Nucleotides - RNA / BOC Sciences

N4-Ac-CTP, Tris Salt

Description: N4-Acetylcytidine 5'-triphosphate tris salt (N4-Ac-CTP tris salt) is a nucleotide derivative where cytidine is phosphorylated at the 5' position and acetylated at the N4 position of the cytosine base. This compound is stabilized with Tris to form its salt. N4-Ac-CTP is used in biochemical and molecular biology research, particularly in studies involving RNA modification, enzymatic assays, and nucleic acid labeling.

CAT: BRP-01065

MF: C11H18N3O15P3 (free acid)

MF: 525.19 (free acid)

Purity: ≥95% by HPLC

Appearance: Clear colorless to light yellow liquid

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IUPAC Name: [[(2R,3S,4R,5R)-5-(4-acetamido-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate;2-amino-2-(hydroxymethyl)propane-1,3-diol

Synonyms: N4-Acetyl-Cytidine-5'-O-triphosphate, Tris Salt; N-Acetylcytidine 5'-(tetrahydrogen triphosphate) Tris salt (1:x); N4-Acetylcytidine triphosphate Tris salt; ac4CTP Tris salt; N4-Acetyl-CTP Tris Salt

Related CAS: 1428903-57-4 (free base)

A-5'-O-(1-Boranotriphosphate), Tris Salt

Description: A-5'-O-(1-Boranotriphosphate) tris salt is a modified nucleotide derivative where adenosine is linked to a boron-containing triphosphate group at the 5'-position. This compound is stabilized with Tris to form its salt. It is used in biochemical research as a non-hydrolyzable analog of ATP to study ATP-dependent processes, enzyme kinetics, and interactions with ATP-binding proteins.

CAT: BRP-01066

MF: C10H17BN5O12P3 (free acid)

MF: 503.00 (free acid)

Purity: ≥95% by HPLC

Appearance: Clear colorless to light yellow liquid

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IUPAC Name: (((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl boraneylphosphonic) diphosphoric anhydride;2-amino-2-(hydroxymethyl)propane-1,3-diol

Synonyms: Adenosine-5'-O-(1-Boranotriphosphate), Tris Salt; Adenosine, 5'-[hydrogen P-borylphosphonate], anhydride with diphosphoric acid Tris Salt

C-5'-O-(1-Boranotriphosphate), Tris Salt

Description: C-5'-O-(1-Boranotriphosphate) tris salt is a modified nucleotide derivative where cytidine is linked to a boron-containing triphosphate group at the 5'-position. This compound is stabilized with Tris to form its salt. It is used in biochemical research as a non-hydrolyzable analog of CTP to study CTP-dependent processes, enzyme kinetics, and interactions with CTP-binding proteins.

CAT: BRP-01067

MF: C9H17BN3O13P3 (free acid)

MF: 478.97 (free acid)

Purity: ≥95% by HPLC

Appearance: Clear colorless to light yellow liquid

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IUPAC Name: (((2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl boraneylphosphonic) diphosphoric anhydride;2-amino-2-(hydroxymethyl)propane-1,3-diol

Synonyms: Cytidine-5'-O-(1-Boranotriphosphate), Tris Salt; Cytidine, 5'-(hydrogen borylphosphonate), monoanhydride with diphosphoric acid, Tris Salt

Related CAS: 199116-93-3 (free base)

9-alpha-L-Arabinofuranosylguanine-5'-triphosphate sodium salt

Description: 9-alpha-L-Arabinofuranosylguanine 5'-triphosphate sodium salt is a nucleotide derivative where guanine is linked to an arabinofuranosyl sugar and phosphorylated at the 5' position with a triphosphate group. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and pharmacological research as a substrate analog for studying nucleoside metabolism and as a potential therapeutic agent.

