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GMP Tris Salt
Description: GMP Tris Salt is guanosine 5'-monophosphate (GMP), a nucleotide consisting of guanosine linked to a single phosphate group at the 5' position of the ribose sugar. GMP is essential in molecular biology and biochemistry as a precursor for RNA synthesis and as a substrate in enzymatic reactions involving GMP-binding proteins. Its use spans from fundamental research to practical applications in biotechnology and pharmaceutical development.
CAT: BRP-01206
MF: C10H14N5O8P (free acid)
MF: 363.22 (free acid)
Purity: ≥97% by HPLC
Appearance: Clear colorless to yellow 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 dihydrogen phosphate;2-amino-2-(hydroxymethyl)propane-1,3-diol
Synonyms: Guanosine 5'-monohosphate tris salt; 5'-Guanylic acid tris salt; Guanosine monophosphate tris salt; Guanosine 5'-phosphate tris salt; Guanosine 5'-(dihydrogen phosphate) tris salt
Related CAS: 85-32-5 (free base)
Guanosine 5'-tetraphosphate, tetrasodium salt
Description: Guanosine 5'-tetraphosphate, tetrasodium salt, is a chemical compound consisting of guanosine linked to four phosphate groups at the 5' position of the ribose sugar. In its tetrasodium salt form, the phosphate groups are complexed with sodium ions to enhance stability and solubility. This compound is utilized in biochemical and biotechnological research, particularly in studies involving nucleotide signaling, enzymatic reactions, and as a substrate or cofactor in various cellular processes. Its properties make it valuable in understanding RNA and DNA metabolism, as well as in applications ranging from molecular biology to pharmaceutical development.
CAT: BRP-01207
MF: C10H13Na4N5O17P4
MF: 691.09
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Storage: Store at -20 °C
InChIKey: QXHMFINSYFFJAG-ZVQJTLEUSA-J
CanonicalSMILES: [Na].[Na].[Na].[Na].O=C1N=C(N)NC2=C1N=CN2C3OC(COP(=O)(O)OP(=O)(O)OP(=O)(O)OP(=O)(O)O)C(O)C3O
IUPAC Name: tetrasodium;((2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl hydrogen tetraphosphate
InChI: InChI=1S/C10H17N5O17P4.4Na/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(29-9)1-28-34(22,23)31-36(26,27)32-35(24,25)30-33(19,20)21;;;;/h2-3,5-6,9,16-17H,1H2,(H,22,23)(H,24,25)(H,26,27)(H2,19,20,21)(H3,11,13,14,18);;;;/q;4*+1/p-4/t3-,5-,6-,9-;;;;/m1..../s1
Synonyms: Guanosine 5'-tetraphosphate, sodium salt; GrP4.Na4; Guanosine 5'-(pentahydrogen tetraphosphate) tetrasodium salt; Guanosine tetraphosphate tetrasodium salt
Related CAS: 3369-85-5 (free acid) ; 1402828-40-3 (pentasodium salt) ; 1434288-53-5 (tetraammonium salt)
Inosine 5'-tetraphosphate, tetrasodium salt
Description: Inosine 5'-tetraphosphate, tetrasodium salt, is a chemical compound composed of inosine linked to four phosphate groups at the 5' position of the ribose sugar. In its tetrasodium salt form, the phosphate groups are complexed with sodium ions to enhance stability and solubility. This compound is used primarily in biochemical and biotechnological research, where it serves various roles such as a substrate or cofactor in enzymatic reactions, particularly those involving nucleotide metabolism and signaling pathways. Its applications extend to studies of RNA and DNA structure, function, and modification, making it a valuable tool in molecular biology and related fields of research.
