Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Magie M. Kapojos is active.

Publication


Featured researches published by Magie M. Kapojos.


Phytochemistry | 2017

Oleanane triterpenes with protein tyrosine phosphatase 1B inhibitory activity from aerial parts of Lantana camara collected in Indonesia and Japan

Delfly B. Abdjul; Hiroyuki Yamazaki; Wilmar Maarisit; Henki Rotinsulu; Defny S. Wewengkang; Deiske A. Sumilat; Magie M. Kapojos; Fitje Losung; Kazuyo Ukai; Michio Namikoshi

During the search for new protein tyrosine phosphatase (PTP) 1B inhibitors, EtOH extracts from the aerial parts of Lantana camara L. (lantana) collected at Manado (Indonesia) and two subtropical islands in Japan (Ishigaki and Iriomote Islands, Okinawa) exhibited potent inhibitory activities against PTP1B in an enzyme assay. Four previously undescribed oleanane triterpenes were isolated together with known triterpenes and flavones from the Indonesian lantana. The EtOH extracts of lantana collected in Ishigaki and Iriomote Islands exhibited different phytochemical profiles from each other and the Indonesian lantana. Triterpenes with a 24-OH group were isolated from the Indonesian lantana only. Five known triterpene compounds were detected in the Ishigaki lantana, and two oleanane triterpenes with an ether linkage between 3β and 25 were the main components together with five known triterpenes as minor components in the Iriomote lantana. The structures of previously undescribed compounds were assigned on the basis of their spectroscopic data. Among the compounds obtained in this study, oleanolic acid exhibited the most potent activity against PTP1B, and is used as a positive control in studies on PTP1B.


Bioorganic & Medicinal Chemistry Letters | 2017

A tetramic acid derivative with protein tyrosine phosphatase 1B inhibitory activity and a new nortriterpene glycoside from the Indonesian marine sponge Petrosia sp.

Wilmar Maarisit; Hiroyuki Yamazaki; Syu-ichi Kanno; Ayako Tomizawa; Henki Rotinsulu; Defny S. Wewengkang; Deiske A. Sumilat; Kazuyo Ukai; Magie M. Kapojos; Michio Namikoshi

During the search for protein tyrosine phosphatase 1B (PTP1B) inhibitors from marine organisms, the known tetramic acid derivative, melophlin C (1), was isolated as an active component together with the new nortriterpenoid saponin, sarasinoside S (2), and three homologues: sarasinosides A1 (3), I1 (4), and J (5), from the Indonesian marine sponge Petrosia sp. The structure of 2 was elucidated on the basis of its spectroscopic data. Compound 1 inhibited PTP1B activity with an IC50 value of 14.6μM, while compounds 2-5 were not active at 15.2-16.0μM. This is the first study to report the inhibitory effects of a tetramic acid derivative on PTP1B activity.


Bioorganic & Medicinal Chemistry Letters | 2017

Anti-mycobacterial alkaloids, cyclic 3-alkyl pyridinium dimers, from the Indonesian marine sponge Haliclona sp.

Wilmar Maarisit; Delfly B. Abdjul; Hiroyuki Yamazaki; Hajime Kato; Henki Rotinsulu; Defny S. Wewengkang; Deiske A. Sumilat; Magie M. Kapojos; Kazuyo Ukai; Michio Namikoshi

Three new dimeric 3-alkyl pyridinium alkaloids, named haliclocyclamines A-C (1-3), were isolated together with five known congeners, cyclostellettamines A (4), B (5), C (6), E (7), and F (8), from the Indonesian marine sponge Haliclona sp. The structures of 1-3 were assigned based on their spectroscopic data (1D and 2D NMR, HRFABMS, ESIMS/MS, UV, and IR). Compounds 1-8 exhibited antimicrobial activities against Mycobacterium smegmatis with inhibition zones of 17, 10, 13, 14, 8, 8, 12, and 12mm, respectively, at 10μg/disc. Compounds 3 and 8 also modestly inhibited the activity of vaccinia H-1-related phosphatase (VHR), a dual-specificity phosphatase, at 17-18μM.


Chemical & Pharmaceutical Bulletin | 2018

Absolute Structures of Wedelolide Derivatives and Structure–Activity Relationships of Protein Tyrosine Phosphatase 1B Inhibitory ent-Kaurene Diterpenes from Aerial Parts of Wedelia spp. Collected in Indonesia and Japan

Delfly B. Abdjul; Hiroyuki Yamazaki; Syu-ichi Kanno; Ryota Kirikoshi; Ayako Tomizawa; Ohgi Takahashi; Wilmar Maarisit; Fitje Losung; Henki Rotinsulu; Defny S. Wewengkang; Deiske A. Sumilat; Magie M. Kapojos; Michio Namikoshi

Two sesquiterpene lactones with the (9R)-eudesman-9,12-olide framework, wedelolides I and J, have been isolated together with five eudesmanolide sesquiterpenes and twelve ent-kaurene diterpenes from the aerial parts of Indonesian Wedelia prostrata. The absolute configurations of wedelolides I and J, proposed in the previous communication, were proven by comparing their experimental Electronic Circular Dichroism (ECD) spectra with the calculated ECD spectrum of wedelolide I. The phytochemical study on the aerial parts of Okinawan Wedelia chinensis led to the isolation of three other eudesmanolide sesquiterpenes in addition to the three sesquiterpenes and eleven diterpenes isolated from the Indonesian W. prostrata as above. However, the wedelolide derivatives found in the Indonesian plant were not detected. Among these compounds, most of the diterpenes inhibited protein tyrosine phosphatase (PTP) 1B activity, and a structure-activity relationship study revealed that the cinnamoyl group enhanced inhibitory activity. Therefore, two ent-kaurene derivatives with and without a cinnamoyl group were examined for the ability to accumulate phosphorylated-Akt (p-Akt) because PTP1B dephosphorylates signal transduction from the insulin receptor such as phosphorylated Akt, a key downstream effector. However, neither compound enhanced insulin-stimulated p-Akt levels in two human hepatoma cell lines (Huh-7 and HepG2) at non-cytotoxic doses.


