
NMS-E973
CAS No. 1253584-84-7
NMS-E973( NMS-E973 | NMSE973 )
Catalog No. M17906 CAS No. 1253584-84-7
NMS-E973 is a potent and selective Hsp90 inhibitor with DC50 of <10 nM for Hsp90 binding, no activiy against a panel of 52 diverse protein kinases.
Purity : >98% (HPLC)






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Biological Information
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Product NameNMS-E973
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NoteResearch use only, not for human use.
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Brief DescriptionNMS-E973 is a potent and selective Hsp90 inhibitor with DC50 of <10 nM for Hsp90 binding, no activiy against a panel of 52 diverse protein kinases.
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DescriptionNMS-E973 is a novel, selective and potent inhibitor of heat shock protein 90 (Hsp90). NMS-E973 displays significant efficacy in a human ovarian A2780 xenograft tumor model, with a mechanism of action confirmed in vivo by typical modulation of known Hsp90 client proteins, and with a favorable pharmacokinetic and safety profile. The efficacy profile of NMS-E973 suggests a potential for development in different clinical settings, including tumors that have become resistant to molecular targeted agents, particularly in cases of tumors which reside beyond the blood-brain barrier (BBB).
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In VitroNMS-E973 inhibits cancer cell proliferation. NMS-E973 shows a widespread antiproliferative activity, with an average IC50 of 1.6 μM and 15 cell lines with an IC50 <100 nM. Cell Proliferation Assay Cell Line:Carcinoma breast DU-4475, EVSA-T, CAL-51, HCC1954, BT-474, HCC1419, HDQ-P1 cells; Leukemia MV-4-11 and MOLM-13 cells; Melanoma A-375 cellsConcentration:Incubation Time:24, 48, 72 hours Result:IC50s of 13, 16, 56, 61, 73, 76, and 89 nM for DU-4475, EVSA-T, CAL-51, HCC1954, BT-474, HCC1419, HDQ-P1 cells, respectively.IC50s of 29 and 35 nM for MV-4-11, MOLM-13 cells, respectively.The IC50 of 133 nM for A-375 cell.
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In VivoNMS-E973 (60 mg/kg; i.v.) inhibits the growth of A375 tumors subcutaneously or intracranially implanted in mice. NMS-E973 exhibits moderate elimination half-lives (5.55±1.07 h) due to high plasma clearance (39.9±1.70 mL/min/kg) combined with large volumes of distribution (5.83±3.18 L/kg) following intravenous administration (10 mg/kg) in mice. Animal Model:Balb/c male nude mice (aged 6 to 8 weeks) xenografted with the A375 tumors Dosage:60 mg/kg Administration:Administered twice daily i.v. according to 2 schedules: (i) every other day for 12 days and (ii) 3 days on/1 day off/3 days on (3-1-3, one cycle). Result:Both schedules resulted in tumor shrinkage and TGI of 74% and 89%, respectively.
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SynonymsNMS-E973 | NMSE973
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PathwayOthers
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TargetPlatelet aggregation
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RecptorHSP90
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Research AreaCancer
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Indication——
Chemical Information
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CAS Number1253584-84-7
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Formula Weight454.43
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Molecular FormulaC22H22N4O7
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 50 mg/mL (110.03 mM)
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SMILESCN1CCC(CC1)NC(=O)C2=C/C(=C\3/C(=CC(=O)C=C3OC4=CC=C(C=C4)[N+](=O)[O-])O)/ON2
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Chemical Name5-[2,4-Dihydroxy-6-(4-nitrophenoxy)phenyl]-N-(1-methyl-4-piperidinyl)-3-isoxazolecarboxamide
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Fogliatto G, et al. Clin Cancer Res. 2013, 19(13), 3520-3532.
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