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Nucleotides

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CTP potassium salt

Description: CTP (Cytidine 5'-triphosphate) potassium salt is a compound where CTP, a nucleotide consisting of cytidine, ribose sugar, and three phosphate groups, is stabilized and solubilized by complexing with potassium 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 potassium 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-01219
Molecular Formula: C9H16N3O14P3 (free acid)
Molecular Weight: 483.16 (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: potassium;[[(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, potassium salt; Cytidine 5'-(tetrahydrogen triphosphate), potassium salt (1:x); 5'-CTP potassium salt; Cytidine triphosphate, potassium salt
Related CAS: 65-47-4 (free acid)

ATP potassium salt

Description: ATP (Adenosine 5'-triphosphate) potassium salt is a stabilized form of ATP where the nucleotide is complexed with potassium 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-01220
CAS: 29622-22-8
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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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: potassium;[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate
Synonyms: Adenosine 5'-triphosphate, potassium salt; Adenosine triphosphate, potassium salt; Adenosine, 5'-(tetrahydrogen triphosphate), potassium salt; 5'-ATP potassium salt; Adenosine 5'-(tetrahydrogen triphosphate), potassium salt (1:x)
Related CAS: 56-65-5 (free acid)

Guanosine 5'-diphosphate, tris salt

Description: Guanosine 5'-diphosphate, tris salt, is a nucleotide compound consisting of guanosine, a nucleoside made up of guanine attached to a ribose sugar. In this compound, the guanosine is phosphorylated at the 5' position, forming guanosine diphosphate (GDP). The tris salt form indicates that the nucleotide is stabilized with tris(hydroxymethyl)aminomethane (Tris), a common buffering agent. GDP is essential in various biochemical processes, serving as a critical intermediate in cellular energy metabolism, particularly in the synthesis of guanine nucleotides and as a substrate for GTP (guanosine 5'-triphosphate)-binding proteins involved in signal transduction pathways. Its stable tris salt form ensures solubility in aqueous solutions, facilitating its use in enzymatic assays, studies of nucleotide-protein interactions, and other biochemical investigations.
CAT: BRP-01246
Molecular Formula: C10H15N5O11P2 (free acid)
Molecular Weight: 443.20 (free acid)
Purity: ≥97% by HPLC
Appearance: Clear colorless liquid
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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]methyl phosphono hydrogen phosphate;2-amino-2-(hydroxymethyl)propane-1,3-diol
Synonyms: GDP, Tris Salt; Guanosine diphosphate, tris salt; 2-amino-9-{5-O-[hydroxy(phosphonooxy)phosphoryl]-β-D-ribofuranosyl}-9H-purin-6-ol tris salt; Guanosine 5'-(trihydrogen diphosphate) tris salt; 5'-GDP, Tris Salt
Related CAS: 146-91-8 (free base)

Guanosine 5'-diphosphate, ammonium salt

Description: Guanosine 5'-diphosphate, ammonium salt, is a nucleotide compound comprising guanosine, a nucleoside with a guanine base attached to a ribose sugar, which is phosphorylated at the 5' position to form guanosine diphosphate (GDP). The compound is stabilized as an ammonium salt, enhancing its solubility and stability in aqueous solutions. GDP plays a pivotal role in cellular energy metabolism and signal transduction. It serves as a substrate for the synthesis of GTP (guanosine triphosphate), which is essential for protein synthesis, cell signaling, and other critical biochemical pathways. The ammonium salt form makes GDP particularly useful in enzymatic assays, studies of nucleotide-protein interactions, and various biochemical research applications.
CAT: BRP-01247
CAS: 96013-01-3
Molecular Formula: C10H15N5O11P2 (free acid)
Molecular Weight: 443.20 (free acid)
Purity: ≥98% by HPLC
Appearance: Clear colorless liquid
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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]methyl phosphono hydrogen phosphate;ammonium salt
Synonyms: GDP, Ammonium Salt; Guanosine diphosphate, ammonium salt; 2-Amino-9-{5-O-[hydroxy(phosphonooxy)phosphoryl]-β-D-ribofuranosyl}-9H-purin-6-ol ammonium salt; Guanosine 5'-(trihydrogen diphosphate) ammonium salt; 5'-GDP, ammonium Salt
Related CAS: 146-91-8 (free acid)

