US4529796A
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Method for making chromogenic and/or fluorogenic substrates for use in monitoring catalytic or enzymatic activity
Assignee: Roche Diagnostics Corp
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Filing: 1982-02-22
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Granted: 1985-07-16
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Expires: 2002-02-22
Abstract
Abstract A method for preparing a substrate capable of undergoing catalytic-induced hydrolysis of the phosphate ester at the 3' position, to yield a species capable of being monitored spectrophotometrically or fluorometrically, comprises (a) forming a mononucleotide 20', 3' cyclic phosphate of the formula: ##STR1## wherein B is a nucleotide base, and wherein the CH 2 OH group at the 4'-position is either cis or trans to the cyclic phosphate; (b) blocking said mononucleotide 2', 3'-cyclic phosphate at the 5'-hydroxyl with a suitable 5'-blocking member to form a mononucleotide 5'-O-blocked-2', 3'-cyclic phosphate; (c) opening said cyclic phosphate so that essentially only a mononucleotide 5'-O-blocked-2'-hydroxyl-3'-phosphate is formed under conditions leaving the 5'-position essentially blocked; (d) blocking said mononucleotide 5'-O-blocked 3'-phosphate at the 2'-hydroxyl with a suitable 2'-O-blocking member to form a mononucleotide 2'-blocked-5'-blocked-3'-phosphate; and (e) forming a 2'-O-blocked-5'-O-blocked phosphodiester by bonding said mononucleotide 2'-O-blocked-5'-O-blocked-3'-phosphate with a moiety selected from the group consisting of a chromophore or fluorophore. The 2'-blocking member is removed from said 2'-blocked-5'-blocked phosphodiester so as to provide a substrate characterized by the ability to undergo catalytic-induced hydrolysis of the phosphodiester to yield a species capable of being monitored spectrophotometrically or fluorometrically.
Inventors
- 👤 Jemo Kang
- 👤 Glen L. Tolman
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-05 19:32
CPC Classifications
C; C07; C07H; C07H21/00; C07H19/00; C07H19/02; C07H19/04
Claims Analysis
Total Claims: 33
Claim 1
Independent Claim
280 words
A method for preparing a substrate capable of undergoing catalytic-induced hydrolysis of the phosphate ester at the 3'-position to yield a species capable of being monitored spectrophometrically or fluorometrically, comprising (a) forming a mononucleotide 2',3'-cylic phosphate of the formula ##STR13## wherein B is a nucleotide base, and wherein the CH 2 OH group at the 4'-position is either cis or trans to the cyclic phosphate, by reacting a mixture of 2'- and 3'-phosphate mononucleotide isomers with a condensation reagent; (b) reacting said mononucleotide 2',3'-cyclic phosphate with a 5'-blocking reagent to form a mononucleotide 5'-O-blocked-2',3'-cyclic phosphate of the formula ##STR14## wherein R is selected from the group consisting of alkyl, alkenyl, cycloalkyl, aryl, araalkyl, acyl, oxaalkyl, thioalkyl, oxacycloalkyl and thiocycloalkyl; (c) opening the phosphate ring of said mononucleotide 5'-O-blocked-2',3'-cyclic phosphate by reaction thereof with a suitable catalyst so that essentially only a mononucleotide 5'-O-blocked 2'-hydroxyl 3'-phosphate of the formula ##STR15## is formed; (d) reacting said mononucleotide 5'-O-blocked 2'-hydroxyl 3'-phosphate with a 2'-O-blocking reagent to form a mononucleotide 2'-O-blocked-5'-O-blocked-3'-phosphate of the formula ##STR16## wherein R' is selected from the group consisting of oxaalkyl, thioalkyl, oxacycloalkyl, silyl derivatives and thiocycloalkyl; and (e) esterifying said mononucleotide 2'-O-blocked-5'-O-blocked-3'-phosphate with a chromophore or fluorophore to form a mononucleotide 2'-O-blocked-5'-O-blocked phosphodiester of the formula ##STR17## wherein R" is selected from the group consisting of a chromophore or fluorophore moiety; said 2'-blocking member being capable of at least essentially blocking medium-induced hydrolysis of the phosphate ester at the 3'-position, and said 2'-blocking member being capable of being removed to provide a substrate characterized by the ability to undergo catalytic-induced hydrolysis of the phosphate ester at the 3'-position to yield a species capable of being monitored spectrophotometrically or fluorometrically.
