Isopetrosynol, a New Protein Tyrosine Phosphatase 1B Inhibitor, from the Marine Sponge Halichondria cf. panicea Collected at Iriomote Island

被引:13
作者
Abdjul, Delfly Booby [1 ,2 ]
Yamazaki, Hiroyuki [1 ]
Takahashi, Ohgi [1 ]
Kirikoshi, Ryota [1 ]
Ukai, Kazuyo [1 ]
Namikoshi, Michio [1 ]
机构
[1] Tohoku Med & Pharmaceut Univ, Fac Pharmaceut Sci, Sendai, Miyagi 9818558, Japan
[2] Sam Ratulangi Univ, Fac Fisheries & Marine Sci, Kampus Bahu, Manado 95115, Indonesia
关键词
isopetrosynol; polyacetylene; marine sponge; Halichondria cf. panicea; protein tyrosine phosphatase 1B (PTP1B) inhibitor; PETROSIA SP; NATURAL-PRODUCTS; POLYACETYLENES; PETROSTEROL; METABOLITES; DERIVATIVES; TARGET; PTP1B; ACID;
D O I
10.1248/cpb.c16-00061
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A new polyacetylene compound, isopetrosynol (1), was isolated from the Okinawan marine sponge Halichondria cf. panicea together with petrosynol (2), adociacetylene D (3), (5R)-3,15,27-triacontatriene-1,29-diyn-5-ol (4), and petrosterol (5). The structure of 1 was assigned on the basis of spectroscopic data for 1 and 2. Compound 1 inhibited protein tyrosine phosphatase 1B (PTP1B) activity with an IC50 value of 8.2+/-0.3 mu M, while compound 2, a diastereomer of 1, showed only 28.9+/-4.5% inhibition at 21.6 mu M. The IC50 values of compounds 3 and 4 were 7.8+/-0.5 and 12.2+/-0.5 mu M, respectively. Oleanolic acid, a positive control, inhibited PTP1B activity at 0.7+/-0.1 mu M (IC50) in the same experiment. The inhibitory activity of 1 was stronger than that of its diastereomer (2). This is the first study to show the inhibitory effects of polyacetylene compounds on PTP1B.
引用
收藏
页码:733 / 736
页数:4
相关论文
共 19 条
[1]   Two new protein tyrosine phosphatase 1B inhibitors, hyattellactones A and B, from the Indonesian marine sponge Hyattella sp. [J].
Abdjul, Delfly B. ;
Yamazaki, Hiroyuki ;
Takahashi, Ohgi ;
Kirikoshi, Ryota ;
Mangindaan, Remy E. P. ;
Namikoshi, Michio .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2015, 25 (04) :904-907
[2]   Protein tyrosine phosphatases as drug targets: strategies and challenges of inhibitor development [J].
Barr, Alastair J. .
FUTURE MEDICINAL CHEMISTRY, 2010, 2 (10) :1563-1576
[3]   Protein tyrosine phosphatase 1B inhibitors from Morus root bark [J].
Cui, L ;
Na, MK ;
Oh, M ;
Bae, EY ;
Jeong, DG ;
Ryu, SE ;
Kim, S ;
Kim, BY ;
Oh, WK ;
Ahn, JS .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2006, 16 (05) :1426-1429
[4]   BIOACTIVE MARINE METABOLITES .20. PETROSYNOL AND PETROSYNONE, ANTIMICROBIAL C30 POLYACETYLENES FROM THE MARINE SPONGE PETROSIA SP - DETERMINATION OF THE ABSOLUTE-CONFIGURATION [J].
FUSETANI, N ;
SHIRAGAKI, T ;
MATSUNAGA, S ;
HASHIMOTO, K .
TETRAHEDRON LETTERS, 1987, 28 (37) :4313-4314
[5]   BIOACTIVE MARINE METABOLITES .3. A NOVEL POLYACETYLENE ALCOHOL, INHIBITOR OF CELL-DIVISION IN FERTILIZED SEA-URCHIN EGGS, FROM THE MARINE SPONGE TETROSIA SP [J].
FUSETANI, N ;
KATO, Y ;
MATSUNAGA, S ;
HASHIMOTO, K .
TETRAHEDRON LETTERS, 1983, 24 (27) :2771-2774
[6]   PETROSYNOL AND PETROSOLIC ACID, 2 NOVEL NATURAL INHIBITORS OF THE REVERSE-TRANSCRIPTASE OF HUMAN-IMMUNODEFICIENCY-VIRUS FROM PETROSIA SP [J].
ISAACS, S ;
KASHMAN, Y ;
LOYA, S ;
HIZI, A ;
LOYA, Y .
TETRAHEDRON, 1993, 49 (45) :10435-10438
[7]   Natural products possessing protein tyrosine phosphatase 1B (PTP1B) inhibitory activity found in the last decades [J].
Jiang, Cheng-shi ;
Liang, Lin-fu ;
Guo, Yue-wei .
ACTA PHARMACOLOGICA SINICA, 2012, 33 (10) :1217-1245
[8]   Structure Elucidation and Cytotoxic Evaluation of New Polyacetylenes from a Marine Sponge Petrosia sp. [J].
Juan, Yung-Shun ;
Lee, Chien-Chih ;
Tsao, Chia-Wei ;
Lu, Mei-Chin ;
El-Shazly, Mohamed ;
Shih, Huei-Chuan ;
Chen, Yu-Cheng ;
Wu, Yang-Chang ;
Su, Jui-Hsin .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2014, 15 (09) :16511-16521
[9]  
Kobayashi M, 1996, CHEM PHARM BULL, V44, P720
[10]   Strongylophorines, new protein tyrosine phosphatase 1B inhibitors, from the marine sponge Strongylophora strongilata collected at Iriomote Island [J].
Lee, Jong-Soo ;
Abdjul, Delfly B. ;
Yamazaki, Hiroyuki ;
Takahashi, Ohgi ;
Kirikoshi, Ryota ;
Ukai, Kazuyo ;
Namikoshi, Michio .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2015, 25 (18) :3900-3902