Phosphoramidites

ANA 2'-OMe U amidite

Description: ANA 2'-OMe U amidite is a modified phosphoramidite used in oligonucleotide synthesis. It serves as a building block during solid-phase oligonucleotide synthesis, allowing the incorporation of uridine residues modified with 2'-O-methyl into the oligonucleotide sequence. This compound is essential for synthesizing oligonucleotides with specific modifications, which can be utilized in various applications such as molecular biology research, diagnostics, and therapeutics.

CAT: BRP-00901

CAS: 1239669-77-2

Molecular Formula: C40H49N4O9P

Molecular Weight: 760.83

Purity: >98%

Appearance: Off-white solid

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InChIKey: UVUOJOLPNDCIHL-LYEFJPEKSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: CC(C)N(C(C)C)P(OCCC#N)OC1C(OC(C1OC)N2C=CC(=O)NC2=O)COC(C3=CC=CC=C3)(C4=CC=C(C=C4)OC)C5=CC=C(C=C5)OC

IUPAC Name: 3-[[(2R,3R,4S,5R)-2-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-5-(2,4-dioxopyrimidin-1-yl)-4-methoxyoxolan-3-yl]oxy-[di(propan-2-yl)amino]phosphanyl]oxypropanenitrile

InChI: InChI=1S/C40H49N4O9P/c1-27(2)44(28(3)4)54(51-25-11-23-41)53-36-34(52-38(37(36)49-7)43-24-22-35(45)42-39(43)46)26-50-40(29-12-9-8-10-13-29,30-14-18-32(47-5)19-15-30)31-16-20-33(48-6)21-17-31/h8-10,12-22,24,27-28,34,36-38H,11,25-26H2,1-7H3,(H,42,45,46)/t34-,36-,37+,38-,54?/m1/s1

Synonyms: 1-[5-O-[Bis(4-methoxyphenyl)phenylmethyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-2-O-methyl-β-D-arabinofuranosyl]-2,4(1H,3H)-pyrimidinedione; 2'-OMe-U-ANA-CE-Phosphoramidite; (2R,3R,4S,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-methoxytetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite; 5-O-(4,4'-dimethoxytrityl)-3-O-(diisopropylamino-2-cyanoethoxyphosphanyl)-1-deoxy-2-O-methyl-1-uracil-1-yl-beta-D-arabino-pentofuranose; DMTr-2'-ara-OMe-U-3'-CE-Phosphoramidite; 5'-O-DMTr-2'-ara-OMe-U-3'-CE-Phosphoramidite; 5'-O-(4,4'-dimethoxytrityl)-2'-O-methyl-arabinouridine-3'-[(2-cyanoethyl)-(N,N-diisopropropyl)]-Phosphoramidite

ANA 2'-OMe A(Bz) amidite

Description: ANA 2'-OMe A(Bz) amidite is a modified phosphoramidite used in oligonucleotide synthesis. It serves as a building block during solid-phase oligonucleotide synthesis, enabling the incorporation of adenine residues modified with 2'-O-methyl and protected with benzoyl (Bz) into the oligonucleotide sequence. This compound is crucial for synthesizing oligonucleotides with specific modifications, which can be utilized in various applications such as molecular biology research, diagnostics, and therapeutics.

CAT: BRP-00902

CAS: 1239669-70-5

Molecular Formula: C48H54N7O8P

Molecular Weight: 887.98

Purity: >98%

Appearance: Off-white solid

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InChIKey: AZCGOTUYEPXHMJ-VOJYYREFSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: CC(C)N(C(C)C)P(OCCC#N)OC1C(OC(C1OC)N2C=NC3=C(N=CN=C32)NC(=O)C4=CC=CC=C4)COC(C5=CC=CC=C5)(C6=CC=C(C=C6)OC)C7=CC=C(C=C7)OC

IUPAC Name: N-[9-[(2R,3S,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-3-methoxyoxolan-2-yl]purin-6-yl]benzamide

InChI: InChI=1S/C48H54N7O8P/c1-32(2)55(33(3)4)64(61-28-14-27-49)63-42-40(62-47(43(42)59-7)54-31-52-41-44(50-30-51-45(41)54)53-46(56)34-15-10-8-11-16-34)29-60-48(35-17-12-9-13-18-35,36-19-23-38(57-5)24-20-36)37-21-25-39(58-6)26-22-37/h8-13,15-26,30-33,40,42-43,47H,14,28-29H2,1-7H3,(H,50,51,53,56)/t40-,42-,43+,47-,64?/m1/s1

Synonyms: DMTr-2'-ara-OMe-A(Bz)-3'-CE-Phosphoramidite; 2'-OMe-A(Bz)-ANA-CE-Phosphoramidite; Benzamide, N-[9-[5-O-[bis(4-methoxyphenyl)phenylmethyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-2-O-methyl-β-D-arabinofuranosyl]-9H-purin-6-yl]-; (2R,3R,4S,5R)-5-(6-benzamido-9H-purin-9-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-methoxytetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite; 5'-O-DMTr-2'-ara-OMe-A(Bz)-3'-CE-Phosphoramidite; N6-benzoyl-(5'-O-(4,4'-dimethoxytrityl)-2'-O-methyl-arabinoadenosine-3'-[(2-cyanoethyl)-(N, N-diisopropropyl)]-Phosphoramidite

aTNA A(Bz) amidite

Description: aTNA A(Bz) amidite is a modified phosphoramidite used in oligonucleotide synthesis. This compound is essential for synthesizing oligonucleotides with specific modifications, which can be utilized in various applications such as molecular biology research, diagnostics, and therapeutics.