Claim 2
Independent Claim
280 words
A method for preparing a substrate capable of undergoing catalytic-induced hydrolysis of the phosphate ester at the 3'-position to yield a species capable of being monitored spectrophometrically or fluorometrically, comprising (a) forming a mononucleotide 2',3'-cylic phosphate of the formula ##STR13## wherein B is a nucleotide base, and wherein the CH 2 OH group at the 4'-position is either cis or trans to the cyclic phosphate, by reacting a mixture of 2'- and 3'-phosphate mononucleotide isomers with a condensation reagent; (b) reacting said mononucleotide 2',3'-cyclic phosphate with a 5'-blocking reagent to form a mononucleotide 5'-O-blocked-2',3'-cyclic phosphate of the formula ##STR14## wherein R is selected from the group consisting of alkyl, alkenyl, cycloalkyl, aryl, araalkyl, acyl, oxaalkyl, thioalkyl, oxacycloalkyl and thiocycloalkyl; (c) opening the phosphate ring of said mononucleotide 5'-O-blocked-2',3'-cyclic phosphate by reaction thereof with a suitable catalyst so that essentially only a mononucleotide 5'-O-blocked 2'-hydroxyl 3'-phosphate of the formula ##STR15## is formed; (d) reacting said mononucleotide 5'-O-blocked 2'-hydroxyl 3'-phosphate with a 2'-O-blocking reagent to form a mononucleotide 2'-O-blocked-5'-O-blocked-3'-phosphate of the formula ##STR16## wherein R' is selected from the group consisting of oxaalkyl, thioalkyl, oxacycloalkyl, silyl derivatives and thiocycloalkyl; and (e) esterifying said mononucleotide 2'-O-blocked-5'-O-blocked-3'-phosphate with a chromophore or fluorophore to form a mononucleotide 2'-O-blocked-5'-O-blocked phosphodiester of the formula ##STR17## wherein R" is selected from the group consisting of a chromophore or fluorophore moiety; said 2'-blocking member being capable of at least essentially blocking medium-induced hydrolysis of the phosphate ester at the 3'-position, and said 2'-blocking member being capable of being removed to provide a substrate characterized by the ability to undergo catalytic-induced hydrolysis of the phosphate ester at the 3'-position to yield a species capable of being monitored spectrophotometrically or fluorometrically.
Claim 3
Independent Claim
301 words
A method for preparing a substrate capable of undergoing catalytic-induced hydrolysis of the phosphate ester at the 3'-position to yield a species capable of being monitored spectrophotometrically or fluorometrically, comprising (a) forming a mononucleotide 2',3'-cyclic phosphate of the formula ##STR18## wherein B is a nucleotide base, and wherein the CH 2 OH group at the 4'-position is either cis or trans to the cyclic phosphate, by reacting a mixture of 2'- and 3'-phosphate mononucleotide isomers with a condensation reagent; (b) reacting said mononucleotide 2',3'-cyclic phosphate with a 5'-blocking reagent to form a mononucleotide 5'-O-blocked-2',3'-cyclic phosphate of the formula ##STR19## wherein R is selected from the group consisting of alkyl, alkenyl, cycloalkyl, aryl, araalkyl, acyl, oxaalkyl, thioalkyl, oxacycloalkyl, and thiocycloalkyl; (c) opening the phosphate ring of said mononucleotide 5'-O-blocked-2-,3'-cyclic phosphate by reacting thereof with a suitable catalyst so that essentially only a mononucleotide 5'-O-blocked 2'-hydroxyl 3'-phosphate of the formula ##STR20## is formed; (d) reacting said mononucleotide 5'-O-blocked-2'-hydroxyl 3'-phosphate with a 2'-O-blocking reagent to form a mononucleotide 2'-O-blocked-5'-O-blocked-3'-phosphate of the formula ##STR21## wherein R' is selected from the group consisting of oxaalkyl, thioalkyl, oxacycloalkyl, silyl derivatives and thiocycloalkyl; and (e) reacting said mononucleotide 2'-O-blocked-5-O-blocked-3'-phosphate with a dephosphorylating agent to cleave the 3'-phosphate to form a 2',5'-diblocked mononucleotide and reacting said 2,5-diblocked mononucleotide with a phosphorylated derivative of a chromophore or fluorophore to form a mononucleotide 2'-O-blocked-5'-O-blocked phosphodiester of the formula ##STR22## wherein R" is selected from the group consisting of a chromophore or fluorophore moiety; said 2'-blocking member being capable of at least essentially blocking medium-induced hydrolysis of the phosphate ester at the 3'-position, and said 2'-blocking member being capable of being removed to provide a substrate characterized by the ability to undergo catalytic-induced hydrolysis of the phosphate ester at the 3'-position to yield a species capable of being monitored spectrophotometrically or fluorometrically.
