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KI1275DEAB (diethylaminobenzaldehyde)100 g$88

Chemical Characteristic

Product NameDEAB (diethylaminobenzaldehyde)
CAS No.120-21-8
Molecular Weight 177.24
FormulaC11H15NO
Chemical Name4-Diethylaminobenzaldehyde
Smilesc1(ccc(cc1)N(CC)CC)C=O
Chemical Structure

Biological activities

DEAB is a specific inhibitor for ALDH1. DEAB is widely used in the treatment of tumor. DEAB shows an ability to bind to the AR. DEAB hasa potent anti-androgenic effects with an IC50 of 1.7 µM. [1]The IC50 of DEAB is 277 µM against P. falciparum.[2]DEAB treatment between 0 and 18 hpf (hour-postfertilization) increases gene expression associated with hematopoietic stem and progenitor cells(scl, lmo2), erythropoiesis (gata1, α- and β-eHb) and myelopoiesis (spi1) as well as gfp(+) cells in dissociated Tg(gata1:gfp) embryos.DEAB expands HSPC population during primitive hematopoiesis through inhibition of aldh and retinoic acid synthesis.[3]Treatment of L1210/CPA cells in vitro with 50 µM DEAB abolishes the tumor cells' resistance to 4-HC. Co-injections of DEAB and cyclophosphamide produces the toxicity against intestinalcrypt cells in mice. [4]

Protocols

In vitro: DEAB is prepared in sterile dimethyl sulfoxide.[4]

References

[1]Araki N, et al. Screening for androgen receptor activities in 253 industrial chemicals by in vitro reporter gene assays using AR-EcoScreen cells.ToxicolIn Vitro. 2005, 19(6), 831-842.
[2]Graves PR, et al.Discovery of novel targets of quinoline drugs in the human purine binding proteome.MolPharmacol. 2002, 62(6), 1364-1372.
[3]Ma AC, et al. A DEAB-sensitive aldehyde dehydrogenase regulates hematopoieticstem and progenitor cells development during primitive hematopoiesis in zebrafish embryos. Leukemia. 2010, 24(12), 2090-2099.
[4]Russo J, et al. 4-(N,N-dipropylamino)benzaldehyde inhibits the oxidation of all-trans retinal to all-trans retinoic acid by ALDH1A1, but not the differentiation of HL-60 promyelocytic leukemia cells exposed to all-trans retinal.BMC Pharmacol. 2002, 2:4.

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