PlantaeDB Logo
Login Sign-up

Elateriospermum tapos

Elateriospermum tapos - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID6440390b76a30243614868
Scientific name Elateriospermum tapos
Authority Blume
First published in Bijdr. Fl. Ned. Ind. : 621 (1826)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Elateriospermum rhizophorum Boerl. & Koord. Syst. Verz. 2: 28 (1910)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Spanish elateriospermeae
Malay pokok perah
Malay tapus
Malay perah
su tapos

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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
    • Indo-China
      • Thailand
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000948026
Tropicos 50266297
KEW urn:lsid:ipni.org:names:345259-1
The Plant List kew-66382
Open Tree Of Life 370208
NCBI Taxonomy 212299
IPNI 345259-1
iNaturalist 427576
GBIF 3071462
Freebase /m/079tbw
EOL 1145601

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
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Editorial: Obesity, hyperglycemia, and pregnancy: from pathophysiology to clinical practice - volume II Succurro E, Vitacolonna E Front Endocrinol (Lausanne) 07-Sep-2023
PMCID:PMC10520456
doi:10.3389/fendo.2023.1283609
PMID:37766677
Made in the Womb: Maternal Programming of Offspring Cardiovascular Function by an Obesogenic Womb Diniz MS, Grilo LF, Tocantins C, Falcão-Pires I, Pereira SP Metabolites 13-Jul-2023
PMCID:PMC10386510
doi:10.3390/metabo13070845
PMID:37512552
The role of Elateriospermum tapos yoghurt in mitigating high-fat dietary cause of maternal obesity—an experimental study Naomi R, Rusli RN, Othman F, Balan SS, Abidin AZ, Embong H, Teoh SH, Jasni AS, Jumidil SH, Bahari H, Yazid MD Front Endocrinol (Lausanne) 21-Jun-2023
PMCID:PMC10321599
doi:10.3389/fendo.2023.1131830
PMID:37415666
Elateriospermum tapos Yoghurt as a Therapeutic Intervention for Obesity-Associated Cognitive Impairments and Anxiety-like Behaviour in a High Fat Diet Maternal Obese Rat Model Naomi R, Teoh SH, Rusli RN, Embong H, Bahari H, Kumar J Nutrients 15-May-2023
PMCID:PMC10223143
doi:10.3390/nu15102312
PMID:37242195
Remodulation Effect of Elateriospermum tapos Yoghurt on Metabolic Profile of Maternal Obesity Induced Cognitive Dysfunction and Anxiety-like Behavior in Female Offspring—An In Vivo Trial on Sprague Dawley Rats Naomi R, Rusli RN, Teoh SH, Bahari H, Zakaria ZA Foods 11-Apr-2023
PMCID:PMC10137489
doi:10.3390/foods12081613
PMID:37107408
Elateriospermum tapos Yogurt Supplement in Maternal Obese Dams during Pregnancy Modulates the Body Composition of F1 Generation Naomi R, Rusli RN, Othman F, Balan SS, Abidin AZ, Embong H, Teoh SH, Jasni AS, Jumidil SH, Matraf KS, Zakaria ZA, Bahari H, Yazid MD Nutrients 02-Mar-2023
PMCID:PMC10005445
doi:10.3390/nu15051258
PMID:36904258
Neuroprotective Potential of Biflavone Ginkgetin: A Review Tatlı Çankaya İİ, Devkota HP, Zengin G, Šamec D Life (Basel) 16-Feb-2023
PMCID:PMC9964866
doi:10.3390/life13020562
PMID:36836918
Kaempferol: Antimicrobial Properties, Sources, Clinical, and Traditional Applications Periferakis A, Periferakis K, Badarau IA, Petran EM, Popa DC, Caruntu A, Costache RS, Scheau C, Caruntu C, Costache DO Int J Mol Sci 30-Nov-2022
PMCID:PMC9740324
doi:10.3390/ijms232315054
PMID:36499380
Free Linoleic Acid and Oleic Acid Reduce Fat Digestion and Absorption In Vivo as Potent Pancreatic Lipase Inhibitors Derived from Sesame Meal Li X, Morita S, Yamada H, Koga K, Ota W, Furuta T, Yamatsu A, Kim M Molecules 01-Aug-2022
PMCID:PMC9370031
doi:10.3390/molecules27154910
PMID:35956860
E. tapos Yoghurt—A View from Nutritional Composition and Toxicological Evaluation Naomi R, Rusli RN, Balan SS, Othman F, Jasni AS, Jumidil SH, Bahari H, Yazid MD Foods 27-Jun-2022
PMCID:PMC9265303
doi:10.3390/foods11131903
PMID:35804719
In vitro α-glucosidase inhibitory activity of Tamarix nilotica shoot extracts and fractions Daou M, Elnaker NA, Ochsenkühn MA, Amin SA, Yousef AF, Yousef LF PLoS One 14-Mar-2022
PMCID:PMC8920278
doi:10.1371/journal.pone.0264969
PMID:35286313
Hydroethanolic Extract of Prunus domestica L.: Metabolite Profiling and In Vitro Modulation of Molecular Mechanisms Associated to Cardiometabolic Diseases Ullah H, Sommella E, Santarcangelo C, D’Avino D, Rossi A, Dacrema M, Minno AD, Di Matteo G, Mannina L, Campiglia P, Magni P, Daglia M Nutrients 14-Jan-2022
PMCID:PMC8778072
doi:10.3390/nu14020340
PMID:35057523
High-throughput sequencing reveals dietary segregation in Malaysian babblers Mansor MS, Rozali FZ, Davies S, Nor SM, Ramli R Curr Zool 03-Sep-2021
PMCID:PMC9450176
doi:10.1093/cz/zoab074
PMID:36090137
A Review on Obesity Management through Natural Compounds and a Green Nanomedicine-Based Approach Bhardwaj M, Yadav P, Vashishth D, Sharma K, Kumar A, Chahal J, Dalal S, Kataria SK Molecules 28-May-2021
PMCID:PMC8198321
doi:10.3390/molecules26113278
PMID:34071722

