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Sarcolobus globosus

Sarcolobus globosus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643ffc068798d208778745
Scientific name Sarcolobus globosus
Authority Wall.
First published in Asiat. Res. 12: 568 (1816)

Description Top

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Sarcolobus globosus is a twining shrub native to tropical regions of Asia. It is found in mangrove forests of India, China, Thailand, Malaysia, Myanmar-Burma, the Philippines and Indonesia. The leaves and rhizomes are used as medicine, while the seeds are poisonous and used as bait to kill dogs and wild animals. Chemical constituents of the plant include flavonoids, rotenoids, phenolyc glycosides, isoflavones, and barbigerone. It is listed by the FDA as poisonous and has been used to kill cats and tigers. It is also used as an herbal medicine for treatment of rheumatism, dengue and fever, and is known to have significant antioxidant and anti-cancer properties.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
mnw ခရာမ်၊ တၞံ
Thai เถาหัวลิง
Chinese 球状毒虎藤

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Sarcolobus globosus subsp. globosus Unknown
Sarcolobus globosus subsp. peregrinus (Blanco) Rintz Blumea 26: 76 (1980)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Area

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© OpenStreetMap
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
    • Indo-China
      • Andaman Islands
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000431188
Tropicos 2602211
KEW urn:lsid:ipni.org:names:100926-1
The Plant List kew-2473339
Open Tree Of Life 5784551
NCBI Taxonomy 2306791
IPNI 100926-1
iNaturalist 426597
GBIF 7311731
Freebase /m/0bs8px7
Elurikkus 586965
USDA GRIN 418466
Wikipedia Sarcolobus_globosus

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
Barbigerone prevents scopolamine-induced memory impairment in rats by inhibiting oxidative stress and acetylcholinesterase levels AlGhamdi SA, Al-Abbasi FA, Alghamdi AM, Omer AB, Afzal O, Altamimi AS, Alamri A, Alzarea SI, Almalki WH, Kazmi I R Soc Open Sci 12-Apr-2023
PMCID:PMC10090886
doi:10.1098/rsos.230013
PMID:37063992
Bioprospecting of underutilized mangrove fruits used by coastal communities in the Odisha coast, India: a review Rout P Food Sci Biotechnol 09-Dec-2021
PMCID:PMC8817954
doi:10.1007/s10068-021-01013-8
PMID:35186345
Anti-Bacterial, Anti-Diarrheal, and Cytotoxic Activities of Edible Fruits in the Sundarbans Mangrove Forest of Bangladesh Hosen MZ, Biswas A, Islam MR, Hossain SJ Prev Nutr Food Sci 30-Jun-2021
PMCID:PMC8276707
doi:10.3746/pnf.2021.26.2.192
PMID:34316484
S N/A Saunders Comprehensive Veterinary Dictionary 16-Oct-2020
PMCID:PMC9771675
doi:10.1016/B978-0-7020-7463-9.50027-6
P N/A Saunders Comprehensive Veterinary Dictionary 16-Oct-2020
PMCID:PMC9771673
doi:10.1016/B978-0-7020-7463-9.50024-0
Phytochemicals: Extraction, Isolation, and Identification of Bioactive Compounds from Plant Extracts Altemimi A, Lakhssassi N, Baharlouei A, Watson DG, Lightfoot DA Plants (Basel) 22-Sep-2017
PMCID:PMC5750618
doi:10.3390/plants6040042
PMID:28937585
Molecular understanding of lung cancers-A review Singh CR, Kathiresan K Asian Pac J Trop Biomed 01-May-2014
PMCID:PMC4025309
doi:10.12980/APJTB.4.2014C597
PMID:25183110
Biological activities and chemical constituents of some mangrove species from Sundarban estuary: An overview Simlai A, Roy A Pharmacogn Rev 01-Jul-2013
PMCID:PMC3841995
doi:10.4103/0973-7847.120518
PMID:24347925
Chemical, Antioxidant and Antimicrobial Investigations of Pinus cembra L. Bark and Needles Apetrei CL, Tuchilus C, Aprotosoaie AC, Oprea A, Malterud KE, Miron A Molecules 13-Sep-2011
PMCID:PMC6264604
doi:10.3390/molecules16097773
PMID:22143542
Rotenoids and isoflavones from Sarcolobus globosus. Wangensteen H, Alamgir M, Rajia S, Samuelsen AB, Malterud KE Planta Med 01-Aug-2005
doi:10.1055/S-2005-864182
PMID:16142641

