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2'-Modified Nucleotides
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(10/10) Base Protected Nucleotides
(16/16) Dinucleosides Phosphate
(76/76) Fluorescent Nucleotides
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(90/90) Other Protected Nucleotides
(50/50) Phosphate Modified Nucleotides (93/93) Ribonucleotides
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(64/64) 3'-Modified Nucleotides
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(76/76) Fluorescent Nucleotides
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Cy3-CTP sodium salt
Description: Cy3-CTP Sodium Salt is a derivative of cytidine triphosphate (CTP) with a Cy3 fluorophore attached to the 5-position of the pyrimidine ring. Cy3 is a cyanine dye commonly used as a fluorescent label in molecular biology applications such as fluorescence in situ hybridization (FISH), microarray analysis, and RNA labeling. The sodium salt form enhances its solubility and stability, making it suitable for enzymatic reactions involving RNA synthesis or modification, where fluorescently labeled nucleotides are required for visualization or detection purposes.
CAT: BRP-00687
MF: C43H57N6O21P3S2 (free acid)
MF: 1151.00 (free acid)
Purity: >95%
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles and avoid direct sunlight
IUPAC Name: sodium;(E)-2-((E)-3-(1-(6-(((E)-3-(4-amino-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(((hydroxy((hydroxy(phosphonooxy)phosphoryl)oxy)phosphoryl)oxy)methyl)tetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-5-yl)allyl)amino)-6-oxohexyl)-3,3-dimethyl-5-sulfo-3H-indol-1-ium-2-yl)allylidene)-1-ethyl-3,3-dimethylindoline-5-sulfonate
Synonyms: Cyanine 3-AA-CTP sodium salt
Related CAS: 2478618-70-9 (free acid)
5-Me-UTP Sodium Salt
Description: 5-Me-UTP Sodium Salt is a derivative of uridine triphosphate (UTP) with a methyl group attached to the 5-position of the uracil base. It is commonly used in enzymatic reactions for RNA synthesis, where the 5-methyl modification can confer altered biochemical properties to the resulting RNA molecule. The sodium salt form ensures its solubility and stability, making it suitable for various molecular biology techniques such as RNA labeling, structural studies, and functional assays.
CAT: BRP-00688
CAS: 24905-72-4
MF: C10H17N2O15P3 (free acid)
MF: 498.17 (free acid)
Purity: >98%
| Size | Price | Stock | Quantity |
|---|---|---|---|
| -- | -- | -- |
Storage: Store at -20 °C, Avoid direct sunlight and keep in dry place
IUPAC Name: sodium;((2R,3S,4R,5R)-3,4-dihydroxy-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate
Synonyms: Uridine 5'-(tetrahydrogen triphosphate), 5-methyl-, sodium salt (1:x); Uridine, 5-methyl-, 5'-(tetrahydrogen triphosphate), sodium salt; 5-Methyluridine 5'-(tetrahydrogen triphosphate) sodium salt; 5-Methyl-UTP sodium salt; 5-Methyluridine 5'-triphosphate sodium salt; Ribothymidine 5'-triphosphate sodium salt
Related CAS: 23198-01-8 (free acid) ; 1801968-79-5 (tetrasodium salt)
2-Thio-UTP sodium salt
Description: 2-Thio-UTP Sodium Salt is a derivative of uridine triphosphate (UTP) where a thiol (sulfhydryl) group is substituted for the oxygen at the 2-position of the ribose sugar moiety. The thiol group confers unique reactivity, making it useful in various biochemical applications such as RNA labeling, RNA-protein crosslinking, and RNA structural probing. The sodium salt form enhances its solubility and stability, facilitating its use in enzymatic reactions for RNA synthesis or modification.
CAT: BRP-00689
MF: C9H15N2O14P3S (free acid)
MF: 500.21 (free acid)
Purity: >98%
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|---|---|---|---|
| -- | -- | -- |
Storage: Store at -20 °C, Always avoid freeze-thaw cycles
Synonyms: ((2R,3S,4R,5R)-3,4-dihydroxy-5-(4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate sodium salt; 2-Thiouridine 5'-(tetrahydrogen triphosphate) sodium salt; 2-Thiouridine 5'-triphosphate sodium salt; 2-thioUTP sodium salt; 2-thio-1-β-D-ribofuranosyl(3H)pyrimidine-2,4-dione 5'-triphosphate sodium salt; 1-[5-O-(Hydroxy{[hydroxy(phosphonooxy)phosphoryl]oxy}phosphoryl)-β-D-ribofuranosyl]-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone sodium salt
Related CAS: 35763-29-2 (free acid) ; 1343364-70-4 (tetrasodium salt)
Biotin-16-UTP sodium salt
Description: Biotin-16-UTP Sodium Salt is a derivative of uridine triphosphate (UTP) with a biotin moiety attached to the 5-position of the ribose sugar moiety via a linker arm. Biotin is a small molecule that exhibits strong, specific binding to avidin or streptavidin, making it a popular choice for labeling nucleic acids in various molecular biology applications such as RNA labeling, affinity purification, and detection assays. The sodium salt form improves its solubility and stability, enabling efficient incorporation into RNA molecules during enzymatic reactions.
