Nucleotides - RNA / BOC Sciences

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

MF: C18H24N6NaO12P

MF: 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

MF: C19H23N7NaO13P

MF: 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

MF: C22H30N10O14P2 (free acid)

MF: 720.49 (free acid)

Purity: ≥97% by HPLC

Appearance: White, off-white to light yellow powder

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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

MF: C20H24N10NaO11P

MF: 634.43

Purity: ≥98%

Appearance: Colorless to light yellow liquid

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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

MF: C22H30N10O14P2 (free acid)

MF: 720.48 (free acid)

Purity: ≥98% by HPLC

Appearance: Clear and colorless to slightly yellow liquid

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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

MF: C22H30N10O14P2

MF: 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

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

MF: C19H24N8NaO11P

MF: 594.41

Purity: ≥98%

Appearance: Colorless to light yellow liquid

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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

MF: C19H23N7NaO12P

MF: 595.39

Purity: ≥98%

Appearance: Colorless to light yellow liquid

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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

MF: C21H28N10O13P2S (free acid)

MF: 722.52 (free acid)

Purity: ≥95% by HPLC

Appearance: White, off-white to faint 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)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

MF: C18H22N4NaO14P

MF: 572.35

Purity: ≥98%

Appearance: Colorless to light yellow liquid

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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

MF: C19H25N7O15P2 (free acid)

MF: 653.39 (free acid)

Purity: ≥95% by HPLC

Appearance: White, off-white to faint yellow powder

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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

MF: C23H32N10O15P2 (free acid)

MF: 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

MF: C20H27N7O15P2 (free acid)

MF: 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))

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

Description: Adenylyl-(3'-5')-uridine sodium salt is a dinucleotide derivative where adenosine 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 study RNA capping mechanisms, mRNA processing, and interactions with RNA-binding proteins. This nucleotide derivative serves as a tool to understand RNA structure, function, and enzymatic reactions involving RNA molecules.

CAT: BRP-01098

CAS: 43150-64-7

MF: C19H23N7NaO12P

MF: 595.39

Purity: ≥98%

Appearance: Colorless to light yellow liquid

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InChIKey: VIJAZWBPDRETEC-ANTYETTRSA-M

CanonicalSMILES: [Na].O=C1C=CN(C(=O)N1)C2OC(COP(=O)(O)OC3C(O)C(OC3CO)N4C=NC=5C(=NC=NC54)N)C(O)C2O

IUPAC Name: sodium;(2R,3S,4R,5R)-5-(6-amino-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/C19H24N7O12P.Na/c20-15-10-16(22-5-21-15)26(6-23-10)18-13(31)14(7(3-27)36-18)38-39(33,34)35-4-8-11(29)12(30)17(37-8)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: AmpU sodium salt; AmpU Na salt; Adenylyl-(3'→5')-uridine sodium salt; 3'-Adenylic acid, ester with uridine-(3'→5') sodium salt; Adenosine, uridylyl-(5'→3')-, sodium salt; Adenylyluridine sodium salt; Uridylyl-(5'→3')-adenosine sodium salt; Uridine, adenylyl-(3'→5')-, sodium salt (1:1); Adenosine, uridylyl-(5'→3')-, monosodium salt; Uridine, adenylyl-(3'→5')-, monosodium salt

Related CAS: 3051-84-1 (free acid)

Cytidylyl(3'-5')uridine sodium salt

Description: Cytidylyl-(3'-5')-uridine sodium salt is a dinucleotide derivative where cytidine is linked via a 3',5'-phosphodiester bond to uridine. 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 critical role in understanding RNA structure, function, and enzymatic reactions involving RNA molecules.

CAT: BRP-01099

MF: C18H23N5NaO13P

MF: 571.37

Purity: ≥98%

Appearance: Colorless to light yellow liquid

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InChIKey: BEGNGJBTEUONPW-ZNFCZCJPSA-M

CanonicalSMILES: [Na].C1=CN(C(=O)N=C1N)C2C(C(C(O2)CO)OP(=O)(O)OCC3C(C(C(O3)N4C=CC(=O)NC4=O)O)O)O

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-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl) phosphate

InChI: InChI=1S/C18H24N5O13P.Na/c19-9-1-3-22(17(29)20-9)16-13(28)14(7(5-24)34-16)36-37(31,32)33-6-8-11(26)12(27)15(35-8)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: CmpU sodium salt; CmpU Na salt; Cytidylyl-(3',5')-uridine sodium salt; CpU RNA Dinucleotide (5'-3') sodium salt; 5'-Uridylic acid, 3'-ester with cytidine sodium salt; Cytidylyl-(3'→5')-uridine sodium salt

