| Weight | 297.34 g/mol |
|---|---|
| Formula | C11H15N5O3S |
| Hydrogen Acceptors | 9 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
Methylthioadenosine (2457-80-9)
Score:
#1302 in Biochemistry
,
#3191 in Biology
,
#3992 in Chemistry
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- Trends in the biochemical pharmacology of 5-deoxy-5-methylthioadenosine (Biochemical Pharmacology, 1982)
- Homozygous Deletion of CDKN2A and Codeletion of the Methylthioadenosine Phosphorylase Gene in the Majority of Pleural Mesotheliomas (Clinical Cancer Research, 2003)
- Phosphate-stimulated breakdown of 5-methylthioadenosine by rat ventral prostate (Biochemical Journal, 1969)
- Methionine synthesis from 5'-methylthioadenosine in rat liver. (Journal of Biological Chemistry, 1981)
- Methylthioadenosine Phosphorylase, a Gene Frequently Codeleted with p16cdkN2a/ARF, Acts as a Tumor Suppressor in a Breast Cancer Cell Line (Cancer Research, 2002)
- Methylthioadenosine/S-adenosylhomocysteine nucleosidase, a critical enzyme for bacterial metabolism. (Molecular Microbiology, 2011)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCSCC1C(C(C(O1)N2C=NC3=C2N=CN=C3N)O)O
-
InChIKeyWUUGFSXJNOTRMR-UHFFFAOYSA-N
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Methylthioadenosine
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