SYNTHESIS OF 11,12-LEUKOTRIENE-A4, 11S,12S-OXIDO-5Z,7E,9E,14Z-EICOSATETRAENOIC ACID, A NOVEL LEUKOTRIENE OF THE 12-LIPOXYGENASE PATHWAY

被引：9

作者：

KITAMURA, S ^{[1
]}

SHIMIZU, T ^{[1
]}

IZUMI, T ^{[1
]}

SEYAMA, Y ^{[1
]}

机构：

[1] UNIV TOKYO,FAC MED,DEPT PHYSIOL CHEM & NUTR,BUNKYO KU,TOKYO 113,JAPAN

来源：

FEBS LETTERS | 1987年 / 213卷 / 01期

关键词：

D O I：

10.1016/0014-5793(87)81485-0

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：169 / 173

页数：5

共 50 条

[1] STEREOSPECIFIC SYNTHESIS OF 11S, 12S-OXIDO 5Z,7E,9E,14Z-EICOSATETRAENOIC ACID
ZAMBONI, R
MILETTE, S
ROKACH, J
TETRAHEDRON LETTERS, 1984, 25 (51) : 5835 - 5838
[2] IDENTIFICATION OF 5-KETO-(7E,9E,11Z,14Z)-EICOSATETRAENOIC ACID AS A NOVEL NONENZYMATIC REARRANGEMENT PRODUCT OF LEUKOTRIENE-A(4)
GRAVEL, J
FALGUEYRET, JP
YERGEY, J
TRIMBLE, L
RIENDEAU, D
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 306 (02) : 469 - 475
[3] STEREOSELECTIVE SYNTHESIS OF (11R,12S)-(5Z,7E,9E,14Z)-11,12-DIHYDROXY 5,7,9,14-EICOSATETRAENOIC ACID FROM DIACETONE GLUCOSE
SHARMA, GVM
RAO, SM
TETRAHEDRON LETTERS, 1994, 35 (24) : 4231 - 4232
[4] SYNTHESIS OF (+/-)-5,6-EPOXY-7E,9E,11Z,14Z-EICOSATETRAENOIC ACID METHYL-ESTER
TOLSTIKOV, GA
MIFTAKHOV, MS
TOLSTIKOV, AG
BULLETIN OF THE ACADEMY OF SCIENCES OF THE USSR DIVISION OF CHEMICAL SCIENCE, 1984, 33 (02): : 442 - 443
[5] Non-enzymatic rearrangement of leukotriene A4 to 5-keto-(7E,9E,11Z,14Z)-eicosatetraenoic acid in aqueous media
Riendeau, D
Falgueyret, JP
Gravel, J
Trimble, L
Yergey, J
EICOSANOIDS AND OTHER BIOACTIVE LIPIDS IN CANCER, INFLAMMATION, AND RADIATION INJURY 2, PTS A AND B, 1997, 400 : 71 - 76
[6] PREPARATION OF TETRADEUTERATED LEUKOTRIENE-A4 METHYL-ESTER - METHYL-[11,12,14,15-2H4]-(5S,6S)-OXIDO-(7E,9E,11Z,14Z)-EICOSATETRAENOATE
LELLOUCHE, JP
BEAUCOURT, JP
VANHOVE, A
METHODS IN ENZYMOLOGY, 1990, 187 : 70 - 76
[7] STEREOCONTROLLED TOTAL SYNTHESIS OF (5S,6R)-(7E,9E,11Z,14Z)-5-6-DIHYDROXY-7,9,11,14-ICOSATETRAENOIC, (5S,6S)-(7E,9E,11Z,14Z)-5-6-DIHYDROXY-7,9,11,14-ICOSATETRAENOIC, (5R,6R)-(7E,9E,11Z,14Z)-5-6-DIHYDROXY-7,9,11,14-ICOSATETRAENOIC, AND (5R,6S)-(7E,9E,11Z,14Z)-5,6-DIHYDROXY-7,9,11,14-ICOSATETRAENOIC ACID (5,6-DIHETE) METHYL-ESTERS
NICOLAOU, KC
RAMPHAL, JY
PALAZON, JM
SPANEVELLO, RA
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1989, 28 (05): : 587 - 588
[8] THE STEREOSPECIFIC SYNTHESIS OF 14S,15S-OXIDO 5Z,8Z,10E,12E-EICOSATETRAENOIC ACID
ZAMBONI, R
MILETTE, S
ROKACH, J
TETRAHEDRON LETTERS, 1983, 24 (45) : 4899 - 4902
[9] Synthesis of the conjugated trienes 5E,7E,9E,14Z,17Z-eicosapentaenoic acid and 5Z,7E,9E,14Z,17Z-eicosapentaenoic acid, and their induction of apoptosis in DLD-1 colorectal adenocarcinorna cells
Tsuzuki, T
Tanaka, K
Kuwahara, S
Miyazawa, T
LIPIDS, 2005, 40 (02) : 147 - 154
[10] Synthesis of (9Z,12E)-, (9E,12Z)-[1-C-14]-linoleic acid, (92,12Z,15E)-, (9E,12Z,15Z)-[1-C-14]-linolenic acid and (5Z,8Z,11Z,14E)-[1-C-14]-arachidonic acid
Eynard, T
Vatele, JM
Berdeaux, O
Poullain, D
Noel, JP
GRASAS Y ACEITES, 1996, 47 (1-2) : 81 - 85

← 1 2 3 4 5 →