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Bolbostemma paniculatum

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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 UUID64400d6676075574680215
Scientific name Bolbostemma paniculatum
Authority Franquet
First published in Bull. Mus. Natl. Hist. Nat. , sér. 2, 2: 327 (1930)

Description Top

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Synonyms Top

Scientific name Authority First published in
Mitrosicyos paniculatus Maxim. Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 113 (1859)
Schizopepon fargesii Gagnep. Bull. Mus. Natl. Hist. Nat. 24: 377 (1918)
Actinostemma multilobum Harms Bot. Jahrb. Syst. 29: 602 (1901)
Actinostemma paniculatum Maxim. ex Cogn. Monogr. Phan. 3: 920 (1881)

Common names Top

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Language Common/alternative name
Chinese 假贝母
Chinese 土贝母

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-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000568244
UNII 1775OPK1YG
Tropicos 50043457
KEW urn:lsid:ipni.org:names:291523-1
The Plant List kew-2678947
Open Tree Of Life 351037
NCBI Taxonomy 381652
IPNI 291523-1
GBIF 3623332
EOL 5736742

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 and therapeutic potential of SIRTs in sepsis You J, Li Y, Chong W Front Immunol 16-Apr-2024
PMCID:PMC11058839
doi:10.3389/fimmu.2024.1394925
PMID:38690282
Merremia emarginata Extract Potentiates the Inhibition of Human Colon Cancer Cells (HT-29) via the Modulation of Caspase-3/Bcl-2-Mediated Pathways Benedict A, Suresh V, Selvamani M, Jayaraman S, Hussein MA Cureus 16-Mar-2024
PMCID:PMC11019472
doi:10.7759/cureus.56300
PMID:38629020
The complete chloroplast genome sequence of Thladiantha nudiflora Hemsl. ex F.B.Forbes & Hemsl. 1887 (Cucurbitaceae) Zhao YY, Chen MM, Duan BL, Xie QZ, Miao Q Mitochondrial DNA B Resour 25-Jan-2024
PMCID:PMC10812858
doi:10.1080/23802359.2024.2305402
PMID:38282981
Unraveling the Action Mechanism of Tubeimoside-1 against Tumor Microvessels via Network Pharmacology and Experimental Validation Yang Y, Wang Q, Zhan F J Cancer 01-Jan-2024
PMCID:PMC10788730
doi:10.7150/jca.90391
PMID:38230220
Natural Anticancer Molecules and Their Therapeutic Potential Zhang J, Leung EL Int J Mol Sci 08-Nov-2023
PMCID:PMC10671740
doi:10.3390/ijms242216066
PMID:38003270
Advances in Immunotherapy for Hepatocellular Carcinoma (HCC) Bicer F, Kure C, Ozluk AA, El-Rayes BF, Akce M Curr Oncol 07-Nov-2023
PMCID:PMC10670350
doi:10.3390/curroncol30110711
PMID:37999131
Recent Advances in the Application of Cucurbitacins as Anticancer Agents Zieniuk B, Pawełkowicz M Metabolites 14-Oct-2023
PMCID:PMC10608718
doi:10.3390/metabo13101081
PMID:37887406
Tubeimoside-1 Enhances TRAIL-Induced Apoptotic Cell Death through STAMBPL1-Mediated c-FLIP Downregulation Song SR, Seo SU, Woo SM, Yoon JY, Yook S, Kwon TK Int J Mol Sci 24-Jul-2023
PMCID:PMC10380985
doi:10.3390/ijms241411840
PMID:37511599
Triterpenes as Potential Drug Candidates for Rheumatoid Arthritis Treatment Faustino C, Pinheiro L, Duarte N Life (Basel) 05-Jul-2023
PMCID:PMC10381804
doi:10.3390/life13071514
PMID:37511889
The Recent Research Progress of NF-κB Signaling on the Proliferation, Migration, Invasion, Immune Escape and Drug Resistance of Glioblastoma Shi P, Xu J, Cui H Int J Mol Sci 19-Jun-2023
PMCID:PMC10298967
doi:10.3390/ijms241210337
PMID:37373484
Progress in the discovery and development of small molecule methuosis inducers Ye T, Shan P, Zhang H RSC Med Chem 25-May-2023
PMCID:PMC10429883
doi:10.1039/d3md00155e
PMID:37593581
Wnt/β‐catenin signaling pathway inhibitors, glycyrrhizic acid, solanine, polyphyllin I, crocin, hypericin, tubeimoside‐1, diosmin, and rutin in medicinal plants have better binding affinities and anticancer properties: Molecular docking and ADMET study Egbuna C, Patrick‐Iwuanyanwu KC, Onyeike EN, Uche CZ, Ogoke UP, Riaz M, Ibezim EN, Khan J, Adedokun KA, Imodoye SO, Bello IO, Awuchi CG Food Sci Nutr 04-May-2023
PMCID:PMC10345731
doi:10.1002/fsn3.3405
PMID:37457177
Pyrrole-2-carboxaldehydes: Origins and Physiological Activities Matsugo S, Nakamura Y Molecules 13-Mar-2023
PMCID:PMC10058459
doi:10.3390/molecules28062599
PMID:36985566
Inhibiting Angiogenesis by Anti-Cancer Saponins: From Phytochemistry to Cellular Signaling Pathways Majnooni MB, Fakhri S, Ghanadian SM, Bahrami G, Mansouri K, Iranpanah A, Farzaei MH, Mojarrab M Metabolites 22-Feb-2023
PMCID:PMC10052344
doi:10.3390/metabo13030323
PMID:36984763
Adjuvant activity of tubeimosides by mediating the local immune microenvironment Han Z, Jin J, Chen X, He Y, Sun H Front Immunol 10-Feb-2023
PMCID:PMC9950507
doi:10.3389/fimmu.2023.1108244
PMID:36845089

