Skip to Content
Merck
All Photos(1)

Key Documents

A7435

Sigma-Aldrich

Adenylyl(3′→5′)cytidine

≥98%

Synonym(s):

ApC

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C19H25N8O11P
CAS Number:
Molecular Weight:
572.42
EC Number:
MDL number:
UNSPSC Code:
41106305
PubChem Substance ID:

Assay

≥98%

storage temp.

−20°C

SMILES string

NC1=NC(=O)N(C=C1)C2OC(CO)C(OP(O)(=O)OCC3OC(C(O)C3O)n4cnc5c(N)ncnc45)C2O

Looking for similar products? Visit Product Comparison Guide


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

R K Dubey et al.
Hypertension (Dallas, Tex. : 1979), 35(1 Pt 2), 267-272 (2000-01-21)
Adenosine inhibits growth of vascular smooth muscle cells. The goals of this study were to determine which adenosine receptor subtype mediates the antimitogenic effects of adenosine and to investigate the signal transduction mechanisms involved. In rat aortic vascular smooth muscle
B S Parker et al.
Nucleic acids research, 28(4), 982-990 (2000-01-29)
Recently we have found that mitoxantrone, like Adria-mycin, can be activated by formaldehyde and subsequently form adducts which stabilise double-stranded DNA in vitro. This activation by formaldehyde may be biologically relevant since formaldehyde levels are elevated in those tumours in
Adenosine, blood pressure and NREM delta.
I Feinberg et al.
Sleep, 22(1), 7-7 (1999-02-16)
Dabashree Bandyopadhyay et al.
Journal of biomolecular structure & dynamics, 19(4), 659-667 (2002-02-15)
Effect of flanking base pairs on CA and AA dinluceotide step-geometry has been studied using molecular dynamics method. Sixteen dodecameric sequences are constructed for each doublet with all possible bases at their 5' and 3' positions along with their complementary
A M Vicentini et al.
Biochemistry, 35(28), 9128-9132 (1996-07-16)
RNase PL3 is a structurally highly conserved, pyrimidine-specific RNase, which strongly prefers to cleave at the 3'-side of uridine. Here, question of which residues are involved in determining substrate specificity is addressed. The difference in the rate of cleavage of

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service