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
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
6,7-Dimethoxychroman-4-one 11469836 Click to see COC1=C(C=C2C(=C1)C(=O)CCO2)OC 208.21 unknown https://doi.org/10.1055/S-2005-864182
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
13-Homo-13-oxa-6a,12a-dehydrodeguelin 10092854 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)OC5=CC(=C(C=C5OC4)OC)OC)C 408.40 unknown https://doi.org/10.1055/S-2005-864182
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
(3S,5R)-4,4-dimethyl-12-(2,4,5-trimethoxyphenyl)-6,14-dioxatetracyclo[8.4.0.02,7.03,5]tetradeca-1(10),2(7),8,12-tetraen-11-one 163003906 Click to see CC1(C2C1OC3=C2C4=C(C=C3)C(=O)C(=CO4)C5=CC(=C(C=C5OC)OC)OC)C 394.40 unknown https://doi.org/10.1055/S-2005-864182
4,4-Dimethyl-12-(2,4,5-trimethoxyphenyl)-6,14-dioxatetracyclo[8.4.0.02,7.03,5]tetradeca-1(10),2(7),8,12-tetraen-11-one 102180655 Click to see CC1(C2C1OC3=C2C4=C(C=C3)C(=O)C(=CO4)C5=CC(=C(C=C5OC)OC)OC)C 394.40 unknown https://doi.org/10.1055/S-2005-864182
Barbigerone 156793 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC=C(C3=O)C4=CC(=C(C=C4OC)OC)OC)C 394.40 unknown https://doi.org/10.1055/S-2005-864182
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(1)Benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(6aH)-one,12,12a-dihydro-6a-hydroxy-8,9-dimethoxy-, (6aS-cis)- 183157 Click to see COC1=C(C=C2C(=C1)C3(C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)O)OC 368.30 unknown https://doi.org/10.1055/S-2005-864182
(1R,14R)-11,14-dihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.0^{3,12.0^{4,9.0^{15,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one 13846202 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C 426.40 unknown https://doi.org/10.1055/S-2005-864182
(1R,14S)-14-hydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one 11962145 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C 410.40 unknown https://doi.org/10.1055/S-2005-864182
(1R,5R,7S,14R)-14-hydroxy-17,18-dimethoxy-6,6-dimethyl-2,8,21-trioxahexacyclo[12.8.0.03,12.04,9.05,7.015,20]docosa-3(12),4(9),10,15,17,19-hexaen-13-one 26203653 Click to see CC1(C2C1OC3=C2C4=C(C=C3)C(=O)C5(C(O4)COC6=CC(=C(C=C65)OC)OC)O)C 410.40 unknown https://doi.org/10.1055/S-2005-864182
(Rac)-Tephrosin 4485131 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C 410.40 unknown https://doi.org/10.1055/S-2005-864182
11-Hydroxytephrosin 155725 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C 426.40 unknown https://doi.org/10.1055/S-2005-864182
13-Hydroxy-16,17-dimethoxy-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),5,9,14,16,18-heptaen-12-one 13846201 Click to see COC1=C(C=C2C(=C1)C3(C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)O)OC 368.30 unknown https://doi.org/10.1055/S-2005-864182
14-Hydroxy-17,18-dimethoxy-6,6-dimethyl-2,8,21-trioxahexacyclo[12.8.0.03,12.04,9.05,7.015,20]docosa-3(12),4(9),10,15,17,19-hexaen-13-one 45359663 Click to see CC1(C2C1OC3=C2C4=C(C=C3)C(=O)C5(C(O4)COC6=CC(=C(C=C65)OC)OC)O)C 410.40 unknown https://doi.org/10.1055/S-2005-864182
CID 303992 303992 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC 410.40 unknown https://doi.org/10.1055/S-2005-864182
Dehydrodeguelin 3083803 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)C 392.40 unknown https://doi.org/10.1055/S-2005-864182
Rotenolon II 99189 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC 410.40 unknown https://doi.org/10.1055/S-2005-864182
Rotenolone 68184 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC 410.40 unknown https://doi.org/10.1055/S-2005-864182
Tephrosin 114909 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C 410.40 unknown https://doi.org/10.1055/S-2005-864182

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