CAT: BRP-00690
MF: C32H52N7O19P3S (free acid)
MF: 963.78 (free acid)
Purity: >95%
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|---|---|---|---|
| -- | -- | -- |
Storage: Store at -20 °C, Always avoid freeze-thaw cycles and avoid direct sunlight
IUPAC Name: sodium;((2R,3S,4R,5R)-5-(2,4-dioxo-5-((E)-3-(4-(6-(5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)hexanamido)butanamido)prop-1-en-1-yl)-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate
Synonyms: Biotin-16-uridine-5'-triphosphate, sodium salt; Biotin-16-AA-UTP sodium salt; Biotin-16-Aminoallyluridine-5'-Triphosphate sodium salt
Related CAS: 280549-77-1 (free acid) ; 186033-13-6 (tetralithium salt）
CTPαS sodium salt
Description: CTPαS sodium salt is a modified form of cytidine triphosphate (CTP) where the oxygen at the α-phosphate position is replaced by a sulfur atom. This modification alters the properties of CTP, potentially affecting its biological activity and interactions with enzymes. It finds utility in biochemical research, particularly in studies related to RNA synthesis, RNA modification, and enzymology. The sodium salt form enhances its solubility and stability, facilitating its use in enzymatic reactions or structural studies.
CAT: BRP-00691
MF: C9H16N3O13P3S (free acid)
MF: 499.21 (free acid)
Purity: >98%
Appearance: Colorless to light yellow liquid
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: sodium;[[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphinothioyl] phosphono hydrogen phosphate
Synonyms: Cytidine, 5'→P''-ester with thiotriphosphoric acid sodium salt; Cytidine-5'-O-(1-thiotriphosphate) sodium salt; CTP-αS sodium salt; Cytidine-5'-(α-thio)-triphosphate, sodium salt (1:1 Mixture of Rp and Sp isomers); Alpha Thiol CTP (1-Thio-CTP) sodium salt
Related CAS: 110972-40-2 (free acid)
UDP-glucosamine Disodium Salt
Description: UDP-glucosamine disodium salt is a nucleotide derivative containing uridine diphosphate (UDP) linked to glucosamine. It serves as a key precursor in the biosynthesis of various glycoconjugates, including glycoproteins, glycolipids, and peptidoglycans. This compound is crucial in cellular processes such as cell wall biosynthesis, protein glycosylation, and immune responses. The disodium salt form improves its solubility and bioavailability, making it suitable for biochemical studies and metabolic labeling experiments.
CAT: BRP-00692
CAS: 1355005-51-4
MF: C15H23N3Na2O16P2
MF: 609.28
Purity: >98%
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| -- | -- | -- |
Storage: Store at -20 °C, Avoid direct sunlight and keep in dry place
InChIKey: OYUJNUWEWMWPBM-CZILZAFRSA-L
CanonicalSMILES: C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)([O-])OP(=O)([O-])OC3C(C(C(C(O3)CO)O)O)N)O)O.[Na+].[Na+]
IUPAC Name: disodium;[(2R,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] phosphate
InChI: InChI=1S/C15H25N3O16P2.2Na/c16-8-11(23)9(21)5(3-19)32-14(8)33-36(28,29)34-35(26,27)30-4-6-10(22)12(24)13(31-6)18-2-1-7(20)17-15(18)25;;/h1-2,5-6,8-14,19,21-24H,3-4,16H2,(H,26,27)(H,28,29)(H,17,20,25);;/q;2*+1/p-2/t5-,6-,8-,9-,10-,11-,12-,13-,14-;;/m1../s1
Synonyms: Uridine 5'-(trihydrogen diphosphate), P'-(2-amino-2-deoxy-α-D-glucopyranosyl) ester, sodium salt (1:2); UDP-glucosamine (disodium); UDP-D-glucosamine Disodium Salt; UDP-N-glucosamine Disodium Salt; Uridine 5'-diphosphate glucosamine Disodium Salt; Uridine 5'-diphospho-2-amino-2-deoxy-α-D-glucopyranose Disodium Salt; Uridine diphosphate glucosamine Disodium Salt; Uridine diphosphoglucosamine Disodium Salt
Related CAS: 17479-04-8 (free acid)
O6-Me-GTP sodium salt
Description: O6-Me-GTP sodium salt is a modified form of guanosine triphosphate (GTP) with a methyl group attached to the O6 position of the guanine base. This modification alters the chemical properties of GTP, potentially influencing its interactions with enzymes and proteins involved in signal transduction, nucleic acid synthesis, and post-translational modifications. The sodium salt form enhances its solubility and stability, making it suitable for various biochemical applications, including enzymology studies and nucleotide analog screening assays.
