2015
DOI: 10.6023/cjoc201505044
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Secondary Metabolites of aBruguiera sexangula var.Rhynchopetala-Derived FungusPhomopsis longicollaHL-2232

Abstract: Under the guidance of bioassay, five alkaloids, one chromone and four steroids were isolated from the Phomopsis longicolla HL-2232, a fungus isolated from a mangrove Bruguiera sexangula var. Rhynchopetala. Their structures were identified as 6-aminopurine-9-carboxylic acid methyl ester (1), adenine riboside (2), uridine (3), N,N'-diphenyl urea (4), (2S,2'R,3R,4E,8E,3'E)-2-(2'-hydroxy-3'-octadecenoylamino)-9-methyl-4,8-octadecadiene-l,3-diol (5), 2-(2'S-hydroxypropyl)-5methyl-7-hydroxychromone (6), fortisterol … Show more

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Cited by 5 publications
(3 citation statements)
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“…The diversity of diterpenoids in plants playing important roles in plant development, stress resistance, and interactions with environmental microorganisms, depends on the various skeletons biosynthesized by terpene synthases and the substrate promiscuity of cytochrome P450 monooxygenases (P450s), along with other postmodification enzymes [38]. In the genus Bruguiera, researchers have isolated five different skeletal types of diterpenoid (Table 2 and Figure 3), namely ent-pimarane (79-82), isopi-marane (83)(84), ent-beyerane (85-86), ent-kaurane (62)(63)(64)(65)(66)(67)(68)(69)(70)(71)(72)(73)(74)(75)(76)(77)(78), and ent-gibberellane (59-61), with the key intermediate pimarane in their biosynthesis. Most sesterpenoids are sourced from marine organisms, with approximately 15% of these compounds having been isolated from plants [44].…”
Section: Diterpenoidsmentioning
confidence: 99%
See 1 more Smart Citation
“…The diversity of diterpenoids in plants playing important roles in plant development, stress resistance, and interactions with environmental microorganisms, depends on the various skeletons biosynthesized by terpene synthases and the substrate promiscuity of cytochrome P450 monooxygenases (P450s), along with other postmodification enzymes [38]. In the genus Bruguiera, researchers have isolated five different skeletal types of diterpenoid (Table 2 and Figure 3), namely ent-pimarane (79-82), isopi-marane (83)(84), ent-beyerane (85-86), ent-kaurane (62)(63)(64)(65)(66)(67)(68)(69)(70)(71)(72)(73)(74)(75)(76)(77)(78), and ent-gibberellane (59-61), with the key intermediate pimarane in their biosynthesis. Most sesterpenoids are sourced from marine organisms, with approximately 15% of these compounds having been isolated from plants [44].…”
Section: Diterpenoidsmentioning
confidence: 99%
“…189(2S,2′R,3R,4E,8E,3′E)-2-(2′-hydroxy-3′octadecenoylamino)-9-methyl-4,8-octadecadiene-l,3-diol P. longicolla HL-2232 (the leaf B. sexangula var. rhynchopetala, endophytic fungus)[67] …”
mentioning
confidence: 99%
“…rhynchopetala . The compounds 20 and 21 exhibited cytotoxicity against MCF-7 and A549 cell lines with IC 50 values of 14.9 and 8.6 μM, respectively [ 23 ].…”
Section: Bioactive Compounds In Mangrove Plantsmentioning
confidence: 99%