Marrubiin

The ethno-medicinal approach to drug discovery represents one of the most important sources of new and safe therapeutic agents to the challenges confronting modern medicine and daily life. Many of the traditionally important medicinal plants contain active molecules or ones that serve as precursors...

Full description

Saved in:
Bibliographic Details
Published in:Molecules (Basel, Switzerland) Vol. 18; no. 8; pp. 9049 - 9060
Main Authors: Popoola, Olugbenga K, Elbagory, Abdulrahman M, Ameer, Farouk, Hussein, Ahmed A
Format: Journal Article Book Review
Language:English
Published: Switzerland MDPI AG 29-07-2013
MDPI
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract The ethno-medicinal approach to drug discovery represents one of the most important sources of new and safe therapeutic agents to the challenges confronting modern medicine and daily life. Many of the traditionally important medicinal plants contain active molecules or ones that serve as precursors to biosynthesised secondary metabolites to which the biological activity could be attributed. Marrubiin is one such compound and is a potential valuable compound which exists in high concentrations in many traditionally important Lamiaceae species which have demonstrated excellent pharmacological properties with commendably high safety margins. Marrubiin's attributes include a low turnover, high stability and little catabolism, which are core characteristics required for therapeutic compounds and nutraceuticals of economic importance. In addition, marrubiin is considered a potential substrate for potent active compounds viz; marrubiinic acid, and marrubenol. The contribution of marrubiin to drug discovery thus needs to be put into prospective due to its ready availability, high potential applications and ease of modification. In this short review we highlight the most important chemical and pharmacological aspects reported on marrubiin since it was discovered.
AbstractList The ethno-medicinal approach to drug discovery represents one of the most important sources of new and safe therapeutic agents to the challenges confronting modern medicine and daily life. Many of the traditionally important medicinal plants contain active molecules or ones that serve as precursors to biosynthesised secondary metabolites to which the biological activity could be attributed. Marrubiin is one such compound and is a potential valuable compound which exists in high concentrations in many traditionally important Lamiaceae species which have demonstrated excellent pharmacological properties with commendably high safety margins. Marrubiin’s attributes include a low turnover, high stability and little catabolism, which are core characteristics required for therapeutic compounds and nutraceuticals of economic importance. In addition, marrubiin is considered a potential substrate for potent active compounds viz; marrubiinic acid, and marrubenol. The contribution of marrubiin to drug discovery thus needs to be put into prospective due to its ready availability, high potential applications and ease of modification. In this short review we highlight the most important chemical and pharmacological aspects reported on marrubiin since it was discovered.
The ethno-medicinal approach to drug discovery represents one of the most important sources of new and safe therapeutic agents to the challenges confronting modern medicine and daily life. Many of the traditionally important medicinal plants contain active molecules or ones that serve as precursors to biosynthesised secondary metabolites to which the biological activity could be attributed. Marrubiin is one such compound and is a potential valuable compound which exists in high concentrations in many traditionally important Lamiaceae species which have demonstrated excellent pharmacological properties with commendably high safety margins. Marrubiin’s attributes include a low turnover, high stability and little catabolism, which are core characteristics required for therapeutic compounds and nutraceuticals of economic importance. In addition, marrubiin is considered a potential substrate for potent active compounds viz ; marrubiinic acid, and marrubenol. The contribution of marrubiin to drug discovery thus needs to be put into prospective due to its ready availability, high potential applications and ease of modification. In this short review we highlight the most important chemical and pharmacological aspects reported on marrubiin since it was discovered.
Author Ameer, Farouk
Popoola, Olugbenga K
Elbagory, Abdulrahman M
Hussein, Ahmed A
AuthorAffiliation Chemistry Department, University of Western Cape, Private Bag X17, Belleville 7535, South Africa; E-Mails: 3318925@uwc.ac.za (O.K.P.); 3376881@uwc.ac.za (A.M.E.); fameer@uwc.ac.za (F.A.)
AuthorAffiliation_xml – name: Chemistry Department, University of Western Cape, Private Bag X17, Belleville 7535, South Africa; E-Mails: 3318925@uwc.ac.za (O.K.P.); 3376881@uwc.ac.za (A.M.E.); fameer@uwc.ac.za (F.A.)
