| Weight | 237.292 g/mol |
|---|---|
| Formula | C8H11N7S |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
Ambazone (6011-12-7, 539-21-9)
1,4-benzoquinone guanylhydrazone thiosemicarbazone monohydrochloride · 1,4-benzoquinone guanylhydrazone thiosemicarbazone
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- Ambazone as a membrane active antitumor drug (Biophysical Chemistry, 1990)
- Voltammetric behavior and quantitative determination of ambazone concentrations in urine and in a pharmaceutical formulation (Central European Journal of Chemistry, 2014)
- Spectroscopic and physical-chemical characterization of ambazone-glutamate salt (Spectroscopy, 2011)
- Carcinogenesis and aging: VIII. Effect of host age on tumour growth, metastatic potential, and chemotherapeutic sensitivity to 1.4-benzoquinone-guanylhydrazonethiosemicarbazone (ambazone) and 5-fluorouracil in mice and rats (Experimental pathology, 1988)
- Influence of age on antileukemic action, subacute toxicity and tissue distribution of ambazone in B6D2F1 mice. (Archiv fur Geschwulstforschung, 1990)
- Influence of murine melanoma B16 on the distribution of ambazone in B6D2F1 mice. (Die Pharmazie, 1990)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1,4-benzoquinone guanylhydrazone thiosemicarbazone monohydrochloride
- 1,4-benzoquinone guanylhydrazone thiosemicarbazone
-
SMILESC1=CC(=CC=C1NN=C(N)N)N=NC(=S)N
-
InChIKeyANZIOUQAFBXNHU-UHFFFAOYSA-N
- Pubchem - Ambazone
- Wikipedia - Ambazone
Ambazone is an oral antiseptic. Ambazon was patented in 1957 by Bayer under the trade name Iversal, and briefly used in Germany. It is still used in Russia, countries of the former Soviet Union, Poland and Romania.
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