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
TBMS1 saponin 3034097 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC(CC3C5=CCC6C(C5(C=C4)C)(CCC7C6(CC(C(C7(C)C)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(CO9)OC(=O)CC(C)(CC(=O)O)O)O)O)O)C)C)(C)C)O)OC1C(C(C(CO1)O)O)O)O)O)O 1319.40 unknown https://doi.org/10.1055/S-2006-957831
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,4S,7S,8S,9R,11S,13S,14S,18S,23R,24S,25S,26R,27S,29R,30S,31S,32R,34R,36R,37S,39R,40R,43R,44R,48S,53R,55S,58S,59R)-7,8,18,24,25,26,30,31,37,53,59-undecahydroxy-32,56-bis(hydroxymethyl)-13,18,39,43,50,50,55,56-octamethyl-58-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-3,5,10,12,15,21,28,33,35,57-decaoxadecacyclo[41.9.3.211,14.123,27.136,40.01,48.04,9.029,34.039,44.047,55]nonapentacont-46-ene-2,16,20-trione 146014459 Click to see CC1C2C(C(C(O1)OC3C(C(COC3OC(=O)C45CCC(CC4C6=CCC7C(C6(CC5O)C)(CCC8C7(CC(C(C8(C)CO)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)COC(=O)CC(CC(=O)O2)(C)O)O)O)O)O)C)C)(C)C)O)O)O)OC1C(C(C(CO1)O)O)O 1365.50 unknown https://doi.org/10.1002/CJOC.19880060316
https://doi.org/10.1016/0031-9422(88)80212-7
7,8,18,28,29,35,55,56,58-nonahydroxy-30,54-bis(hydroxymethyl)-13,18,37,41,48,48,53,54-octamethyl-57-[(3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy]-3,5,10,12,15,21,24,26,31,33-decaoxadecacyclo[39.9.3. 6110917 Click to see CC1C2C(C(C(O1)OC3C(C(COC3OC(=O)C45CCC(CC4C6=CCC7C(C6(CC5)C)(CCC8C7(CC(C(C8(C)CO)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(CO1)OC(=O)CC(CC(=O)O2)(C)O)O)O)O)C)C)(C)C)O)O)O)OC1C(C(C(CO1)O)O)O 1319.40 unknown https://doi.org/10.1055/S-2006-959459
https://doi.org/10.1016/0031-9422(88)80212-7
https://doi.org/10.1002/IJC.2910500425
https://doi.org/10.1248/CPB.34.3974
https://doi.org/10.1016/S0040-4039(00)85321-6
Lobatoside H 5462420 Click to see CC1C2C(C(C(O1)OC3C(C(COC3OC(=O)C45CCC(CC4C6=CCC7C(C6(CC5)C)(CCC8C7(CC(C(C8(C)CO)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(CO1)OC(=O)CC(CC(=O)O2)(C)O)O)O)O)C)C)(C)C)O)O)O)OC1C(C(C(CO1)O)O)O 1319.40 unknown https://doi.org/10.1248/CPB.34.3974
https://doi.org/10.1002/IJC.2910500425
https://doi.org/10.1016/0031-9422(88)80212-7
https://doi.org/10.1016/S0040-4039(00)85321-6
https://doi.org/10.1055/S-2006-959459
tubeimoside II 14037387 Click to see CC1C2C(C(C(O1)OC3C(C(COC3OC(=O)C45CCC(CC4C6=CCC7C(C6(CC5O)C)(CCC8C7(CC(C(C8(C)CO)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(CO1)OC(=O)CC(CC(=O)O2)(C)O)O)O)O)C)C)(C)C)O)O)O)OC1C(C(C(CO1)O)O)O 1335.40 unknown https://doi.org/10.1016/0031-9422(88)80212-7
https://doi.org/10.1002/CJOC.19880060316
Tubeimoside III 5489425 Click to see CC1C2C(C(C(O1)OC3C(C(COC3OC(=O)C45CCC(CC4C6=CCC7C(C6(CC5O)C)(CCC8C7(CC(C(C8(C)CO)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)COC(=O)CC(CC(=O)O2)(C)O)O)O)O)O)C)C)(C)C)O)O)O)OC1C(C(C(CO1)O)O)O 1365.50 unknown https://doi.org/10.1016/0031-9422(88)80212-7
https://doi.org/10.1002/CJOC.19880060316
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
beta-D-Glucopyranose, 4-O-beta-D-galactopyranosyl- 294 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1016/S0040-4039(00)85321-6
Gal(a1-4)a-Ido 131632347 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1016/S0040-4039(00)85321-6
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Maltol 8369 Click to see CC1=C(C(=O)C=CO1)O 126.11 unknown https://doi.org/10.1016/S0040-4039(00)85321-6

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