PeptideDB

GB1908

CAS: F: C18H18Cl2N4O5S2 W: 505.40

GB1908 is a selective and orally active galectin-1 inhibitor with Ki values of 57 nM and 72 nM for human and mouse galec
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Bioactivity GB1908 is a selective and orally active galectin-1 inhibitor with Ki values of 57 nM and 72 nM for human and mouse galectin-1, respectively. GB1908 displays >50-fold selectivity over galectin-3. GB1908 can be used for the study of lung cancer[1].
Invitro GB1908(0.1-10 μM;16 小时)可抑制 Jurkat 细胞中半乳糖凝集素-1 诱导的细胞凋亡(IC50 为 850 nM)[1]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. 0 --> GB1908 相关抗体: Apoptosis Analysis[1] Cell Line:
In Vivo GB1908(化合物 5d;30 mg/kg;口服;每天两次;持续 21 天)在同源小鼠模型中降低了原发性肺癌 LL/2 的生长[1]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
Formula C18H18Cl2N4O5S2
Molar Mass 505.40
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]. Fredrik R Zetterberg, et al. Discovery of the Selective and Orally Available Galectin-1 Inhibitor GB1908 as a Potential Treatment for Lung Cancer. J Med Chem. 2024 May 28.