MedKoo Cat#: 412763 | Name: CGS 12066A

Description:

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

CGS 12066A is a drug which acts as a potent and selective agonist for the 5-HT1B receptor with lower affinity for the three 5-HT₂ receptor subtypes. It is used for studying the role of the 5-HT1B receptor in various processes including perception of pain and the sleep-wake cycle.

Chemical Structure

CGS 12066A
CGS 12066A
CAS#121741-03-5

Theoretical Analysis

MedKoo Cat#: 412763

Name: CGS 12066A

CAS#: 121741-03-5

Chemical Formula: C19H19F3N4O4

Exact Mass: 424.1358

Molecular Weight: 424.38

Elemental Analysis: C, 53.77; H, 4.51; F, 13.43; N, 13.20; O, 15.08

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 #
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Synonym
CGS 12066A; CGS12066A; CGS-12066A
IUPAC/Chemical Name
Pyrrolo(1,2-a)quinoxaline, 4-(4-methyl-1-piperazinyl)-7-(trifluoromethyl)-, ethanedioate (1:1)
InChi Key
RRTXUQKIVYYULV-UHFFFAOYSA-N
InChi Code
InChI=1S/C17H17F3N4.C2H2O4/c1-22-7-9-23(10-8-22)16-15-3-2-6-24(15)14-5-4-12(17(18,19)20)11-13(14)21-16;3-1(4)2(5)6/h2-6,11H,7-10H2,1H3;(H,3,4)(H,5,6)
SMILES Code
FC(C1=CC2=C(N3C(C(N4CCN(C)CC4)=N2)=CC=C3)C=C1)(F)F.O=C(O)C(O)=O
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 424.38 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: Brumley MR, Robinson SR. The serotonergic agonists quipazine, CGS-12066A, and alpha-methylserotonin alter motor activity and induce hindlimb stepping in the intact and spinal rat fetus. Behav Neurosci. 2005 Jun;119(3):821-33. doi: 10.1037/0735-7044.119.3.821. PMID: 15998204. 2: Monti JM. Serotonin control of sleep-wake behavior. Sleep Med Rev. 2011 Aug;15(4):269-81. doi: 10.1016/j.smrv.2010.11.003. Epub 2011 Apr 2. PMID: 21459634. 3: Bagdy E, Kiraly I, Harsing LG Jr. Reciprocal innervation between serotonergic and GABAergic neurons in raphe nuclei of the rat. Neurochem Res. 2000 Nov;25(11):1465-73. doi: 10.1023/a:1007672008297. PMID: 11071365. 4: Sershen H, Hashim A, Lajtha A. Effect of ibogaine on cocaine-induced efflux of [3H] dopamine and [3H] serotonin from mouse striatum. Pharmacol Biochem Behav. 1996 Apr;53(4):863-9. doi: 10.1016/0091-3057(95)02098-5. PMID: 8801590. 5: Jeong HS, Jang MJ, Park JS. Effects of CGS-12066A on medial vestibular nuclear neurons. Brain Res. 2005 Mar 15;1038(1):118-21. doi: 10.1016/j.brainres.2005.01.025. PMID: 15748881. 6: Paul D, Yao D, Zhu P, Minor LD, Garcia MM. 5-hydroxytryptamine3 (5-HT3) receptors mediate spinal 5-HT antinociception: an antisense approach. J Pharmacol Exp Ther. 2001 Aug;298(2):674-8. PMID: 11454930. 7: Granados-Soto V, Argüelles CF, Rocha-González HI, Godínez-Chaparro B, Flores- Murrieta FJ, Villalón CM. The role of peripheral 5-HT1A, 5-HT1B, 5-HT1D, 5-HT1E and 5-HT1F serotonergic receptors in the reduction of nociception in rats. Neuroscience. 2010 Jan 20;165(2):561-8. doi: 10.1016/j.neuroscience.2009.10.020. PMID: 19837141. 8: Joppa MA, Rowe RK, Meisel RL. Effects of serotonin 1A or 1B receptor agonists on social aggression in male and female Syrian hamsters. Pharmacol Biochem Behav. 1997 Oct;58(2):349-53. doi: 10.1016/s0091-3057(97)00277-3. PMID: 9300591. 9: Middlemiss DN, Hutson PH. The 5-HT1B receptors. Ann N Y Acad Sci. 1990;600:132-47; discussion 347-48. doi: 10.1111/j.1749-6632.1990.tb16878.x. PMID: 2252306. 10: Lu CW, Lin TY, Huang SK, Wang SJ. 5-HT1B receptor agonist CGS12066 presynaptically inhibits glutamate release in rat hippocampus. Prog Neuropsychopharmacol Biol Psychiatry. 2018 Aug 30;86:122-130. doi: 10.1016/j.pnpbp.2018.05.019. Epub 2018 May 24. PMID: 29803926.