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606-25-7 | naphthalene-1-sulfonamide
CAS No: 606-25-7 Catalog No: AG01B15L MDL No:MFCD00985933
Product Description
Catalog Number:
AG01B15L
Chemical Name:
naphthalene-1-sulfonamide
CAS Number:
606-25-7
Molecular Formula:
C10H9NO2S
Molecular Weight:
207.2490
MDL Number:
MFCD00985933
IUPAC Name:
naphthalene-1-sulfonamide
InChI:
InChI=1S/C10H9NO2S/c11-14(12,13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,(H2,11,12,13)
InChI Key:
ZFIFHAKCBWOSRN-UHFFFAOYSA-N
SMILES:
NS(=O)(=O)c1cccc2c1cccc2
Properties
Complexity:
294
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
207.035g/mol
Formal Charge:
0
Heavy Atom Count:
14
Hydrogen Bond Acceptor Count:
3
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
207.247g/mol
Monoisotopic Mass:
207.035g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
68.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.9
Literature
| Title | Journal |
|---|---|
| Decolorization of Textile Dyes and Degradation of Mono-Azo Dye Amaranth by Acinetobacter calcoaceticus NCIM 2890. | Indian journal of microbiology 20111001 |
| Crystal structures of two aminoglycoside kinases bound with a eukaryotic protein kinase inhibitor. | PloS one 20110101 |
| Synthesis of N-[2-(2,4-Difluorophenoxy)trifluoromethyl-3-pyridyl]sulfonamides and their inhibitory activities against secretory phospholipase A₂. | Chemical & pharmaceutical bulletin 20110101 |
| Neuroprotective effects of calmodulin peptide 76-121aa: disruption of calmodulin binding to mutant huntingtin. | Brain pathology (Zurich, Switzerland) 20100101 |
| Structure of the inhibitor W7 bound to the regulatory domain of cardiac troponin C. | Biochemistry 20090623 |
| New fluorescent probes for carbonic anhydrases. | Chemical communications (Cambridge, England) 20070714 |
| Membrane-permeable calmodulin inhibitors (e.g. W-7/W-13) bind to membranes, changing the electrostatic surface potential: dual effect of W-13 on epidermal growth factor receptor activation. | The Journal of biological chemistry 20070316 |
| Design, synthesis, and evaluation of naphthalene-sulfonamide antagonists of human CCR8. | Journal of medicinal chemistry 20070208 |
| Functional, genetic and bioinformatic characterization of a calcium/calmodulin kinase gene in Sporothrix schenckii. | BMC microbiology 20070101 |
| Chemically modified dansyl probes: a fluorescent diagnostic for ion and proton detection in solution and in polymers. | Organic letters 20060413 |
| Phenolic P2/P3 core motif as thrombin inhibitors--design, synthesis, and X-ray co-crystal structure. | Bioorganic & medicinal chemistry letters 20060215 |
| Carbonic anhydrase inhibitors: the first QSAR study on inhibition of tumor-associated isoenzyme IX with aromatic and heterocyclic sulfonamides. | Bioorganic & medicinal chemistry letters 20040621 |
| Ground and excited-state electronic interactions in poly(propylene amine) dendrimers functionalized with naphthyl units: effect of protonation and metal complexation. | Chemphyschem : a European journal of chemical physics and physical chemistry 20040419 |
| Caffeoyl naphthalenesulfonamide derivatives as HIV integrase inhibitors. | Bioorganic & medicinal chemistry 20030815 |
| Carbonic anhydrase inhibitors: inhibition of the tumor-associated isozyme IX with aromatic and heterocyclic sulfonamides. | Bioorganic & medicinal chemistry letters 20030324 |
| Development of novel copper(II) complexes of benzothiazole- N-sulfonamides as protective agents against superoxide anion. Crystal structures of [Cu( N-2-(4-methylbenzothiazole)benzenesulfonamidate)(2)(py)(2)] and [Cu( N-2-(6-nitrobenzothiazole)naphthalenesulfonamidate)(2)(py)(2)]. | Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry 20030101 |
| Novel potent antagonists of human neuropeptide Y Y5 receptors. Part 3: 7-methoxy-1-hydroxy-1-substituted tetraline derivatives. | Bioorganic & medicinal chemistry letters 20020311 |
| Assembly of gap junction channels: mechanism, effects of calmodulin antagonists and identification of connexin oligomerization determinants. | European journal of biochemistry 20010801 |
| Naphthalenesulphonamides block neutrophil superoxide production by intact cells and in a cell-free system: is myosin light chain kinase responsible for these effects? | The Biochemical journal 19951001 |
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