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418800-15-4

418800-15-4 Structure

418800-15-4 Structure
IdentificationBack Directory
[Name]

1H-INDOLE-3-CARBALDEHYDE N-(8-QUINOLINYL)HYDRAZONE
[CAS]

418800-15-4
[Synonyms]

LDK
Lenaldekar
1H-INDOLE-3-CARBALDEHYDE N-(8-QUINOLINYL)HYDRAZONE
8-[(E)-2-[(1H-indol-3-yl)methylidene]hydrazin-1-yl]quinoline
[Molecular Formula]

C18H14N4
[MDL Number]

MFCD00409836
[MOL File]

418800-15-4.mol
[Molecular Weight]

286.33
Chemical PropertiesBack Directory
[Boiling point ]

549.8±38.0 °C(Predicted)
[density ]

1.26±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO: 100mg/mL
[form ]

powder
[pka]

11.02±0.70(Predicted)
[color ]

yellow
Hazard InformationBack Directory
[Description]

Lenaldekar is a inhibitor of T-cell expansion and autoimmune encephalomyelitis.
[Uses]

Lenaldekar (LDK) inhibits human and murine T-cell expansiomn. Lenaldekar inhibits autoimmune T cell response. Lenaldekar also induces cancer cell apoptosis. Lenaldekar can be used for T-cell mediated autoimmune diseases research[1][2].
[in vivo]

Lenaldekar (40 mg/kg per day, i.p.) inhibits experimental autoimmune encephalomyelitis (EAE) relapse in mice sensitized with the encephalitogenic PLP139-151 peptide[1].
Lenaldekar (16 mg/kg, i.p., twice daily) inhibits tumor progession in a mouse xenograft model of T-cell acute lymphoblastic leukemia (T-ALL)[2].

[References]

[1] Cusick MF, et al. Human T cell expansion and experimental autoimmune encephalomyelitis inhibited by Lenaldekar, a small molecule discovered in a zebrafish screen. J Neuroimmunol. 2012 Mar;244(1-2):35-44. DOI:10.1016/j.jneuroim.2011.12.024
[2] Ridges S, et al, et al. Zebrafish screen identifies novel compound with selective toxicity against leukemia. Blood. 2012 Jun 14;119(24):5621-31. DOI:10.1182/blood-2011-12-398818
Spectrum DetailBack Directory
[Spectrum Detail]

1H-INDOLE-3-CARBALDEHYDE N-(8-QUINOLINYL)HYDRAZONE(418800-15-4)1HNMR
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