Weight | 471.518 g/mol |
---|---|
Formula | C22H29N7O5 |
Hydrogen Acceptors | 11 |
Hydrogen Donors | 4 |
Aromatic Rings | 3 |
Rotatable Bonds | 8 |
puromycin (53-79-2)
Score:
#1289 in Biochemistry
,
#3161 in Biology
,
#3957 in Chemistry
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- Memory in Mice as Affected by Intracerebral Puromycin (Science, 1963)
- Podoplanin, novel 43-kd membrane protein of glomerular epithelial cells, is down-regulated in puromycin nephrosis. (American Journal of Pathology, 1997)
- In vitro virus: Bonding of mRNA bearing puromycin at the 3-terminal end to the C-terminal end of its encoded protein on the ribosome in vitro (FEBS Letters, 1997)
- INHIBITION BY PUROMYCIN OF AMINO ACID INCORPORATION INTO PROTEIN (Proceedings of the National Academy of Sciences of the United States of America, 1959)
- Cultured animal cells exposed to amino acid analogues or puromycin rapidly synthesize several polypeptides (Journal of Cellular Physiology, 1980)
- THE PUROMYCIN REACTION AND ITS RELATION TO PROTEIN SYNTHESIS. (Journal of Molecular Biology, 1964)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN(C)C1=NC=NC2=C1N=CN2C3C(C(C(O3)CO)NC(=O)C(CC4=CC=C(C=C4)OC)N)O
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InChIKeyRXWNCPJZOCPEPQ-UHFFFAOYSA-N
- Pubchem - puromycin
- Wikipedia - puromycin
Puromycin is an antibiotic protein synthesis inhibitor which causes premature chain termination during translation.
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