CAT: BRP-01208
CAS: 14356-95-7
MF: C10H11N4Na4O14P3
MF: 596.09
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Storage: Store at -20 °C
InChIKey: KOPCSZLOQBLCSK-KWIZKVQNSA-J
CanonicalSMILES: C1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])[O-])O)O.[Na+].[Na+].[Na+].[Na+]
IUPAC Name: tetrasodium;[[[(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-1H-purin-9-yl)oxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphoryl] phosphate
InChI: InChI=1S/C10H15N4O14P3.4Na/c15-6-4(1-25-30(21,22)28-31(23,24)27-29(18,19)20)26-10(7(6)16)14-3-13-5-8(14)11-2-12-9(5)17;;;;/h2-4,6-7,10,15-16H,1H2,(H,21,22)(H,23,24)(H,11,12,17)(H2,18,19,20);;;;/q;4*+1/p-4/t4-,6-,7-,10-;;;;/m1..../s1
Synonyms: 5'-ITP.Na4; Inosine 5'-(tetrahydrogen triphosphate), sodium salt (1:4); Inosine 5'-(tetrahydrogen triphosphate), tetrasodium salt; Inosine 5'-triphosphate sodium salt; ITP tetrasodium salt; Inosine triphosphate tetrasodium salt
Related CAS: 132-06-9 (free acid) ; 35908-31-7 (trisodium salt)
ATP ammonium salt
Description: ATP (Adenosine 5'-triphosphate) ammonium salt is a stabilized form of ATP where the nucleotide is complexed with ammonium ions. It is widely used in biochemical research due to its enhanced solubility and utility in enzymatic assays. ATP serves as a crucial energy carrier in cells, powering processes like muscle contraction, biosynthesis, and active transport. Its role in phosphorylation reactions also makes it essential for studying cellular metabolism and signaling pathways.
CAT: BRP-01209
CAS: 79670-88-5
MF: C10H16N5O13P3 (free acid)
MF: 507.18 (free acid)
Purity: ≥97% by HPLC
Appearance: Clear colorless liquid
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: [[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate;ammonium salt
Synonyms: Adenosine-5'-triphosphate, ammonium salt; Adenosine triphosphate, ammonium salt; Adenosine, 5'-(tetrahydrogen triphosphate), ammonium salt; 5'-ATP ammonium salt
Related CAS: 56-65-5 (free acid)
ATP lithium salt
Description: ATP (Adenosine 5'-triphosphate) lithium salt is a stabilized form of ATP where the nucleotide is complexed with lithium ions. It is widely used in biochemical research due to its enhanced solubility and utility in enzymatic assays. ATP serves as a crucial energy carrier in cells, powering processes like muscle contraction, biosynthesis, and active transport. Its role in phosphorylation reactions also makes it essential for studying cellular metabolism and signaling pathways.
CAT: BRP-01210
CAS: 16610-49-4
MF: C10H16N5O13P3 (free acid)
MF: 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: lithium;[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate
Synonyms: Adenosine 5'-triphosphate, lithium salt; Adenosine triphosphate, lithium salt; Adenosine, 5'-(tetrahydrogen triphosphate), lithium salt; 5'-ATP lithium salt
Related CAS: 56-65-5 (free acid)
GTP ammonium salt
Description: GTP (Guanosine 5'-triphosphate) ammonium salt is a compound where GTP, a nucleotide composed of guanine, ribose sugar, and three phosphate groups, is stabilized and solubilized by complexing with ammonium ions. This form of GTP is utilized in biochemical and molecular biology research for its improved properties in aqueous solutions, making it suitable for enzymatic assays and studies involving protein synthesis and cellular signaling pathways. GTP ammonium salt is essential for understanding fundamental biological processes and exploring therapeutic targets related to nucleotide metabolism and signal transduction mechanisms in cells.
CAT: BRP-01211
MF: C10H16N5O14P3 (free acid)
MF: 523.18 (free acid)
Purity: ≥97% by HPLC
Appearance: Clear colorless liquid
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: [[(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate;ammonium salt
Synonyms: Guanosine 5'-triphosphate, ammonium salt; 5'-GTP ammonium Salt; Ammonium GTP; Guanosine 5'-(tetrahydrogen triphosphate), ammonium salt (1:x); Guanosine 5'-triphosphate ammonium salt; Guanosine triphosphate ammonium salt
Related CAS: 86-01-1 (free acid)
GTP potassium salt
Description: GTP (Guanosine 5'-triphosphate) potassium salt is a compound where GTP, a nucleotide composed of guanine, ribose sugar, and three phosphate groups, is stabilized and solubilized by complexing with potassium ions. This form of GTP is utilized in biochemical and molecular biology research for its improved properties in aqueous solutions, making it suitable for enzymatic assays and studies involving protein synthesis and cellular signaling pathways. GTP potassium salt is essential for understanding fundamental biological processes and exploring therapeutic targets related to nucleotide metabolism and signal transduction mechanisms in cells.
