Nucleotides

N1-Me-pUMP ammonium salt

Description: N1-Methylpseudouridine 5'-monophosphate ammonium salt (N1-Me-pUMP ammonium salt) is a nucleotide derivative where N1-methylpseudouridine is phosphorylated at the 5' position and combined with ammonium ions to form its salt. This compound is used in biochemical and molecular biology research, particularly in studies involving RNA modification, RNA structure, RNA-protein interactions, and investigations into the biological roles and functions of modified nucleosides within RNA molecules.

CAT: BRP-01038

Molecular Formula: C10H15N2O9P (free acid)

Molecular Weight: 338.21 (free acid)

Size	Price	Stock	Quantity
--	--	--

Inquiry

IUPAC Name: [(2R,3S,4R,5S)-3,4-dihydroxy-5-(1-methyl-2,4-dioxopyrimidin-5-yl)oxolan-2-yl]methyl dihydrogen phosphate;ammonium salt

Synonyms: N1-methyl-pseudouridine-5'-monophosphate, ammonium salt; N1-Me-pUMP NH4 salt; N1-methylpseudouridine 5'-monophosphate ammonium salt; N(1)-methylpseudouridine 5'-monophosphate ammonium salt; N(1)-methylpseudouridylic acid ammonium salt; N(1)-methylpseudouridine 5'-phosphate ammonium salt; (1S)-1,4-anhydro-1-(1-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)-5-O-phosphono-D-ribitol ammonium salt

Related CAS: 1446012-27-6 (free acid)

N6-Aminohexyl-AMP

Description: N6-Aminohexyladenosine 5'-monophosphate (N6-Aminohexyl-AMP) is a nucleotide derivative where adenosine is phosphorylated at the 5' position and modified with aminohexyl group at the N6 position. This compound is used in biochemical and molecular biology research, particularly in studies involving nucleic acid labeling, RNA-protein interactions, and other applications requiring modified nucleotides.

CAT: BRP-01039

CAS: 38198-98-0

Molecular Formula: C16H27N6O7P

Molecular Weight: 446.40

Size	Price	Stock	Quantity
--	--	--

Inquiry

InChIKey: MIMJOEOVYXMMPO-XNIJJKJLSA-N

CanonicalSMILES: C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O)NCCCCCCN

IUPAC Name: [(2R,3S,4R,5R)-5-[6-(6-aminohexylamino)purin-9-yl]-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate

InChI: InChI=1S/C16H27N6O7P/c17-5-3-1-2-4-6-18-14-11-15(20-8-19-14)22(9-21-11)16-13(24)12(23)10(29-16)7-28-30(25,26)27/h8-10,12-13,16,23-24H,1-7,17H2,(H,18,19,20)(H2,25,26,27)/t10-,12-,13-,16-/m1/s1

Synonyms: N6-aminohexyl-adenosine-5'-monophosphate; N(6)-Aminohexyladenosine monophosphate; AH-Amp; ((2R,3S,4R,5R)-5-(6-((6-Aminohexyl)amino)-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl dihydrogen phosphate; 5'-Adenylic acid, N-(6-aminohexyl)-; N-(6-Aminohexyl)-9-(5-O-phosphonopentofuranosyl)-9H-purin-6-amine

5-OMe-UMP disodium salt

Description: 5-Methoxyuridine 5'-monophosphate disodium salt (5-OMe-UMP disodium salt) is a nucleotide compound where 5-methoxyuridine is phosphorylated at the 5' position and combined with two sodium ions to form its salt. This compound is utilized in biochemical and molecular biology research, particularly in studies involving RNA modification, RNA structure, RNA-protein interactions, and investigations into the roles of modified nucleosides in RNA function.