Related CAS: 2382-64-1 (free acid)

pGmpC ammonium salt

Description: pGmpC ammonium salt is a modified nucleotide composed of guanosine monophosphate (GMP's 3'-hydroxyl group) linked to cytidine monophosphate (CMP's 5'-phosphate group) via a phosphoester bond. This compound is stabilized with ammonium ions in its salt form. It is used in biochemical research to study RNA structure, RNA-protein interactions, and enzymatic reactions involving RNA molecules.

CAT: BRP-01100

MF: C19H26N8O15P2 (free acid)

MF: 668.40 (free acid)

Purity: ≥95% by HPLC

Appearance: White, off-white to faint yellow powder

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IUPAC Name: ((2R,3S,4R,5R)-3-(((((2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)oxidophosphoryl)oxy)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-4-hydroxytetrahydrofuran-2-yl)methyl phosphate;ammonium salt

Synonyms: pGmpC NH4 salt; 5'-Guanylic acid, cytidylyl-(5'→3')-, ammonium salt; 5'-O-Phosphonoguanylyl-(3'→5')-cytidine ammonium salt; Guanosine, cytidylyl-(5'→3')-, 5'-(dihydrogen phosphate) ammonium salt; Guanosine, cytidylyl-(5'→3')-, 5'-phosphate ammonium salt

Related CAS: 28079-00-7 (free acid)

[2'-O-TBDMS-A(Bz)](pCyEt)[2',3'-di-TBDMS-U]

Description: [2'-O-TBDMS-A(Bz)](pCyEt)[2',3'-di-TBDMS-U] is a nucleotide structure where adenosine (A) is modified at the 2'-position with tert-butyldimethylsilyl (TBDMS) and benzoyl (Bz) groups. It is linked via a phosphoramide linkage (pCyEt) to a uridine (U) nucleotide that is protected with TBDMS groups at both the 2'- and 3'-positions. This structure is used in oligonucleotide synthesis to introduce modified adenosine and uridine residues, enhancing stability and specificity in nucleic acid interactions.

CAT: BRP-01195

MF: C47H73N8O13PSi3

MF: 1073.37

Purity: ≥97% by HPLC

Appearance: White, off-white to faint yellow powder

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InChIKey: ARWJDNJCTMYJRQ-JVZNXEAPSA-N

IUPAC Name: (2R,3R,4R,5R)-5-(6-benzamido-9H-purin-9-yl)-4-((tert-butyldimethylsilyl)oxy)-2-(hydroxymethyl)tetrahydrofuran-3-yl (((2R,3R,4R,5R)-3,4-bis((tert-butyldimethylsilyl)oxy)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl) (2-cyanoethyl) phosphate

InChI: InChI=1S/C47H73N8O13PSi3/c1-45(2,3)70(10,11)66-36-32(64-42(54-24-22-33(57)52-44(54)59)38(36)68-72(14,15)47(7,8)9)27-62-69(60,61-25-19-23-48)65-35-31(26-56)63-43(37(35)67-71(12,13)46(4,5)6)55-29-51-34-39(49-28-50-40(34)55)53-41(58)30-20-17-16-18-21-30/h16-18,20-22,24,28-29,31-32,35-38,42-43,56H,19,25-27H2,1-15H3,(H,52,57,59)(H,49,50,53,58)/t31-,32-,35-,36-,37-,38-,42-,43-,69?/m1/s1

Synonyms: N-Benzoyl-P-(2-cyanoethyl)-2'-O-[(1,1-dimethylethyl)dimethylsilyl]adenylyl-(3'→5')-2',3'-bis-O-[(1,1-dimethylethyl)dimethylsilyl]uridine

[2'-O-TBDMS-G(iBu)](pCyEt)[2',3'-diTBDMS-C(Ac)]

Description: [2'-O-TBDMS-G(iBu)](pCyEt)[2',3'-diTBDMS-C(Ac)] features a guanosine (G) nucleotide modified with TBDMS and isobutyryl (iBu) groups at the 2'-position, linked via a phosphoramide linkage (pCyEt) to a cytidine (C) nucleotide protected with TBDMS groups at both the 2'- and 3'-positions, with an acetyl (Ac) group attached. This compound is used in oligonucleotide synthesis to incorporate modified guanosine and cytidine residues, enhancing stability and functionality for specific nucleic acid interactions.

