Language:
English
繁體中文
Help
Login
Back
Switch To:
Labeled
|
MARC Mode
|
ISBD
Progress in the Chemistry of Organic...
~
Liu, Ji-Kai.
Progress in the Chemistry of Organic Natural Products 115
Record Type:
Language materials, printed : Monograph/item
Title/Author:
Progress in the Chemistry of Organic Natural Products 115/ edited by A. Douglas Kinghorn, Heinz Falk, Simon Gibbons, Yoshinori Asakawa, Ji-Kai Liu, Verena M. Dirsch.
other author:
Dirsch, Verena M.
Description:
VII, 203 p. 144 illus., 42 illus. in color.online resource. :
Contained By:
Springer Nature eBook
Subject:
Pharmaceutical Sciences/Technology. -
Online resource:
https://doi.org/10.1007/978-3-030-64853-4
ISBN:
9783030648534
Progress in the Chemistry of Organic Natural Products 115
Progress in the Chemistry of Organic Natural Products 115
[electronic resource] /edited by A. Douglas Kinghorn, Heinz Falk, Simon Gibbons, Yoshinori Asakawa, Ji-Kai Liu, Verena M. Dirsch. - 1st ed. 2021. - VII, 203 p. 144 illus., 42 illus. in color.online resource. - Progress in the Chemistry of Organic Natural Products,1152192-4309 ;. - Progress in the Chemistry of Organic Natural Products,100.
Total Synthesis of Decanolides (Nonanolides) with a Special Focus on Olefin Metathesis -- From Plant to Patient: Thapsigargin -- Antileishmanial Activity of Lignans and Neolignans -- Cryptolepine as a Lead to new Antiprotozoal Agents -- Biologically Active Constituents from Plants of the Genus Xanthium.
This book describes current understandings and recent progress into a varied group of natural products. In the first chapter the role that total synthesis may play in revising the structures proposed for decanolides, which are ten-membered lactones found primarily in fungi, frogs, and termites is presented. The following chapter presents the development of the intriguing plant-derived sesquiterpene lactone, thapsigargin, a potent inhibitor of the enzyme, SERCA (sarco-endoplasmic Ca2+ ATPase), which has potential as a lead compound to treat cancer. The third chapter covers the potential of various plant phenolic compounds for treating the tropical and sub-tropical infectious disease, leishmaniasis. In addition the volume presents recent advances related to the plant alkaloid, cryptolepine, which is of particular interest as a lead for the treatment of malaria, trypanosomiasis, and cancer.
ISBN: 9783030648534
Standard No.: 10.1007/978-3-030-64853-4doiSubjects--Topical Terms:
768561
Pharmaceutical Sciences/Technology.
LC Class. No.: QD415-436
Dewey Class. No.: 547
Progress in the Chemistry of Organic Natural Products 115
LDR
:02753nam a22004095i 4500
001
1052309
003
DE-He213
005
20210920131245.0
007
cr nn 008mamaa
008
220103s2021 sz | s |||| 0|eng d
020
$a
9783030648534
$9
978-3-030-64853-4
024
7
$a
10.1007/978-3-030-64853-4
$2
doi
035
$a
978-3-030-64853-4
050
4
$a
QD415-436
072
7
$a
PNN
$2
bicssc
072
7
$a
SCI013040
$2
bisacsh
072
7
$a
PNN
$2
thema
082
0 4
$a
547
$2
23
245
1 0
$a
Progress in the Chemistry of Organic Natural Products 115
$h
[electronic resource] /
$c
edited by A. Douglas Kinghorn, Heinz Falk, Simon Gibbons, Yoshinori Asakawa, Ji-Kai Liu, Verena M. Dirsch.
250
$a
1st ed. 2021.
264
1
$a
Cham :
$b
Springer International Publishing :
$b
Imprint: Springer,
$c
2021.
300
$a
VII, 203 p. 144 illus., 42 illus. in color.
$b
online resource.