CAT: BRP-01040

Molecular Formula: C10H13N2Na2O10P

Molecular Weight: 398.17

Size	Price	Stock	Quantity
--	--	--

Inquiry

InChIKey: ZWFDQWCBGKXIAF-ORXGBHRDSA-L

CanonicalSMILES: [Na].[Na].COC1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)O)O)O

IUPAC Name: disodium;((2R,3S,4R,5R)-3,4-dihydroxy-5-(5-methoxy-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl phosphate

InChI: InChI=1S/C10H15N2O10P.2Na/c1-20-4-2-12(10(16)11-8(4)15)9-7(14)6(13)5(22-9)3-21-23(17,18)19;;/h2,5-7,9,13-14H,3H2,1H3,(H,11,15,16)(H2,17,18,19);;/q;2*+1/p-2/t5-,6-,7-,9-;;/m1../s1

Synonyms: 5-O-methyl-uridine-5'-monophosphate, disodium salt; 5-OMe-UMP Na2; 5-Methoxyuridine 5'-monophosphate disodium salt

Related CAS: 36908-07-3 (free acid)

N6-(6-hexylamidobiotin)-AMP

Description: N6-(6-Hexylamidobiotin)adenosine 5'-monophosphate (N6-(6-hexylamidobiotin)-AMP) is a nucleotide derivative where adenosine is phosphorylated at the 5' position and modified with a 6-hexylamidobiotin group at the N6 position. This compound is used in biochemical and molecular biology research, particularly in studies involving affinity labeling, nucleic acid-protein interactions, and other applications requiring modified nucleotides.

CAT: BRP-01041

CAS: 689279-71-8

Molecular Formula: C26H41N8O9PS

Molecular Weight: 672.69

Size	Price	Stock	Quantity
--	--	--

Inquiry

Density: 1.76±0.1 g/cm3

InChIKey: JHPPUZXTSWNMKQ-LDAIXZEYSA-N

CanonicalSMILES: O=C1NC2CSC(CCCCC(=O)NCCCCCCNC3=NC=NC4=C3N=CN4C5OC(COP(=O)(O)O)C(O)C5O)C2N1

IUPAC Name: ((2R,3S,4R,5R)-3,4-dihydroxy-5-(6-((6-(5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)hexyl)amino)-9H-purin-9-yl)tetrahydrofuran-2-yl)methyl dihydrogen phosphate

InChI: InChI=1S/C26H41N8O9PS/c35-18(8-4-3-7-17-19-15(12-45-17)32-26(38)33-19)27-9-5-1-2-6-10-28-23-20-24(30-13-29-23)34(14-31-20)25-22(37)21(36)16(43-25)11-42-44(39,40)41/h13-17,19,21-22,25,36-37H,1-12H2,(H,27,35)(H,28,29,30)(H2,32,33,38)(H2,39,40,41)/t15-,16+,17-,19-,21+,22+,25+/m0/s1

Synonyms: N6-(6-hexylamidobiotin)-adenosine-5'-monophosphate; 5'-Adenylic acid, N-[6-[[5-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-1-oxopentyl]amino]hexyl]-

7-Me-2'-OMe-GMP TEA salt

Description: 7-Methyl-2'-O-methylguanosine 5'-monophosphate TEA salt is a nucleotide compound where 7-methyl-2'-O-methylguanosine is phosphorylated at the 5' position and combined with triethylamine (TEA) to form its salt. This compound is utilized in biochemical and molecular biology research, particularly in studies concerning RNA modification, RNA structure, RNA-protein interactions, and the roles of modified nucleosides in RNA function.

CAT: BRP-01042

CAS: 1186316-98-2

Molecular Formula: C18H33N6O8P

Molecular Weight: 492.46

Size	Price	Stock	Quantity
--	--	--

Inquiry

InChIKey: UFDVSISXKIBZJZ-YCSZXMBFSA-N

CanonicalSMILES: O=C1N=C(N)NC2=C1[N+](=CN2C3OC(COP(=O)([O-])O)C(O)C3OC)C.N(CC)(CC)CC

IUPAC Name: ((2R,3R,4R,5R)-5-(2-amino-7-methyl-6-oxo-1,6-dihydro-9H-purin-7-ium-9-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl hydrogen phosphate;N,N-diethylethanamine

