Nucleotides - RNA / BOC Sciences

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

MF: C10H15N5O11P2 (free acid)

MF: 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

MF: C10H14N4O11P2 (free acid)

MF: 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

MF: C13H15N7NaO7P

MF: 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

MF: C13H16N7O7P

MF: 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

MF: C10H14N5Na2O14P3

MF: 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

MF: C11H16N5Na2O13P3

MF: 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

MF: C10H16N3Na2O14P3

MF: 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

MF: C11H16N5Na2O14P3

MF: 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

MF: C10H15N2Na2O15P3

MF: 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

MF: C9H11FLi3N2O14P3

MF: 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

MF: C11H15N5Na3O13P3

MF: 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

MF: C12H15N3Na3O14P3

MF: 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

MF: C10H13FN5O7P

MF: 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)

Inosine 5'-monophosphate monopotassium salt

Description: Inosine 5'-monophosphate monopotassium salt (IMP-K) is a valuable nucleotide derivative used in biochemical, pharmacological, and nutritional research. Its role in nucleotide metabolism makes it an important substrate for enzyme studies and drug development. Additionally, its application as a flavor enhancer highlights its versatility in both scientific and industrial contexts. This compound provides insights into purine metabolism and aids in the development of therapeutic agents targeting related metabolic pathways.

CAT: BRP-01503

CAS: 909272-79-3

MF: C10H12KN4O8P

MF: 386.30

Purity: 98%

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InChIKey: AWOLVHQZOSVDSL-MCDZGGTQSA-M

CanonicalSMILES: C1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)COP(=O)(O)[O-])O)O.[K+]

IUPAC Name: potassium;[(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-1H-purin-9-yl)oxolan-2-yl]methyl hydrogen phosphate

InChI: InChI=1S/C10H13N4O8P.K/c15-6-4(1-21-23(18,19)20)22-10(7(6)16)14-3-13-5-8(14)11-2-12-9(5)17;/h2-4,6-7,10,15-16H,1H2,(H,11,12,17)(H2,18,19,20);/q;+1/p-1/t4-,6-,7-,10-;/m1./s1

Synonyms: 5'-Inosinic acid, potassium salt (1:1); Inosinic acid, potassium salt; IMP potassium salt; 5'-IMP potassium salt; Inosine 5'-(dihydrogen phosphate) potassium salt; Inosine 5'-phosphate potassium salt; Inosine-5'-monophosphoric acid potassium salt; ((2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-1,6-dihydro-9H-purin-9-yl)tetrahydrofuran-2-yl)methyl hydrogen phosphate potassium salt; Inosine 5'-monophosphate potassium salt

Related CAS: 20262-26-4 (dipotassium salt) ; 96286-05-4 (x-potassium salt) ; 131-99-7 (free acid)

2'-F-m7GMP sodium salt

Description: 2'-F-m7GMP sodium salt is a modified nucleotide derivative used in biochemical and pharmaceutical research. It consists of 7-methylguanosine monophosphate (m7GMP) with a fluorine substitution at the 2' carbon of the ribose sugar, and it is in its sodium salt form for improved solubility and stability in aqueous solutions. This compound is primarily employed to investigate RNA modifications and their biological implications. The fluorine substitution at the 2' position can potentially alter the base-pairing properties and interactions of the nucleotide with RNA-binding proteins or enzymes involved in RNA metabolism. It serves as a valuable tool in studies aiming to understand the role of modified nucleotides in gene expression regulation, RNA structure-function relationships, and as a potential therapeutic target in RNA-related diseases.

CAT: BRP-01536

MF: C11H15FN5O7P (free acid)

MF: 379.24 (free acid)

Purity: >98%

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

Synonyms: ((2R,3R,4R,5R)-5-(2-amino-7-methyl-6-oxo-1,6-dihydro-9H-purin-7-ium-9-yl)-4-fluoro-3-hydroxytetrahydrofuran-2-yl)methyl hydrogen phosphate sodium salt; 5'-Guanylic acid, 7-methyl-2'-deoxy-2'-fluoro-, inner salt, sodium salt

2'-F-m7GMP ammonium salt

Description: 2'-F-m7GMP ammonium salt is a modified nucleotide derivative used in biochemical and pharmaceutical research. It consists of 7-methylguanosine monophosphate (m7GMP) with a fluorine substitution at the 2' carbon of the ribose sugar, and it is in its ammonium salt form for improved solubility and stability in aqueous solutions. This compound is primarily employed to investigate RNA modifications and their biological implications. The fluorine substitution at the 2' position can potentially alter the base-pairing properties and interactions of the nucleotide with RNA-binding proteins or enzymes involved in RNA metabolism. It serves as a valuable tool in studies aiming to understand the role of modified nucleotides in gene expression regulation, RNA structure-function relationships, and as a potential therapeutic target in RNA-related diseases.

