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Sarcophyte sanguinea

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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 UUID64404ee76b8b8620627982
Scientific name Sarcophyte sanguinea
Authority Sparrm.
First published in Kongl. Vetensk. Acad. Handl. 27: 300 (1776)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ichthyosma weinmannii Harv. Gen. S. Afr. Pl. : 300 (1838)
Ichthyosma wehdemanni Schltdl. Linnaea 2: 674 (1827)

Common names Top

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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
  • Africa
    • South Tropical Africa
      • Mozambique
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001140462
Tropicos 3000041
KEW urn:lsid:ipni.org:names:103400-1
The Plant List tro-3000041
Open Tree Of Life 5729548
NCBI Taxonomy 1618143
IPNI 103400-1
iNaturalist 337669
GBIF 7309825
USDA GRIN 451139

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
Extreme plastomes in holoparasitic Balanophoraceae are not the norm Kim W, Lautenschläger T, Bolin JF, Rees M, Nzuzi A, Zhou R, Wanke S, Jost M BMC Genomics 15-Jun-2023
PMCID:PMC10268348
doi:10.1186/s12864-023-09422-1
PMID:37322447
Ethnobotany and Toxicity Status of Medicinal Plants with Cosmeceutical Relevance from Eastern Cape, South Africa Ndhlala AR, Thibane VS, Masehla CM, Mokwala PW Plants (Basel) 30-May-2022
PMCID:PMC9182599
doi:10.3390/plants11111451
PMID:35684224
Ethnopharmacological Study of Medicinal Plants Used for the Treatment of Cardiovascular Diseases and Their Associated Risk Factors in sub-Saharan Africa Odukoya JO, Odukoya JO, Mmutlane EM, Ndinteh DT Plants (Basel) 23-May-2022
PMCID:PMC9143319
doi:10.3390/plants11101387
PMID:35631812
A review study on the anti-trichomonas activities of medicinal plants Hashemi N, Ommi D, Kheyri P, Khamesipour F, Setzer WN, Benchimol M Int J Parasitol Drugs Drug Resist 12-Feb-2021
PMCID:PMC7902805
doi:10.1016/j.ijpddr.2021.01.002
PMID:33610966
Are plants used in the Eastern Cape province for cosmetics fully commercialized? Sagbo IJ, Mbeng WO Indian J Pharmacol 01-May-2019
PMCID:PMC6644182
doi:10.4103/ijp.IJP_262_18
PMID:31391681
Elephantorrhiza elephantina: Traditional Uses, Phytochemistry, and Pharmacology of an Important Medicinal Plant Species in Southern Africa Maroyi A Evid Based Complement Alternat Med 14-May-2017
PMCID:PMC5446883
doi:10.1155/2017/6403905
PMID:28588639
Ethnopharmacological Survey of Plants Used in the Traditional Treatment of Gastrointestinal Pain, Inflammation and Diarrhea in Africa: Future Perspectives for Integration into Modern Medicine Stark TD, Mtui DJ, Balemba OB Animals (Basel) 04-Mar-2013
PMCID:PMC4495512
doi:10.3390/ani3010158
PMID:26487315
Exocarpic acid and other compounds from tubers and inflorescences of Sarcophyte sanguinea Lovina A.C. Naidoo Siegfried E.^Drewes, J.Van Staden, Anne Hutchings Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97556-3

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
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Lariciresinol dimethyl ether 14237703 Click to see COC1=C(C=C(C=C1)CC2COC(C2CO)C3=CC(=C(C=C3)OC)OC)OC 388.50 unknown https://doi.org/10.1016/S0031-9422(00)97556-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Exocarpic acid 5312684 Click to see CCCCC=CC#CC#CCCCCCCCC(=O)O 274.40 unknown https://doi.org/10.1016/S0031-9422(00)97556-3
Octadec-13-ene-9,11-diynoic acid 53635328 Click to see CCCCC=CC#CC#CCCCCCCCC(=O)O 274.40 unknown https://doi.org/10.1016/S0031-9422(00)97556-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
2-(Hydroxymethyl)-6-[3-(4-hydroxyphenyl)prop-2-enoxy]oxane-3,4,5-triol 72726662 Click to see C1=CC(=CC=C1C=CCOC2C(C(C(C(O2)CO)O)O)O)O 312.31 unknown https://doi.org/10.1016/S0031-9422(00)97556-3
Sachaliside 14048613 Click to see C1=CC(=CC=C1C=CCOC2C(C(C(C(O2)CO)O)O)O)O 312.31 unknown https://doi.org/10.1016/S0031-9422(00)97556-3
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
6-Methoxycyclohexane-1,2,3,4,5-pentol 230881 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1016/S0031-9422(00)97556-3
D-Pinitol 164619 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1016/S0031-9422(00)97556-3
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-(4-Hydroxyphenyl)prop-2-enal 440733 Click to see C1=CC(=CC=C1C=CC=O)O 148.16 unknown https://doi.org/10.1016/S0031-9422(00)97556-3
p-Coumaraldehyde 641301 Click to see C1=CC(=CC=C1C=CC=O)O 148.16 unknown https://doi.org/10.1016/S0031-9422(00)97556-3
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(00)97556-3
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/S0031-9422(00)97556-3
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/S0031-9422(00)97556-3
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(00)97556-3

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