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Arenaria kansuensis

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64400a65785fa789877127
Scientific name Arenaria kansuensis
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 26: 428 (1880)

Description Top

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Synonyms Top

Scientific name Authority First published in
Arenaria kansuensis var. acropetala Tsui & L.H.Zhou Acta Phytotax. Sin. 18: 360 (1980)
Arenaria kansuensis var. ovatipetala Tsui & L.H.Zhou Acta Phytotax. Sin. 18: 359 (1980)

Common names Top

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Language Common/alternative name
Chinese 雪灵芝
Chinese 甘肃雪灵芝甘肃蚤缀、卵瓣蚤缀）
Chinese 甘肃蚤缀
Chinese 甘肃雪灵芝

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000546067
Tropicos 50065148
KEW urn:lsid:ipni.org:names:151324-1
The Plant List kew-2649588
NCBI Taxonomy 2604645
IPNI 151324-1
GBIF 7267527

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
The Role of Nrf2 in Pulmonary Fibrosis: Molecular Mechanisms and Treatment Approaches Wang Y, Wei J, Deng H, Zheng L, Yang H, Lv X Antioxidants (Basel) 29-Aug-2022
PMCID:PMC9495339
doi:10.3390/antiox11091685
PMID:36139759
Natural Product-Based Potential Therapeutic Interventions of Pulmonary Fibrosis Hasan M, Paul NC, Paul SK, Saikat AS, Akter H, Mandal M, Lee SS Molecules 22-Feb-2022
PMCID:PMC8911636
doi:10.3390/molecules27051481
PMID:35268581
Phylogenetic and Physiological Diversity of Cultivable Actinomycetes Isolated From Alpine Habitats on the Qinghai-Tibetan Plateau Ma A, Zhang X, Jiang K, Zhao C, Liu J, Wu M, Wang Y, Wang M, Li J, Xu S Front Microbiol 02-Oct-2020
PMCID:PMC7566193
doi:10.3389/fmicb.2020.555351
PMID:33117304
Natural products as home‐based prophylactic and symptom management agents in the setting of COVID‐19 Thota SM, Balan V, Sivaramakrishnan V Phytother Res 17-Aug-2020
PMCID:PMC7461159
doi:10.1002/ptr.6794
PMID:32881214
Plant density and life history traits of Aconitum spicatum in North-central Nepal: effects of elevation and anthropogenic disturbances Chapagain DJ, Meilby H, Ghimire SK PeerJ 10-Sep-2019
PMCID:PMC6743441
doi:10.7717/peerj.7574
PMID:31565560
A comparative study on shared-use medicines in Tibetan and Chinese medicine Zhao MM, Wang KR, Gu R, Zhong SH J Ethnobiol Ethnomed 23-Aug-2019
PMCID:PMC6706903
doi:10.1186/s13002-019-0320-5
PMID:31443668
Terpenoids and flavonoids from Arenaria kansuensis. Feng-E WU, Kazuo KOIKE, Tamotsu NIKAIDO, Kiyoshi ISHII, Taichi OHMOTO, Keiji IKEDA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.38.2281
New .BETA.-carboline alkaloids from a chinese medicinal plant, Arenaria kansuensis. Structures of arenarines A, B, C, and D. Feng-E Wu, Kazuo KOIKE, Tamotsu NIKAIDO, Yohko SAKAMOTO, Taichi OHMOTO, Keiji IKEDA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.37.1808

