80173-30-4

Basic information

• Product Name: (3aS,10aS)-3aα,4,9,10-Tetrahydro-2,6-diamino-4α-[[(sulfoaminocarbonyl)oxy]methyl]-1H,8H-pyrrolo[1,2-c]purine-9β,10,10-triol 9-sulfate
• Synonyms: (3aS,10aS)-3aα,4,9,10-Tetrahydro-2,6-diamino-4α-[[(sulfoaminocarbonyl)oxy]methyl]-1H,8H-pyrrolo[1,2-c]purine-9β,10,10-triol 9-sulfate;11-Epigonyautoxin VIII;11-Epi-GTX8;Protogonyautoxin I;PX1;Toxin C1;N-Sulfocarbamoyl-gonyautoxin-2 and -3
• CAS NO: 80173-30-4
• Molecular Formula: C23H26FN3O2
• Molecular Weight: 395.4698432
• Mol File: 80173-30-4.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Density: 2.61g/cm³
• Refractive Index: 1.962
• PKA: -3.88±0.18(Predicted)
• CAS DataBase Reference: (3aS,10aS)-3aα,4,9,10-Tetrahydro-2,6-diamino-4α-[[(sulfoaminocarbonyl)oxy]methyl]-1H,8H-pyrrolo[1,2-c]purine-9β,10,10-triol 9-sulfate(CAS DataBase Reference)
• NIST Chemistry Reference: (3aS,10aS)-3aα,4,9,10-Tetrahydro-2,6-diamino-4α-[[(sulfoaminocarbonyl)oxy]methyl]-1H,8H-pyrrolo[1,2-c]purine-9β,10,10-triol 9-sulfate(80173-30-4)
• EPA Substance Registry System: (3aS,10aS)-3aα,4,9,10-Tetrahydro-2,6-diamino-4α-[[(sulfoaminocarbonyl)oxy]methyl]-1H,8H-pyrrolo[1,2-c]purine-9β,10,10-triol 9-sulfate(80173-30-4)

Safety Data

• Hazardous Substances Data: 80173-30-4(Hazardous Substances Data)

Usage

Uses

N-Sulfocarbamoylgonyautoxin 2 is a paralytic shellfish toxins. C1. EU regulated marine toxin.

InChI:InChI=1/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

Upstream product

• 80173-30-4 gonyautoxin VIII 
• 80173-30-4 C₁₀H₁₇N₇O₁₁S₂ 

Downstream Products

• 80173-30-4 gonyautoxin VIII 
• 80173-30-4 C₁₀H₁₇N₇O₁₁S₂ 

Relevant articles and documents

Isolation of side-chain sulfated saxitoxin analogs. Their significance in interpretation of the mechanism of action

A newly discovered toxin, gonyautoxin-VIII, and two previously reported toxins, gonyautoxin-V and -VI, have been found to have carbamoyl N-sulfate conjugation. The exceptionally low toxic nature of the derivatives seems to support the hypothesis that the toxins interact on the surface of excitable membranes.