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Zosuquidar hydrochloride

SIGMA/SML1044 - ≥98% (HPLC)

Synonym: (2R)-Anti-5-[3-[4-(10,11-difluoromethanodibenzosuber-5-yl)piperazin-1-yl]-2-hydroxypropoxy]quinoline hydrochloride; LY-335979; RS-33295-198

CAS Number: 167354-41-8 (free base)
Empirical Formula (Hill Notation): C32H31F2N3O2 · xHCl
Molecular Weight: 527.60 (free base basis)
Linear Formula: C32H31F2N3O2 · xHCl
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-SML1044-5MG 5 mg
 $242.00
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45-SML1044-25MG 25 mg
 $817.00
1/EA		 Add To Favorites

 

assay ≥98% (HPLC)
color white to beige
form powder
InChI 1S/C32H31F2N3O2.ClH/c33-32(34)29-22-7-1-3-9-24(22)31(25-10-4-2-8-23(25)30(29)32)37-17-15-36(16-18-37)19-21(38)20-39-28-13-5-12-27-26(28)11-6-14-35-27;/h1-14,21,29-31,38H,15-20H2;1H/t21-,29-,30+,31-;/m1./s1
InChI key VQJFFWJUYDGTQZ-FCNWNIDBSA-N
Quality Level 100 
SMILES string O[C@@H](COC1=C(C=CC=N2)C2=CC=C1)CN(CC3)CCN3[C@@H]4C5=C(C=CC=C5)[C@@H]6[C@@H](C6(F)F)C7=C4C=CC=C7.Cl
solubility H2O: 4 mg/mL, clear (warmed)
storage condition desiccated
storage temp. −20°C
Biochem/physiol Actions: Zosuqidar is a potent inhibitor of P-glycoprotein (P-gp, MDR1) a transporter protein that is a key modulator of cellular drug efflux.
Biochem/physiol Actions: Zosuqidar is a potent inhibitor of P-glycoprotein (P-gp, MDR1) a transporter protein that is a key modulator of cellular drug efflux. Zosuquidar sensitizes AML, and other cancer cell lines to cytotoxic drugs.
Features and Benefits: This compound is a featured product for ADME Tox research. Click here  to discover more featured ADME Tox products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm .
Packaging: 5 mg in glass bottle
Purity ≥98% (HPLC)
Storage Temp. −20°C
UNSPSC 12161501

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