WARNING: This product is for research use only, not for human or veterinary use.
Hodoodo CAT#: H526570
CAS#: 139047-48-6
Description: Way 125971 is a bioactive chemcial.
Hodoodo Cat#: H526570
Name: Way 125971
CAS#: 139047-48-6
Chemical Formula: C22H28N4O5S2
Exact Mass: 492.15
Molecular Weight: 492.609
Elemental Analysis: C, 53.64; H, 5.73; N, 11.37; O, 16.24; S, 13.02
This product is not in stock, which may be available by custom synthesis.
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Synonym: Way 125971; Way125971; Way-125971
IUPAC/Chemical Name: N-(4-(3-(methyl((6-(methylsulfonamido)quinolin-2-yl)methyl)amino)propoxy)phenyl)methanesulfonamide
InChi Key: HIIKPWFGIGTCBP-UHFFFAOYSA-N
InChi Code: InChI=1S/C22H28N4O5S2/c1-26(13-4-14-31-21-10-7-18(8-11-21)24-32(2,27)28)16-20-6-5-17-15-19(25-33(3,29)30)9-12-22(17)23-20/h5-12,15,24-25H,4,13-14,16H2,1-3H3
SMILES Code: CS(=O)(NC1=CC=C(OCCCN(C)CC2=NC3=CC=C(NS(=O)(C)=O)C=C3C=C2)C=C1)=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:
Biological target: | |
In vitro activity: | |
In vivo activity: |
The following data is based on the product molecular weight 492.61 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: | |
In vitro protocol: | |
In vivo protocol: |
1: Butera JA, Spinelli W, Anantharaman V, Marcopulos N, Parsons RW, Moubarak IF, Cullinan C, Bagli JF. Synthesis and selective class III antiarrhythmic activity of novel N-heteroaralkyl-substituted 1-(aryloxy)-2-propanolamine and related propylamine derivatives. J Med Chem. 1991 Nov;34(11):3212-28. PubMed PMID: 1956040.