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111 results for “Saponins”

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Fig. 7. Sprengerinin C in Spirostane saponins with a rearranged A/B ring system isolated from the rhizomes of Ophiopogon japonicus

Fig. 7. Sprengerinin C (19) induces cell cycle arrest in G2/M in NCI–H460 cells.

opennotspecifiedJan 2022View details →
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Fig. 6. Sprengerinin C in Spirostane saponins with a rearranged A/B ring system isolated from the rhizomes of Ophiopogon japonicus

Fig. 6. Sprengerinin C (19) induces apoptosis of NCI–H460 cells.

opennotspecifiedJan 2022View details →
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Fig. 5 in Spirostane saponins with a rearranged A/B ring system isolated from the rhizomes of Ophiopogon japonicus

Fig. 5. Cytotoxic effects of sprengerinin C (19).

opennotspecifiedJan 2022View details →
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Fig. 4. Plausible biogenetic pathway for compounds 1 and 2 in Spirostane saponins with a rearranged A/B ring system isolated from the rhizomes of Ophiopogon japonicus

Fig. 4. Plausible biogenetic pathway for compounds 1 and 2.

opennotspecifiedJan 2022View details →
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Fig. 3 in Spirostane saponins with a rearranged A/B ring system isolated from the rhizomes of Ophiopogon japonicus

Fig. 3. Key NOESY correlations of compounds 1–4.

opennotspecifiedJan 2022View details →
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Fig. 1 in Spirostane saponins with a rearranged A/B ring system isolated from the rhizomes of Ophiopogon japonicus

Fig. 1. Structures of compounds 1–23.

opennotspecifiedJan 2022View details →
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Fig. 3 in Acylated saponins and flavonoid glycosides from the fruits of Stewartia koreana

Fig. 3. Key HMBC (from H to C) correlation for compounds 4–6.

opennotspecifiedJan 2022View details →
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Fig. 1 in Acylated saponins and flavonoid glycosides from the fruits of Stewartia koreana

Fig. 1. Chemical structures of isolated compounds 1–6 from the dried fruits of Stewartia koreana.

opennotspecifiedJan 2022View details →
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Fig. 3 in Dammarane-type saponins with proprotein convertase subtilisin/kexin type 9 inhibitory activity from Gynostemma pentaphyllum

Fig. 3. Key NOESY correlations of the dammarane skeletons of compounds 1, 2, 4 and 7.

opennotspecifiedFeb 2022View details →
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Fig. 2. Key 1H–1H in Dammarane-type saponins with proprotein convertase subtilisin/kexin type 9 inhibitory activity from Gynostemma pentaphyllum

Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–7.

opennotspecifiedFeb 2022View details →
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Fig. 1 in Dammarane-type saponins with proprotein convertase subtilisin/kexin type 9 inhibitory activity from Gynostemma pentaphyllum

Fig. 1. Chemical structures of compounds 1–11.

opennotspecifiedFeb 2022View details →
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Fig. 4 in Eight undescribed steroidal saponins including an unprecedented 16, 26-epoxy-furostanol saponin from Solanum xanthocarpum and their cytotoxic activities

Fig. 4. Plausible biosynthesis pathway of 16,26-epoxy-furostanol saponins.

opennotspecifiedJul 2022View details →
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Fig. 1 in Eight undescribed steroidal saponins including an unprecedented 16, 26-epoxy-furostanol saponin from Solanum xanthocarpum and their cytotoxic activities

Fig. 1. Chemical structures of compounds 1–8.

opennotspecifiedJul 2022View details →
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Fig. 3 in Eight undescribed steroidal saponins including an unprecedented 16, 26-epoxy-furostanol saponin from Solanum xanthocarpum and their cytotoxic activities

Fig. 3. Key NOESY correlations of compounds 1, 2, 4 and 7.

opennotspecifiedJul 2022View details →
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Fig. 2. 1H–1H in Eight undescribed steroidal saponins including an unprecedented 16, 26-epoxy-furostanol saponin from Solanum xanthocarpum and their cytotoxic activities

Fig. 2. 1H–1H COSY of the aglycones and key HMBC correlations of compounds 1–8.

opennotspecifiedJul 2022View details →
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Fig. 3 in Furostanol saponins from Asparagus racemosus as potential hypoglycemic agents

Fig. 3. Key HMBC (H C) and ROESY (H H) correlations of compound 1.

opennotspecifiedSep 2022View details →
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Fig. 2 in Furostanol saponins from Asparagus racemosus as potential hypoglycemic agents

Fig. 2. Proposed mass fragmentation of furoasparoside A (1).

opennotspecifiedSep 2022View details →
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Fig. 2. Key HMBC and COSY correlations for compound 1a in Ingadosides A-C, acacic acid-type saponins from Inga sapindoides with potent inhibitory activity against downy mildew

Fig. 2. Key HMBC and COSY correlations for compound 1a.

opennotspecifiedJul 2022View details →
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Fig. 1. Saponins isolated from I in Ingadosides A-C, acacic acid-type saponins from Inga sapindoides with potent inhibitory activity against downy mildew

Fig. 1. Saponins isolated from I. sapindoides.

opennotspecifiedJul 2022View details →
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Fig. 2 in Phytochemical and biological diversity of triterpenoid saponins from family Sapotaceae: A comprehensive review

Fig. 2. (continued).

opennotspecifiedOct 2022View details →

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International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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Last verified 2026-04-29Open record

OpenNeuro

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neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record