Phytochemical Profile Top

Add a new one!
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 / Tetralins
2-[(1R,2S)-1-(carboxymethyl)-5-ethenyl-7-hydroxy-1,6-dimethyl-3,4-dihydro-2H-naphthalen-2-yl]-2-methylpropanoic acid 162970036 Click to see CC1=C(C=C2C(=C1C=C)CCC(C2(C)CC(=O)O)C(C)(C)C(=O)O)O 346.40 unknown https://doi.org/10.1021/NP070629G
2-[1-(carboxymethyl)-5-ethenyl-7-hydroxy-1,6-dimethyl-3,4-dihydro-2H-naphthalen-2-yl]-2-methylpropanoic acid 74318680 Click to see CC1=C(C=C2C(=C1C=C)CCC(C2(C)CC(=O)O)C(C)(C)C(=O)O)O 346.40 unknown https://doi.org/10.1021/NP070629G
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4S,6R,7S,9S,10R,13S)-5,5,6,7,9,13-hexamethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-12-one 162882946 Click to see CC1CC2(C(CCC34C2CC(=O)C(C3)(C=C4)C)C(C1C)(C)C)C 314.50 unknown https://doi.org/10.1021/NP070629G
5,5,6,7,9,13-Hexamethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-12-one 162882945 Click to see CC1CC2(C(CCC34C2CC(=O)C(C3)(C=C4)C)C(C1C)(C)C)C 314.50 unknown https://doi.org/10.1021/NP070629G
yucalexin B-22 44448252 Click to see CC1(C2CCC34CC(C=C3)(C(=O)CC4C2(CC(C1O)O)C)C)C 318.40 unknown https://doi.org/10.1021/NP070629G
yucalexin P-15 44448251 Click to see CC1(C2CC=C3C(C(C(=O)C=C3C2(CC(=O)C1O)C)(C)C=C)O)C 330.40 unknown https://doi.org/10.1021/NP070629G
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
5a,5b,8,8,11a,13b-Hexamethyl-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-9-ol 604951 Click to see CC(=C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP070629G
hopenol B 10093995 Click to see CC(=C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP070629G
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(4aS,6aR,6bR,8aR,10S,12aR,14aS,14bR)-10-hydroxy-2,2,6b,9,9,12a,14a-heptamethyl-1,3,4,5,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydropicene-4a-carboxylic acid 637268 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C(=O)O)C 456.70 unknown https://doi.org/10.1021/NP070629G
10-Hydroxy-2,2,6b,9,9,12a,14a-heptamethyl-1,3,4,5,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydropicene-4a-carboxylic acid 14313023 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C(=O)O)C 456.70 unknown https://doi.org/10.1021/NP070629G
Acetyl aleuritolic acid 161616 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1021/NP070629G
Acetylaleuritolic acid 429885 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1021/NP070629G
Maprounic acid 161527 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C(=O)O)C 456.70 unknown https://doi.org/10.1021/NP070629G
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicen-3-yl) hexadecanoate 163100987 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5=CC(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)(C)C)C 665.10 unknown https://doi.org/10.1016/S0031-9422(00)85245-0
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 345510 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)85245-0
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) hexadecanoate 13915598 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 665.10 unknown https://doi.org/10.1016/S0031-9422(00)85245-0
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate 163187379 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)85245-0
[(3S,4aR,6aR,6bS,8aR,12aS,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 51398128 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)85245-0
beta-Amyrin palmitate 13915599 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 665.10 unknown https://doi.org/10.1016/S0031-9422(00)85245-0
Germanicol acetate 14167342 Click to see CC(=O)OC1CCC2(C3CCC4C5=CC(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)(C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)85245-0
