| Weight | 144.177 g/mol |
|---|---|
| Formula | C9H8N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
6-AMINOQUINOLINE (580-15-4)
Score:
#2851 in Biochemistry
,
#6987 in Chemistry
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- Review of key knowledge gaps in glucose-6-phosphate dehydrogenase deficiency detection with regard to the safe clinical deployment of 8-aminoquinoline treatment regimens: a workshop report (Malaria Journal, 2013)
- A sensitive fluorimetric rate assay for biotinidase using a new derivative of biotin, biotinyl-6-aminoquinoline (Analytical Biochemistry, 1984)
- Antiparasitic activities and toxicities of individual enantiomers of the 8-aminoquinoline 8-[(4-amino-1-methylbutyl)amino]-6-methoxy-4-methyl-5-[3,4- dichlorophenoxy]quinoline succinate (Antimicrobial Agents and Chemotherapy, 2008)
- Inhibitors of Tumor Progression Loci-2 (Tpl2) Kinase and Tumor Necrosis Factor (TNF-) Production: Selectivity and in Vivo Antiinflammatory Activity of Novel 8-Substituted-4-anilino-6-aminoquinoline-3-carbonitriles (Journal of Medicinal Chemistry, 2007)
- Enthalpies of combustion, vapour pressures, and enthalpies of sublimation of 3-, 5-, 6-, and 8-aminoquinoline (The Journal of Chemical Thermodynamics, 1993)
- 6-Aminoquinoline as a fluorogenic leaving group in peptide cleavage reactions: A new fluorogenic substrate for chymotrypsin (Analytical Biochemistry, 1981)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C=CC(=C2)N)N=C1
-
InChIKeyRJSRSRITMWVIQT-UHFFFAOYSA-N
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6-AMINOQUINOLINE
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