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Structure via PubChem · Public domain (PubChem)
ambuphylline
Sign in to saveAmbuphylline (or bufylline) is a combination of theophylline and aminoisobutanol used as a bronchodilator. It also acts and may be used as a diuretic.
Chemical data
- Formula
- C11H19N5O3
- Molecular weight
- 269.3 g/mol
- IUPAC name
- 2-amino-2-methylpropan-1-ol;1,3-dimethyl-7H-purine-2,6-dione
- SMILES
- CC(C)(CO)N.CN1C2=C(C(=O)N(C1=O)C)NC=N2
- InChIKey
- SEIRRUDMPNNSCY-UHFFFAOYSA-N
- Polar surface area
- 116 Ų
- H-bond donors
- 3
- H-bond acceptors
- 5
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
- Indications
- Airway obstruction
via ChEMBL · EBI
Research
7 papers- Acute and chronic toxicity studies on theophylline aminoisobutanol and theophylline ethylenediamine.The Journal of laboratory and clinical medicine · 1946
- A study of the clinical effects and tolerance of theophylline aminoisobutanol.Proceedings [of the] annual meeting. Central Society for Clinical Research (U.S.) · 1946
- DETERMINATION OF IN VIVO AND IN VITRO RELEASE OF THEOPHYLLINE AMINOISOBUTANOL IN A PROLONGED-ACTION SYSTEM.Journal of pharmaceutical sciences · 1965
- The effect of theophylline aminoisobutanol in the failing experimental heart.Proceedings [of the] annual meeting. Central Society for Clinical Research (U.S.) · 1945
- The effect of theophylline aminoisobutanol in the failing experimental heart.The Journal of laboratory and clinical medicine · 1946
via PubMed
Wikidata facts
- Instance of
- combination drug
- Has part
- aminomethylpropanol
- Mass
- 269.149
Show 3 more facts
- chemical formula
- C₁₁H₁₉N₅O₃
- canonical SMILES
- CC(C)(CO)N.CN1C2=C(C(=O)N(C1=O)C)NC=N2
- subject has role
- bronchodilator
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Ambuphylline (or bufylline) is a combination of theophylline and aminoisobutanol used as a bronchodilator. It also acts and may be used as a diuretic.
==References==
Excerpted from Wikipedia’s “ambuphylline” article, available under the CC BY-SA 4.0 licence.