Chemistry:Nitensidine D
From HandWiki
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| IUPAC name
(E)-2-(3,7-dimethylocta-2,6-dien-1-yl)guanidine
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Other names
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C11H21N3 | |
| Molar mass | 195.310 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Tracking categories (test):
Nitensidine D is a toxic alkaloid natural product that was isolated from the leaves of the South American legume Pterogyne nitens.[2] It is also hypothesized to be a possible intermediate in the still unknown, seemingly monoterpene based, terrestrial biosynthetic pathway for tetrodotoxin.[3]
See also
References
- ↑ "KNApSAcK Metabolite Information - C00047317". http://www.knapsackfamily.com/knapsack_core/information.php?sname=C_ID&word=C00047317.
- ↑ Regasini, Luis Octávio; Castro-Gamboa, Ian; Silva, Dulce Helena Siqueira; Furlan, Maysa; Barreiro, Eliezer Jesus; Ferreira, Paulo Michel Pinheiro; Pessoa, Cláudia; Lotufo, Letícia Veras Costa et al. (2009-03-27). "Cytotoxic Guanidine Alkaloids fromPterogyne nitens△". Journal of Natural Products (American Chemical Society (ACS)) 72 (3): 473–476. doi:10.1021/np800612x. ISSN 0163-3864. PMID 19159272.
- ↑ Kudo, Yuta; Yotsu-Yamashita, Mari (2019-05-22). "Isolation and Biological Activity of 8-Epitetrodotoxin and the Structure of a Possible Biosynthetic Shunt Product of Tetrodotoxin, Cep-226A, from the Newt Cynops ensicauda popei". Journal of Natural Products (American Chemical Society (ACS)) 82 (6): 1656–1663. doi:10.1021/acs.jnatprod.9b00178. ISSN 0163-3864. PMID 31117524.
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