Weight | 251.246 g/mol |
---|---|
Formula | C10H13N5O3 |
Hydrogen Acceptors | 8 |
Hydrogen Donors | 3 |
Aromatic Rings | 2 |
Rotatable Bonds | 2 |
Cordycepin (75808-67-2, 73-03-0)
3'-deoxyadenosine
Score:
#1731 in Biochemistry
,
#3825 in Biology
,
#4817 in Chemistry
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- Cordycepin inhibits lipopolysaccharide-induced inflammation by the suppression of NF-B through Akt and p38 inhibition in RAW 264.7 macrophage cells (European Journal of Pharmacology, 2006)
- The selective interruption of nucleolar RNA synthesis in HeLa cells by cordycepin. (Journal of Cell Biology, 1969)
- Messenger and Heterogeneous Nuclear RNA in HeLa Cells: Differential Inhibition by Cordycepin (Proceedings of the National Academy of Sciences of the United States of America, 1970)
- Cordycepin, a metabolic product isolated from cultures of Cordyceps militaris (Linn.) Link. (Nature, 1950)
- 3-End labeling of DNA with [-32P] cordycepin-5-triphosphate (Gene, 1980)
- Cordycepin : Selective growth inhibitor derived from liquid culture of Cordyceps militaris against Clostridium spp. (Journal of Agricultural and Food Chemistry, 2000)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3'-deoxyadenosine
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SMILESC1C(OC(C1O)N2C=NC3=C2N=CN=C3N)CO
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InChIKeyOFEZSBMBBKLLBJ-UHFFFAOYSA-N
- Pubchem - Cordycepin
- Wikipedia - cordycepin
Cordycepin, or 3'-deoxyadenosine, is a derivative of the nucleoside adenosine, differing from the latter by the absence of the hydroxy group in the 3' position of its ribose part. It was initially extracted from the fungus Cordyceps militaris, but is now produced synthetically. Because cordycepin is similar to adenosine, some enzymes cannot discriminate between the two.
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