Guanosine 5'-diphosphate, Imidazolate

Description: Guanosine 5'-diphosphate, imidazolate is a nucleotide compound in which guanosine, consisting of a guanine base attached to a ribose sugar, is phosphorylated at the 5' position to form guanosine diphosphate (GDP). In this structure, the imidazolate group is covalently linked to the phosphate moiety. This compound is significant in various biochemical applications, including the study of cellular energy metabolism and signal transduction pathways. GDP serves as a precursor to GTP (guanosine triphosphate), which is crucial for processes such as protein synthesis and cell signaling. The imidazolate linkage enhances the stability and utility of GDP in enzymatic assays, nucleotide-protein interaction studies, and other biochemical research contexts.
CAT: BRP-01248
CAS: 94102-61-1
Molecular Formula: C13H17N7O10P2
Molecular Weight: 493.26
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Storage: Store at -20 °C
Density: 2.39±0.1 g/cm3
InChIKey: WNASQXDYNREIBF-WOUKDFQISA-N
CanonicalSMILES: C1=CN(C=N1)P(=O)(O)OP(=O)(O)OCC2C(C(C(O2)N3C=NC4=C3N=C(NC4=O)N)O)O
IUPAC Name: [[(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-imidazol-1-ylphosphinic acid
InChI: InChI=1S/C13H17N7O10P2/c14-13-17-10-7(11(23)18-13)16-5-20(10)12-9(22)8(21)6(29-12)3-28-32(26,27)30-31(24,25)19-2-1-15-4-19/h1-2,4-6,8-9,12,21-22H,3H2,(H,24,25)(H,26,27)(H3,14,17,18,23)/t6-,8-,9-,12-/m1/s1
Synonyms: GDP Im; 5'-Guanylic acid, anhydride with P-1H-imidazol-1-ylphosphonic acid (1:1); 5'-Guanylic acid, monoanhydride with 1H-imidazol-1-ylphosphonic acid
Related CAS: 1199264-75-9 (disodium salt) ; 109611-43-0 (dilithium salt) ; 1787255-41-7 (TEA salt (1:2))

Guanosine 5'-diphosphate, Imidazolate disodium salt

Description: Guanosine 5'-diphosphate, Imidazolate disodium salt is a nucleotide compound in which guanosine, consisting of a guanine base attached to a ribose sugar, is phosphorylated at the 5' position to form guanosine diphosphate (GDP). In this structure, the imidazolate group is covalently linked to the phosphate moiety. This compound is significant in various biochemical applications, including the study of cellular energy metabolism and signal transduction pathways. GDP serves as a precursor to GTP (guanosine triphosphate), which is crucial for processes such as protein synthesis and cell signaling. The imidazolate linkage enhances the stability and utility of GDP in enzymatic assays, nucleotide-protein interaction studies, and other biochemical research contexts.
CAT: BRP-01249
CAS: 1199264-75-9
Molecular Formula: C13H15N7Na2O10P2
Molecular Weight: 537.23
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Storage: Store at -20 °C
InChIKey: NLJLFSUCHFQBLU-CMUBXXRSSA-L
CanonicalSMILES: [Na].[Na].O=C1N=C(N)NC2=C1N=CN2C3OC(COP(=O)(O)OP(=O)(O)N4C=NC=C4)C(O)C3O
IUPAC Name: disodium;[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-imidazol-1-ylphosphate
InChI: InChI=1S/C13H17N7O10P2.2Na/c14-13-17-10-7(11(23)18-13)16-5-20(10)12-9(22)8(21)6(29-12)3-28-32(26,27)30-31(24,25)19-2-1-15-4-19;;/h1-2,4-6,8-9,12,21-22H,3H2,(H,24,25)(H,26,27)(H3,14,17,18,23);;/q;2*+1/p-2/t6-,8-,9-,12-;;/m1../s1
Synonyms: 5'-Guanylic acid, anhydride with P-1H-imidazol-1-ylphosphonic acid, sodium salt (1:1:2); GDP Im disodium salt; 5'-Guanylic acid, monoanhydride with 1H-imidazol-1-ylphosphonic acid disodium salt
Related CAS: 94102-61-1 (free acid)

