Nucleotides

3'-O-Methylguanosine-5'-diphosphate

Description: 3'-O-Methylguanosine-5'-diphosphate (3'-OMeGDP) is a modified nucleotide molecule composed of guanosine, with a methyl group attached to the 3' carbon of the ribose, and phosphorylated at the 5' carbon of the ribose with two phosphate groups, forming a diphosphate. This molecule plays important roles in RNA metabolism, often serving as an intermediate or substrate in RNA modification or signaling pathways.

CAT: BRP-00781

CAS: 78771-34-3

Molecular Formula: C11H17N5O11P2

Molecular Weight: 457.23

Purity: ≥98%

Appearance: White solid

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

Density: 2.37±0.1 g/cm3

Boiling Point: 906.0±75.0 °C at 760 mmHg

InChIKey: LBHMDBPTFLRYQU-KQYNXXCUSA-N

CanonicalSMILES: COC1C(OC(C1O)N2C=NC3=C2N=C(NC3=O)N)COP(=O)(O)OP(=O)(O)O

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

InChI: InChI=1S/C11H17N5O11P2/c1-24-7-4(2-25-29(22,23)27-28(19,20)21)26-10(6(7)17)16-3-13-5-8(16)14-11(12)15-9(5)18/h3-4,6-7,10,17H,2H2,1H3,(H,22,23)(H2,19,20,21)(H3,12,14,15,18)/t4-,6-,7-,10-/m1/s1

Synonyms: 3'-O-Methyl GDP; 3'-OMe-GDP; Guanosine 5'-(trihydrogen diphosphate), 3'-O-methyl-; 3'-O-Methylguanosine-5'-trihydrogen diphosphate

7-Methyl-3'-O-methylguanosine-5'-monophosphate

Description: 7-Methyl-3'-O-methylguanosine-5'-monophosphate is a modified nucleotide where guanosine has a methyl group attached to the 7th position of the base and a methyl group attached to the 3' carbon of the ribose sugar. It has a single phosphate group attached to the 5' carbon of the ribose. This molecule is important in RNA biology, playing roles in RNA modification processes.

CAT: BRP-00782

CAS: 94889-79-9

Molecular Formula: C12H18N5O8P

Molecular Weight: 391.27

Purity: ≥98%

Appearance: White solid

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InChIKey: FHSYAAQTDTXBME-IOSLPCCCSA-N

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

IUPAC Name: [(2R,3R,4R,5R)-5-(2-amino-7-methyl-6-oxo-1H-purin-9-ium-9-yl)-3-hydroxy-4-methoxyoxolan-2-yl]methyl hydrogen phosphate

InChI: InChI=1S/C12H18N5O8P/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/h4-5,7-8,11,18H,3H2,1-2H3,(H4-,13,14,15,19,20,21,22)/t5-,7-,8-,11-/m1/s1

Synonyms: 5'-Guanylic acid, 7-methyl-2'-O-methyl-, inner salt; 1H-Purinium, 2-amino-6,9-dihydro-7-methyl-9-(2-O-methyl-5-O-phosphono-β-D-ribofuranosyl)-6-oxo-, inner salt; ((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; 7-Me-3'-OMe-GMP

α-Thio-1-methylpseudouridine-5'-triphosphate, trisodium salt

Description: α-Thio-1-methylpseudouridine-5'-triphosphate, trisodium salt is a modified nucleotide compound used in biochemical research. It contains a thio-modified pseudouridine base with a methyl group at the 1st position, linked to a triphosphate group at the 5' carbon of the ribose sugar. It is in the form of a trisodium salt. This compound is often utilized in studies related to RNA modification and structure-function analyses.

CAT: BRP-00785

Molecular Formula: C10H14N2Na3O14P3S

Molecular Weight: 580.17

Purity: ≥98%

Appearance: Colorless transparent liquid

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InChIKey: VLACZZDERVSXNN-APBPHFBHSA-K

CanonicalSMILES: CN1C=C(C(=O)NC1=O)C2C(C(C(O2)COP(=S)([O-])OP(=O)([O-])OP(=O)(O)[O-])O)O.[Na+].[Na+].[Na+]

IUPAC Name: trisodium;[[[(2R,3S,4R,5S)-3,4-dihydroxy-5-(1-methyl-2,4-dioxopyrimidin-5-yl)oxolan-2-yl]methoxy-oxidophosphinothioyl]oxy-oxidophosphoryl] hydrogen phosphate