InChI: InChI=1S/C12H18N5O8P.C6H15N/c1-16-4-17(9-6(16)10(19)15-12(13)14-9)11-8(23-2)7(18)5(25-11)3-24-26(20,21)22;1-4-7(5-2)6-3/h4-5,7-8,11,18H,3H2,1-2H3,(H4-,13,14,15,19,20,21,22);4-6H2,1-3H3/t5-,7-,8-,11-;/m1./s1

Synonyms: 7-methyl-2'-O-methyl-guanosine-5'-monophosphate, triethylamine salt; 5'-Guanylic acid, 7-methyl-2'-O-methyl-, inner salt, compd. with N,N-diethylethanamine (1:1)

Related CAS: 94889-79-9 (free acid)

N6-(6-hexylamidobiotin)-AMP IM

Description: N6-(6-Hexylamidobiotin)adenosine 5'-monophosphate IM (imidazole) is a nucleotide derivative where adenosine is phosphorylated at the 5' position and modified with a 6-hexylamidobiotin group. This compound forms a salt with imidazole. It is used in biochemical and molecular biology research, particularly in studies involving affinity labeling, nucleic acid-protein interactions, and other applications requiring modified nucleotides.

CAT: BRP-01043

Molecular Formula: C29H43N10O8PS

Molecular Weight: 722.76

Size	Price	Stock	Quantity
--	--	--

Inquiry

InChIKey: IUNZQSXAEFYGII-WAPAMYMSSA-N

InChI: InChI=1S/C29H43N10O8PS/c40-21(8-4-3-7-20-22-18(14-49-20)36-29(43)37-22)31-9-5-1-2-6-10-32-26-23-27(34-15-33-26)39(17-35-23)28-25(42)24(41)19(47-28)13-46-48(44,45)38-12-11-30-16-38/h11-12,15-20,22,24-25,28,41-42H,1-10,13-14H2,(H,31,40)(H,44,45)(H,32,33,34)(H2,36,37,43)/t18-,19+,20-,22-,24+,25+,28+/m0/s1

Synonyms: N6-(6-hexylamidobiotin)-AMP, Imidazolate; N6-(6-hexylamidobiotin)-AMP.IM

7-Me-2'-OMe-GMP IM sodium salt

Description: 7-Methyl-2'-O-methylguanosine 5'-monophosphate IM sodium salt is a nucleotide derivative where 7-methyl-2'-O-methylguanosine is phosphorylated at the 5' position and combined with IM (imidazole) and sodium ions to form its salt. This compound is used in biochemical and molecular biology research, particularly in studies involving RNA modification, RNA structure, RNA-protein interactions, and the roles of modified nucleosides in RNA function.

CAT: BRP-01044

CAS: 1201817-80-2

Molecular Formula: C15H19N7NaO7P

Molecular Weight: 463.32

Size	Price	Stock	Quantity
--	--	--

Inquiry

InChIKey: PBPRXJIUTKNQGF-ZBMQJGODSA-N

CanonicalSMILES: [Na].O=C1N=C(N)NC2=C1[N+](=CN2C3OC(COP(=O)([O-])N4C=NC=C4)C(O)C3OC)C

IUPAC Name: sodium;((2R,3R,4R,5R)-5-(2-amino-7-methyl-6-oxido-9H-purin-7-ium-9-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl (1H-imidazol-1-yl)phosphonate

InChI: InChI=1S/C15H20N7O7P.Na/c1-20-7-22(12-9(20)13(24)19-15(16)18-12)14-11(27-2)10(23)8(29-14)5-28-30(25,26)21-4-3-17-6-21;/h3-4,6-8,10-11,14,23H,5H2,1-2H3,(H3-,16,18,19,24,25,26);/t8-,10-,11-,14-;/m1./s1

