Viburnum utile 15 claims

species · family Adoxaceae · green plant · NCBI Taxonomy ↗

2 spellings

Viburnum utile
Viburnum utileAnRo0002 · CC0 · Wikimedia Commons ↗
Observationobservedoriginal resultmeasured

Claim · model-written summary

Viburnum utile extract yielded identified compounds viburnumide A, vitamin E and α-amyrin.

Taxon
Viburnum utileViburnum utilet0
Outcome
viburnumide A(1), vitamin E(2), α-amyrin(3)e0

Verbatim

e0

“Sixteen compounds were obtained and identified as viburnumide A(1), vitamin E(2), α-amyrin(3), α-tocoquinone(4), narjatamanin B(5), ethyl caffeate(6), naringenin(7), apigenin(8), ethyl β-D-ribo-hex-3-ulopyranoside(9), trans-p-hydroxycinnamic acid(10), amentoflavone(11), apigenin-7-O-β-D-glucoside(12), luteolin-7-O-β-D-glucoside(13), henryoside(14), ursolic acid(15), and 2α-hydroxy-oleanolic acid(16).”

✓ located verbatim in the source · abstract, characters 334–737
t0

“Viburnum utile”

✓ located verbatim in the source · title, characters 26–40

Title

[Chemical constituents of Viburnum utile and their inhibitory activities against α-glucosidase].

Chu-Yi Long; Qi-Ji Li; Lang Zhou; et al. PubMed 2024. doi:10.19540/j.cnki.cjcmm.20240607.201

Other claims from this paper (8)
Observationobservedoriginal resultmeasured

Claim · model-written summary

The extract contained α-tocoquinone, narjatamanin B and ethyl caffeate.

Taxon
Viburnum utileViburnum utilet0
Outcome
α-tocoquinone(4), narjatamanin B(5), ethyl caffeate(6)e0

Verbatim

e0

“α-tocoquinone(4), narjatamanin B(5), ethyl caffeate(6)”

✓ located verbatim in the source · abstract, characters 429–483
t0

“Viburnum utile”

✓ located verbatim in the source · title, characters 26–40

Title

[Chemical constituents of Viburnum utile and their inhibitory activities against α-glucosidase].

Chu-Yi Long; Qi-Ji Li; Lang Zhou; et al. PubMed 2024. doi:10.19540/j.cnki.cjcmm.20240607.201

Other claims from this paper (8)
Observationobservedoriginal resultmeasured

Claim · model-written summary

The extract contained naringenin, apigenin and ethyl β-D-ribo-hex-3-ulopyranoside.

Taxon
Viburnum utileViburnum utilet0
Outcome
naringenin(7), apigenin(8), ethyl β-D-ribo-hex-3-ulopyranoside(9)e0

Verbatim

e0

“naringenin(7), apigenin(8), ethyl β-D-ribo-hex-3-ulopyranoside(9)”

✓ located verbatim in the source · abstract, characters 485–550
t0

“Viburnum utile”

✓ located verbatim in the source · title, characters 26–40

Title

[Chemical constituents of Viburnum utile and their inhibitory activities against α-glucosidase].

Chu-Yi Long; Qi-Ji Li; Lang Zhou; et al. PubMed 2024. doi:10.19540/j.cnki.cjcmm.20240607.201

Other claims from this paper (8)
Observationobservedoriginal resultmeasured

Claim · model-written summary

The extract contained trans-p-hydroxycinnamic acid, amentoflavone and apigenin-7-O-β-D-glucoside.

Taxon
Viburnum utileViburnum utilet0
Outcome
trans-p-hydroxycinnamic acid(10), amentoflavone(11), apigenin-7-O-β-D-glucoside(12)e0

Verbatim

e0

“trans-p-hydroxycinnamic acid(10), amentoflavone(11), apigenin-7-O-β-D-glucoside(12)”

✓ located verbatim in the source · abstract, characters 552–635
t0

“Viburnum utile”

✓ located verbatim in the source · title, characters 26–40

Title

[Chemical constituents of Viburnum utile and their inhibitory activities against α-glucosidase].

Chu-Yi Long; Qi-Ji Li; Lang Zhou; et al. PubMed 2024. doi:10.19540/j.cnki.cjcmm.20240607.201

Other claims from this paper (8)
Observationobservedoriginal resultmeasured

Claim · model-written summary

The extract contained luteolin-7-O-β-D-glucoside, henryoside and ursolic acid.

