1.0 2010-04-08 22:09:43 UTC 2025-11-18 23:29:12 UTC FDB011568 Gonyautoxin V Production by Gonyaulax and Protogonyaulax subspecies Gonyautoxin V is found in mollusks. Gonyautoxin V Gonyautoxin-v Toxin B1 C10H17N7O7S 379.35 379.091016623 2,6-diimino-4-({[(sulfoamino)carbonyl]oxy}methyl)-decahydropyrrolo[1,2-c]purine-10,10-diol 2,6-diimino-4-({[(sulfoamino)carbonyl]oxy}methyl)-hexahydro-1H-pyrrolo[1,2-c]purine-10,10-diol 64296-25-9 OC1(O)CCN2C(=N)NC(COC(=O)NS(O)(=O)=O)C3NC(=N)NC123 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) JKKCSFJSULZNDN-UHFFFAOYSA-N 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. Saxitoxins, gonyautoxins, and derivatives Organic compounds Phenylpropanoids and polyketides Saxitoxins, gonyautoxins, and derivatives Aliphatic heteropolycyclic compounds Alkaloids and derivatives Azacyclic compounds Carbonyl hydrates Carboximidamides Diazinanes Guanidines Hydrocarbon derivatives Imidazolidines Imidazopyrimidines Imines Organic oxides Organic sulfuric acids and derivatives Organopnictogen compounds Pyrrolidines 1,3-diazinane Aliphatic heteropolycyclic compound Alkaloid or derivatives Azacycle Carbonyl hydrate Carboximidamide Guanidine Hydrocarbon derivative Imidazolidine Imidazopyrimidine Imine Organic nitrogen compound Organic oxide Organic oxygen compound Organic sulfuric acid or derivatives Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Pyrrolidine Saxitoxin-gonyautoxin skeleton logp -2.26 ALOGPS logs -2.35 ALOGPS solubility 1.70e+00 g/l ALOGPS logp -5.3 ChemAxon pka_strongest_acidic -1.6 ChemAxon pka_strongest_basic 10.15 ChemAxon iupac 2,6-diimino-4-({[(sulfoamino)carbonyl]oxy}methyl)-decahydropyrrolo[1,2-c]purine-10,10-diol ChemAxon average_mass 379.35 ChemAxon mono_mass 379.091016623 ChemAxon smiles OC1(O)CCN2C(=N)NC(COC(=O)NS(O)(=O)=O)C3NC(=N)NC123 ChemAxon formula C10H17N7O7S ChemAxon inchi 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) ChemAxon inchikey JKKCSFJSULZNDN-UHFFFAOYSA-N ChemAxon polar_surface_area 220.19 ChemAxon refractivity 98.83 ChemAxon polarizability 32.7 ChemAxon rotatable_bond_count 3 ChemAxon acceptor_count 12 ChemAxon donor_count 9 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 10531 Specdb::CMs 43336 Specdb::CMs 167302 Specdb::NmrOneD 120378 Specdb::NmrOneD 120379 Specdb::NmrOneD 120380 Specdb::NmrOneD 120381 Specdb::NmrOneD 120382 Specdb::NmrOneD 120383 Specdb::NmrOneD 120384 Specdb::NmrOneD 120385 Specdb::NmrOneD 120386 Specdb::NmrOneD 120387 Specdb::NmrOneD 120388 Specdb::NmrOneD 120389 Specdb::NmrOneD 120390 Specdb::NmrOneD 120391 Specdb::NmrOneD 120392 Specdb::NmrOneD 120393 Specdb::NmrOneD 120394 Specdb::NmrOneD 120395 Specdb::NmrOneD 120396 Specdb::NmrOneD 120397 Specdb::MsMs 289213 Specdb::MsMs 289214 Specdb::MsMs 289215 Specdb::MsMs 328579 Specdb::MsMs 328580 Specdb::MsMs 328581 Specdb::MsMs 2299332 Specdb::MsMs 2299333 Specdb::MsMs 2299334 Specdb::MsMs 2639605 Specdb::MsMs 2639606 Specdb::MsMs 2639607 HMDB33513 #<Reference:0x000055ce31eb9178> Mollusks Unknown generic 6447