SML2978
d9A-2
≥98% (HPLC)
别名:
N-(14-{[2-(2,6-dioxopiperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl]amino}-3,6,9,12-tetraoxatetradecan-1-yl)-4′-fluoro-3′-methyl-2-[4-(4-methyl-1H-imidazol-5-yl)piperidin-1-yl]-[1,1′-biphenyl]-4-carboxamide
InChI key
WMBSSRAFHKGIRA-UHFFFAOYSA-N
SMILES string
O=C(CCC1N2C(C(C=CC=C3NCCOCCOCCOCCOCCNC(C4=CC(N5CCC(C6=C(C)N=CN6)CC5)=C(C7=CC=C(F)C(C)=C7)C=C4)=O)=C3C2=O)=O)NC1=O
assay
≥98% (HPLC)
form
powder
color
white to beige
solubility
DMSO: 2 mg/mL, clear
storage temp.
2-8°C
Quality Level
Biochem/physiol Actions
d9A-2 is a potent degrader (PROTAC) of the solute carrier SLC9A1 impairs recovery from acid load and is potently cytotoxic to multiple cancer cell lines. Also, d9A-2 incites degradation of some SLC9 members including closely related SLC9A2 and SLC9A4, distant SLC9A7 and SLC9B1. d9A-2 comprise w9A ligand binding to SLC9A1 and the phthalimide-based CRBN binder.
potent degrader (PROTAC) of the solute carrier SLC9A1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Ariel Bensimon et al.
Cell chemical biology, 27(6), 728-739 (2020-05-11)
With more than 450 members, the solute carrier (SLC) group of proteins represents the largest class of transporters encoded in the human genome. Their several-pass transmembrane domain structure and hydrophobicity contribute to the orphan status of many SLCs, devoid of
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