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ly-294002 Hydrochloride

  Cat. No.:  DCC3181   Featured
Chemical Structure
934389-88-5
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More than 5000 active chemicals with high quality for research!
Field of application
Selective cell permeable phosphatidylinositol 3-kinase (PI3K) inhibitor
Cas No.: 934389-88-5
Chemical Name: LY 294002 Hydrochloride
Synonyms: 4H-1-Benzopyran-4-one,2-(4-morpholinyl)-8-phenyl-, hydrochloride (1:1);2-morpholin-4-yl-8-phenylchromen-4-one,hydrochloride;LY 294002 hydrochloride;LY 294002, HYDROCHLORIDE SALT;LY 294002, HYDROCHLORIDE SALT, >99;2-(4-Morpholinyl)-8-phenyl-1(4H)-benzopyran-4-one hydrochloride;LY294002 hydrochloride;2-(4-Morpholinyl)-8-phenyl-4H-1-benzopyran-4-one hydrochloride;2-(Morpholin-4-yl)-8-phenyl-4H-chromen-4-one hydrochloride;EX-A1710;HY-10108A;934389-88-5;LY-294002 hydrochloride;2-?(4-?Morpholinyl)?-?8-?phenyl-4H-?1-?benzopyran-?4-?one Hydrochloride;;SR-01000076245;CCG-222014;DS-016248;NCGC00261395-01;C19H17NO3.HCl;2-(4-Morpholinyl)-8-phenyl-4H-1-benzopyran-4-one hydrochloride;NSC 697286; SF 1101;LY-294,002 hydrochloride;SR-01000076245-3;SR-01000076245-1;Tox21_500710;SCHEMBL5078472;AC-32574;CHEMBL1398499;EN300-657176;LP00710;L 9908;DTXSID50474691;CS-0021282;HB2266;CU-00000000012-1;OQZQSRICUOWBLW-UHFFFAOYSA-N;LY294002 (hydrochloride);NCGC00094060-01;2-(4-Morpholinyl)-8-phenyl-4H-1-ben zopyran-4-one hydrochloride;NCGC00094060-02;AKOS024456404;EU-0100710;GLXC-03300;AT34063;BCP17476;2-(MORPHOLIN-4-YL)-8-PHENYLCHROMEN-4-ONE HYDROCHLORIDE;2-morpholin-4-yl-8-phenylchromen-4-one;hydrochloride;AS-58350
SMILES: Cl.O=C1C2C=CC=C(C=2OC(N2CCOCC2)=C1)C1C=CC=CC=1
Formula: C19H18ClNO3
M.Wt: 343.804124355316
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
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DC75816 Nisoxetine Nisoxetine acts as a highly selective and potent noradrenaline transporter (NET) antagonist, exhibiting a binding affinity (Kd) of 0.76 nM. In addition to its antidepressant properties, nisoxetine functions as a local anesthetic by inhibiting voltage-gated sodium channels. This dual pharmacological activity makes it a compound of interest for both neurological and pain management research.
DC75641 GENZ-644282 TFA salt Genz-644282, also known as SAR402674, is a non-camptothecin inhibitor of topoisomerase I with potential antineoplastic activity. Topoisomerase I inhibitor Genz-644282 binds to and inhibits the enzyme topoisomerase I, which may result in the inhibition of repair of single-strand DNA breaks, DNA replication, and tumor cell growth in susceptible tumor cell populations.
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