Claim 4
Independent Claim
301 words
A method for preparing a substrate capable of undergoing catalytic-induced hydrolysis of the phosphate ester at the 3'-position to yield a species capable of being monitored spectrophotometrically or fluorometrically, comprising (a) forming a mononucleotide 2',3'-cyclic phosphate of the formula ##STR18## wherein B is a nucleotide base, and wherein the CH 2 OH group at the 4'-position is either cis or trans to the cyclic phosphate, by reacting a mixture of 2'- and 3'-phosphate mononucleotide isomers with a condensation reagent; (b) reacting said mononucleotide 2',3'-cyclic phosphate with a 5'-blocking reagent to form a mononucleotide 5'-O-blocked-2',3'-cyclic phosphate of the formula ##STR19## wherein R is selected from the group consisting of alkyl, alkenyl, cycloalkyl, aryl, araalkyl, acyl, oxaalkyl, thioalkyl, oxacycloalkyl, and thiocycloalkyl; (c) opening the phosphate ring of said mononucleotide 5'-O-blocked-2-,3'-cyclic phosphate by reacting thereof with a suitable catalyst so that essentially only a mononucleotide 5'-O-blocked 2'-hydroxyl 3'-phosphate of the formula ##STR20## is formed; (d) reacting said mononucleotide 5'-O-blocked-2'-hydroxyl 3'-phosphate with a 2'-O-blocking reagent to form a mononucleotide 2'-O-blocked-5'-O-blocked-3'-phosphate of the formula ##STR21## wherein R' is selected from the group consisting of oxaalkyl, thioalkyl, oxacycloalkyl, silyl derivatives and thiocycloalkyl; and (e) reacting said mononucleotide 2'-O-blocked-5-O-blocked-3'-phosphate with a dephosphorylating agent to cleave the 3'-phosphate to form a 2',5'-diblocked mononucleotide and reacting said 2,5-diblocked mononucleotide with a phosphorylated derivative of a chromophore or fluorophore to form a mononucleotide 2'-O-blocked-5'-O-blocked phosphodiester of the formula ##STR22## wherein R" is selected from the group consisting of a chromophore or fluorophore moiety; said 2'-blocking member being capable of at least essentially blocking medium-induced hydrolysis of the phosphate ester at the 3'-position, and said 2'-blocking member being capable of being removed to provide a substrate characterized by the ability to undergo catalytic-induced hydrolysis of the phosphate ester at the 3'-position to yield a species capable of being monitored spectrophotometrically or fluorometrically.
Claim 5
Dependent Claim
59 words
The method of claim 2 comprising the further step of reacting said mononucleotide 2'-O-blocked-5'-O-blocked phosphodiester with a deblocking agent to remove said 2'-blocking member to provide an enzyme substrate of the formula ##STR23## wherein said substrate is characterized by the ability to undergo catalytic-induced hydrolysis of said phosphodiester to yield a species capable of being monitored spectrophotometrically or fluorometrically.
Claim 6
Dependent Claim
59 words
The method of claim 1 comprising the further step of reacting said mononucleotide 2'-O-blocked-5'-O-blocked phosphodiester with a deblocking agent to remove the 2'-blocking member to provide an enzyme substrate of the formula ##STR24## wherein said substrate is characterized by the ability to undergo catalytic-induced hydrolysis of said phosphodiester to yield a species capable of being monitored spectrophotometrically or fluorometrically.
Claim 7
Dependent Claim
12 words
The method of claim 1 wherein said base is a pyrimidine analog.
Claim 8
Dependent Claim
12 words
The method of claim 1 wherein said base is a purine analog.
Claim 9
Dependent Claim
24 words
The method of claim 1 wherein said base is a member selected from the group consisting of uracil, dihydrouracil, cytosine, dihydrocytosine and halogenated uracils.
Claim 10
Dependent Claim
10 words
A method of claim 1 wherein said base is uracil.