InChI: InChI=1S/C10H17N2O14P3S.3Na/c1-12-2-4(9(15)11-10(12)16)8-7(14)6(13)5(24-8)3-23-29(22,30)26-28(20,21)25-27(17,18)19;;;/h2,5-8,13-14H,3H2,1H3,(H,20,21)(H,22,30)(H,11,15,16)(H2,17,18,19);;;/q;3*+1/p-3/t5-,6-,7-,8+,29?;;;/m1.../s1

Synonyms: 5-[5-O-[[[Hydroxy(phosphonooxy)phosphinyl]oxy]mercaptophosphinyl]-β-D-ribofuranosyl]-1-methyl-2,4(1H,3H)-pyrimidinedione Trisodium Salt; alpha-Thio-1-methylpseudouridine-5'-triphosphate, trisodium salt

Related CAS: 1443686-60-9 (free acid)

β-Thio-1-methylpseudouridine-5'-triphosphate, trisodium salt

Description: β-Thio-1-methylpseudouridine-5'-triphosphate, trisodium salt is a modified nucleotide compound used in biochemical research. It contains a thio-modified pseudouridine base with a methyl group at the 1st position, linked to a triphosphate group at the 5' carbon of the ribose sugar. It is in the form of a trisodium salt. This compound is commonly employed in studies related to RNA modification and structure-function analyses.

CAT: BRP-00786

Molecular Formula: C10H14N2Na3O14P3S

Molecular Weight: 580.17

Purity: ≥98%

Appearance: Colorless transparent liquid

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InChIKey: NKOUYZJTNSUGSQ-APBPHFBHSA-K

CanonicalSMILES: CN1C=C(C(=O)NC1=O)C2C(C(C(O2)COP(=O)([O-])OP(=S)([O-])OP(=O)(O)[O-])O)O.[Na+].[Na+].[Na+]

IUPAC Name: trisodium;[[[(2R,3S,4R,5S)-3,4-dihydroxy-5-(1-methyl-2,4-dioxopyrimidin-5-yl)oxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphinothioyl] hydrogen phosphate

InChI: InChI=1S/C10H17N2O14P3S.3Na/c1-12-2-4(9(15)11-10(12)16)8-7(14)6(13)5(24-8)3-23-28(20,21)26-29(22,30)25-27(17,18)19;;;/h2,5-8,13-14H,3H2,1H3,(H,20,21)(H,22,30)(H,11,15,16)(H2,17,18,19);;;/q;3*+1/p-3/t5-,6-,7-,8+,29?;;;/m1.../s1

Synonyms: beta-Thio-1-methylpseudouridine-5'-triphosphate, trisodium salt

β-Thio-pseudouridine-5'-triphosphate, trisodium salt

Description: β-Thio-pseudouridine-5'-triphosphate, trisodium salt is a modified nucleotide compound used in biochemical research. It contains a thio-modified pseudouridine base linked to a triphosphate group at the 5' carbon of the ribose sugar. It is in the form of a trisodium salt. This compound is commonly used in studies related to RNA modification and structure-function analyses.

CAT: BRP-00787

Molecular Formula: C9H12N2Na3O14P3S

Molecular Weight: 566.15

Purity: ≥98%

Appearance: Colorless transparent liquid

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InChIKey: OMPHCMHZOYGFSX-XMRXGGJWSA-K

CanonicalSMILES: C1=C(C(=O)NC(=O)N1)C2C(C(C(O2)COP(=O)([O-])OP(=S)([O-])OP(=O)(O)[O-])O)O.[Na+].[Na+].[Na+]

IUPAC Name: trisodium;[[[(2R,3S,4R,5S)-5-(2,4-dioxo-1H-pyrimidin-5-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphinothioyl] hydrogen phosphate

InChI: InChI=1S/C9H15N2O14P3S.3Na/c12-5-4(2-22-27(19,20)25-28(21,29)24-26(16,17)18)23-7(6(5)13)3-1-10-9(15)11-8(3)14;;;/h1,4-7,12-13H,2H2,(H,19,20)(H,21,29)(H2,16,17,18)(H2,10,11,14,15);;;/q;3*+1/p-3/t4-,5-,6-,7+,28?;;;/m1.../s1

Synonyms: beta-Thio-pseudouridine-5'-triphosphate, trisodium salt

5-Methyl-CTP-βS

Description: 5-Methyl-CTP-βS is a modified nucleotide compound used in biochemical research. It consists of a cytidine base with a methyl group at the 5th position, linked to a cytidine triphosphate (CTP) moiety, and containing a sulfur (S) atom at the β position. This modification alters the reactivity of the nucleotide. It is often used as a substrate analog in enzymatic assays and studies related to RNA labeling and structural analysis.