Guanosine 5'-diphosphate, triethylamine salt

Description: Guanosine 5'-diphosphate, triethylamine salt, is a nucleotide compound consisting of guanosine, a nucleoside with a guanine base attached to a ribose sugar, phosphorylated at the 5' position to form guanosine diphosphate (GDP). In this form, the nucleotide is stabilized with triethylamine, enhancing its solubility and stability in aqueous solutions. This compound is essential in various biochemical processes, including cellular energy metabolism and signal transduction. GDP serves as a precursor for GTP (guanosine triphosphate), which is critical for protein synthesis, cell signaling, and other important cellular functions. The triethylamine salt form makes it particularly useful in enzymatic assays, studies of nucleotide-protein interactions, and other biochemical research applications.
CAT: BRP-01250
CAS: 83209-71-6
Molecular Formula: C16H30N6O11P2
Molecular Weight: 544.39
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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]methyl phosphono hydrogen phosphate;N,N-diethylethanamine
Synonyms: GDP TEA salt; Guanosine diphosphate, triethylamine salt; 2-Amino-9-{5-O-[hydroxy(phosphonooxy)phosphoryl]-β-D-ribofuranosyl}-9H-purin-6-ol triethylamine salt; Guanosine 5'-(trihydrogen diphosphate) triethylamine salt; 5'-GDP, triethylamine Salt; Guanosine 5'-(trihydrogen diphosphate), compd. with N,N-diethylethanamine (1:1); GDP triethylammonium salt
Related CAS: 146-91-8 (free base)

Guanosine 5'-diphosphate, dimethylhexylammonium salt

Description: Guanosine 5'-diphosphate, dimethylhexylammonium salt, is a nucleotide compound composed of guanosine, which is guanine attached to a ribose sugar, phosphorylated at the 5' position to form guanosine diphosphate (GDP). In this compound, the GDP is stabilized with dimethylhexylammonium, enhancing its solubility and stability in aqueous solutions. This compound plays a vital role in various biochemical processes, including cellular energy metabolism and signal transduction pathways. GDP is an intermediate in the synthesis of GTP (guanosine triphosphate), which is crucial for protein synthesis, cell signaling, and other essential cellular functions. The dimethylhexylammonium salt form is particularly beneficial for its use in enzymatic assays, studies of nucleotide-protein interactions, and other biochemical research applications.
CAT: BRP-01251
Molecular Formula: C10H15N5O11P2 (free acid)
Molecular Weight: 443.20 (free acid)
Purity: ≥98% by HPLC
Appearance: White to off-white powder
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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]methyl phosphono hydrogen phosphate;N,N-dimethylhexan-1-amine
Synonyms: GDP DMHA salt; Guanosine diphosphate, dimethylhexylammonium salt; 2-Amino-9-{5-O-[hydroxy(phosphonooxy)phosphoryl]-β-D-ribofuranosyl}-9H-purin-6-ol dimethylhexylammonium salt; Guanosine 5'-(trihydrogen diphosphate) dimethylhexylammonium salt; 5'-GDP, dimethylhexylammonium Salt; Guanosine 5'-(trihydrogen diphosphate), compd. with N,N-dimethyl-1-hexanamine (1:x)
Related CAS: 146-91-8 (free base)

IDP sodium salt

Description: IDP sodium salt is a pivotal constituent in the biomedical field, serving as a precursor for crucial molecules engaged in cellular processes. Its applied scope encompasses the synthesis of paramount compounds pertinent to studying viral invasions, immune disorders, and select cancerous conditions.
CAT: BRP-01252
CAS: 51192-98-4
Molecular Formula: C10H14N4O11P2 (free acid)
Molecular Weight: 428.18 (free acid)
Purity: ≥95% by HPLC
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Storage: Store at -20 °C
IUPAC Name: sodium;[(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-1H-purin-9-yl)oxolan-2-yl]methyl phosphono hydrogen phosphate
Synonyms: Inosine 5'-diphosphate sodium salt; Inosine 5'-(trihydrogen diphosphate), sodium salt (1:x); Inosine 5'-(trihydrogen diphosphate), sodium salt; 5'-IDP sodium salt; Inosine 5-diphosphate sodium salt; Inosine diphosphate sodium salt
Related CAS: 86-04-4 (free acid)