Author_xml – sequence: 1
  givenname: Olugbenga K
  surname: Popoola
  fullname: Popoola, Olugbenga K
  organization: Chemistry Department, University of Western Cape, Private Bag X17, Belleville 7535, South Africa
– sequence: 2
  givenname: Abdulrahman M
  surname: Elbagory
  fullname: Elbagory, Abdulrahman M
– sequence: 3
  givenname: Farouk
  surname: Ameer
  fullname: Ameer, Farouk
– sequence: 4
  givenname: Ahmed A
  surname: Hussein
  fullname: Hussein, Ahmed A
BackLink https://www.ncbi.nlm.nih.gov/pubmed/23899837$$D View this record in MEDLINE/PubMed
BookMark eNplkctOwzAQRS1URB_wAWzYsGFT8Dv2BglVPCoVsYG15bjjkiqJi50g8fektFQtrDzy3Dlz7TtEvTrUgNA5wdeMaXxThRJcW0IiCiuNuT5CA8IpHrOu7u3VfTRMaYkxJZyIE9SnTGmtWDZAg2cbY5sXRX2Kjr0tE5xtzxF6e7h_nTyNZy-P08ndbOyE0M3YOc5Fpp0GrJX3JJdKSu4FWO9ySgUBbj0ICdJ5mnnulRBW55bBnJOcSTZC0w13HuzSrGJR2fhlgi3Mz0WIC2NjU7gSjLJeWpVLTtbG59BxOFcqy3nGtZWuY91uWKs2r2DuoG6iLQ-gh526eDeL8GkklVpR2gGutoAYPlpIjamK5KAsbQ2hTaZbK6UWUq6ll3-ky9DGuvsqQwSjhEnMs05FNioXQ0oR_M4MwWYdmvkXWjdzsf-K3cRvSuwbPmuVBA
CitedBy_id crossref_primary_10_1248_yakushi_21_00126
crossref_primary_10_1590_0103_8478cr20200855
crossref_primary_10_1016_j_colsurfb_2018_01_046
crossref_primary_10_1016_j_fitote_2019_02_027
crossref_primary_10_1021_acs_orglett_6b01602
crossref_primary_10_1155_2018_7801543
crossref_primary_10_3390_plants11172309
crossref_primary_10_3390_molecules22111851
crossref_primary_10_1016_j_sciaf_2022_e01510
crossref_primary_10_1021_acs_joc_8b00882
crossref_primary_10_1002_pca_2820
crossref_primary_10_1039_D4RA01834F
crossref_primary_10_1007_s13205_020_2126_5
crossref_primary_10_1155_2022_4457973
crossref_primary_10_34172_jcvtr_2023_31704
crossref_primary_10_5010_JPB_2022_49_1_003
crossref_primary_10_1016_j_jep_2015_08_013
crossref_primary_10_1080_15376516_2024_2364191
crossref_primary_10_34172_PS_2020_35
crossref_primary_10_1111_tpj_12589
crossref_primary_10_3390_metabo14010027
crossref_primary_10_1002_2211_5463_12755
crossref_primary_10_55355_snv2022113113
crossref_primary_10_3390_ijms25084496
crossref_primary_10_1007_s12033_023_00728_9
crossref_primary_10_1186_s12870_019_1702_5
crossref_primary_10_4081_monaldi_2021_1821
crossref_primary_10_1155_2022_8442734
crossref_primary_10_1002_cbdv_202201188
crossref_primary_10_1016_j_chroma_2019_460602
crossref_primary_10_1177_1934578X1400900705
crossref_primary_10_3390_molecules25122898
crossref_primary_10_3390_pharmaceutics11100523
crossref_primary_10_1016_j_phytol_2015_07_005
crossref_primary_10_3390_ijms18122665
crossref_primary_10_1039_D0RA10253A
crossref_primary_10_1093_plphys_kiac056
crossref_primary_10_3390_molecules25071610
crossref_primary_10_3390_cosmetics5010019
crossref_primary_10_3390_molecules26123712
crossref_primary_10_3389_fmolb_2018_00030
crossref_primary_10_2174_1389201022666210122125854
crossref_primary_10_2174_1574893618666221019092212
crossref_primary_10_1016_j_flora_2017_04_001
crossref_primary_10_34172_jhp_2022_14
crossref_primary_10_3233_JAD_231011
crossref_primary_10_3923_ijp_2024_269_278
crossref_primary_10_3390_biology13060426
Cites_doi 10.1300/J044v03n01_02
10.1016/j.jep.2011.08.041
10.1016/j.phytochem.2007.03.027
10.1111/j.2042-7158.2011.01321.x
10.1016/0021-9673(92)85036-S
10.1016/j.phytochem.2005.02.029
10.1016/j.phytochem.2012.02.021
10.1111/j.1399-3054.1997.tb01049.x
10.3109/10641963.2011.601383
10.1007/s10725-008-9286-3
10.1039/a709175c
10.1016/j.farmac.2005.01.003
10.1016/S0305-1978(01)00148-X
10.1055/s-2006-957451
10.1007/BF02466478
10.1016/j.phytochem.2012.07.014
10.1055/s-0028-1101585
10.1002/mrc.1136
10.1016/S0944-7113(98)80005-6
10.1042/bj3260449
10.1016/j.phytochem.2009.03.011
10.1016/j.fct.2011.08.026
10.1016/j.jep.2006.05.023
10.1002/1521-4079(200208)37:8<896::AID-CRAT896>3.0.CO;2-F
10.1080/10286020.2012.672975
10.1016/S0944-7113(00)80082-3
10.1128/JB.182.20.5841-5848.2000
10.1016/0031-9422(93)85464-3
10.1039/j39690002014
10.1016/S0895-7061(03)00168-7
10.1016/j.bse.2010.12.021
10.1016/j.phymed.2011.12.008
10.1002/cbdv.201000215
10.1021/np9700782
10.1016/0031-9422(91)83073-T
10.1007/BF02167631
10.2174/138161210793563392
10.1055/s-2003-37042
10.1021/np50124a010
10.1248/cpb.48.1234
ContentType Journal Article
Book Review
Copyright Copyright MDPI AG 2013
2013 by the authors; licensee MDPI, Basel, Switzerland. 2013
Copyright_xml – notice: Copyright MDPI AG 2013
– notice: 2013 by the authors; licensee MDPI, Basel, Switzerland. 2013
DBID CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
3V.
