PeptideDB

iBFAR2

CAS: 353484-02-3 F: C19H15F3N2O2 W: 360.33

iBFAR2, a BFAR inhibitor, restores the CD8+ TRM cell subset against solid tumors. iBFAR2 promotes JAK2-STAT1 association
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Bioactivity iBFAR2, a BFAR inhibitor, restores the CD8+ TRM cell subset against solid tumors. iBFAR2 promotes JAK2-STAT1 association and STAT1 phosphorylation[1].
Invitro iBFAR2 在小鼠初级 CD8+ T细胞中,消除了 USP39 的泛素化,抑制了 JAK2-USP39 的相互作用,从而抑制了 JAK2 的去泛素化,进而促进了 JAK2-STAT1 的结合并增强了 STAT1 的磷酸化。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. 0 --> iBFAR2 相关抗体:
In Vivo iBFAR2 (ip;1, 5, 10 mg/kg;once every 2 days starting from day 7 (n = 9 mice/group)) 以剂量依赖的方式抑制 MB49 肿瘤的生长。 MCE has not independently confirmed the accuracy of these methods. They are for reference only.
CAS 353484-02-3
Formula C19H15F3N2O2
Molar Mass 360.33
Transport Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Reference [1]. Siyu Pei, et al. Age-related decline in CD8+ tissue resident memory T cells compromises antitumor immunity. Nat Aging. 2024 Dec;4(12):1828-1844.