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• 试剂商城
• 直接询价

分类

• {SNA} Building Blocks, C7 to C9, Chemical Synthesis, Heterocyclic Building Blocks, Indoles
• {uni_hamburg} no charge; nitrogen heterocycle; carbocycle; aromatic; large ring; fused rings; 5ring; 6ring; 9ring; amide; ketone; lactame; 1fragment
• Building Blocks, C7 to C9, Chemical Synthesis, Heterocyclic Building Blocks, Indoles

产品应用

• Reactant for preparation of:
• Potential antibacterial and antifungal agents;
• spiro[indole-thiazolidi?nones] as a medicinally important scaffold;
• Potential antimycobacterial agents;
• Anticonvulsant agents;
• Inhibitors of human transglutaminase 2;
• Anthelmintic agents;
• Anti-human immunodeficiency virus (HIV) agents;
• Antimicrobial agents;
• Potential antitubercular agents;
• Inhibitors of acetylcholinesterase.

相关文献及参考

• Short: III/31a Title: Nuclear Quadrupole Resonance Spectroscopy Data: Nuclei D ... Cu Author: Chihara, H.; Nakamura, N. Editor: Hellwege, K.-H.; Hellwege, A.M. Source: Landolt-Börnstein, New Series Volume: III/31a Year: 1993 Keyword: NQR ISBN: 3-540-55146-8 ISBN: 978-3-540-55146-1 Internet Resource: DOI:10.1007/b43999 RefComment: VIII, 437 pages. Hardcover Abstract: Volume III/31 continues the compilation of nuclear quadrupole resonance spectroscopy data of solid substances which started in with volume III/20 in 1987 covering the literature from the beginning of nuclear quadrupole resonance spectroscopy in 1951 to 1982 and containing the data for 8000 substances in the solid state, distributed among three subvolumes III/20 a, b, and c. Volume III/31 covers the literature published in the period from the end of 1982
• 4. Praveen, C.; et al. Bioorg. Med. Chem. Lett. 21 , 4072, (2011)
• Beil. 21 ,456
• 8. Bhardwaj, S.; et al. J. Pharm. Res. 3 , 2983, (2010)
• 1. Ozil, M.; et al. J. Chem. Res. (M) 35 , 268, (2011)
• 6. Suresh, C. H.; et al. Int. Res. J. Pharm. 2 , 257, (2011)
• FT-IR 2 (2), 3054:C / FT-IR 1 (2), 395:A / FT-NMR 1 (2), 1440:B / IR-Spectra (3), 1094:C / IR-Spectra (2), 955:E / NMR-Reference 2 (2), 374:A / RegBook 1 (2), 2059:D / Sax 6 , 2029 / Structure Index 1 , 327:A:5
• 9. Prasanna, P.; et al. Eur. J. Med. Chem. 45 , 5653, (2010)
• 3. Aboul-Fadl, T.; et al. Molecules 16 , 5194, (2011) 摘要
• 2. Dandia, A.; et al. Green Chem. 13 , 1852, (2011)
• 7. Kumari, G.; et al. Eur. J. Med. Chem. 46 , 1181, (2011)
• 10. Ali, M. A.; et al. Bioorg. Med. Chem. Lett. 20 , 7064, (2010)
• 5. Kloeck, C.; et al. Bioorg. Med. Chem. Lett. 21 , 2692, (2011)

安全信息

GHS Symbol

TYPE OF TEST            : Mutation in microorganisms
TEST SYSTEM             : Bacteria - Salmonella typhimurium
DOSE/DURATION           : 100 nmol/plate
REFERENCE :
   MUREAV Mutation Research.  (Elsevier Science Pub. B.V., POB 211, 1000 AE
   Amsterdam, Netherlands) V.1-    1964-  Volume(issue)/page/year: 58,11,1978

其他信息

• Acros Organics:5-硝基靛红 5-Nitroisatin, 97%(611-09-6)
• 5-硝基靛红价格(试剂级):更新日期 产品编号 产品名称 包装 价格 2014/06/02 N0572 5-硝基靛红 5-Nitroisatin 5G 357元 2014/06/02 N0572 5-硝基靛红 5-Nitroisatin 25G 1200元 2010/06/21 128720250 5-硝基靛红 5-Nitroisatin 97% 25 GR 1225元
• MOL 文件:611-09-6.mol
• 图谱信息:5-硝基靛红(611-09-6)红外图谱(IR2) 5-硝基靛红(611-09-6)红外图谱(IR1) 5-硝基靛红(611-09-6)质谱(MS) 5-硝基靛红(611-09-6)核磁图( 13 CNMR) 5-硝基靛红(611-09-6)核磁图( 1 HNMR)
• MSDS 信息:5-Nitroisatin(611-09-6).msds
• Sigma Aldrich:611-09-6(sigmaaldrich)
• 5-Nitroisatin is a useful reactant for the synthesis of antibacterial, antifungal, antimycobacterial, antimicrobial, ans antitubercular agents. 5-Nitroisatin is also used to synthesize spiro[indole-thiazolidinones], anticonvulsant agents, human transglutaminase 2 inhibitors, anthelmic agents, acetylcholinesterase inhibitors, and anti-HIV agents.
• Alfa Aesar:5-硝基靛红,98% 5-Nitroisatin, 98%(611-09-6)
• TCI Shanghai:5-硝基靛红 5-Nitroisatin,>;98.0%(LC)(T)(611-09-6)