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Nucleotides

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Adenylyl-(3'-5')-cytidine sodium salt

Description: Adenylyl-(3'-5')-cytidine sodium salt is a dinucleotide derivative where adenosine and cytidine are linked via a 3',5'-phosphodiester bond. This compound is stabilized with sodium ions to form its salt. Adenylyl-(3'-5')-cytidine sodium salt is used in biochemical and molecular biology research to study RNA-related processes, including RNA capping mechanisms, mRNA processing, and interactions with enzymes involved in RNA metabolism. This compound serves as a model substrate to investigate RNA modification dynamics and its impact on RNA stability and function.
CAT: BRP-01078
CAS: 25763-55-7
Molecular Formula: C19H24N8NaO11P
Molecular Weight: 594.41
Purity: ≥98%
Appearance: Colorless to light yellow liquid
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Storage: Store at -20 °C
InChIKey: CQLGPTQGNINUMX-ANTYETTRSA-M
CanonicalSMILES: [Na].C1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)(O)OC3C(OC(C3O)N4C=NC5=C(N=CN=C54)N)CO)O)O
IUPAC Name: sodium;((2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl ((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-2-(hydroxymethyl)tetrahydrofuran-3-yl) phosphate
InChI: InChI=1S/C19H25N8O11P.Na/c20-9-1-2-26(19(32)25-9)17-12(30)11(29)8(37-17)4-35-39(33,34)38-14-7(3-28)36-18(13(14)31)27-6-24-10-15(21)22-5-23-16(10)27;/h1-2,5-8,11-14,17-18,28-31H,3-4H2,(H,33,34)(H2,20,25,32)(H2,21,22,23);/q;+1/p-1/t7-,8-,11-,12-,13-,14-,17-,18-;/m1./s1
Synonyms: AmpC sodium salt; AmpC Na salt; Cytidylyl(5'->3')adenosine sodium salt; 3'-Adenylic acid, 5'-ester with cytidine sodium salt; Adenosine, cytidylyl-(5'→3')-, sodium salt; Adenylyl-(3'→5')-cytidine sodium salt; Adenylylcytosine sodium salt; ApC sodium salt
Related CAS: 4833-63-0 (free acid)

Cytidylyl-(3'-5')-guanosine sodium salt

Description: Cytidylyl-(3'-5')-guanosine sodium salt is a dinucleotide derivative where cytidine and guanosine are linked via a 3',5'-phosphodiester bond. This compound is stabilized with sodium ions to form its salt. Cytidylyl-(3'-5')-guanosine sodium salt is a valuable tool in RNA research, contributing to advancements in our understanding of RNA biology and its therapeutic potential.
CAT: BRP-01079
CAS: 172793-57-6
Molecular Formula: C19H24N8NaO12P
Molecular Weight: 610.41
Purity: ≥98%
Appearance: Colorless to light yellow liquid
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Storage: Store at -20 °C
InChIKey: FTZJFXCZHMRECV-ORIIHXKDSA-M
CanonicalSMILES: [Na].O=C1N=C(N)NC2=C1N=CN2C3OC(COP(=O)(O)OC4C(O)C(OC4CO)N5C=CC(=NC5=O)N)C(O)C3O
IUPAC Name: sodium;(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-4-hydroxy-2-(hydroxymethyl)tetrahydrofuran-3-yl (((2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl) phosphate
InChI: InChI=1S/C19H25N8O12P.Na/c20-8-1-2-26(19(33)23-8)17-12(31)13(6(3-28)37-17)39-40(34,35)36-4-7-10(29)11(30)16(38-7)27-5-22-9-14(27)24-18(21)25-15(9)32;/h1-2,5-7,10-13,16-17,28-31H,3-4H2,(H,34,35)(H2,20,23,33)(H3,21,24,25,32);/q;+1/p-1/t6-,7-,10-,11-,12-,13-,16-,17-;/m1./s1
Synonyms: CmpG sodium salt; CmpG Na salt; Guanosine, cytidylyl-(3'→5')-, monosodium salt; Cytidylyl-3'-5'-guanosine sodium salt; CpG RNA Dinucleotide (5'-3') sodium salt; Cytidylyl-(3'→5')-guanosine sodium salt; (3'-5')CpG sodium salt; Cytidylylguanosine sodium salt; Guanosine cytidine 3',5'-monophosphate sodium salt; CpG sodium salt
Related CAS: 2382-65-2 (free acid)

