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US5352803A
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5(6)-methyl substituted fluorescein derivatives
Assignee: Abbott Laboratories
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Filing: 1992-03-30
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Granted: 1994-10-04
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Expires: 2012-03-30
Abstract
Abstract 5(6)-methyl substituted fluorescein derivatives and a process for producing 5(6)-methyl substituted derivatives. Also provided are methods for these utilizing these derivatives as indicator reagents in assays for analytes, indicator reagents which comprise specific binding members attached to these derivatives and test kits which contain these derivatives.
Inventors
- 👤 Phillip G. Mattingly
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-31 16:23
CPC Classifications
C; C07; C07D; C07D493/00; C07D493/02; C07D493/10; C07F; C07F9/00; C07F9/02; C07F9/547; C07F9/6561; C07K; C07K16/00; C07K16/18; C07K16/44; C09; C09B; C09B11/00; C09B11/04; C09B11/06; C09B11/08; G; G01; G01N; G01N33/00; G01N33/48; G01N33/50; G01N33/53; G01N33/531; G01N33/532; G01N33/533; G01N33/74; G01N33/78; Y; Y10; Y10S; Y10S436/00; Y10S436/80; Y10S530/00; Y10S530/807
Claims Analysis
Total Claims: 7
Claim 1
Independent Claim
51 words
Fluorescein derivatives of the following formulas: ##STR47## wherein R is selected from the group consisting of hydroxy and protected hydroxy; and wherein X is selected from the group consisting of hydroxy, protected hydroxy, amino, protected amino, thiol, protected thiol, a leaving group, a Michael acceptor, phosphoramidite, phosphonate and a linking group.
Claim 2
Dependent Claim
51 words
Fluorescein derivatives of the following formulas: ##STR47## wherein R is selected from the group consisting of hydroxy and protected hydroxy; and wherein X is selected from the group consisting of hydroxy, protected hydroxy, amino, protected amino, thiol, protected thiol, a leaving group, a Michael acceptor, phosphoramidite, phosphonate and a linking group.
Claim 3
Dependent Claim
29 words
The fluorescein derivative according to claim 1 wherein the protected hydroxyl groups are selected from the group consisting of alkyl esters, aryl ethers, silyl ethers, esters, carbonates, and carbamates.
Claim 4
Dependent Claim
32 words
The fluorescein derivative according to claim 1 wherein the protected amino groups are selected from the group consisting of carbamates, amides, cyclic imides, N-benzyl derivatives, imine derivatives, silyl derivatives, and N-sulfonyl derivatives.
Claim 5
Dependent Claim
24 words
The fluorescein derivative according to claim 1 wherein the thiol groups are selected from the group consisting of thioethers, thioesters, thiocarbonates, thiocarbamates and disulfides.
Claim 6
Dependent Claim
72 words
The fluorescein derivative according to claim 1 wherein the Michael acceptor is of the formula --O--"MA" or --N(H) n "MA", wherein "MA" is the Michael acceptor of the formula: ##STR48## wherein a, b and c independently can be hydrogen, alkyl, and aryl and wherein U is chosen from --CH(═O), --C(═O)R 1 , --C(═O)NH 2 , --CN, --NO 2 , --S(═O)R 1 --S(═O) 2 R 1 , and n is 0 or 1.
Claim 7
Dependent Claim
175 words
The fluorescein derivative according to claim 5 wherein said ##STR49## Michael acceptor is wherein when X is a linking group it is selected from the group consisting of the formula --O--A--B and --N(H) n --A--B, wherein n=0 or 1 to satisfy the nitrogen valency; wherein A is a spacer group consisting of from 0 to 50 carbon atoms and heteroatoms, including not more than ten heteroatoms, arranged in a straight or branched chain, saturated or unsaturated, with the provisos that: (a) not more than two heteroatoms may be directly linked in the sequence --O--A--B or --N(H) n --A--B, (b) the sequence --O--A--B or --N(H) n --A--B cannot contain --O--O--, and (c) in the sequence --N(H) n --A--B, when n=0, then N--A taken together may comprise a ring of not more that 6 atoms; and (d) that branchings may occur only on carbon atoms; and wherein B is a reactive functional group selected from --C(═O)OH, --NH 2 , --CH(═O), halo (--Cl, --Br, --I), sulfonate ester(OS(═O) 2 -alkyl, --OS(≡0 O) 2 -aryl), Michael acceptor, phosphoramidite, and phosphonate.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
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| 3.5 Years (Year 4) | 1997-10-03 | 1998-04-04 | 1998-10-04 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 2001-10-03 | 2002-04-04 | 2002-10-04 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2005-10-03 | 2006-04-04 | 2006-10-04 | $7700.00 | Window Closed / Lapsed |