| Weight | 145.161 g/mol |
|---|---|
| Formula | C9H7NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
1-Hydroxyisoquinoline (491-30-5)
isocarbostyril
Score:
#36 in Medicinal chemistry
,
#606 in Microbiology
,
#2497 in Biochemistry
,
#4879 in Biology
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- Structure-activity relationship analysis of novel derivatives of narciclasine (an Amaryllidaceae isocarbostyril derivative) as potential anticancer agents. (Journal of Medicinal Chemistry, 2009)
- The Amaryllidaceae Isocarbostyril Narciclasine Induces Apoptosis By Activation of the Death Receptor and/or Mitochondrial Pathways in Cancer Cells But Not in Normal Fibroblasts (Neoplasia, 2007)
- Design, synthesis, and biological evaluation of a series of 2-hydroxyisoquinoline-1,3(2H,4H)-diones as dual inhibitors of human immunodeficiency virus type 1 integrase and the reverse transcriptase RNase H domain. (Journal of Medicinal Chemistry, 2008)
- Magnesium Chelating 2-Hydroxyisoquinoline-1,3(2H,4H)-diones, as Inhibitors of HIV-1 Integrase and/or the HIV-1 Reverse Transcriptase Ribonuclease H Domain: Discovery of a Novel Selective Inhibitor of the Ribonuclease H Function (Journal of Medicinal Chemistry, 2011)
- Isocarbostyril alkaloids from Haemanthus kalbreyeri (Phytochemistry, 1989)
- Amaryllidaceae Isocarbostyril Alkaloids and Their Derivatives as Promising Antitumor Agents (Translational Oncology, 2008)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - isocarbostyril
-
SMILESC1=CC=C2C(=C1)C=CNC2=O
-
InChIKeyVDBNYAPERZTOOF-UHFFFAOYSA-N
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