Nucleotides

2'-OMe-2-amino-ATP

Description: 2'-OMe-2-amino-ATP is a modified nucleotide used in biochemical and molecular biology research. It contains an adenosine base with a 2'-O-methyl modification and an amino group at the 2' position, linked to a triphosphate group. This modified nucleotide can be incorporated into RNA during transcription or into DNA during synthesis, allowing researchers to study its effects on RNA or DNA structure, stability, and function. It is particularly useful in investigations of RNA modification, RNA-protein interactions, and RNA catalysis due to its unique properties compared to natural nucleotides.

CAT: BRP-00924

CAS: 215942-59-9

Molecular Formula: C11H19N6O13P3

Molecular Weight: 536.22

Purity: 95%

Appearance: Lyophilized white powder

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Storage: Store at -20 °C

Density: 2.51±0.1 g/cm3

Boiling Point: 995.1±75.0 °C at 760 mmHg

InChIKey: HZIXZQRCKAUTNV-KQYNXXCUSA-N

Solubility: Soluble in Water

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

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

InChI: InChI=1S/C11H19N6O13P3/c1-26-7-6(18)4(2-27-32(22,23)30-33(24,25)29-31(19,20)21)28-10(7)17-3-14-5-8(12)15-11(13)16-9(5)17/h3-4,6-7,10,18H,2H2,1H3,(H,22,23)(H,24,25)(H2,19,20,21)(H4,12,13,15,16)/t4-,6-,7-,10-/m1/s1

Synonyms: Adenosine 5'-(tetrahydrogen triphosphate), 2-amino-2'-O-methyl-; 2-Amino-2'-O-methyladenosine 5'-(tetrahydrogen triphosphate); 2-Amino-2'-O-methyl-ATP; 2-Amino-2'-O-methyladenosine 5'-triphosphate

4-F-UTP

Description: 4-F-UTP, or 4-Fluoro-uridine triphosphate, is a modified nucleotide used in biochemical and molecular biology research. It contains a uridine base with a fluorine atom substituted at the 4th position, linked to a triphosphate group. This modified nucleotide is employed in RNA labeling, where the fluorine substitution can be detected using fluorescence-based techniques. It is useful for studying RNA synthesis, processing, and degradation, as well as for labeling RNA probes in various molecular biology applications such as in situ hybridization and RNA imaging.

CAT: BRP-00925

CAS: 1251838-93-3

Molecular Formula: C9H14FN2O15P3

Molecular Weight: 502.13

Purity: 95%

Appearance: Lyophilized white powder

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Storage: Store at -20 °C

Density: 2.13±0.1 g/cm3

InChIKey: JICLDCHIWOEHQY-JVZYCSMKSA-N

Solubility: Soluble in Water

CanonicalSMILES: C1=CN(C(=O)NC1=O)C2C(C(C(O2)(COP(=O)(O)OP(=O)(O)OP(=O)(O)O)F)O)O

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

InChI: InChI=1S/C9H14FN2O15P3/c10-9(3-24-29(20,21)27-30(22,23)26-28(17,18)19)6(15)5(14)7(25-9)12-2-1-4(13)11-8(12)16/h1-2,5-7,14-15H,3H2,(H,20,21)(H,22,23)(H,11,13,16)(H2,17,18,19)/t5-,6+,7-,9-/m1/s1

Synonyms: Uridine 5'-(tetrahydrogen triphosphate), 4'-C-fluoro-; 4'-C-Fluorouridine 5'-(tetrahydrogen triphosphate); ((2S,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-fluoro-3,4-dihydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate; 4'-fluorouridine 5'-O-triphosphate

LNA-ATP

Description: LNA-ATP, or Locked Nucleic Acid-adenosine triphosphate, is a modified nucleotide used in biochemical and molecular biology research. It contains an adenosine base modified with a locked nucleic acid (LNA) backbone and linked to a triphosphate group. This modified nucleotide is utilized in studies related to RNA and DNA research, where LNA modifications enhance the stability and specificity of oligonucleotides. LNA-ATP can be incorporated into RNA or DNA strands during synthesis, allowing researchers to investigate various aspects of nucleic acid structure, function, and interactions.

