Nucleotides

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

Molecular Formula: C19H23N7NaO12P

Molecular Weight: 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

Molecular Formula: C18H23N5NaO13P

Molecular Weight: 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

Molecular Formula: C19H26N8O15P2 (free acid)

Molecular Weight: 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

Molecular Formula: C47H73N8O13PSi3

Molecular Weight: 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

Molecular Formula: C46H78N9O14PSi3

Molecular Weight: 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

Molecular Formula: C10H15N5O11P2 (free acid)

Molecular Weight: 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

Molecular Formula: C10H12N5Na3O11P2

Molecular Weight: 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)

GMP Tris Salt

Description: GMP Tris Salt is guanosine 5'-monophosphate (GMP), a nucleotide consisting of guanosine linked to a single phosphate group at the 5' position of the ribose sugar. GMP is essential in molecular biology and biochemistry as a precursor for RNA synthesis and as a substrate in enzymatic reactions involving GMP-binding proteins. Its use spans from fundamental research to practical applications in biotechnology and pharmaceutical development.

CAT: BRP-01206

Molecular Formula: C10H14N5O8P (free acid)

Molecular Weight: 363.22 (free acid)

Purity: ≥97% by HPLC

Appearance: Clear colorless to 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 dihydrogen phosphate;2-amino-2-(hydroxymethyl)propane-1,3-diol

Synonyms: Guanosine 5'-monohosphate tris salt; 5'-Guanylic acid tris salt; Guanosine monophosphate tris salt; Guanosine 5'-phosphate tris salt; Guanosine 5'-(dihydrogen phosphate) tris salt

Related CAS: 85-32-5 (free base)

Guanosine 5'-tetraphosphate, tetrasodium salt

Description: Guanosine 5'-tetraphosphate, tetrasodium salt, is a chemical compound consisting of guanosine linked to four phosphate groups at the 5' position of the ribose sugar. In its tetrasodium salt form, the phosphate groups are complexed with sodium ions to enhance stability and solubility. This compound is utilized in biochemical and biotechnological research, particularly in studies involving nucleotide signaling, enzymatic reactions, and as a substrate or cofactor in various cellular processes. Its properties make it valuable in understanding RNA and DNA metabolism, as well as in applications ranging from molecular biology to pharmaceutical development.

CAT: BRP-01207

Molecular Formula: C10H13Na4N5O17P4

Molecular Weight: 691.09

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InChIKey: QXHMFINSYFFJAG-ZVQJTLEUSA-J

CanonicalSMILES: [Na].[Na].[Na].[Na].O=C1N=C(N)NC2=C1N=CN2C3OC(COP(=O)(O)OP(=O)(O)OP(=O)(O)OP(=O)(O)O)C(O)C3O

IUPAC Name: tetrasodium;((2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl hydrogen tetraphosphate

InChI: InChI=1S/C10H17N5O17P4.4Na/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(29-9)1-28-34(22,23)31-36(26,27)32-35(24,25)30-33(19,20)21;;;;/h2-3,5-6,9,16-17H,1H2,(H,22,23)(H,24,25)(H,26,27)(H2,19,20,21)(H3,11,13,14,18);;;;/q;4*+1/p-4/t3-,5-,6-,9-;;;;/m1..../s1

Synonyms: Guanosine 5'-tetraphosphate, sodium salt; GrP4.Na4; Guanosine 5'-(pentahydrogen tetraphosphate) tetrasodium salt; Guanosine tetraphosphate tetrasodium salt

Related CAS: 3369-85-5 (free acid) ; 1402828-40-3 (pentasodium salt) ; 1434288-53-5 (tetraammonium salt)

Inosine 5'-tetraphosphate, tetrasodium salt

Description: Inosine 5'-tetraphosphate, tetrasodium salt, is a chemical compound composed of inosine linked to four phosphate groups at the 5' position of the ribose sugar. In its tetrasodium salt form, the phosphate groups are complexed with sodium ions to enhance stability and solubility. This compound is used primarily in biochemical and biotechnological research, where it serves various roles such as a substrate or cofactor in enzymatic reactions, particularly those involving nucleotide metabolism and signaling pathways. Its applications extend to studies of RNA and DNA structure, function, and modification, making it a valuable tool in molecular biology and related fields of research.