CAT: BRP-00693
MF: C11H18N5O14P3
MF: 537.21 (free acid)
Purity: >98%
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| -- | -- | -- |
Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: sodium;((2R,3S,4R,5R)-5-(2-amino-6-methoxy-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate
Synonyms: 6-O-Methylguanosine 5'-triphosphate sodium salt; 6-O-Methylguanosine 5'-(tetrahydrogen triphosphate) sodium salt
Related CAS: 99404-63-4 (free acid)
5-Formyl-CTP sodium salt
Description: 5-Formyl-CTP sodium salt is a modified form of cytidine triphosphate (CTP) with a formyl group attached to the 5-position of the pyrimidine ring. This modification can mimic the structure of transition state analogs, making it useful in studies of enzyme mechanisms and inhibitor design. It can also serve as a substrate for enzymes involved in RNA modification and nucleotide metabolism. The sodium salt form improves its solubility and stability, enabling its use in biochemical assays and enzymatic reactions.
CAT: BRP-00694
MF: C10H16N3O15P3 (free acid)
MF: 511.17 (free acid)
Purity: >98%
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: sodium;((2R,3S,4R,5R)-5-(4-amino-5-formyl-2-oxopyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate
Synonyms: 5-Formylcytidine-5'-Triphosphate sodium salt; 5-fCTP sodium salt; 5-FoCTP sodium salt
Related CAS: 1428903-58-5 (free acid)
6-Fu-ATP Sodium Salt
Description: 6-Fu-ATP sodium salt is a modified form of adenosine triphosphate (ATP) with 6-Furfuryl (6-Fu) attached to the adenine base. This modification can affect the base-pairing properties of ATP and its interactions with enzymes involved in nucleic acid metabolism and signaling pathways. It is commonly used in biochemical and pharmacological studies, including investigations of DNA replication, repair, and synthesis of nucleotide analogs. The sodium salt form enhances its solubility and stability, making it suitable for various experimental applications.
CAT: BRP-00695
MF: C15H20N5O14P3 (free acid)
MF: 587.27 (free acid)
Purity: >98%
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Storage: Store at -20 °C, Avoid direct sunlight and keep in dry place
IUPAC Name: sodium;[[(2R,3S,4R,5R)-5-[6-(furan-2-ylmethylamino)purin-9-yl]-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate
Synonyms: N6-Furfuryladenosine-5'-O-triphosphate, sodium salt; N-(2-Furanylmethyl)adenosine 5'-(tetrahydrogen triphosphate) sodium salt; Kinetin triphosphate sodium salt; Kinetin triphosphate KTP sodium salt; N6-Furfuryl-ATP sodium salt
Related CAS: 1450894-16-2 (free acid)
Carboxyaminoimidazole ribotide sodium salt
Description: Carboxyaminoimidazole ribotide sodium salt, also known as CAIR, is an intermediate in the de novo purine biosynthesis pathway. It serves as a precursor for the synthesis of inosine monophosphate (IMP), an essential precursor for purine nucleotide synthesis. CAIR is involved in regulating cellular purine levels and is crucial for cell proliferation and nucleotide metabolism. The sodium salt form ensures its solubility and stability, facilitating its use in biochemical studies and metabolic labeling experiments.