Guanosine-5'-monophosphate, Imidazolate sodium salt

Description: Guanosine-5'-monophosphate, imidazolate sodium salt is an important nucleotide with various crucial functions in organisms, including involvement in protein synthesis, cell signaling, and energy metabolism. Research indicates that Guanosine-5'-monophosphate, imidazolate also has potential medicinal value in treating certain diseases, serving as a potential drug target.
CAT: BRP-01253
CAS: 886753-16-8
Molecular Formula: C13H15N7NaO7P
Molecular Weight: 435.26
Purity: ≥95%
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Storage: Store at 2-8 °C, in tightly closed container, protected from light and humidity
InChIKey: KMOMTSXNMLAONG-OUTCZKRVSA-M
CanonicalSMILES: C1=CN(C=N1)P(=O)(O)OCC2C(C(C(O2)N3C=NC4=C3N=C(N=C4[O-])N)O)O.[Na+]
IUPAC Name: sodium;2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-[[hydroxy(imidazol-1-yl)phosphoryl]oxymethyl]oxolan-2-yl]purin-6-olate
InChI: InChI=1S/C13H16N7O7P.Na/c14-13-17-10-7(11(23)18-13)16-5-20(10)12-9(22)8(21)6(27-12)3-26-28(24,25)19-2-1-15-4-19;/h1-2,4-6,8-9,12,21-22H,3H2,(H,24,25)(H3,14,17,18,23);/q;+1/p-1/t6-,8-,9-,12-;/m1./s1
Synonyms: GMP-Im sodium salt; Guanosine, 5'-(hydrogen P-1H-imidazol-1-ylphosphonate), sodium salt (1:1); Guanosine, 5'-(hydrogen 1H-imidazol-1-ylphosphonate), monosodium salt; Guanosine 5'-phosphorimidazolide sodium salt; ImpG sodium salt
Related CAS: 69281-33-0 (free acid)

Guanosine-5'-monophosphate, Imidazolate

Description: Guanosine-5'-monophosphate, imidazolate is an important nucleotide with various crucial functions in organisms, including involvement in protein synthesis, cell signaling, and energy metabolism. Research indicates that Guanosine-5'-monophosphate, imidazolate also has potential medicinal value in treating certain diseases, serving as a potential drug target.
CAT: BRP-01254
CAS: 69281-33-0
Molecular Formula: C13H16N7O7P
Molecular Weight: 413.28
Purity: ≥95%
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Storage: Store at 2-8 °C, in tightly closed container, protected from light and humidity
Density: 2.23±0.1 g/cm3
InChIKey: YVUZUNMTEUIDKC-WOUKDFQISA-N
CanonicalSMILES: C1=CN(C=N1)P(=O)(O)OCC2C(C(C(O2)N3C=NC4=C3N=C(NC4=O)N)O)O
IUPAC Name: [(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-imidazol-1-ylphosphinic acid
InChI: InChI=1S/C13H16N7O7P/c14-13-17-10-7(11(23)18-13)16-5-20(10)12-9(22)8(21)6(27-12)3-26-28(24,25)19-2-1-15-4-19/h1-2,4-6,8-9,12,21-22H,3H2,(H,24,25)(H3,14,17,18,23)/t6-,8-,9-,12-/m1/s1
Synonyms: Guanosine, 5'-(hydrogen P-1H-imidazol-1-ylphosphonate); Guanosine, 5'-(hydrogen 1H-imidazol-1-ylphosphonate); Guanosine 5'-phosphorimidazolide; ImpG
Related CAS: 886753-16-8 (monosodium salt)

