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Brachystemma calycinum

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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 UUID64400db728aff444244775
Scientific name Brachystemma calycinum
Authority D.Don
First published in Prodr. Fl. Nepal. : 216 (1825)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 白牛膝
Chinese 短瓣花
Chinese 抽筋藤
Chinese 活抽筋
Chinese 生筋藤

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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • Nepal
      • West Himalaya
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000570662
Tropicos 50065151
KEW urn:lsid:ipni.org:names:151926-1
The Plant List kew-2681703
Open Tree Of Life 109659
NCBI Taxonomy 1205701
IPNI 151926-1
iNaturalist 1182131
GBIF 3815492
EOL 2873158

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
Phylogenetic analysis and temporal diversification of the tribe Alsineae (Caryophyllaceae) with the description of three new genera, Hesperostellaria, Reniostellaria and Torreyostellaria Xue B, Song Z, Cai J, Ma Z, Huang J, Li Y, Yao G Front Plant Sci 21-Jun-2023
PMCID:PMC10321415
doi:10.3389/fpls.2023.1127443
PMID:37416878
Chemistry and Pharmacology of Bergenin or Its Derivatives: A Promising Molecule Salimo ZM, Yakubu MN, da Silva EL, de Almeida AC, Chaves YO, Costa EV, da Silva FM, Tavares JF, Monteiro WM, de Melo GC, Koolen HH Biomolecules 21-Feb-2023
PMCID:PMC10046151
doi:10.3390/biom13030403
PMID:36979338
A 2022 Systematic Review and Meta-Analysis of Enriched Therapeutic Diets and Nutraceuticals in Canine and Feline Osteoarthritis Barbeau-Grégoire M, Otis C, Cournoyer A, Moreau M, Lussier B, Troncy E Int J Mol Sci 08-Sep-2022
PMCID:PMC9499673
doi:10.3390/ijms231810384
PMID:36142319
Classifying natural products from plants, fungi or bacteria using the COCONUT database and machine learning Capecchi A, Reymond JL J Cheminform 18-Oct-2021
PMCID:PMC8524952
doi:10.1186/s13321-021-00559-3
PMID:34663470
Ethnobotanical study on wild edible plants used by three trans-boundary ethnic groups in Jiangcheng County, Pu’er, Southwest China Cao Y, Li R, Zhou S, Song L, Quan R, Hu H J Ethnobiol Ethnomed 27-Oct-2020
PMCID:PMC7590688
doi:10.1186/s13002-020-00420-1
PMID:33109239
Pharmacological and Predicted Activities of Natural Azo Compounds Dembitsky VM, Gloriozova TA, Poroikov VV Nat Prod Bioprospect 04-Jan-2017
PMCID:PMC5315673
doi:10.1007/s13659-016-0117-3
PMID:28054247
Effect of a diet enriched with green-lipped mussel on pain behavior and functioning in dogs with clinical osteoarthritis Rialland P, Bichot S, Lussier B, Moreau M, Beaudry F, del Castillo JR, Gauvin D, Troncy E Can J Vet Res 01-Jan-2013
PMCID:PMC3525174
PMID:23814358
Brachystemma calycinum D. Don Effectively Reduces the Locomotor Disability in Dogs with Naturally Occurring Osteoarthritis: A Randomized Placebo-Controlled Trial Moreau M, Lussier B, Pelletier JP, Martel-Pelletier J, Bédard C, Gauvin D, Troncy E Evid Based Complement Alternat Med 15-Jul-2012
PMCID:PMC3403515
doi:10.1155/2012/646191
PMID:22844335
Brachystemols A-C, three new furan derivatives from Brachystemma calycinum. Zhao J, Zeng LH, Li X, Dong XP, Yan YM, Cheng YX J Asian Nat Prod Res 01-Oct-2011
doi:10.1080/10286020.2011.600250
PMID:21972806
Bioactive compounds from the aerial parts of Brachystemma calycinum and structural revision of an octacyclopeptide. Zhao J, Zhou LL, Li X, Xiao HB, Hou FF, Cheng YX J Nat Prod 24-Jun-2011