CAT: BRP-00788

Molecular Formula: C10H18N3O13P3S

Molecular Weight: 513.25

Purity: ≥98%

Appearance: Colorless transparent liquid

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InChIKey: YFZJJCOYJMDNDY-GWKANUBMSA-N

CanonicalSMILES: CC1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)(O)OP(=S)(O)OP(=O)(O)O)O)O

IUPAC Name: [(2R,3S,4R,5R)-5-(4-amino-5-methyl-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl [hydroxy(phosphonooxy)phosphinothioyl] hydrogen phosphate

InChI: InChI=1S/C10H18N3O13P3S/c1-4-2-13(10(16)12-8(4)11)9-7(15)6(14)5(24-9)3-23-28(20,21)26-29(22,30)25-27(17,18)19/h2,5-7,9,14-15H,3H2,1H3,(H,20,21)(H,22,30)(H2,11,12,16)(H2,17,18,19)/t5-,6-,7-,9-,29?/m1/s1

Synonyms: β-Thio-((2R,3S,4R,5R)-5-(4-amino-5-methyl-2-oxopyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl triphosphate; 5-Methylcytidine-5'-O-(2-thiotriphosphate); 5-Methyl-CTPβS

2'-O-Methyl-ATP-βS

Description: 2'-O-Methyl-ATP-βS is a modified nucleotide compound used in biochemical research. It consists of an adenosine base with a methyl group at the 2'-position, linked to an adenosine triphosphate (ATP) moiety, and containing a sulfur (S) atom at the β position. This modification alters the reactivity of the nucleotide. It is commonly utilized as a substrate analog in enzymatic assays and studies related to RNA modification, structural analysis, and RNA-protein interactions.

CAT: BRP-00789

CAS: 926631-25-6

Molecular Formula: C11H18N5O12P3S

Molecular Weight: 537.28

Purity: ≥98%

Appearance: Colorless transparent liquid

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

Density: 2.35±0.1 g/cm3

Boiling Point: 864.5±75.0 °C at 760 mmHg

InChIKey: MGIWZFGDBWCPJG-YOLSTXSHSA-N

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

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

InChI: InChI=1S/C11H18N5O12P3S/c1-24-8-7(17)5(2-25-30(21,22)28-31(23,32)27-29(18,19)20)26-11(8)16-4-15-6-9(12)13-3-14-10(6)16/h3-5,7-8,11,17H,2H2,1H3,(H,21,22)(H,23,32)(H2,12,13,14)(H2,18,19,20)/t5-,7-,8-,11-,31?/m1/s1

Synonyms: β-Thio-((2R,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl triphosphate; 5'-Adenylic acid, 2'-O-methyl-, P'-anhydride with thiodiphosphoric acid ((HO)2P(O)OP(O)(OH)(SH)); 2'-O-Methyladenosine-5'-O-(2-Thiotriphosphate); 2'-O-Methyl-ATP-β-S; 2'-O-Methyl-ATPβS

2'-O-Methyl-GTP-βS

Description: 2'-O-Methyl-GTP-βS is a modified nucleotide compound used in biochemical research. It consists of a guanosine base with a methyl group at the 2'-position, linked to a guanosine triphosphate (GTP) moiety, and containing a sulfur (S) atom at the β position. This modification alters the reactivity of the nucleotide. It is frequently employed as a substrate analog in enzymatic assays and studies related to RNA modification, structural analysis, and RNA-protein interactions.

CAT: BRP-00790

Molecular Formula: C11H18N5O13P3S

Molecular Weight: 553.28

Purity: ≥98%

Appearance: Colorless transparent liquid

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

Density: 2.45±0.1 g/cm3

Boiling Point: 931.1±75.0 °C at 760 mmHg

InChIKey: VJCFJRASRRBLIU-NRSRKINISA-N

CanonicalSMILES: COC1C(C(OC1N2C=NC3=C2N=C(NC3=O)N)COP(=O)(O)OP(=S)(O)OP(=O)(O)O)O

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

InChI: InChI=1S/C11H18N5O13P3S/c1-25-7-6(17)4(2-26-31(22,23)29-32(24,33)28-30(19,20)21)27-10(7)16-3-13-5-8(16)14-11(12)15-9(5)18/h3-4,6-7,10,17H,2H2,1H3,(H,22,23)(H,24,33)(H2,19,20,21)(H3,12,14,15,18)/t4-,6-,7-,10-,32?/m1/s1

Synonyms: β-Thio-((2R,3R,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl triphosphate; 2'-O-Methyl-GTPβS

α-Thio-pseudouridine-5'-triphosphate, trisodium salt

Description: α-Thio-pseudouridine-5'-triphosphate, trisodium salt is a modified nucleotide compound used in biochemical research. It contains a thio-modified pseudouridine base linked to a triphosphate group at the 5' carbon of the ribose sugar. This modification introduces a sulfur (S) atom at the α position of the pseudouridine. It is in the form of a trisodium salt. This compound is commonly utilized as a substrate analog in enzymatic assays and studies related to RNA modification, RNA structure-function relationships, and RNA-protein interactions.

