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Journal of Clinical & Experimental Pharmacology | ISSN: 2161-1459 | Volume: 8

International Conference on

July 18-19, 2018 | Atlanta, USA

Pharmacology and Ethnopharmacology

11

th

International Conference and Exhibition on

Pharmaceutical Oncology

&

Isolation and identification of antifungal compounds from turmeric (Ryudai gold) and their activities

against

Fusarium solani

Jesmin Akter, Md Amzad Hossain

and

Sano Ayako

University of the Ryukyus, Japan

R

ecently, synthetic fungicide is gradually restricted due to its undesirable impacts on the environment and human health. Turmeric

(

Curcuma

spp.) has numerous biological activities including anticancer, antibacterial, antifungal and insecticidal properties.

There are more than 80 species of turmeric and 70 strains/varieties of

Curcuma

longa

with different chemical properties which

may possess different activities.

Fusarium solani sensu lato

(FSSL), pathogenic fungal species, causes several diseases in human,

animals, and plants. To date, there has been no report that addresses the effect of turmeric on F. solani. Therefore, we evaluated

antifungal activities of 3

Curcuma

longa strains (Ryudai gold: RD, Okinawa ukon, and BK2),

C. xanthorrhiza, C. aromatica, C.

amada and C. zedoaria

on 4 isolates of FSSL derived from American manatees (Trichechus manatus) with 3 different genotypes.

The methanol extract of all turmeric inhibited fungal growth concentration-dependently. Among different species and varieties

of turmeric,

Curcuma

longa

(Ryudai gold) had a highest inhibitory effect on fungal growth. For this, Ryudai gold was chosen for

isolation of antifungal compounds using silica gel column and high-performance liquid chromatography. Structural identification

of the antifungal compounds was conducted using

1

H NMR,

13

C NMR, and liquid chromatography-tandem mass spectrometry. The

purified antifungal compounds were curcumin (1), demethoxycurcumin (2), bisdemethoxycurcumin (3) and (

E

)-α-atlantone (4).

The order of the IC

50

against

F. solani

was curcumin (65-76 µM) > demethoxycurcumin (76-88 µM) > (E)-α-atlantone (91-118 µM)

>bisdemethoxycurcumin (711-746 µM). The results suggested that turmeric strain Ryudai gold developed by the University of the

Ryukyus showed excellent antifungal activities against FSSL and could be used for an antifungal agent.

jesminbau02@gmail.com

Clin Exp Pharmacol 2018, Volume: 8

DOI: 10.4172/2161-1459-C1-029