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Table 1 Inhibitory activity of 2′-hydroxyflavanone and other 13 flavonoids against AeNobo. Fifteen flavonoids, including the subclasses of flavonone, flavone, isoflavone, flavonol, isoflavan, and anthocyanidin, are illustrated in Additional file 1: Figure S3. “No inhibition” means that the IC50 value of a compound is greater than 25 μM. Among the examined chemicals, biochanin A is the only estrogenic chemical that inhibits the in vitro enzymatic activity of AeNobo. s.d. standard deviation, - not determined

From: Molecular action of larvicidal flavonoids on ecdysteroidogenic glutathione S-transferase Noppera-bo in Aedes aegypti

Compound

Subclass

IC50 to AeNobo-WT (μM) (mean ± s.d.)

IC50 to AeNobo-E113A (μM) (mean ± s.d.)

2′-Hydroxyflavanone

Flavanone

4.76 ± 0.37

No inhibition

Naringenin

Flavanone

No inhibition

-

Luteolin

Flavone

3.99 ± 0.46

35.8 ± 5.73

Biochanin A

Isoflavone

1.84 ± 0.06

No inhibition

Daidzein

Isoflavone

3.87 ± 0.52

No inhibition

(+) Catechin hydrate

Flavonol

No inhibition

-

Fisetin

Flavonol

1.69 ± 0.04

No inhibition

Kaempferol

Flavonol

4.91 ± 1.69

No inhibition

Myricetin

Flavonol

2.91 ± 0.27

No inhibition

Quercetin

Flavonol

0.963 ± 0.094

No inhibition

Tamarixetin

Flavonol

No inhibition

-

S-equol

Isoflavan

No inhibition

-

Cyanidin chloride

Anthocyanidin

2.15 ± 0.24

No inhibition

Petunidin

Anthocyanidin

14.9 ± 2.01

No inhibition