CAT: BRP-00791

Molecular Formula: C9H12N2Na3O14P3S

Molecular Weight: 566.15

Purity: ≥98%

Appearance: Colorless transparent liquid

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InChIKey: MMSUJHCLVGJXAW-XMRXGGJWSA-K

CanonicalSMILES: C1=C(C(=O)NC(=O)N1)C2C(C(C(O2)COP(=S)([O-])OP(=O)([O-])OP(=O)(O)[O-])O)O.[Na+].[Na+].[Na+]

IUPAC Name: trisodium;[[[(2R,3S,4R,5S)-5-(2,4-dioxo-1H-pyrimidin-5-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphinothioyl]oxy-oxidophosphoryl] hydrogen phosphate

InChI: InChI=1S/C9H15N2O14P3S.3Na/c12-5-4(2-22-28(21,29)25-27(19,20)24-26(16,17)18)23-7(6(5)13)3-1-10-9(15)11-8(3)14;;;/h1,4-7,12-13H,2H2,(H,19,20)(H,21,29)(H2,16,17,18)(H2,10,11,14,15);;;/q;3*+1/p-3/t4-,5-,6-,7+,28?;;;/m1.../s1

Synonyms: alpha-Thio-pseudouridine-5'-triphosphate, trisodium salt

5-Methyl-CTP-αS

Description: 5-Methyl-CTP-αS is a modified nucleotide compound used in biochemical research. It consists of a cytidine base with a methyl group at the 5th position, linked to a cytidine triphosphate (CTP) moiety, and containing a sulfur (S) atom at the α position. This modification alters the reactivity of the nucleotide. It is often utilized as a substrate analog in enzymatic assays and studies related to RNA modification, RNA labeling, and RNA-protein interactions.

CAT: BRP-00792

Molecular Formula: C10H18N3O13P3S

Molecular Weight: 513.25

Purity: ≥98%

Appearance: Colorless transparent liquid

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InChIKey: PQLJKNQISGQQDR-GWKANUBMSA-N

CanonicalSMILES: CC1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=S)(O)OP(=O)(O)OP(=O)(O)O)O)O

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

InChI: InChI=1S/C10H18N3O13P3S/c1-4-2-13(10(16)12-8(4)11)9-7(15)6(14)5(24-9)3-23-29(22,30)26-28(20,21)25-27(17,18)19/h2,5-7,9,14-15H,3H2,1H3,(H,20,21)(H,22,30)(H2,11,12,16)(H2,17,18,19)/t5-,6-,7-,9-,29?/m1/s1

Synonyms: α-Thio-((2R,3S,4R,5R)-5-(4-amino-5-methyl-2-oxopyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl triphosphate; 5-Methylcytidine, 5'→P''-ester with thiotriphosphoric acid; 5-Methylcytidine-5'-O-(1-thiotriphosphate); 5-Methyl-CTPαS

2'-O-Methyl-ATP-αS

Description: 2'-O-Methyl-ATP-αS is a modified nucleotide compound used in biochemical research. It consists of an adenosine base with a methyl group at the 2'-position, linked to an adenosine triphosphate (ATP) moiety, and containing a sulfur (S) atom at the α position. This modification alters the reactivity of the nucleotide. It is commonly employed as a substrate analog in enzymatic assays and studies related to RNA modification, RNA labeling, and RNA-protein interactions.

CAT: BRP-00793

CAS: 926631-26-7

Molecular Formula: C11H18N5O12P3S

Molecular Weight: 537.28

Purity: ≥98%

Appearance: Colorless transparent liquid

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

Density: 2.35±0.1 g/cm3

Boiling Point: 864.5±75.0 °C at 760 mmHg

InChIKey: PPIGLURRZVMGQO-YOLSTXSHSA-N

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

IUPAC Name: [[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-3-hydroxy-4-methoxyoxolan-2-yl]methoxy-hydroxyphosphinothioyl] phosphono hydrogen phosphate

InChI: InChI=1S/C11H18N5O12P3S/c1-24-8-7(17)5(2-25-31(23,32)28-30(21,22)27-29(18,19)20)26-11(8)16-4-15-6-9(12)13-3-14-10(6)16/h3-5,7-8,11,17H,2H2,1H3,(H,21,22)(H,23,32)(H2,12,13,14)(H2,18,19,20)/t5-,7-,8-,11-,31?/m1/s1