CAT: BRP-00903

CAS: 1654757-57-9

Molecular Formula: C48H55N8O7P

Molecular Weight: 886.99

Purity: >98%

Appearance: White solid

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InChIKey: IHMRCPNOGYPCLE-BZSGYPRQSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: N#CCCOP(OC(C)C(NC(=O)CN1C=NC=2C(=NC=NC21)NC(=O)C=3C=CC=CC3)COC(C=4C=CC=CC4)(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)N(C(C)C)C(C)C

IUPAC Name: (2R,3R)-3-(2-(6-benzamido-9H-purin-9-yl)acetamido)-4-(bis(4-methoxyphenyl)(phenyl)methoxy)butan-2-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C48H55N8O7P/c1-33(2)56(34(3)4)64(62-28-14-27-49)63-35(5)42(53-43(57)29-55-32-52-44-45(50-31-51-46(44)55)54-47(58)36-15-10-8-11-16-36)30-61-48(37-17-12-9-13-18-37,38-19-23-40(59-6)24-20-38)39-21-25-41(60-7)26-22-39/h8-13,15-26,31-35,42H,14,28-30H2,1-7H3,(H,53,57)(H,50,51,54,58)/t35-,42-,64?/m1/s1

Synonyms: Phosphoramidous acid, N,N-bis(1-methylethyl)-, (1R,2R)-2-[[2-[6-(benzoylamino)-9H-purin-9-yl]acetyl]amino]-3-[bis(4-methoxyphenyl)phenylmethoxy]-1-methylpropyl 2-cyanoethyl ester; (1R,2R)-2-[[2-[6-(Benzoylamino)-9H-purin-9-yl]acetyl]amino]-3-[bis(4-methoxyphenyl)phenylmethoxy]-1-methylpropyl 2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite

2'-OTBS 5-I-C(Bz) amidite

Description: 2'-OTBS 5-I-C(Bz) amidite is used in the synthesis of oligonucleotides where specific modifications are required for various research or therapeutic applications. The iodine atom at the 5-position allows for further functionalization or labeling, the TBDMS group protects the 2'-hydroxyl during synthesis, and the benzoyl group protects the exocyclic amino group. This reagent is particularly useful in applications that demand modified nucleotides for enhanced properties such as increased stability or specific binding characteristics.

CAT: BRP-00907

CAS: 256493-91-1

Molecular Formula: C52H65IN5O9PSi

Molecular Weight: 1090.08

Purity: >95%

Appearance: Off-white solid

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InChIKey: UVIALSKMICAVNV-ZQRHXHOESA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: CC(C)N(C(C)C)P(OCCC#N)OC1C(OC(C1O[Si](C)(C)C(C)(C)C)N2C=C(C(=NC2=O)NC(=O)C3=CC=CC=C3)I)COC(C4=CC=CC=C4)(C5=CC=C(C=C5)OC)C6=CC=C(C=C6)OC

IUPAC Name: N-[1-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-3-[tert-butyl(dimethyl)silyl]oxy-4-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxyoxolan-2-yl]-5-iodo-2-oxopyrimidin-4-yl]benzamide

InChI: InChI=1S/C52H65IN5O9PSi/c1-35(2)58(36(3)4)68(64-32-18-31-54)66-45-44(34-63-52(38-21-16-13-17-22-38,39-23-27-41(61-8)28-24-39)40-25-29-42(62-9)30-26-40)65-49(46(45)67-69(10,11)51(5,6)7)57-33-43(53)47(56-50(57)60)55-48(59)37-19-14-12-15-20-37/h12-17,19-30,33,35-36,44-46,49H,18,32,34H2,1-11H3,(H,55,56,59,60)/t44-,45-,46-,49-,68?/m1/s1

Synonyms: Cytidine, N-benzoyl-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-[(1,1-dimethylethyl)dimethylsilyl]-5-iodo-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]; (2R,3R,4R,5R)-5-(4-benzamido-5-iodo-2-oxopyrimidin-1(2H)-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite; 5-Iodo Cytidine CED phosphoramidite; 5-Iodo 2'-TBDMS C(Bz) 3'-CE phosphoramidite

2'-OMe PseudoIsoCytidine(dmf) amidite

Description: 2'-OMe PseudoIsoCytidine(dmf) amidite is a modified phosphoramidite used in oligonucleotide synthesis. It serves as a building block during solid-phase oligonucleotide synthesis, enabling the incorporation of pseudoisocytidine modified with 2'-O-methyl and protected with dimethylformamidine (dmf) into the oligonucleotide sequence. This compound is essential for synthesizing oligonucleotides with specific modifications, which can be utilized in various applications such as RNA research, antisense oligonucleotide design, and therapeutics.

CAT: BRP-00908

CAS: 141411-21-4

Molecular Formula: C43H55N6O8P

Molecular Weight: 814.92

Purity: >95%

Appearance: Off-white solid

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InChIKey: SGBFUZIGEGJKFA-SAAFSQBVSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: N#CCCOP(OC1C(OC(C2=CN=C(N=CN(C)C)NC2=O)C1OC)COC(C=3C=CC=CC3)(C4=CC=C(OC)C=C4)C5=CC=C(OC)C=C5)N(C(C)C)C(C)C

IUPAC Name: (2R,3R,4S,5S)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2-(((dimethylamino)methylene)amino)-6-oxo-1,6-dihydropyrimidin-5-yl)-4-methoxytetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C43H55N6O8P/c1-29(2)49(30(3)4)58(55-25-13-24-44)57-39-37(56-38(40(39)53-9)36-26-45-42(47-41(36)50)46-28-48(5)6)27-54-43(31-14-11-10-12-15-31,32-16-20-34(51-7)21-17-32)33-18-22-35(52-8)23-19-33/h10-12,14-23,26,28-30,37-40H,13,25,27H2,1-9H3,(H,45,47,50)/t37-,38+,39-,40+,58?/m1/s1

