MedKoo Cat#: 584421 | Name: Hgg 12

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Hgg 12 is used therapeutically in organophosphate poisoning.

Chemical Structure

Hgg 12
Hgg 12
CAS#83972-73-0

Theoretical Analysis

MedKoo Cat#: 584421

Name: Hgg 12

CAS#: 83972-73-0

Chemical Formula: C20H19Cl2N3O3

Exact Mass: 419.0803

Molecular Weight: 420.29

Elemental Analysis: C, 57.16; H, 4.56; Cl, 16.87; N, 10.00; O, 11.42

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
Hgg 12; Hgg12; Hgg-12
IUPAC/Chemical Name
Pyridinium, 1-(((3-benzoylpyridinio)methoxy)methyl)-2-((hydroxyimino)methyl)-, dichloride
InChi Key
WEOUPFRRXAHWCD-UHFFFAOYSA-M
InChi Code
InChI=1S/C20H18N3O3.2ClH/c24-20(17-7-2-1-3-8-17)18-9-6-11-22(14-18)15-26-16-23-12-5-4-10-19(23)13-21-25;;/h1-14H,15-16H2;2*1H/q+1;;/p-1
SMILES Code
O/N=C/C1=CC=CC=[N+]1COC[N+]2=CC=CC(C(C3=CC=CC=C3)=O)=C2.[Cl-].[Cl-]
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 420.29 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Hauser W, Weger N. Therapeutic effects of the bis-pyridinium salts HGG-12, HGG-42, and atropine, benactyzine in organophosphate poisoning of dogs. Arch Toxicol Suppl. 1979;(2):393-6. PubMed PMID: 288351. 2: van Helden HP, van der Wiel HJ, Zijlstra JJ, Melchers BP, Busker RW. Comparison of the therapeutic effects and pharmacokinetics of HI-6, HLö-7, HGG-12, HGG-42 and obidoxime following non-reactivatable acetylcholinesterase inhibition in rats. Arch Toxicol. 1994;68(4):224-30. PubMed PMID: 8067894. 3: Cetković S, Cvetković M, Jandrić D, Cosić M, Bosković B. Effect of PAM-2 Cl, HI-6, and HGG-12 in poisoning by tabun and its thiocholine-like analog in the rat. Fundam Appl Toxicol. 1984 Apr;4(2 Pt 2):S116-23. PubMed PMID: 6547103. 4: Bosković B, Kovacević V, Jovanović D. PAM-2 Cl, HI-6, and HGG-12 in soman and tabun poisoning. Fundam Appl Toxicol. 1984 Apr;4(2 Pt 2):S106-15. PubMed PMID: 6724203. 5: Klimmek R, Eyer P. Pharmacokinetics and toxicity of the oxime HGG 12 in dogs. Arch Toxicol. 1985 Sep;57(4):237-42. PubMed PMID: 4091648. 6: Reithmann C, Berger HJ, Hilf G, Werdan K. The oxime HGG-12 as a muscarinic acetylcholine receptor antagonist without intrinsic activity in cardiac membranes. Arch Toxicol. 1991;65(6):518-23. PubMed PMID: 1929874. 7: Pantelić D. [Comparative reactivation efficacy of the oximes HI-6 and HGG-12 in the central nervous system and blood of rats poisoned with nerve gases used in warfare]. God Vojnomed Akad. 1986;28:35-40. Croatian. PubMed PMID: 3482058. 8: Kloog Y, Galron R, Balderman D, Sokolovsky M. Reversible and irreversible inhibition of rat brain muscarinic receptors is related to different substitutions on bisquaternary pyridinium oximes. Arch Toxicol. 1985 Oct;58(1):37-9. PubMed PMID: 3907590. 9: Eyer P, Hell W. The metabolism of 3-benzoylpyridine. Xenobiotica. 1983 Nov;13(11):649-59. PubMed PMID: 6673376. 10: van Helden HP, van der Wiel HJ, Wolthuis OL. Therapy of organophosphate poisoning: the marmoset as a model for man. Br J Pharmacol. 1983 Mar;78(3):579-89. PubMed PMID: 6301602; PubMed Central PMCID: PMC2044728. 11: Clement JG. Efficacy of mono- and bis-pyridinium oximes versus soman, sarin and tabun poisoning in mice. Fundam Appl Toxicol. 1983 Nov-Dec;3(6):533-5. PubMed PMID: 6662294. 12: van Helden HP, de Lange J, Busker RW, Melchers BP. Therapy of organophosphate poisoning in the rat by direct effects of oximes unrelated to ChE reactivation. Arch Toxicol. 1991;65(7):586-93. PubMed PMID: 1664202. 13: Schlagmann C, Ulbrich H, Remien J. Bispyridinium (oxime) compounds antagonize the "ganglion blocking" effect of pyridostigmine in isolated superior cervical ganglia of the rat. Arch Toxicol. 1990;64(6):482-9. PubMed PMID: 1980409. 14: Jovanović D. The effect of bis-pyridinium oximes on neuromuscular blockade induced by highly toxic organophosphates in rat. Arch Int Pharmacodyn Ther. 1983 Apr;262(2):231-41. PubMed PMID: 6307195. 15: Lundy PM, Tremblay KP. Ganglion blocking properties of some bispyridinium soman antagonists. Eur J Pharmacol. 1979 Nov 23;60(1):47-53. PubMed PMID: 42547. 16: Kuhnen-Clausen D, Hagedorn I, Gross G, Bayer H, Hucho F. Interactions of bisquaternary pyridine salts (H-oximes) with cholinergic receptors. Arch Toxicol. 1983 Nov;54(3):171-9. PubMed PMID: 6661028. 17: Eyer P, Kawan A, Ladstetter B. Formation of cyanide after i.v. administration of the oxime HI 6 to dogs. Arch Toxicol. 1987;61(1):63-9. PubMed PMID: 3439876. 18: Endres W, Spuler A, ten Bruggencate G. Acetylcholinesterase reactivators antagonize epileptiform bursting induced by paraoxon in guinea pig hippocampal slices. J Pharmacol Exp Ther. 1989 Dec;251(3):1181-6. PubMed PMID: 2600810. 19: Hauser W, Kirsch D, Weger N. Therapeutic effects of new oximes, benactyzine and atropine in Soman poisoning: Part II. effect of HGG12, HGG42, and obidoxime in poisoning with various anticholinesterase agents in Beagle dogs. Fundam Appl Toxicol. 1981 Mar-Apr;1(2):164-8. PubMed PMID: 6764202. 20: Kloog Y, Galron R, Sokolovsky M. Bisquaternary pyridinium oximes as presynaptic agonists and postsynaptic antagonists of muscarinic receptors. J Neurochem. 1986 Mar;46(3):767-72. PubMed PMID: 3950607.