Synonyms: α-Thio-((2R,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl triphosphate; 2'-O-Methyladenosine-5'-O-(1-Thiotriphosphate); 2'-O-Methyl-ATP-α-S; 2'-O-Methyl-ATPαS; Adenosine, 2'-O-methyl-, 5'→P''-ester with thiotriphosphoric acid ((HO)2P(O)OP(O)(OH)OP(O)(OH)(SH))

2'-O-Methyl-GTP-αS

Description: 2'-O-Methyl-GTP-αS is a modified nucleotide compound used in biochemical research. It contains a guanosine base with a methyl group at the 2'-position, linked to a guanosine triphosphate (GTP) moiety, and containing a sulfur (S) atom at the α position. This modification alters the reactivity of the nucleotide. It is frequently used as a substrate analog in enzymatic assays and studies related to RNA modification, RNA labeling, and RNA-protein interactions.

CAT: BRP-00794

CAS: 847648-38-8

Molecular Formula: C11H18N5O13P3S

Molecular Weight: 553.28

Purity: ≥98%

Appearance: Colorless transparent liquid

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

Density: 2.45±0.1 g/cm3

Boiling Point: 931.1±75.0 °C at 760 mmHg

InChIKey: PTDOTKSKFQMXQJ-NRSRKINISA-N

CanonicalSMILES: COC1C(C(OC1N2C=NC3=C2N=C(NC3=O)N)COP(=S)(O)OP(=O)(O)OP(=O)(O)O)O

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

InChI: InChI=1S/C11H18N5O13P3S/c1-25-7-6(17)4(2-26-32(24,33)29-31(22,23)28-30(19,20)21)27-10(7)16-3-13-5-8(16)14-11(12)15-9(5)18/h3-4,6-7,10,17H,2H2,1H3,(H,22,23)(H,24,33)(H2,19,20,21)(H3,12,14,15,18)/t4-,6-,7-,10-,32?/m1/s1

Synonyms: α-Thio-((2R,3R,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl triphosphate; Guanosine, 2'-O-methyl-, 5'→P''-ester with thiotriphosphoric acid ((HO)2P(O)OP(O)(OH)OP(O)(OH)(SH)); 2'-O-Methyl-GTPαS

5-Methoxyuridine 5'-monophosphate

Description: 5-Methoxyuridine 5'-monophosphate is a modified nucleotide used in biochemical research. It consists of a uridine base with a methoxy group at the 5th position and a monophosphate group attached to the 5' carbon of the ribose sugar. This compound is commonly employed in studies of RNA synthesis, modification, and function, helping to elucidate the roles of modified nucleotides in biological processes and potential therapeutic applications.

CAT: BRP-00806

CAS: 36908-07-3

Molecular Formula: C10H15N2O10P

Molecular Weight: 354.21

Purity: 98%

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Density: 1.82±0.1 g/cm3

InChIKey: UAVXJXAREPXQGC-JXOAFFINSA-N

CanonicalSMILES: COC1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)O)O)O

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

InChI: InChI=1S/C10H15N2O10P/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)/t5-,6-,7-,9-/m1/s1

Synonyms: ((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; 5-Methoxy UMP; 5'-Uridylic acid, 5-methoxy-; 5-Methoxy-5'-uridylic acid; 5-Methoxyuridine 5'-phosphate; 5-OMe-UMP; 5-O-methyl-uridine-5'-monophosphate; 5-O-methyluridine-5'-monophosphate

Related CAS: 70406-74-5 (homopolymer)

6-Fluoro-3,4-dihydro-3-oxo-4-(5-O-phosphono-β-D-ribofuranosyl)-2-pyrazinecarboxamide ammonium salt

Description: 6-Fluoro-3,4-dihydro-3-oxo-4-(5-O-phosphono-β-D-ribofuranosyl)-2-pyrazinecarboxamide ammonium salt is a modified nucleoside phosphate used in biochemical and pharmaceutical research. The ammonium salt form enhances its solubility and stability. This nucleoside analog is often employed in studies of nucleic acid metabolism, enzyme interactions, and as a potential antiviral or anticancer agent, providing insights into therapeutic mechanisms and applications.