7X7
7XB
88E
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BENPR
CCPQU
DWQXO
FYUFA
GHDGH
K9.
M0S
M1P
PIMPY
PQEST
PQQKQ
PQUKI
7X8
5PM
DOA
DOI 10.3390/molecules18089049
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
CrossRef
ProQuest Central (Corporate)
Health & Medical Complete (ProQuest Database)
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central
ProQuest Central Essentials
ProQuest Central
ProQuest One Community College
ProQuest Central
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Health & Medical Complete (Alumni)
Health & Medical Collection (Alumni Edition)
PML(ProQuest Medical Library)
Publicly Available Content Database
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
MEDLINE - Academic
PubMed Central (Full Participant titles)
Directory of Open Access Journals
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
CrossRef
Publicly Available Content Database
ProQuest Central Essentials
ProQuest One Academic Eastern Edition
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Hospital Collection (Alumni)
ProQuest Central
ProQuest Health & Medical Complete
Health Research Premium Collection
ProQuest Medical Library
ProQuest One Academic UKI Edition
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
ProQuest One Academic
ProQuest Medical Library (Alumni)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList CrossRef
MEDLINE
Publicly Available Content Database


Database_xml – sequence: 1
  dbid: DOA
  name: Directory of Open Access Journals
  url: http://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: ECM
  name: MEDLINE
  url: https://search.ebscohost.com/login.aspx?direct=true&db=cmedm&site=ehost-live
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1420-3049
EndPage 9060
ExternalDocumentID oai_doaj_org_article_8af6a8b6412141dea9b44887b4749a6c
3324396801
10_3390_molecules18089049
23899837
Genre Journal Article
Review
GroupedDBID ---
0R~
123
2WC
3V.
53G
5VS
7X7
88E
8FE
8FG
8FH
8FI
8FJ
A8Z
AADQD
AAFWJ
AAHBH
ABDBF
ABJCF
ABUWG
ACGFO
ACIWK
ACPRK
AEGXH
AENEX
AFKRA
AFPKN
AFRAH
AFZYC
AIAGR
ALIPV
ALMA_UNASSIGNED_HOLDINGS
BBNVY
BENPR
BHPHI
BPHCQ
BVXVI
CCPQU
CGR
CS3
CUY
CVF
D1I
DIK
DU5
E3Z
EBD
ECM
EIF
EMOBN
ESTFP
ESX
FYUFA
GROUPED_DOAJ
GX1
HCIFZ
HH5
HMCUK
HYE
HZ~
I09
IPNFZ
KB.
KQ8
LK8
M1P
M7P
MODMG
M~E
NPM
O-U
O9-
OK1
P2P
PDBOC
PIMPY
PQQKQ
PROAC
PSQYO
RIG
RPM
SV3
TR2
TUS
UKHRP
~8M
AAYXX
CITATION
7XB
8FK
AZQEC
DWQXO
K9.
PQEST
PQUKI
7X8
5PM
ID FETCH-LOGICAL-c559t-cc44579c9e098ff1b68664f5eafcb2251e4afe56e6cf27f4f855a9ba3ed41b363
IEDL.DBID RPM
ISSN 1420-3049
IngestDate Tue Oct 22 15:15:29 EDT 2024
Tue Sep 17 21:06:48 EDT 2024
Fri Jun 28 00:44:09 EDT 2024
Tue Nov 19 04:35:18 EST 2024
Fri Aug 23 02:34:09 EDT 2024
Sat Sep 28 08:39:44 EDT 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 8
Language English
License This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c559t-cc44579c9e098ff1b68664f5eafcb2251e4afe56e6cf27f4f855a9ba3ed41b363
Notes ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
ORCID 0000-0002-3877-9959
OpenAccessLink https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269822/
PMID 23899837
PQID 1532136047
PQPubID 2032355
PageCount 12
ParticipantIDs doaj_primary_oai_doaj_org_article_8af6a8b6412141dea9b44887b4749a6c
pubmedcentral_primary_oai_pubmedcentral_nih_gov_6269822
proquest_miscellaneous_1416695662
proquest_journals_1532136047
crossref_primary_10_3390_molecules18089049
pubmed_primary_23899837
PublicationCentury 2000
PublicationDate 20130729
PublicationDateYYYYMMDD 2013-07-29
PublicationDate_xml – month: 7
  year: 2013
  text: 20130729
  day: 29
PublicationDecade 2010
PublicationPlace Switzerland
PublicationPlace_xml – name: Switzerland
– name: Basel
PublicationTitle Molecules (Basel, Switzerland)
PublicationTitleAlternate Molecules
PublicationYear 2013
Publisher MDPI AG
MDPI
Publisher_xml – name: MDPI AG
– name: MDPI
References ref_50
Santin (ref_7) 2011; 63