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1021/NP070629G
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1021/NP070629G
https://doi.org/10.1016/S0031-9422(00)85245-0
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1021/NP070629G
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1021/NP070629G
Oleana-18-ene-3beta-ol hexadecanoate 102272876 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5=CC(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)(C)C)C 665.10 unknown https://doi.org/10.1016/S0031-9422(00)85245-0
Taraxasterol acetate 13889352 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)85245-0
Taraxasterol, acetate 344468 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)85245-0
Taraxerol, acetate 345509 Click to see CC(=O)OC1CCC2(C3CCC4C5=CC(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)(C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)85245-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids / 3-carboxy steroids
(1R,2R,4aR,6aS,10aS,10bS,12aR)-1-(carboxymethyl)-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1,4a,9,9,10b-pentamethyl-3,4,6,7,8,10,10a,11,12,12a-decahydro-2H-chrysene-6a-carboxylic acid 101844037 Click to see CC1(CCC2(CC=C3C4(CCC(C(C4CCC3(C2C1)C)(C)CC(=O)O)C(C)(C)C(=O)OC)C)C(=O)O)C 516.70 unknown https://doi.org/10.1021/NP070629G
(1R,4aR,6aS,10bS)-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1-(2-methoxy-2-oxoethyl)-1,4a,9,9,10b-pentamethyl-3,4,6,7,8,10,10a,11,12,12a-decahydro-2H-chrysene-6a-carboxylic acid 44448123 Click to see CC1(CCC2(CC=C3C4(CCC(C(C4CCC3(C2C1)C)(C)CC(=O)OC)C(C)(C)C(=O)OC)C)C(=O)O)C 530.70 unknown https://doi.org/10.1021/NP070629G
1-(carboxymethyl)-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1,4a,9,9,10b-pentamethyl-3,4,6,7,8,10,10a,11,12,12a-decahydro-2H-chrysene-6a-carboxylic acid 74318628 Click to see CC1(CCC2(CC=C3C4(CCC(C(C4CCC3(C2C1)C)(C)CC(=O)O)C(C)(C)C(=O)OC)C)C(=O)O)C 516.70 unknown https://doi.org/10.1021/NP070629G
2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1-(2-methoxy-2-oxoethyl)-1,4a,9,9,10b-pentamethyl-3,4,6,7,8,10,10a,11,12,12a-decahydro-2H-chrysene-6a-carboxylic acid 74318627 Click to see CC1(CCC2(CC=C3C4(CCC(C(C4CCC3(C2C1)C)(C)CC(=O)OC)C(C)(C)C(=O)OC)C)C(=O)O)C 530.70 unknown https://doi.org/10.1021/NP070629G
2,3-Secotaraxera-14-ene-2,3,28-trioic acid 2,3-dimethyl ester 101844036 Click to see CC1(CCC2(CC=C3C4(CCC(C(C4CCC3(C2C1)C)(C)CC(=O)OC)C(C)(C)C(=O)OC)C)C(=O)O)C 530.70 unknown https://doi.org/10.1021/NP070629G
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / 2-deoxystreptamine aminoglycosides / 4,6-disubstituted 2-deoxystreptamines
Kanamycin 6032 Click to see C1C(C(C(C(C1N)OC2C(C(C(C(O2)CN)O)O)O)O)OC3C(C(C(C(O3)CO)O)N)O)N 484.50 unknown https://doi.org/10.1021/NP070629G
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
Ellipticine 3213 Click to see CC1=C2C=CN=CC2=C(C3=C1NC4=CC=CC=C43)C 246.31 unknown https://doi.org/10.1021/NP070629G
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives
Isoniazid 3767 Click to see C1=CN=CC=C1C(=O)NN 137.14 unknown https://doi.org/10.1021/NP070629G
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown https://doi.org/10.1021/NP070629G
Ginkgetin 5271805 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O 566.50 unknown https://doi.org/10.1021/NP070629G
Putraflavone 5320646 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)OC)O)O 566.50 unknown https://doi.org/10.1021/NP070629G
Sequoiaflavone 5484010 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O)O 552.50 unknown https://doi.org/10.1021/NP070629G
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1021/NP070629G

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.