CAT: BRP-00809

CAS: 2096342-42-4

Molecular Formula: C10H16FN4O9P

Molecular Weight: 386.23

Purity: 98%

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InChIKey: LMKFDJHKHJFIBX-MGVVQUQWSA-N

CanonicalSMILES: O=C(N)C1=NC(F)=CN(C1=O)C2OC(COP(=O)(O)O)C(O)C2O.N

IUPAC Name: azanium;[(2R,3S,4R,5R)-5-(3-carbamoyl-5-fluoro-2-oxopyrazin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl hydrogen phosphate

InChI: InChI=1S/C10H13FN3O9P.H3N/c11-4-1-14(9(18)5(13-4)8(12)17)10-7(16)6(15)3(23-10)2-22-24(19,20)21;/h1,3,6-7,10,15-16H,2H2,(H2,12,17)(H2,19,20,21);1H3/t3-,6-,7-,10-;/m1./s1

Synonyms: 2-Pyrazinecarboxamide, 6-fluoro-3,4-dihydro-3-oxo-4-(5-O-phosphono-β-D-ribofuranosyl)-, ammonium salt (1:1); T-705RMP (ammonium); T 705RMP ammonium salt

Related CAS: 356783-08-9 (free base)

NaMTP

Description: NaMTP is a compound used in biochemical research and drug development. This compound is often studied for its potential biological activities and interactions, particularly in nucleotide metabolism and signaling pathways. Its structural complexity suggests possible roles in enzymatic processes or as a therapeutic target.

CAT: BRP-00819

CAS: 1135561-87-3

Molecular Formula: C16H21O14P3

Molecular Weight: 530.25

Purity: 95%

Appearance: Lyophilized white powder

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Storage: Store at -20 °C

Density: 1.775±0.06 g/cm3

Boiling Point: 824.3±75.0 °C at 760 mmHg

InChIKey: CCJNXXZRNQFAFA-FPCVCCKLSA-N

Solubility: Soluble in Water

CanonicalSMILES: COC1=CC2=CC=CC=C2C=C1C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O

IUPAC Name: [[(2R,3S,4R,5S)-3,4-dihydroxy-5-(3-methoxynaphthalen-2-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate

InChI: InChI=1S/C16H21O14P3/c1-26-12-7-10-5-3-2-4-9(10)6-11(12)16-15(18)14(17)13(28-16)8-27-32(22,23)30-33(24,25)29-31(19,20)21/h2-7,13-18H,8H2,1H3,(H,22,23)(H,24,25)(H2,19,20,21)/t13-,14-,15-,16+/m1/s1

Synonyms: (1S)-1,4-anhydro-5-O-[(R)-hydroxy{[(S)-hydroxy(phosphonooxy)phosphoryl]oxy}phosphoryl]-1-(3-methoxynaphthalen-2-yl)-D-ribitol; ((2R,3S,4R,5S)-3,4-dihydroxy-5-(3-methoxynaphthalen-2-yl)tetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate; D-Ribitol, 1,4-anhydro-1-C-(3-methoxy-2-naphthalenyl)-, 5-(tetrahydrogen triphosphate), (1S)-

NaMTP-CF2

Description: NaMTP-CF2 is a compound used in biochemical research and drug development. This compound is often studied for its potential biological activities and interactions, particularly in nucleotide metabolism and signaling pathways. Its structural complexity suggests possible roles in enzymatic processes or as a therapeutic target.

CAT: BRP-00820

Molecular Formula: C17H21F2O13P3

Molecular Weight: 564.26

Purity: 95%

Appearance: Lyophilized white powder

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InChIKey: QPQQKBQSGWQWPC-FPCVCCKLSA-N

Solubility: Soluble in Water

IUPAC Name: (((((((2R,3S,4R,5S)-3,4-dihydroxy-5-(3-methoxynaphthalen-2-yl)tetrahydrofuran-2-yl)methoxy)(hydroxy)phosphoryl)oxy)(hydroxy)phosphoryl)difluoromethyl)phosphonic acid

InChI: InChI=1S/C17H21F2O13P3/c1-29-12-7-10-5-3-2-4-9(10)6-11(12)16-15(21)14(20)13(31-16)8-30-35(27,28)32-34(25,26)17(18,19)33(22,23)24/h2-7,13-16,20-21H,8H2,1H3,(H,25,26)(H,27,28)(H2,22,23,24)/t13-,14-,15-,16+/m1/s1

Related CAS: 2095501-89-4 (2'-deoxy-NaMTP-CF2)

D-FMAUTP

Description: D-FMAUTP is a nucleotide analog compound with potential applications in antiviral drug development and nucleic acid chemistry research.