pA(2-NH2-2'-OMe)mpG TEA salt

Description: pA(2-NH2-2'-OMe)mpG TEA salt is a modified nucleotide composed of adenosine monophosphate (AMP's 3'-hydroxyl group) linked to guanosine monophosphate (GMP's 5'-phosphate group) through a phosphoester bond. The adenosine nucleoside is specifically modified with a 2-amino and 2'-O-methyl (2-NH2-2'-OMe) group, imparting unique properties to the molecule. Triethylamine (TEA) is used as a counter ion to stabilize the compound in its salt form. This modified nucleotide is utilized in biochemical and molecular biology research to study RNA structure, function, and RNA-protein interactions. Its specific modifications can influence RNA stability, enzymatic reactions involving RNA, and various cellular processes related to gene expression and RNA metabolism.
CAT: BRP-01080
Molecular Formula: C21H29N11O14P2 (free acid)
Molecular Weight: 721.47 (free acid)
Purity: ≥98% by UPLC
Appearance: White, off-white to light yellow powder
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IUPAC Name: ((2R,3R,4R,5R)-3-(((((2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(hydroxy)phosphoryl)oxy)-5-(2,6-diamino-9H-purin-9-yl)-4-methoxytetrahydrofuran-2-yl)methyl dihydrogen phosphate;N,N-diethylethanamine
Synonyms: pA(2-NH2-2'-O-Methyl)mpG TEA salt
Related CAS: 2892150-53-5 (free base) ; 2956650-49-8 (TEA salt (1:2)) ; 2892150-54-6 (TEA salt (1:3))

Adenylyl-(3'-5')-adenosine sodium salt

Description: Adenylyl-(3'-5')-adenosine sodium salt is a dinucleotide derivative where adenosine is linked via a 3',5'-phosphodiester bond to another adenosine molecule. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and molecular biology research to study RNA capping, mRNA processing, RNA metabolism, and enzymatic reactions.
CAT: BRP-01081
CAS: 61240-16-2
Molecular Formula: C20H24N10NaO10P
Molecular Weight: 618.44
Purity: ≥98%
Appearance: Colorless to light yellow liquid
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InChIKey: BFGXEXPKOZLNPD-AHKIGRPSSA-M
CanonicalSMILES: [Na].O=P(O)(OCC1OC(N2C=NC=3C(=NC=NC32)N)C(O)C1O)OC4C(O)C(OC4CO)N5C=NC=6C(=NC=NC65)N
IUPAC Name: sodium;((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl ((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-2-(hydroxymethyl)tetrahydrofuran-3-yl) phosphate
InChI: InChI=1S/C20H25N10O10P.Na/c21-15-9-17(25-3-23-15)29(5-27-9)19-12(33)11(32)8(39-19)2-37-41(35,36)40-14-7(1-31)38-20(13(14)34)30-6-28-10-16(22)24-4-26-18(10)30;/h3-8,11-14,19-20,31-34H,1-2H2,(H,35,36)(H2,21,23,25)(H2,22,24,26);/q;+1/p-1/t7-,8-,11-,12-,13-,14-,19-,20-;/m1./s1
Synonyms: AmpA Na salt; ApA RNA Dinucleotide (5'-3') sodium salt; 5'-Adenylic acid, 3'-ester with adenosine sodium salt; Adenylyl-(3'→5')-adenosine sodium salt; 3',5'-ApA sodium salt; D-Adenylyl-(3'-5')-D-adenosine sodium salt; Adenylyl-(5'→3')-adenosine sodium salt; Adenylyladenosine sodium salt; Diadenosine 3',5'-monophosphate sodium salt; AmpA sodium salt; Adenosine, adenylyl-(3'→5')-, monosodium salt; ApA sodium salt
Related CAS: 2391-46-0 (free acid)

Guanylyl-(3'-5')-cytidine sodium salt

Description: Guanylyl-(3'-5')-cytidine sodium salt is a dinucleotide derivative where guanosine is linked via a 3',5'-phosphodiester bond to cytidine. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and molecular biology research to study RNA-related processes, including RNA capping mechanisms, mRNA processing, and interactions with RNA-binding proteins.
CAT: BRP-01082
CAS: 98046-66-3
Molecular Formula: C19H24N8NaO12P
Molecular Weight: 610.41
Purity: ≥98%
Appearance: White, off-white to faint yellow powder
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Storage: Store at -20 °C
InChIKey: AIQIHLOTMLLFGR-ORIIHXKDSA-M
CanonicalSMILES: C1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)(O)OC3C(OC(C3O)N4C=NC5=C4N=C(N=C5[O-])N)CO)O)O.[Na+]
IUPAC Name: sodium;2-amino-9-[(2R,3R,4S,5R)-4-[[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]purin-6-olate
InChI: InChI=1S/C19H25N8O12P.Na/c20-8-1-2-26(19(33)23-8)16-11(30)10(29)7(38-16)4-36-40(34,35)39-13-6(3-28)37-17(12(13)31)27-5-22-9-14(27)24-18(21)25-15(9)32;/h1-2,5-7,10-13,16-17,28-31H,3-4H2,(H,34,35)(H2,20,23,33)(H3,21,24,25,32);/q;+1/p-1/t6-,7-,10-,11-,12-,13-,16-,17-;/m1./s1
Synonyms: GmpC Sodium salt; GmpC Na salt; Guanylyl-3',5'-cytidine Sodium salt; Guanylyl-(3',5')-cytidine Sodium salt; GpC RNA Dinucleotide (5'-3') Sodium salt; Cytidylyl-(5'->3')-guanosine Sodium salt; 3'-Guanylic acid, 5'-ester with cytidine Sodium salt; Guanylyl-(3'→5')-cytidine Sodium salt; GC Sodium salt; GpC Sodium salt; Cytidine, guanylyl-(3'→5')-, monosodium salt
Related CAS: 4785-04-0 (free acid)

