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5-carbamoylmethyluridine

  • Name 5-carbamoylmethyluridine
  • CAS 29569-30-0
  • Purity 99%
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1.What is the 5-carbamoylmethyluridine ?

5-Carbamoylmethyluridine, also known as 5-Uridineacetamide, is a modified nucleoside belonging to the class of uridines. It is uridine in which the hydrogen at position 5 of the pyrimidine ring is substituted by a 2-amino-2-oxoethyl group. This modification makes it a putative cancer biomarker, indicating its potential role in cancer research and therapeutics.

5-Uridineacetamide is a modified nucleoside, and a putative cancer biomarker.

2.What is the CAS number for 5-carbamoylmethyluridine ?

The CAS number of 5-carbamoylmethyluridine is 29569-30-0.

More information of 5-carbamoylmethyluridine 29569-30-0 are:

CAS?Number

29569-30-0

Density

1.653g/cm3

Boiling Point

°Cat760mmHg

Flash Point

°C

Refractive Index

1.639

PSA

169.12000

LogP

-2.26210

3.What is the molecular formula of 5-carbamoylmethyluridine ?

The chemical formula of?5-carbamoylmethyluridine is C11H15 N3 O7 which containing 11 Carbon atoms,15 Hydrogen atoms,3 Nitrogen atoms and 7 Oxygen atoms,and the molecular weight, and the molecular weight of 5-carbamoylmethyluridine is 301.256

4.What is 5-carbamoylmethyluridine(29569-30-0)used for?

5-Carbamoylmethyluridine, also known as 5-Uridineacetamide, is a modified nucleoside belonging to the class of uridines. It is uridine in which the hydrogen at position 5 of the pyrimidine ring is substituted by a 2-amino-2-oxoethyl group. This modification makes it a putative cancer biomarker, indicating its potential role in cancer research and therapeutics.

InChI:InChI=1/C11H15N3O7/c12-6(16)1-4-2-14(11(20)13-9(4)19)10-8(18)7(17)5(3-15)21-10/h2,5,7-8,10,15,17-18H,1,3H2,(H2,12,16)(H,13,19,20)/t5-,7-,8-,10-/m1/s1

Relevant articles related to 5-carbamoylmethyluridine:

Article

Source

Isolation and characterization of 5-carbamoylmethyluridine and 5- carbamoylmethyl-2-thiouridine from human urine

Chheda,Patrzyc,Tworek,Dutta

, p. 2155 - 2173 (1999)

MODIFIED NUCLEIC ACID MOLECULES AND USES THEREOF

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Page/Page column 293, (2014/07/07)

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