CAT: BRP-00696
MF: C9H14N3O9P (free acid)
MF: 339.20 (free acid)
Purity: >95%
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Storage: Store at -20 °C, Avoid direct sunlight and keep in dry place
IUPAC Name: sodium;5-amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]imidazole-4-carboxylic acid
Synonyms: Carboxyaminoimidazole ribotide; 5-Amino-4-carboxyimidazole ribonucleotide sodium salt; Carboxy-AIR sodium salt; CAIR sodium salt; 5-Aminoimidazole-4-carboxylic acid-1-b-D-ribofuranose 5'-monophosphate sodium salt; 5-amino-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-((phosphonooxy)methyl)tetrahydrofuran-2-yl)-1H-imidazole-4-carboxylic acid sodium salt
Related CAS: 6001-14-5 (free acid)
6-Aza-UTP Ammonium Salt
Description: 6-Aza-UTP ammonium salt is a modified form of uridine triphosphate (UTP) with a 6-Aza moiety attached to the uracil base. This modification alters the base-pairing properties of UTP and can affect its interactions with enzymes involved in RNA synthesis and modification. It is utilized in various biochemical and molecular biology applications, including RNA labeling, structural studies, and enzymatic assays. The ammonium salt form improves its solubility and stability, making it suitable for experimental use.
CAT: BRP-00697
MF: C8H14N3O15P3 (free acid)
MF: 485.13 (free acid)
Purity: >95%
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Storage: Store at -20 °C, Avoid direct sunlight and keep in dry place
Synonyms: ((2R,3S,4R,5R)-5-(3,5-dioxo-4,5-dihydro-1,2,4-triazin-2(3H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate Ammonium Salt; 6-Azauridine 5'-triphosphoric acid Ammonium Salt
Related CAS: 6198-30-7 (free acid)
TFMU-ADPr Ammonium Salt
Description: TFMU-ADPr ammonium salt is a modified form of adenosine diphosphate ribose (ADPr) with TFMU modification. ADPr is a key molecule involved in the regulation of cellular processes such as DNA repair, gene expression, and calcium signaling. The TFMU modification can alter the chemical properties and biological activities of ADPr, potentially affecting its interactions with enzymes and proteins. The ammonium salt form enhances its solubility and stability, making it suitable for biochemical and pharmacological studies, including investigations of ADP-ribosylation pathways and enzyme mechanisms.
CAT: BRP-00698
MF: C25H26F3N5O16P2 (free acid)
MF: 771.44 (free acid)
Purity: >98%
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|---|---|---|---|
| -- | -- | -- |
Storage: Store at -20 °C, Avoid direct sunlight and keep in dry place
Synonyms: [[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2R,3S,4R,5R)-3,4-dihydroxy-5-[2-oxo-4-(trifluoromethyl)chromen-7-yl]oxyoxolan-2-yl]methyl hydrogen phosphate Ammonium Salt
Related CAS: 2412923-11-4 (free acid)
Quemliclustat
Description: Quemliclustat is a highly potent, reversible and selective CD73 (an ecto-nucleotidase) inhibitor with Ki of 5 pM.
CAT: BRP-00699
CAS: 2105904-82-1
MF: C20H24ClFN4O9P2
MF: 580.8
Purity: 98% by HPLC
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|---|---|---|---|
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Storage: Store at -20 °C, Avoid direct sunlight and keep in dry place
Density: 1.86±0.1 g/cm3 (Predicted)
Boiling Point: 867.0±75.0 °C at 760 mmHg
InChIKey: MFYLCAMJNGIULC-KCVUFLITSA-N
Solubility: Soluble in DMSO
CanonicalSMILES: CC(C1=CC=CC=C1F)NC2=CC(=NC3=C2C=NN3C4C(C(C(O4)COP(=O)(CP(=O)(O)O)O)O)O)Cl
IUPAC Name: [[(2R,3S,4R,5R)-5-[6-chloro-4-[[(1S)-1-(2-fluorophenyl)ethyl]amino]pyrazolo[3,4-b]pyridin-1-yl]-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]methylphosphonic acid
InChI: InChI=1S/C20H24ClFN4O9P2/c1-10(11-4-2-3-5-13(11)22)24-14-6-16(21)25-19-12(14)7-23-26(19)20-18(28)17(27)15(35-20)8-34-37(32,33)9-36(29,30)31/h2-7,10,15,17-18,20,27-28H,8-9H2,1H3,(H,24,25)(H,32,33)(H2,29,30,31)/t10-,15+,17+,18+,20+/m0/s1
Synonyms: AB-680; AB 680; AB680
-sodium-salt.gif)
ATPαS (Rp isomer) sodium salt
Description: ATPαS (Rp isomer) sodium salt is a stereoisomer of adenosine 5'-O-(1-thiotriphosphate) (ATPαS), where the sulfur atom replaces one of the non-bridging oxygen atoms at the α-phosphate position in the Rp configuration. This modification alters the molecule's interaction with enzymes and proteins, making it a valuable tool in studying ATP-dependent processes, enzyme mechanisms, and signal transduction pathways. The sodium salt form improves its solubility and stability for experimental use.
