Phytochemical Constituents of Artemisia dubia var. longeracemosa Forma tonkinensis

Giang, Phan Minh; Nhan, Tran Thi Thanh; Chinh, Truong Thi To; Sơn, Phan Tống; Matsunami, Katsuyoshi

doi:10.1007/s10600-015-1290-z

Cited by 4 publications

(4 citation statements)

References 8 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…dubia and A . herba ‐ alba by Bourgou et al () and Giang, Nhan, Chinh, Son, and Matsunami (), respectively. Burnamicine is a cryptopine like the analog of corynantheol as a new class of indole alkaloids called yohimbine, where the eburnamine groups and the quaternary diastereoisomeric N ‐methyl derivatives of hunterburnine are present.…”

Section: The Chemistry and Pharmacology Of Artemisia Alkaloids/alliedmentioning

confidence: 95%

“…References are numbered as follows: 1 (Su et al, ), 2 (He at el. 2012), 3 (Su et al, ), 4 (Fontaine et al, ), 5 (Sham'yanov et al, ), 6 (Wang et al, ), 7 (Ma, Sun, Zhou, Hong, & Pei, ), 8 (Shukla et al, ), 9 (Lu et al, ), 10 (Liu et al, & 2017), 11 (Zou et al, ), 12 (Choi et al, ), 13 (Mamun et al, ), 14 (Giang et al, ), 15 (Bourgou et al, ), 16 (Nguyen et al, ), 17 (Jakupovic et al, ), 18 (Lin et al, 2014), 19 (Tu et al, ), 20 (Nakamura & Hattori, ), 21 (Saadali et al, ), 22 (Yamada et al, ), 23 (Wheeler et al, ), 24 (Rashid et al, ), 25 (Umano et al, ), 26 (Bak et al, ), 27 (Kavvadias et al, ), 28 (Megdiche‐Ksouri et al, ), 29 (Kim et al, ), 30 (Choi et al, ), 31 (Geng et al, ), and 32 (Mizushina et al, ).…”

Section: Introductionmentioning

confidence: 99%

See 1 more Smart Citation

The chemistry and pharmacology of alkaloids and allied nitrogen compounds fromArtemisiaspecies: A review

Rashid

Alamzeb²,

Ali³

et al. 2019

Phytotherapy Research

View full text Add to dashboard Cite

Several reviews have been published on Artemisia's derived natural products, but it is the first attempt to review the chemistry and pharmacology of more than 80 alkaloids and allied nitrogen compounds obtained from various Artemisia species (covering the literature up to June 2018). The pharmacological potential and unique skeleton types of certain Artemisia's alkaloids provoke the importance of analyzing Artemisia species for bioactive alkaloids and allied nitrogen compounds. Among the various types of bioactive Artemisia's alkaloids, the main classes were the derivatives of rupestine (pyridine–sesquiterpene), lycoctonine (diterpene), pyrrolizidine, purines, polyamine, peptides, indole, piperidine, pyrrolidine, alkamides, and flavoalkaloids. The rupestine derivatives are Artemisia's characteristic alkaloids, whereas the rest are common alkaloids found in the family Asteraceae and chemotaxonomically links the genus Artemisia with the tribes Anthemideae. The most important biological activities of Artemisia's alkaloids are including hepatoprotective, local anesthetic, β‐galactosidase, and antiparasitic activities; treatment of angina pectoris, opening blocked arteries, as a sleep‐inducing agents and inhibition of HIV viral protease, CYP450, melanin biosynthesis, human carbonic anhydrase, [3H]‐AEA metabolism, kinases, and DNA polymerase β1. Some of the important nitrogen metabolites of Artemisia include pellitorine, zeatin, tryptophan, rupestine, and aconitine analogs, which need to be optimized and commercialized further.

show abstract

Section: The Chemistry and Pharmacology Of Artemisia Alkaloids/alliedmentioning

confidence: 95%

Section: Introductionmentioning

confidence: 99%

The chemistry and pharmacology of alkaloids and allied nitrogen compounds fromArtemisiaspecies: A review

Rashid

Alamzeb²,

Ali³

et al. 2019

Phytotherapy Research

View full text Add to dashboard Cite

show abstract

“…Eudesmane sesquiterpenes are chemotaxonomic compounds of A. japonica; three new eudesmanes, named artemisidiols A-C (46-48) with an unusual 1α,6α,8α-oxygenated pattern, were obtained from the leaves of A. japonica in Vietnam. 39) Oxygenated guaianolides and dicaffeoylquinic acids were obtained as main constituents from A. dubia WALL. ex BESS.…”

Section: The Genusmentioning

confidence: 99%

“…24) Two new 2-C-β-D-glucopyranosyl benzoic acid derivatives, mallonanosides A (37) and B (38), were isolated from the methanol extract of the leaves of M. nanus. 25) A new lignan dimer, bilariciresinol (39), was isolated from the leaves of M. philippensis. 26) The methanol leaf extract of M. macrostachyus yielded two new cycloartanes, macrostachyosides A (40) and B (41).…”

Section: Introductionmentioning

confidence: 99%

New Compounds and Potential Candidates for Drug Discovery from Medicinal Plants of Vietnam

Giang

Otsuka

2018

Chem. Pharm. Bull.

Self Cite

View full text Add to dashboard Cite

The study of natural products introduces interesting new bioorganic structures and potential candidates for the drug discovery stage in the development of innovative drugs. Vietnam enjoys a broad biodiversity of native plant species, microorganisms, marine organisms, and a long tradition of using herbal remedies. Thus, the study of medicinal plants in determining the basis of their efficacy and safety is an important task for modern researchers in Vietnam. The present review covers literature on new compounds elucidated from the systematic study of medicinal plants within some popular genera in Vietnam, as well as their significant biological activities.

show abstract

Artemidubolides A−T, cytotoxic unreported guaiane-type sesquiterpenoid dimers against three hepatoma cell lines from Artemisia dubia

Gao

et al. 2022

Phytochemistry

View full text Add to dashboard Cite

Phytochemical Constituents of Artemisia dubia var. longeracemosa Forma tonkinensis

Cited by 4 publications

References 8 publications

The chemistry and pharmacology of alkaloids and allied nitrogen compounds fromArtemisiaspecies: A review

The chemistry and pharmacology of alkaloids and allied nitrogen compounds fromArtemisiaspecies: A review

New Compounds and Potential Candidates for Drug Discovery from Medicinal Plants of Vietnam

Artemidubolides A−T, cytotoxic unreported guaiane-type sesquiterpenoid dimers against three hepatoma cell lines from Artemisia dubia

Contact Info

Product

Resources

About