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Stellaria yunnanensis

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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 UUID6440550f7ea2f851935000
Scientific name Stellaria yunnanensis
Authority Franch.
First published in Pl. Delavay. : 98 (1889)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 筋骨草
Chinese 千针万线草
Chinese 千针万线草（云南繁缕）
Chinese 钱针万线草
Chinese 云南繁缕
Chinese 麦参

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001238181
Tropicos 50097895
KEW urn:lsid:ipni.org:names:159544-1
The Plant List tro-50097895
Open Tree Of Life 5728503
NCBI Taxonomy 2653284
IPNI 159544-1
GBIF 7268115
EOL 2904032

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
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C J Ethnobiol Ethnomed 15-Jan-2024
PMCID:PMC10790445
doi:10.1186/s13002-023-00638-9
PMID:38225656
Cancer Treatment by Caryophyllaceae-Type Cyclopeptides Houshdar Tehrani MH, Gholibeikian M, Bamoniri A, Mirjalili BB Front Endocrinol (Lausanne) 14-Jan-2021
PMCID:PMC7841296
doi:10.3389/fendo.2020.600856
PMID:33519710
The genetic origin of evolidine, the first cyclopeptide discovered in plants, and related orbitides Fisher MF, Payne CD, Chetty T, Crayn D, Berkowitz O, Whelan J, Rosengren KJ, Mylne JS J Biol Chem 19-Aug-2020
PMCID:PMC7573267
doi:10.1074/jbc.RA120.014781
PMID:32817170
Photo-induced synthesis, structure and in vitro bioactivity of a natural cyclic peptide Yunnanin A analog Jiang S, Zhao L, Wu J, Bao Y, Wang Z, Jin Y RSC Adv 24-Dec-2019
PMCID:PMC9047273
doi:10.1039/c9ra09163g
PMID:35492554
Medicinal plants of the family Caryophyllaceae: a review of ethno-medicinal uses and pharmacological properties Chandra S, Rawat DS Integr Med Res 04-Jul-2015
PMCID:PMC5481791
doi:10.1016/j.imr.2015.06.004
PMID:28664118
Two new cyclopeptides from <i>stellaria yunnanensis</i> Yu‐Rui Zhao, Xian‐Kai Wang, Tong‐Fang Zhao, Jun Zhou, Xiao‐Lin Huang, Hou‐Ming Wu Wiley 09-Sep-2010
doi:10.1002/CJOC.19950130312
Cyclic Peptides from Higher Plants. Part 30. Three Novel Cyclic Peptides, Yunnanins D, E and F from Stellaria yunnanensis Hideji Itokawa, Hiroshi Morita, Takashi Kayashita, Masako Shimomura, Koichi Takeya The Japan Institute of Heterocyclic Chemistry 31-Mar-2009
doi:10.3987/COM-96-7459
Revision of the structure of escholidine. Chudík S, Marek R, Seckárová P, Necas M, Dostál J, Slavík J J Nat Prod 01-Jun-2006
doi:10.1021/NP060078E
PMID:16792417
Two Novel Cyclic Peptides, Yunnanins A and B from <i>Stellaria yunnanensis</i> Hiroshi Morita, Akira Shishido, Takashi Kayashita, Masako Shimomura, Koichi Takeya, Hideji Itokawa Oxford University Press (OUP) 26-Apr-2006
doi:10.1246/CL.1994.2415
Cyclic peptides from higher plants. 24.1 yunnanin C, a novel cyclic heptapeptide from Stellaria yunnanensis. Morita H, Kayashita T, Shimomura M, Takeya K, Itokawa H J Nat Prod 01-Mar-1996
doi:10.1021/NP960123Q
PMID:8882429
Cyclopeptides from Stellaria yunnanensis. Zhao YR, Zhou J, Wang XK, Huang XL, Wu HM, Zou C Phytochemistry 01-Nov-1995
doi:10.1016/0031-9422(95)00351-7
PMID:8534403