Synonyms: Methanimidamide, N'-[5-[5-O-[bis(4-methoxyphenyl)phenylmethyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-2-O-methyl-β-D-ribofuranosyl]-1,4-dihydro-4-oxo-2-pyrimidinyl]-N,N-dimethyl-; Phosphoramidous acid, bis(1-methylethyl)-, mono(2-cyanoethyl) ester, ester with N'-[5-[5-O-[bis(4-methoxyphenyl)phenylmethyl]-2-O-methyl-β-D-ribofuranosyl]-1,4-dihydro-4-oxo-2-pyrimidinyl]-N,N-dimethylmethanimidamide

2'-OTBS PseudoIsoCytidine(dmf) amidite

Description: 2'-OTBS PseudoIsoCytidine(dmf) amidite is a modified phosphoramidite used in oligonucleotide synthesis. It serves as a building block during solid-phase oligonucleotide synthesis, enabling the incorporation of pseudoisocytidine modified with a tert-butyldimethylsilyl (OTBS) protecting group and protected with dimethylformamidine (dmf) into the oligonucleotide sequence. This compound is crucial for synthesizing oligonucleotides with specific modifications, which can be utilized in various applications such as RNA research, antisense oligonucleotide design, and therapeutics.

CAT: BRP-00909

CAS: 1192344-93-6

Molecular Formula: C48H67N6O8PSi

Molecular Weight: 915.16

Purity: >95%

Appearance: Off-white solid

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InChIKey: LSKHQLXTKWPBJC-LHBYQZGQSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: N#CCCOP(OC1C(OC(C2=CN=C(N=CN(C)C)NC2=O)C1O[Si](C)(C)C(C)(C)C)COC(C=3C=CC=CC3)(C4=CC=C(OC)C=C4)C5=CC=C(OC)C=C5)N(C(C)C)C(C)C

IUPAC Name: (2R,3R,4S,5S)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)-5-(2-(((dimethylamino)methylene)amino)-6-oxo-1,6-dihydropyrimidin-5-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C48H67N6O8PSi/c1-33(2)54(34(3)4)63(59-29-17-28-49)61-43-41(60-42(44(43)62-64(12,13)47(5,6)7)40-30-50-46(52-45(40)55)51-32-53(8)9)31-58-48(35-18-15-14-16-19-35,36-20-24-38(56-10)25-21-36)37-22-26-39(57-11)27-23-37/h14-16,18-27,30,32-34,41-44H,17,29,31H2,1-13H3,(H,50,52,55)/t41-,42+,43-,44+,63?/m1/s1

Synonyms: Methanimidamide, N'-[5-[5-O-[bis(4-methoxyphenyl)phenylmethyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-2-O-[(1,1-dimethylethyl)dimethylsilyl]-β-D-ribofuranosyl]-1,6-dihydro-6-oxo-2-pyrimidinyl]-N,N-dimethyl-; N'-[5-[5-O-[Bis(4-methoxyphenyl)phenylmethyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-2-O-[(1,1-dimethylethyl)dimethylsilyl]-β-D-ribofuranosyl]-1,6-dihydro-6-oxo-2-pyrimidinyl]-N,N-dimethylmethanimidamide

Cyanine 3 amidite (iodide)

Description: Cyanine 3 amidite (iodide) is a fluorescent dye-labeled phosphoramidite used in oligonucleotide synthesis. It serves as a building block during solid-phase oligonucleotide synthesis, allowing the incorporation of Cyanine 3 (Cy3) fluorophore into the oligonucleotide sequence. This compound is widely used in various applications such as fluorescence in situ hybridization (FISH), microarray analysis, and fluorescence-based detection assays in molecular biology and diagnostics due to its strong and stable fluorescence properties.

CAT: BRP-00910

Molecular Formula: C58H70IN4O4P

Molecular Weight: 1045.10

Purity: >95%

Appearance: Dark-purple solid

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InChIKey: GTLRVZNKJSCYOV-UHFFFAOYSA-M

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: CC1(C)C(C=CC=C2N(CCCOP(OCCC#N)N(C(C)C)C(C)C)C3=C(C=CC=C3)C2(C)C)=[N+](CCCOC(C4=CC=CC=C4)(C5=CC=C(OC)C=C5)C6=CC=CC=C6)C7=C1C=CC=C7.[I-]

IUPAC Name: 2-(3-(1-(3-(((2-cyanoethoxy)(diisopropylamino)phosphaneyl)oxy)propyl)-3,3-dimethylindolin-2-ylidene)prop-1-en-1-yl)-1-(3-((4-methoxyphenyl)diphenylmethoxy)propyl)-3,3-dimethyl-3H-indol-1-ium;iodide

InChI: InChI=1S/C58H70N4O4P.HI/c1-44(2)62(45(3)4)67(65-42-21-38-59)66-43-23-40-61-53-31-19-17-29-51(53)57(7,8)55(61)33-20-32-54-56(5,6)50-28-16-18-30-52(50)60(54)39-22-41-64-58(46-24-12-10-13-25-46,47-26-14-11-15-27-47)48-34-36-49(63-9)37-35-48;/h10-20,24-37,44-45H,21-23,39-43H2,1-9H3;1H/q+1;/p-1

Synonyms: 3H-Indolium, 2-[3-[1-[3-[[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]oxy]propyl]-1,3-dihydro-3,3-dimethyl-2H-indol-2-ylidene]-1-propen-1-yl]-1-[3-[(4-methoxyphenyl)diphenylmethoxy]propyl]-3,3-dimethyl-, iodide (1:1); Cyanine 3 amidite

Related CAS: 182873-76-3 (chloride) ; 718594-66-2 (free base)

ENA MeC(Bz) amidite

Description: ENA MeC(Bz) amidite is a modified phosphoramidite used in oligonucleotide synthesis. This compound is crucial for synthesizing oligonucleotides with specific modifications, which can be utilized in various applications such as antisense technology, RNA research, and diagnostics.