Isoguanosine 5'-triphosphate disodium salt

Description: Isoguanosine 5'-triphosphate disodium salt is a nucleotide analog used in biochemical research. It consists of isoguanosine, an analog of guanosine, attached to a ribose sugar and a triphosphate group. This compound is commonly used to study RNA synthesis, nucleotide interactions, and enzymatic activity. As a disodium salt, it is water-soluble and suitable for various biological assays.
CAT: BRP-01328
Molecular Formula: C10H14N5Na2O14P3
Molecular Weight: 567.14
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InChIKey: WHILFBHYVTYXCP-LGVAUZIVSA-L
CanonicalSMILES: [Na].[Na].O=C1N=C(N)C=2N=CN(C2N1)C3OC(COP(=O)(O)OP(=O)(O)OP(=O)(O)O)C(O)C3O
IUPAC Name: disodium;((2R,3S,4R,5R)-5-(6-amino-2-oxo-2,3-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl dihydrogen triphosphate
InChI: InChI=1S/C10H16N5O14P3.2Na/c11-7-4-8(14-10(18)13-7)15(2-12-4)9-6(17)5(16)3(27-9)1-26-31(22,23)29-32(24,25)28-30(19,20)21;;/h2-3,5-6,9,16-17H,1H2,(H,22,23)(H,24,25)(H2,19,20,21)(H3,11,13,14,18);;/q;2*+1/p-2/t3-,5-,6-,9-;;/m1../s1
Synonyms: Adenosine 5'-(tetrahydrogen triphosphate), 2,3-dihydro-2-oxo-, disodium salt; 2,3-Dihydro-2-oxoadenosine 5'-(tetrahydrogen triphosphate) disodium salt; Isoguanosine 5'-triphosphate disodium salt; 2-hydroxy-ATP disodium salt; 2-oxo-2-hydroadenosine 5'-(tetrahydrogen triphosphate) disodium salt; isoGTP disodium salt; Iso-GTP disodium salt
Related CAS: 58083-93-5 (free acid)

2'-O-Methyladenosine-5'-triphosphate disodium salt

Description: 2'-O-Methyladenosine-5'-triphosphate disodium salt is a modified nucleotide used in biochemical research. It consists of adenosine with a methyl group attached to the 2'-oxygen of the ribose sugar and a triphosphate group. This compound is utilized to study RNA synthesis, nucleotide interactions, and the role of methylation in biological processes. As a disodium salt, it is water-soluble, making it suitable for various biological and biochemical assays.
CAT: BRP-01329
Molecular Formula: C11H16N5Na2O13P3
Molecular Weight: 565.17
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InChIKey: SEILEHTYIWXZNM-LYYWGVPGSA-L
CanonicalSMILES: [Na].[Na].COC1C(C(OC1N2C=NC3=C(N=CN=C32)N)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O
IUPAC Name: disodium;((2R,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl dihydrogen triphosphate
InChI: InChI=1S/C11H18N5O13P3.2Na/c1-25-8-7(17)5(2-26-31(21,22)29-32(23,24)28-30(18,19)20)27-11(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,23,24)(H2,12,13,14)(H2,18,19,20);;/q;2*+1/p-2/t5-,7-,8-,11-;;/m1../s1
Synonyms: 2'-(O-Methyl)-Adenosine 5'-triphosphate disodium salt; 2'-O-methyl-adenosine-5'-triphosphate, disodium salt; 2'-O-Me-ATP disodium Salt; Adenosine, 2'-O-methyl-, 5'-(tetrahydrogen triphosphate), sodium salt (1:2); 2'-O-Methyladenosine 5'-(tetrahydrogen triphosphate) disodium salt; 2'-O-Methyl-ATP disodium salt
Related CAS: 30948-06-2 (free acid)