Uridylyl-(3'-5')-cytidine sodium salt

Description: Uridylyl-(3'-5')-cytidine sodium salt is a dinucleotide derivative where uridine is linked via a 3',5'-phosphodiester bond to cytidine. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and molecular biology research to study RNA-related processes, including RNA capping mechanisms, mRNA processing, and interactions with RNA-binding proteins.
CAT: BRP-01083
CAS: 108347-78-0
Molecular Formula: C18H23N5NaO13P
Molecular Weight: 571.37
Purity: ≥98%
Appearance: Colorless to light yellow liquid
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InChIKey: VURZOPNHTCBXDR-ZNFCZCJPSA-M
CanonicalSMILES: [Na].O=C1N=C(N)C=CN1C2OC(COP(=O)(O)OC3C(O)C(OC3CO)N4C=CC(=O)NC4=O)C(O)C2O
IUPAC Name: sodium;((2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl ((2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-hydroxy-2-(hydroxymethyl)tetrahydrofuran-3-yl) phosphate
InChI: InChI=1S/C18H24N5O13P.Na/c19-9-1-3-22(17(29)20-9)15-12(27)11(26)8(35-15)6-33-37(31,32)36-14-7(5-24)34-16(13(14)28)23-4-2-10(25)21-18(23)30;/h1-4,7-8,11-16,24,26-28H,5-6H2,(H,31,32)(H2,19,20,29)(H,21,25,30);/q;+1/p-1/t7-,8-,11-,12-,13-,14-,15-,16-;/m1./s1
Synonyms: UmpC Sodium salt; UmpC Na salt; UpC RNA Dinucleotide (5'-3') sodium salt; Cytidylyl-(5',3')-uridine sodium salt; 3'-Uridylic acid, 5'-ester with cytidine sodium salt; Uridine, cytidylyl-(5'→3')-, sodium salt; Uridylyl-(3'→5')-cytidine sodium salt; Cytidylyl-(5'→3')-uridine sodium salt; Uridine, cytidylyl-(5'→3')-, monosodium salt
Related CAS: 3013-97-6 (free acid)

Guanylyl-(3'-5')-guanosine sodium salt

Description: Guanylyl-(3'-5')-guanosine sodium salt is a dinucleotide derivative where guanosine is linked via a 3',5'-phosphodiester bond to another guanosine molecule. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and molecular biology research to study RNA-related processes, such as RNA capping mechanisms, mRNA processing, and interactions with RNA-binding proteins.
CAT: BRP-01084
Molecular Formula: C20H24N10NaO12P
Molecular Weight: 650.43
Purity: ≥98%
Appearance: Colorless to light yellow liquid
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Storage: Store at -20 °C
InChIKey: GXRIXMJPGDBQDY-AORRWANRSA-M
CanonicalSMILES: [Na].O=C1N=C(N)NC2=C1N=CN2C3OC(COP(=O)(O)OC4C(O)C(OC4CO)N5C=NC=6C(=O)N=C(N)NC65)C(O)C3O
IUPAC Name: sodium;((2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl ((2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-4-hydroxy-2-(hydroxymethyl)tetrahydrofuran-3-yl) phosphate
InChI: InChI=1S/C20H25N10O12P.Na/c21-19-25-13-7(15(35)27-19)23-3-29(13)17-10(33)9(32)6(41-17)2-39-43(37,38)42-12-5(1-31)40-18(11(12)34)30-4-24-8-14(30)26-20(22)28-16(8)36;/h3-6,9-12,17-18,31-34H,1-2H2,(H,37,38)(H3,21,25,27,35)(H3,22,26,28,36);/q;+1/p-1/t5-,6-,9-,10-,11-,12-,17-,18-;/m1./s1
Synonyms: GmpG sodium salt; GmpG Na salt; GpG RNA Dinucleotide (5'-3') sodium salt; 3'-Guanylic acid, 3',5'-ester with guanosine sodium salt; Guanylyl-(3'→5')-guanosine sodium salt; GmpG sodium salt; GpG sodium salt; Guanosyl(3',5')guanosine sodium salt
Related CAS: 3353-33-1 (free acid)

