Neoxaline
Code | Size | Price |
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TAR-T33641-5mg | 5mg | £850.00 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Overview
Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃
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Further Information
Bioactivity:
Neoxaline is an alkaloid isolated from fermentation broth of Aspergillus japonicus.
CAS:
71812-10-7
Formula:
C23H25N5O4
Molecular Weight:
435.484
Purity:
0.98
SMILES:
CON1c2ccccc2C2(CC(O)C(=O)N3C(=C/c4c[nH]cn4)C(=O)NC123)C(C)(C)C=C
References
Sunazuka T, Shirahata T, Tsuchiya S, Hirose T, Mori R, Harigaya Y, Kuwajima I, Omura S. A concise stereoselective route to the indoline spiroaminal framework of neoxaline and oxaline. Org Lett. 2005 Mar 3;7(5):941-3. PubMed PMID: 15727480.
Hirano A, Iwai Y, Masuma R, Tei K, Omura S. Neoxaline, a new alkaloid produced by Aspergillus japonicus. Production, isolation and properties. J Antibiot (Tokyo). 1979 Aug;32(8):781-5. PubMed PMID: 500498.
Mart?n JF, Liras P. Evolutionary formation of gene clusters by reorganization: the meleagrin/roquefortine paradigm in different fungi. Appl Microbiol Biotechnol. 2016 Feb;100(4):1579-87. doi: 10.1007/s00253-015-7192-y. Epub 2015 Dec 15. Review. PubMed PMID: 26668029.
Ideguchi T, Yamada T, Shirahata T, Hirose T, Sugawara A, Kobayashi Y, ?mura S, Sunazuka T. Asymmetric total synthesis of neoxaline. J Am Chem Soc. 2013 Aug 28;135(34):12568-71. doi: 10.1021/ja406657v. Epub 2013 Aug 19. PubMed PMID: 23957424.