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1338320-94-7

1338320-94-7 structure
1338320-94-7 structure
  • Name: MPT0E028
  • Chemical Name: (E)-3-[1-(benzenesulfonyl)-2,3-dihydroindol-5-yl]-N-hydroxyprop-2-enamide
  • CAS Number: 1338320-94-7
  • Molecular Formula: C17H16N2O4S
  • Molecular Weight: 344.38500
  • Catalog: Signaling Pathways Apoptosis Apoptosis
  • Create Date: 2016-06-21 04:40:16
  • Modify Date: 2024-01-10 11:07:41
  • MPT0E028 is an orally active and selective HDAC inhibitor with IC50s of 53.0 nM, 106.2 nM, 29.5 nM for HDAC1, HDAC2 and HDAC6, respectively[1]. MPT0E028 reduces the viability of B-cell lymphomas by inducing apoptosis and possesses potent direct Akt targeting ability and reduces Akt phosphorylation in B-cell lymphoma. MPT0E028 has good anticancer activity[2].

Name (E)-3-[1-(benzenesulfonyl)-2,3-dihydroindol-5-yl]-N-hydroxyprop-2-enamide
Synonyms 3-(1-(Benzenesulfonyl)-2,3-dihydro-1H-indol-5-yl)-N-hydroxyacrylamide
2-Propenamide,3-(2,3-dihydro-1-(phenylsulfonyl)-1H-indol-5-yl)-N-hydroxy
UNII-T65L58FI65
Description MPT0E028 is an orally active and selective HDAC inhibitor with IC50s of 53.0 nM, 106.2 nM, 29.5 nM for HDAC1, HDAC2 and HDAC6, respectively[1]. MPT0E028 reduces the viability of B-cell lymphomas by inducing apoptosis and possesses potent direct Akt targeting ability and reduces Akt phosphorylation in B-cell lymphoma. MPT0E028 has good anticancer activity[2].
Related Catalog
Target

HDAC1:53.0 nM (IC50)

HDAC2:106.2 nM (IC50)

HDAC6:29.5 nM (IC50)

HDAC8:2532.6 nM (IC50)

Akt

References

[1]. Huang HL, et al. Anticancer activity of MPT0E028, a novel potent histone deacetylase inhibitor, in human colorectal cancer HCT116 cells in vitro and in vivo. PLoS One. 2012;7(8):e43645.

[2]. Huang HL, et al. Novel oral histone deacetylase inhibitor, MPT0E028, displays potent growth-inhibitory activity against human B-cell lymphoma in vitro and in vivo. Oncotarget. 2015 Mar 10;6(7):4976-91.

Molecular Formula C17H16N2O4S
Molecular Weight 344.38500
Exact Mass 344.08300
PSA 98.58000
LogP 3.94270
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