2'-O-Methylcytidine-5'-triphosphate disodium salt

Description: 2'-O-Methylcytidine-5'-triphosphate disodium salt is a modified nucleotide used in biochemical research. It consists of cytidine with a methyl group attached to the 2'-oxygen of the ribose sugar and a triphosphate group. This modification is important for studying RNA synthesis, nucleotide interactions, and methylation's role in biological processes. As a disodium salt, it is water-soluble, making it suitable for various biological and biochemical assays.
CAT: BRP-01330
Molecular Formula: C10H16N3Na2O14P3
Molecular Weight: 541.15
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InChIKey: USYUJUVBMIQNPS-BAZBJWKESA-L
CanonicalSMILES: [Na].[Na].O=C1N=C(N)C=CN1C2OC(COP(=O)(O)OP(=O)(O)OP(=O)(O)O)C(O)C2OC
IUPAC Name: disodium;((2R,3R,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl dihydrogen triphosphate
InChI: InChI=1S/C10H18N3O14P3.2Na/c1-23-8-7(14)5(25-9(8)13-3-2-6(11)12-10(13)15)4-24-29(19,20)27-30(21,22)26-28(16,17)18;;/h2-3,5,7-9,14H,4H2,1H3,(H,19,20)(H,21,22)(H2,11,12,15)(H2,16,17,18);;/q;2*+1/p-2/t5-,7-,8-,9-;;/m1../s1
Synonyms: 2'-(O-Methyl)-Cytidine 5'-triphosphate disodium salt; 2'-O-methyl-cytidine-5'-triphosphate, disodium salt; 2'-O-Me-CTP disodium salt; Cytidine, 2'-O-methyl-, 5'-(tetrahydrogen triphosphate), sodium salt (1:2); 2'-O-Methylcytidine 5'-(tetrahydrogen triphosphate) disodium salt; 2'-O-Methyl-CTP disodium salt
Related CAS: 143028-98-2 (free acid)

2'-O-Methylguanosine-5'-triphosphate disodium salt

Description: 2'-O-Methylguanosine-5'-triphosphate disodium salt is a modified nucleotide used in biochemical research. It consists of guanosine with a methyl group attached to the 2'-oxygen of the ribose sugar and a triphosphate group. This compound is utilized to study RNA synthesis, nucleotide interactions, and the effects of methylation in biological processes. As a disodium salt, it is water-soluble, making it suitable for various biological and biochemical assays.
CAT: BRP-01331
Molecular Formula: C11H16N5Na2O14P3
Molecular Weight: 581.17
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Storage: Store at -20 °C
IUPAC Name: disodium;((2R,3R,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl dihydrogen triphosphate
Synonyms: 2'-(O-Methyl)-Guanosine 5'-triphosphate disodium salt; 2'-O-Methylguanosine 5'-(tetrahydrogen triphosphate); 2'-O-Methyl-GTP; 2'-O-Methylguanosine triphosphate; 2'-O-Me-GTP
Related CAS: 61556-44-3 (free acid)

2'-O-Methyluridine-5'-triphosphate disodium salt

Description: 2'-O-Methyluridine-5'-triphosphate disodium salt is a nucleotide analog commonly used in biochemistry research. It can be used as a substrate for RNA polymerases or as a terminator analog in RNA synthesis reactions. Its effectiveness as an antiviral and antitumor agent is also being investigated.
CAT: BRP-01332
Molecular Formula: C10H15N2Na2O15P3
Molecular Weight: 542.13
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Storage: Store at -20 °C
InChIKey: UNWQAQYAFNLTDC-BAZBJWKESA-L
CanonicalSMILES: [Na].[Na].O=C1C=CN(C(=O)N1)C2OC(COP(=O)(O)OP(=O)(O)OP(=O)(O)O)C(O)C2OC
IUPAC Name: disodium;((2R,3R,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl dihydrogen triphosphate
InChI: InChI=1S/C10H17N2O15P3.2Na/c1-23-8-7(14)5(25-9(8)12-3-2-6(13)11-10(12)15)4-24-29(19,20)27-30(21,22)26-28(16,17)18;;/h2-3,5,7-9,14H,4H2,1H3,(H,19,20)(H,21,22)(H,11,13,15)(H2,16,17,18);;/q;2*+1/p-2/t5-,7-,8-,9-;;/m1../s1
Synonyms: 2'-(O-Methyl)-Uridine 5'-triphosphate disodium salt; 2'-OMe-UTP disodium salt; Uridine, 2'-O-methyl-, 5'-(tetrahydrogen triphosphate), sodium salt (1:2); 2'-methoxy-UTP disodium salt; 2'-O-Methyluridine 5'-(tetrahydrogen triphosphate) disodium salt; 2'-O-Methyl-UTP disodium salt
Related CAS: 143028-99-3 (free acid)

