PeptideDB

SPDZi1

CAS: F: C22H19N3O5 W: 405.40

SPDZi1 is a potent and selective syntenin inhibitor that binds to PDZ1 and PDZ2 domains of syntenin. SPDZi1 binds to the
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Bioactivity SPDZi1 is a potent and selective syntenin inhibitor that binds to PDZ1 and PDZ2 domains of syntenin. SPDZi1 binds to the syntenin PDZ tandem (STNPDZ) with a Kd of 3.6 μM. SPDZi1 suppresses glioblastoma and reduces the activation of NF-κB, a downstream effector of syntenin[1].
Invitro SPDZi1 (Z3322068027;20 μM;24 小时) 可抑制人类多形性胶质母细胞瘤 (GBM) 细胞增殖,同时降低 NF-κB 的活化[1]。 在胶质母细胞瘤类器官 (GBO) 中,SPDZi1 可有效抑制小 GBO 的生长[1]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. 0 --> SPDZi1 相关抗体: Cell Proliferation Assay[1] Cell Line:
Formula C22H19N3O5
Molar Mass 405.40
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]. Yunseok Heo, et al. Discovery of a potent inhibitor that suppresses glioblastoma by dual targeting of both syntenin PDZ domains. bioRxiv preprint. April 04, 2024.