Hussain (ref_5) 2011; 4
Citoglu (ref_27) 2002; 30
Yunes (ref_10) 2005; 60
Krejci (ref_51) 1959; 7
Uzma (ref_30) 2012; 14
Abbondanza (ref_1) 1964; 67
Sagitdinova (ref_29) 1996; 1
Paseshnichenko (ref_35) 1998; 63
(ref_25) 2010; 16
Piccoli (ref_8) 2008; 56
Rey (ref_19) 1992; 605
Lichtenthaler (ref_32) 1997; 101
Rustaiyan (ref_40) 1992; 31
Schlemper (ref_15) 1998; 5
Rodrigues (ref_14) 1998; 47
Knoess (ref_13) 1998; 64
Karioti (ref_23) 2007; 68
Naidoo (ref_47) 2011; 39
Bergeron (ref_38) 1995; 3
Zaabat (ref_6) 2011; 49
He (ref_45) 2012; 83
Mohamed (ref_18) 1993; 9
Rohmer (ref_33) 1999; 16
Tasdemir (ref_42) 1995; 58
Wu (ref_46) 2013; 91
Mnonopi (ref_3) 2011; 138
Argyropoulou (ref_22) 2011; 8
Knoess (ref_17) 1994; 32
Hussein (ref_37) 2003; 41
Govindasamy (ref_44) 2002; 37
Busby (ref_49) 1983; 83B
Takeda (ref_28) 2000; 48
Marrelli (ref_2) 2013; 8
ref_31
Morel (ref_11) 2003; 69
Ruzicka (ref_48) 1953; 9
Oliveira (ref_12) 2000; 7
Savona (ref_20) 1979; 18
Hellen (ref_9) 2006; 108
Taboada (ref_16) 1995; 23
Knoss (ref_34) 1997; 326
Hon (ref_39) 1993; 33
Cunningham (ref_36) 2000; 118
Tasdemir (ref_43) 1997; 60
Mnonopi (ref_24) 2012; 19
Ojewole (ref_52) 2003; 16
Khan (ref_53) 2012; 34
Henderson (ref_41) 1969; 15
Karioti (ref_26) 2005; 66
Laonigro (ref_4) 1979; 109
Argyropoulou (ref_21) 2009; 70
References_xml – volume: 8
  start-page: 567
  year: 2013
  ident: ref_2
  article-title: Cytotoxic properties of Marrubium globosum ssp. libanoticum and its bioactive components
  publication-title: Nat. Prod. Comm.
  contributor:
    fullname: Marrelli
– volume: 3
  start-page: 3
  year: 1995
  ident: ref_38
  article-title: Influence of supplemental lighting and irrigation on mineral composition growth and premarrubin content of horehound, Marrubium vulgare L
  publication-title: J. Herbs, Spices Med. Plants
  doi: 10.1300/J044v03n01_02
  contributor:
    fullname: Bergeron
– volume: 138
  start-page: 67
  year: 2011
  ident: ref_3
  article-title: The cardioprotective effects of marrubiin, a diterpenoid found in Leonotis leonurus extracts
  publication-title: J. Ethnopharmacol.
  doi: 10.1016/j.jep.2011.08.041
  contributor:
    fullname: Mnonopi
– volume: 68
  start-page: 1587
  year: 2007
  ident: ref_23
  article-title: Cytotoxicity and immunomodulating characteristics of labdane diterpenes from Marrubium cylleneum and Marrubium velutinum
  publication-title: Phytochemistry
  doi: 10.1016/j.phytochem.2007.03.027
  contributor:
    fullname: Karioti
– volume: 63
  start-page: 1230
  year: 2011
  ident: ref_7
  article-title: Gastroprotective activity of methanol extract and marrubiin obtained from leaves of Marrubium vulgare L. (Lamiaceae)
  publication-title: J. Pharm. Pharmacol.
  doi: 10.1111/j.2042-7158.2011.01321.x
  contributor:
    fullname: Santin
– volume: 605
  start-page: 124
  year: 1992
  ident: ref_19
  article-title: Extraction and high-performance liquid chromatographic methods for the γ-lactones parthenolide (Chrysanthemum parthenium Bernh.), marrubiin (Marrubium vulgare L.) and artemisinin (Artemisia annua L.)
  publication-title: J. Chromatogr. A
  doi: 10.1016/0021-9673(92)85036-S
  contributor:
    fullname: Rey
– volume: 66
  start-page: 1060
  year: 2005
  ident: ref_26
  article-title: Labdane diterpenes from Marrubium velutinum and Marrubium cylleneum
  publication-title: Phytochemistry.
  doi: 10.1016/j.phytochem.2005.02.029
  contributor:
    fullname: Karioti
– volume: 91
  start-page: 229
  year: 2013
  ident: ref_46
  article-title: Diterpenoids from Leonotis leonurus
  publication-title: Phytochemistry
  doi: 10.1016/j.phytochem.2012.02.021
  contributor:
    fullname: Wu
– volume: 32
  start-page: 785
  year: 1994
  ident: ref_17
  article-title: Furaniclabdane diterpenes in differentiated and undifferentiated cultures of Marrubium vulgare and Leonurus cardiac
  publication-title: Plant Physiol. Biochem.
