Identification Common Name Gonyautoxin 5 Class Small Molecule Description Gonyautoxin 5 is a paralytic shellfish toxin. It can breaks the vicious circle of pain and spasm that leads to anal fissure.
Read more Contaminant Sources FooDB Chemicals
STOFF IDENT Compounds
T3DB toxins Contaminant Type Amide
Amine
Animal Toxin
Ether
Food Toxin
Marine Toxin
Natural Compound
Organic Compound
PFAS Chemical Structure Synonyms Value Source Gonyautoxin V Kegg GTX5 Kegg Toxin b1 Kegg N-Sulfo{[(4R,10as,10BS)-10,10-dihydroxy-2,6-diimino-decahydropyrrolo[1,2-c]purin-4-yl]methoxy}carboximidate Generator N-Sulpho{[(4R,10as,10BS)-10,10-dihydroxy-2,6-diimino-decahydropyrrolo[1,2-c]purin-4-yl]methoxy}carboximidate Generator N-Sulpho{[(4R,10as,10BS)-10,10-dihydroxy-2,6-diimino-decahydropyrrolo[1,2-c]purin-4-yl]methoxy}carboximidic acid Generator
Chemical Formula C10 H17 N7 O7 S Average Molecular Mass 379.350 g/mol Monoisotopic Mass 379.091 g/mol CAS Registry Number 64296-25-9 IUPAC Name N-sulfo{[(4R,10aS,10bS)-10,10-dihydroxy-2,6-diimino-decahydropyrrolo[1,2-c]purin-4-yl]methoxy}carboximidic acid Traditional Name N-sulfo{[(4R,10aS,10bS)-10,10-dihydroxy-2,6-diimino-hexahydro-1H-pyrrolo[1,2-c]purin-4-yl]methoxy}carboximidic acid SMILES [H][C@@]12NC(=N)N[C@]11N(CCC1(O)O)C(=N)N[C@@]2([H])COC(O)=NS(O)(=O)=O InChI Identifier InChI=1S/C10H17N7O7S/c11-6-14-5-4(3-24-8(18)16-25(21,22)23)13-7(12)17-2-1-9(19,20)10(5,17)15-6/h4-5,19-20H,1-3H2,(H2,12,13)(H,16,18)(H3,11,14,15)(H,21,22,23)/t4-,5-,10-/m0/s1 InChI Key JKKCSFJSULZNDN-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
Hydropyrimidine
1,4,5,6-tetrahydropyrimidine
2-imidazoline
Organic sulfuric acid or derivatives
Pyrrolidine
Guanidine
Carbonic acid derivative
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carbonyl hydrate
Carboximidamide
Hydrocarbon derivative
Organopnictogen compound
Carbonyl group
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
Organic oxide
Organic oxygen compound
Aliphatic heteropolycyclic compound Molecular Framework Aliphatic heteropolycyclic compounds External Descriptors Not Available 