Synonyms: 7-methyl-2'-O-methyl-guanosine-5'-monophosphate, Imidazolate sodium salt; 7-Me-2'-OMe-GMP.IM; Guanosine, 7-methyl-2'-O-methyl-, 5'-(hydrogen P-1H-imidazol-1-ylphosphonate), inner salt, sodium salt (1:1)

Related CAS: 1003839-69-7 (free acid)

N1-Me-pUMP

Description: N1-Methylpseudouridine 5'-monophosphate (N1-Me-pUMP) is a nucleotide derivative where N1-methylpseudouridine is phosphorylated at the 5' position. This compound is used in biochemical and molecular biology research, particularly in studies involving RNA modification, RNA structure, RNA-protein interactions, and investigations into the biological roles and functions of modified nucleosides within RNA molecules.

CAT: BRP-01045

CAS: 1446012-27-6

Molecular Formula: C10H15N2O9P

Molecular Weight: 338.21

Size	Price	Stock	Quantity
--	--	--

Inquiry

Density: 1.763±0.06 g/cm3

InChIKey: VORAOZTXNOXTGQ-XUTVFYLZSA-N

CanonicalSMILES: CN1C=C(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)O)O)O

IUPAC Name: [(2R,3S,4R,5S)-3,4-dihydroxy-5-(1-methyl-2,4-dioxopyrimidin-5-yl)oxolan-2-yl]methyl dihydrogen phosphate

InChI: InChI=1S/C10H15N2O9P/c1-12-2-4(9(15)11-10(12)16)8-7(14)6(13)5(21-8)3-20-22(17,18)19/h2,5-8,13-14H,3H2,1H3,(H,11,15,16)(H2,17,18,19)/t5-,6-,7-,8+/m1/s1

Synonyms: N1-methyl-pseudouridine-5'-monophosphate, free acid; N1-methylpseudouridine 5'-monophosphate; N(1)-methylpseudouridine 5'-monophosphate; N(1)-methylpseudouridylic acid; N(1)-methylpseudouridine 5'-phosphate; N1-Me-pUMP.H2; (1S)-1,4-anhydro-1-(1-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)-5-O-phosphono-D-ribitol; ((2R,3S,4R,5S)-3,4-dihydroxy-5-(1-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)tetrahydrofuran-2-yl)methyl dihydrogen phosphate; 1-Methyl-5-(5-O-phosphono-β-D-ribofuranosyl)-2,4(1H,3H)-pyrimidinedione

5-OMe-UMP ammonium salt

Description: 5-Methoxyuridine 5'-monophosphate ammonium salt (5-OMe-UMP ammonium salt) is a nucleotide compound where 5-methoxyuridine is phosphorylated at the 5' position and combined with ammonium ions to form its salt. This compound is utilized in biochemical and molecular biology research, particularly in studies involving RNA modification, RNA structure, RNA-protein interactions, and investigations into the roles of modified nucleosides in RNA function.

CAT: BRP-01046

Molecular Formula: C10H15N2O10P (free acid)

Molecular Weight: 354.21 (free acid)

Size	Price	Stock	Quantity
--	--	--

Inquiry

IUPAC Name: [(2R,3S,4R,5R)-3,4-dihydroxy-5-(5-methoxy-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl dihydrogen phosphate;ammonium salt

Synonyms: 5-O-methyl-uridine-5'-monophosphate, ammonium salt; 5-OMe-UMP NH4 salt; ((2R,3S,4R,5R)-3,4-Dihydroxy-5-(5-methoxy-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl dihydrogen phosphate ammonium salt; 5-Methoxyuridine 5'-monophosphate ammonium salt

Related CAS: 36908-07-3 (free acid)

2'-O-Methyladenosine 5'-monophosphate

Description: 2'-O-Methyladenosine 5'-monophosphate (2'-O-Me-A-MP) is a nucleotide derivative where adenosine is phosphorylated at the 5' position and modified with a methyl group at the 2'-hydroxyl (2'-OH) position of the ribose sugar. This modification alters the RNA molecule's structure and function, affecting RNA stability, translation efficiency, and interactions with RNA-binding proteins. 2'-O-Methyladenosine 5'-monophosphate is used in biochemical and molecular biology research to study RNA modification dynamics, RNA-protein interactions, and the regulatory roles of modified nucleotides in RNA biology.

