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HTH-01-091 , CAS No.2000209-42-5

COA

Cas Number: 2000209-42-5
Molecular Weight: 499.43

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Item Number

H650200

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SKU	Size	Availability	Price	Qty
H650200-5mg	5mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$880.90
H650200-10mg	10mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$1,400.90

View related series

Apoptosis (4276) Cell Cycle (2830) DYRK (39) Extrinsic Pathway (436) GSK-3 (104) JAK/STAT Signaling (507) MELK (11) mTOR (145) Non-receptor Tyrosine Kinase (643) PI3K/Akt/mTOR (765) Pim (31) Protein Tyrosine Kinase/RTK (1314) RIP kinase (65) Stem Cell/Wnt (1019)

Basic Description

Biochemical and Physiological Mechanisms	HTH-01-091 is a potent and selective maternal embryonic leucine zipper kinase (MELK) inhibitor, with an IC 50 of 10.5 nM. HTH-01-091 also inhibits PIM1/2/3 , RIPK2 , DYRK3 , smMLCK and CLK2 . HTH-01-091 can be uesd for breast cancer research.
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	HTH-01-091 is a potent and selective maternal embryonic leucine zipper kinase (MELK) inhibitor, with an IC 50 of 10.5 nM. HTH-01-091 also inhibits PIM1/2/3 , RIPK2 , DYRK3 , smMLCK and CLK2 . HTH-01-091 can be uesd for breast cancer research In Vitro HTH-01-091 (1 μM) selectively inhibits 4% of the kinases over 90%. HTH-01-091 (0-10 μM, 1 h) is cell permeable and causes MELK degradation. HTH-01-091 (0-10 μM, 3 day) exhibits minor antiproliferative effects in breast cancer cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot AnalysisCell Line: MDA-MB-468 cells Concentration: 0, 0.1, 1.0, and 10 μM Incubation Time: 1 h Result: Reduced MELK protein levels in MDA-MB-468 cells; Dose-dependently decreased MELK pull-down by streptavidin beads, demonstrating that the compound is cell permeable and binds to MELK in an ATP-competitive fashion. Had no effect on ERK1/2 pull-down, showing no binding affinity of HTH-01-091 to ERK1/2. Cell Proliferation AssayCell Line: MDA-MB-468, BT-549, HCC70, ZR-75-1, MCF7, and T-47D cells Concentration: 0, 0.001, 0.01, 0.1, 1.0, and 10 μM Incubation Time: 3 day Result: Showed antiproliferative activities in a panel of breast cancer cell lines, including MDA-MB-468, BT-549, HCC70, ZR-75-1, MCF7, and T-47D cells, with IC 50 values of 4.00 μM, 6.16 μM, 8.80 μM, >10 μM, 8.75 μM, and 3.87 μM, respectively. IC50& Target:DYRK4 41.8 nM (IC 50 ) PIM1 60.6 nM (IC 50 ) mTOR 632 nM (IC 50 ) CDK7 1230 nM (IC 50 ) PIM2 PIM3

Names and Identifiers

Smiles	O=C1N([C@H]2CC[C@H](CN(C)C)CC2)C3=C(CN1)C=NC4=CC=C(C5=CC(Cl)=C(O)C(Cl)=C5)C=C34
Molecular Weight	499.43

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