AT-IAP

Modify Date: 2024-04-04 18:05:56

AT-IAP Structure
AT-IAP structure
Common Name AT-IAP
CAS Number 1403898-55-4 Molecular Weight 509.659
Density 1.1±0.1 g/cm3 Boiling Point 678.3±55.0 °C at 760 mmHg
Molecular Formula C29H40FN5O2 Melting Point N/A
MSDS N/A Flash Point 364.0±31.5 °C

 Use of AT-IAP


A potent, orally bioavailable, dual XIAP/cIAP1 inhibitor with EC50 of 5.1/0.32 nM, respectively; exhibits MDA-MB-231 cell proliferation inhibition with IC50 of 4.4 nM; decreases basal and TNF-α-induced cIAP-1 expression in CaP cells, switches TNF-α signaling from pro-survival to pro-apoptotic and increases radiation sensitivity of CaP cells in co-culture with THP-1 cells; shows in vivo efficacy in Balb/c scid mice bearing MDA-MB-231 xenografts.

 Names

Name 1-[6-(4-Fluorobenzyl)-3,3-dimethyl-2,3-dihydro-1H-pyrrolo[3,2-b]pyridin-1-yl]-2-[(2R,5R)-5-methyl-2-{[(3R)-3-methyl-4-morpholinyl]methyl}-1-piperazinyl]ethanone
Synonym More Synonyms

 AT-IAP Biological Activity

Description A potent, orally bioavailable, dual XIAP/cIAP1 inhibitor with EC50 of 5.1/0.32 nM, respectively; exhibits MDA-MB-231 cell proliferation inhibition with IC50 of 4.4 nM; decreases basal and TNF-α-induced cIAP-1 expression in CaP cells, switches TNF-α signaling from pro-survival to pro-apoptotic and increases radiation sensitivity of CaP cells in co-culture with THP-1 cells; shows in vivo efficacy in Balb/c scid mice bearing MDA-MB-231 xenografts.
References References 1. Tamanini E, et al. J Med Chem. 2017 Jun 8;60(11):4611-4625. 2. Armstrong CW, et al. Oncotarget. 2016 Feb 16;7(7):7885-98. View Related Products by Target IAP

 Chemical & Physical Properties

Density 1.1±0.1 g/cm3
Boiling Point 678.3±55.0 °C at 760 mmHg
Molecular Formula C29H40FN5O2
Molecular Weight 509.659
Flash Point 364.0±31.5 °C
Exact Mass 509.316589
LogP 4.23
Vapour Pressure 0.0±2.1 mmHg at 25°C
Index of Refraction 1.549

 Synonyms

Ethanone, 1-[6-[(4-fluorophenyl)methyl]-2,3-dihydro-3,3-dimethyl-1H-pyrrolo[3,2-b]pyridin-1-yl]-2-[(2R,5R)-5-methyl-2-[[(3R)-3-methyl-4-morpholinyl]methyl]-1-piperazinyl]-
1-[6-(4-Fluorobenzyl)-3,3-dimethyl-2,3-dihydro-1H-pyrrolo[3,2-b]pyridin-1-yl]-2-[(2R,5R)-5-methyl-2-{[(3R)-3-methyl-4-morpholinyl]methyl}-1-piperazinyl]ethanone
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