CAT: BRP-01047

CAS: 24121-00-4

Molecular Formula: C11H16N5O7P

Molecular Weight: 361.25

Purity: ≥95% by HPLC

Appearance: White to faint yellow powder

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at 2-8 °C, Keep in a dark and dry place

Density: 2.07±0.1 g/cm3

Boiling Point: 746.4±70.0 °C at 760 mmHg

InChIKey: TVGFEBXIZUYVFR-IOSLPCCCSA-N

CanonicalSMILES: COC1C(C(OC1N2C=NC3=C(N=CN=C32)N)COP(=O)(O)O)O

IUPAC Name: [(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-3-hydroxy-4-methoxyoxolan-2-yl]methyl dihydrogen phosphate

InChI: InChI=1S/C11H16N5O7P/c1-21-8-7(17)5(2-22-24(18,19)20)23-11(8)16-4-15-6-9(12)13-3-14-10(6)16/h3-5,7-8,11,17H,2H2,1H3,(H2,12,13,14)(H2,18,19,20)/t5-,7-,8-,11-/m1/s1

Synonyms: 2'-O-methyl-2'-adenosine-5'-monophosphate; 2'-O-Me-AMP; 2'-O-Methyladenosine 5'-(dihydrogen phosphate); ((2R,3R,4R,5R)-5-(6-Amino-9H-purin-9-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl dihydrogen phosphate; 2'-O-Methyl-AMP

Related CAS: 28516-86-1 (homopolymer) ; 1231158-15-8 (TEA salt)

2'-O-Me-GMP disodium salt

Description: 2'-O-Methylguanosine 5'-monophosphate disodium salt (2'-O-Me-GMP disodium salt) is a nucleotide derivative where guanosine is phosphorylated at the 5' position and modified with a methyl group at the 2'-hydroxyl (2'-OH) position of the ribose sugar. This compound forms a salt with two sodium ions. It is used in biochemical and molecular biology research to investigate RNA modification dynamics, RNA structure, RNA-protein interactions, and the regulatory functions of modified nucleotides in RNA biology. Specifically, 2'-O-Me-GMP disodium salt is valuable in studies exploring how 2'-O-methylation influences RNA stability, translation processes, and interactions with RNA-binding proteins.

CAT: BRP-01048

Molecular Formula: C11H14N5Na2O8P

Molecular Weight: 421.21

Purity: ≥98% by HPLC

Appearance: White to faint yellow powder

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at 2-8 °C, Keep in a dark and dry place

InChIKey: OCMMAIFXIKRNGT-IDIVVRGQSA-L

CanonicalSMILES: COC1C(C(OC1N2C=NC3=C2N=C(NC3=O)N)COP(=O)([O-])[O-])O.[Na+].[Na+]

IUPAC Name: disodium;[(2R,3R,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxy-4-methoxyoxolan-2-yl]methyl phosphate

InChI: InChI=1S/C11H16N5O8P.2Na/c1-22-7-6(17)4(2-23-25(19,20)21)24-10(7)16-3-13-5-8(16)14-11(12)15-9(5)18;;/h3-4,6-7,10,17H,2H2,1H3,(H2,19,20,21)(H3,12,14,15,18);;/q;2*+1/p-2/t4-,6-,7-,10-;;/m1../s1

Synonyms: 2'-O-methyl-2'-guanosine-5'-monophosphate, disodium salt; 2'-O-Methyl-guanosine-5'-monophosphate, disodium salt; 2'-O-Me-GMP.Na2; 2'-O-Methylguanosine 5'-(dihydrogen phosphate) disodium salt; 2'-O-Methylguanosine 5'-monophosphate disodium salt

Related CAS: 24121-01-5 (free acid)

CTPαS Tris salt

Description: CTPαS (cytidine 5'-O-(1-thiotriphosphate)) Tris salt is a modified nucleotide derivative where cytidine is linked to a sulfur atom at the α-phosphate position of the triphosphate group. This compound is combined with Tris (tris(hydroxymethyl)aminomethane) to form its salt. CTPαS is often used in biochemical and molecular biology research as a non-hydrolyzable analog of CTP to study enzymatic reactions, RNA synthesis, and other processes where CTP is involved.