Cytidylyl-(3'-5')-cytidine sodium salt

Description: Cytidylyl-(3'-5')-cytidine sodium salt is a dinucleotide derivative where cytidine is linked via a 3',5'-phosphodiester bond to another cytidine molecule. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and molecular biology research to study RNA-related processes, including RNA capping mechanisms, mRNA processing, and interactions with RNA-binding proteins.
CAT: BRP-01085
Molecular Formula: C18H24N6NaO12P
Molecular Weight: 570.38
Purity: ≥98%
Appearance: Colorless to light yellow liquid
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InChIKey: AQOPRPMSNZJVLS-ZNFCZCJPSA-M
CanonicalSMILES: [Na].C1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)(O)OC3C(OC(C3O)N4C=CC(=NC4=O)N)CO)O)O
IUPAC Name: sodium;((2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl ((2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-4-hydroxy-2-(hydroxymethyl)tetrahydrofuran-3-yl) phosphate
InChI: InChI=1S/C18H25N6O12P.Na/c19-9-1-3-23(17(29)21-9)15-12(27)11(26)8(35-15)6-33-37(31,32)36-14-7(5-25)34-16(13(14)28)24-4-2-10(20)22-18(24)30;/h1-4,7-8,11-16,25-28H,5-6H2,(H,31,32)(H2,19,21,29)(H2,20,22,30);/q;+1/p-1/t7-,8-,11-,12-,13-,14-,15-,16-;/m1./s1
Synonyms: CmpC sodium salt; CmpC Na salt; CpC RNA Dinucleotide (5'-3') sodium salt; 3'-Cytidylic acid, 5'-ester with cytidine sodium salt; Cytidylyl-(3'→5')-cytidine sodium salt; CpC sodium salt
Related CAS: 2536-99-4 (free acid)

Guanylyl-(3'-5')-uridine sodium salt

Description: Guanylyl-(3'-5')-uridine sodium salt is a dinucleotide derivative where guanosine is linked via a 3',5'-phosphodiester bond to uridine. This compound is stabilized with sodium ions to form its salt. It is utilized in biochemical and molecular biology research to investigate RNA-related processes, including RNA capping mechanisms, mRNA processing, and interactions with RNA-binding proteins. This compound serves as a valuable tool in elucidating the roles of modified nucleotides in RNA biology and in studying enzymatic reactions involving RNA molecules.
CAT: BRP-01086
Molecular Formula: C19H23N7NaO13P
Molecular Weight: 611.39
Purity: ≥98%
Appearance: Colorless to light yellow liquid
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InChIKey: ARFFYXAWJAGGOQ-ORIIHXKDSA-M
CanonicalSMILES: [Na].C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)OC3C(OC(C3O)N4C=NC5=C4N=C(NC5=O)N)CO)O)O
IUPAC Name: sodium;(2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-4-hydroxy-2-(hydroxymethyl)tetrahydrofuran-3-yl (((2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl) phosphate
InChI: InChI=1S/C19H24N7O13P.Na/c20-18-23-14-9(15(32)24-18)21-5-26(14)17-12(31)13(6(3-27)37-17)39-40(34,35)36-4-7-10(29)11(30)16(38-7)25-2-1-8(28)22-19(25)33;/h1-2,5-7,10-13,16-17,27,29-31H,3-4H2,(H,34,35)(H,22,28,33)(H3,20,23,24,32);/q;+1/p-1/t6-,7-,10-,11-,12-,13-,16-,17-;/m1./s1
Synonyms: GmpU Na salt; GmpU sodium salt; Guanylyl(3'-5')uridine sodium salt; 3'-Guanylic acid, 5'-ester with uridine sodium salt; Guanylyl-(3'→5')-uridine sodium salt; GU sodium salt; Guanosyl-(3',5')-uridine sodium salt; Guanylyl-(3',5')-uridine sodium salt
Related CAS: 4785-07-3 (free acid)

