Collected mass spectrometry data on monoterpene indole alkaloids from natural product chemistry research

被引：43

作者：

Ramos, Alexander E. Fox ^{[1
]}

Le Pogam, Pierre ^{[1
]}

Alcover, Charlotte Fox ^{[1
]}

N'Nang, Elvis Otogo ^{[1
]}

Cauchie, Gaela ^{[1
]}

Hazni, Hazrina ^{[1
,2
]}

Awang, Khalijah ^{[2
]}

Breard, Dimitri ^{[3
]}

Echavarren, Antonio M. ^{[4
,5
]}

Frederich, Michel ^{[6
]}

Gaslonde, Thomas ^{[7
]}

Girardot, Marion ^{[8
]}

Grougnet, Raphael ^{[7
]}

Kirillova, Mariia S. ^{[4
]}

Kritsanida, Marina ^{[7
]}

Lemus, Christelle ^{[7
]}

Le Ray, Anne-Marie ^{[3
]}

Lewin, Guy ^{[1
]}

Litaudon, Marc ^{[9
]}

Mambu, Lengo ^{[10
]}

Michel, Sylvie ^{[7
]}

Miloserdov, Fedor M. ^{[4
]}

Muratore, Michael E. ^{[4
]}

Richomme-Peniguel, Pascal ^{[3
]}

Roussi, Fanny ^{[9
]}

Evanno, Laurent ^{[1
]}

Poupon, Erwan ^{[1
]}

Champy, Pierre ^{[1
]}

Beniddir, Mehdi A. ^{[1
]}

机构：

[1] Univ Paris Saclay, Univ Paris Sud, Equipe Pharmacognosie Chim Subst Nat BioCIS, CNRS, 5 Rue JB Clement, F-92290 Chatenay Malabry, France

[2] Univ Malaya, Ctr Nat Prod & Drug Discovery, Kuala Lumpur 50603, Malaysia

[3] UBL Angers Univ, SFR QUASAV, SONAS, EA921, Campus Vegetal,42 Rue Georges Morel, F-49070 Beaucouze, France

[4] Barcelona Inst Sci & Technol, Inst Chem Res Catalonia ICIQ, Ave Paisos Catalans 16, Tarragona 43007, Spain

[5] Univ Rovira & Virgili, Dept Quim Organ & Analit, C Marcelli Domingo S-N, Tarragona 43007, Spain

[6] Univ Liege, CIRM, Lab Pharmacognosy, Quartier Hop, 15 Ave Hippocrate, B-4000 Liege, Belgium

[7] Univ Paris 05, Sorbonne Paris Cite, CNRS, UMR 8638,Lab Pharmacognosie,COMETE,Fac Pharm Pari, 4 Ave Observ, F-75006 Paris, France

[8] Univ Poitiers, CNRS, UMR 7267, Lab Ecol & Biol Interact,Equipe Microbiol Eau, 5 Rue Albert Turpain, F-86073 Poitiers 09, France

[9] Univ Paris Saclay, CNRS, ICSN, UPR 2301, 1 Ave Terrasse, F-91198 Gif Sur Yvette, France

[10] Univ Limoges, Fac Pharm, Lab PEIRENE, Dept Pharmacognosie,EA 7500, 2 Rue Dr Marcland, F-87025 Limoges, France

来源：

SCIENTIFIC DATA | 2019年 / 6卷 / 1期

关键词：

MOLECULAR NETWORKING; CATHARANTHUS-ROSEUS; STEP;

D O I：

10.1038/s41597-019-0028-3

中图分类号：

O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

This Data Descriptor announces the submission to public repositories of the monoterpene indole alkaloid database (MIADB), a cumulative collection of 172 tandem mass spectrometry (MS/MS) spectra from multiple research projects conducted in eight natural product chemistry laboratories since the 1960s. All data have been annotated and organized to promote reuse by the community. Being a unique collection of these complex natural products, these data can be used to guide the dereplication and targeting of new related monoterpene indole alkaloids within complex mixtures when applying computer-based approaches, such as molecular networking. Each spectrum has its own accession number from CCMSLIB00004679916 to CCMSLIB00004680087 on the GNPS. The MIADB is available for download from MetaboLights under the identifier: MTBLS142 (https://www.ebi.ac.uk/metabolights/MTBLS142).