CAT: BRP-00700
MF: C10H16N5O12P3S (free acid)
MF: 523.24 (free acid)
Purity: >98%
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|---|---|---|---|
| -- | -- | -- |
Storage: Store at -20 °C, Always avoid freeze-thaw cycles
Synonyms: Adenosine, 5'→P''-ester with [P''(R)]-thiotriphosphoric acid sodium salt; Adenosine, 5'→P''-ester with thiotriphosphoric acid ((HO)2P(O)OP(O)(OH)OP(S)(OH)2), (R)-, sodium salt; (R)-ATPαS sodium salt; Adenosine-5'-O-(1-thiotriphosphate), Rp-isomer sodium salt; Rp-ATP-alpha-S sodium salt
Related CAS: 58976-49-1 (free acid)
-sodium-salt.gif)
ATPαS (Sp isomer) sodium salt
Description: ATPαS (Sp isomer) sodium salt is another stereoisomer of adenosine 5'-O-(1-thiotriphosphate) (ATPαS), where the sulfur atom replaces one of the non-bridging oxygen atoms at the α-phosphate position in the Sp configuration. This modification affects the molecule's interaction with enzymes differently compared to the Rp isomer. It is useful for dissecting the stereospecificity of enzyme mechanisms and studying ATP-dependent biochemical pathways. The sodium salt form enhances its solubility and stability.
CAT: BRP-00701
MF: C10H16N5O12P3S (free acid)
MF: 523.24 (free acid)
Purity: >98%
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|---|---|---|---|
| -- | -- | -- |
Storage: Store at -20 °C, Always avoid freeze-thaw cycles
Synonyms: Adenosine, 5'→P''-ester with [P''(S)]-thiotriphosphoric acid sodium salt; Adenosine, 5'→P''-ester with thiotriphosphoric acid ((HO)2P(O)OP(O)(OH)OP(S)(OH)2), (S)-, sodium salt; (S)-ATPαS sodium salt; Adenosine-5'-O-(1-thiotriphosphate), Sp-isomer sodium salt; Sp-ATP-alpha-S sodium salt
Related CAS: 58976-48-0 (free acid)
GTPαS sodium salt
Description: GTPαS sodium salt is a modified form of guanosine triphosphate (GTP) where one of the non-bridging oxygen atoms at the α-phosphate position is replaced by a sulfur atom. This modification makes GTPαS resistant to hydrolysis by GTPases, allowing it to act as a non-hydrolyzable analog of GTP. It is commonly used in studies of G-protein signaling, enzymatic regulation, and molecular biology research. The sodium salt form improves its solubility and stability for experimental applications.
CAT: BRP-00702
MF: C10H16N5O13P3S (free acid)
MF: 539.25 (free acid)
Purity: >98%
Appearance: Colorless to light yellow liquid
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|---|---|---|---|
| -- | -- | -- |
Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: sodium;[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphinothioyl] phosphono hydrogen phosphate
Synonyms: Guanosine, 5'→P''-ester with thiotriphosphoric acid sodium salt; GTP-αS sodium salt; Guanosine-5'-Rp-Alpha-Thio-Triphosphate sodium salt; Guanosine 5'-O-(1-thiotriphosphate) sodium salt; Guanosine 5'-O-thiotriphosphate sodium salt; Alpha Thiol GTP (1-Thio-GTP) sodium salt
Related CAS: 71376-96-0 (free acid)
5-hme-CTP sodium salt
Description: 5-hme-CTP sodium salt is a modified form of cytidine triphosphate (CTP) with a hydroxymethyl group attached to the 5-position of the cytosine ring. This modification can impact the molecule's interactions with enzymes involved in nucleic acid synthesis and repair. It is used in biochemical research to study DNA methylation, epigenetic modifications, and nucleotide metabolism. The sodium salt form enhances its solubility and stability for various experimental purposes.