CAT: BRP-00926

CAS: 941597-09-7

Molecular Formula: C11H16N5O13P3

Molecular Weight: 519.19

Purity: 95%

Appearance: Lyophilized white powder

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Storage: Store at -20 °C

Density: 2.66±0.1 g/cm3

Boiling Point: 938.3±75.0 °C at 760 mmHg

InChIKey: IYXWSFFOIIMVHP-LRMGWDNHSA-N

Solubility: Soluble in Water

CanonicalSMILES: C1C2(C(C(O1)C(O2)N3C=NC4=C(N=CN=C43)N)O)COP(=O)(O)OP(=O)(O)OP(=O)(O)O

IUPAC Name: [[(1R,3R,4R,7S)-3-(6-aminopurin-9-yl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-1-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate

InChI: InChI=1S/C11H16N5O13P3/c12-8-5-9(14-3-13-8)16(4-15-5)10-6-7(17)11(27-10,1-25-6)2-26-31(21,22)29-32(23,24)28-30(18,19)20/h3-4,6-7,10,17H,1-2H2,(H,21,22)(H,23,24)(H2,12,13,14)(H2,18,19,20)/t6-,7+,10-,11-/m1/s1

Synonyms: 9H-Purin-6-amine, 9-[2,5-anhydro-4-C-(3,5,7,7-tetrahydroxy-3,5,7-trioxido-2,4,6-trioxa-3,5,7-triphosphahept-1-yl)-α-L-lyxofuranosyl]-; 9-[2,5-Anhydro-4-C-(3,5,7,7-tetrahydroxy-3,5,7-trioxido-2,4,6-trioxa-3,5,7-triphosphahept-1-yl)-α-L-lyxofuranosyl]-9H-purin-6-amine; ((1R,3R,4R,7S)-3-(6-amino-9H-purin-9-yl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-1-yl)methyl tetrahydrogen triphosphate; LNA-A-TP

LNA-GTP

Description: LNA-GTP, or Locked Nucleic Acid-guanosine triphosphate, is a modified nucleotide used in biochemical and molecular biology research. It contains a guanosine base modified with a locked nucleic acid (LNA) backbone and linked to a triphosphate group. This modified nucleotide is employed in studies related to RNA and DNA research, where LNA modifications enhance the stability and specificity of oligonucleotides. LNA-GTP can be incorporated into RNA or DNA strands during synthesis, enabling researchers to investigate various aspects of nucleic acid structure, function, and interactions.

CAT: BRP-00927

CAS: 1233876-29-3

Molecular Formula: C11H16N5O14P3

Molecular Weight: 535.19

Purity: 95%

Appearance: Lyophilized white powder

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Storage: Store at -20 °C

Density: 2.79±0.1 g/cm3

Boiling Point: 1013.6±75.0 °C at 760 mmHg

InChIKey: PYKYQYMIAMREBH-HLJYALQUSA-N

Solubility: Soluble in Water

CanonicalSMILES: C1C2(C(C(O1)C(O2)N3C=NC4=C3N=C(NC4=O)N)O)COP(=O)(O)OP(=O)(O)OP(=O)(O)O

IUPAC Name: [[(1R,3R,4R,7S)-3-(2-amino-6-oxo-1H-purin-9-yl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-1-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate

InChI: InChI=1S/C11H16N5O14P3/c12-10-14-7-4(8(18)15-10)13-3-16(7)9-5-6(17)11(28-9,1-26-5)2-27-32(22,23)30-33(24,25)29-31(19,20)21/h3,5-6,9,17H,1-2H2,(H,22,23)(H,24,25)(H2,19,20,21)(H3,12,14,15,18)/t5-,6+,9-,11-/m1/s1

