| Weight | 130.15 g/mol |
|---|---|
| Formula | C8H6N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
1,8-Naphthyridine (254-60-4)
Score:
#6472 in Chemistry
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- 1,8-NAPHTHYRIDINE DERIVATIVES. A NEW CLASS OF CHEMOTHERAPEUTIC AGENTS. (Journal of Medicinal Chemistry, 1962)
- 1,8-Naphthyridines IV. 9-Substituted N,N-dialkyl-5-(alkylamino or cycloalkylamino) [1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities (European Journal of Medicinal Chemistry, 2000)
- Synthesis and structure-activity relationships of novel 7-substituted 1,4-dihydro-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acids as antitumor agents. Part 1. (Journal of Medicinal Chemistry, 2002)
- Recognition of a Single Guanine Bulge by 2-Acylamino-1,8-naphthyridine (Journal of the American Chemical Society, 2000)
- A 1,8-naphthyridine-based fluorescent chemodosimeter for the rapid detection of Zn2+ and Cu2+. (Organic Letters, 2008)
- Recognition of guanine-guanine mismatches by the dimeric form of 2-amino-1,8-naphthyridine. (Journal of the American Chemical Society, 2001)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(N=C1)N=CC=C2
-
InChIKeyFLBAYUMRQUHISI-UHFFFAOYSA-N
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