CAT: BRP-00911

CAS: 287737-53-5

Molecular Formula: C49H56N5O9P

Molecular Weight: 889.99

Purity: >95%

Appearance: Off-white solid

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InChIKey: ALWJTTIHWFLNHB-ABEMJPNPSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: CC1=CN(C(=O)N=C1NC(=O)C2=CC=CC=C2)C3C4C(C(O3)(CCO4)COC(C5=CC=CC=C5)(C6=CC=C(C=C6)OC)C7=CC=C(C=C7)OC)OP(N(C(C)C)C(C)C)OCCC#N

IUPAC Name: N-[1-[(1R,5R,7R,8S)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-8-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-2,6-dioxabicyclo[3.2.1]octan-7-yl]-5-methyl-2-oxopyrimidin-4-yl]benzamide

InChI: InChI=1S/C49H56N5O9P/c1-33(2)54(34(3)4)64(61-29-14-28-50)63-43-42-46(53-31-35(5)44(52-47(53)56)51-45(55)36-15-10-8-11-16-36)62-48(43,27-30-59-42)32-60-49(37-17-12-9-13-18-37,38-19-23-40(57-6)24-20-38)39-21-25-41(58-7)26-22-39/h8-13,15-26,31,33-34,42-43,46H,14,27,29-30,32H2,1-7H3,(H,51,52,55,56)/t42-,43+,46-,48-,64?/m1/s1

Synonyms: Benzamide, N-[1-[2,6-anhydro-4-C-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-5-deoxy-α-L-lyxo-hexofuranosyl]-1,2-dihydro-5-methyl-2-oxo-4-pyrimidinyl]-; ENA-5MeC (bz) Phosphoramidite; (1R,5R,7R,8S)-7-(4-benzamido-5-methyl-2-oxopyrimidin-1(2H)-yl)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-2,6-dioxabicyclo[3.2.1]octan-8-yl (2-cyanoethyl) diisopropylphosphoramidite

ENA MeC(dmf) amidite

Description: ENA MeC(dmf) amidite is a modified phosphoramidite used in oligonucleotide synthesis. This compound is crucial for synthesizing oligonucleotides with ENA backbone modifications, which can impart enhanced stability and other properties for applications such as antisense technology, RNA research, and diagnostics.

CAT: BRP-00912

Molecular Formula: C45H57N6O8P

Molecular Weight: 840.96

Purity: >95%

Appearance: Off-white solid

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InChIKey: UXKOVGOMMGRMCZ-GIEZTROHSA-N

Solubility: Soluble in Acetonitrile, DMF

IUPAC Name: (1R,5R,7R,8S)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-7-(4-(((dimethylamino)methylene)amino)-5-methyl-2-oxopyrimidin-1(2H)-yl)-2,6-dioxabicyclo[3.2.1]octan-8-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C45H57N6O8P/c1-31(2)51(32(3)4)60(57-26-13-25-46)59-40-39-42(50-28-33(5)41(48-43(50)52)47-30-49(6)7)58-44(40,24-27-55-39)29-56-45(34-14-11-10-12-15-34,35-16-20-37(53-8)21-17-35)36-18-22-38(54-9)23-19-36/h10-12,14-23,28,30-32,39-40,42H,13,24,26-27,29H2,1-9H3/t39-,40+,42-,44-,60?/m1/s1

Synonyms: ENA MeC(dmf) Phosphoramidite

ENA A(dmf) amidite

Description: ENA A(dmf) amidite is a modified phosphoramidite used in oligonucleotide synthesis. This compound is essential for synthesizing oligonucleotides with ENA backbone modifications, which can impart enhanced stability and other desirable properties for applications such as antisense technology, RNA research, and diagnostics.

CAT: BRP-00913

Molecular Formula: C45H55N8O7P

Molecular Weight: 850.96

Purity: >95%

Appearance: Off-white solid

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InChIKey: AQCTXDYCTBALJS-XCDQGDGNSA-N

Solubility: Soluble in Acetonitrile, DMF

IUPAC Name: (1R,5R,7R,8S)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-7-(6-(((dimethylamino)methylene)amino)-9H-purin-9-yl)-2,6-dioxabicyclo[3.2.1]octan-8-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C45H55N8O7P/c1-31(2)53(32(3)4)61(58-25-12-24-46)60-40-39-43(52-30-49-38-41(50-29-51(5)6)47-28-48-42(38)52)59-44(40,23-26-56-39)27-57-45(33-13-10-9-11-14-33,34-15-19-36(54-7)20-16-34)35-17-21-37(55-8)22-18-35/h9-11,13-22,28-32,39-40,43H,12,23,25-27H2,1-8H3/t39-,40+,43-,44-,61?/m1/s1

Synonyms: ENA A(dmf) Phosphoramidite

FNA A(Bz) amidite

Description: FNA A(Bz) amidite is a phosphoramidite reagent used in solid-phase oligonucleotide synthesis, specifically for the incorporation of FNA monomers into oligonucleotide sequences. FNA A(Bz) amidite contains a benzoyl (Bz) protecting group on the adenine base. It is utilized for the synthesis of modified oligonucleotides containing FNA nucleotide analogs, which confer enhanced nuclease resistance and stability to the oligonucleotide duplexes. It finds applications in antisense technology, RNA interference (RNAi), and other nucleic acid-based research fields.