  contributor:
    fullname: Knoess
– volume: 101
  start-page: 643
  year: 1997
  ident: ref_32
  article-title: Two independent biochemical pathways for isopentenyl diphosphate and isoprenoid biosynthesis in higher plants
  publication-title: Physiol. Plant.
  doi: 10.1111/j.1399-3054.1997.tb01049.x
  contributor:
    fullname: Lichtenthaler
– volume: 34
  start-page: 132
  year: 2012
  ident: ref_53
  article-title: Vasodilator effect of phlomis bracteosa constituents is mediated through dual endothelium-dependent and endothelium-independent pathways
  publication-title: Clin. Exp. Hypertension
  doi: 10.3109/10641963.2011.601383
  contributor:
    fullname: Khan
– volume: 109
  start-page: 145
  year: 1979
  ident: ref_4
  article-title: The configuration of the diterpene spiro ethers from Marrubium vulgare and from Leonotis leonurus
  publication-title: Gazz. Chim. Ital.
  contributor:
    fullname: Laonigro
– volume: 56
  start-page: 71
  year: 2008
  ident: ref_8
  article-title: Accumulation of the labdane diterpene marrubiin in glandular trichome cells along the ontogeny of Marrubium vulgare plants
  publication-title: Plant Growth Regul.
  doi: 10.1007/s10725-008-9286-3
  contributor:
    fullname: Piccoli
– ident: ref_31
– volume: 16
  start-page: 565
  year: 1999
  ident: ref_33
  article-title: The discovery of a mevalonate-independent pathway for isoprenoid biosynthesis in bacteria, algae and higher plants
  publication-title: Nat. Prod. Rep.
  doi: 10.1039/a709175c
  contributor:
    fullname: Rohmer
– volume: 60
  start-page: 321
  year: 2005
  ident: ref_10
  article-title: Analgesic potential of marrubiin derivatives, a bioactive diterpene present in Marrubium vulgare (Lamiaceae)
  publication-title: Farmaco
  doi: 10.1016/j.farmac.2005.01.003
  contributor:
    fullname: Yunes
– volume: 30
  start-page: 885
  year: 2002
  ident: ref_27
  article-title: Occurrence of marrubiin and ladanein in Marrubium trachyticumboiss
  publication-title: Biochem. Syst. Ecol.
  doi: 10.1016/S0305-1978(01)00148-X
  contributor:
    fullname: Citoglu
– volume: 64
  start-page: 357
  year: 1998
  ident: ref_13
  article-title: Accumulation of furan labdane diterpenes in Marrubium vulgare and Leonurus cardiaca
  publication-title: Planta Med.
  doi: 10.1055/s-2006-957451
  contributor:
    fullname: Knoess
– volume: 47
  start-page: 449
  year: 1998
  ident: ref_14
  article-title: An improved extraction of marrubiin from Marrubium vulgare
  publication-title: Chromatographia
  doi: 10.1007/BF02466478
  contributor:
    fullname: Rodrigues
– volume: 67
  start-page: 95
  year: 1964
  ident: ref_1
  article-title: Crespi. Biosynthesis of labeled molecules: mechanism of biosynthetic reactions of precursors of furanicterpenes and phytosterol
  publication-title: Prepn. Bio-Med. Appl. Labeled Mol. Proc. Symp. Venice
  contributor:
    fullname: Abbondanza
– volume: 1
  start-page: 54
  year: 1996
  ident: ref_29
  article-title: Labdanoids of Marrubium anisodon
  publication-title: Khim.Prir.Soedin.
  contributor:
    fullname: Sagitdinova
– volume: 83
  start-page: 168
  year: 2012
  ident: ref_45
  article-title: Leonurenones A–C: Labdane diterpenes from Leonotis leonurus
  publication-title: Phytochemistry
  doi: 10.1016/j.phytochem.2012.07.014
  contributor:
    fullname: He
– volume: 7
  start-page: 1
  year: 1959
  ident: ref_51
  article-title: Die Gallentreiben de wirkung von marrubiin und marrabinsäure
  publication-title: Planta Med.
  doi: 10.1055/s-0028-1101585
  contributor:
    fullname: Krejci
– volume: 41
  start-page: 147
  year: 2003
  ident: ref_37
  article-title: Complete 1H and 13C NMR assignments of three labdane diterpenoids isolated from Leonotis ocymifolia and six other related compounds
  publication-title: Magn. Reson. Chem.
  doi: 10.1002/mrc.1136
  contributor:
    fullname: Hussein
– volume: 5
  start-page: 103
  year: 1998
  ident: ref_15
  article-title: Analgesic profile of hydroalcoholic extract obtained from Marrubium vulgare
  publication-title: Phytomedicine
  doi: 10.1016/S0944-7113(98)80005-6
  contributor:
    fullname: Schlemper
– volume: 63
  start-page: 139
  year: 1998
  ident: ref_35
  article-title: A new alternative non-mevalonate pathway for isoprenoid biosynthesis ineubacteria and plants
  publication-title: Biochemistry (Mosc.)
