N-Sulfocarbamoyl-Gonyautoxin-1 and -4

Inquiry

Description

N-sulfocarbamoyl-gonyautoxin-1 and -4 are N-sulfonylcarbamoyl analogs of gonyautoxin I (GTX1) and IV (GTX4). These compounds belong to a class of substances known for their high affinity for sodium channels in nerve cells, leading to inhibition of neuronal signaling and muscle paralysis. The introduction of sulfocarbamoyl groups in their structure enhances their stability and biological activity, making them significant both for scientific research and for understanding the mechanisms of toxin action in marine ecosystems.

Specification

Item	N-Sulfocarbamoyl-Gonyautoxin-1	N-Sulfocarbamoyl-Gonyautoxin-4
Catalog	MC89614459	MC89674986
CAS	89614-45-9	89674-98-6
Molecular Formula	C₁₀H₁₇N₇O₁₂S₂	C₁₀H₁₇N₇O₁₂S₂
Molecular Weight	491.40	491.40
Purity	>97%	>97%
Concentration	12.6±0.9 µg/g	3.35±0.32 µg/g
Solvent	AcOH pH5 (aq)	AcOH pH5 (aq)
SMILES	ON1[C@@H](COC(=O)NS(=O)(=O)[O-])[C@@H]2NC(=[NH2+])N[C@]23N(C[C@H](OS(=O)(=O)[O-])C3(O)O)C1=[NH2+]	ON1[C@@H](COC(=O)NS(=O)(=O)[O-])[C@@H]2NC(=[NH2+])N[C@]23N(C[C@@H](OS(=O)(=O)[O-])C3(O)O)C1=[NH2+]
InChi Code	InChI=1S/C10H17N7O12S2/c11-6-13-5-3(2-28-8(18)15-30(22,23)24)17(21)7(12)16-1-4(29-31(25,26)27)10(19,20)9(5,16)14-6/h3-5,12,19-21H,1-2H2,(H,15,18)(H3,11,13,14)(H,22,23,24)(H,25,26,27)/t3-,4-,5-,9-/m0/s1	InChI=1S/C10H17N7O12S2/c11-6-13-5-3(2-28-8(18)15-30(22,23)24)17(21)7(12)16-1-4(29-31(25,26)27)10(19,20)9(5,16)14-6/h3-5,12,19-21H,1-2H2,(H,15,18)(H3,11,13,14)(H,22,23,24)(H,25,26,27)/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.