Paper · 1967 · Bulletin of the Chemical Society of Japan

Altenin. V. Pathogenic Activity of Reductones to the Pear

Noboru Sugiyama; Choji Kashima; Makoto Yamamoto; et al.

2
claims
4
verbatim quotes
1
citations
2
research areas
—
Not open access

Abstract

Abstract The three reductones, 3-hydroxy-2, 4-dioxopentane, ethyl 2-hydroxy-1, 3-dioxovalerate and ethyl 2-hydroxy-3-oxobutyrate, were synthesized. These compounds were examined for the pathogenic activities to the pear. The pathogenic activities of reductones have some relations with the endiol contents. The center of pathogenic activity in altenin is shown to be the endiol carbonyl grouping.

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The text the model read, with the source record’s inline markup (italics, sub- and superscripts) rendered and its character entities decoded; quote offsets refer to the raw text.

Claims 2

Associationobservedoriginal resultmeasured

Claim · model-written summary

Reductone pathogenic activity to pear relates to endiol content.

Compound
endiol contentse0
Outcome
pathogenic activities of reductonese0

Not reportedDirection

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Pyrus communis
Pyrus communis · TaxonDidier Descouens · CC BY-SA 4.0 · Wikimedia Commons ↗

Verbatim

e0

“The pathogenic activities of reductones have some relations with the endiol contents”

✓ located verbatim in the source · abstract, characters 221–305 · show in text ↑
t0

“Pear”

✓ located verbatim in the source · title, characters 53–57 · show in text ↑
Mechanismobservedoriginal resultmeasured

Claim · model-written summary

The endiol carbonyl grouping is identified as the center of altenin pathogenic activity.

Compound
endiol carbonyl groupinge0
Outcome
pathogenic activity in altenine0

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Pyrus communis
Pyrus communis · TaxonDidier Descouens · CC BY-SA 4.0 · Wikimedia Commons ↗

Verbatim

e0

“The center of pathogenic activity in altenin is shown to be the endiol carbonyl grouping”

✓ located verbatim in the source · abstract, characters 307–395 · show in text ↑
t0

“Pear”

✓ located verbatim in the source · title, characters 53–57 · show in text ↑