Bioorganic & Medicinal Chemistry Letters | 2018

Callyspongiamides A and B, sterol O -acyltransferase inhibitors, from the Indonesian marine sponge Callyspongia sp.

Magie M. Kapojos; Delfly B. Abdjul; Hiroyuki Yamazaki; Taichi Ohshiro; Henki Rotinsulu; Defny S. Wewengkang; Deiske A. Sumilat; Hiroshi Tomoda; Michio Namikoshi; Ryuji Uchida

Callyspongiamides A (1) and B (2), two new sterol O-acyltransferase (SOAT) inhibitors, were isolated from the Indonesian marine sponge Callyspongia sp. together with a known congener, dysamide A (3). The structures of 1 and 2 were elucidated to be polychlorine-containing modified dipeptides based on their spectroscopic data. Compounds 1-3 inhibited both of the SOAT isozymes, SOAT1 and SOAT2, in cell-based and enzyme-based assays.


Omni-Akuatika | 2015

AKTIVITAS ANTIMITOTIK DARI EKSTRAK KARANG LUNAK GENUS SINULARIA

Wendy Alexander Tanod; Remy E. P. Mangindaan; Magie M. Kapojos

Soft coral genus Sinularia be a sources of terpenoid compounds that show efficacy in vitro cytotoxic test using cancer cell lines. The study looked at the morphological changes that occur in fungal mycelial growth of Pyricularia oryzae, such as curling effect indicating antimitotic activity. Four extracts of soft coral genus Sinularia have been examination and this is an primary test to obtain information about the soft coral genus Sinularia that used as sources of compound antimitotic. This research was conducted in several stages, ie extraction of bioactive substances, P. oryzae fungal culture test, and biological testing antimitotic activity with a qualitative assessment methods. From the examination the Sinularia 3 ethyl acetate fraction show the strongest antimitotic activity (to concentration 1,5 μg/ml). Ethyl acetate fraction was purified using column chromatography. From the examination show that fraction of ethyl acetate 1 is the best fraction because still show curling effect on concentration 0,7 μg/ml. Keywords : Antimitotic, Soft Coral, Sinularia, microtubule, Pyricularia oryzae


Tetrahedron | 2010

Two unprecedented cembrene-type terpenes from an indonesian soft coral sarcophyton sp.

Magie M. Kapojos; Jong Soo Lee; Taiko Oda; Takahiro Nakazawa; Ohgi Takahashi; Kazuyo Ukai; Remy E. P. Mangindaan; Henki Rotinsulu; Defny S. Wewengkang; Sachiko Tsukamoto; Hisayoshi Kobayashi; Michio Namikoshi


Journal of Natural Medicines | 2017

An anti-mycobacterial bisfunctionalized sphingolipid and new bromopyrrole alkaloid from the Indonesian marine sponge Agelas sp.

Delfly B. Abdjul; Hiroyuki Yamazaki; Syu-ichi Kanno; Ayako Tomizawa; Henki Rotinsulu; Defny S. Wewengkang; Deiske A. Sumilat; Kazuyo Ukai; Magie M. Kapojos; Michio Namikoshi


Phytochemistry Letters | 2018

Protein tyrosine phosphatase 1B inhibitory polybromobiphenyl ethers and monocyclofarnesol-type sesquiterpenes from the Indonesian marine sponge Lamellodysidea cf. herbacea

Magie M. Kapojos; Delfly B. Abdjul; Hiroyuki Yamazaki; Ryota Kirikoshi; Ohgi Takahashi; Henki Rotinsulu; Defny S. Wewengkang; Deiske A. Sumilat; Kazuyo Ukai; Michio Namikoshi


Phytochemistry Letters | 2018

Protein tyrosine phosphatase 1B inhibitory components and a new unique N-alkylamide derivative with an endoperoxide bridge from aerial parts of Indonesian Spilanthes paniculata

Delfly B. Abdjul; Hiroyuki Yamazaki; Wilmar Maarisit; Ryota Kirikoshi; Ohgi Takahashi; Fitje Losung; Magie M. Kapojos; Michio Namikoshi

Collaboration


Dive into the Magie M. Kapojos's collaboration.

Top Co-Authors

Avatar

Michio Namikoshi

Tokyo University of Marine Science and Technology

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Kazuyo Ukai

Tohoku Pharmaceutical University

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Ohgi Takahashi

Tohoku Pharmaceutical University

View shared research outputs
Top Co-Authors

Avatar

Fitje Losung

Sam Ratulangi University

View shared research outputs
Researchain Logo
Decentralizing Knowledge