CAT: BRP-00914

Molecular Formula: C46H52N7O7P

Molecular Weight: 845.94

Purity: >98%

Appearance: Off-white solid

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InChIKey: JDILKNZRQTXVQP-DFVFTTOBSA-N

Solubility: Soluble in Acetonitrile, DMF

IUPAC Name: (R)-2-((6-benzamido-9H-purin-9-yl)methoxy)-3-(bis(4-methoxyphenyl)(phenyl)methoxy)propyl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C46H52N7O7P/c1-33(2)53(34(3)4)61(59-27-13-26-47)60-29-41(57-32-52-31-50-42-43(48-30-49-44(42)52)51-45(54)35-14-9-7-10-15-35)28-58-46(36-16-11-8-12-17-36,37-18-22-39(55-5)23-19-37)38-20-24-40(56-6)25-21-38/h7-12,14-25,30-31,33-34,41H,13,27-29,32H2,1-6H3,(H,48,49,51,54)/t41-,61?/m1/s1

Synonyms: DMTr-FNA-A(Bz)phosphoramidite

FNA G(Ac) amidite

Description: FNA G(Ac) amidite is a phosphoramidite reagent used in solid-phase oligonucleotide synthesis, specifically for the incorporation of FNA monomers into oligonucleotide sequences. FNA G(Ac) amidite contains an acetyl (Ac) protecting group on the guanine base. It is utilized for the synthesis of modified oligonucleotides containing FNA nucleotide analogs, which confer enhanced nuclease resistance and stability to the oligonucleotide duplexes. It finds applications in antisense technology, RNA interference (RNAi), and other nucleic acid-based research fields.

CAT: BRP-00915

CAS: 208758-63-8

Molecular Formula: C41H50N7O8P

Molecular Weight: 799.87

Purity: >98%

Appearance: Off-white solid

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InChIKey: WYKRXWSAMISEIB-COURYUFRSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: N#CCCOP(OCC(OCN1C=NC=2NC(=NC(=O)C21)NC(=O)C)COC(C=3C=CC=CC3)(C4=CC=C(OC)C=C4)C5=CC=C(OC)C=C5)N(C(C)C)C(C)C

IUPAC Name: (R)-2-((2-acetamido-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy)-3-(bis(4-methoxyphenyl)(phenyl)methoxy)propyl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C41H50N7O8P/c1-28(2)48(29(3)4)57(55-23-11-22-42)56-25-36(53-27-47-26-43-38-37(47)39(50)46-40(45-38)44-30(5)49)24-54-41(31-12-9-8-10-13-31,32-14-18-34(51-6)19-15-32)33-16-20-35(52-7)21-17-33/h8-10,12-21,26,28-29,36H,11,23-25,27H2,1-7H3,(H2,44,45,46,49,50)/t36-,57?/m1/s1

Synonyms: Phosphoramidous acid, bis(1-methylethyl)-, (2R)-2-[[2-(acetylamino)-1,6-dihydro-6-oxo-7H-purin-7-yl]methoxy]-3-[bis(4-methoxyphenyl)phenylmethoxy]propyl 2-cyanoethyl ester; DMTr-FNA-G(Ac)phosphoramidite

2'-OTBS O6-NPE-G(Me) amidite

Description: 2'-OTBS O6-NPE-G(Me) amidite is a modified phosphoramidite used in oligonucleotide synthesis. It features a guanosine nucleotide modified at the 2' position with a tert-butyldimethylsilyl (OTBS) protecting group and at the O6 position with a nitrophenylethyl (NPE) group, along with a methyl group modification. This compound is utilized in solid-phase oligonucleotide synthesis to incorporate specifically modified nucleosides into oligonucleotide sequences. Such modifications are important for studies in molecular biology, diagnostics, and therapeutic applications, providing enhanced stability and specific properties to the synthesized oligonucleotides.

CAT: BRP-00916

CAS: 219648-40-5

Molecular Formula: C55H71N8O10PSi

Molecular Weight: 1063.28

Purity: >95%

Appearance: Off-white solid

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InChIKey: DFBXNVVGLXNLNJ-UVQCDVNLSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: CC(C)N(C(C)C)P(OCCC#N)OC1C(OC(C1O[Si](C)(C)C(C)(C)C)N2C=NC3=C2N=C(N=C3OCCC4=CC=C(C=C4)[N+](=O)[O-])NC)COC(C5=CC=CC=C5)(C6=CC=C(C=C6)OC)C7=CC=C(C=C7)OC

IUPAC Name: 3-[[(2R,3R,4R,5R)-2-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-[tert-butyl(dimethyl)silyl]oxy-5-[2-(methylamino)-6-[2-(4-nitrophenyl)ethoxy]purin-9-yl]oxolan-3-yl]oxy-[di(propan-2-yl)amino]phosphanyl]oxypropanenitrile

InChI: InChI=1S/C55H71N8O10PSi/c1-37(2)62(38(3)4)74(70-33-16-32-56)72-48-46(35-69-55(40-17-14-13-15-18-40,41-21-27-44(66-9)28-22-41)42-23-29-45(67-10)30-24-42)71-52(49(48)73-75(11,12)54(5,6)7)61-36-58-47-50(61)59-53(57-8)60-51(47)68-34-31-39-19-25-43(26-20-39)63(64)65/h13-15,17-30,36-38,46,48-49,52H,16,31,33-35H2,1-12H3,(H,57,59,60)/t46-,48-,49-,52-,74?/m1/s1