Synonyms: 6H-Purin-6-one, 2-amino-9-[2,5-anhydro-4-C-(3,5,7,7-tetrahydroxy-3,5,7-trioxido-2,4,6-trioxa-3,5,7-triphosphahept-1-yl)-α-L-lyxofuranosyl]-1,9-dihydro-; 2-Amino-9-[2,5-anhydro-4-C-(3,5,7,7-tetrahydroxy-3,5,7-trioxido-2,4,6-trioxa-3,5,7-triphosphahept-1-yl)-α-L-lyxofuranosyl]-1,9-dihydro-6H-purin-6-one; LNA-G-TP; ((1R,3R,4R,7S)-3-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-1-yl)methyl tetrahydrogen triphosphate

LNA-CTP

Description: LNA-CTP, or Locked Nucleic Acid-cytidine triphosphate, is a modified nucleotide used in biochemical and molecular biology research. It contains a cytidine base modified with a locked nucleic acid (LNA) backbone and linked to a triphosphate group. This modified nucleotide is utilized in studies related to RNA and DNA research, where LNA modifications enhance the stability and specificity of oligonucleotides. LNA-CTP can be incorporated into RNA or DNA strands during synthesis, allowing researchers to investigate various aspects of nucleic acid structure, function, and interactions.

CAT: BRP-00928

CAS: 847650-98-0

Molecular Formula: C10H16N3O14P3

Molecular Weight: 495.17

Purity: 95%

Appearance: Lyophilized white powder

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Storage: Store at -20 °C

Density: 2.54±0.1 g/cm3

Boiling Point: 837.7±75.0 °C at 760 mmHg

InChIKey: LSTGCLQXGYREJT-IBCQBUCCSA-N

Solubility: Soluble in Water

CanonicalSMILES: C1C2(C(C(O1)C(O2)N3C=CC(=NC3=O)N)O)COP(=O)(O)OP(=O)(O)OP(=O)(O)O

IUPAC Name: [[(1R,3R,4R,7S)-3-(4-amino-2-oxopyrimidin-1-yl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-1-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate

InChI: InChI=1S/C10H16N3O14P3/c11-5-1-2-13(9(15)12-5)8-6-7(14)10(25-8,3-23-6)4-24-29(19,20)27-30(21,22)26-28(16,17)18/h1-2,6-8,14H,3-4H2,(H,19,20)(H,21,22)(H2,11,12,15)(H2,16,17,18)/t6-,7+,8-,10-/m1/s1

Synonyms: 2(1H)-Pyrimidinone, 4-amino-1-[2,5-anhydro-4-C-(3,5,7,7-tetrahydroxy-3,5,7-trioxido-2,4,6-trioxa-3,5,7-triphosphahept-1-yl)-α-L-lyxofuranosyl]-; 4-Amino-1-[2,5-anhydro-4-C-(3,5,7,7-tetrahydroxy-3,5,7-trioxido-2,4,6-trioxa-3,5,7-triphosphahept-1-yl)-α-L-lyxofuranosyl]-2(1H)-pyrimidinone; LNA-C-TP; ((1R,3R,4R,7S)-3-(4-amino-2-oxopyrimidin-1(2H)-yl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-1-yl)methyl tetrahydrogen triphosphate

LNA-UTP

Description: LNA-UTP, or Locked Nucleic Acid-uridine triphosphate, is a modified nucleotide used in biochemical and molecular biology research. It contains a uridine base modified with a locked nucleic acid (LNA) backbone and linked to a triphosphate group. This modified nucleotide is employed in studies related to RNA and DNA research, where LNA modifications enhance the stability and specificity of oligonucleotides. LNA-UTP can be incorporated into RNA strands during synthesis, allowing researchers to investigate various aspects of nucleic acid structure, function, and interactions.

CAT: BRP-00929

CAS: 1258616-54-4

Molecular Formula: C10H15N2O15P3

Molecular Weight: 496.15

Purity: 95%

Appearance: Lyophilized white powder

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Storage: Store at -20 °C

Density: 2.109±0.06 g/cm3

InChIKey: RSSDTUFQOLIPRO-IBCQBUCCSA-N

Solubility: Soluble in Water

CanonicalSMILES: C1C2(C(C(O1)C(O2)N3C=CC(=O)NC3=O)O)COP(=O)(O)OP(=O)(O)OP(=O)(O)O

IUPAC Name: [[(1R,3R,4R,7S)-3-(2,4-dioxopyrimidin-1-yl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-1-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate

InChI: InChI=1S/C10H15N2O15P3/c13-5-1-2-12(9(15)11-5)8-6-7(14)10(25-8,3-23-6)4-24-29(19,20)27-30(21,22)26-28(16,17)18/h1-2,6-8,14H,3-4H2,(H,19,20)(H,21,22)(H,11,13,15)(H2,16,17,18)/t6-,7+,8-,10-/m1/s1

Synonyms: 2,4(1H,3H)-Pyrimidinedione, 1-[2,5-anhydro-4-C-(3,5,7,7-tetrahydroxy-3,5,7-trioxido-2,4,6-trioxa-3,5,7-triphosphahept-1-yl)-α-L-lyxofuranosyl]-; 1-[2,5-Anhydro-4-C-(3,5,7,7-tetrahydroxy-3,5,7-trioxido-2,4,6-trioxa-3,5,7-triphosphahept-1-yl)-α-L-lyxofuranosyl]-2,4(1H,3H)-pyrimidinedione; LNA-U-TP; ((1R,3R,4R,7S)-3-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-1-yl)methyl tetrahydrogen triphosphate

5'-Ethyl dimethyl phosphonate-2'-OMe-U

Description: 5'-Ethyl dimethyl phosphonate-2'-OMe-U includes an ethyl dimethyl phosphonate group replaced to the 5' hydroxyl, along with a methyl (Me) group at the 2' position of ribose. It is used in oligonucleotide synthesis to introduce phosphonate modifications.

CAT: BRP-01014

Molecular Formula: C13H21N2O8P

Molecular Weight: 364.29

Purity: ≥98% by UPLC

Appearance: White, off-white to light yellow powder

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Storage: Store at -20 °C

InChIKey: HHIFIFUUIMPUDT-HJQYOEGKSA-N

IUPAC Name: dimethyl (2-((2R,3R,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)ethyl)phosphonate

InChI: InChI=1S/C13H21N2O8P/c1-20-11-10(17)8(5-7-24(19,21-2)22-3)23-12(11)15-6-4-9(16)14-13(15)18/h4,6,8,10-12,17H,5,7H2,1-3H3,(H,14,16,18)/t8-,10-,11-,12-/m1/s1

Synonyms: 5'-ethyl dimethyl phosphonate-2'-O-methyl-uridine

N7-Me-GDP TEA salt

Description: N7-Me-GDP TEA salt is a modified nucleotide analog. It contains a methyl group (Me) at the N7 position of guanosine diphosphate (GDP) and exists in the triethylammonium (TEA) salt form. This modified nucleotide is utilized in various biochemical and enzymatic studies, particularly in RNA research, to investigate the effects of N7 methylation on RNA structure, function, or interactions with proteins or enzymes.

CAT: BRP-01025

CAS: 2173378-02-2

Molecular Formula: C17H32N6O11P2

Molecular Weight: 558.42

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InChIKey: UZIQIBOSSFOGCK-MCDZGGTQSA-N

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

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;N,N-diethylethanamine

InChI: InChI=1S/C11H17N5O11P2.C6H15N/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;1-4-7(5-2)6-3/h3-4,6-7,10,17-18H,2H2,1H3,(H5-,12,13,14,19,20,21,22,23,24);4-6H2,1-3H3/t4-,6-,7-,10-;/m1./s1

Synonyms: 7-methyl-guanosine-5'-diphosphate, triethylamine salt (1:1); Guanosine 5'-(trihydrogen diphosphate), 7-methyl-, inner salt, compd. with N,N-diethylethanamine (1:1); 7-Methyl-GDP triethylamine salt; 7-Methylguanosine 5'-diphosphate triethylamine salt; 7-Methylguanosine diphosphate triethylamine salt; m7GDP triethylamine salt

Related CAS: 26467-11-8 (free base)

GDP-α-S tris salt

Description: GDP-α-S tris salt is a modified nucleotide analog where the oxygen atom in the alpha position of guanosine diphosphate (GDP) is replaced by a sulfur atom (α-S). It exists in the form of a tris(hydroxymethyl)aminomethane (tris) salt. This modification is used in biochemical and molecular biology studies to investigate nucleotide-binding proteins and enzymes, as it can act as a non-hydrolyzable analog of GDP. This property makes it useful for studying G-protein signaling and other processes involving GDP/GTP binding and hydrolysis.