CAT: BRP-01208

CAS: 14356-95-7

Molecular Formula: C10H11N4Na4O14P3

Molecular Weight: 596.09

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InChIKey: KOPCSZLOQBLCSK-KWIZKVQNSA-J

CanonicalSMILES: C1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])[O-])O)O.[Na+].[Na+].[Na+].[Na+]

IUPAC Name: tetrasodium;[[[(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-1H-purin-9-yl)oxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphoryl] phosphate

InChI: InChI=1S/C10H15N4O14P3.4Na/c15-6-4(1-25-30(21,22)28-31(23,24)27-29(18,19)20)26-10(7(6)16)14-3-13-5-8(14)11-2-12-9(5)17;;;;/h2-4,6-7,10,15-16H,1H2,(H,21,22)(H,23,24)(H,11,12,17)(H2,18,19,20);;;;/q;4*+1/p-4/t4-,6-,7-,10-;;;;/m1..../s1

Synonyms: 5'-ITP.Na4; Inosine 5'-(tetrahydrogen triphosphate), sodium salt (1:4); Inosine 5'-(tetrahydrogen triphosphate), tetrasodium salt; Inosine 5'-triphosphate sodium salt; ITP tetrasodium salt; Inosine triphosphate tetrasodium salt

Related CAS: 132-06-9 (free acid) ; 35908-31-7 (trisodium salt)

ATP ammonium salt

Description: ATP (Adenosine 5'-triphosphate) ammonium salt is a stabilized form of ATP where the nucleotide is complexed with ammonium ions. It is widely used in biochemical research due to its enhanced solubility and utility in enzymatic assays. ATP serves as a crucial energy carrier in cells, powering processes like muscle contraction, biosynthesis, and active transport. Its role in phosphorylation reactions also makes it essential for studying cellular metabolism and signaling pathways.

CAT: BRP-01209

CAS: 79670-88-5

Molecular Formula: C10H16N5O13P3 (free acid)

Molecular Weight: 507.18 (free acid)

Purity: ≥97% by HPLC

Appearance: Clear colorless liquid

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

Synonyms: Adenosine-5'-triphosphate, ammonium salt; Adenosine triphosphate, ammonium salt; Adenosine, 5'-(tetrahydrogen triphosphate), ammonium salt; 5'-ATP ammonium salt

Related CAS: 56-65-5 (free acid)

ATP lithium salt

Description: ATP (Adenosine 5'-triphosphate) lithium salt is a stabilized form of ATP where the nucleotide is complexed with lithium ions. It is widely used in biochemical research due to its enhanced solubility and utility in enzymatic assays. ATP serves as a crucial energy carrier in cells, powering processes like muscle contraction, biosynthesis, and active transport. Its role in phosphorylation reactions also makes it essential for studying cellular metabolism and signaling pathways.

CAT: BRP-01210

CAS: 16610-49-4

Molecular Formula: C10H16N5O13P3 (free acid)

Molecular Weight: 507.18 (free acid)

Purity: ≥97% by HPLC

Appearance: Clear colorless to faint yellow liquid

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

Synonyms: Adenosine 5'-triphosphate, lithium salt; Adenosine triphosphate, lithium salt; Adenosine, 5'-(tetrahydrogen triphosphate), lithium salt; 5'-ATP lithium salt

Related CAS: 56-65-5 (free acid)

GTP ammonium salt

Description: GTP (Guanosine 5'-triphosphate) ammonium salt is a compound where GTP, a nucleotide composed of guanine, ribose sugar, and three phosphate groups, is stabilized and solubilized by complexing with ammonium ions. This form of GTP is utilized in biochemical and molecular biology research for its improved properties in aqueous solutions, making it suitable for enzymatic assays and studies involving protein synthesis and cellular signaling pathways. GTP ammonium salt is essential for understanding fundamental biological processes and exploring therapeutic targets related to nucleotide metabolism and signal transduction mechanisms in cells.

CAT: BRP-01211

Molecular Formula: C10H16N5O14P3 (free acid)

Molecular Weight: 523.18 (free acid)

Purity: ≥97% by HPLC

Appearance: Clear colorless 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]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate;ammonium salt

Synonyms: Guanosine 5'-triphosphate, ammonium salt; 5'-GTP ammonium Salt; Ammonium GTP; Guanosine 5'-(tetrahydrogen triphosphate), ammonium salt (1:x); Guanosine 5'-triphosphate ammonium salt; Guanosine triphosphate ammonium salt

Related CAS: 86-01-1 (free acid)

GTP potassium salt

Description: GTP (Guanosine 5'-triphosphate) potassium salt is a compound where GTP, a nucleotide composed of guanine, ribose sugar, and three phosphate groups, is stabilized and solubilized by complexing with potassium ions. This form of GTP is utilized in biochemical and molecular biology research for its improved properties in aqueous solutions, making it suitable for enzymatic assays and studies involving protein synthesis and cellular signaling pathways. GTP potassium salt is essential for understanding fundamental biological processes and exploring therapeutic targets related to nucleotide metabolism and signal transduction mechanisms in cells.

