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1800405-30-4

1800405-30-4 Structure

1800405-30-4 Structure
IdentificationBack Directory
[Name]

KL-1333
[CAS]

1800405-30-4
[Synonyms]

KL-1333
NQO1 ACTIVATOR 1
KL-1333(NQO1 activator 1)
2-(1-Methylethyl)-3H-naphth[1,2-d]imidazole-4,5-dione
3H-Naphth[1,2-d]imidazole-4,5-dione, 2-(1-methylethyl)-
[Molecular Formula]

C14H12N2O2
[MOL File]

1800405-30-4.mol
[Molecular Weight]

240.26
Chemical PropertiesBack Directory
[Boiling point ]

517.3±19.0 °C(Predicted)
[density ]

1.329±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 250 mg/mL (1040.54 mM)
[form ]

Solid
[pka]

8.58±0.20(Predicted)
[color ]

Reddish brown to red
[InChI]

InChI=1S/C14H12N2O2/c1-7(2)14-15-10-8-5-3-4-6-9(8)12(17)13(18)11(10)16-14/h3-7H,1-2H3,(H,15,16)
[InChIKey]

AJFWITSBVLLDCC-UHFFFAOYSA-N
[SMILES]

C1(C(C)C)NC2C(=O)C(=O)C3=C(C=2N=1)C=CC=C3
Hazard InformationBack Directory
[Uses]

KL1333, a derivative of β-lapachone, is an orally available NAD+ modulator. KL1333 reacts with NAD(P)H:quinone oxidoreductase 1 (NQO1) as a substrate, resulting in increases in intracellular NAD+ levels via NADH oxidation. KL1333 improves energy metabolism and mitochondrial dysfunction in MELAS fibroblasts. KL1333 protects against Cisplatin-induced ototoxicity in mouse cochlear cultures[1][2].
[storage]

Store at -20°C
[References]

[1] Seo KS, et al. KL1333, a Novel NAD+ Modulator, Improves Energy Metabolism and Mitochondrial Dysfunction in MELAS Fibroblasts. Front Neurol. 2018;9:552. Published 2018 Jul 5. DOI:10.3389/fneur.2018.00552
[2] Lee HS, et al. KL1333, a derivative of β-lapachone, protects against cisplatin-induced ototoxicity in mouse cochlear cultures. Biomed Pharmacother. 2020;126:110068. DOI:10.1016/j.biopha.2020.110068
Spectrum DetailBack Directory
[Spectrum Detail]

KL-1333(1800405-30-4)1HNMR
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