| Weight | 372.808 g/mol |
|---|---|
| Formula | C19H17ClN2O4 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 6 |
glafenine (3820-67-5)
Glafenin · Glaphenine · Glycerylaminophenaquine
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- Correction of the Phe508 Cystic Fibrosis Transmembrane Conductance Regulator Trafficking Defect by the Bioavailable Compound Glafenine (Molecular Pharmacology, 2010)
- Determination of some aminobenzoic acid derivatives : glafenine and metoclopramide (Journal of Pharmaceutical and Biomedical Analysis, 2000)
- Glafenine-induced intestinal injury in zebrafish is ameliorated by -opioid signaling via enhancement of Atf6-dependent cellular stress responses (Disease Models & Mechanisms, 2013)
- Application of H-point standard additions method to spectrophotometric and spectrofluorimetric determinations of glafenine and glafenic acid in mixtures (Talanta, 2000)
- Glafenine-associated hepatic injury: analysis of 38 cases and review of the literature (Liver, 2008)
- Glafenine-associated anaphylaxis as a cause of hospital admission in the Netherlands (European Journal of Clinical Pharmacology, 1991)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Glafenin
- Glaphenine
- Glycerylaminophenaquine
- Exidol
-
SMILESC1=CC=C(C(=C1)C(=O)OCC(CO)O)NC2=C3C=CC(=CC3=NC=C2)Cl
-
InChIKeyGWOFUCIGLDBNKM-UHFFFAOYSA-N
- Pubchem - glafenine
- Wikipedia - glafenine
Glafenine is a nonsteroidal anti-inflammatory drug (NSAID). Use of glafenine is limited due to the risk of anaphylaxis and acute kidney failure.
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