CAT: BRP-01212

Molecular Formula: C10H16N5O14P3 (free acid)

Molecular Weight: 523.18 (free acid)

Purity: ≥97% by HPLC

Appearance: Clear colorless to faint yellow liquid

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

Synonyms: Guanosine 5'-triphosphate, potassium salt; 5'-GTP potassium Salt; Potassium GTP; Guanosine 5'-(tetrahydrogen triphosphate), potassium salt (1:x); Guanosine 5'-triphosphate potassium salt; Guanosine triphosphate potassium salt

Related CAS: 86-01-1 (free acid)

UTP potassium salt

Description: UTP (Uridine 5'-triphosphate) potassium salt is a form of UTP where the nucleotide is stabilized and solubilized by complexing with potassium ions. This salt is widely used in biochemical and molecular biology research for its enhanced stability and solubility in aqueous solutions. UTP is essential for RNA synthesis, serving as a substrate for RNA polymerases during transcription and participating in various RNA modification processes. UTP potassium salt is crucial for studying nucleic acid metabolism, gene expression regulation, and other cellular processes where RNA plays a pivotal role. Its use facilitates the investigation of RNA-related mechanisms in both basic biological research and pharmaceutical development contexts.

CAT: BRP-01213

Molecular Formula: C9H15N2O15P3 (free acid)

Molecular Weight: 484.14 (free acid)

Purity: ≥97% by HPLC

Appearance: Clear colorless to faint yellow liquid

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

Synonyms: Uridine 5'-triphosphate, potassium salt; Uridine 5'-(tetrahydrogen triphosphate) potassium salt; Uridine 5'-trisphosphate potassium salt (1:x); 5'-UTP potassium salt; Uridine triphosphate, potassium salt

Related CAS: 63-39-8 (free acid)

GTP lithium salt

Description: GTP (Guanosine 5'-triphosphate) lithium salt is a compound where GTP, a nucleotide composed of guanine, ribose sugar, and three phosphate groups, is stabilized and solubilized by complexing with lithium ions. This form of GTP is utilized in biochemical and molecular biology research for its improved properties in aqueous solutions, making it suitable for enzymatic assays and studies involving protein synthesis and cellular signaling pathways. GTP lithium salt is essential for understanding fundamental biological processes and exploring therapeutic targets related to nucleotide metabolism and signal transduction mechanisms in cells.

CAT: BRP-01214

CAS: 96012-99-6

Molecular Formula: C10H16N5O14P3 (free acid)

Molecular Weight: 523.18 (free acid)

Purity: ≥97% by HPLC

Appearance: Clear colorless to faint yellow liquid

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Storage: Store at -20 °C, Always avoid freeze-thaw cycles

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

Synonyms: Guanosine 5'-triphosphate, lithium salt; 5'-GTP lithium Salt; Lithium GTP; Guanosine 5'-(tetrahydrogen triphosphate), lithium salt (1:x); Guanosine triphosphate lithium salt; Guanosine 5'-(tetrahydrogen triphosphate), lithium salt

Related CAS: 86-01-1 (free acid)

UTP lithium salt

Description: UTP (Uridine 5'-triphosphate) lithium salt is a form of UTP where the nucleotide is stabilized and solubilized by complexing with lithium ions. This salt is widely used in biochemical and molecular biology research for its enhanced stability and solubility in aqueous solutions. UTP is essential for RNA synthesis, serving as a substrate for RNA polymerases during transcription and participating in various RNA modification processes. UTP lithium salt is crucial for studying nucleic acid metabolism, gene expression regulation, and other cellular processes where RNA plays a pivotal role. Its use facilitates the investigation of RNA-related mechanisms in both basic biological research and pharmaceutical development contexts.

CAT: BRP-01215

CAS: 27821-52-9

Molecular Formula: C9H15N2O15P3 (free acid)

Molecular Weight: 484.14 (free acid)

Purity: ≥97% by HPLC

Appearance: Clear colorless to faint yellow liquid

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Storage: Store at -20 °C, Always avoid freeze-thaw cycles

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

Synonyms: Uridine 5'-triphosphate, lithium salt; Uridine 5'-(tetrahydrogen triphosphate) lithium salt; Uridine 5'-trisphosphate lithium salt (1:x); 5'-UTP lithium salt; Uridine triphosphate, lithium salt

Related CAS: 63-39-8 (free acid)

UTP ammonium salt

Description: UTP (Uridine 5'-triphosphate) ammonium salt is a form of UTP where the nucleotide is stabilized and solubilized by complexing with ammonium ions. This salt is widely used in biochemical and molecular biology research for its enhanced stability and solubility in aqueous solutions. UTP is essential for RNA synthesis, serving as a substrate for RNA polymerases during transcription and participating in various RNA modification processes. UTP ammonium salt is crucial for studying nucleic acid metabolism, gene expression regulation, and other cellular processes where RNA plays a pivotal role. Its use facilitates the investigation of RNA-related mechanisms in both basic biological research and pharmaceutical development contexts.