CAT: BRP-01026

Molecular Formula: C10H15N5O10P2S (free acid)

Molecular Weight: 459.27 (free acid)

Purity: ≥90% by HPLC

Appearance: Clear colorless to yellow liquid

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

Synonyms: Guanosine 5'-[α-thio] diphosphate tris salt; Guanosine 5'-O-(1-thiodiphosphate) tris salt; GDPαS tris salt; Guanosine-5'-O-thiodiphosphate tris salt; Guanosine, 5'-P'-ester with thiodiphosphoric acid ((HO)2P(O)OP(O)(OH)(SH)) tris salt (1:x)

Related CAS: 77481-24-4 (free base)

GDP-β-S tris salt

Description: GDP-β-S tris salt is a modified nucleotide analog where a sulfur atom replaces one of the non-bridging oxygen atoms on the beta phosphate group of guanosine diphosphate (GDP), and it exists in the tris(hydroxymethyl)aminomethane (tris) salt form. This modified nucleotide is used in biochemical and molecular biology studies to explore enzyme mechanisms, protein-nucleotide interactions, and signaling pathways, offering insights into the role of phosphorylation and sulfur substitution in various biochemical processes.

CAT: BRP-01027

Molecular Formula: C10H15N5O10P2S (free acid)

Molecular Weight: 459.27 (free acid)

Purity: ≥90% by HPLC

Appearance: Clear colorless to yellow liquid

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

Synonyms: Guanosine 5'-[β-thio] diphosphate tris salt; GDP-βS; Guanosine 5'-(β-thiodiphosphate) tris salt; Guanosine 5'-O-(2-thiodiphosphate) tris salt; Guanosine 5'-O-(β-thiodiphosphate) tris salt; Guanyl-5'-yl thiophosphate tris salt; GDP-β-S

Related CAS: 71376-97-1 (free base)

2'-OMe-AMP IM

Description: 2'-OMe-AMP IM is a modified nucleotide analog where a methyl group (Me) is attached to the 2' position of adenosine monophosphate (AMP), and it includes an imidazolate (IM) group. This modified nucleotide is used in oligonucleotide synthesis and various biochemical studies to investigate RNA stability, structure, and function, as well as to introduce specific properties or functionalities into nucleic acid sequences for research or therapeutic purposes.

CAT: BRP-01028

CAS: 1516676-65-5

Molecular Formula: C14H18N7O6P

Molecular Weight: 411.31

Purity: ≥90% by HPLC

Appearance: White to faint yellow powder

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Storage: Store at -20 °C

Density: 1.94±0.1 g/cm3

Boiling Point: 769.8±70.0 °C at 760 mmHg

InChIKey: WQKFXPOUCFBMBQ-IDTAVKCVSA-N

CanonicalSMILES: O=P(O)(OCC1OC(N2C=NC=3C(=NC=NC32)N)C(OC)C1O)N4C=NC=C4

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

InChI: InChI=1S/C14H18N7O6P/c1-25-11-10(22)8(4-26-28(23,24)20-3-2-16-6-20)27-14(11)21-7-19-9-12(15)17-5-18-13(9)21/h2-3,5-8,10-11,14,22H,4H2,1H3,(H,23,24)(H2,15,17,18)/t8-,10-,11-,14-/m1/s1

Synonyms: 2'-O-Methyl-Adenosine-5'-monophosphate-Imidazolate; Adenosine, 2'-O-methyl-, 5'-(hydrogen P-1H-imidazol-1-ylphosphonate); 2'-OMe-AMP-IMZ; 2'-OMe-AMP.Im

Related CAS: 1231158-18-1 (triethylamine salt (1:x)) ; 1516676-66-6 (triethylamine salt (1:1))

2'-OMe-AMP IM sodium salt

Description: 2'-OMe-AMP IM sodium salt is a modified nucleotide analog where a methyl group (Me) is attached to the 2' position of adenosine monophosphate (AMP), and it includes an imidazolate (IM) group. This modified nucleotide is used in oligonucleotide synthesis and various biochemical studies to investigate RNA stability, structure, and function, as well as to introduce specific properties or functionalities into nucleic acid sequences for research or therapeutic purposes.