CAT: BRP-01049

Molecular Formula: C9H16N3O13P3S (free acid)

Molecular Weight: 499.22 (free acid)

Purity: ≥95% by HPLC

Appearance: Clear colorless to light yellow liquid

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

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

Synonyms: Cytidine-5'-O-(1-Thiotriphosphate), Tris Salt (Mixture of Rp and Sp isomers); Cytidine, 5'→P''-ester with thiotriphosphoric acid Tris salt; Cytidine-5'-O-(1-thiotriphosphate) Tris salt; CTP-αS Tris salt; CTPαS; Cytidine-5'-(α-thio)-triphosphate, Tris salt (1:1 Mixture of Rp and Sp isomers)

Related CAS: 110972-40-2 (free base)

N1-Me-ATP, tetralithium salt

Description: N1-Methyladenosine 5'-triphosphate, tetralithium salt (N1-Me-ATP tetralithium salt) is a nucleotide derivative where adenosine is phosphorylated at the 5' position and methylated at the N1 position of the adenine base. This compound is combined with four lithium ions to form its salt. It is used in biochemical and molecular biology research, particularly in studies involving ATP-dependent processes, nucleic acid labeling, and investigations into ATP-binding proteins.

CAT: BRP-01050

Molecular Formula: C11H14Li4N5O13P3

Molecular Weight: 544.94

Purity: ≥98% by HPLC

Appearance: Clear colorless to yellow liquid

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: OJDHBBFBWGGDQB-WHEJUCFXSA-J

CanonicalSMILES: O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC1OC(N2C=NC=3C(=N)N(C=NC32)C)C(O)C1O.Li.Li.Li.Li

IUPAC Name: tetralithium;((2R,3S,4R,5R)-3,4-dihydroxy-5-(6-imino-1-methyl-1,6-dihydro-9H-purin-9-yl)tetrahydrofuran-2-yl)methyl triphosphate

InChI: InChI=1S/C11H18N5O13P3.4Li/c1-15-3-14-10-6(9(15)12)13-4-16(10)11-8(18)7(17)5(27-11)2-26-31(22,23)29-32(24,25)28-30(19,20)21;;;;/h3-5,7-8,11-12,17-18H,2H2,1H3,(H,22,23)(H,24,25)(H2,19,20,21);;;;/q;4*+1/p-4/t5-,7-,8-,11-;;;;/m1..../s1

Synonyms: N1-Methyl-adenosine-5'-triphosphate, tetralithium salt; 1-Methyladenosine 5'-(tetrahydrogen triphosphate) tetralithium salt; 1-Methyladenosine 5'-triphosphate tetralithium salt; N1-Methyl-ATP tetralithium salt

Related CAS: 68643-11-8 (free acid)

ATPαS Tris salt

Description: ATPαS (adenosine 5'-O-(1-thiotriphosphate)) Tris salt is a modified nucleotide derivative where adenosine is linked to a sulfur atom at the α-phosphate position of the triphosphate group. This compound is combined with Tris to form its salt. ATPαS is commonly used as a non-hydrolyzable analog of ATP in biochemical and molecular biology research to study ATP-dependent processes, enzyme kinetics, and ATP-binding proteins.