pA(2'-O-ethyl)mpG TEA salt

Description: pA(2'-O-ethyl)mpG TEA salt is a modified nucleotide composed of adenosine monophosphate (AMP's 3'-hydroxyl group) linked to guanosine monophosphate (GMP's 5'-phosphate group) through a phosphoester bond. The adenosine nucleoside is specifically modified with a 2'-O-ethyl group, enhancing its stability and affecting its biological activity. This compound is crucial in biochemical and molecular biology research for studying RNA structure, function, and RNA-protein interactions. It serves as a valuable tool to elucidate the roles of modified nucleotides in RNA stability, enzymatic reactions involving RNA, and the regulation of gene expression pathways.
CAT: BRP-01087
Molecular Formula: C22H30N10O14P2 (free acid)
Molecular Weight: 720.49 (free acid)
Purity: ≥97% by HPLC
Appearance: White, off-white to light yellow powder
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Storage: Store at -20 °C
IUPAC Name: [(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl [(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-4-ethoxy-2-(phosphonooxymethyl)oxolan-3-yl] hydrogen phosphate;N,N-diethylethanamine
Synonyms: pA(2'-O-ethyl)mpG TEA salt; ((2R,3R,4R,5R)-3-(((((2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(hydroxy)phosphoryl)oxy)-5-(6-amino-9H-purin-9-yl)-4-ethoxytetrahydrofuran-2-yl)methyl dihydrogen phosphate TEA salt

Adenylyl-(3'-5')-guanosine sodium salt

Description: Adenylyl-(3'-5')-guanosine sodium salt is a dinucleotide derivative where adenosine is linked via a 3',5'-phosphodiester bond to guanosine. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and molecular biology research to study RNA capping, mRNA processing, RNA metabolism, and enzymatic reactions.
CAT: BRP-01088
Molecular Formula: C20H24N10NaO11P
Molecular Weight: 634.43
Purity: ≥98%
Appearance: Colorless to light yellow liquid
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Storage: Store at -20 °C
InChIKey: DLGZYSANFJSDKP-VSBWEBIMSA-M
CanonicalSMILES: [Na].C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)OP(=O)(O)OCC4C(C(C(O4)N5C=NC6=C5N=C(NC6=O)N)O)O)O)N
IUPAC Name: sodium;((2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl ((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-2-(hydroxymethyl)tetrahydrofuran-3-yl) phosphate
InChI: InChI=1S/C20H25N10O11P.Na/c21-14-8-15(24-3-23-14)29(4-25-8)19-12(34)13(6(1-31)39-19)41-42(36,37)38-2-7-10(32)11(33)18(40-7)30-5-26-9-16(30)27-20(22)28-17(9)35;/h3-7,10-13,18-19,31-34H,1-2H2,(H,36,37)(H2,21,23,24)(H3,22,27,28,35);/q;+1/p-1/t6-,7-,10-,11-,12-,13-,18-,19-;/m1./s1
Synonyms: AmpG Sodium salt; AmpG Na salt; 3'-Adenylic acid, 5'-ester with guanosine Sodium salt; Adenylyl-(3'→5')-guanosine Sodium salt; A-G Sodium salt; Adenosine, guanylyl-(5'→3')-, Sodium salt
Related CAS: 3352-23-6 (free acid)

pA(N6-Me-2'-OMe)mpG TEA salt

Description: pA(N6-Me-2'-OMe)mpG TEA salt is a modified nucleotide composed of adenosine monophosphate (AMP's 3'-hydroxyl group) linked to guanosine monophosphate (GMP's 5'-phosphate group) via a phosphoester bond. The adenosine nucleoside is specifically modified with a methyl group at the N6 position of adenine and a methoxy group at the 2'-position of the ribose (2'-OMe). Triethylamine (TEA) is used as a counter ion to stabilize the compound in its salt form. This modification affects the nucleotide's biological activity and stability, making it useful for studying RNA structure, function, and interactions with RNA-binding proteins.
CAT: BRP-01089
Molecular Formula: C22H30N10O14P2 (free acid)
Molecular Weight: 720.48 (free acid)
Purity: ≥98% by HPLC
Appearance: Clear and colorless to slightly yellow liquid
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Storage: Store at -20 °C
IUPAC Name: [(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl [(2R,3R,4R,5R)-4-methoxy-5-[6-(methylamino)purin-9-yl]-2-(phosphonooxymethyl)oxolan-3-yl] hydrogen phosphate;N,N-diethylethanamine
Synonyms: pA(N6-Methyl-2'-O-methyl)mpG TEA salt; (2'OMe-5'p-m6A)pG TEA salt; N-Methyl-2'-O-methyl-5'-O-phosphonoadenylyl-(3'→5')-guanosine TEA salt; ((2R,3R,4R,5R)-3-(((((2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(hydroxy)phosphoryl)oxy)-4-methoxy-5-(6-(methylamino)-9H-purin-9-yl)tetrahydrofuran-2-yl)methyl dihydrogen phosphate TEA salt
Related CAS: 1207283-40-6 (free base)