2'-Deoxy-2'-fluorouridine-5'-triphosphate trilithium salt

Description: 2'-Deoxy-2'-fluorouridine-5'-triphosphate trilithium salt is a vital compound in biomedicine used for various research purposes. It serves as a nucleotide analog that incorporates into DNA during synthesis, aiding in the study of DNA replication, repair, and mutagenesis. This compound can also be utilized in the development of antiviral drugs targeting RNA viruses such as hepatitis C and HIV.
CAT: BRP-01495
Molecular Formula: C9H11FLi3N2O14P3
Molecular Weight: 503.93
Purity: ≥97%
Appearance: Clear colorless Liquid
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Storage: Store at -20 °C
InChIKey: PFCPHBRAVUMWNK-LLWADOMFSA-K
CanonicalSMILES: [Li+].[Li+].[Li+].C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)([O-])OP(=O)([O-])OP(=O)(O)[O-])O)F
IUPAC Name: trilithium;[[[(2R,3R,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-4-fluoro-3-hydroxyoxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphoryl] hydrogen phosphate
InChI: InChI=1S/C9H14FN2O14P3.3Li/c10-6-7(14)4(24-8(6)12-2-1-5(13)11-9(12)15)3-23-28(19,20)26-29(21,22)25-27(16,17)18;;;/h1-2,4,6-8,14H,3H2,(H,19,20)(H,21,22)(H,11,13,15)(H2,16,17,18);;;/q;3*+1/p-3/t4-,6-,7-,8-;;;/m1.../s1
Synonyms: 2'-F-dUTP Lithium Salt; 2'-Deoxy-2'-fluorouridine 5'-(tetrahydrogen triphosphate) trilithium salt; 2'-Fluoro UTP trilithium salt; 2'-Fluoro-2'-deoxyuridine 5'-triphosphate trilithium salt; 2'-Fluoro-2'-deoxyuridine triphosphate trilithium salt; 2'-Fluoro-dUTP trilithium salt; 2'-Fluorodeoxy-UTP trilithium salt
Related CAS: 66840-02-6 (free acid)

N6-Me-ATP trisodium salt

Description: N6-Me-ATP trisodium salt is a modified nucleotide where a methyl group is attached to the nitrogen at the 6th position of the adenine base. It is used in various biochemical applications, including studies on enzyme kinetics, nucleotide binding assays, and as a substrate for certain kinase reactions. The trisodium salt form ensures solubility and stability in aqueous solutions, making it suitable for experimental and research purposes.
CAT: BRP-01496
Molecular Formula: C11H15N5Na3O13P3
Molecular Weight: 587.15
Purity: ≥97%
Appearance: Clear colorless liquid
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Storage: Store at -20 °C
InChIKey: HBLZVYQIAJLSKJ-MTQUBGKESA-K
CanonicalSMILES: CNC1=C2C(=NC=N1)N(C=N2)C3C(C(C(O3)COP(=O)([O-])OP(=O)([O-])OP(=O)(O)[O-])O)O.[Na+].[Na+].[Na+]
IUPAC Name: trisodium;[[[(2R,3S,4R,5R)-3,4-dihydroxy-5-[6-(methylamino)purin-9-yl]oxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphoryl] hydrogen phosphate
InChI: InChI=1S/C11H18N5O13P3.3Na/c1-12-9-6-10(14-3-13-9)16(4-15-6)11-8(18)7(17)5(27-11)2-26-31(22,23)29-32(24,25)28-30(19,20)21;;;/h3-5,7-8,11,17-18H,2H2,1H3,(H,22,23)(H,24,25)(H,12,13,14)(H2,19,20,21);;;/q;3*+1/p-3/t5-,7-,8-,11-;;;/m1.../s1
Synonyms: N6-Me-ATP.3Na; N6-Methyl ATP trisodium salt; m6A trisodium salt; N6-Methyladenosine-5'-triphosphate trisodium salt; m6ATP trisodium salt; Adenosine, N-methyl-, 5'-(tetrahydrogen triphosphate), trisodium salt; N-Methyladenosine 5'-(tetrahydrogen triphosphate) trisodium salt; 6-N-Methyladenosine 5'-triphosphate trisodium salt; 6-Me-ATP trisodium
Related CAS: 3130-39-0 (free acid)

