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Journal : Indonesian Journal of Chemistry

A TRITERPENOID SAPONIN FROM SEEDS OF KOLOWE (Chydenanthus excelsus) Laode Rijai; Supriyatna Sutardjo; Husein Hernandi Bahti; Unang Supratman; Rymond J. Rumampuk; W.C. Taylor
Indonesian Journal of Chemistry Vol 4, No 3 (2004)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (182.279 KB) | DOI: 10.22146/ijc.21854

Abstract

A triterpenoid saponin have been isolated from n-butanol fraction of the seeds of kolowe (Chydenanthus excelsus). The structure was determined as 3-O-[β-D-glucopyranosyl(1→3)-β-D-xylopyranosyl(1→3)- β - D-glucuronopyranosyloxy]- 22α -O-(2-methylbutiroyloxyolean-12-en-15α,16α,28-tri-hydroxy. Structure elucidation was accomplished by NMR (HMBC, HMQC/HSQC, ROE, ROESY, TOCSY) methods, ESIMS, and IR spectroscopic.
ISOLATION OF AN ANTIFEEDANT TRITERPENOID FROM THE SEED OF Barringtonia asiatica Emma J Pongoh; Rymond J Rumampuk; Ponis Tarigan; Anthony J Herlt; Lewis N Mander
Indonesian Journal of Chemistry Vol 4, No 1 (2004)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (95.76 KB) | DOI: 10.22146/ijc.21873

Abstract

An antifeedant triterpenoid saponin has been isolated from the seed of Barringtonia asiatica and its structure elucidated mainly by two dimensional NMR spectroscopy is identified as 3-O-{[β-D-galactopyranosyl(1→3)-β-D-glucopyranosyl (1→2)]-β-D-glucuronopyranosyloxy}-22-O-[2-(E)-methyl-2-butenyloyloxy]-15, 16,28-trihydroxy-(3β,15α,16α,22α)-olean-12-ene. This compound showed antifeedant activity towards Epilachna sp larvae
A TRITERPENE ESTER SAPONIN FROM THE SEED OF Barringtonia asiatica Rymond J Rumampuk; Emma J Pongoh; Ponis Tarigan; Anthony J Herlt; Lewis N Mander
Indonesian Journal of Chemistry Vol 3, No 3 (2003)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (76.507 KB) | DOI: 10.22146/ijc.21880

Abstract

A triterpene ester saponin has been isolated from the seed of Barringtonia asiatica and its structure has been established by extensive application of high-resolution FABMS and two dimensional NMR techniques to be 3-O-{[β-D-galactopyranosyl(1→3)-β-D-glucopyranosyl(1→2)]-β-D-glucuronopyranosyloxy}-22-O-[2-methylbutyroyloxy]-15,16,28-trihydroxy-(3β,15α,16α,22α)-olean-12-ene.
ISOLATION AND STRUCTURE DETERMINATION OF BISDEMTHYLAAPTAMINE FROM BUNAKEN MARINE PARK SPONGE Aaptos, sp. Wilson AR Rombang; Rymond J Rumampuk; Ponis Tarigan; Anthony J Herlt; Lewis N Mander
Indonesian Journal of Chemistry Vol 3, No 3 (2003)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (50.507 KB) | DOI: 10.22146/ijc.21881

Abstract

Bisdemethylaaptamine, an alkaloid naphtyridine with molecular weight 200 and formulae molecule C11H8N2O2 has been isolated from Bunaken Marine Park sponge Aaptos sp. Isolation was done by using several stages of column chromatography and high performance liquid chromatography. Molecular weight of this naphtyridine alkaloid was determined by electron ionization (EI) and electrospray ionization (ESI) mass spectroscopies and its structure assigned to be 8,9-dihydroxy-1H-benzo[d,e][1,6]naphtyridine by proton and carbon nuclear magnetic resonances (1H and 13C-NMR).
IDENTIFICATION AND SEQUENCING BY NMR SPECTROSCOPY OF THE CARBOHYDRATE MOIETY IN A SAPONIN FROM Barringtonia asiatica Rymond J Rumampuk
Indonesian Journal of Chemistry Vol 1, No 3 (2001)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (87.941 KB) | DOI: 10.22146/ijc.21936

Abstract

A trisaccharide chain in a saponin from the seeds of Barringtonia asiatica has been identified and sequenced as {[b-D-galactopyranosyl(1®3)- b-D-glucopyranosyl(1®2)]-b-D-glucuronopyranosyloxy} using a combination of homonuclear and heteronuclear correlation NMR spectroscopy. The 1H and 13C NMR signals of the sugar residues can be determined and distinguished from one other by use of the HMQC-TOCSY technique. Anomeric configurations were unambiguously assigned from the vicinal coupling constants 3JH-1,H-2 of the anomeric protons. Inter-glycosidic linkage assignments were elucidated using  HMBC.
CHEMICAL CONSTITUENTS FROM THE STEM BARK OF Alangium kurzi, Craib Sofyan M Nur; Soetijoso Soemitro; Husein Hernandi Bahti; Ponis Tarigan; Yue Mao Shen; Rymond J Rumampuk
Indonesian Journal of Chemistry Vol 1, No 3 (2001)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (54.61 KB) | DOI: 10.22146/ijc.21938

Abstract

Three new chemical constituents have been isolated from the stem bark of Alangium kurzii Craib. The structures were respectively determined to be 4-cyclohexene-1,2,3-triol 1, 3-β-stigmast-5-en-3-ol (β-sitosterol 2), and 3-O-β-D-glucopyranosyl-stigmast-5-ene (daucosterol 3). These compounds are preliminary isolated from this plant.