PeptideDB

DN401

CAS: 2135749-60-7 F: C13H9BrClN5O2 W: 382.60

DN401 is a potent TRAP1 inhibitor with an IC50 of 79 nM. DN401 shows a weak inhibition of Hsp90 (IC50 of 698 nM). DN401
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Bioactivity DN401 is a potent TRAP1 inhibitor with an IC50 of 79 nM. DN401 shows a weak inhibition of Hsp90 (IC50 of 698 nM). DN401 inactivates mitochondrial TRAP1 and has potent anticancer activities[1].
Invitro DN401(5-20 µM;24 小时)具有优异的癌症特异性细胞毒性,但在正常细胞中的细胞毒性作用降低[1]。DN401(20 µM;6 小时)抑制 HeLa 细胞中 Chk1 和 Akt 的表达[1]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. 0 --> DN401 相关抗体: Cell Viability Assay[1] Cell Line:
In Vivo DN401(30 mg/kg;腹腔注射;每天一次;持续 14 天)可减少肿瘤生长并增加肿瘤组织中的细胞凋亡,并且不会导致体重减轻或组织学异常[1]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
CAS 2135749-60-7
Formula C13H9BrClN5O2
Molar Mass 382.60
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]. Hye-Kyung Park, et al. Paralog Specificity Determines Subcellular Distribution, Action Mechanism, and Anticancer Activity of TRAP1 Inhibitors. J Med Chem. 2017 Sep 14;60(17):7569-7578.