Identification Common Name Gonyautoxin 6 Class Small Molecule Description Gonyautoxin 6 is paralytic shellfish toxin. It can breaks the vicious circle of pain and spasm that leads to anal fissure. It is the most unstable toxin in any condition and at temperatures lower than 4 °C there is no important change in the other toxins in the first year of storage.
Read more Contaminant Sources FooDB Chemicals
T3DB toxins Contaminant Type Amide
Amine
Animal Toxin
Ether
Food Toxin
Marine Toxin
Natural Compound
Organic Compound
PFAS Chemical Structure Synonyms Value Source Gonyautoxin VI Kegg GTX6 Kegg Toxin b2 Kegg N-Sulfo{[(4R,10as,10BS)-5,10,10-trihydroxy-2,6-diimino-decahydropyrrolo[1,2-c]purin-4-yl]methoxy}carboximidate Generator N-Sulpho{[(4R,10as,10BS)-5,10,10-trihydroxy-2,6-diimino-decahydropyrrolo[1,2-c]purin-4-yl]methoxy}carboximidate Generator N-Sulpho{[(4R,10as,10BS)-5,10,10-trihydroxy-2,6-diimino-decahydropyrrolo[1,2-c]purin-4-yl]methoxy}carboximidic acid Generator Gonyautoxin-VI MeSH
Chemical Formula C10 H17 N7 O8 S Average Molecular Mass 395.349 g/mol Monoisotopic Mass 395.086 g/mol CAS Registry Number 82810-44-4 IUPAC Name N-sulfo{[(4R,10aS,10bS)-5,10,10-trihydroxy-2,6-diimino-decahydropyrrolo[1,2-c]purin-4-yl]methoxy}carboximidic acid Traditional Name N-sulfo{[(4R,10aS,10bS)-5,10,10-trihydroxy-2,6-diimino-hexahydropyrrolo[1,2-c]purin-4-yl]methoxy}carboximidic acid SMILES [H][C@@]12NC(=N)N[C@]11N(CCC1(O)O)C(=N)N(O)[C@@]2([H])COC(O)=NS(O)(=O)=O InChI Identifier InChI=1S/C10H17N7O8S/c11-6-13-5-4(3-25-8(18)15-26(22,23)24)17(21)7(12)16-2-1-9(19,20)10(5,16)14-6/h4-5,12,19-21H,1-3H2,(H,15,18)(H3,11,13,14)(H,22,23,24)/t4-,5-,10-/m0/s1 InChI Key ALRRPAKWGUBPBK-HGRQIUPRSA-N Chemical Taxonomy Description Belongs to the class of organic compounds known as saxitoxins, gonyautoxins, and derivatives. Saxitoxins, gonyautoxins, and derivatives are compounds with a structure based on a 2,6-diamino-4-methyl-pyrrolo[1,2-c]purin-10-ol skeleton. Kingdom Organic compounds Super Class Phenylpropanoids and polyketides Class Saxitoxins, gonyautoxins, and derivatives Sub Class Not Available Direct Parent Saxitoxins, gonyautoxins, and derivatives Alternative Parents Substituents Saxitoxin-gonyautoxin skeleton
Imidazopyrimidine
Alkaloid or derivatives
1,3-diazinane
N-hydroxyguanidine
Imidazolidine
Organic sulfuric acid or derivatives
Pyrrolidine
Guanidine
Azacycle
Carbonyl hydrate
Polyol
Organoheterocyclic compound
Carboximidamide
Organonitrogen compound
Organopnictogen compound
Imine
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Organic nitrogen compound
Organic oxygen compound
Aliphatic heteropolycyclic compound Molecular Framework Aliphatic heteropolycyclic compounds External Descriptors Not Available