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2070014-90-1

2070014-90-1 Structure

2070014-90-1 Structure
IdentificationBack Directory
[Name]

LY 303511 (hydrochloride)
[CAS]

2070014-90-1
[Synonyms]

CS-1207
LY 303511 (hydrochloride)
[Molecular Formula]

C19H19ClN2O2
[MDL Number]

MFCD28167798
[MOL File]

2070014-90-1.mol
[Molecular Weight]

342.82
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

Solid
[color ]

White to light yellow
Hazard InformationBack Directory
[Uses]

LY 303511 hydrochloride is a structural analogue of LY294002. LY303511 does not inhibit PI3K. LY303511 enhances TRAIL sensitivity of SHEP-1 neuroblastoma cells. LY303511 reversibly blocks K+ currents (IC50=64.6±9.1 μM) in MIN6 insulinoma cells.
[in vivo]

Intraperitoneal administration of vehicle or LY303511 (10 mg/kg/day) is performed when tumors reach a volume of ~150 mm3, at which time 35 mice have developed a tumor. After 21 days, >15% of the mice require euthanasia because of excessive tumor growth, and these data are censored due to unreliable estimates of average tumor volume. The administration of LY303511, 10 mg/kg/day, is sufficient to inhibit PC-3 tumor growth in vivo[4].

[References]

[1] Bodenstine TM, et al. Homotypic gap junctional communication associated with metastasis suppression increases with PKA activity and is unaffected by PI3K inhibition. Cancer Res. 2010 Dec 1;70(23):10002-11. DOI:10.1158/0008-5472.CAN-10-2606
[2] El-Kholy W, Macdonald PE, Lin JH, The phosphatidylinositol 3-kinase inhibitor LY294002 potently blocks K(V) currents via a direct mechanism. FASEB J. 2003 Apr;17(6):720-2. DOI:10.1096/fj.02-0802fje
[3] Shenoy K, et al. LY303511 enhances TRAIL sensitivity of SHEP-1 neuroblastoma cells via hydrogen peroxide-mediated mitogen-activated protein kinase activation and up-regulation of death receptors. Cancer Res. 2009 Mar 1;69(5):1941-50. DOI:10.1158/0008-5472.CAN-08-1996
[4] Kristof AS, et al. LY303511 (2-piperazinyl-8-phenyl-4H-1-benzopyran-4-one) acts via phosphatidylinositol 3-kinase-independent pathways to inhibit cell proliferation via mammalian target of rapamycin (mTOR)- and non-mTOR-dependent mechanisms. J Pharmacol E DOI:10.1124/jpet.105.083550
Spectrum DetailBack Directory
[Spectrum Detail]

LY 303511 (hydrochloride)(2070014-90-1)1HNMR
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