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]
^"KNApSAcK Metabolite Information - C00047317". www.knapsackfamily.com.
^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; de Moraes, Manoel Odorico; Young, Maria Claudia Marx; Bolzani, Vanderlan da Silva (2009-03-27). "Cytotoxic Guanidine Alkaloids fromPterogyne nitens△". Journal of Natural Products. 72 (3). American Chemical Society (ACS): 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. 82 (6). American Chemical Society (ACS): 1656–1663. doi:10.1021/acs.jnatprod.9b00178. ISSN 0163-3864. PMID 31117524. S2CID 162180379.
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nitensidine, toxic, alkaloid, natural, product, that, isolated, from, leaves, south, american, legume, pterogyne, nitens, also, hypothesized, possible, intermediate, still, unknown, seemingly, monoterpene, based, terrestrial, biosynthetic, pathway, tetrodotoxi. 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 Nitensidine D NamesIUPAC name E 2 3 7 dimethylocta 2 6 dien 1 yl guanidineOther names geranyl guanidineIdentifiersCAS Number 1107631 55 9 N 1 3D model JSmol Interactive imageChEMBL ChEMBL556739ChemSpider 24623230PubChem CID 45269644InChI InChI 1S C11H21N3 c1 9 2 5 4 6 10 3 7 8 14 11 12 13 h5 7H 4 6 8H2 1 3H3 H4 12 13 14 b10 7 Key WDTUVHUDPPUQMN JXMROGBWSA NSMILES CC CCC C C CN C N N C CPropertiesChemical formula C 11H 21N 3Molar mass 195 310 g mol 1Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa Infobox referencesSee also editGalegineReferences edit KNApSAcK Metabolite Information C00047317 www knapsackfamily com Regasini Luis Octavio Castro Gamboa Ian Silva Dulce Helena Siqueira Furlan Maysa Barreiro Eliezer Jesus Ferreira Paulo Michel Pinheiro Pessoa Claudia Lotufo Leticia Veras Costa de Moraes Manoel Odorico Young Maria Claudia Marx Bolzani Vanderlan da Silva 2009 03 27 Cytotoxic Guanidine Alkaloids fromPterogyne nitens Journal of Natural Products 72 3 American Chemical Society ACS 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 82 6 American Chemical Society ACS 1656 1663 doi 10 1021 acs jnatprod 9b00178 ISSN 0163 3864 PMID 31117524 S2CID 162180379 nbsp This article about an alkaloid is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Nitensidine D amp oldid 1166496870, wikipedia, wiki, book, books, library,