  contributor:
    fullname: Paseshnichenko
– volume: 326
  start-page: 449
  year: 1997
  ident: ref_34
  article-title: Biosynthesis of the labdane diterpene marrubiin in Marrubium vulgare via a non-mevalonate pathway
  publication-title: Biochem. J.
  doi: 10.1042/bj3260449
  contributor:
    fullname: Knoss
– volume: 70
  start-page: 635
  year: 2009
  ident: ref_21
  article-title: Labdane Diterpenes from Marrubium thessalum
  publication-title: Phytochemistry
  doi: 10.1016/j.phytochem.2009.03.011
  contributor:
    fullname: Argyropoulou
– volume: 49
  start-page: 3328
  year: 2011
  ident: ref_6
  article-title: Antioxidant and antigenotoxic properties of compounds isolated from Marrubium deserti de Noe
  publication-title: J. Food Chem. Toxicol.
  doi: 10.1016/j.fct.2011.08.026
  contributor:
    fullname: Zaabat
– volume: 9
  start-page: 92
  year: 1993
  ident: ref_18
  article-title: Constituents of the aerial parts of Marrubium vulgare L
  publication-title: J. Pharm. Sci.
  contributor:
    fullname: Mohamed
– volume: 108
  start-page: 379
  year: 2006
  ident: ref_9
  article-title: Antioedematogenic effect of marrubiin obtained from Marrubium vulgare
  publication-title: J. Ethnopharmacol.
  doi: 10.1016/j.jep.2006.05.023
  contributor:
    fullname: Hellen
– volume: 18
  start-page: 859
  year: 1979
  ident: ref_20
  article-title: Diterpenes from Marrubium sericeum, Marrubium supinum and Marrubium alysson
  publication-title: Phytomedicine
  contributor:
    fullname: Savona
– volume: 37
  start-page: 896
  year: 2002
  ident: ref_44
  article-title: Structural studies on three plant diterpenoids from Leonotis nepetaefolia
  publication-title: Cryst. Res. Tech.
  doi: 10.1002/1521-4079(200208)37:8<896::AID-CRAT896>3.0.CO;2-F
  contributor:
    fullname: Govindasamy
– volume: 14
  start-page: 601
  year: 2012
  ident: ref_30
  article-title: Spiraeamide, New sphingolipid from Spiraea brahuica
  publication-title: J. Asian. Nat. Prod. Res.
  doi: 10.1080/10286020.2012.672975
  contributor:
    fullname: Uzma
– volume: 7
  start-page: 111
  year: 2000
  ident: ref_12
  article-title: Analysis of the antinociceptive properties of marrubiin isolated from Marrubium vulgare
  publication-title: Phytomedicine
  doi: 10.1016/S0944-7113(00)80082-3
  contributor:
    fullname: Oliveira
– volume: 118
  start-page: 5841
  year: 2000
  ident: ref_36
  article-title: Evidence of a role for LytB in the non-mevalonate pathway of isoprenoid biosynthesis
  publication-title: J. Bacteriol.
  doi: 10.1128/JB.182.20.5841-5848.2000
  contributor:
    fullname: Cunningham
– volume: 33
  start-page: 639
  year: 1993
  ident: ref_39
  article-title: Preleoheterin and leoheterin, two labdane diterpenes from Leonurus heterophyllus
  publication-title: Phytochemistry
  doi: 10.1016/0031-9422(93)85464-3
  contributor:
    fullname: Hon
– volume: 15
  start-page: 2014
  year: 1969
  ident: ref_41
  article-title: Premarrubiin. A diterpenoid from Marrubium vulgare
  publication-title: J. Chem. Soc. C
  doi: 10.1039/j39690002014
  contributor:
    fullname: Henderson
– volume: 16
  start-page: 213
  year: 2003
  ident: ref_52
  article-title: Hypotensive effect of Leonotis leonurus
  publication-title: Amer. J. Hypertens.
  doi: 10.1016/S0895-7061(03)00168-7
  contributor:
    fullname: Ojewole
– volume: 39
  start-page: 216
  year: 2011
  ident: ref_47
  article-title: New labdane-type diterpenoids from Leonotis leonurus support circumscription of Lamiaceae
  publication-title: Biochem. Syst. Ecol.
  doi: 10.1016/j.bse.2010.12.021
  contributor:
    fullname: Naidoo
– volume: 4
  start-page: 178
  year: 2011
  ident: ref_5
  article-title: Antispasmodic and Ca++ antagonist potential of marrubiin, a labdane type diterpene from Phlomis bracteosa
  publication-title: J. Pharmacy Res.
  contributor:
    fullname: Hussain
– ident: ref_50
– volume: 19
  start-page: 488
  year: 2012
  ident: ref_24
  article-title: Marrubiin, a constituent of Leonotus leonurus, alleviates diabetic symptoms
  publication-title: Phytomedicine
  doi: 10.1016/j.phymed.2011.12.008
  contributor:
    fullname: Mnonopi
– volume: 8
  start-page: 1880
  year: 2011
  ident: ref_22
  article-title: Minor labdane diterpenes from Marrubium thessalum
  publication-title: Chem. Biodivers.
