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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)-

3H-Imidazo[2,1-i]purine, 3-(2-deoxy-b-D-erythro-pentofuranosyl)-

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Chemical Name: 3H-Imidazo[2,1-i]purine, 3-(2-deoxy-b-D-erythro-pentofuranosyl)-
CAS Number: 68498-25-9
Product Number: AG01CB5W(AGN-PC-0TSRZG)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
275.268g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
275.102g/mol
Monoisotopic Mass:
275.102g/mol
Topological Polar Surface Area:
97.7A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
373
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
3
Undefined Atom Stereocenter Count:
0
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


Ethenodeoxyadenosine, commonly referred to as εdA, is a modified nucleoside that plays a valuable role in chemical synthesis. Due to its unique structure which includes an additional etheno bridge between the base and the sugar moiety, εdA has been utilized as a tool in the study of DNA damage and repair mechanisms. In chemical synthesis, εdA serves as a versatile building block for the creation of advanced DNA analogs and modified nucleic acid constructs. Its presence in synthetic oligonucleotides provides valuable insights into the effects of DNA lesions and how they can impact biological processes. Additionally, εdA has been employed in the development of new pharmaceuticals and diagnostic agents. Its ability to mimic damaged DNA makes it a valuable asset in studying molecular interactions and developing targeted therapies. Ultimately, the application of Ethenodeoxyadenosine in chemical synthesis continues to expand our understanding of DNA structure and function, paving the way for innovative advancements in biotechnology and medicine.