Taxon
Viburnum utileViburnum utilet0
Outcome
luteolin-7-O-β-D-glucoside(13), henryoside(14), ursolic acid(15)e0

Verbatim

e0

“luteolin-7-O-β-D-glucoside(13), henryoside(14), ursolic acid(15)”

✓ located verbatim in the source · abstract, characters 637–701
t0

“Viburnum utile”

✓ located verbatim in the source · title, characters 26–40

Title

[Chemical constituents of Viburnum utile and their inhibitory activities against α-glucosidase].

Chu-Yi Long; Qi-Ji Li; Lang Zhou; et al. PubMed 2024. doi:10.19540/j.cnki.cjcmm.20240607.201

Other claims from this paper (8)
Observationobservedoriginal resultmeasured

Claim · model-written summary

The extract contained 2α-hydroxy-oleanolic acid.

Taxon
Viburnum utileViburnum utilet0
Outcome
2α-hydroxy-oleanolic acid(16)e0

Verbatim

e0

“2α-hydroxy-oleanolic acid(16)”

✓ located verbatim in the source · abstract, characters 707–736
t0

“Viburnum utile”

✓ located verbatim in the source · title, characters 26–40

Title

[Chemical constituents of Viburnum utile and their inhibitory activities against α-glucosidase].

Chu-Yi Long; Qi-Ji Li; Lang Zhou; et al. PubMed 2024. doi:10.19540/j.cnki.cjcmm.20240607.201

Other claims from this paper (8)
Observationobservedoriginal resultmeasured

Claim · model-written summary

Viburnumide A was identified as a new compound.

Taxon
Viburnum utileViburnum utilet0
Outcome
new compounde0

Verbatim

e0

“compound 1 was a new compound”

✓ located verbatim in the source · abstract, characters 750–779
t0

“Viburnum utile”

✓ located verbatim in the source · title, characters 26–40

Title

[Chemical constituents of Viburnum utile and their inhibitory activities against α-glucosidase].

Chu-Yi Long; Qi-Ji Li; Lang Zhou; et al. PubMed 2024. doi:10.19540/j.cnki.cjcmm.20240607.201

Other claims from this paper (8)
Observationobservedoriginal resultmeasured

Claim · model-written summary

Compounds 2–16 were first isolated from V. utile.

Taxon
V. utileViburnum utilee0
Outcome
isolated from V. utile for the first timee0

Verbatim

e0

“compounds 2-16 were isolated from V. utile for the first time.”

✓ located verbatim in the source · abstract, characters 785–847

Title

[Chemical constituents of Viburnum utile and their inhibitory activities against α-glucosidase].

Chu-Yi Long; Qi-Ji Li; Lang Zhou; et al. PubMed 2024. doi:10.19540/j.cnki.cjcmm.20240607.201

Other claims from this paper (8)
Observationobservedoriginal resultpositivemeasured

Claim · model-written summary

Amentoflavone inhibited α-glucosidase with IC50 of 4.0 μmol·L~(-1), comparable to acarbose.

Taxon
Viburnum utileViburnum utilet0
Outcome
inhibitory activitye0
Value
4.0 μmol·L~(-1)e0
Qualifier
2.3 μmol·L~(-1)e0
Comparator
positive control acarbosee0

Verbatim

e0

“The inhibitory activity(IC_(50) of 4.0 μmol·L~(-1)) of compound 11 against α-glucosidase was comparable to that of the positive control acarbose(IC_(50) of 2.3 μmol·L~(-1)).”

✓ located verbatim in the source · abstract, characters 848–1021
t0

“Viburnum utile”

✓ located verbatim in the source · title, characters 26–40

Title

[Chemical constituents of Viburnum utile and their inhibitory activities against α-glucosidase].

Chu-Yi Long; Qi-Ji Li; Lang Zhou; et al. PubMed 2024. doi:10.19540/j.cnki.cjcmm.20240607.201

Other claims from this paper (8)
Observationobservedoriginal resultmeasured

Claim · model-written summary

Viburnum utile used both soil and subcutaneous water in slight and non-desertified grades, but only soil water in medium and severe grades.

Taxon
Viburnum utileViburnum utilee0
Outcome
extracted water from both soil layers and subcutaneous zonee0

Verbatim

e0

“Pyracantha fortuneana,Rhamnus davurica and Viburnum utile in slight and non karst desertification grade extracted water from both soil layers and subcutaneous zone,while these plants only used water form soil layers in medium and severe grade”

✓ located verbatim in the source · abstract, characters 2051–2293

Title

CHARACTERISTICS OF WATER SOURCES OF COMMON PLANT SPECIES IN VARIOUS MICROHABITATS IN KARST ROCKY DESERTIFICATION AREA IN CENTRAL GUIZHOU PROVINCE

DU Xue-lia Changjiang liuyu ziyuan yu huanjing 2015

Other claims from this paper (6)