  doi: 10.1002/cbdv.201000215
  contributor:
    fullname: Argyropoulou
– volume: 60
  start-page: 874
  year: 1997
  ident: ref_43
  article-title: Further Labdane diterpenoids isolated from Leonurus persicus
  publication-title: J. Nat. Prod.
  doi: 10.1021/np9700782
  contributor:
    fullname: Tasdemir
– volume: 31
  start-page: 344
  year: 1992
  ident: ref_40
  article-title: Furanolabdanes and related compounds from Ballota aucheri
  publication-title: Phytochemistry
  doi: 10.1016/0031-9422(91)83073-T
  contributor:
    fullname: Rustaiyan
– volume: 9
  start-page: 357
  year: 1953
  ident: ref_48
  article-title: The isoprene rule and the biogenesis of terpenic compounds
  publication-title: Experientia
  doi: 10.1007/BF02167631
  contributor:
    fullname: Ruzicka
– volume: 16
  start-page: 3503
  year: 2010
  ident: ref_25
  article-title: A review of the chemical and pharmacological aspects of the genus Marrubium
  publication-title: Curr. Pharm. Design
  doi: 10.2174/138161210793563392
– volume: 69
  start-page: 75
  year: 2003
  ident: ref_11
  article-title: The vasorelaxant activity of marrubenol and marrubiin from Marrubium vulgare
  publication-title: Planta Med.
  doi: 10.1055/s-2003-37042
  contributor:
    fullname: Morel
– volume: 23
  start-page: 120
  year: 1995
  ident: ref_16
  article-title: Antifeedant activity of marrubiin and reduced marrubiin
  publication-title: Rev. Lat. Am. Quim.
  contributor:
    fullname: Taboada
– volume: 83B
  start-page: 21
  year: 1983
  ident: ref_49
  article-title: The stereochemistry and conformation of marrubiin: An X-Ray Study
  publication-title: Proc. R. Ir. Acad.
  contributor:
    fullname: Busby
– volume: 58
  start-page: 1543
  year: 1995
  ident: ref_42
  article-title: Detailed 1H- and 13C-NMR investigations of some diterpenes isolated from Leonurus persicus
  publication-title: J. Nat. Prod.
  doi: 10.1021/np50124a010
  contributor:
    fullname: Tasdemir
– volume: 48
  start-page: 1234
  year: 2000
  ident: ref_28
  article-title: Labdane diterpenoids from Marrubium globosum ssp
  publication-title: Globosum. Chem. Pharmaceut. Bull.
  doi: 10.1248/cpb.48.1234
  contributor:
    fullname: Takeda
SSID ssj0021415
Score 2.3484128
SecondaryResourceType review_article
Snippet The ethno-medicinal approach to drug discovery represents one of the most important sources of new and safe therapeutic agents to the challenges confronting...
SourceID doaj
pubmedcentral
proquest
crossref
pubmed
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
StartPage 9049
SubjectTerms anti-inflammatory
Anti-Inflammatory Agents - therapeutic use
biological activity
Diterpenes - chemistry
Diterpenes - metabolism
Diterpenes - therapeutic use
Drug Discovery
Furans - chemistry
Furans - metabolism
Humans
Lamiaceae
Lamiaceae - chemistry
Lead - chemistry
lead compound
marrubiin
Review
SummonAdditionalLinks – databaseName: Directory of Open Access Journals
  dbid: DOA
  link: http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV09T8MwED1Bl7IgvglfKhITUlTHcfwxQmnVBRZAYotsxxYdSFHb_H_OSVq1gMTCGns4v4vt92T7HcCN9MQ4aniMVJTGyG-z2FDJY1akBulpkSobhOL4WTy9yYdhsMlZlfoKd8Iae-AGuL7UnmtpOEtowpLCaWVQUUhhmGBKc1uvvkQuxVQrtbBrVr8rCu-DkQQ355kpCvz-R1N21s0TSaQiwURzbUeqjft_Y5vfL02u7UKjPdht6WPvrgl7H7ZceQDdwbJq2yF0H_VsVpnJpDyC19HwZTCO23IHsUVav4itZSwTyipHlPQ-MVxyznzmtLcGp13imPYu445bT4VnXmYZoqFTV7DEpDw9hk45Ld0p9HD8RSa0R4wIMi6rrCCqcB7hIDr1PoLb5ZDzz8bVIkc1EPDJf-ATwX0AZdUxGFLXHzBNeZum_K80RXCxhDRvZ8k8x9WWJiknTERwvWpGwMKhhS7dtMI-GD9HEcdpBCdNBlaR0GAOiAo7ArGRm41QN1vKyXvtoY06LjgXnv3H2M5hh9ZFMkRM1QV0FrPKXcL2vKiu6r_yC35h5HA
