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Home > Nitro Compounds > 863637-28-9
863637-28-9 | 2H-Indazole, 3-nitro-
CAS No: 863637-28-9 Catalog No: AG00IE13 MDL No:
Product Description
Catalog Number:
AG00IE13
Chemical Name:
2H-Indazole, 3-nitro-
CAS Number:
863637-28-9
IUPAC Name:
3-nitro-2H-indazole
InChI:
InChI=1S/C7H5N3O2/c11-10(12)7-5-3-1-2-4-6(5)8-9-7/h1-4H,(H,8,9)
InChI Key:
OWIRCRREDNEXTA-UHFFFAOYSA-N
Properties
Complexity:
192
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
163.038g/mol
Formal Charge:
0
Heavy Atom Count:
12
Hydrogen Bond Acceptor Count:
3
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
163.136g/mol
Monoisotopic Mass:
163.038g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
74.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.7
Literature
| Title | Journal |
|---|---|
| Biological and chemical study of fused tri- and tetracyclic indazoles and analogues with important antiparasitic activity. | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20120901 |
| Involvement of nitric oxide in learning & memory processes. | The Indian journal of medical research 20110501 |
| The mitochondrial permeability transition pore regulates nitric oxide-mediated apoptosis of neurons induced by target deprivation. | The Journal of neuroscience : the official journal of the Society for Neuroscience 20110105 |
| Production of bioactive secondary metabolites by marine vibrionaceae. | Marine drugs 20110101 |
| Aqabamycins A-G: novel nitro maleimides from a marine Vibrio species: II. Structure elucidation. | The Journal of antibiotics 20100601 |
| Aqabamycins A-G: novel nitro maleimides from a marine Vibrio species. I. Taxonomy, fermentation, isolation and biological activities. | The Journal of antibiotics 20100601 |
| ESR and electrochemical study of 1,2-disubstituted 5-nitroindazolin-3-ones and 2-substituted 3-alkoxy-5-nitro-2H-indazoles: reactivity and free radical production capacity in the presence of biological systems. | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20100101 |
| Nitroindazole compounds inhibit the oxidative activation of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) neurotoxin to neurotoxic pyridinium cations by human monoamine oxidase (MAO). | Free radical research 20091001 |
| BOLD response during uncoupling of neuronal activity and CBF. | NeuroImage 20060801 |
| Neuronal nitric oxide synthase and splanchnic blood flow in anaesthetized rats. | Acta physiologica Scandinavica 20050301 |
| Stimulation of nitric oxide synthase in cerebral cortex due to elevated partial pressures of oxygen: an oxidative stress response. | Journal of neurobiology 20020501 |
| Crystal structure of nitric oxide synthase bound to nitro indazole reveals a novel inactivation mechanism. | Biochemistry 20011113 |
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