Weight | 233.311 g/mol |
---|---|
Formula | C14H19NO2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
Piperoxan (59-39-2)
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- USE OF PIPEROXAN AND REGITINE AS ROUTINE TESTS IN PATIENTS WITH HYPERTENSION (JAMA, 1951)
- ACCIDENTAL ADRENALINE OVERDOSAGE AND ITS TREATMENT WITH PIPEROXAN (The Lancet, 1955)
- The -2 antagonists idazoxan and rauwolscine but not yohimbine or piperoxan are anxiolytic in the vogel lick-shock conflict paradigm following intravenous administration (Life Sciences, 1994)
- Lack of specificity of piperoxan hydrochloride test for adrenal medullary tumors. (JAMA, 1951)
- Chemoenzymatic synthesis of piperoxan, prosympal, dibozane, and doxazosin (Tetrahedron-asymmetry, 2012)
- TREATMENT OF LOCAL ISCHEMIA DUE TO LEVARTERENOL (LEVOPHED) LEAKAGE WITH PIPEROXAN (JAMA, 1957)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CCN(CC1)CC2COC3=CC=CC=C3O2
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- Pubchem - Piperoxan
- Wikipedia - piperoxan
Piperoxan, also known as benodaine, is a drug which was the very first antihistamine to be discovered. This compound, derived from benzodioxan, was prepared in the early 1930s by Daniel Bovet and Ernest Fourneau at the Pasteur Institute in France. Formerly investigated by Fourneau as an -adrenergic-blocking agent, they demonstrated that it also antagonized histamine-induced bronchospasm in guinea pigs, and published their findings in 1933.
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