  priority: 102
  providerName: Directory of Open Access Journals
Title Marrubiin
URI https://www.ncbi.nlm.nih.gov/pubmed/23899837
https://www.proquest.com/docview/1532136047
https://search.proquest.com/docview/1416695662
https://pubmed.ncbi.nlm.nih.gov/PMC6269822
https://doaj.org/article/8af6a8b6412141dea9b44887b4749a6c
Volume 18
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3JTsMwEB3RXuCC2AlLBRInpDSb4-UIpYgLCAmQuEW2Y0MlmlYp-X_GWSoKnLjGjjSeGcfvyZM3ABfchsrEivoIRWMf8W3qq5hTn-SJQniaJ0I7onj3xB5e-c3YyeSk3b8wddG-VpNh8TEdFpP3urZyPtVBVycWPN6PEIQ72bmgBz3Ehh1Fb1lWhEdSc32ZIJ8Ppk2XWbOIeMgF4mEn_-tE5bhrff7tLKol-__CmT_LJb-dP7dbsNkCx7OrxsBtWDPFDqyPun5tu7B-L8uyUpNJsQcvt-Pn0Z3fNjrwNQL6T19rQlImtDCh4NZGinJKiU2NtFrhhosMkdak1FBtY2aJ5WkqhZKJyUmkEprsQ7-YFeYQznD5ecqkJYyEiLW00CwUubEEd4NMrPXgsltyNm_0LDLkAc5V2S9XeXDtnLKc6KSo6wez8i1rA5JxaankipLIuT43aBhSPs4UmiAk1R6cdC7N2v2xyPA7G0cJDQnz4Hw5jA5z1xWyMLMK56D9FOkbjT04aCKwtKSLoAdsJTYrpq6OYDLV6tlt8hz9-81j2IjrnhjMj8UJ9D_LypxCb5FXg5rRD-p8_AIhduRZ
link.rule.ids 230,314,315,729,782,786,794,866,887,2108,27933,27935,27936,53803,53805
linkProvider National Library of Medicine
linkToHtml http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LT9tAEB4VOKQXHn2AKW2p1BOSE9u73sexpKBUTSIkgsTN2l3vQiTioAT_f2b9iBLaU65eWxrN5_F-n3b8DcBP4SJtE81CpKJJiPw2DXUiWEhzopGe5kQaLxQHt3x8L35feZuctP0XpmraN3raLZ5m3WL6WPVWPs9Mr-0T692M-kjCve1cbwf2sF4j0or0RmfFuCnVB5gEFX1vVs-ZtctYREIiI_YGwN5WTvjh52u7UWXa_z-m-bZhcm0Huj7YMvZD2G8o5_mvevkI3tniA3T67aS3j9AZqcWi1NNp8Qnurq8m_UHYjEgIDUqBl9AYSlMujbSRFM7FmgnGqEutckZjqcaWKmdTZplxCXfUiTRVUiticxprwshn2C3mhT2Bc0xbnnLlKKcRsjQjDY9kbh3FOlLEuQAu2lRlz7UTRoYKwqc4-yfFAVz6ZK5u9CbW1YX54iFr0pEJ5ZgSmtHYQ5ZbDAzFouAaQ5CKmQDOWiiyprKWGX6hk5iwiPIAfqyWMWH-oEMVdl7iPRg_Q-HHkgCOa-RWkbTIB8A3MN0IdXMFoax8txvoTrd-8jt0BpPRMBv-Gf_9Au-TarIGDxN5Brsvi9J-hZ1lXn6r3uZXHZr48g
linkToPdf http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1ZS8QwEB48QH3xPuot-CTUXmmOR11dFA8EFXwrSZrogttddt3_76TH4qpP-tqkMMzXab6PDN8AHHMbKhMr6iMVjX3kt6mvYk59kicK6WmeCO2E4tUju3_hF5fOJmc86qts2teqc1q8d0-LzlvZW9nv6qDpEwse7lpIwp3tXNDPbTANs1izYdoI9VprRXgwVZeYCar6oFvNmjXDiIdcICt2JsDOWo67AehfTqTSuP83tvm9afLLKdRe-kf8y7BYU8_Ds2rLCkyZYhXmW83EtzWYv5ODwUh1OsU6PLcvn1pXfj0qwdcoCT58rQlJmdDChIJbGynKKSU2NdJqhSUbGSKtSamh2sbMEsvTVAolE5OTSCU02YCZoleYLTjE1OUpk5YwEiJb00KzUOTGEqwnmVjrwUmTrqxfOWJkqCRcmrMfafbg3CV0vNGZWZcPeoPXrE5JxqWlkitKIgdbbjAwFI2cKQxBSKo92G3gyOoKG2b4p46jhIaEeXA0XsaEuQsPWZjeCPdg_BQFII092KzQG0fSoO8Bm8B1ItTJFYSz9N-u4dv-85sHMPdw0c5ur-9vdmAhLgdsMD8WuzDzMRiZPZge5qP98oP-BANR-3I
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Marrubiin&rft.jtitle=Molecules+%28Basel%2C+Switzerland%29&rft.au=Popoola%2C+Olugbenga+K&rft.au=Elbagory%2C+Abdulrahman+M&rft.au=Ameer%2C+Farouk&rft.au=Hussein%2C+Ahmed+A&rft.date=2013-07-29&rft.pub=MDPI+AG&rft.eissn=1420-3049&rft.volume=18&rft.issue=8&rft.spage=9049&rft_id=info:doi/10.3390%2Fmolecules18089049&rft.externalDBID=HAS_PDF_LINK&rft.externalDocID=3324396801
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1420-3049&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1420-3049&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1420-3049&client=summon