Nye 3'modificerede oligonucleotid-derivater

3'-Derivatised oligonucleotide analogues of formula (I) and (II) and their salts are new: R -(A )n'-(B )m'-(A )n-(B )m-B (I); R -(A )n'-(B )m'-(A )n-A (II); A and A = gps. of formula (i); B and B = gps. of formula (ii); B = a gp. of formula (iii); and A = a gp. of formula (i...

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Main Authors CAROLUS, CAROLIN, UHLMANN, EUGEN, PEYMAN, ANUSCHIRWAN
Format Patent
LanguageDanish
Published 18.04.2006
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Abstract 3'-Derivatised oligonucleotide analogues of formula (I) and (II) and their salts are new: R -(A )n'-(B )m'-(A )n-(B )m-B (I); R -(A )n'-(B )m'-(A )n-A (II); A and A = gps. of formula (i); B and B = gps. of formula (ii); B = a gp. of formula (iii); and A = a gp. of formula (iv); a and b = 0 to 20; R = H, 1-18C alkyl, 2-18C alkenyl, 3-18C alkynyl, 2-19C alkanoyl, 3-20C alkenoyl, 4-20C alkynoyl, 6-20C aryl, (6-14C)aryl(1-8C)alkyl or P(W)ZZ'; R = H, OH, 1-18C alkoxy, halogen, azido or NH2; D = OH or OPO3<2->; B = a natural or unnatural nucleotide base; n = 1-100; n' = 0-50; m = 0-5; m' = 0-5 in (I) or 1-5 in (II); A = O, S or CH2; W = O, S or Se; V = O or S; T = O, S or NH; Y = O, S, NH or CH2; X = OH or SH; U = OH, SH, BH3 (sic), SeH, 1-18C alkoxy, 1-18C alkyl, 6-20C aryl, (6-14C)aryl(1-8C)alkyl, NHR , NR R or (OCH2CH2)pO(CH2)qCH2R ; R = 1-18C alkyl, 6-20C aryl, (6-14C)aryl(1-8C)alkyl or (CH2)c(NH(CH2)c)dNR R ; c = 2-6; d = 0-6; R = H, 1-6C alkyl or (1-4C)alkoxy(1-6C)alkyl; R = 1-18C alkyl, 6-20C aryl or (6-14C)aryl(1-8C)alkyl; or NR R = a 5- or 6-membered ring opt. contg. another N, O or S atom; p = 1-100; q = 0-22; R = H or a functional gp. such as OH, NH2, NHR , COOH, CONH2, COOR or halogen; R = 1-6C alkyl, R = 1-4C alkyl; Z and Z' = OH, SH, SeH, 1-22C alkoxy, O(CH2)bNHR 'R ', 1-18C alkyl, 6-20C aryl, (6-14)aryl(1-8C)alkyl (where aryl includes heteroaryl and is opt. substd. by 1-3 of COOH, NH2, NO2, 1-4C alkylamino, 1-6C alkoxy, OH, halogen and CN), 1-18C alkylthio, NHR , NR R , a 3'- or 5'-linked nucleoside or oligonucleotide, or a gp. which enhances intracellular uptake, serves as a DNA probe label or binds to, crosslinks with or cleaves a target nucleic acid after hybridisation; R 'R ' = as R , R ; or NR 'R = a 3- to 6-membered ring.
AbstractList 3'-Derivatised oligonucleotide analogues of formula (I) and (II) and their salts are new: R -(A )n'-(B )m'-(A )n-(B )m-B (I); R -(A )n'-(B )m'-(A )n-A (II); A and A = gps. of formula (i); B and B = gps. of formula (ii); B = a gp. of formula (iii); and A = a gp. of formula (iv); a and b = 0 to 20; R = H, 1-18C alkyl, 2-18C alkenyl, 3-18C alkynyl, 2-19C alkanoyl, 3-20C alkenoyl, 4-20C alkynoyl, 6-20C aryl, (6-14C)aryl(1-8C)alkyl or P(W)ZZ'; R = H, OH, 1-18C alkoxy, halogen, azido or NH2; D = OH or OPO3<2->; B = a natural or unnatural nucleotide base; n = 1-100; n' = 0-50; m = 0-5; m' = 0-5 in (I) or 1-5 in (II); A = O, S or CH2; W = O, S or Se; V = O or S; T = O, S or NH; Y = O, S, NH or CH2; X = OH or SH; U = OH, SH, BH3 (sic), SeH, 1-18C alkoxy, 1-18C alkyl, 6-20C aryl, (6-14C)aryl(1-8C)alkyl, NHR , NR R or (OCH2CH2)pO(CH2)qCH2R ; R = 1-18C alkyl, 6-20C aryl, (6-14C)aryl(1-8C)alkyl or (CH2)c(NH(CH2)c)dNR R ; c = 2-6; d = 0-6; R = H, 1-6C alkyl or (1-4C)alkoxy(1-6C)alkyl; R = 1-18C alkyl, 6-20C aryl or (6-14C)aryl(1-8C)alkyl; or NR R = a 5- or 6-membered ring opt. contg. another N, O or S atom; p = 1-100; q = 0-22; R = H or a functional gp. such as OH, NH2, NHR , COOH, CONH2, COOR or halogen; R = 1-6C alkyl, R = 1-4C alkyl; Z and Z' = OH, SH, SeH, 1-22C alkoxy, O(CH2)bNHR 'R ', 1-18C alkyl, 6-20C aryl, (6-14)aryl(1-8C)alkyl (where aryl includes heteroaryl and is opt. substd. by 1-3 of COOH, NH2, NO2, 1-4C alkylamino, 1-6C alkoxy, OH, halogen and CN), 1-18C alkylthio, NHR , NR R , a 3'- or 5'-linked nucleoside or oligonucleotide, or a gp. which enhances intracellular uptake, serves as a DNA probe label or binds to, crosslinks with or cleaves a target nucleic acid after hybridisation; R 'R ' = as R , R ; or NR 'R = a 3- to 6-membered ring.
Author CAROLUS, CAROLIN
PEYMAN, ANUSCHIRWAN
UHLMANN, EUGEN
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Snippet 3'-Derivatised oligonucleotide analogues of formula (I) and (II) and their salts are new: R -(A )n'-(B )m'-(A )n-(B )m-B (I); R -(A )n'-(B )m'-(A )n-A (II); A...
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SubjectTerms ACYCLIC OR CARBOCYCLIC COMPOUNDS
ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM
BEER
BIOCHEMISTRY
CHEMISTRY
COMPOSITIONS BASED THEREON
COMPOSITIONS OR TEST PAPERS THEREFOR
CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES
DERIVATIVES THEREOF
ENZYMOLOGY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS
MEDICAL OR VETERINARY SCIENCE
METALLURGY
MICROBIOLOGY
MUTATION OR GENETIC ENGINEERING
NUCLEIC ACIDS
NUCLEOSIDES
NUCLEOTIDES
ORGANIC CHEMISTRY
ORGANIC MACROMOLECULAR COMPOUNDS
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
PROCESSES OF PREPARING SUCH COMPOSITIONS
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
SPIRITS
STEROIDS
SUGARS
THEIR PREPARATION OR CHEMICAL WORKING-UP
VINEGAR
WINE
Title Nye 3'modificerede oligonucleotid-derivater
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