CAT: BRP-01068

MF: C10H16N5O14P3 (free acid)

MF: 523.18 (free acid)

Purity: ≥98% by HPLC

Appearance: Clear colorless liquid

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

Synonyms: 9-alpha-L-Arabinofuranosylguanine-5'-triphosphate Na salt; ((2S,3R,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate sodium salt

UTPαS sodium salt

Description: Uridine 5'-O-(1-thiotriphosphate) sodium salt (UTPαS sodium salt) is a nucleotide derivative where uridine is linked to a sulfur atom at the α-phosphate position of the triphosphate group. This compound is stabilized with sodium ions to form its salt. UTPαS is used in biochemical and molecular biology research as a non-hydrolyzable analog of UTP to study RNA synthesis, RNA polymerase activity, and other UTP-dependent processes.

CAT: BRP-01069

MF: C9H15N2O14P3S (free acid)

MF: 500.20 (free acid)

Purity: ≥98% by HPLC

Appearance: Colorless to light yellow liquid

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IUPAC Name: sodium;[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphinothioyl] phosphono hydrogen phosphate

Synonyms: Uracil-5'-O-(1-Thiotriphosphate), Sodium Salt; Alpha Thiol UTP (1-Thio-UTP) Sodium Salt; Alpha Thiol UTP Sodium salt; 1-Thio-UTP Sodium salt; Uridine-5'-O-(1-Thiotriphosphate) Sodium salt; Uridine, 5'→P''-ester with thiotriphosphoric acid Sodium salt; UTP-αS Sodium salt

Related CAS: 18875-71-3 (free acid)

9-alpha-L-Arabinofuranosyladenine-5'-triphosphate sodium salt

Description: 9-alpha-L-Arabinofuranosyladenine 5'-triphosphate sodium salt is a nucleotide derivative where adenine is linked to an arabinofuranosyl sugar and phosphorylated at the 5' position with a triphosphate group. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and pharmacological research as a substrate analog for studying nucleoside metabolism and as a potential therapeutic agent.

CAT: BRP-01070

MF: C10H16N5O13P3 (free acid)

MF: 507.18 (free acid)

Purity: ≥98% by HPLC

Appearance: Clear colorless liquid

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IUPAC Name: sodium;[[(2S,3R,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate

Synonyms: 9-alpha-L-Arabinofuranosyladenine-5'-triphosphate Na salt; ((2S,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate sodium salt

1-alpha-L-Arabinofuranosylcytosine-5'-triphosphate, sodium salt

Description: 1-alpha-L-Arabinofuranosylcytosine 5'-triphosphate sodium salt is a nucleotide derivative where cytosine is linked to an arabinofuranosyl sugar and phosphorylated at the 5' position with a triphosphate group. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and molecular biology research, particularly in studies involving RNA synthesis, nucleoside metabolism, and enzymatic assays.

CAT: BRP-01071

MF: C9H16N3O14P3 (free acid)

MF: 483.16 (free acid)

Purity: ≥98% by HPLC

Appearance: Clear colorless liquid

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IUPAC Name: sodium;[[(2S,3R,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate

Synonyms: 1-alpha-L-Arabinofuranosylcytosine-5'-triphosphate, Na salt; ((2S,3R,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate sodium salt; 4-Amino-1-[5-O-[hydroxy[[hydroxy(phosphonooxy)phosphinyl]oxy]phosphinyl]-α-L-arabinofuranosyl]-2(1H)-pyrimidinone sodium salt

Related CAS: 847650-30-0 (free acid)

1-alpha-L-Arabinofuranosyluracil-5'-triphosphate sodium salt

Description: 1-alpha-L-Arabinofuranosyluracil 5'-triphosphate sodium salt is a nucleotide derivative where uracil is linked to an arabinofuranosyl sugar and phosphorylated at the 5' position with a triphosphate group. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and molecular biology research, similar to 1-alpha-L-Arabinofuranosylcytosine-5'-triphosphate, for studies involving RNA synthesis, nucleoside metabolism, and enzymatic assays.

