Holoptelea integrifolia - Unknown
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Internal ID UUID644020c3c68da262144642
Scientific name Holoptelea integrifolia
Authority (Roxb.) Planch.
First published in Ann. Sci. Nat., Bot. , sér. 3, 10: 259 (1848)

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Synonyms Top

Scientific name Authority First published in
Ulmus integrifolia Roxb. Pl. Coromandel 1: 56 (1796)

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Language Common/alternative name
Arabic دردار كامل متكامل الأوراق
Hindi चिरोल
Malayalam ആവൽ
Marathi वावळा
Burmese ဖျောက်ဆိပ်
Tamil ஆவு மரம்
Thai กระเชา
Chinese 全叶榆

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Nepal
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000724298
KEW urn:lsid:ipni.org:names:854174-1
Open Tree Of Life 582840
NCBI Taxonomy 63066
IPNI 854174-1
iNaturalist 553635
GBIF 4160169
USDA GRIN 19236
Wikipedia Holoptelea_integrifolia

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
Biosynthesis, characterization and study of the application of silver nanoparticle for 4-nitrophenol reduction, and antimicrobial activities Mulu M, Tefera M, Guadie A, Basavaiah K Biotechnol Rep (Amst) 21-Mar-2024
PMCID:PMC10999826
doi:10.1016/j.btre.2024.e00838
PMID:38590717
Ayurvedic clinical decision-making methods to predict, prevent and manage childhood allergic disorders Karthik KP, Dileep A, Rajagopala S, Arun Kumar M, Dharmarajan P, Vellela J J Ayurveda Integr Med 18-Jan-2024
PMCID:PMC10828817
doi:10.1016/j.jaim.2023.100857
PMID:38237455
Casearia tomentosa fruit extracts exposed larvicidal activity and morphological alterations in Culex quinquefasciatus and Aedes albopictus under in vitro and semi field conditions Mandal P, Chandra G BMC Res Notes 02-Jan-2024
PMCID:PMC10762963
doi:10.1186/s13104-023-06663-x
PMID:38167220
The Characterization and Study of Antibacterial, Free Radical Scavenging, and Anticancer Potential of Livistona chinensis-Mediated Silver Nanoparticles Saleem A, Ali S, Aftab MN, Shami A, Al-Saeed FA, Mustafa B, Paray BA Molecules 25-Nov-2023
PMCID:PMC10708060
doi:10.3390/molecules28237773
PMID:38067504
Antimicrobial and antiviral evaluation of compounds from Holoptelea integrifolia: in silico supported in vitro study Mohammed HS, Taha EF, Mahrous FS, Sabour R, Abdel-Aziz MM, Ismail LD RSC Adv 03-Nov-2023
PMCID:PMC10624013
doi:10.1039/d3ra05978b
PMID:37928846
Exploring the Potential of Extracts from Sloanea medusula and S. calva: Formulating Two Skincare Gels with Antioxidant, Sun Protective Factor, and Anti-Candida albicans Activities Quintero-Rincón P, Mesa-Arango AC, Flórez-Acosta OA, Zapata-Zapata C, Stashenko EE, Pino-Benítez N Pharmaceuticals (Basel) 11-Jul-2023
PMCID:PMC10384365
doi:10.3390/ph16070990
PMID:37513902
Editorial: A Feasible Approach for Natural Products to Treatment of Diseases Ooi SL, Pak SC Molecules 28-Apr-2023
PMCID:PMC10180473
doi:10.3390/molecules28093791
PMID:37175201
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
Green Biofabrication of Silver Nanoparticles of Potential Synergistic Activity with Antibacterial and Antifungal Agents against Some Nosocomial Pathogens Al-Otibi FO, Yassin MT, Al-Askar AA, Maniah K Microorganisms 04-Apr-2023
PMCID:PMC10144991
doi:10.3390/microorganisms11040945
PMID:37110368
Phytochemical cocktail of Asanadi ganaextract in the management of diabetes Dulala RK, Balraj M, Chandrashekar S, N M, Rajapandiyan N, Badrachalam R, Mani V Bioinformation 31-Mar-2023
PMCID:PMC10557453
doi:10.6026/97320630019299
PMID:37808369
Molecular Phylogeny and Morphology Reveal Four Novel Species of Corynespora and Kirschsteiniothelia (Dothideomycetes, Ascomycota) from China: A Checklist for Corynespora Reported Worldwide Liu J, Hu Y, Luo X, Castañeda-Ruíz RF, Xia J, Xu Z, Cui R, Shi X, Zhang L, Ma J J Fungi (Basel) 12-Jan-2023
PMCID:PMC9863821
doi:10.3390/jof9010107
PMID:36675928
Pharmacodynamic appraisal of wound-healing herbs of Sushruta Samhita Kumar V, Nesari TM, Ghildiyal S, Sherkhane R Ayu 07-Dec-2022
PMCID:PMC9893898
doi:10.4103/ayu.AYU_34_20
PMID:36743272
Effect of Holoptelea integrifolia (Roxb.) Planch. n-Hexane Extract and Its Bioactive Compounds on Wound Healing and Anti-Inflammatory Activity Somwong K, Lertpatipanpong P, Nimlamool W, Panya A, Tragoolpua Y, Yongsawas R, Gritsanapan W, Pandith H, Baek SJ Molecules 04-Dec-2022
PMCID:PMC9738392
doi:10.3390/molecules27238540
PMID:36500633
Ionizing Radiation: Effective Physical Agents for Economic Crop Seed Priming and the Underlying Physiological Mechanisms Wang J, Zhang Y, Zhou L, Yang F, Li J, Du Y, Liu R, Li W, Yu L Int J Mol Sci 02-Dec-2022
PMCID:PMC9737873
doi:10.3390/ijms232315212
PMID:36499532
Evaluation of Wound Healing Activity of 80% Hydromethanolic Crude Extract and Solvent Fractions of the Leaves of Urtica simensis in Mice Abeje BA, Bekele T, Getahun KA, Asrie AB J Exp Pharmacol 17-Jul-2022
PMCID:PMC9304411
doi:10.2147/JEP.S363676
PMID:35875331

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 / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCO 382.70 unknown https://doi.org/10.1055/S-0028-1099406
1-Octacosanol 68406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO 410.80 unknown https://doi.org/10.1055/S-0028-1099406
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(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-ol 12358398 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1099406
(4aS,6aR,6aR,6bS,8aS,10R,12aS,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162942879 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1055/S-0028-1097519
(4aS,6aS,6aS,6bR,8aR,9S,10R,12aS,14bR)-10-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162902760 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1055/S-0028-1097519
2,3-Dihydroxyolean-12-en-28-oic acid 3694932 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1055/S-0028-1097804
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1055/S-0028-1097519
alpha-Hederagenin 258538 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1055/S-0028-1097519
epi-Maslinic acid 25564831 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1055/S-0028-1097804
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1055/S-0028-1099406
Epifriedelin 15559350 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1099406
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1099406
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1055/S-0028-1099406
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1099406
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1099406
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1099406

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