pA(N6-Me-2'-OMe)mpG

Description: pA(N6-Me-2'-OMe)mpG is a modified nucleotide composed of adenosine monophosphate (AMP's 3'-hydroxyl group) linked to guanosine monophosphate (GMP's 5'-phosphate group) via a phosphoester bond. The adenosine nucleoside is specifically modified with a methyl group at the N6 position of adenine and a methoxy group at the 2'-position of the ribose (2'-OMe). This modification affects the nucleotide's biological activity and stability, making it useful for studying RNA structure, function, and interactions with RNA-binding proteins.
CAT: BRP-01090
CAS: 1207283-40-6
Molecular Formula: C22H30N10O14P2
Molecular Weight: 720.48
Purity: ≥98% by HPLC
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Storage: Store at -20 °C
Density: 2.23±0.1 g/cm3
Boiling Point: 1145.4±75.0 °C at 760 mmHg
InChIKey: ZSLVBXJFRJQSDL-NAGRZYTCSA-N
CanonicalSMILES: CNC1=C2C(=NC=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)OP(=O)(O)OCC4C(C(C(O4)N5C=NC6=C5N=C(NC6=O)N)O)O)OC
IUPAC Name: [(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl [(2R,3R,4R,5R)-4-methoxy-5-[6-(methylamino)purin-9-yl]-2-(phosphonooxymethyl)oxolan-3-yl] hydrogen phosphate
InChI: InChI=1S/C22H30N10O14P2/c1-24-16-10-17(26-5-25-16)31(6-27-10)21-15(41-2)14(9(45-21)4-42-47(36,37)38)46-48(39,40)43-3-8-12(33)13(34)20(44-8)32-7-28-11-18(32)29-22(23)30-19(11)35/h5-9,12-15,20-21,33-34H,3-4H2,1-2H3,(H,39,40)(H,24,25,26)(H2,36,37,38)(H3,23,29,30,35)/t8-,9-,12-,13-,14-,15-,20-,21-/m1/s1
Synonyms: pA(N6-Methyl-2'-O-methyl)mpG; (2'OMe-5'p-m6A)pG; N-Methyl-2'-O-methyl-5'-O-phosphonoadenylyl-(3'→5')-guanosine; ((2R,3R,4R,5R)-3-(((((2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(hydroxy)phosphoryl)oxy)-4-methoxy-5-(6-(methylamino)-9H-purin-9-yl)tetrahydrofuran-2-yl)methyl dihydrogen phosphate
Related CAS: 2638447-56-8 (TEA salt (1:3)) ; 3031475-41-6 (TEA salt (1:1)) ; 2956650-43-2 (TEA salt (1:2))

Adenylyl-3',5'-cytidine sodium salt

Description: Adenylyl-3',5'-cytidine sodium salt is a dinucleotide derivative where adenosine is linked via a 3',5'-phosphodiester bond to cytidine. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and molecular biology research to study RNA capping mechanisms, RNA metabolism, mRNA processing, and interactions with RNA-binding proteins.
CAT: BRP-01091
CAS: 25602-07-7
Molecular Formula: C19H24N8NaO11P
Molecular Weight: 594.41
Purity: ≥98%
Appearance: Colorless to light yellow liquid
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Storage: Store at -20 °C
InChIKey: VHMIQUJTVKVUMO-ANTYETTRSA-M
CanonicalSMILES: [Na].O=C1N=C(N)C=CN1C2OC(CO)C(OP(=O)(O)OCC3OC(N4C=NC=5C(=NC=NC54)N)C(O)C3O)C2O
IUPAC Name: sodium;(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-4-hydroxy-2-(hydroxymethyl)tetrahydrofuran-3-yl (((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl) phosphate
InChI: InChI=1S/C19H25N8O11P.Na/c20-9-1-2-26(19(32)25-9)18-13(31)14(7(3-28)36-18)38-39(33,34)35-4-8-11(29)12(30)17(37-8)27-6-24-10-15(21)22-5-23-16(10)27;/h1-2,5-8,11-14,17-18,28-31H,3-4H2,(H,33,34)(H2,20,25,32)(H2,21,22,23);/q;+1/p-1/t7-,8-,11-,12-,13-,14-,17-,18-;/m1./s1
Synonyms: CmpA sodium salt; CmpA Na salt; Adenosine, cytidylyl-(3'→5')-, monosodium salt; 5'-Adenylic acid, 3'-ester with cytidine sodium salt; Cytidylyl-(3'→5')-adenosine sodium salt; Cytidylyl adenosine sodium salt; Cytidylyl-3',5'-adenosine phosphate sodium salt; (3'-5')CpA sodium salt; Cytidylyl-(3'-5')-adenosine sodium salt; CpA sodium salt; Cytidylyl(3',5')adenosine sodium salt
Related CAS: 2382-66-3 (free acid)