CAT: BRP-01072

MF: C9H15N2O15P3 (free acid)

MF: 484.14 (free acid)

Purity: ≥98% by HPLC

Appearance: Clear colorless liquid

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IUPAC Name: sodium;[[(2S,3R,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate

Synonyms: 1-alpha-L-Arabinofuranosyluracil-5'-triphosphate Na salt; ((2S,3R,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate sodium salt

3'-OMe-GTP sodium salt

Description: 3'-O-Methylguanosine 5'-triphosphate sodium salt (3'-OMe-GTP sodium salt) is a nucleotide derivative where guanosine is phosphorylated at the 5' position and modified with a methyl group at the 3'-hydroxyl (3'-OH) position of the ribose sugar. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and molecular biology research to study RNA modification, RNA structure, RNA-protein interactions, and regulatory roles of modified nucleotides in RNA biology.

CAT: BRP-01073

MF: C11H18N5O14P3 (free acid)

MF: 537.21 (free acid)

Purity: ≥95% by HPLC

Appearance: Clear colorless to yellow liquid

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IUPAC Name: sodium;[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-4-hydroxy-3-methoxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate

Synonyms: 3'-O-methyl-guanosine-5'-triphosphate, sodium salt; (3'Ome)GTP sodium salt; 3'-O-Methylguanosine-5'-triphosphate sodium salt; 3'-O-Methylguanosine 5'-(tetrahydrogen triphosphate) sodium salt; 3'-O-methyl-GTP sodium salt; 3'-O-Methylguanosine triphosphate sodium salt

Related CAS: 61556-45-4 (free acid)

8-Br-GTP sodium salt

Description: 8-Bromo-guanosine 5'-triphosphate sodium salt (8-Br-GTP sodium salt) is a nucleotide derivative where guanosine is phosphorylated at the 5' position and modified with a bromine atom at the 8-position of the purine ring. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and molecular biology research as a substrate analog to study GTP-dependent processes, enzyme kinetics, and interactions with GTP-binding proteins.

CAT: BRP-01074

MF: C10H15BrN5O14P3 (free acid)

MF: 602.08 (free acid)

Purity: ≥95% by HPLC

Appearance: Clear colorless to yellow liquid

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IUPAC Name: sodium;[[(2R,3S,4R,5R)-5-(2-amino-8-bromo-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate

Synonyms: 8-Bromo-guanosine-5'-triphosphate, sodium salt; 8-Bromoguanosine 5'-triphosphate sodium salt; 8-Bromo-GTP sodium salt; 8-Bromoguanosine triphosphate sodium salt; 8-Br-GTP; Guanosine 5'-(tetrahydrogen triphosphate), 8-bromo-; 8-Bromoguanosine 5'-(tetrahydrogen triphosphate)

Related CAS: 23197-98-0 (free acid)

2-F-ATP sodium salt

Description: 2-Fluoro-adenosine 5'-triphosphate sodium salt (2-F-ATP sodium salt) is a nucleotide derivative where adenosine is phosphorylated at the 5' position and modified with a fluorine atom at the 2-position of the adenine base. This compound is stabilized with sodium ions to form its salt. It is used in biochemical and molecular biology research as a substrate analog to study ATP-dependent processes, enzymatic reactions, and interactions with ATP-binding proteins.

CAT: BRP-01075

MF: C10H15FN5O13P3 (free acid)

MF: 525.17 (free acid)

Purity: ≥95% by HPLC

Appearance: Clear colorless to yellow liquid

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Synonyms: 2-Fluoro-adenosine-5'-triphosphate, sodium salt; (2F-ATP) sodium salt; 2-Fluoroadenosine 5'-(tetrahydrogen triphosphate) sodium salt; Adenosine, 2-fluoro-, 5'-(tetrahydrogen triphosphate) sodium salt; Adenosine, 2-fluoro-, 5'-triphosphate sodium salt; 2-Fluoroadenine-9β-D-ribofuranoside 5'-triphosphate sodium salt; 2-Fluoroadenosine 5'-triphosphate sodium salt; 2-Fluoroadenosine triphosphate sodium salt; 2-Fluoro-ATP sodium salt

Related CAS: 1492-62-2 (free acid)

5-[(Trpytamino) carbonyl]-2'-OMe-C-5'-triphosphate, trilithium salt

Description: 5-[(Trpytamino) carbonyl]-2'-O-methylcytidine 5'-triphosphate trilithium salt is a nucleotide derivative where 2'-O-methylcytidine is linked to a ((Trpytamino) carbonyl) group at the 5-position and phosphorylated at the 5' position with a triphosphate group. This compound is stabilized with lithium ions to form its salt. It is used in biochemical research to study RNA modification, RNA structure, and RNA-protein interactions.

