2019
DOI: 10.1021/acs.jnatprod.9b00648
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Glechomanamides A–C, Germacrane Sesquiterpenoids with an Unusual Δ8-7,12-Lactam Moiety from Salvia scapiformis and Their Antiangiogenic Activity

Abstract: Three new germacrane sesquiterpenoid-type alkaloids with an unusual Δ8-7,12-lactam moiety, glechomanamides A–C (1–3), and two pairs of 7,12-hemiketal sesquiterpenoid epimers (4a/b, 5a/b) were isolated from Salvia scapiformis. Their structures were elucidated by spectroscopic methods including HRESIMS, IR, UV, and 1D and 2D NMR and also confirmed by single-crystal X-ray diffraction analysis. The chemical transformation of compounds 1–5 in a solution environment was analyzed by 2D NMR spectroscopy. The aza aceta… Show more

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Cited by 8 publications
(7 citation statements)
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“…These images were measured with the Angiogenesis Analyzer of the ImageJ program. The total segment lengths of the structures were used to calculate the tube-formation activity and to evaluate the degree of tube formation [ 68 ].…”
Section: Methodsmentioning
confidence: 99%
“…These images were measured with the Angiogenesis Analyzer of the ImageJ program. The total segment lengths of the structures were used to calculate the tube-formation activity and to evaluate the degree of tube formation [ 68 ].…”
Section: Methodsmentioning
confidence: 99%
“…One γ-elemene-type sesquiterpenes, 8β(H)-elema-1,3,7(11)-trien-8,12-lactam (330) (Figure 8) was obtained from the rhizomes of Curcuma phaeocaulis [63]. Three new germacrane sesquiterpenoid-typealkaloids with an unusual ∆ 8 -7,12-lactam moiety, glechomanamides A-C (331-333) (Figure 8) were isolated from Salvia scapiformis [78]. In a tube formation assay, 332 showed the most potent antiangiogenic activity in primary screening, and its IC 50 value was determined to be 40.4 µM [78].…”
Section: Germacrane Elemaneand Iresane Sesquiterpenoidsmentioning
confidence: 99%
“…Three new germacrane sesquiterpenoid-typealkaloids with an unusual ∆ 8 -7,12-lactam moiety, glechomanamides A-C (331-333) (Figure 8) were isolated from Salvia scapiformis [78]. In a tube formation assay, 332 showed the most potent antiangiogenic activity in primary screening, and its IC 50 value was determined to be 40.4 µM [78]. In addition to VEGFR2, 332 decreased BMP4 expression, which regulates tube formation, and glycolysisrelated proteins, including GLUT1 and HK2, which suggests that the novel compound 332 is worthy of additional investigation for angiogenesis-associated pathological conditions [78].…”
Section: Germacrane Elemaneand Iresane Sesquiterpenoidsmentioning
confidence: 99%
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“…In recent years, substituted lactams have emerged as an important pharmacophore for several drug classes, with a large spectrum of biological outcomes and various therapeutic applications [6][7][8]. From a structural standpoint, they can be four-, five-, six-and seven-membered rings, called β-lactams, γ-lactam, δ-lactam and ε-lactam, respectively.…”
Section: Introductionmentioning
confidence: 99%