doi:10.1021/NP200048U
PMID:21634415
Cucubalactam and Brachystemin E, Two New Compounds from Caryophyllaceae Jun Zhou, Yong-Xian Cheng, Ning-Hua Tan, Yang Lu, Xu-Ying Liu, Qi-Tai Zheng The Japan Institute of Heterocyclic Chemistry 09-Mar-2009
doi:10.3987/COM-01-9276
Study on the spatial structure of brachystemin C, a new cyclic peptide from Brachystemma calycinum Cheng Wang, Li-Li Zhang, Yang Lu, Qi-Tai Zheng, Yong-Xian Cheng, Jun Zhou, Ning-Hua Tan Elsevier BV 20-Nov-2003
doi:10.1016/J.MOLSTRUC.2003.09.012
Isolation and characterization of Brachystemidines A-E, novel alkaloids from Brachystemma calycinum. Cheng YX, Zhou J, Tan NH, Teng RW, Lu Y, Wang C, Zheng QT J Nat Prod 01-May-2002
doi:10.1021/NP010330C
PMID:12027759

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one 2356 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)O)O)OC2=O)O 328.27 unknown https://doi.org/10.1080/10286020.2011.600250
Bergenin 66065 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)O)O)OC2=O)O 328.27 unknown https://doi.org/10.1080/10286020.2011.600250
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1080/10286020.2011.600250
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
4-Hydroxy-3,5,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one 73815023 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown https://doi.org/10.1080/10286020.2011.600250
Roseoside 9930064 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown https://doi.org/10.1080/10286020.2011.600250
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(6S)-vomifoliol 12444927 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown https://doi.org/10.1021/NP200048U
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol 191 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown https://doi.org/10.1080/10286020.2011.600250
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown https://doi.org/10.1080/10286020.2011.600250
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
cyclo[Ala-Ala-Tyr-Pro-Pro-aIle-Gly-Val] 163041975 Click to see CCC(C)C1C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)N3CCCC3C(=O)N1)CC4=CC=C(C=C4)O)C)C)C(C)C 768.90 unknown https://doi.org/10.1016/J.MOLSTRUC.2003.09.012
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
cyclo[DL-Ala-DL-Ala-DL-Tyr-DL-Pro-DL-Pro-DL-xiIle-Gly-DL-Val] 163041974 Click to see CCC(C)C1C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)N3CCCC3C(=O)N1)CC4=CC=C(C=C4)O)C)C)C(C)C 768.90 unknown https://doi.org/10.1016/J.MOLSTRUC.2003.09.012
Iizlikhgmwghpv-obrbypsjsa- 11147317 Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NCC(=O)N3CCCC3C(=O)N1)C(C)CC)CC(C)C)CC(=O)N)CC4=CNC5=CC=CC=C54 891.10 unknown https://doi.org/10.3987/COM-01-9276
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
(2R,3S,4S,5R)-2,5-bis(hydroxymethyl)-2-pentoxyoxolane-3,4-diol 102443008 Click to see CCCCCOC1(C(C(C(O1)CO)O)O)CO 250.29 unknown https://doi.org/10.1080/10286020.2011.600250
(2S,3S,4S,5R)-2,5-bis(hydroxymethyl)-2-methoxyoxolane-3,4-diol 6325664 Click to see COC1(C(C(C(O1)CO)O)O)CO 194.18 unknown https://doi.org/10.1080/10286020.2011.600250
(2S,3S,4S,5R)-2,5-bis(hydroxymethyl)-2-pentoxyoxolane-3,4-diol 123294240 Click to see CCCCCOC1(C(C(C(O1)CO)O)O)CO 250.29 unknown https://doi.org/10.1080/10286020.2011.600250
alpha-D-Fructofuranoside, ethyl 14057170 Click to see CCOC1(C(C(C(O1)CO)O)O)CO 208.21 unknown https://doi.org/10.1080/10286020.2011.600250
