| Weight | 166.958 g/mol |
|---|---|
| Formula | C3H3BrO3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
3-bromopyruvic acid (1113-59-3)
bromopyruvate · 3-bromopyruvate
Score:
#2443 in Biochemistry
,
#6111 in Chemistry
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- Advanced cancers: eradication in all cases using 3-bromopyruvate therapy to deplete ATP (Biochemical and Biophysical Research Communications, 2004)
- Bromopyruvate Inactivation of 2-Keto-3-deoxy-6-phosphogluconic Aldolase. I. Kinetic Evidence for Active Site Specificity* (Biochemistry, 1967)
- Role of mitochondria-associated hexokinase II in cancer cell death induced by 3-bromopyruvate (Biochimica et Biophysica Acta, 2009)
- 3-Bromopyruvate: A New Targeted Antiglycolytic Agent and a Promise for Cancer Therapy (Current Pharmaceutical Biotechnology, 2010)
- 3-Bromopyruvate as inhibitor of tumour cell energy metabolism and chemopotentiator of platinum drugs (Molecular Oncology, 2008)
- Glyceraldehyde-3-phosphate Dehydrogenase (GAPDH) Is Pyruvylated during 3-Bromopyruvate Mediated Cancer Cell Death (Anticancer Research, 2009)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - bromopyruvate
- 3-bromopyruvate
-
SMILESC(C(=O)C(=O)O)Br
-
InChIKeyPRRZDZJYSJLDBS-UHFFFAOYSA-N
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Alternate Names
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
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3-bromopyruvic acid
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