CAT: BRP-01051

Molecular Formula: C10H16N5O12P3S (free acid)

Molecular Weight: 523.25 (free acid)

Purity: ≥95% by HPLC

Appearance: Clear colorless to light yellow liquid

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

IUPAC Name: [[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphinothioyl] phosphono hydrogen phosphate;2-amino-2-(hydroxymethyl)propane-1,3-diol

Synonyms: Adenosine-5'-O-(1-Thiotriphosphate), Tris Salt (Mixture of Rp and Sp isomers); Adenosine, 5'→P''-ester with thiotriphosphoric acid ((HO)2P(O)OP(O)(OH)OP(O)(OH)(SH)), Tris Salt; Adenosine-5'-O-(1-Thiotriphosphate) Tris salt; ATP-α-S Tris salt; α-Thio-dATP Tris salt; ATP-αS Tris salt

Related CAS: 29220-54-0 (free base)

GTPαS Tris salt

Description: GTPαS (guanosine 5'-O-(1-thiotriphosphate)) Tris salt is a modified nucleotide derivative where guanosine is linked to a sulfur atom at the α-phosphate position of the triphosphate group. This compound is combined with Tris to form its salt. GTPαS is utilized in biochemical and molecular biology research as a non-hydrolyzable analog of GTP to study GTP-dependent processes, GTPase activity, and interactions with GTP-binding proteins.

CAT: BRP-01052

Molecular Formula: C10H16N5O13P3S (free acid)

Molecular Weight: 539.25 (free acid)

Purity: ≥95% by HPLC

Appearance: Clear colorless to light yellow liquid

Size	Price	Stock	Quantity
--	--	--

Inquiry

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]methoxy-hydroxyphosphinothioyl] phosphono hydrogen phosphate;2-amino-2-(hydroxymethyl)propane-1,3-diol

Synonyms: Guanosine-5'-O-(1-Thiotriphosphate), Tris Salt (Mixture of Rp and Sp isomers); Guanosine, 5'→P''-ester with thiotriphosphoric acid Tris salt; GTP-αS Tris salt; Guanosine-5'-Alpha-Thio-Triphosphate Tris salt; Guanosine 5'-O-(1-thiotriphosphate) Tris salt; Guanosine 5'-O-thiotriphosphate Tris salt; Alpha Thiol GTP (1-Thio-GTP) Tris salt

Related CAS: 71376-96-0 (free base)

UTPγS sodium salt

Description: UTPγS (uridine 5'-O-(3-thiotriphosphate)) sodium salt is a modified nucleotide derivative where uridine is linked to a sulfur atom at the γ-phosphate position of the triphosphate group. This compound is combined with sodium ions to form its salt. UTPγS 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-01053

Molecular Formula: C9H15N2O14P3S (free acid)

Molecular Weight: 500.20 (free acid)

Purity: ≥95% by HPLC

Appearance: Colorless to slightly yellow liquid

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

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

Synonyms: Uridine-5'-O-(γ-Thio)-triphosphate sodium salt; UTP-γS sodium salt; Uridine 5'-O-(3-thiotriphosphate) sodium salt

Related CAS: 79049-97-1 (free acid)

N1-Me-pUTPαS Tris salt

Description: N1-Me-pUTPαS Tris salt is a modified nucleotide derivative where N1-methyl-pseudouridine is phosphorylated at the 5' position and linked to a sulfur atom at the α-phosphate position of the triphosphate group. This compound is combined with Tris to form its salt. N1-Me-pUTPαS is used in biochemical and molecular biology research as a non-hydrolyzable analog of UTP (uridine 5'-triphosphate) to study RNA synthesis, RNA modification, and RNA-protein interactions.

CAT: BRP-01054

Molecular Formula: C10H17N2O14P3S (free acid)

Molecular Weight: 514.23 (free acid)

Purity: ≥95% by HPLC

Appearance: Clear colorless to light yellow liquid

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

IUPAC Name: [[(2R,3S,4R,5S)-3,4-dihydroxy-5-(1-methyl-2,4-dioxopyrimidin-5-yl)oxolan-2-yl]methoxy-hydroxyphosphinothioyl] phosphono hydrogen phosphate;2-amino-2-(hydroxymethyl)propane-1,3-diol