Synonyms: Guanosine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-[(1,1-dimethylethyl)dimethylsilyl]-N-methyl-6-O-[2-(4-nitrophenyl)ethyl]-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]; (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)-5-(2-(methylamino)-6-(4-nitrophenethoxy)-9H-purin-9-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

2'-OTBS O6-NPE-G(di-Me) amidite

Description: 2'-OTBS O6-NPE-G(di-Me) amidite is a modified phosphoramidite used in oligonucleotide synthesis. It features a guanosine nucleotide modified at the 2' position with a tert-butyldimethylsilyl (OTBS) protecting group and at the O6 position with a nitrophenylethyl (NPE) group, along with two methyl (di-Me) group modifications. This compound is utilized in solid-phase oligonucleotide synthesis to incorporate specifically modified nucleosides into oligonucleotide sequences. Such modifications are important for studies in molecular biology, diagnostics, and therapeutic applications, providing enhanced stability and specific properties to the synthesized oligonucleotides.

CAT: BRP-00917

CAS: 2104647-87-0

Molecular Formula: C56H73N8O10PSi

Molecular Weight: 1077.31

Purity: >98%

Appearance: Off-white solid

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InChIKey: ZEHMGNXQYCLVHJ-UTZPLLLRSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: N#CCCOP(OC1C(OC(N2C=NC=3C(=NC(=NC32)N(C)C)OCCC4=CC=C(C=C4)N(=O)=O)C1O[Si](C)(C)C(C)(C)C)COC(C=5C=CC=CC5)(C6=CC=C(OC)C=C6)C7=CC=C(OC)C=C7)N(C(C)C)C(C)C

IUPAC Name: (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)-5-(2-(dimethylamino)-6-(4-nitrophenethoxy)-9H-purin-9-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C56H73N8O10PSi/c1-38(2)63(39(3)4)75(71-34-17-33-57)73-49-47(36-70-56(41-18-15-14-16-19-41,42-22-28-45(67-10)29-23-42)43-24-30-46(68-11)31-25-43)72-53(50(49)74-76(12,13)55(5,6)7)62-37-58-48-51(62)59-54(61(8)9)60-52(48)69-35-32-40-20-26-44(27-21-40)64(65)66/h14-16,18-31,37-39,47,49-50,53H,17,32,34-36H2,1-13H3/t47-,49-,50-,53-,75?/m1/s1

Synonyms: Guanosine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-[(1,1-dimethylethyl)dimethylsilyl]-N,N-dimethyl-6-O-[2-(4-nitrophenyl)ethyl]-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]

2'-OTBS N1-Me-I amidite

Description: 2'-OTBS N1-Me-I amidite is a modified phosphoramidite used in oligonucleotide synthesis. It features a nucleoside with a tert-butyldimethylsilyl (OTBS) protecting group at the 2' position and a methyl group at the N1 position of the base. This specific modification involves inosine (I), a purine nucleoside. This compound is employed in solid-phase oligonucleotide synthesis to incorporate modified nucleosides into oligonucleotide sequences, providing enhanced stability and specific properties. These modifications are valuable for applications in molecular biology, diagnostics, and therapeutic development.

CAT: BRP-00918

CAS: 236752-21-9

Molecular Formula: C47H63N6O8PSi

Molecular Weight: 899.11

Purity: >95%

Appearance: Off-white solid

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InChIKey: USHFHCSKQCIRHW-UTZPQXNGSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: N#CCCOP(OC1C(OC(N2C=NC=3C(=O)N(C=NC32)C)C1O[Si](C)(C)C(C)(C)C)COC(C=4C=CC=CC4)(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)N(C(C)C)C(C)C

IUPAC Name: (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)-5-(1-methyl-6-oxo-1,6-dihydro-9H-purin-9-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C47H63N6O8PSi/c1-32(2)53(33(3)4)62(58-28-16-27-48)60-41-39(59-45(42(41)61-63(11,12)46(5,6)7)52-31-49-40-43(52)50-30-51(8)44(40)54)29-57-47(34-17-14-13-15-18-34,35-19-23-37(55-9)24-20-35)36-21-25-38(56-10)26-22-36/h13-15,17-26,30-33,39,41-42,45H,16,28-29H2,1-12H3/t39-,41-,42-,45-,62?/m1/s1

Synonyms: Inosine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-[(1,1-dimethylethyl)dimethylsilyl]-1-methyl-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]

isoGNA A(Bz) amidite

Description: isoGNA A(Bz) amidite is a modified phosphoramidite used in oligonucleotide synthesis. It features an adenine (A) base protected with a benzoyl (Bz) group, incorporated into an isoglycerol nucleic acid (isoGNA) backbone. This compound is utilized in solid-phase oligonucleotide synthesis to incorporate modified nucleosides with isoGNA backbones into oligonucleotide sequences. Such modifications are important for enhancing the stability, binding affinity, and specificity of synthetic oligonucleotides, making them useful for applications in molecular biology, diagnostics, and therapeutic research.