CAT: BRP-01029

Molecular Formula: C14H17N7NaO6P

Molecular Weight: 433.30

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Storage: Store at -20 °C

InChIKey: HWUZIMVCPBEJHS-ZBMQJGODSA-M

CanonicalSMILES: O=P(O)(OCC1OC(N2C=NC=3C(=NC=NC32)N)C(OC)C1O)N4C=NC=C4.Na

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

InChI: InChI=1S/C14H18N7O6P.Na/c1-25-11-10(22)8(4-26-28(23,24)20-3-2-16-6-20)27-14(11)21-7-19-9-12(15)17-5-18-13(9)21;/h2-3,5-8,10-11,14,22H,4H2,1H3,(H,23,24)(H2,15,17,18);/q;+1/p-1/t8-,10-,11-,14-;/m1./s1

Synonyms: 2'-O-Methyl-Adenosine-5'-monophosphate-Imidazolate sodium salt; Adenosine, 2'-O-methyl-, 5'-(hydrogen P-1H-imidazol-1-ylphosphonate) sodium salt; 2'-OMe-AMP-IMZ sodium salt; 2'-OMe-AMP.Im sodium salt

Related CAS: 1516676-65-5 (free acid)

pUMP TEA salt

Description: Pseudouridine 5'-monophosphate, triethylamine salt, is a nucleotide where pseudouridine, a modified nucleoside, is phosphorylated at the 5' position and combined with triethylamine to form its salt. Pseudouridine 5'-monophosphate, triethylamine salt, can be used in research involving RNA modification and structure, RNA-protein interactions, and the role of pseudouridine in RNA stability and function. It is also useful in studies aiming to understand the biochemistry of RNA and its various modifications.

CAT: BRP-01030

Molecular Formula: C15H28N3O9P

Molecular Weight: 425.37

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IUPAC Name: [(2R,3S,4R,5S)-5-(2,4-dioxo-1H-pyrimidin-5-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate;N,N-diethylethanamine

Synonyms: Pseudouridine 5'-monophosphate, triethylamine salt; Pseudouridine 5'-phosphate triethylamine salt; pUMP TEA; 5-(5-O-Phosphono-beta-D-ribofuranosyl)-2,4(1H,3H)-pyrimidinedione triethylamine salt

Related CAS: 1157-60-4 (free base)

pUMP ammonium salt

Description: Pseudouridine 5'-monophosphate, ammonium salt, is a nucleotide where pseudouridine, a modified nucleoside, is phosphorylated at the 5' position and combined with ammonium to form its salt. Pseudouridine 5'-monophosphate, ammonium salt, can be used in research involving RNA modification and structure, RNA-protein interactions, and the role of pseudouridine in RNA stability and function. It is also useful in studies aiming to understand the biochemistry of RNA and its various modifications.

CAT: BRP-01031

Molecular Formula: C9H13N2O9P (free acid)

Molecular Weight: 324.19 (free acid)

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IUPAC Name: [(2R,3S,4R,5S)-5-(2,4-dioxo-1H-pyrimidin-5-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate;ammonium salt

Synonyms: Pseudouridine 5'-monophosphate, ammonium salt; pUMP.NH4; Pseudouridine 5'-phosphate ammonium salt; 5-(5-O-Phosphono-beta-D-ribofuranosyl)-2,4(1H,3H)-pyrimidinedione ammonium salt

Related CAS: 1157-60-4 (free base)

N7-Me-GMP IM sodium salt

Description: N7-Methylguanosine 5'-monophosphate, imidazole sodium salt (N7-Me-GMP IM sodium salt), is a nucleotide derivative where 7-methylguanosine is phosphorylated at the 5' position and combined with imidazole and sodium ions to form its salt. This compound is utilized in biochemical research, particularly in studies related to RNA capping mechanisms, RNA modification and structure, RNA-protein interactions, and the broader roles of modified nucleosides in RNA stability and function.

