(-) -Luteoskyrin

CAT: 0804-HY-129900Size: 1 EachDry Ice: NoHazardous: No

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Description

(-) -Luteoskyrin has a wide range of antibacterial activity, such as against malaria (with an IC50 of 0.51 μg/mL), tuberculosis (MIC of 6.25 μg/mL), and it also shows antibacterial effects (with MIC for Gram-positive bacteria ranging from 0.39 to 1.56 μg/mL, and for Gram-negative bacteria from 3.13 to 12.50 μg/mL), as well as antifungal activity (with MIC against plant pathogens ranging from 3.13 to 50μg/mL) . (-) -Luteoskyrin exhibits cytotoxicity against NCI-H187 cells, with an IC50 range of 0.16–17.99 μg/mL[1].

CAS Number

21884-44-6

UNSPSC

12352005

Target

Bacterial; Fungal

Related Pathways

Anti-infection

Field of Research

Infection

Smiles

O=C1[C@]23[C@]([C@]4([H])O)([H])[C@]5([H])[C@@](O)([H])[C@@]2([H])C(O)=C6C5(C(C7=C(C(O)=CC(C)=C7O)C6=O)=O)[C@]4([H])C(O)=C3C(C8=C(O)C=C(C)C(O)=C18)=O

Molecular Formula

C30H22O12

Molecular Weight

574.49

References & Citations

[1]Karoon Sadorn, et al. Phenolic glucosides and chromane analogs from the insect fungus Conoideocrella krungchingensis BCC53666. Tetrahedron. Volume 75, Issue 25, 21 June 2019, Pages 3463-3471.

Shipping Conditions

Room temperature

Scientific Category

Reference compound1

Clinical Information

No Development Reported

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(-) -Luteoskyrin

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