Ethyl beta-D-fructofuranoside 11769694 Click to see CCOC1(C(C(C(O1)CO)O)O)CO 208.21 unknown https://doi.org/10.1080/10286020.2011.600250
methyl beta-D-fructofuranoside 128889 Click to see COC1(C(C(C(O1)CO)O)O)CO 194.18 unknown https://doi.org/10.1080/10286020.2011.600250
Methylbeta-D-fructofuranoside 14055124 Click to see COC1(C(C(C(O1)CO)O)O)CO 194.18 unknown https://doi.org/10.1080/10286020.2011.600250
> Organoheterocyclic compounds / Benzofurans
6-Hydroxy-4,4,7a-trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one 14334 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1021/NP200048U
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1021/NP200048U
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(2R)-2-hydroxy-3-(hydroxymethyl)-2H-furan-5-one 162867978 Click to see C1=C(C(OC1=O)O)CO 130.10 unknown https://doi.org/10.1080/10286020.2011.600250
> Organoheterocyclic compounds / Furans / Furoic acid and derivatives / Furoic acids
3-Furoic acid 10268 Click to see C1=COC=C1C(=O)O 112.08 unknown https://doi.org/10.1080/10286020.2011.600250
> Organoheterocyclic compounds / Oxepanes
4-(4-Hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]hept-1-yl)-3-buten-2-one 181574 Click to see CC(=O)C=CC12C(CC(CC1(O2)C)O)(C)C 224.30 unknown https://doi.org/10.1021/NP200048U
Annuionone D 14605579 Click to see CC(=O)C=CC12C(CC(CC1(O2)C)O)(C)C 224.30 unknown https://doi.org/10.1021/NP200048U
> Organoheterocyclic compounds / Pyrroles / Pyrrole carboxylic acids and derivatives
[(2R)-2-(3,5-dihydroxy-2-oxopyrrolidin-1-yl)-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 11066790 Click to see C1C=C(C(O1)N2C(CC(C2=O)O)O)COC(=O)C3=CC=CN3 308.29 unknown https://doi.org/10.1021/NP010330C
[(2R)-2-[(2R)-2-hydroxy-5-oxopyrrolidin-1-yl]-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 162847682 Click to see C1CC(=O)N(C1O)C2C(=CCO2)COC(=O)C3=CC=CN3 292.29 unknown https://doi.org/10.1021/NP010330C
[(2R)-2-[(2R)-2-methoxy-5-oxopyrrolidin-1-yl]-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 163019005 Click to see COC1CCC(=O)N1C2C(=CCO2)COC(=O)C3=CC=CN3 306.31 unknown https://doi.org/10.1021/NP010330C
[(2R)-2-[(3R,5R)-3-hydroxy-5-methoxy-2-oxopyrrolidin-1-yl]-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 163195669 Click to see COC1CC(C(=O)N1C2C(=CCO2)COC(=O)C3=CC=CN3)O 322.31 unknown https://doi.org/10.1021/NP010330C
[(2R)-2-[(3R,5S)-3,5-dihydroxy-2-oxopyrrolidin-1-yl]-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 163185248 Click to see C1C=C(C(O1)N2C(CC(C2=O)O)O)COC(=O)C3=CC=CN3 308.29 unknown https://doi.org/10.1021/NP010330C
[(2S)-2-[(2R)-2-hydroxy-5-oxopyrrolidin-1-yl]-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 162847680 Click to see C1CC(=O)N(C1O)C2C(=CCO2)COC(=O)C3=CC=CN3 292.29 unknown https://doi.org/10.1021/NP200048U
[(2S)-2-[(2R)-2-methoxy-5-oxopyrrolidin-1-yl]-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 163019004 Click to see COC1CCC(=O)N1C2C(=CCO2)COC(=O)C3=CC=CN3 306.31 unknown https://doi.org/10.1021/NP200048U
https://doi.org/10.1021/NP010330C
[(2S)-2-[(2S)-2-hydroxy-5-oxopyrrolidin-1-yl]-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 162847681 Click to see C1CC(=O)N(C1O)C2C(=CCO2)COC(=O)C3=CC=CN3 292.29 unknown https://doi.org/10.1021/NP010330C
