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DASA-58
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
DASA-58图片
CAS NO:1203494-49-8
规格:≥98%
包装与价格:
包装价格(元)
5mg询价
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25mg询价
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理化性质和储存条件
Molecular Weight (MW)453.53
FormulaC19H23N3O6S2
CAS No.1203494-49-8
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 91 mg/mL (200.6 mM)
Water: <1 mg/mL
Ethanol: <1 mg/mL
Other info

Chemical Name: 3-[[4-[(2,3-dihydro-1,4-benzodioxin-6-yl)sulfonyl]hexahydro-1H-1,4-diazepin-1-yl]sulfonyl]-benzenamine

InChi Key: GMHIOMMKSMSRLY-UHFFFAOYSA-N

InChi Code: InChI=1S/C19H23N3O6S2/c20-15-3-1-4-16(13-15)29(23,24)21-7-2-8-22(10-9-21)30(25,26)17-5-6-18-19(14-17)28-12-11-27-18/h1,3-6,13-14H,2,7-12,20H2

SMILES Code: O=S(N1CCN(S(C2=CC=C(OCCO3)C3=C2)(=O)=O)CCC1)(C4=CC(N)=CC=C4)=O

SynonymsML-203; ML 203; ML203; DASA-58; DASA 58; DASA58; NCGC00185916; NCGC-00185916; NCGC 00185916
实验参考方法
In Vitro

In vitro activity: DASA-58 inhibits LPS-induced Hif-1α and IL-1β, as well as the expression of a range of other Hif-1α-dependent genes in primary BMDMs, and also inhibits glycolysis and the accumulation of succinate in LPS-activated macrophages. In PC3 cells, DASA-58 impairs stromal-induced EMT program by restoring PK activity and abrogating the nuclear translocation of PKM2, as well as its association with HIF-1α. DASA-58 also dramatically reduces (~6-fold) CAFs-induced lung metastases formation in PC3 cells.


Cell Assay: In A549-PKM1/kd and A549-PKM2/kd cells, Flag-PKM1 and Flag-PKM2 were expressed, respectively. Endogenous PKM2 was knockdowned. Treatment with DMSO resulted in 233±27% more pyruvate kinase activity in lysates from A549-PKM1/kd cells than that in lysates from A549-PKM2/kd cells. Treatment with DASA-58 did not increase the pyruvate kinase activity in A549-PKM1/kd cells, but it resulted in a 248 ±21% pyruvate kinase activity increase in the lysate of A549-PKM2/kd cells. In cells, 0-100 μM of DASA-58 dose-dependently activated PKM2 with an EC50 value of 19.6 μM.

In VivoDASA-58 (40 μM) affects EMT of prostate cancers and tumor dissemination in SCID mice.
Animal modelMale SCID-bg/bg mice bearing PC3 tumors
Formulation & DosageDissolved in DMSO; 40 μM; i.v. injection
References

Cell Metab. 2015 Jan 6;21(1):65-80; Oncotarget. 2015 Sep 15;6(27):24061-74.

 
 
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