SITOTOKSISITAS DARI BEBERAPA SENYAWA TURUNAN KURKUMIN PADA SEL P388

Eryanti, Yum; Nurulita, Yuana; Yuharmen; Hendra, Rudi; Zamri, Adel

dc.contributor.author	Eryanti, Yum
dc.contributor.author	Nurulita, Yuana
dc.contributor.author	Yuharmen
dc.contributor.author	Hendra, Rudi
dc.contributor.author	Zamri, Adel
dc.date.accessioned	2014-05-21T04:40:58Z
dc.date.available	2014-05-21T04:40:58Z
dc.date.issued	2014-05-21
dc.identifier.isbn	978-602-18936-0-9
dc.identifier.other	wahyu sari yeni
dc.identifier.uri	http://repository.unri.ac.id/xmlui/handle/123456789/6278
dc.description.abstract	Four analogue curcumins (3b, 3e, 3h and 3i) have been synthesized from aldehyde and ketone by using Claisen-Schmidt condensation under base condition. All the compounds have been confirmed their structure by using UN, IR, 1HNMR and 13CNMR spectroscopy analysis. Generally, all the compounds showed cytotoxicity activity with IC50 value 15 – 80 ppm against murine leukemia (P-388) cell lines. The results showed that 3i could inhibit the highest P-388 cell line growth percentage.	en_US
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dc.description.provenance	Made available in DSpace on 2014-05-21T04:40:58Z (GMT). No. of bitstreams: 1 16 makalah oral.pdf: 341586 bytes, checksum: 6abf80718818270868c1e26c83f49be3 (MD5)	en
dc.description.sponsorship	Seminar UR-UKM ke-7 2012	en_US
dc.language.iso	en	en_US
dc.subject	curcumin	en_US
dc.subject	condensation	en_US
dc.subject	Claisen-Schmidt	en_US
dc.subject	cytotoxicity	en_US
dc.subject	P388	en_US
dc.title	SITOTOKSISITAS DARI BEBERAPA SENYAWA TURUNAN KURKUMIN PADA SEL P388	en_US
dc.type	UR-Proceedings	en_US