[(2S)-2-[(3R,5S)-3-hydroxy-5-methoxy-2-oxopyrrolidin-1-yl]-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 162931521 Click to see COC1CC(C(=O)N1C2C(=CCO2)COC(=O)C3=CC=CN3)O 322.31 unknown https://doi.org/10.1021/NP200048U
[(2S)-2-[(3R,5S)-3,5-dihydroxy-2-oxopyrrolidin-1-yl]-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 162945751 Click to see C1C=C(C(O1)N2C(CC(C2=O)O)O)COC(=O)C3=CC=CN3 308.29 unknown https://doi.org/10.1021/NP010330C
[(2S)-2-[(3S,5S)-3-hydroxy-5-methoxy-2-oxopyrrolidin-1-yl]-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 162931520 Click to see COC1CC(C(=O)N1C2C(=CCO2)COC(=O)C3=CC=CN3)O 322.31 unknown https://doi.org/10.1021/NP010330C
[(5S)-5-[(2R)-2-methoxy-5-oxopyrrolidin-1-yl]-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 636754 Click to see COC1CCC(=O)N1C2C=C(CO2)COC(=O)C3=CC=CN3 306.31 unknown https://doi.org/10.1021/NP010330C
https://doi.org/10.1021/NP200048U
[(5S)-5-[(2S)-2-methoxy-5-oxopyrrolidin-1-yl]-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 162852807 Click to see COC1CCC(=O)N1C2C=C(CO2)COC(=O)C3=CC=CN3 306.31 unknown https://doi.org/10.1021/NP010330C
[2-(2-hydroxy-5-oxopyrrolidin-1-yl)-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 73820776 Click to see C1CC(=O)N(C1O)C2C(=CCO2)COC(=O)C3=CC=CN3 292.29 unknown https://doi.org/10.1021/NP010330C
https://doi.org/10.1021/NP200048U
[2-(2-methoxy-5-oxopyrrolidin-1-yl)-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 21672074 Click to see COC1CCC(=O)N1C2C(=CCO2)COC(=O)C3=CC=CN3 306.31 unknown https://doi.org/10.1021/NP010330C
https://doi.org/10.1021/NP200048U
[2-(3-hydroxy-5-methoxy-2-oxopyrrolidin-1-yl)-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 21672075 Click to see COC1CC(C(=O)N1C2C(=CCO2)COC(=O)C3=CC=CN3)O 322.31 unknown https://doi.org/10.1021/NP200048U
https://doi.org/10.1021/NP010330C
[2-(3,5-dihydroxy-2-oxopyrrolidin-1-yl)-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 21672077 Click to see C1C=C(C(O1)N2C(CC(C2=O)O)O)COC(=O)C3=CC=CN3 308.29 unknown https://doi.org/10.1021/NP010330C
[5-(2-methoxy-5-oxopyrrolidin-1-yl)-2,5-dihydrofuran-3-yl]methyl 1H-pyrrole-2-carboxylate 21672073 Click to see COC1CCC(=O)N1C2C=C(CO2)COC(=O)C3=CC=CN3 306.31 unknown https://doi.org/10.1021/NP010330C
https://doi.org/10.1021/NP200048U
Brachystemidine A 10892118 Click to see COC1CCC(=O)N1C2C=C(CO2)COC(=O)C3=CC=CN3 306.31 unknown https://doi.org/10.1021/NP010330C
Brachystemidine B 10859738 Click to see COC1CCC(=O)N1C2C(=CCO2)COC(=O)C3=CC=CN3 306.31 unknown https://doi.org/10.1021/NP010330C
Brachystemidine C 11023697 Click to see COC1CC(C(=O)N1C2C(=CCO2)COC(=O)C3=CC=CN3)O 322.31 unknown https://doi.org/10.1021/NP010330C
Brachystemidine D 21672076 Click to see C1CC(=O)N(C1O)C2C(=CCO2)COC(=O)C3=CC=CN3 292.29 unknown https://doi.org/10.1021/NP010330C
> Organoheterocyclic compounds / Pyrroles / Pyrrole carboxylic acids and derivatives / Pyrrole carboxylic acids / Pyrrole 2-carboxylic acids
Pyrrole-2-carboxylic acid 12473 Click to see C1=CNC(=C1)C(=O)O 111.10 unknown https://doi.org/10.1021/NP200048U
https://doi.org/10.1080/10286020.2011.600250
> Organoheterocyclic compounds / Tetrahydrofurans
[(2R,3S,4S)-2,4-diethoxyoxolan-3-yl]methanol 162918830 Click to see CCOC1COC(C1CO)OCC 190.24 unknown https://doi.org/10.1080/10286020.2011.600250
[(3S,4R,5R)-4,5-diethoxyoxolan-3-yl]methanol 162881460 Click to see CCOC1C(COC1OCC)CO 190.24 unknown https://doi.org/10.1080/10286020.2011.600250

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