 18 words
A compound, as claimed in claim 2, wherein the one or two carboxylic acid terminated residues is/are linear.
Claim 5
Dependent Claim 28 words
A compound, as claimed in claim 1, wherein no more than two of substituents R 1 , R 4 , and R 7 are carboxylic acid terminated residues.
Claim 6
Dependent Claim 16 words
A compound, as claimed in claim 4, wherein R 1 is one carboxylic acid terminated residue.
Claim 7
Dependent Claim 17 words
A compound, as claimed in claim 5, wherein said carboxylic acid terminated residue is linear and saturated.
Claim 8
Dependent Claim 16 words
A compound, as claimed in claim 4, wherein R 4 is one carboxylic acid terminated residue.
Claim 9
Dependent Claim 17 words
A compound, as claimed in claim 7, wherein said carboxylic acid terminated residue is linear and saturated.
Claim 10
Dependent Claim 47 words
A compound, as claimed in claim 1, wherein R 1 , R 2 , or R 3 , is one carboxylic acid terminated residue and R 5 , R 6 , or R 7 is one alkyl or arylalkyl residue containing 1 to 16 aliphatic carbon atoms.
Claim 11
Dependent Claim 23 words
A compound, as claimed in claim 9, wherein R 1 is one carboxylic acid terminated residue and R 7 is one alkyl residue.
Claim 12
Dependent Claim 28 words
A compound, as claimed in claim 9, wherein one carboxylic acid terminated residue contains n carbon atoms and one alkyl or arylalkyl residue contains (13-n) aliphatic carbon atoms.
Claim 13
Dependent Claim 33 words
A compound, as claimed in claim 11, wherein R 1 is one carboxylic acid terminated residue containing n carbon atoms, where n is greater than 8; and R 7 is one alkyl residue.
Claim 14
Dependent Claim 40 words
A compound, as claimed in claim 1, wherein R 1 , R 2 , or R 3 , is one carboxylic acid terminated residue; and R 5 , R 6 , or R 7 is one aryl or heteroaryl residue.
Claim 15
Dependent Claim 25 words
A compound, as claimed in claim 13, wherein R 1 is one carboxylic acid terminated residue and R 7 is one aryl or heteroaryl residue.
Claim 16
Dependent Claim 50 words
A compound, as claimed in claim 1, wherein R 4 is one carboxylic acid terminated residue; and R 1 and R 7 , or R 2 and R 6 , or R 3 and R 5 , are identical alkyl or arylalkyl residues containing 1 to 16 aliphatic carbon atoms.
Claim 17
Dependent Claim 28 words
A compound, as claimed in claim 15, wherein R 4 is one carboxylic acid terminated residue; and R 1 and R 7 are identical alkyl or arylalkyl residues.
Claim 18
Dependent Claim 43 words
A compound, as claimed in claim 1, wherein R 4 is one carboxylic acid terminated residue; and R 1 and R 7 , or R 2 and R 6 , or R 3 and R 5 , are identical aryl or heteroaryl residues.
Claim 19
Dependent Claim 28 words
A compound, as claimed in claim 17, wherein R 4 is one carboxylic acid terminated residue; and R 1 and R 7 are identical aryl or heteroaryl residues.
Claim 20
Dependent Claim 30 words
A compound, as claimed in claim 1, wherein R 1 and R 7 are identical; R 2 and R 6 are identical; and R 3 and R 5 are identical.
Claim 21
Dependent Claim 26 words
A compound, as claimed in claim 19, wherein R 4 is one carboxylic acid terminated residue; and R 1 and R 7 are identical alkyl residues.

References Cited (Backward Citations)

US4774339A Cited
US4916711A Cited
US5262545A Cited
US5248782A Cited
US5187288A Cited
US5274113A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1997-08-15 1998-02-14 1998-08-16 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 2001-08-15 2002-02-14 2002-08-16 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2005-08-15 2006-02-14 2006-08-16 $7700.00 Window Closed / Lapsed

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