CAT: BRP-01537

MF: C11H15FN5O7P (free acid)

MF: 379.24 (free acid)

Purity: >98%

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

Synonyms: 5'-Guanylic acid, 7-methyl-2'-deoxy-2'-fluoro-, inner salt, ammonium salt; ((2R,3R,4R,5R)-5-(2-amino-7-methyl-6-oxo-1,6-dihydro-9H-purin-7-ium-9-yl)-4-fluoro-3-hydroxytetrahydrofuran-2-yl)methyl hydrogen phosphate ammonium salt

2'-F-m7GMP TEA Salt

Description: 2'-F-m7GMP TEA Salt is a modified nucleotide derivative used in biochemical and pharmaceutical research. It consists of 7-methylguanosine monophosphate (m7GMP) with a fluorine substitution at the 2' carbon of the ribose sugar, and it is in its TEA salt form for improved solubility and stability in aqueous solutions. This compound is primarily employed to investigate RNA modifications and their biological implications. The fluorine substitution at the 2' position can potentially alter the base-pairing properties and interactions of the nucleotide with RNA-binding proteins or enzymes involved in RNA metabolism. It serves as a valuable tool in studies aiming to understand the role of modified nucleotides in gene expression regulation, RNA structure-function relationships, and as a potential therapeutic target in RNA-related diseases.

CAT: BRP-01538

MF: C11H15FN5O7P (free base)

MF: 379.24 (free base)

Purity: >98%

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

Synonyms: 5'-Guanylic acid, 7-methyl-2'-deoxy-2'-fluoro-, inner salt, triethylammonium salt; ((2R,3R,4R,5R)-5-(2-amino-7-methyl-6-oxo-1,6-dihydro-9H-purin-7-ium-9-yl)-4-fluoro-3-hydroxytetrahydrofuran-2-yl)methyl hydrogen phosphate triethylammonium salt

2'-Deoxy-2'-fluoro-2'-C-methyluridine 5'-triphosphate, ammonium salt

Description: 2'-Deoxy-2'-fluoro-2'-C-methyluridine 5'-triphosphate, ammonium salt is a modified nucleotide derivative utilized in molecular biology research to introduce modified nucleotides into DNA and RNA molecules. Its unique structure, featuring fluorine and methyl substitutions on the ribose sugar of uridine, enhances stability and resistance to enzymatic degradation, making it valuable for studying nucleic acid structure, function, and interactions. This modified nucleotide serves as a substrate for DNA and RNA polymerases, facilitating the synthesis of modified nucleic acids and enabling the development of novel molecular tools and techniques in genetic engineering and RNA biology research.

CAT: BRP-01549

MF: C10H28FN6O14P3

MF: 568.28

Purity: ≥98% by HPLC

Appearance: White powder

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Storage: Store at -20 °C

InChIKey: GXUQVMFGQHPIPU-DLULJLDFSA-N

CanonicalSMILES: O=C1C=CN(C(=O)N1)C2OC(COP(=O)(O)OP(=O)(O)OP(=O)(O)O)C(O)C2(F)C.[NH4+].[NH4+].[NH4+].[NH4+]

IUPAC Name: tetraammonium;((2R,3R,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-fluoro-3-hydroxy-4-methyltetrahydrofuran-2-yl)methyl triphosphate

InChI: InChI=1S/C10H16FN2O14P3.4H3N/c1-10(11)7(15)5(25-8(10)13-3-2-6(14)12-9(13)16)4-24-29(20,21)27-30(22,23)26-28(17,18)19;;;;/h2-3,5,7-8,15H,4H2,1H3,(H,20,21)(H,22,23)(H,12,14,16)(H2,17,18,19);4*1H3/t5-,7-,8-,10-;;;;/m1..../s1

