N-Sulfocarbamoyl-Gonyautoxin-2 and -3

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Description

N-sulfocarbamoyl-gonyautoxin-2 and -3 are analogs of gonyautoxins found in marine microalgae and freshwater cyanobacteria. These compounds specifically feature a sulfonyl group, which enhances their hydrophilicity and alters their interaction with voltage-gated sodium channels in nerve cells, resulting in neurotoxic effects. Due to their potent biological activity and the ecological implications of their presence, these toxins are subjects of significant research within marine biology, toxicology, and environmental science.

Specification

Item	N-Sulfocarbamoyl-Gonyautoxin-2	N-Sulfocarbamoyl-Gonyautoxin-3
Catalog	MC80173304	MC80226626
CAS	80173-30-4	80226-62-6
Molecular Formula	C10H17N7O11S2	C10H17N7O11S2
Molecular Weight	475.41	475.41
Purity	>99%	>99%
Concentration	40.1±2.4 µg/g	11.5±0.9 µg/g
Solvent	AcOH pH5 (aq)	AcOH pH5 (aq)
SMILES	NC1=N[C@H]2[C@H](COC(=O)NS(=O)(=O)O)N=C(N)N3C[C@@H](OS(=O)(=O)O)C(O)(O)[C@]23N1	NC1=N[C@H]2[C@H](COC(=O)NS(=O)(=O)O)N=C(N)N3C[C@H](OS(=O)(=O)O)C(O)(O)[C@]23N1
InChi Code	InChI=1S/C10H17N7O11S2/c11-6-14-5-3(2-27-8(18)16-29(21,22)23)13-7(12)17-1-4(28-30(24,25)26)10(19,20)9(5,17)15-6/h3-5,19-20H,1-2H2,(H2,12,13)(H,16,18)(H3,11,14,15)(H,21,22,23)(H,24,25,26)/t3-,4+,5-,9-/m0/s1	InChI=1S/C10H17N7O11S2/c11-6-14-5-3(2-27-8(18)16-29(21,22)23)13-7(12)17-1-4(28-30(24,25)26)10(19,20)9(5,17)15-6/h3-5,19-20H,1-2H2,(H2,12,13)(H,16,18)(H3,11,14,15)(H,21,22,23)(H,24,25,26)/t3-,4-,5-,9-/m0/s1
Storage Temperature	Store at -20 °C.	Store at -20 °C.

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For Research Use Only. Not for use in diagnostic or therapeutic procedures.