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869650-21-5

869650-21-5 Structure

869650-21-5 Structure
IdentificationBack Directory
[Name]

Ethanone, 1-[3-[6-[(cyclopropylmethyl)amino]imidazo[1,2-b]pyridazin-3-yl]phenyl]-
[CAS]

869650-21-5
[Synonyms]

K00135
K-00135
K 00135
Ethanone, 1-[3-[6-[(cyclopropylmethyl)amino]imidazo[1,2-b]pyridazin-3-yl]phenyl]-
[Molecular Formula]

C18H18N4O
[MOL File]

869650-21-5.mol
[Molecular Weight]

306.36
Chemical PropertiesBack Directory
[density ]

1.33±0.1 g/cm3(Predicted)
[pka]

4.91±0.30(Predicted)
Hazard InformationBack Directory
[Description]

K00135 is a potent and selective inhibitor of PIM kinases. K00135 was shown to impair survival and clonogenic growth of a panel of human acute leukemia cells. Exposure to K00135 also significantly suppressed in vitro growth of leukemic blasts from five acute myelogenous leukemia patients but not of normal umbilical cord blood mononuclear cells.
[Uses]

K00135 is a potent and selective inhibitor of PIM kinases. K00135 inhibits survival and clonogenic growth of acute leukemia cells. K00135 inhibits the phosphorylation of PIM downstream targets[1].
[References]

[1] Pogacic V, et al. Structural analysis identifies imidazo [1, 2-b] pyridazines as PIM kinase inhibitors with in vitro antileukemic activity[J]. Cancer research, 2007, 67(14): 6916-6924.
Spectrum DetailBack Directory
[Spectrum Detail]

Ethanone, 1-[3-[6-[(cyclopropylmethyl)amino]imidazo[1,2-b]pyridazin-3-yl]phenyl]-(869650-21-5)1HNMR
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869650-21-5