CAT: BRP-00703
MF: C10H18N3O15P3 (free acid)
MF: 513.18 (free acid)
Purity: >98%
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|---|---|---|---|
| -- | -- | -- |
Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: sodium;((2R,3S,4R,5R)-5-(4-amino-5-(hydroxymethyl)-2-oxopyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate
Synonyms: hm5C sodium salt; 5-Hydroxymethylcytidine-5'-Triphosphate sodium salt; 5-hm-CTP sodium salt; 5-HmCTP sodium salt; 5-Hydroxymethyl-CTP sodium salt; 5-(Hydroxymethyl)cytidine 5'-triphosphoric acid sodium salt; 5-Hydroxymethyl CTP sodium salt; 5-(Hydroxymethyl)cytidine 5'-(tetrahydrogen triphosphate) sodium salt; 5-(Hydroxymethyl)-CTP sodium salt; 5-(Hydroxymethyl)cytidine 5'-triphosphate sodium salt
Related CAS: 39749-90-1 (free acid)
m7-ITP sodium salt
Description: m7-ITP sodium salt is a modified form of inosine triphosphate (ITP) with a methyl group attached to the N7 position of the inosine base. This modification can influence the molecule's interactions with enzymes and proteins involved in nucleotide metabolism and RNA synthesis. It is useful for investigating the mechanisms of RNA modification, transcriptional regulation, and enzymatic activity. The sodium salt form improves its solubility and stability for use in biochemical studies.
CAT: BRP-00704
CAS: 2414283-39-7
MF: C11H17N4O14P3 (free acid)
MF: 522.19 (free acid)
Purity: >95%
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Storage: Store at -20 °C, Avoid direct sunlight and keep in dry place
IUPAC Name: sodium;9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(((((hydroxy(phosphonooxy)phosphoryl)oxy)oxidophosphoryl)oxy)methyl)tetrahydrofuran-2-yl)-7-methyl-6-oxo-6,9-dihydro-1H-purin-7-ium
Synonyms: 7-Methyl-ITP sodium salt; 7-Methylinosine 5'-(tetrahydrogen triphosphate) sodium salt; 7-Methylinosine 5'-triphosphate sodium salt; m7 ITP sodium salt
Related CAS: 1446012-56-1 (free acid)
-vinyl-phosphonate-3'-o-me-rg.gif)
5'-Me-(E)-vinyl phosphonate-3'-O-Me-rG
Description: 5'-Me-(E)-vinyl phosphonate-3'-O-Me-rG is a modified nucleotide. This compound is used in the synthesis of RNA oligonucleotides, providing unique properties that can influence RNA stability and interactions with enzymes, useful in biochemical research and the development of nucleotide-based therapeutics.
CAT: BRP-00710
MF: C14H20N5O7P
MF: 401.32
Purity: ≥98% by HPLC
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|---|---|---|---|
| -- | -- | -- |
Storage: Store at 2-8 °C
InChIKey: SSOSIAOMHJATPR-LNAVCVTKSA-N
IUPAC Name: dimethyl ((E)-2-((2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-4-hydroxy-3-methoxytetrahydrofuran-2-yl)vinyl)phosphonate
InChI: InChI=1S/C14H20N5O7P/c1-23-10-7(4-5-27(22,24-2)25-3)26-13(9(10)20)19-6-16-8-11(19)17-14(15)18-12(8)21/h4-7,9-10,13,20H,1-3H3,(H3,15,17,18,21)/b5-4+/t7-,9-,10-,13-/m1/s1
-vinyl-phosphonate-rg.gif)
5'-Me-(E)-vinyl phosphonate-rG
Description: 5'-Me-(E)-vinyl phosphonate-rG is a modified nucleotide where a methyl group and an (E)-vinyl phosphonate group are attached to the 5' position of guanine (rG). This modification alters the chemical properties of the ribonucleoside, enhancing its potential applications in biochemical research and the development of nucleic acid-based therapeutics.
CAT: BRP-00713
MF: C13H18N5O7P
MF: 387.29
Purity: ≥98% by HPLC
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Storage: Store at 2-8 °C
InChIKey: NDLBDKPYAJHVCG-XJHNSCJASA-N
IUPAC Name: dimethyl ((E)-2-((2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)vinyl)phosphonate
InChI: InChI=1S/C13H18N5O7P/c1-23-26(22,24-2)4-3-6-8(19)9(20)12(25-6)18-5-15-7-10(18)16-13(14)17-11(7)21/h3-6,8-9,12,19-20H,1-2H3,(H3,14,16,17,21)/b4-3+/t6-,8-,9-,12-/m1/s1
