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LEQ506LEQ506 is a second generation inhibitor of smoothened (Smo) with IC50s of 2 and 4 nM in human and mouse, respectively. Product information CAS Number: 1204975 42 7 Molecular Weight: 432. 56 Formula: C25H32N6O Chemical Name: 2 {5 [(2R) 4 (6 benzyl 4,5 dimethylpyridazin 3 yl) 2 methylpiperazin 1 yl]pyrazin 2 yl}propan 2 ol Smiles: C[C@@H]1CN(CCN1C1=CN=C(C=N1)C(C)(C)O)C1=NN=C(CC2C=CC=CC=2)C(C)=C1C InChiKey: POERAARDVFVDLO QGZVFWFLSA N InChi: InChI=1S
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LEQ506 is a second-generation inhibitor of smoothened (Smo) with IC50s of 2 and 4 nM in human and mouse, respectively.

Product information

CAS Number: 1204975-42-7

Molecular Weight: 432.56

Formula: C25H32N6O

Chemical Name: 2-{5-[(2R)-4-(6-benzyl-4,5-dimethylpyridazin-3-yl)-2-methylpiperazin-1-yl]pyrazin-2-yl}propan-2-ol

Smiles: C[C@@H]1CN(CCN1C1=CN=C(C=N1)C(C)(C)O)C1=NN=C(CC2C=CC=CC=2)C(C)=C1C

InChiKey: POERAARDVFVDLO-QGZVFWFLSA-N

InChi: InChI=1S/C25H32N6O/c1-17-16-30(11-12-31(17)23-15-26-22(14-27-23)25(4,5)32)24-19(3)18(2)21(28-29-24)13-20-9-7-6-8-10-20/h6-10,14-15,17,32H,11-13,16H2,1-5H3/t17-/m1/s1

Technical Data

Appearance: Solid Power

Purity: ≥98% (or refer to the Certificate of Analysis)

Solubility: DMSO : ≥ 100 mg/mL (231.18 mM).

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis

Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.

Shelf Life: ≥12 months if stored properly.

Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.

Drug Formulation: To be determined

HS Tariff Code: 382200

How to use

In Vitro:

LEQ506 is a second-generation inhibitor of smoothened (Smo) with IC50s of 2 and 4 nM in human and mouse, respectively. LEQ506 inhibits Hedgehog (Hh) signaling in a human cell line (HEPM) as measured by the amount of Gli mRNA with an IC50 ~6-fold lower than that of Compound 2. LEQ506 is an efficacious compound by consistently decreasing Gli1 mRNA by about 70 to 80%. LEQ506 shows a tendency to preferentially inhibit Gli1 rather than Ptch1 mRNA. LEQ506 (at 1%) is also an efficacious compound with an inhibition of 80 to 90% for Gli1 and of 60 to 70% for Ptch1.

Products are for research use only. Not for human use.

LEQ506

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