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Biochemical Systematics and Ecology 29 (2001) 213}214

A minor coumarino-lignoid from

Jatropha gossypifolia

q

Biswanath Das

*

, B. Venkataiah

Organic Chemistry Division-I, Indian Institute of Chemical Technology, Hyderabad-500 007, India

Received 11 February 2000; accepted 26 April 2000

Keywords: Jatropha gossypifolia; Euphorbiaceae; Whole plant; Propacin; Coumarino-lignoid

1. Subject and source

Jatropha gossypifolia

Linn. (Euporbiaceae) is a small shrub which grows widely in

India. The plant has been used ethnomedically for the treatment of cancerous growths

(Hartwell, 1969).

The whole plant was collected from the campus in September 1997. A voucher

specimen of the plant material (IICP-2048) is preserved in the herbarium of the Indian

Institute of Chemical Technology.

2. Previous work

Several novel diterpenes (jatrophone and its analogues (Kupchan et al., 1970;

Taylor et al., 1983) and jatropholones A and B (Purushothaman et al., 1979)) as well as

lignans (jatrophan and gadain (Banerji et al., 1984) and venkatasin (Das et al., 1999))

have previously been reported.

3. Present study

The dried whole plant of

J. gossypifolia

was extracted with CH

2

Cl

2

}

MeOH (1 : 1)

for 120 h. The concentrated extract was subjected to column chromatography over

q

Studies on Phytochemicals: Part XXXI; IICT Communication No. 4498

(2)

silica gel to produce propacin (

1

) (yield 0.0011%). The physical (m.p., [

a

]

D

) and

spectral (IR,

1H NMR and MS) properties of the compound and its acetyl derivative

were found to be identical to those recorded earlier (Zoghbi et al., 1981; Arnoldi et al.,

1984; Chatterjee et al., 1994). This is the

"

rst report of the isolation of propacin from

J. gossypifolia.

4. Chemotaxonomic signi

5

cance

Coumarino-lignoids have previously been isolated (Parthasarathy and Saradhi,

1984; Das et al., 1999) from various

Jatropha

species. These compounds may be useful

taxonomic markers within the genus.

Acknowledgements

The authors thank CSIR (New Delhi) for

"

nancial assistance.

References

Arnoldi, A., Arnone, A., Merlini, L., 1984. Heterocycles 22, 1537.

Banerji, J., Das, R., Chatterjee, A., Shoolery, J.N., 1984. Phytochemistry 23, 2323. Chatterjee, A., Das, P.C., Joshi, P.C., Mondal, S., 1994. J. Ind. Chem. Soc. 71, 475. Das, B., Venkataiah, B., Kashinatham, A., 1999. Nat. Prod. Lett. 13, 293. Hartwell, J.L., 1969. Lloydia 32, 153.

Kupchan, S.M., Sigel, C.W., Matz, M.J., Renauld, J.A.S., Haltiwanger, R.C., Bryan, R.F., 1970. J. Am. Chem. Soc. 92, 4476.

Parthasarathy, M.R., Saradhi, K.P., 1984. Phytochemistry 23, 867.

Purushothaman, K.K., Chandrasekharan, J., Cameron, A.F., Connoly, J.D., Labbe, C., Maltz, A., Rycorft, D.S., 1979. Tetrahedron Lett.

Taylor, M.D., Smith, A.B. III, Furst, G.T., Gunasekara, S.P., Bevelle, C.A., Cordell, G.A., Farnsworth, N.R., Kupchan, S.M., Uchida, H., Branfman, A.R., Daily, R.G. Jr., Sneden, A.T., 1983. J. Am. Chem. Soc. 105, 3177.

Zoghbi, M.D.G.B., Roque, N.E., Gottilieb, O.R., 1981. Phytochemistry 20, 180.

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