CAT: BRP-01212
MF: C10H16N5O14P3 (free acid)
MF: 523.18 (free acid)
Purity: ≥97% by HPLC
Appearance: Clear colorless to faint yellow liquid
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| -- | -- | -- |
Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: potassium;[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate
Synonyms: Guanosine 5'-triphosphate, potassium salt; 5'-GTP potassium Salt; Potassium GTP; Guanosine 5'-(tetrahydrogen triphosphate), potassium salt (1:x); Guanosine 5'-triphosphate potassium salt; Guanosine triphosphate potassium salt
Related CAS: 86-01-1 (free acid)
UTP potassium salt
Description: UTP (Uridine 5'-triphosphate) potassium salt is a form of UTP where the nucleotide is stabilized and solubilized by complexing with potassium ions. This salt is widely used in biochemical and molecular biology research for its enhanced stability and solubility in aqueous solutions. UTP is essential for RNA synthesis, serving as a substrate for RNA polymerases during transcription and participating in various RNA modification processes. UTP potassium salt is crucial for studying nucleic acid metabolism, gene expression regulation, and other cellular processes where RNA plays a pivotal role. Its use facilitates the investigation of RNA-related mechanisms in both basic biological research and pharmaceutical development contexts.
CAT: BRP-01213
MF: C9H15N2O15P3 (free acid)
MF: 484.14 (free acid)
Purity: ≥97% by HPLC
Appearance: Clear colorless to faint yellow liquid
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: potassium;[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate
Synonyms: Uridine 5'-triphosphate, potassium salt; Uridine 5'-(tetrahydrogen triphosphate) potassium salt; Uridine 5'-trisphosphate potassium salt (1:x); 5'-UTP potassium salt; Uridine triphosphate, potassium salt
Related CAS: 63-39-8 (free acid)
GTP lithium salt
Description: GTP (Guanosine 5'-triphosphate) lithium salt is a compound where GTP, a nucleotide composed of guanine, ribose sugar, and three phosphate groups, is stabilized and solubilized by complexing with lithium ions. This form of GTP is utilized in biochemical and molecular biology research for its improved properties in aqueous solutions, making it suitable for enzymatic assays and studies involving protein synthesis and cellular signaling pathways. GTP lithium salt is essential for understanding fundamental biological processes and exploring therapeutic targets related to nucleotide metabolism and signal transduction mechanisms in cells.
CAT: BRP-01214
CAS: 96012-99-6
MF: C10H16N5O14P3 (free acid)
MF: 523.18 (free acid)
Purity: ≥97% by HPLC
Appearance: Clear colorless to faint yellow liquid
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| -- | -- | -- |
Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: lithium;[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate
Synonyms: Guanosine 5'-triphosphate, lithium salt; 5'-GTP lithium Salt; Lithium GTP; Guanosine 5'-(tetrahydrogen triphosphate), lithium salt (1:x); Guanosine triphosphate lithium salt; Guanosine 5'-(tetrahydrogen triphosphate), lithium salt
Related CAS: 86-01-1 (free acid)
UTP lithium salt
Description: UTP (Uridine 5'-triphosphate) lithium salt is a form of UTP where the nucleotide is stabilized and solubilized by complexing with lithium ions. This salt is widely used in biochemical and molecular biology research for its enhanced stability and solubility in aqueous solutions. UTP is essential for RNA synthesis, serving as a substrate for RNA polymerases during transcription and participating in various RNA modification processes. UTP lithium salt is crucial for studying nucleic acid metabolism, gene expression regulation, and other cellular processes where RNA plays a pivotal role. Its use facilitates the investigation of RNA-related mechanisms in both basic biological research and pharmaceutical development contexts.