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Harmala alkaloids
(1R)-2-methoxy-1-(9H-pyrido[3,4-b]indol-1-yl)ethanol 101726885 Click to see COCC(C1=NC=CC2=C1NC3=CC=CC=C23)O 242.27 unknown https://doi.org/10.1248/CPB.37.1808
(1S)-2-methoxy-1-(9H-pyrido[3,4-b]indol-1-yl)ethanol 101726886 Click to see COCC(C1=NC=CC2=C1NC3=CC=CC=C23)O 242.27 unknown https://doi.org/10.1248/CPB.37.1808
1-(7-Methoxy-9H-pyrido[3,4-b]indol-1-yl)ethan-1-one 188439 Click to see CC(=O)C1=NC=CC2=C1NC3=C2C=CC(=C3)OC 240.26 unknown https://doi.org/10.1248/CPB.37.1808
1-(9H-pyrido[3,4-b]indol-1-yl)ethanone 638667 Click to see CC(=O)C1=NC=CC2=C1NC3=CC=CC=C23 210.23 unknown https://doi.org/10.1248/CPB.37.1808
2-Methoxy-1-(9H-pyrido(3,4-b)indol-1-yl)ethanol 5491732 Click to see COCC(C1=NC=CC2=C1NC3=CC=CC=C23)O 242.27 unknown https://doi.org/10.1248/CPB.37.1808
2-Methoxy-1-(9H-pyrido(3,4-b)indol-1-yl)ethanone 183645 Click to see COCC(=O)C1=NC=CC2=C1NC3=CC=CC=C23 240.26 unknown https://doi.org/10.1248/CPB.37.1808
methyl 9H-pyrido[3,4-b]indole-1-carboxylate 597266 Click to see COC(=O)C1=NC=CC2=C1NC3=CC=CC=C23 226.23 unknown https://doi.org/10.1248/CPB.37.1808
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(3S,3aR,5aR,5bR,7S,7aS,11aR,11bR,13aS,13bS)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-7-ol 162968339 Click to see CC1(CCCC2(C1C(CC3(C2CCC4C3(CCC5C4(CCC5C(C)(C)O)C)C)C)O)C)C 444.70 unknown https://doi.org/10.1248/CPB.38.2281
3-(2-Hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-7-ol 4603262 Click to see CC1(CCCC2(C1C(CC3(C2CCC4C3(CCC5C4(CCC5C(C)(C)O)C)C)C)O)C)C 444.70 unknown https://doi.org/10.1248/CPB.38.2281
Zeorin 159931 Click to see CC1(CCCC2(C1C(CC3(C2CCC4C3(CCC5C4(CCC5C(C)(C)O)C)C)C)O)C)C 444.70 unknown https://doi.org/10.1248/CPB.38.2281
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,3aR,5aR,5bR,7aR,11aS,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-2,3,4,5,5b,6,7,7a,10,11,13,13b-dodecahydro-1H-cyclopenta[a]chrysen-9-one 12305184 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(=O)C5(C)C)C)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.38.2281
[(3S,5S,9S,10S,13R,14R,17R)-17-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] hexadecanoate 162910609 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3=CCC2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown https://doi.org/10.1248/CPB.38.2281
[17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] hexadecanoate 14683201 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3=CCC2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown https://doi.org/10.1248/CPB.38.2281
3a,5a,8,8,11a,13a-Hexamethyl-3-(propan-2-yl)-1,2,3,3a,4,5,5a,5b,6,7,7a,8,10,11,11a,13,13a,13b-octadecahydro-9h-cyclopenta[a]chrysen-9-one 185590 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(=O)C5(C)C)C)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.38.2281
Eburicol 9803310 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 440.70 unknown https://doi.org/10.1248/CPB.38.2281
Euphorbol 634628 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 440.70 unknown https://doi.org/10.1248/CPB.38.2281
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
17-(3,4-Dihydroxy-5,6-dimethylheptan-2-yl)-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one 73229503 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CCC4C3(CCC(=O)C4)C)C)O)O 432.70 unknown https://doi.org/10.1248/CPB.37.1808
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
(1S,2R,5R,6R,9S,10R,13S,15S)-5-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-ol 124406528 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C 428.60 unknown https://doi.org/10.1248/CPB.38.2281
5-(5,6-Dimethylhept-3-en-2-yl)-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-ol 633877 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C 428.60 unknown https://doi.org/10.1248/CPB.38.2281
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
22,23-Dihydro-alpha-spinasterone 14160308 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown https://doi.org/10.1248/CPB.38.2281
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/CPB.38.2281
delta7Stigmastenol 521367 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.38.2281
Schottenol 441837 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.38.2281
Schottenone 129681578 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown https://doi.org/10.1248/CPB.38.2281
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/CPB.38.2281
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 102059373 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1248/CPB.38.2281
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 163025843 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1248/CPB.38.2281
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 3549959 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1248/CPB.38.2281
Isoscoparin 442611 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1248/CPB.38.2281
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown https://doi.org/10.1248/CPB.38.2281

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