Uridylyl-(3'-5')-adenosine sodium salt

Description: Uridylyl-(3'-5')-adenosine sodium salt is a dinucleotide derivative where uridine is linked via a 3',5'-phosphodiester bond to adenosine. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and molecular biology research to study RNA-related processes, including RNA capping mechanisms, mRNA processing, and interactions with RNA-binding proteins. This nucleotide plays a crucial role in understanding RNA structure, function, and enzymatic reactions involving RNA molecules.
CAT: BRP-01092
CAS: 160509-67-1
Molecular Formula: C19H23N7NaO12P
Molecular Weight: 595.39
Purity: ≥98%
Appearance: Colorless to light yellow liquid
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Storage: Store at -20 °C
InChIKey: DVNDUHYSCGFVEL-ANTYETTRSA-M
CanonicalSMILES: [Na].O=C1C=CN(C(=O)N1)C2OC(CO)C(OP(=O)(O)OCC3OC(N4C=NC=5C(=NC=NC54)N)C(O)C3O)C2O
IUPAC Name: sodium;((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl ((2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-hydroxy-2-(hydroxymethyl)tetrahydrofuran-3-yl) phosphate
InChI: InChI=1S/C19H24N7O12P.Na/c20-15-10-16(22-5-21-15)26(6-23-10)17-12(30)11(29)8(37-17)4-35-39(33,34)38-14-7(3-27)36-18(13(14)31)25-2-1-9(28)24-19(25)32;/h1-2,5-8,11-14,17-18,27,29-31H,3-4H2,(H,33,34)(H2,20,21,22)(H,24,28,32);/q;+1/p-1/t7-,8-,11-,12-,13-,14-,17-,18-;/m1./s1
Synonyms: UmpA sodium salt; Adenosine, uridylyl-(3'→5')-, monosodium salt; UmpA Na salt; UpA RNA Dinucleotide (5'-3') sodium salt; Uridylyladenosine sodium salt; Uridine-3',5'-adenosine phosphate sodium salt; (3',5')-Uridylyladenosine sodium salt; 5'-Adenylic acid, ester with uridine-(5'→3') sodium salt; Uridylyl-(3'→5')-adenosine sodium salt; (3'-5')UpA sodium salt; Adenosine 5',3'-phosphouridine sodium salt
Related CAS: 3256-24-4 (free acid)

pA(2'-OMe)(thio-p)G ammonium salt

Description: pA(2'-OMe)(thio-p)G ammonium salt refers to a modified nucleotide composed of adenosine monophosphate (AMP's 3'-hydroxyl group) linked to guanosine monophosphate (GMP's 5'-phosphate group) via a phosphoester bond. Ammonium ions are used to stabilize the compound in its salt form. This modified nucleotide is utilized in biochemical and molecular biology research to study RNA structure, function, and interactions with RNA-binding proteins. Its specific modifications can influence RNA stability, enzymatic reactions involving RNA, and various cellular processes related to gene expression and RNA metabolism.
CAT: BRP-01093
Molecular Formula: C21H28N10O13P2S (free acid)
Molecular Weight: 722.52 (free acid)
Purity: ≥95% by HPLC
Appearance: White, off-white to faint yellow powder
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Storage: Store at -20 °C
IUPAC Name: ((2R,3R,4R,5R)-3-(((((2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)oxidophosphorothioyl)oxy)-5-(6-amino-9H-purin-9-yl)-4-methoxytetrahydrofuran-2-yl)methyl phosphate;ammonium salt
Synonyms: pA(2'-OMe)(thio-p)G NH4 salt

Uridylyl-(3'-5')-uridine sodium salt

Description: Uridylyl-(3'-5')-uridine sodium salt is a dinucleotide derivative where uridine is linked via a 3',5'-phosphodiester bond to another uridine molecule. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and molecular biology research to study RNA-related processes, including RNA capping mechanisms, mRNA processing, and interactions with RNA-binding proteins. This nucleotide derivative plays a significant role in investigating RNA structure, function, and enzymatic reactions involving RNA molecules.
CAT: BRP-01094
CAS: 18531-27-6
Molecular Formula: C18H22N4NaO14P
Molecular Weight: 572.35
Purity: ≥98%
Appearance: Colorless to light yellow liquid
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Storage: Store at -20 °C
InChIKey: QFVHIDIYJLBZCL-ZNFCZCJPSA-M
CanonicalSMILES: [Na].O=C1C=CN(C(=O)N1)C2OC(COP(=O)(O)OC3C(O)C(OC3CO)N4C=CC(=O)NC4=O)C(O)C2O
IUPAC Name: sodium;((2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl ((2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-hydroxy-2-(hydroxymethyl)tetrahydrofuran-3-yl) phosphate
InChI: InChI=1S/C18H23N4O14P.Na/c23-5-7-14(13(28)16(34-7)22-4-2-10(25)20-18(22)30)36-37(31,32)33-6-8-11(26)12(27)15(35-8)21-3-1-9(24)19-17(21)29;/h1-4,7-8,11-16,23,26-28H,5-6H2,(H,31,32)(H,19,24,29)(H,20,25,30);/q;+1/p-1/t7-,8-,11-,12-,13-,14-,15-,16-;/m1./s1
Synonyms: UmpU sodium salt; UmpU Na salt; UpU RNA Dinucleotide (5'-3') sodium salt; Uridine monophosphate-uridine sodium salt; Uridylyl-(3'→5')-uridine sodium salt; 5'-Uridylic acid, 3'-ester with uridine sodium salt; (3',5')-Uridylyluridine sodium salt; Uridylyl-3',5'-uridine sodium salt; Uridine, uridylyl-(3'→5')-, monosodium salt; UpU sodium salt
Related CAS: 2415-43-2 (free acid)