CAT: BRP-01216

CAS: 96013-00-2

Molecular Formula: C9H15N2O15P3 (free acid)

Molecular Weight: 484.14 (free acid)

Purity: ≥97% by HPLC

Appearance: Clear colorless liquid

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Storage: Store at -20 °C, Always avoid freeze-thaw cycles

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

Synonyms: Uridine 5'-triphosphate, ammonium salt; Uridine 5'-(tetrahydrogen triphosphate) ammonium salt; Uridine 5'-trisphosphate ammonium salt (1:x); 5'-UTP ammonium salt; Uridine triphosphate, ammonium salt

Related CAS: 63-39-8 (free acid)

CTP ammonium salt

Description: CTP (Cytidine 5'-triphosphate) ammonium salt is a compound where CTP, a nucleotide consisting of cytidine, ribose sugar, and three phosphate groups, is stabilized and solubilized by complexing with ammonium ions. This form of CTP is particularly useful in biochemical and molecular biology research due to its enhanced stability and solubility in aqueous solutions. CTP ammonium salt is crucial for studying RNA synthesis and metabolism, serving as a substrate for RNA polymerases during transcription. It is also involved in various biochemical pathways where cytidine triphosphate is a necessary cofactor or substrate. This compound enables researchers to investigate RNA-related processes, such as mRNA production and modification, RNA turnover, and regulatory mechanisms in gene expression. Its use in experiments helps elucidate the molecular mechanisms underlying cellular functions and disease processes.

CAT: BRP-01217

Molecular Formula: C9H16N3O14P3 (free acid)

Molecular Weight: 483.16 (free acid)

Purity: ≥97% by HPLC

Appearance: Clear colorless liquid

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Storage: Store at -20 °C, Always avoid freeze-thaw cycles

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

Synonyms: Cytidine-5'-triphosphate, ammonium salt; Cytidine 5'-(tetrahydrogen triphosphate), ammonium salt (1:x); 5'-CTP ammonium salt; Cytidine triphosphate, ammonium salt

Related CAS: 65-47-4 (free acid)

CTP lithium salt

Description: CTP (Cytidine 5'-triphosphate) lithium salt is a compound where CTP, a nucleotide consisting of cytidine, ribose sugar, and three phosphate groups, is stabilized and solubilized by complexing with lithium ions. This form of CTP is particularly useful in biochemical and molecular biology research due to its enhanced stability and solubility in aqueous solutions. CTP lithium salt is crucial for studying RNA synthesis and metabolism, serving as a substrate for RNA polymerases during transcription. It is also involved in various biochemical pathways where cytidine triphosphate is a necessary cofactor or substrate. This compound enables researchers to investigate RNA-related processes, such as mRNA production and modification, RNA turnover, and regulatory mechanisms in gene expression. Its use in experiments helps elucidate the molecular mechanisms underlying cellular functions and disease processes.

CAT: BRP-01218

Molecular Formula: C9H16N3O14P3 (free acid)

Molecular Weight: 483.16 (free acid)

Purity: ≥97% by HPLC

Appearance: Clear colorless to faint yellow liquid

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C, Always avoid freeze-thaw cycles

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

Synonyms: Cytidine 5'-triphosphate, lithium salt; Cytidine 5'-(tetrahydrogen triphosphate), lithium salt (1:x); 5'-CTP lithium salt; Cytidine triphosphate, lithium salt

Related CAS: 65-47-4 (free acid)

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

Cytidylyl(3'-5')uridine sodium salt

pGmpC ammonium salt

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

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

GDP, tributylamine salt

Guanosine 5'-diphosphate trisodium salt

GMP Tris Salt

Guanosine 5'-tetraphosphate, tetrasodium salt

Inosine 5'-tetraphosphate, tetrasodium salt

ATP ammonium salt

ATP lithium salt

GTP ammonium salt

GTP potassium salt

UTP potassium salt

GTP lithium salt

UTP lithium salt

UTP ammonium salt

CTP ammonium salt

CTP lithium salt

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