CAT: BRP-00829

CAS: 79551-89-6

Molecular Formula: C10H16FN2O14P3

Molecular Weight: 500.16

Purity: 95%

Appearance: Lyophilized white powder

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Storage: Store at -20 °C

Density: 1.97±0.1 g/cm3

InChIKey: RUKRVHYQIIURNV-JVZYCSMKSA-N

Solubility: Soluble in Water

CanonicalSMILES: CC1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)F

IUPAC Name: [[(2R,3R,4S,5R)-4-fluoro-3-hydroxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate

InChI: InChI=1S/C10H16FN2O14P3/c1-4-2-13(10(16)12-8(4)15)9-6(11)7(14)5(25-9)3-24-29(20,21)27-30(22,23)26-28(17,18)19/h2,5-7,9,14H,3H2,1H3,(H,20,21)(H,22,23)(H,12,15,16)(H2,17,18,19)/t5-,6+,7-,9-/m1/s1

Synonyms: 2,4(1H,3H)-Pyrimidinedione, 1-[2-deoxy-2-fluoro-5-O-[hydroxy[[hydroxy(phosphonooxy)phosphinyl]oxy]phosphinyl]-β-D-arabinofuranosyl]-5-methyl-; (((2R,3R,4S,5R)-4-fluoro-3-hydroxy-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl)triphosphoric acid; 1-(2-Deoxy-2-fluoro-5-O-(hydroxy((hydroxy(phosphonooxy)phosphinyl)oxy)phosphinyl)-beta-D-arabinofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione

(2'OMe-5'P-A)pG

Description: (2'OMe-5'P-A)pG is a modified nucleotide compound used in biochemical research. It consists of an adenosine nucleotide with a phosphonate group attached to the 5' carbon and a guanosine nucleotide linked to the 3' carbon via a phosphodiester bond. Additionally, the 2' position of the adenosine ribose is methylated. This compound is often utilized in studies related to RNA modification, enzymology, and nucleic acid chemistry, providing insights into RNA structure, function, and enzymatic mechanisms.

CAT: BRP-00904

CAS: 62828-60-8

Molecular Formula: C21H28N10O14P2

Molecular Weight: 706.46

Purity: >99%

Appearance: Lyophilized white powder

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Storage: Store at -20 °C

Density: 2.36±0.1 g/cm3

InChIKey: XQBFQZRTNDQTOK-XPWFQUROSA-N

Solubility: Soluble in Water

CanonicalSMILES: COC1C(C(OC1N2C=NC3=C(N=CN=C32)N)COP(=O)(O)O)OP(=O)(O)OCC4C(C(C(O4)N5C=NC6=C5N=C(NC6=O)N)O)O

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-methoxy-2-(phosphonooxymethyl)oxolan-3-yl] hydrogen phosphate

InChI: InChI=1S/C21H28N10O14P2/c1-40-14-13(8(3-41-46(35,36)37)44-20(14)30-5-26-9-15(22)24-4-25-16(9)30)45-47(38,39)42-2-7-11(32)12(33)19(43-7)31-6-27-10-17(31)28-21(23)29-18(10)34/h4-8,11-14,19-20,32-33H,2-3H2,1H3,(H,38,39)(H2,22,24,25)(H2,35,36,37)(H3,23,28,29,34)/t7-,8-,11-,12-,13-,14-,19-,20-/m1/s1

Synonyms: pApG dimer; 5'-phosphono-O2'-methyl-adenylyl-(3'->5')-guanosine; ((2R,3R,4R,5R)-3-(((((2R,3S,4R,5R)-5-(2-Amino-6-oxo-3,6-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(hydroxy)phosphoryl)oxy)-5-(6-amino-9H-purin-9-yl)-4-methoxytetrahydrofuran-2-yl)methyl dihydrogen phosphate; Guanosine, 2'-O-methyl-5'-O-phosphonoadenylyl-(3'→5')-; 2'-O-Methyl-5'-O-phosphonoadenylyl-(3'→5')-guanosine; (2'OMe5'P A)pG; pA(2'-OMe)mpG

Related CAS: 2638447-50-2 (triethylamine salt (1:3)) ; 2894815-57-5 (triethylamine salt (1:2)) ; 2645354-91-0 (ammonium salt)

N7-Me-3'-OMe GDP

Description: N7-Me-3'-OMe GDP is a modified nucleotide compound used in biochemical research. It consists of guanosine diphosphate (GDP) with methylation at the N7 position of the guanine base and methylation at the 3' position of the ribose sugar. This modified nucleotide is used in studies related to RNA modification, RNA processing, and as a substrate analog in enzymatic assays, providing insights into RNA biology and enzymatic mechanisms.