CAT: BRP-01196

MF: C46H78N9O14PSi3

MF: 1096.41

Purity: ≥97% by HPLC

Appearance: White, off-white to faint yellow powder

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InChIKey: YEDZJCYVUAXCEM-RLXQEWBKSA-N

IUPAC Name: ((2R,3R,4R,5R)-5-(4-acetamido-2-oxopyrimidin-1(2H)-yl)-3,4-bis((tert-butyldimethylsilyl)oxy)tetrahydrofuran-2-yl)methyl ((2R,3R,4R,5R)-4-((tert-butyldimethylsilyl)oxy)-2-(hydroxymethyl)-5-(2-isobutyramido-6-oxo-1,6-dihydro-9H-purin-9-yl)tetrahydrofuran-3-yl) (2-cyanoethyl) phosphate

InChI: InChI=1S/C46H78N9O14PSi3/c1-27(2)38(58)52-42-51-37-32(39(59)53-42)48-26-55(37)41-35(68-72(15,16)45(7,8)9)33(29(24-56)64-41)66-70(61,62-23-19-21-47)63-25-30-34(67-71(13,14)44(4,5)6)36(69-73(17,18)46(10,11)12)40(65-30)54-22-20-31(49-28(3)57)50-43(54)60/h20,22,26-27,29-30,33-36,40-41,56H,19,23-25H2,1-18H3,(H,49,50,57,60)(H2,51,52,53,58,59)/t29-,30-,33-,34-,35-,36-,40-,41-,70?/m1/s1

GDP, tributylamine salt

Description: GDP, tributylamine salt is guanosine 5'-diphosphate, a nucleotide consisting of guanosine linked to a diphosphate group at the 5' position of the ribose sugar. In its tributylamine salt form, it is stabilized and solubilized by tributylamine, a tertiary amine, which forms a salt with GDP. This compound is commonly used in biochemical and biotechnological research, particularly in studies involving GTP-binding proteins and signal transduction pathways.

CAT: BRP-01204

MF: C10H15N5O11P2 (free acid)

MF: 443.20 (free acid)

Purity: ≥98% by HPLC

Appearance: White, off-white to light yellow powder

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IUPAC Name: [(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphono hydrogen phosphate;N,N-dibutylbutan-1-amine

Synonyms: Guanosine-5'-diphosphate, tributylamine salt; 2-amino-9-{5-O-[hydroxy(phosphonooxy)phosphoryl]-β-D-ribofuranosyl}-9H-purin-6-ol tributylamine salt; Guanosine 5'-(trihydrogen diphosphate) tributylamine salt

Related CAS: 146-91-8 (free base)

Guanosine 5'-diphosphate trisodium salt

Description: Guanosine 5'-diphosphate trisodium salt is guanosine 5'-diphosphate (GDP), a nucleotide composed of guanosine linked to a diphosphate group at the 5' position of the ribose sugar. In this trisodium salt form, the phosphate groups are complexed with sodium ions to enhance stability and solubility. It is widely employed as a substrate or cofactor in enzymatic reactions, protein synthesis, and various cellular processes involving GTP-dependent signaling and metabolism.

CAT: BRP-01205

CAS: 59652-27-6

MF: C10H12N5Na3O11P2

MF: 509.15

Purity: ≥98% by HPLC

Appearance: White to off-white powder

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InChIKey: PBVNHDMBCZSEMD-CYCLDIHTSA-K

CanonicalSMILES: C1=NC2=C(N1C3C(C(C(O3)COP(=O)([O-])OP(=O)([O-])[O-])O)O)N=C(NC2=O)N.[Na+].[Na+].[Na+]

IUPAC Name: trisodium;[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] phosphate

InChI: InChI=1S/C10H15N5O11P2.3Na/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(25-9)1-24-28(22,23)26-27(19,20)21;;;/h2-3,5-6,9,16-17H,1H2,(H,22,23)(H2,19,20,21)(H3,11,13,14,18);;;/q;3*+1/p-3/t3-,5-,6-,9-;;;/m1.../s1

Synonyms: Guanosine-5'-diphosphate, trisodium salt; Guanosine 5'-(trihydrogen diphosphate), trisodium salt; 5'-GDP.Na3; Guanosine 5'-(trihydrogen diphosphate), sodium salt (1:3)

Related CAS: 146-91-8 (free acid)