[CAS NO. 801985-13-7]  BPH-1358 free base

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PRODUCTS SPECIFICATIONS [801985-13-7]

Fulfillment
Catalog
HY-118946A
Brand
MCE
CAS
801985-13-7

DESCRIPTION [801985-13-7]

Overview

MDL-
Molecular Weight528.60
Molecular FormulaC32H28N6O2
SMILESO=C(C1=CC=C(C2=CC=C(C(NC3=CC=CC(C4=NCCN4)=C3)=O)C=C2)C=C1)NC5=CC=CC(C6=NCCN6)=C5

For research use only. We do not sell to patients.

Summary

BPH-1358 free base (NSC50460 free base) is a potent human farnesyl diphosphate synthase (FPPS) and undecaprenyl diphosphate synthase (UPPS) inhibitor with IC 50 s of 1.8 μM and 110 nM, respectively, and is active against S. aureus in vitro (MIC ~250 ng/mL) [1] [2] .


IC50 & Target

IC50: 1.8 μM (human bisphosphonate farnesyl diphosphate synthase) [1] ; 100 nM (undecaprenyl diphosphate synthase) [2]


In Vitro

BPH-1358 is the most potent inhibitor of both E. coli UPPS (EcUPPS) as well as S. aureus UPPS (SaUPPS) with an IC 50 of 110 nM. BPH-1358 against E. coli and S. aureus with EC 50 of 300 nM and 290 nM, respectively [1] .

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.


In Vivo

BPH-1358 is active against S. aureus in vivo (20/20 mice survived in an i.p. infection model with a MRSA strain) [1] .

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.


Shipping

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Storage

Please store the product under the recommended conditions in the Certificate of Analysis.