5-ap-2'-dUTP trisodium salt

Description: 5-ap-2'-dUTP trisodium salt is a C5-modified nucleotide that can be incorporated into DNA nanoparticles (DNPs) for the delivery of photosensitizers.
CAT: BRP-01497
Molecular Formula: C12H15N3Na3O14P3
Molecular Weight: 587.15
Purity: ≥97%
Appearance: Colorless to slightly yellow liquid
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Storage: Store at -20 °C
InChIKey: KBEOGKSFRATPCV-SDZJWQATSA-K
Solubility: Soluble in Water
CanonicalSMILES: [Na].[Na].[Na].O=C1NC(=O)N(C=C1C#CCN)C2OC(COP(=O)(O)OP(=O)(O)OP(=O)(O)O)C(O)C2
IUPAC Name: trisodium;((2R,3S,5R)-5-(5-(3-aminoprop-1-yn-1-yl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3-hydroxytetrahydrofuran-2-yl)methyl hydrogen triphosphate
InChI: InChI=1S/C12H18N3O14P3.3Na/c13-3-1-2-7-5-15(12(18)14-11(7)17)10-4-8(16)9(27-10)6-26-31(22,23)29-32(24,25)28-30(19,20)21;;;/h5,8-10,16H,3-4,6,13H2,(H,22,23)(H,24,25)(H,14,17,18)(H2,19,20,21);;;/q;3*+1/p-3/t8-,9+,10+;;;/m0.../s1
Synonyms: 5-(3-Amino-1-propyn-1-yl)-2'-deoxyuridine 5'-(Tetrahydrogen Triphosphate) trisodium salt; 5-Propargylamino-dUTP trisodium salt; 5-Propargylamino-2'-deoxyuridine-5'-Triphosphate trisodium salt; 5-(3-Amino-1-propyn-1-yl)-2'-deoxyuridine 5'-triphosphate sodium salt; 5-PA-dUTP trisodium salt
Related CAS: 179101-49-6 (free acid)

2-Fluoroadenosine-5'-monophosphate

Description: 2-Fluoroadenosine-5'-monophosphate is a valuable tool in biochemical and pharmacological research. Its modified structure allows scientists to study the effects of fluorine substitution on nucleotide function, enzyme interactions, and potential therapeutic applications in cancer and antiviral treatments.
CAT: BRP-01500
CAS: 1492-60-0
Molecular Formula: C10H13FN5O7P
Molecular Weight: 365.21
Purity: ≥95%
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Storage: Store at 2-8 °C, sealed storage, away from moisture and light
Density: 2.39±0.1 g/cm3
Boiling Point: 864.2±75.0 °C at 760 mmHg
InChIKey: GIUYCYHIANZCFB-UUOKFMHZSA-N
CanonicalSMILES: C1=NC2=C(N=C(N=C2N1C3C(C(C(O3)COP(=O)(O)O)O)O)F)N
IUPAC Name: [(2R,3S,4R,5R)-5-(6-amino-2-fluoropurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate
InChI: InChI=1S/C10H13FN5O7P/c11-10-14-7(12)4-8(15-10)16(2-13-4)9-6(18)5(17)3(23-9)1-22-24(19,20)21/h2-3,5-6,9,17-18H,1H2,(H2,12,14,15)(H2,19,20,21)/t3-,5-,6-,9-/m1/s1
Synonyms: 2-Fluoro-5'-adenylic acid; Adenosine, 2-fluoro-, 5'-(dihydrogen phosphate); 2-Fluoro-AMP; 2-Fluoroadenine-9β-D-ribofuranoside 5'-monophosphate; 2-Fluoroadenosine monophosphate
Related CAS: 71261-44-4 (homopolymer)
* Only for research. Not suitable for any diagnostic or therapeutic use.

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