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12,346 results for “derivatives”

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Fig. 5. Single-crystal X in Prenylated C -C derivatives from the stems and branches of Illicium ternstroemioides A. C. Smith with antiviral activity

Fig. 5. Single-crystal X-ray structure of compound 1.

opennotspecifiedDec 2021View details →
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Fig. 2 in Prenylated C -C derivatives from the stems and branches of Illicium ternstroemioides A. C. Smith with antiviral activity

Fig. 2. Key HMBC correlations of compounds 1–5.

opennotspecifiedDec 2021View details →
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Fig. 3 in Prenylated C -C derivatives from the stems and branches of Illicium ternstroemioides A. C. Smith with antiviral activity

Fig. 3. Key ROESY and NOE correlations of compounds 1–5.

opennotspecifiedDec 2021View details →
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Fig. 9. Key 1H–1H in Prenylated C -C derivatives from the stems and branches of Illicium ternstroemioides A. C. Smith with antiviral activity

Fig. 9. Key 1H–1H COSY and HMBC correlations of compounds 11 12.

opennotspecifiedDec 2021View details →
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Fig. 4 in Prenylated C -C derivatives from the stems and branches of Illicium ternstroemioides A. C. Smith with antiviral activity

Fig. 4. CD spectra of compounds 1–5, 7, 8, 10a, 11, 12, and 13 in MeOH.

opennotspecifiedDec 2021View details →
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Fig. 5. X in Phloroglucinol derivatives rhotomensones A-G from Rhodomyrtus tomentosa

Fig. 5. X-ray crystal structure of compound 5.

opennotspecifiedOct 2021View details →
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Fig. 4 in Phloroglucinol derivatives rhotomensones A-G from Rhodomyrtus tomentosa

Fig. 4. The calculated and experimental ECD spectra of 2–4.

opennotspecifiedOct 2021View details →
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Fig. 3 in Phloroglucinol derivatives rhotomensones A-G from Rhodomyrtus tomentosa

Fig. 3. Calculated and experimental ECD spectra of (±)-1.

opennotspecifiedOct 2021View details →
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Fig. 6 in Phloroglucinol derivatives rhotomensones A-G from Rhodomyrtus tomentosa

Fig. 6. Hypothetical biosynthetic pathways of 1–7.

opennotspecifiedOct 2021View details →
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Fig. 11 in Thirteen undescribed diterpenoid quinones derived from the rhizomes of Salvia miltiorrhiza and their anti-tumor activities

Fig. 11. The antitumor activities of 3, 4.

opennotspecifiedNov 2021View details →
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Fig. 9 in Thirteen undescribed diterpenoid quinones derived from the rhizomes of Salvia miltiorrhiza and their anti-tumor activities

Fig. 9. Experimental and calculated ECD spectra of 11.

opennotspecifiedNov 2021View details →
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Fig. 10 in Thirteen undescribed diterpenoid quinones derived from the rhizomes of Salvia miltiorrhiza and their anti-tumor activities

Fig. 10. Experimental and calculated ECD spectra of 12.

opennotspecifiedNov 2021View details →
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Fig. 7 in Thirteen undescribed diterpenoid quinones derived from the rhizomes of Salvia miltiorrhiza and their anti-tumor activities

Fig. 7. Experimental and calculated ECD spectra of 8.

opennotspecifiedNov 2021View details →
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Fig. 3 in Thirteen undescribed diterpenoid quinones derived from the rhizomes of Salvia miltiorrhiza and their anti-tumor activities

Fig. 3. Experimental and calculated ECD spectra of 1a, 1b.

opennotspecifiedNov 2021View details →
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Fig. 1 in Thirteen undescribed diterpenoid quinones derived from the rhizomes of Salvia miltiorrhiza and their anti-tumor activities

Fig. 1. The structure of compound 1a/1b‒12.

opennotspecifiedNov 2021View details →
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Fig. 4 in Thirteen undescribed diterpenoid quinones derived from the rhizomes of Salvia miltiorrhiza and their anti-tumor activities

Fig. 4. ORTEP diagram of 1a and 1b.

opennotspecifiedNov 2021View details →
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Fig. 1 in Pestalopyrones A-D, four tricyclic pyrone derivatives from the endophytic fungus Pestalotiopsis neglecta S3

Fig. 1. Chemical structures of pestalopyrones A–D (1–4).

opennotspecifiedNov 2020View details →
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Fig. 4 in Pestalopyrones A-D, four tricyclic pyrone derivatives from the endophytic fungus Pestalotiopsis neglecta S3

Fig. 4. ΔδRS (δ- δ) values of (R)-MPA ester of 2 and (S)-MPA ester of 2.

opennotspecifiedNov 2020View details →
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Fig. 2 in Pestalopyrones A-D, four tricyclic pyrone derivatives from the endophytic fungus Pestalotiopsis neglecta S3

Fig. 2. Key COSY and HMBC correlations of pestalopyrones A–D (1–4).

opennotspecifiedNov 2020View details →
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Fig. 2 in Role of C-H bond in the antioxidant activities of rooperol and its derivatives: A DFT study

Fig. 2. The most stable geometries of ROP and its derivatives.

opennotspecifiedOct 2020View details →

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Allen Brain Atlas

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DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

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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

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

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

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