Description
SJ6986 is a potent, selective and orally active GSPT1/2 degrader, with a DC50 of 2.1 nM (Dmax 99%) for GSPT1.
Product information
Molecular Weight: 497.40
Formula: C20H14F3N3O7S
Chemical Name: N-[2-(2, 6-dioxopiperidin-3-yl)-1, 3-dioxoisoindol-5-yl]-2-(trifluoromethoxy)benzenesulfonamide
Smiles: O=C1CCC(C(=O)N1)N1C(=O)C2=CC=C(C=C2C1=O)NS(=O)(=O)C1=CC=CC=C1OC(F)(F)F
InChiKey: RKAFYSIKAVFVPS-UHFFFAOYSA-N
InChi: InChI=1S/C20H14F3N3O7S/c21-20(22,23)33-14-3-1-2-4-15(14)34(31,32)25-10-5-6-11-12(9-10)19(30)26(18(11)29)13-7-8-16(27)24-17(13)28/h1-6,9,13,25H,7-8H2,(H,24,27,28)
Technical Data
Appearance: Solid Power
Purity: ≥98% (or refer to the Certificate of Analysis)
Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis
Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.
Shelf Life: ≥12 months if stored properly.
Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.
Drug Formulation: To be determined
HS Tariff Code: 382200
How to use
In Vitro:
SJ6986 exhibits EC50 values of 1.5 nM, 0.4 nM, 726 nM, 336 nM and 3583 nM in MV4-11, MHH-CALL-4, MB002, MB004 and HD-MB03 cell lines, respectively.
In Vivo:
SJ6986 exhibits t1/2 of 3.44 h by iv injection of 3 mg/kg and tmax of 0.25 h by oral administration (%F = 84) of 10 mg/kg in CD1 mice.
Products are for research use only. Not for human use.
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