Gacyclidine hydrochloride

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

MedKoo CAT#: 575769

CAS#: 131774-33-9

Description: Gacyclidine hydrochloride is a N-methyl-D-aspartate (NMDA) receptor antagonist potentially for the treatment of tinnitus.


Chemical Structure

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Gacyclidine hydrochloride
CAS# 131774-33-9

Theoretical Analysis

MedKoo Cat#: 575769
Name: Gacyclidine hydrochloride
CAS#: 131774-33-9
Chemical Formula: C16H26ClNS
Exact Mass: 299.15
Molecular Weight: 299.900
Elemental Analysis: C, 64.08; H, 8.74; Cl, 11.82; N, 4.67; S, 10.69

Price and Availability

This product is not in stock, which may be available by custom synthesis. For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge). Quote less than 1g will not be provided. To request quote, please email to sales @medkoo.com or click below button.
Note: Price will be listed if it is available in the future.

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Synonym: (+/-)-Gacyclidine hydrochloride; Gacyclidine hydrochloride; Gacyclidine HCl

IUPAC/Chemical Name: Piperidine, 1-(2-methyl-1-(2-thienyl)cyclohexyl)-, hydrochloride, cis-

InChi Key: AJPKYPDCAXFLDK-KUARMEPBSA-N

InChi Code: InChI=1S/C16H25NS.ClH/c1-14-8-3-4-10-16(14,15-9-7-13-18-15)17-11-5-2-6-12-17;/h7,9,13-14H,2-6,8,10-12H2,1H3;1H/t14-,16+;/m0./s1

SMILES Code: Cl.C[C@H]1CCCC[C@]1(N2CCCCC2)c3cccs3

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:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 299.90 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
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: Chenoweth JA, Gerona RR, Ford JB, Sutter ME, Rose JS, Albertson TE, Clarke SO, Owen KP. Altered mental status and end organ damage associated with the use of gacyclidine: a case series. J Med Toxicol. 2015 Mar;11(1):115-20. doi: 10.1007/s13181-014-0415-2. PubMed PMID: 25048606; PubMed Central PMCID: PMC4371039.

2: Wenzel GI, Warnecke A, Stöver T, Lenarz T. Effects of extracochlear gacyclidine perfusion on tinnitus in humans: a case series. Eur Arch Otorhinolaryngol. 2010 May;267(5):691-9. doi: 10.1007/s00405-009-1126-1. PubMed PMID: 19847455.

3: Gerber YN, Privat A, Perrin FE. Gacyclidine improves the survival and reduces motor deficits in a mouse model of amyotrophic lateral sclerosis. Front Cell Neurosci. 2013 Dec 27;7:280. doi: 10.3389/fncel.2013.00280. PubMed PMID: 24409117; PubMed Central PMCID: PMC3873512.

4: Hoizey G, Kaltenbach ML, Dukic S, Lamiable D, Millart H, D'Arbigny P, Vistelle R. Pharmacokinetics of gacyclidine enantiomers in plasma and spinal cord after single enantiomer administration in rats. Int J Pharm. 2001 Oct 23;229(1-2):147-53. PubMed PMID: 11604267.

5: Hirbec H, Gaviria M, Vignon J. Gacyclidine: a new neuroprotective agent acting at the N-methyl-D-aspartate receptor. CNS Drug Rev. 2001 Summer;7(2):172-98. Review. PubMed PMID: 11474423.