CAT: BRP-00919

CAS: 1443744-41-9

Molecular Formula: C45H50N7O6P

Molecular Weight: 815.91

Purity: >95%

Appearance: Off-white solid

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InChIKey: JAPSRHIYKAJUIR-UOJNEOKMSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: N#CCCOP(OCC(N1C=NC=2C(=NC=NC21)NC(=O)C=3C=CC=CC3)COC(C=4C=CC=CC4)(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)N(C(C)C)C(C)C

IUPAC Name: (S)-2-(6-benzamido-9H-purin-9-yl)-3-(bis(4-methoxyphenyl)(phenyl)methoxy)propyl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C45H50N7O6P/c1-32(2)52(33(3)4)59(57-27-13-26-46)58-29-38(51-31-49-41-42(47-30-48-43(41)51)50-44(53)34-14-9-7-10-15-34)28-56-45(35-16-11-8-12-17-35,36-18-22-39(54-5)23-19-36)37-20-24-40(55-6)25-21-37/h7-12,14-25,30-33,38H,13,27-29H2,1-6H3,(H,47,48,50,53)/t38-,59?/m0/s1

Synonyms: Phosphoramidous acid, N,N-bis(1-methylethyl)-, (2S)-2-[6-(benzoylamino)-9H-purin-9-yl]-3-[bis(4-methoxyphenyl)phenylmethoxy]propyl 2-cyanoethyl ester; (2S)-2-[6-(Benzoylamino)-9H-purin-9-yl]-3-[bis(4-methoxyphenyl)phenylmethoxy]propyl 2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite

isoGNA C(iBu) amidite

Description: isoGNA C(iBu) amidite is a modified phosphoramidite used in oligonucleotide synthesis. It features a cytosine (C) base protected with an isobutyryl (iBu) group, integrated into an isoglycerol nucleic acid (isoGNA) backbone. This compound is employed in solid-phase oligonucleotide synthesis to incorporate modified nucleosides with isoGNA backbones into oligonucleotide sequences. These modifications enhance the stability, binding affinity, and specificity of synthetic oligonucleotides, making them valuable for various applications in molecular biology, diagnostics, and therapeutic development.

CAT: BRP-00920

CAS: 1443744-42-0

Molecular Formula: C41H52N5O7P

Molecular Weight: 757.87

Purity: >95%

Appearance: Off-white solid

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InChIKey: XGLKXRATAYJCHB-XYMJDGAWSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: N#CCCOP(OCC(N1C=CC(=NC1=O)NC(=O)C(C)C)COC(C=2C=CC=CC2)(C3=CC=C(OC)C=C3)C4=CC=C(OC)C=C4)N(C(C)C)C(C)C

IUPAC Name: (S)-3-(bis(4-methoxyphenyl)(phenyl)methoxy)-2-(4-isobutyramido-2-oxopyrimidin-1(2H)-yl)propyl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C41H52N5O7P/c1-29(2)39(47)43-38-23-25-45(40(48)44-38)35(28-53-54(52-26-12-24-42)46(30(3)4)31(5)6)27-51-41(32-13-10-9-11-14-32,33-15-19-36(49-7)20-16-33)34-17-21-37(50-8)22-18-34/h9-11,13-23,25,29-31,35H,12,26-28H2,1-8H3,(H,43,44,47,48)/t35-,54?/m0/s1

Synonyms: Phosphoramidous acid, N,N-bis(1-methylethyl)-, (2S)-3-[bis(4-methoxyphenyl)phenylmethoxy]-2-[4-[(2-methyl-1-oxopropyl)amino]-2-oxo-1(2H)-pyrimidinyl]propyl 2-cyanoethyl ester; (2S)-3-[Bis(4-methoxyphenyl)phenylmethoxy]-2-[4-[(2-methyl-1-oxopropyl)amino]-2-oxo-1(2H)-pyrimidinyl]propyl 2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite

isoGNA O6-DPC-G(iBu) amidite

Description: isoGNA O6-DPC-G(iBu) amidite is a modified phosphoramidite used in oligonucleotide synthesis. It features a guanine (G) base with an O6-DPC (diphenylcarbamoyl) modification and an isobutyryl (iBu) protecting group, integrated into an isoglycerol nucleic acid (isoGNA) backbone. This compound is utilized in solid-phase oligonucleotide synthesis to incorporate specifically modified nucleosides with isoGNA backbones into oligonucleotide sequences. These modifications are important for enhancing the stability, binding affinity, and specificity of synthetic oligonucleotides, making them valuable for applications in molecular biology, diagnostics, and therapeutic research.

CAT: BRP-00921

CAS: 1638739-09-9

Molecular Formula: C55H61N8O8P

Molecular Weight: 993.12

Purity: >98%

Appearance: Off-white solid

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InChIKey: CNQFTLNOLDNADK-IKGLYBOLSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: N#CCCOP(OCC(N1C=NC=2C(=NC(=NC21)NC(=O)C(C)C)OC(=O)N(C=3C=CC=CC3)C=4C=CC=CC4)COC(C=5C=CC=CC5)(C6=CC=C(OC)C=C6)C7=CC=C(OC)C=C7)N(C(C)C)C(C)C

IUPAC Name: 9-((2S)-1-(bis(4-methoxyphenyl)(phenyl)methoxy)-3-(((2-cyanoethoxy)(diisopropylamino)phosphaneyl)oxy)propan-2-yl)-2-isobutyramido-9H-purin-6-yl diphenylcarbamate

InChI: InChI=1S/C55H61N8O8P/c1-38(2)51(64)59-53-58-50-49(52(60-53)71-54(65)62(44-21-14-10-15-22-44)45-23-16-11-17-24-45)57-37-61(50)46(36-70-72(69-34-18-33-56)63(39(3)4)40(5)6)35-68-55(41-19-12-9-13-20-41,42-25-29-47(66-7)30-26-42)43-27-31-48(67-8)32-28-43/h9-17,19-32,37-40,46H,18,34-36H2,1-8H3,(H,58,59,60,64)/t46-,72?/m0/s1

