ApexBio/MI-3/10mM(1mL二甲基亚砜)/A3603

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¥25920.00
货号:A3603
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品牌:ApexBio
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MI-3Menin-MLL Inhibitor

Catalog No.A3603
SizePriceStockQty
10mM (in 1mL DMSO)
$224.00
In stock
5mg
$187.00
In stock
10mg
$302.00
In stock
50mg
$1,008.00
In stock
100mg
$1,296.00
In stock

Tel: +1-832-696-8203

Email: sales@apexbt.com

Worldwide Distributors

Sample solution is provided at 25 µL, 10mM.

Publications citing ApexBio Products

Nature.2017 Jan 19;541(7637):417-420.
Nature.2018 Nov;563(7731):407-411.
Nature.2018 Jun 13.
Nature.2018 Jun 27.
Nature.2018 Mar 29;555(7698):673-677.
Nature.2017 Sep 7;549(7670):96-100.
Nature.2016 Apr 21;532(7599):398-401.
Science.2016 Aug 5;353(6299)594-8
Nat Nanotechnol.2017 Dec;12(12):1190-1198.
Nature Biotechnology.2017 Jun;35(6):569-576
Nat Med.2018 Sep 17.
Cell.2018 Dec 21. pii: S0092-8674(18)31561-7.
Cell.Available online 25 October 2018.
Cell.2018 Sep 27. pii: S0092-8674(18)31183-8.
Cell.2018 Jun 28;174(1):172-186.e21.
Cell.2018 Feb 22;172(5):1007-1021.e17.
Cell.2017 Nov 30;171(6):1284-1300.e21.
Cell.2017 Aug 17. pii: S0092-8674(17)30869-3.
Cell.2017 Jul 13;170(2):312-323
Nat Med.2018 Jan 29.
Nat Med.2017 Nov;23(11):1342-1351.
Cell.2017 Apr 6;169(2):286-300.
Cell.2015 Aug 27;162(5):987-1002.
Cell.2015 Feb 12;160(4):729-44.
Nature Medicine.2017 Apr;23(4):493-500.
Cancer Cell.2018 May 14;33(5):905-921.e5.
Cancer Cell.2018 Apr 9;33(4):752-769.e8.
Cancer Cell.2018 Mar 12;33(3):401-416.e8.
Cancer Cell.2017 Aug 14;32(2):253-267.e5.
Nat Methods.2018 Jul;15(7):523-526.
Cell Stem Cell.2018 May 3;22(5):769-778.e4.
Cell Stem Cell.2017 Nov 20. pii: S1934-5909(17)30375-2.

Quality Control

Quality Control & MSDS

View current batch:
    Purity = 98.00%
  • COA (Certificate Of Analysis)
  • MSDS (Material Safety Data Sheet)
  • Datasheet

Chemical structure

MI-3

MI-3 Dilution Calculator

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MI-3 Molarity Calculator

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Chemical Properties

Cas No. 1271738-59-0SDF Download SDF
Synonyms Menin-MLL inhibitor 3;Thieno[2,3-d]pyrimidine, 4-[4-(4,5-dihydro-5,5-dimethyl-2-thiazolyl)-1-piperazinyl]-6-(1-methylethyl)-
Chemical Name 4-(4-(5,5-dimethyl-4,5-dihydrothiazol-2-yl)piperazin-1-yl)-6-isopropylthieno[2,3-d]pyrimidine
Canonical SMILES CC(C1=CC2=C(N3CCN(C(S4)=NCC4(C)C)CC3)N=CN=C2S1)C
Formula C18H25N5S2 M.Wt 375.55
Solubility Soluble in DMSO Storage Store at -20°C
Shipping ConditionEvaluation sample solution : ship with blue ice.All other available size:ship with RT , or blue ice upon request
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.

Background

MI-3 is an inhibitor of Menin-Mixed linage leukemia (MML) protein interaction with IC50 value of 648 ± 25 nM [1].

MLL protein is a histone methyltransferase that positively regulates gene transcription. However, MLL gene is a common target for chromosomal translocations found in some leukemia. Fusion of MLL gene with one of over 50 different partner genes forms chimeric oncogenes encoding MLL fusion proteins. Translocations will disrupt the regulatory ability of MLL protein on HOX gene, resulting in enhanced cell proliferation and blocked hematopoietic differentiation. Menin is a tumor suppressor protein which directly controls cell growth in endocrine organs. Importantly, menin is also a highly specific partner of MLL. The regulatory function of MLL and MLL fusion protein is facilitated by the association of menin. Therefore, the interaction between MLL fusion protein and menin is critical for the pathology of leukemia [1].

In HEK293 cells expressing menin and MLL-AF9 fusion protein, treatment of MI-3 resulted in significant disruption of menin-MLL-AF9 complex without affecting expression level of menin and MLL-AF9 complex [1]. In mouse bone marrow cells (BMC) transduced with MLL-AF9 and MLL-ENL, MI-3 was observed to effectively inhibit menin-MLL interaction-induced cell proliferation, transformation and hematopoietic differentiation [1].

In human MLL leukemia cell lines harboring different translocations, MI-3 treatment showed an effective and dose-dependent growth inhibition of several cell lines with different MLL translocations [1].

Reference:[1] Grembecka J et al., Menin-MLL inhibitors reverse oncogenic activity of MLL fusion proteins in leukemia. Nature Chemical Biology. 2012, 8(3): 277-284.

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