Claim 11
Dependent Claim
31 words
The method of claim 1 wherein said R is selected from the group consisting of methyl, ethyl, allyl, cyclohexyl, phenyl, benzyl, nitrobenzyl, acetyl, 1-methoxyethyl, 1-ethoxyethyl, 1-ethylthioethyl, tetrahydropyranyl, tetrahydrothiofuranyl, tetrahydrothiopyranyl, and 4-methoxytetrahydropyran-4-yl.
Claim 12
Dependent Claim
9 words
The method of claim 9 wherein R is acetyl.
Claim 13
Dependent Claim
18 words
The method of claim 1 wherein R' is selected from the group consisting of tetrahydropyranyl, 4-methoxytetrahydropyran-4-yl, and tert-butyldimethylsilyl.
Claim 14
Dependent Claim
9 words
The method of claim 11 wherein R' is tetrahydropyranyl.
Claim 15
Dependent Claim
9 words
The method of claim 11 wherein R' is 4-methoxytetrahydropyran-4-yl.
Claim 16
Dependent Claim
23 words
The method of claim 1 wherein said moiety is a member selected from the group consisting of aryl, araalkyl, heteroaryl or heterocyclic compound.
Claim 17
Dependent Claim
32 words
The method of claim 14 wherein said moiety is a member selected from the group consisting of umbelliferonyl, 4-methylumbelliferonyl, 3-flavonyl, 1-napthyl, o-nitrophenyl, m-nitrophenyl, p-nitrophenyl, 2,4-dinitrophenyl, cyanophenyl, acylphenyl, carboxyphenyl, phenylsulfonate, phenylsulfonyl and phenylsulfoxide.
Claim 18
Dependent Claim
10 words
The method of claim 15 wherein said moiety is 1-napthyl.
Claim 19
Dependent Claim
10 words
The method of claim 15 wherein said moiety is 4-methylumbelliferonyl.
Claim 20
Dependent Claim
10 words
The method of claim 15 wherein said moiety is 3-flavonyl.
Claim 21
Dependent Claim
25 words
The method of claim 1 wherein said 2'-O-blocked-5'-O-blocked phosphodiester is formed by an esterification reaction of said 2'-O-blocked-5'-O-blocked-2'-phosphate with an alcohol form of said moiety.
Claim 22
Dependent Claim
42 words
The method of claim 19 wherein said esterification reaction is carried out in the presence of an esterification reagent selected from the group consisting of 2,4,6,-triisopropylbenzenesulfonyl chloride, N, N'-dicyclohexylcarbondimide, mesitylenesulfonyl chloride, toluenesulfonylchloride, mesitylenesulfonyl imidazole, p-toluenesulfonyl imidazole, picryl chloride and 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride.
Claim 23
Dependent Claim
27 words
The method of claim 20 wherein said esterification reaction is carried out in the presence of an additive selected from the group consisting of N-hydroxysuccinimide and N-hydroxyphthalimide.
Claim 24
Dependent Claim
17 words
The method of claim 20 wherein said esterification reaction is carried out in the presence of pyridine.
Claim 25
Dependent Claim
27 words
The method of claim 22 wherein said esterification reaction is carried out at a temperature in the range of from about -20° C. to about 25° C.
Claim 26
Dependent Claim
23 words
The method of claim 23 wherein said esterification reaction is carried out for a time of from about 5 to about 18 hours.
Claim 27
Dependent Claim
19 words
The method of claim 4 wherein said removal of said 2'-blocking member is carried out in a protic solvent.
Claim 28
Dependent Claim
11 words
The method of claim 25 wherein said protic solvent is water.
Claim 29
Dependent Claim
34 words
The method of claim 26 wherein said removal of said 2'-blocking member is carried out in the presence of an acid selected from the group consisting of hydrochloric acid, trifluoroacetic acid and p-toluenesulfonic acid.
Claim 30
Dependent Claim
22 words
The method of claim 27 wherein said acid is hydrochloric acid in a molar concentration of from about 0.01 to about 1.
Claim 31
Dependent Claim
18 words
The method of claim 28 wherein the molar concentration of hydrochloric acid is from about 0.01 to 0.05.
Claim 32
Dependent Claim
14 words
The method of claim 29 wherein the reaction is carried out at ambient temperature.
Claim 33
Dependent Claim
20 words
The method of claim 30 wherein the reaction is carried out for from about 5 minutes to about 24 hours.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1988-07-15 | 1989-01-14 | 1989-07-16 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1992-07-15 | 1993-01-14 | 1993-07-16 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1996-07-15 | 1997-01-14 | 1997-07-16 | $7700.00 | Window Closed / Lapsed |