Synonyms: Carbamic acid, N,N-diphenyl-, 9-[(1S)-2-[bis(4-methoxyphenyl)phenylmethoxy]-1-[[[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]oxy]methyl]ethyl]-2-[(2-methyl-1-oxopropyl)amino]-9H-purin-6-yl ester; 9-[(1S)-2-[Bis(4-methoxyphenyl)phenylmethoxy]-1-[[[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]oxy]methyl]ethyl]-2-[(2-methyl-1-oxopropyl)amino]-9H-purin-6-yl N,N-diphenylcarbamate

2'-MOE A(Bz) MOP-amidite

Description: 2'-MOE A(Bz) MOP-amidite is a modified phosphoramidite used in oligonucleotide synthesis. It features an adenine (A) base protected with a benzoyl (Bz) group and a 2'-O-methoxyethyl (2'-MOE) modification. This compound is employed in solid-phase oligonucleotide synthesis to incorporate nucleosides with 2'-MOE modifications into oligonucleotide sequences. These modifications enhance the stability, binding affinity, and nuclease resistance of synthetic oligonucleotides, making them valuable for various applications in molecular biology, diagnostics, and therapeutic development.

CAT: BRP-00922

CAS: 1821310-27-3

Molecular Formula: C51H63N6O9P

Molecular Weight: 935.07

Purity: >95%

Appearance: Off-white solid

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InChIKey: BZDIHPNWZGXHOG-LTMMGAFGSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: O=C(NC1=NC=NC2=C1N=CN2C3OC(COC(C=4C=CC=CC4)(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)C(OP(N(C(C)C)C(C)C)CCCOC)C3OCCOC)C=7C=CC=CC7

IUPAC Name: N-(9-((2R,3R,4R,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(((diisopropylamino)(3-methoxypropyl)phosphaneyl)oxy)-3-(2-methoxyethoxy)tetrahydrofuran-2-yl)-9H-purin-6-yl)benzamide

InChI: InChI=1S/C51H63N6O9P/c1-35(2)57(36(3)4)67(31-15-28-59-5)66-45-43(32-64-51(38-18-13-10-14-19-38,39-20-24-41(61-7)25-21-39)40-22-26-42(62-8)27-23-40)65-50(46(45)63-30-29-60-6)56-34-54-44-47(52-33-53-48(44)56)55-49(58)37-16-11-9-12-17-37/h9-14,16-27,33-36,43,45-46,50H,15,28-32H2,1-8H3,(H,52,53,55,58)/t43-,45-,46-,50-,67?/m1/s1

Synonyms: Adenosine, N-benzoyl-5'-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-(2-methoxyethyl)-, 3'-[P-(3-methoxypropyl)-N,N-bis(1-methylethyl)phosphonamidite]

2'-MOE G(iBu) MOP-amidite

Description: 2'-MOE G(iBu) MOP-amidite is a modified phosphoramidite used in oligonucleotide synthesis. It features a guanine (G) base protected with an isobutyryl (iBu) group and a 2'-O-methoxyethyl (2'-MOE) modification. This compound is utilized in solid-phase oligonucleotide synthesis to incorporate nucleosides with 2'-MOE modifications into oligonucleotide sequences. These modifications enhance the stability, binding affinity, and nuclease resistance of synthetic oligonucleotides, making them valuable for various applications in molecular biology, diagnostics, and therapeutic development.

CAT: BRP-00923

CAS: 1821310-28-4

Molecular Formula: C48H65N6O10P

Molecular Weight: 917.05

Purity: >95%

Appearance: Off-white solid

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InChIKey: XUVMXOOSPSMHGP-VKFKYRIUSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: O=C1N=C(NC(=O)C(C)C)NC2=C1N=CN2C3OC(COC(C=4C=CC=CC4)(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)C(OP(N(C(C)C)C(C)C)CCCOC)C3OCCOC

InChI: InChI=1S/C48H65N6O10P/c1-31(2)44(55)51-47-50-43-40(45(56)52-47)49-30-53(43)46-42(61-27-26-58-8)41(64-65(28-14-25-57-7)54(32(3)4)33(5)6)39(63-46)29-62-48(34-15-12-11-13-16-34,35-17-21-37(59-9)22-18-35)36-19-23-38(60-10)24-20-36/h11-13,15-24,30-33,39,41-42,46H,14,25-29H2,1-10H3,(H2,50,51,52,55,56)/t39-,41-,42-,46-,65?/m1/s1

Synonyms: Guanosine, 5'-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-(2-methoxyethyl)-N-(2-methyl-1-oxopropyl)-, 3'-[P-(3-methoxypropyl)-N,N-bis(1-methylethyl)phosphonamidite]

ANA 2'-OMe U amidite

ANA 2'-OMe A(Bz) amidite

aTNA A(Bz) amidite

2'-OTBS 5-I-C(Bz) amidite

2'-OMe PseudoIsoCytidine(dmf) amidite

2'-OTBS PseudoIsoCytidine(dmf) amidite

Cyanine 3 amidite (iodide)

ENA MeC(Bz) amidite

ENA MeC(dmf) amidite

ENA A(dmf) amidite

FNA A(Bz) amidite

FNA G(Ac) amidite

2'-OTBS O6-NPE-G(Me) amidite

2'-OTBS O6-NPE-G(di-Me) amidite

2'-OTBS N1-Me-I amidite

isoGNA A(Bz) amidite

isoGNA C(iBu) amidite

isoGNA O6-DPC-G(iBu) amidite

2'-MOE A(Bz) MOP-amidite

2'-MOE G(iBu) MOP-amidite

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