MedKoo Cat#: 562050 | Name: SK609 HCl
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Description:

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

SK609 HCl is a selective dopamine D3 receptor agonist with atypical signaling properties.

Chemical Structure

SK609 HCl
SK609 HCl
CAS#1092797-77-7

Theoretical Analysis

MedKoo Cat#: 562050

Name: SK609 HCl

CAS#: 1092797-77-7

Chemical Formula: C10H15Cl2N

Exact Mass: 0.0000

Molecular Weight: 220.13

Elemental Analysis: C, 54.56; H, 6.87; Cl, 32.21; N, 6.36

Price and Availability

Size Price Availability Quantity
5mg USD 400.00 2 weeks
25mg USD 850.00 2 weeks
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Related CAS #
Synonym
SK609 hydrochloride; SK-609 hydrochloride; SK 609 hydrochloride; SK609 HCl; SK-609 HCl; SK 609 HCl; ES609; ES-609; ES 609;
IUPAC/Chemical Name
4-(2-Chlorophenyl)butan-2-amine hydrochloride
InChi Key
NVCYSMVSGDVJQR-UHFFFAOYSA-N
InChi Code
InChI=1S/C10H14ClN.ClH/c1-8(12)6-7-9-4-2-3-5-10(9)11;/h2-5,8H,6-7,12H2,1H3;1H
SMILES Code
CC(N)CCC1=CC=CC=C1Cl.[H]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 and water
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
Product Data
Biological target:
SK609 is a dopamine D3 receptor (D3R) selective agonist with a bias towards the G-protein-dependent pathway and an EC50 value of 113.9 nM for activation of ERK1/2 phosphorylation. It does not induce desensitization of D3R.
In vitro activity:
To be determined
In vivo activity:
SK609 has the potential to treat sustained attention deficits without affecting dopamine transporter activity, unlike amphetamines and methylphenidate. In naïve rats, systemic SK609 dosing led to a 300% rise in norepinephrine and a 160% increase in dopamine. Notably, cognitive improvement was more pronounced in low-performing animals, and doses associated with this enhancement did not elevate spontaneous locomotor activity, indicating potential absence of side effects related to dopamine transporter activity. Reference: Neuropharmacology. 2019 Apr;148:178-188. https://pubmed.ncbi.nlm.nih.gov/30633928/
Solvent mg/mL mM comments
Solubility
Water 22.0 100.00
DMSO 22.0 100.00
Note: There can be variations in solubility for the same chemical from different vendors or different batches from the same vendor. The following factors can affect the solubility of the same chemical: solvent used for crystallization, residual solvent content, polymorphism, salt versus free form, degree of hydration, solvent temperature. Please use the solubility data as a reference only. Warming and sonication will facilitate dissolving. Still have questions? Please contact our Technical Support scientists.

Preparing Stock Solutions

The following data is based on the product molecular weight 220.13 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:
1. Marshall CA, Brodnik ZD, Mortensen OV, Reith MEA, Shumsky JS, Waterhouse BD, España RA, Kortagere S. Selective activation of Dopamine D3 receptors and norepinephrine transporter blockade enhances sustained attention. Neuropharmacology. 2019 Apr;148:178-188. doi: 10.1016/j.neuropharm.2019.01.003. Epub 2019 Jan 8. PMID: 30633928; PMCID: PMC6424628. 2. Simms SL, Huettner DP, Kortagere S. In vivo characterization of a novel dopamine D3 receptor agonist to treat motor symptoms of Parkinson's disease. Neuropharmacology. 2016 Jan;100:106-15. doi: 10.1016/j.neuropharm.2015.04.004. Epub 2015 Apr 18. PMID: 25896768.
In vitro protocol:
To be determined
In vivo protocol:
1. Marshall CA, Brodnik ZD, Mortensen OV, Reith MEA, Shumsky JS, Waterhouse BD, España RA, Kortagere S. Selective activation of Dopamine D3 receptors and norepinephrine transporter blockade enhances sustained attention. Neuropharmacology. 2019 Apr;148:178-188. doi: 10.1016/j.neuropharm.2019.01.003. Epub 2019 Jan 8. PMID: 30633928; PMCID: PMC6424628. 2. Simms SL, Huettner DP, Kortagere S. In vivo characterization of a novel dopamine D3 receptor agonist to treat motor symptoms of Parkinson's disease. Neuropharmacology. 2016 Jan;100:106-15. doi: 10.1016/j.neuropharm.2015.04.004. Epub 2015 Apr 18. PMID: 25896768.
1: Xu W, Wang X, Tocker AM, Huang P, Reith ME, Liu-Chen LY, Smith AB 3rd, Kortagere S. Functional Characterization of a Novel Series of Biased Signaling Dopamine D3 Receptor Agonists. ACS Chem Neurosci. 2017 Mar 15;8(3):486-500. doi: 10.1021/acschemneuro.6b00221. Epub 2016 Nov 23. PubMed PMID: 27801563. 2: Simms SL, Huettner DP, Kortagere S. In vivo characterization of a novel dopamine D3 receptor agonist to treat motor symptoms of Parkinson's disease. Neuropharmacology. 2016 Jan;100:106-15. doi: 10.1016/j.neuropharm.2015.04.004. Epub 2015 Apr 18. PubMed PMID: 25896768.