CAT: BRP-00905

CAS: 400806-44-2

Molecular Formula: C12H19N5O11P2

Molecular Weight: 471.26

Purity: >99%

Appearance: Lyophilized white powder

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InChIKey: BYYIIJWDJDLPEV-IOSLPCCCSA-N

Solubility: Soluble in Water

CanonicalSMILES: O=C1N=C(N)NC2=C1[N+](=CN2C3OC(COP(=O)([O-])OP(=O)(O)O)C(OC)C3O)C

IUPAC Name: ((2R,3S,4R,5R)-5-(2-amino-7-methyl-6-oxo-1,6-dihydro-9H-purin-7-ium-9-yl)-4-hydroxy-3-methoxytetrahydrofuran-2-yl)methyl dihydrogen diphosphate

InChI: InChI=1S/C12H19N5O11P2/c1-16-4-17(9-6(16)10(19)15-12(13)14-9)11-7(18)8(25-2)5(27-11)3-26-30(23,24)28-29(20,21)22/h4-5,7-8,11,18H,3H2,1-2H3,(H5-,13,14,15,19,20,21,22,23,24)/t5-,7-,8-,11-/m1/s1

Synonyms: Guanosine 5'-(trihydrogen diphosphate), 7-methyl-3'-O-methyl-, inner salt; 3'-OMe-m7GDP

7-Methylguanosine diphosphate

Description: 7-Methylguanosine diphosphate is a modified nucleotide compound used in biochemical research. It consists of guanosine diphosphate (GDP) with methylation at the 7th position of the guanine base. This modified nucleotide is often used in studies related to RNA modification, mRNA capping, and as a substrate analog in enzymatic assays, providing insights into RNA biology and enzymatic mechanisms.

CAT: BRP-00906

CAS: 26467-11-8

Molecular Formula: C11H17N5O11P2

Molecular Weight: 457.23

Purity: >99%

Appearance: Lyophilized white powder

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InChIKey: SBASPRRECYVBRF-KQYNXXCUSA-N

Solubility: Soluble in Water

CanonicalSMILES: CN1C=[N+](C2=C1C(=O)NC(=N2)N)C3C(C(C(O3)COP(=O)([O-])OP(=O)(O)O)O)O

IUPAC Name: [(2R,3S,4R,5R)-5-(2-amino-7-methyl-6-oxo-1H-purin-9-ium-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphono phosphate

InChI: InChI=1S/C11H17N5O11P2/c1-15-3-16(8-5(15)9(19)14-11(12)13-8)10-7(18)6(17)4(26-10)2-25-29(23,24)27-28(20,21)22/h3-4,6-7,10,17-18H,2H2,1H3,(H5-,12,13,14,19,20,21,22,23,24)/t4-,6-,7-,10-/m1/s1

Synonyms: Guanosine 5'-(trihydrogen diphosphate), 7-methyl-, inner salt; 1H-Purinium, 2-amino-6,9-dihydro-9-[5-O-[hydroxy(phosphonooxy)phosphinyl]-β-D-ribofuranosyl]-7-methyl-6-oxo-, inner salt; Purinium, 2-amino-1,6-dihydro-7-methyl-6-oxo-9-β-D-ribofuranosyl-, hydroxide, 5'-(trihydrogen pyrophosphate), inner salt; 7-Methyl-GDP; 7-Methylguanosine 5'-diphosphate; N7-Me GDP; m7GDP

Related CAS: 104809-16-7 (monosodium salt) ; 240137-50-2 (triethylamine salt (1:x)) ; 2173378-02-2 (triethylamine salt (1:1)) ; 1262968-09-1 (triethylamine salt (1:2))

3'-O-Methylguanosine-5'-diphosphate

7-Methyl-3'-O-methylguanosine-5'-monophosphate

α-Thio-1-methylpseudouridine-5'-triphosphate, trisodium salt

β-Thio-1-methylpseudouridine-5'-triphosphate, trisodium salt

β-Thio-pseudouridine-5'-triphosphate, trisodium salt

5-Methyl-CTP-βS

2'-O-Methyl-ATP-βS

2'-O-Methyl-GTP-βS

α-Thio-pseudouridine-5'-triphosphate, trisodium salt

5-Methyl-CTP-αS

2'-O-Methyl-ATP-αS

2'-O-Methyl-GTP-αS

5-Methoxyuridine 5'-monophosphate

6-Fluoro-3,4-dihydro-3-oxo-4-(5-O-phosphono-β-D-ribofuranosyl)-2-pyrazinecarboxamide ammonium salt

NaMTP

NaMTP-CF2

D-FMAUTP

(2'OMe-5'P-A)pG

N7-Me-3'-OMe GDP

7-Methylguanosine diphosphate

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