336
$a
text
$b
txt
$2
rdacontent
337
$a
computer
$b
c
$2
rdamedia
338
$a
online resource
$b
cr
$2
rdacarrier
347
$a
text file
$b
PDF
$2
rda
490
1
$a
Progress in the Chemistry of Organic Natural Products,
$x
2192-4309 ;
$v
115
505
0
$a
Total Synthesis of Decanolides (Nonanolides) with a Special Focus on Olefin Metathesis -- From Plant to Patient: Thapsigargin -- Antileishmanial Activity of Lignans and Neolignans -- Cryptolepine as a Lead to new Antiprotozoal Agents -- Biologically Active Constituents from Plants of the Genus Xanthium.
520
$a
This book describes current understandings and recent progress into a varied group of natural products. In the first chapter the role that total synthesis may play in revising the structures proposed for decanolides, which are ten-membered lactones found primarily in fungi, frogs, and termites is presented. The following chapter presents the development of the intriguing plant-derived sesquiterpene lactone, thapsigargin, a potent inhibitor of the enzyme, SERCA (sarco-endoplasmic Ca2+ ATPase), which has potential as a lead compound to treat cancer. The third chapter covers the potential of various plant phenolic compounds for treating the tropical and sub-tropical infectious disease, leishmaniasis. In addition the volume presents recent advances related to the plant alkaloid, cryptolepine, which is of particular interest as a lead for the treatment of malaria, trypanosomiasis, and cancer.
650
2 4
$a
Pharmaceutical Sciences/Technology.
$3
768561
650
2 4
$a
Plant Sciences.
$3
593902
650
2 4
$a
Chemistry/Food Science, general.
$3
593890
650
2 4
$a
Medicinal Chemistry.
$3
668872
650
2 4
$a
Biochemistry, general.
$3
593881
650
1 4
$a
Organic Chemistry.
$3
673440
650
0
$a
Pharmaceutical technology.
$3
557391
650
0
$a
Botany.
$3
599558
650
0
$a
Plant science.
$3
1249732
650
0
$a
Chemistry.
$3
593913
650
0
$a
Medicinal chemistry.
$3
1253747
650
0
$a
Biochemistry.
$3
582831
650
0
$a
Organic chemistry.
$3
1148722
700
1
$a
Dirsch, Verena M.
$e
editor.
$1
https://orcid.org/0000-0002-9261-5293
$4
edt
$4
http://id.loc.gov/vocabulary/relators/edt
$3
1357012
700
1
$a
Liu, Ji-Kai.
$e
editor.
$1
https://orcid.org/0000-0001-6279-7893
$4
edt
$4
http://id.loc.gov/vocabulary/relators/edt
$3
1282794
700
1
$a
Asakawa, Yoshinori.
$4
edt
$4
http://id.loc.gov/vocabulary/relators/edt
$3
1079863
700
1
$a
Gibbons, Simon.
$e
editor.
$4
edt
$4
http://id.loc.gov/vocabulary/relators/edt
$3
1269908
700
1
$a
Falk, Heinz.
$4
edt
$4
http://id.loc.gov/vocabulary/relators/edt
$3
796060
700
1
$a
Kinghorn, A. Douglas.
$4
edt
$4
http://id.loc.gov/vocabulary/relators/edt
$3
649575
710
2
$a
SpringerLink (Online service)
$3
593884
773
0
$t
Springer Nature eBook
776
0 8
$i
Printed edition:
$z
9783030648527
776
0 8
$i
Printed edition:
$z
9783030648541
776
0 8
$i
Printed edition:
$z
9783030648558
830
0
$a
Progress in the Chemistry of Organic Natural Products,
$x
2191-7043 ;
$v
100
$3
1254704
856
4 0
$u
https://doi.org/10.1007/978-3-030-64853-4
912
$a
ZDB-2-CMS
912
$a
ZDB-2-SXC
950
$a
Chemistry and Materials Science (SpringerNature-11644)
950
$a
Chemistry and Material Science (R0) (SpringerNature-43709)
based on 0 review(s)
Multimedia
Reviews
Add a review
and share your thoughts with other readers
Export
pickup library
Processing
...
Change password
Login