CAT: BRP-01032

CAS: 1199264-77-1

Molecular Formula: C14H17N7NaO7P

Molecular Weight: 449.29

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InChIKey: UCEADIRWQLQNQS-AZUPYXJKSA-M

CanonicalSMILES: [Na].O=C1N=C(N)NC2=C1[N+](=CN2C3OC(COP(=O)([O-])N4C=NC=C4)C(O)C3O)C

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

InChI: InChI=1S/C14H18N7O7P.Na/c1-19-6-21(11-8(19)12(24)18-14(15)17-11)13-10(23)9(22)7(28-13)4-27-29(25,26)20-3-2-16-5-20;/h2-3,5-7,9-10,13,22-23H,4H2,1H3,(H3-,15,17,18,24,25,26);/q;+1/p-1/t7-,9-,10-,13-;/m1./s1

Synonyms: N1-methyl-guanosine-5'-monophosphate, Imidazolate sodium salt; N7-Me-GMP IM; Guanosine, 7-methyl-, 5'-(hydrogen P-1H-imidazol-1-ylphosphonate), sodium salt (1:1)

Related CAS: 88412-11-7 (free acid)

N7-Me-GMP sodium salt

Description: N7-Methylguanosine 5'-monophosphate sodium salt (N7-Me-GMP sodium salt) is a nucleotide compound where 7-methylguanosine, a modified nucleoside, is phosphorylated at the 5' position and combined with sodium ions to form its salt. This compound is used in biochemical and molecular biology research, particularly in studies concerning RNA modification, RNA capping mechanisms, RNA structure, RNA-protein interactions, and the role of modified nucleosides in RNA biology and function.

CAT: BRP-01033

Molecular Formula: C11H16N5O8P (free acid)

Molecular Weight: 377.25 (free acid)

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Synonyms: N1-methyl-guanosine-5'-monophosphate, sodium salt; N7-Me-GMP.Na; 7-Methyl-guanosine-5'-monophosphate, sodium salt; N(7)-methylguanosine 5'-phosphate sodium salt; 7-Methyl-5'-guanylic acid inner salt, sodium salt; 2-Amino-1,6-dihydro-7-methyl-6-oxo-9-beta-D-ribofuranosylpurinium hydroxide, 5'-phosphate, inner salt, sodium salt; 7-Methylguanosine-5'-monophosphate, sodium salt

Related CAS: 10162-58-0 (free acid)

N1-Me-pUMP disodium salt

Description: N1-Methylpseudouridine 5'-monophosphate disodium salt (N1-Me-pUMP disodium salt) is a nucleotide derivative where N1-methylpseudouridine, a modified nucleoside, 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 biological roles and functions of modified nucleosides within RNA molecules.

CAT: BRP-01034

Molecular Formula: C10H13N2Na2O9P

Molecular Weight: 382.17

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InChIKey: VCKFKWJHPVKIOA-VRCPEZRFSA-L

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

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

InChI: InChI=1S/C10H15N2O9P.2Na/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);;/q;2*+1/p-2/t5-,6-,7-,8+;;/m1../s1

Synonyms: N1-methyl-pseudouridine-5'-monophosphate, disodium salt; N1-methylpseudouridine 5'-monophosphate disodium salt; N(1)-methylpseudouridine 5'-monophosphate disodium salt; N(1)-methylpseudouridylic acid disodium salt; N(1)-methylpseudouridine 5'-phosphate disodium salt; N1-Me-pUMP.Na2; (1S)-1,4-anhydro-1-(1-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)-5-O-phosphono-D-ribitol disodium salt

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

pUMP disodium salt

Description: pUMP disodium salt is a nucleotide compound where pseudouridine, a modified nucleoside, is phosphorylated at the 5' position and combined with two 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 investigations into the role of pseudouridine in RNA stability and function.