CAT: BRP-01215
CAS: 27821-52-9
MF: C9H15N2O15P3 (free acid)
MF: 484.14 (free acid)
Purity: ≥97% by HPLC
Appearance: Clear colorless to faint yellow liquid
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| -- | -- | -- |
Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: lithium;[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate
Synonyms: Uridine 5'-triphosphate, lithium salt; Uridine 5'-(tetrahydrogen triphosphate) lithium salt; Uridine 5'-trisphosphate lithium salt (1:x); 5'-UTP lithium salt; Uridine triphosphate, lithium salt
Related CAS: 63-39-8 (free acid)
UTP ammonium salt
Description: UTP (Uridine 5'-triphosphate) ammonium salt is a form of UTP where the nucleotide is stabilized and solubilized by complexing with ammonium ions. This salt is widely used in biochemical and molecular biology research for its enhanced stability and solubility in aqueous solutions. UTP is essential for RNA synthesis, serving as a substrate for RNA polymerases during transcription and participating in various RNA modification processes. UTP ammonium salt is crucial for studying nucleic acid metabolism, gene expression regulation, and other cellular processes where RNA plays a pivotal role. Its use facilitates the investigation of RNA-related mechanisms in both basic biological research and pharmaceutical development contexts.
CAT: BRP-01216
CAS: 96013-00-2
MF: C9H15N2O15P3 (free acid)
MF: 484.14 (free acid)
Purity: ≥97% by HPLC
Appearance: Clear colorless liquid
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| -- | -- | -- |
Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate;ammonium salt
Synonyms: Uridine 5'-triphosphate, ammonium salt; Uridine 5'-(tetrahydrogen triphosphate) ammonium salt; Uridine 5'-trisphosphate ammonium salt (1:x); 5'-UTP ammonium salt; Uridine triphosphate, ammonium salt
Related CAS: 63-39-8 (free acid)
CTP ammonium salt
Description: CTP (Cytidine 5'-triphosphate) ammonium salt is a compound where CTP, a nucleotide consisting of cytidine, ribose sugar, and three phosphate groups, is stabilized and solubilized by complexing with ammonium ions. This form of CTP is particularly useful in biochemical and molecular biology research due to its enhanced stability and solubility in aqueous solutions. CTP ammonium salt is crucial for studying RNA synthesis and metabolism, serving as a substrate for RNA polymerases during transcription. It is also involved in various biochemical pathways where cytidine triphosphate is a necessary cofactor or substrate. This compound enables researchers to investigate RNA-related processes, such as mRNA production and modification, RNA turnover, and regulatory mechanisms in gene expression. Its use in experiments helps elucidate the molecular mechanisms underlying cellular functions and disease processes.
CAT: BRP-01217
MF: C9H16N3O14P3 (free acid)
MF: 483.16 (free acid)
Purity: ≥97% by HPLC
Appearance: Clear colorless liquid
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: [[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate;ammonium salt
Synonyms: Cytidine-5'-triphosphate, ammonium salt; Cytidine 5'-(tetrahydrogen triphosphate), ammonium salt (1:x); 5'-CTP ammonium salt; Cytidine triphosphate, ammonium salt
Related CAS: 65-47-4 (free acid)
CTP lithium salt
Description: CTP (Cytidine 5'-triphosphate) lithium salt is a compound where CTP, a nucleotide consisting of cytidine, ribose sugar, and three phosphate groups, is stabilized and solubilized by complexing with lithium ions. This form of CTP is particularly useful in biochemical and molecular biology research due to its enhanced stability and solubility in aqueous solutions. CTP lithium salt is crucial for studying RNA synthesis and metabolism, serving as a substrate for RNA polymerases during transcription. It is also involved in various biochemical pathways where cytidine triphosphate is a necessary cofactor or substrate. This compound enables researchers to investigate RNA-related processes, such as mRNA production and modification, RNA turnover, and regulatory mechanisms in gene expression. Its use in experiments helps elucidate the molecular mechanisms underlying cellular functions and disease processes.
CAT: BRP-01218
MF: C9H16N3O14P3 (free acid)
MF: 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: lithium;[[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate
Synonyms: Cytidine 5'-triphosphate, lithium salt; Cytidine 5'-(tetrahydrogen triphosphate), lithium salt (1:x); 5'-CTP lithium salt; Cytidine triphosphate, lithium salt
Related CAS: 65-47-4 (free acid)
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
MF: C9H16N3O14P3 (free acid)
MF: 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
MF: C10H16N5O13P3 (free acid)
MF: 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
MF: C10H15N5O11P2 (free acid)
MF: 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
MF: C10H15N5O11P2 (free acid)
MF: 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
MF: C13H17N7O10P2
MF: 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
MF: C13H15N7Na2O10P2
MF: 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
MF: C16H30N6O11P2
MF: 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)