Synonyms: N1-Methyl-Pseudouridine-5'-O-(1-Thiotriphosphate), Tris Salt (Mixture of Rp and Sp isomers); 5-[5-O-[[[Hydroxy(phosphonooxy)phosphinyl]oxy]mercaptophosphinyl]-β-D-ribofuranosyl]-1-methyl-2,4(1H,3H)-pyrimidinedione Tris Salt

Related CAS: 1443686-60-9 (free base) ; 1613529-70-6 (TEA salt (1:4))

N1-Me-pseudo-iso-CTP Sodium Salt

Description: N1-Methyl-pseudo-isocytidine 5'-triphosphate sodium salt (N1-Me-pseudo-iso-CTP sodium salt) is a modified nucleotide derivative where N1-methyl-pseudo-isocytidine is phosphorylated at the 5' position. This compound forms a salt with sodium ions. It is used in biochemical and molecular biology research to investigate RNA modification, RNA structure, and the roles of modified nucleosides in RNA function.

CAT: BRP-01055

Molecular Formula: C10H18N3O14P3 (free acid)

Molecular Weight: 497.18 (free acid)

Purity: ≥98% by HPLC

Appearance: Clear colorless to yellow liquid

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

IUPAC Name: sodium;((2R,3S,4R,5S)-5-(2-amino-1-methyl-4-oxo-1,4-dihydropyrimidin-5-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate

Synonyms: N1-methyl-Pseudoisocytidine-5'-triphosphate, Sodium Salt

3'-OMe GTP Tris Salt

Description: 3'-O-Methylguanosine 5'-triphosphate Tris salt (3'-OMe GTP Tris 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 combined with Tris to form its salt. 3'-OMe GTP is used in biochemical and molecular biology research to study RNA modification, RNA structure, RNA-protein interactions, and the regulatory roles of modified nucleotides in RNA biology.

CAT: BRP-01056

Molecular Formula: C11H18N5O14P3 (free acid)

Molecular Weight: 537.21 (free acid)

Purity: ≥97% by HPLC

Appearance: Clear colorless to yellow liquid

Size	Price	Stock	Quantity
--	--	--

Inquiry

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

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

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

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

Gamma modified 6-azido GTP, ammonium Salt

Description: Gamma modified 6-azido GTP, ammonium salt is used in biochemical and molecular biology research, particularly in studies involving RNA and protein labeling, nucleic acid crosslinking, and probing protein-nucleic acid interactions. The azido group allows for specific chemical conjugation and crosslinking studies, while the gamma phosphorylation retains the nucleotide's functionality in enzymatic assays and other biological contexts.

CAT: BRP-01057

Molecular Formula: C16H27N8O14P3 (free acid)

Molecular Weight: 648.36 (free acid)

Purity: ≥98% by HPLC

Appearance: White to off-white powder

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

Synonyms: Gamma modified 6-azido guanosine-5'-triphosphare, NH4 Salt

N1-Me-pUMP ammonium salt

N6-Aminohexyl-AMP

5-OMe-UMP disodium salt

N6-(6-hexylamidobiotin)-AMP

7-Me-2'-OMe-GMP TEA salt

N6-(6-hexylamidobiotin)-AMP IM

7-Me-2'-OMe-GMP IM sodium salt

N1-Me-pUMP

5-OMe-UMP ammonium salt

2'-O-Methyladenosine 5'-monophosphate

2'-O-Me-GMP disodium salt

CTPαS Tris salt

N1-Me-ATP, tetralithium salt

ATPαS Tris salt

GTPαS Tris salt

UTPγS sodium salt

N1-Me-pUTPαS Tris salt

N1-Me-pseudo-iso-CTP Sodium Salt

3'-OMe GTP Tris Salt

Gamma modified 6-azido GTP, ammonium Salt

Our Products

Liposome Products

MicroRNA Products

mRNA Products

siRNA Products

RNA Synthesis Reagents

Cap Analogs

CPGs for Oligo Synthesis

Nucleosides

Nucleotides

Phosphoramidites