CAT: BRP-01035

Molecular Formula: C9H11N2Na2O9P

Molecular Weight: 368.14

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InChIKey: VDMQJZZVGPBGAT-DDPCOCNQSA-L

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

IUPAC Name: disodium;((2R,3S,4R,5S)-5-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

InChI: InChI=1S/C9H13N2O9P.2Na/c12-5-4(2-19-21(16,17)18)20-7(6(5)13)3-1-10-9(15)11-8(3)14;;/h1,4-7,12-13H,2H2,(H2,16,17,18)(H2,10,11,14,15);;/q;2*+1/p-2/t4-,5-,6-,7+;;/m1../s1

Synonyms: Pseudouridine 5'-monophosphate, disodium salt; pUMP.Na2; Pseudouridine 5'-phosphate disodium salt; 5-(5-O-Phosphono-beta-D-ribofuranosyl)-2,4(1H,3H)-pyrimidinedione disodium salt

Related CAS: 1157-60-4 (free acid)

7-Me-3'-OMe-GMP IM sodium salt

Description: 7-Methyl-3'-O-methylguanosine 5'-monophosphate IM sodium salt is a nucleotide derivative where 7-methyl-3'-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-01036

CAS: 886753-12-4

Molecular Formula: C15H19N7NaO7P

Molecular Weight: 463.32

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InChIKey: GPIGDAMDRKWMDK-ZBMQJGODSA-M

CanonicalSMILES: [Na].O=C1N=C(N)NC2=C1[N+](=CN2C3OC(COP(=O)([O-])N4C=NC=C4)C(OC)C3O)C

IUPAC Name: sodium;((2R,3S,4R,5R)-5-(2-amino-7-methyl-6-oxido-9H-purin-7-ium-9-yl)-4-hydroxy-3-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)14-10(23)11(27-2)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);/q;+1/p-1/t8-,10-,11-,14-;/m1./s1

Synonyms: 7-methyl-3'-O-methyl-guanosine-5'-monophosphate, Imidazolate sodium salt; 7-Me-3'-OMe-GMP IM; Guanosine, 7-methyl-3'-O-methyl-, 5'-(hydrogen P-1H-imidazol-1-ylphosphonate), inner salt, sodium salt (1:1); Guanosine, 7-methyl-3'-O-methyl-, 5'-(hydrogen 1H-imidazol-1-ylphosphonate), inner salt, monosodium salt; N7-Me-3'-OMe-GMP IM sodium salt

Related CAS: 886884-22-6 (free acid)

7-Me-3'-OMe-GMP TEA salt

Description: 7-Methyl-3'-O-methylguanosine 5'-monophosphate TEA salt is a nucleotide compound where 7-methyl-3'-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 biological roles of modified nucleosides in RNA.

CAT: BRP-01037

CAS: 1149746-17-7

Molecular Formula: C18H33N6O8P

Molecular Weight: 492.47

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InChIKey: BXSNVPCPRXXNOQ-YCSZXMBFSA-N

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

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 hydrogen phosphate;N,N-diethylethanamine

InChI: InChI=1S/C12H18N5O8P.C6H15N/c1-16-4-17(9-6(16)10(19)15-12(13)14-9)11-7(18)8(23-2)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-3'-O-methyl-guanosine-5'-monophosphate, triethylamine salt; 7-Me-3'-OMe-GMP TEA; 5'-Guanylic acid, 7-methyl-3'-O-methyl-, inner salt, compd. with N,N-diethylethanamine (1:1)

Related CAS: 94889-80-2 (free base)

2'-OMe-2-amino-ATP

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LNA-GTP

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5'-Ethyl dimethyl phosphonate-2'-OMe-U

N7-Me-GDP TEA salt

GDP-α-S tris salt

GDP-β-S tris salt

2'-OMe-AMP IM

2'-OMe-AMP IM sodium salt

pUMP TEA salt

pUMP ammonium salt

N7-Me-GMP IM sodium salt

N7-Me-GMP sodium salt

N1-Me-pUMP disodium salt

pUMP disodium salt

7-Me-3'-OMe-GMP IM sodium salt

7-Me-3'-OMe-GMP TEA salt

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