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About This Item
Empirical Formula (Hill Notation):
C19H25N8O11P
CAS Number:
Molecular Weight:
572.42
UNSPSC Code:
41106305
PubChem Substance ID:
EC Number:
219-187-7
MDL number:
Product Name
Adenylyl(3′→5′)cytidine, ≥98%
SMILES string
NC1=NC(=O)N(C=C1)C2OC(CO)C(OP(O)(=O)OCC3OC(C(O)C3O)n4cnc5c(N)ncnc45)C2O
assay
≥98%
storage temp.
−20°C
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Adenosine, blood pressure and NREM delta.
I Feinberg et al.
Sleep, 22(1), 7-7 (1999-02-16)
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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
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
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
A Arnon et al.
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In many nonexcitable cells, hormones and neurotransmitters activate Na(+) influx and mobilize Ca(2+) from intracellular stores. The stores are replenished by Ca(2+) influx via "store-operated" Ca(2+) channels (SOC). The main routes of Na(+) entry in these cells are unresolved, and
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