CAT: BRP-01076

MF: C21H25Li3N5O15P3

MF: 701.19

Purity: ≥95% by HPLC

Appearance: White, off-white to faint yellow powder

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InChIKey: TXXJVMAXPDAABE-ARDAPVOKSA-K

IUPAC Name: trilithium;((2R,3R,4R,5R)-5-(5-((2-(1H-indol-3-yl)ethyl)carbamoyl)-4-amino-2-oxopyrimidin-1(2H)-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl hydrogen triphosphate

InChI: InChI=1S/C21H28N5O15P3.3Li/c1-37-17-16(27)15(10-38-43(33,34)41-44(35,36)40-42(30,31)32)39-20(17)26-9-13(18(22)25-21(26)29)19(28)23-7-6-11-8-24-14-5-3-2-4-12(11)14;;;/h2-5,8-9,15-17,20,24,27H,6-7,10H2,1H3,(H,23,28)(H,33,34)(H,35,36)(H2,22,25,29)(H2,30,31,32);;;/q;3*+1/p-3/t15-,16-,17-,20-;;;/m1.../s1

Synonyms: 5-[(trpytamino) carbonyl]-2'-O-methyl-cytidine-5'-triphosphate, trilithium salt

Guanylyl-(3',5')-adenosine sodium salt

Description: Guanylyl-(3',5')-adenosine sodium salt is a dinucleotide derivative where guanosine 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 capping processes, mRNA processing, and interactions with RNA capping enzymes.

CAT: BRP-01077

CAS: 103192-56-9

MF: C20H24N10NaO11P

MF: 634.43

Purity: ≥98%

Appearance: White, off-white to faint yellow powder

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InChIKey: IFPMHHUPJFSNCB-VSBWEBIMSA-M

CanonicalSMILES: [Na].O=C1N=C(N)NC2=C1N=CN2C3OC(CO)C(OP(=O)(O)OCC4OC(N5C=NC=6C(=NC=NC65)N)C(O)C4O)C3O

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-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl) phosphate

InChI: InChI=1S/C20H25N10O11P.Na/c21-14-8-15(24-3-23-14)29(4-25-8)18-11(33)10(32)7(40-18)2-38-42(36,37)41-13-6(1-31)39-19(12(13)34)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: GmpA Na salt; Guanine ribonucleotidyl-(3'-5')-adenosine Sodium salt; Adenylyl-(5',3')-guanosine Sodium salt; GpA RNA Dinucleotide (5'-3') Sodium salt; GpA Sodium salt; Guanylyladenosine Sodium salt; GmpA Sodium salt; Adenosine, guanylyl-(3'→5')-, monosodium salt; Guanosine, adenylyl-(5'→3')-, monosodium salt

Related CAS: 6554-00-3 (free acid)

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

MF: C19H24N8NaO11P

MF: 594.41

Purity: ≥98%

Appearance: Colorless to light yellow liquid

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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

MF: C19H24N8NaO12P

MF: 610.41

Purity: ≥98%

Appearance: Colorless to light yellow liquid

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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

MF: C21H29N11O14P2 (free acid)

MF: 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

MF: C20H24N10NaO10P

MF: 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

MF: C19H24N8NaO12P

MF: 610.41

Purity: ≥98%

Appearance: White, off-white to faint yellow powder

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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

MF: C18H23N5NaO13P

MF: 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

MF: C20H24N10NaO12P

MF: 650.43

Purity: ≥98%

Appearance: Colorless to light yellow liquid

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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)