Synonym
SNU0039; SNU 0039; SNU-0039; DWK1339; DWK 1339; DWK-1339; MDR-1339; MDR 1339; MDR1339
IUPAC/Chemical Name
2-(3,4-Dimethoxyphenyl)-5-(3-methoxypropyl) benzofuran
InChi Key
CUEPJIGXQLIOIK-UHFFFAOYSA-N
InChi Code
InChI=1S/C20H22O4/c1-21-10-4-5-14-6-8-17-16(11-14)13-19(24-17)15-7-9-18(22-2)20(12-15)23-3/h6-9,11-13H,4-5,10H2,1-3H3
SMILES Code
COCCCC1=CC=C(OC(C2=CC=C(OC)C(OC)=C2)=C3)C3=C1
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
>3 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
Biological target:
SNU-0039 is a blood-brain-barrier-permeable Aβ-aggregation inhibitor.
In vivo activity:
SNU-0039 may offer an alternative treatment for Alzheimer’s disease (AD). SNU-0039 restored cellular viability from Aβ-induced cytotoxicity but also improved the learning and memory function of AD model mice by reducing the Aβ aggregates in the brains.
Reference: J Med Chem. 2018 Jan 11;61(1):396-402. https://pubmed.ncbi.nlm.nih.gov/29161514/
|
Solvent |
mg/mL |
mM |
comments |
Solubility |
DMF |
30.0 |
91.91 |
|
DMSO |
30.0 |
91.91 |
|
Ethanol |
2.0 |
6.13 |
|
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
326.39
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.
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. Son JH, Jeong YS, Lee JH, Kim MS, Lee KR, Shim CK, Kim YH, Chung SJ. Identification of metabolites of MDR-1339, an inhibitor of β-amyloid protein aggregation, and kinetic characterization of the major metabolites in rats. J Pharm Biomed Anal. 2018 Mar 20;151:61-70. doi: 10.1016/j.jpba.2017.12.060. Epub 2018 Jan 3. PMID: 29306735.
2. Ha HJ, Kang DW, Kim HM, Kang JM, Ann J, Hyun HJ, Lee JH, Kim SH, Kim H, Choi K, Hong HS, Kim Y, Jo DG, Lee J, Lee J. Discovery of an Orally Bioavailable Benzofuran Analogue That Serves as a β-Amyloid Aggregation Inhibitor for the Potential Treatment of Alzheimer's Disease. J Med Chem. 2018 Jan 11;61(1):396-402. doi: 10.1021/acs.jmedchem.7b00844. Epub 2017 Dec 6. PMID: 29161514.
In vivo protocol:
1. Son JH, Jeong YS, Lee JH, Kim MS, Lee KR, Shim CK, Kim YH, Chung SJ. Identification of metabolites of MDR-1339, an inhibitor of β-amyloid protein aggregation, and kinetic characterization of the major metabolites in rats. J Pharm Biomed Anal. 2018 Mar 20;151:61-70. doi: 10.1016/j.jpba.2017.12.060. Epub 2018 Jan 3. PMID: 29306735.
2. Ha HJ, Kang DW, Kim HM, Kang JM, Ann J, Hyun HJ, Lee JH, Kim SH, Kim H, Choi K, Hong HS, Kim Y, Jo DG, Lee J, Lee J. Discovery of an Orally Bioavailable Benzofuran Analogue That Serves as a β-Amyloid Aggregation Inhibitor for the Potential Treatment of Alzheimer's Disease. J Med Chem. 2018 Jan 11;61(1):396-402. doi: 10.1021/acs.jmedchem.7b00844. Epub 2017 Dec 6. PMID: 29161514.
1. Lee KR, Chae YJ, Maeng HJ, Lee J, Kim DD, Chong S, Shim CK, Chung SJ. Physiologically based pharmacokinetic modeling of SNU-0039, an anti-Alzheimer's agent, in rats. J Pharmacokinet Pharmacodyn. 2011 Oct;38(5):637-51. doi: 10.1007/s10928-011-9212-6. Epub 2011 Aug 25. PubMed PMID: 21866408.
2. Son JH, Jeong YS, Lee JH, Kim MS, Lee KR, Shim CK, Kim YH, Chung SJ. Identification of metabolites of MDR-1339, an inhibitor of β-amyloid protein aggregation, and kinetic characterization of the major metabolites in rats. J Pharm Biomed Anal. 2018 Mar 20;151:61-70. doi: 10.1016/j.jpba.2017.12.060. Epub 2018 Jan 3. PMID: 29306735.
3. Ha HJ, Kang DW, Kim HM, Kang JM, Ann J, Hyun HJ, Lee JH, Kim SH, Kim H, Choi K, Hong HS, Kim Y, Jo DG, Lee J, Lee J. Discovery of an Orally Bioavailable Benzofuran Analogue That Serves as a β-Amyloid Aggregation Inhibitor for the Potential Treatment of Alzheimer's Disease. J Med Chem. 2018 Jan 11;61(1):396-402. doi: 10.1021/acs.jmedchem.7b00844. Epub 2017 Dec 6. PMID: 29161514.