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2226511-77-7

2226511-77-7 Structure

2226511-77-7 Structure
IdentificationBack Directory
[Name]

3,6,9-Acridinetriamine, N9-[3-(dimethylamino)propyl]-N3,N3,N6,N6-tetramethyl-, hydrochloride (1:2)
[CAS]

2226511-77-7
[Synonyms]

3,6-DMAD dihydrochloride
3,6,9-Acridinetriamine, N9-[3-(dimethylamino)propyl]-N3,N3,N6,N6-tetramethyl-, hydrochloride (1:2)
[Molecular Formula]

C22H32ClN5
[MOL File]

2226511-77-7.mol
[Molecular Weight]

401.98
Hazard InformationBack Directory
[Uses]

3,6-DMAD dihydrochloride, an acridine derivative, is a potent IRE1α-XBP1s pathway inhibitor. 3,6-DMAD dihydrochloride promotes IL-6 secretion via the IRE1α-XBP1s pathway. 3,6-DMAD dihydrochloride inhibits IRE1α oligomerization and endoribonuclease (RNase) activity. 3,6-DMAD dihydrochloride can be used for research of cancer[1][2].
[in vivo]

3,6-DMAD dihydrochloride (10 mg/kg; i.p.; three times every 12 hours, for 84 hours; NOD Scid mice with RPMI 8226 xenograft) has inhibition of XBP1 splicing in vivo[1].
3,6-DMAD dihydrochloride (10 mg/kg; 24 h; i.p.; every 48 hours, for 12 days; NOD Scid mice with RPMI 8226 xenograft) suppresses multiple myeloma xenograft growth in vivo[1].

Animal Model:NOD Scid mice (4-6 weeks) with RPMI 8226 xenograft[1]
Dosage:10 mg/kg
Administration:Intraperitoneal injection; three times every 12 hours, for 84 hours
Result:Inhibited XBP1-luciferase activity in NOD Scid mice with RPMI 8226 xenograft.
Animal Model:NOD Scid mice (4-6 weeks) with RPMI 8226 xenograft[1]
Dosage:10 mg/kg
Administration:Intraperitoneal injection; every 48 hours, for 12 days
Result:Inhibited tumor growth in NOD Scid mice with RPMI 8226 xenograft.
[References]

[1] Jiang D, et, al. Acridine Derivatives as Inhibitors of the IRE1α-XBP1 Pathway Are Cytotoxic to Human Multiple Myeloma. Mol Cancer Ther. 2016 Sep;15(9):2055-65. DOI:10.1158/1535-7163.MCT-15-1023
[2] De SY, et, al. SHP-2 specific deletion in macrophages accelerates pathological cardiac hypertrophy through promoting IRE1α-XBP1s pathway regulated by IL-6 secretion. Research Article. 2022 May 3.
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