pAmpU ammonium salt

Description: pAmpU ammonium salt is a modified nucleotide composed of adenosine monophosphate (AMP's 3'-hydroxyl group) linked to uridine monophosphate (UMP's 5'-phosphate group) via a phosphoester bond. This compound is stabilized with ammonium ions to form its salt. It is used in biochemical and molecular biology research to study RNA structure, RNA-protein interactions, and enzymatic reactions involving RNA.
CAT: BRP-01095
Molecular Formula: C19H25N7O15P2 (free acid)
Molecular Weight: 653.39 (free acid)
Purity: ≥95% by HPLC
Appearance: White, off-white to faint yellow powder
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Storage: Store at -20 °C
IUPAC Name: [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-(phosphonooxymethyl)oxolan-3-yl] [(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl hydrogen phosphate;ammonium salt
Synonyms: pAmpU NH4 salt; 5'-Adenylic acid, 3'-ester with 5'-uridylic acid ammonium salt; 5'-Adenylic acid, uridylyl-(5'→3')-, ammonium salt; 5'-O-Phosphonoadenylyl-(3'→5')-uridine ammonium salt; Adenosine, uridylyl-(5'→3')-, 5'-(dihydrogen phosphate) ammonium salt; Adenosine, uridylyl-(5'→3')-, 5'-phosphate ammonium salt
Related CAS: 2676-45-1 (free base)

pA(2'-O-MOE)mpG ammonium salt

Description: pA(2'-O-MOE)mpG ammonium salt is a modified nucleotide composed of adenosine monophosphate (AMP's 3'-hydroxyl group) linked to guanosine monophosphate (GMP's 5'-phosphate group) via a phosphoester bond. This compound is stabilized with ammonium ions to form its salt. It is used in biochemical and molecular biology research to investigate RNA structure, stability, and RNA-protein interactions. This nucleotide derivative plays a crucial role in understanding RNA modifications and their impact on cellular processes.
CAT: BRP-01096
Molecular Formula: C23H32N10O15P2 (free acid)
Molecular Weight: 750.51 (free acid)
Purity: ≥97% by HPLC
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Storage: Store at 2-8 °C
IUPAC Name: [(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl [(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-4-(2-methoxyethoxy)-2-(phosphonooxymethyl)oxolan-3-yl] hydrogen phosphate;ammonium salt
Synonyms: pA(2'-O-MOE)mpG NH4 salt; ((2R,3R,4R,5R)-3-(((((2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)oxidophosphoryl)oxy)-5-(6-amino-9H-purin-9-yl)-4-(2-methoxyethoxy)tetrahydrofuran-2-yl)methyl phosphate ammonium salt

pA(2'-OMe)mpU ammonium salt

Description: pA(2'-OMe)mpU ammonium salt is a modified nucleotide composed of adenosine monophosphate (AMP's 3'-hydroxyl group) linked to uridine monophosphate (UMP's 5'-phosphate group) via a phosphoester bond. This compound is stabilized with ammonium ions to form its salt. It is utilized in biochemical and molecular biology research to study RNA metabolism, RNA modification mechanisms, and interactions with RNA-binding proteins. This nucleotide derivative serves as a valuable tool in investigating the roles of modified nucleotides in RNA-related processes.
CAT: BRP-01097
Molecular Formula: C20H27N7O15P2 (free acid)
Molecular Weight: 667.42 (free acid)
Purity: ≥95% by HPLC
Appearance: White, off-white to faint yellow powder
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Storage: Store at -20 °C
IUPAC Name: [(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-4-methoxy-2-(phosphonooxymethyl)oxolan-3-yl] [(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl hydrogen phosphate;ammonium salt
Synonyms: pA(2'-OMe)mpU NH4 salt; (2'-OMe-5'-MP-A)pU ammonium salt; ((2R,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-3-(((((2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)oxidophosphoryl)oxy)-4-methoxytetrahydrofuran-2-yl)methyl phosphate ammonium salt
Related CAS: 2956650-76-1 (free acid) ; 2956650-77-2 (triethylamine salt (1:2))
* Only for research. Not suitable for any diagnostic or therapeutic use.

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