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Pentamidine Chemical Structure

Pentamidine

Data Sheet For research use only. Not for human use.
Cat. No. :BCP10950CAS No. :100-33-4Purity:98%
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  • Chemical Properties&Biological Activity
CAS No. 100-33-4 Cat. No. BCP10950
Name Pentamidine
Synonyms MP601205;MP 601205;MP-601205;
SMILES
Chemical Name
Formula C19H24N4O2 M. Wt 340.42
Purity 98% Storage Store at 4-8°C
Description Pentamidine has a potent in vitro antiprotozoal activity. Pentamidine displays cytotoxic activity against L. infantum promastigotes with IC50 of 2.5 μM. 2.5 μM Pentamidine induces early programmed cell death in 49.6% of L. infantum promastigotes. 2.5 μM Pentamidine induces a notorious decrease in promastigotes in both G1 and S phases relative to the control-untreated samples (G1:77.0 vs 15.0%; S:11.0 vs 2.4% for control- and pentamidine-treated promastigotes, resp). Pentamidine is able to bind with calf-thymus DNA (CT-DNA) and induces conformational changes in the DNA double helix. Pentamidine also binds with ubiquitin to modifiy the β-cluster of ubiquitin [1]. Pentamidine is an inhibitor of phosphatase of regenerating liver (PRLs). 1 μg/mL of Pentamidine complete inhibits the activity of recombinant PTP1B in dephosphorylating a phos-photyrosine peptide. 10 μg/mL of Pentamidine completely inhibits the activities of recombinant PRL-1, PRL-2 and PRL-3 in dephosphorylating a phosphotyrosi
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