Synonyms: 2'-F-2'-C-Me-dUTP.4NH4; (2'R)-2'-Deoxy-2'-fluoro-2'-methyluridine 5'-(tetrahydrogen triphosphate) ammonium salt; GS 461203 ammonium salt; PSI 7409 ammonium salt; Sofosbuvir triphosphate ammonium salt; Sofosbuvir-TP ammonium salt

Related CAS: 1015073-42-3 (free acid)

2'-Fluoro-2'-deoxyguanosine-5'-monophosphate, disodium salt

Description: 2'-Fluoro-2'-deoxyguanosine-5'-monophosphate, disodium salt is a modified nucleotide derivative used in biochemical and molecular biology research. It is valuable in studying nucleotide metabolism, nucleic acid-protein interactions, and RNA biology, contributing to advancements in genetic engineering, drug discovery, and molecular diagnostics.

CAT: BRP-01550

MF: C10H11FN5Na2O7P

MF: 409.18

Purity: ≥98% by HPLC

Appearance: White powder

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InChIKey: KUVAIZOIRVHUFK-ZOYUQYBOSA-L

CanonicalSMILES: C1=NC2=C(N1C3C(C(C(O3)COP(=O)(O)[O-])O)F)N=C(N=C2[O-])N.[Na+].[Na+]

IUPAC Name: disodium;((2R,3R,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-4-fluoro-3-hydroxytetrahydrofuran-2-yl)methyl phosphate

InChI: InChI=1S/C10H13FN5O7P.2Na/c11-4-6(17)3(1-22-24(19,20)21)23-9(4)16-2-13-5-7(16)14-10(12)15-8(5)18;;/h2-4,6,9,17H,1H2,(H2,19,20,21)(H3,12,14,15,18);;/q;2*+1/p-2/t3-,4-,6-,9-;;/m1../s1

Synonyms: 2'-F-dGMP.Na2; 2'-F-dGMP disodium salt; 2'-Deoxy-2'-fluoroguanosine-5'-monophosphate disodium salt; 9-(2-Deoxy-2-fluoro-β-D-ribofuranosyl)guanine-5'-monophosphate disodium salt; 2'-deoxy-2'-fluoroguanosine 5'-(dihydrogen phosphate) disodium salt

Related CAS: 170784-58-4 (free acid)

Iso-GTP

Description: Iso-GTP, also known as iso-guanosine triphosphate, is a modified nucleotide used in biochemical and molecular biology research. It features an isomer of guanosine linked to a triphosphate group. Iso-GTP can be incorporated into RNA or DNA strands during synthesis, providing a means to study the effects of nucleotide isomerism on nucleic acid structure, function, and interactions. This compound is useful in investigations of nucleotide analogs' roles in enzymatic processes, molecular recognition, and potential therapeutic applications. Its unique structural properties allow researchers to explore variations in nucleotide behavior and stability compared to natural guanosine triphosphate (GTP).

CAT: BRP-01608

CAS: 58083-93-5

MF: C10H16N5O14P3

MF: 523.18

Purity: 95%

Appearance: Lyophilized white powder

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Storage: Store at -20°C

Density: 2.75±0.1 g/cm3

InChIKey: DJHOBIUAJLDRDQ-UUOKFMHZSA-N

Solubility: Soluble in Water

CanonicalSMILES: C1=NC2=C(NC(=O)N=C2N1C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O)N

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

InChI: InChI=1S/C10H16N5O14P3/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)/t3-,5-,6-,9-/m1/s1

Synonyms: Adenosine 5'-(tetrahydrogen triphosphate), 2,3-dihydro-2-oxo-; 2,3-Dihydro-2-oxoadenosine 5'-(tetrahydrogen triphosphate); Adenosine 5'-(tetrahydrogen triphosphate), 1,2-dihydro-2-oxo-; iso-GTP; Isoguanosine 5'-triphosphate; 2-hydroxy-ATP; 2-oxo-2-hydroadenosine 5'-(tetrahydrogen triphosphate); isoGTP; (((2R,3S,4R,5R)-5-(6-amino-2-oxo-1,2-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)triphosphoric acid

Related CAS: 148469-19-6 (tetraammonium salt)