引用

页数：6

共 50 条

[11] Monoterpene Indole Alkaloids from the Twigs of Kopsia arborea
Cheenpracha, Sarot
Raksat, Achara
Ritthiwigrom, Thunwadee
Laphookhieo, Surat
NATURAL PRODUCT COMMUNICATIONS, 2014, 9 (10) : 1441 - 1443
[12] Indole and monoterpene alkaloids from the leaves of Kopsia dasyrachis
Kam, TS
Choo, YM
Chen, W
Yao, JX
PHYTOCHEMISTRY, 1999, 52 (05) : 959 - 963
[13] Bioactive monoterpene indole alkaloids from Nauclea officinalis
Liu, Yan-Ping
Liu, Qing-Long
Zhang, Xiang-Lin
Niu, Hai-Yuan
Guan, Chun-Yan
Sun, Fu-Kang
Xu, Wei
Fu, Yan-Hui
BIOORGANIC CHEMISTRY, 2019, 83 : 1 - 5
[14] A multimodal metabolomics approach using imaging mass spectrometry and liquid chromatography-tandem mass spectrometry for spatially characterizing monoterpene indole alkaloids secreted from roots
Nakabayashi, Ryo
Takeda-Kamiya, Noriko
Yamada, Yutaka
Mori, Tetsuya
Uzaki, Mai
Nirasawa, Takashi
Toyooka, Kiminori
Saito, Kazuki
PLANT BIOTECHNOLOGY, 2021, 38 (03) : 305 - 310
[15] Unusual monoterpene indole alkaloids from Psychotria stachyoides Benth
Torres Pimenta, Antonia Avila
Braz Filho, Raimundo
Delprete, Piero Giuseppe
de Souza, Elnatan Bezerra
Silveira, Edilberto Rocha
Sousa Lima, Mary Anne
BIOCHEMICAL SYSTEMATICS AND ECOLOGY, 2010, 38 (04) : 846 - 849
[16] Boosting Sensitivity in Liquid Chromatography-Fourier Transform Ion Cyclotron Resonance-Tandem Mass Spectrometry for Product Ion Analysis of Monoterpene Indole Alkaloids
Nakabayashi, Ryo
Tsugawa, Hiroshi
Kitajima, Mariko
Takayama, Hiromitsu
Saito, Kazuki
FRONTIERS IN PLANT SCIENCE, 2015, 6
[17] Targeted Isolation of Monoterpene Indole Alkaloids from Palicourea sessilis
Klein-Junior, Luiz C.
Cretton, Sylvian
Allard, Pierre-Marie
Genta-Jouve, Gregory
Passos, Carolina S.
Salton, Juliana
Bertelli, Pablo
Pupier, Marion
Jeannerat, Damien
Vander Heyden, Yvan
Gasper, Andre L.
Wolfender, Jean-Luc
Christen, Philippe
Henriques, Amelia T.
JOURNAL OF NATURAL PRODUCTS, 2017, 80 (11): : 3032 - 3037
[18] Monoterpene indole alkaloids with anticancer activity from Tabernaemontana species
Goncalves, Bruno M. F.
Duarte, Noelia
Ramalhete, Catia
Barbosa, Filipa
Madureira, Ana Margarida
Ferreira, Maria-Jose U.
PHYTOCHEMISTRY REVIEWS, 2024,
[19] New zwitterionic monoterpene indole alkaloids from Uncaria rhynchophylla
Guo, Qiang
Yang, Hongshuai
Liu, Xinyu
Si, Xiali
Liang, Hong
Tu, Pengfei
Zhang, Qingying
FITOTERAPIA, 2018, 127 : 47 - 55
[20] Isolation and structural elucidation of indole alkaloids from Geissospermum vellosii by mass spectrometry
Mbeunkui, Flaubert
Grace, Mary H.
Lila, Mary Ann
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2012, 885 : 83 - 89

← 1 2 3 4 5 →