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
Stellarine A 50993701 Click to see CC(=O)C1=C2C(=CC(=N1)C(=O)N)C3=CC=CC=C3N2 253.26 unknown https://doi.org/10.1021/NP060078E
https://doi.org/10.1016/0031-9422(95)00351-7
https://doi.org/10.1002/CJOC.19950130312
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
(3R,6S,9R,12S,15S)-6,9-dibenzyl-12-[(2R)-4-hydroxybutan-2-yl]-15-(hydroxymethyl)-3-methyl-1,4,7,10,13,16-hexazacyclooctadecane-2,5,8,11,14,17-hexone 162882593 Click to see CC1C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CC2=CC=CC=C2)CC3=CC=CC=C3)C(C)CCO)CO 638.70 unknown https://doi.org/10.1016/0031-9422(95)00351-7
(3R,6S,9R,12S,15S)-6,9-dibenzyl-12-[(2R)-4-hydroxybutan-2-yl]-3,15-bis(hydroxymethyl)-1,4,7,10,13,16-hexazacyclooctadecane-2,5,8,11,14,17-hexone 163195095 Click to see CC(CCO)C1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NCC(=O)NC(C(=O)N1)CO)CO)CC2=CC=CC=C2)CC3=CC=CC=C3 654.70 unknown https://doi.org/10.1016/0031-9422(95)00351-7
(3S,6S,9S,12S,15S)-6,9-dibenzyl-12-[(2R)-4-hydroxybutan-2-yl]-3,15-bis(hydroxymethyl)-1,4,7,10,13,16-hexazacyclooctadecane-2,5,8,11,14,17-hexone 162910160 Click to see CC(CCO)C1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NCC(=O)NC(C(=O)N1)CO)CO)CC2=CC=CC=C2)CC3=CC=CC=C3 654.70 unknown https://doi.org/10.3987/COM-96-7459
cyclo[DL-Arg-DL-Phe-DL-Pro-Gly-DL-xiIle-DL-Ser-DL-Phe] 85278970 Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NCC(=O)N1)CC3=CC=CC=C3)CCCN=C(N)N)CC4=CC=CC=C4)CO 804.90 unknown https://doi.org/10.3987/COM-96-7459
cyclo[Gly-DL-Val-DL-xiThr-DL-Trp-DL-Tyr-DL-Pro-DL-Ser-DL-Ser] 72832656 Click to see CC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NCC(=O)N1)CO)CO)CC3=CC=C(C=C3)O)CC4=CNC5=CC=CC=C54)C(C)O 877.90 unknown https://doi.org/10.3987/COM-96-7459
cyclo[Gly-Gly-DL-Pro-DL-Phe-DL-Pro-Gly-DL-Tyr] 85105436 Click to see C1CC2C(=O)NC(C(=O)N3CCCC3C(=O)NCC(=O)NC(C(=O)NCC(=O)NCC(=O)N2C1)CC4=CC=C(C=C4)O)CC5=CC=CC=C5 675.70 unknown https://doi.org/10.1246/CL.1994.2415
cyclo[Gly-Gly-Pro-Phe-Pro-Gly-Tyr] 10055293 Click to see C1CC2C(=O)NC(C(=O)N3CCCC3C(=O)NCC(=O)NC(C(=O)NCC(=O)NCC(=O)N2C1)CC4=CC=C(C=C4)O)CC5=CC=CC=C5 675.70 unknown https://doi.org/10.1246/CL.1994.2415
cyclo[Gly-Val-D-Thr-Trp-Tyr-Pro-Ser-Ser] 163190055 Click to see CC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NCC(=O)N1)CO)CO)CC3=CC=C(C=C3)O)CC4=CNC5=CC=CC=C54)C(C)O 877.90 unknown https://doi.org/10.3987/COM-96-7459
cyclo[Gly-Val-Thr-Trp-Tyr-Pro-Ser-Ser] 11400297 Click to see CC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NCC(=O)N1)CO)CO)CC3=CC=C(C=C3)O)CC4=CNC5=CC=CC=C54)C(C)O 877.90 unknown https://doi.org/10.3987/COM-96-7459
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
(3S,6R,12S,15S)-6,9-dibenzyl-12-[(2S)-4-hydroxybutan-2-yl]-3,15-bis(hydroxymethyl)-1,4,7,10,13,16-hexazacyclooctadecane-2,5,8,11,14,17-hexone 101682233 Click to see CC(CCO)C1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NCC(=O)NC(C(=O)N1)CO)CO)CC2=CC=CC=C2)CC3=CC=CC=C3 654.70 unknown https://doi.org/10.3987/COM-96-7459
(3S,6S,9S,12S,15S)-6,9-dibenzyl-12-[(2S)-4-hydroxybutan-2-yl]-15-(hydroxymethyl)-3-methyl-1,4,7,10,13,16-hexazacyclooctadecane-2,5,8,11,14,17-hexone 101682232 Click to see CC1C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CC2=CC=CC=C2)CC3=CC=CC=C3)C(C)CCO)CO 638.70 unknown https://doi.org/10.1002/CJOC.19950130312
https://doi.org/10.1016/0031-9422(95)00351-7
https://doi.org/10.1246/CL.1994.2415
6,9-Dibenzyl-12-(4-hydroxybutan-2-yl)-15-(hydroxymethyl)-3-methyl-1,4,7,10,13,16-hexazacyclooctadecane-2,5,8,11,14,17-hexone 162882591 Click to see CC1C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CC2=CC=CC=C2)CC3=CC=CC=C3)C(C)CCO)CO 638.70 unknown https://doi.org/10.1016/0031-9422(95)00351-7
https://doi.org/10.1246/CL.1994.2415
6,9-Dibenzyl-12-(4-hydroxybutan-2-yl)-3,15-bis(hydroxymethyl)-1,4,7,10,13,16-hexazacyclooctadecane-2,5,8,11,14,17-hexone 162910158 Click to see CC(CCO)C1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NCC(=O)NC(C(=O)N1)CO)CO)CC2=CC=CC=C2)CC3=CC=CC=C3 654.70 unknown https://doi.org/10.1016/0031-9422(95)00351-7
https://doi.org/10.3987/COM-96-7459
https://doi.org/10.1002/CJOC.19950130312
cyclo[Arg-Phe-Pro-Gly-Ile-Ser-Phe] 101986179 Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NCC(=O)N1)CC3=CC=CC=C3)CCCN=C(N)N)CC4=CC=CC=C4)CO 804.90 unknown https://doi.org/10.3987/COM-96-7459
Yunnanin A 44584206 Click to see C1CC2C(=O)NC(C(=O)N3CCCC3C(=O)NCC(=O)NCC(=O)NC(C(=O)NCC(=O)N2C1)CC4=CC=C(C=C4)O)CC5=CC=CC=C5 675.70 unknown https://doi.org/10.1246/CL.1994.2415
Yunnanin C 10556828 Click to see CCC(C)C1C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NCC(=O)N1)CO)CC3=CC=C(C=C3)O)CC4=CC=CC=C4 721.80 unknown https://doi.org/10.1021/NP960123Q

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