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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

N-[3-(4-carbamimidoylphenyl)-1-oxo-1-piperidin-1-ylpropan-2-yl]-2-(naphthalen-2-ylsulfonylamino)acetamide

Nc1nc(N)c2c(n1)n(cn2)[C@@H]1O[C@@H]([C@H](C1)O)COP(=O)(OP(=O)(OP(=O)(O)O)O)O Request for Quotation
Chemical Name: N-[3-(4-carbamimidoylphenyl)-1-oxo-1-piperidin-1-ylpropan-2-yl]-2-(naphthalen-2-ylsulfonylamino)acetamide
CAS Number: 86125-48-6
Product Number: AG004TX2(AGN-PC-0JK6VL)
Synonyms:
MDL No:
Molecular Formula: C10H17N6O12P3
Molecular Weight: 506.1963

Identification/Properties

Computed Properties
Molecular Weight:
521.636g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
9
Exact Mass:
521.21g/mol
Monoisotopic Mass:
521.21g/mol
Topological Polar Surface Area:
154A^2
Heavy Atom Count:
37
Formal Charge:
0
Complexity:
906
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-amino-2'-deoxyadenosine 5'-(tetrahydrogen triphosphate), also known as AHTP, is a versatile compound with numerous applications in chemical synthesis. In the field of organic chemistry, AHTP is commonly used as a high-energy phosphorylating agent, serving as a convenient source of phosphate groups for the phosphorylation of various molecules.One key application of AHTP in chemical synthesis is in the enzymatic or non-enzymatic transfer of phosphate groups to nucleoside or nucleotide derivatives. This process is essential in the production of modified nucleic acids, which are valuable tools in molecular biology research and drug development. AHTP facilitates the efficient phosphorylation of nucleoside building blocks, enabling the synthesis of custom nucleotide analogs with diverse functional groups or modifications.Furthermore, AHTP can also be utilized in the synthesis of nucleotide triphosphates, which are crucial intermediates in the production of nucleic acid probes, primers, and substrates for enzymes like polymerases and ligases. By serving as a phosphate donor in enzymatic reactions, AHTP enables the targeted modification of nucleotide sequences for various applications in biotechnology and biochemistry.Overall, the versatility of 2-amino-2'-deoxyadenosine 5'-(tetrahydrogen triphosphate) makes it a valuable tool for researchers and chemists working in the field of nucleic acid chemistry, allowing for the efficient synthesis of custom nucleotide analogs and specialized nucleic acid constructs with tailored properties.