Sabal yapa - Unknown
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Internal ID UUID643feb74e1473537258476
Scientific name Sabal yapa
Authority C.Wright ex Becc.
First published in Webbia 2: 64 (1907)

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Synonyms Top

Scientific name Authority First published in
Inodes yapa (C.Wright ex Becc.) Standl. Publ. Field Columb. Mus., Bot. Ser. 3: 219 (1930)
Sabal peregrina L.H.Bailey Gentes Herbarum 6: 400 (1944)
Sabal yucatanica L.H.Bailey Gentes Herbarum 6: 418 (1944)

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Language Common/alternative name
Arabic سبال اليابا
Persian نخل یاپا
Chinese 对裂菜棕

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000299323
Tropicos 2400617
INPN 706768
KEW urn:lsid:ipni.org:names:60440702-2
The Plant List kew-181072
Open Tree Of Life 180750
Observations.org 209578
NCBI Taxonomy 469734
IUCN Red List 56360782
IPNI 60440702-2
iNaturalist 281548
GBIF 2732498
Freebase /m/05pdcj6
EOL 1131503
Elurikkus 292393
Wikipedia Sabal_yapa

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
Silvicultural Practices in the Management of Diospyros melanoxylon (Tendu) Leaf Production: Options and Trade-offs Date AA, Hiremath AJ, Joshi AA, Lele S Econ Bot 11-Apr-2023
PMCID:PMC10088608
doi:10.1007/s12231-023-09572-z
PMID:37359048
A sulfated polyphenols-rich extract from Sabal yapa exhibits antitumor activities in Ehrlich ascites carcinoma Fahmi AA, El Raey MA, Ibrahim AY, Abdelfattah MA, Abdelmageed AM, Sobeh M Saudi J Biol Sci 21-Feb-2021
PMCID:PMC8117008
doi:10.1016/j.sjbs.2021.02.056
PMID:34012333
Raman Spectroscopy and Chemometric Modeling to Predict Physical-Chemical Honey Properties from Campeche, Mexico Anguebes-Franseschi F, Abatal M, Pat L, Flores A, Córdova Quiroz AV, Ramírez-Elias MA, San Pedro L, May Tzuc O, Bassam A Molecules 13-Nov-2019
PMCID:PMC6891675
doi:10.3390/molecules24224091
PMID:31766131
Application of Multivariable Analysis and FTIR-ATR Spectroscopy to the Prediction of Properties in Campeche Honey Anguebes F, Pat L, Ali B, Guerrero A, Córdova AV, Abatal M, Garduza JP J Anal Methods Chem 14-Dec-2016
PMCID:PMC5192472
doi:10.1155/2016/5427526
PMID:28070445
Effects of Harvest on the Sustainability and Leaf Productivity of Populations of Two Palm Species in Maya Homegardens Martínez-Ballesté A, Martorell C PLoS One 24-Mar-2015
PMCID:PMC4372575
doi:10.1371/journal.pone.0120666
PMID:25803029
Patch Size and Isolation Predict Plant Species Density in a Naturally Fragmented Forest Munguía-Rosas MA, Montiel S PLoS One 27-Oct-2014
PMCID:PMC4210240
doi:10.1371/journal.pone.0111742
PMID:25347818
Round and large: morphological and genetic consequences of artificial selection on the gourd tree Crescentia cujete by the Maya of the Yucatan Peninsula, Mexico Aguirre-Dugua X, Eguiarte LE, González-Rodríguez A, Casas A Ann Bot 12-Apr-2012
PMCID:PMC3359923
doi:10.1093/aob/mcs068
PMID:22499854
Sablacaurin A and B, Two 19‐nor‐3,4‐seco‐Lanostane‐Type Triterpenoids from Sabal causiarum and Sabal blackburniana, Respectively. Rabab El‐Dib, Maki Kaloga, Ibrahim Mahmoud, Hesham S. M. Soliman, Fatma A. Moharram, Herbert Kolodziej Wiley 11-Aug-2004
doi:10.1002/CHIN.200436206
Sablacaurin A and B, two 19-nor-3,4-seco-lanostane-type triterpenoids from Sabal causiarum and Sabal blackburniana, respectively. El-Dib R, Kaloga M, Mahmoud I, Soliman HS, Moharram FA, Kolodziej H Phytochemistry 01-Apr-2004
doi:10.1016/J.PHYTOCHEM.2004.02.026
PMID:15110697
Raphides in Palm Embryos and their Systematic Distribution ZONA S Ann Bot 01-Apr-2004
PMCID:PMC4242339
doi:10.1093/aob/mch060
PMID:14980977

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 / Steroids and steroid derivatives / Cucurbitacins
(8R,9S,13R,17R)-17-(5,6-dimethylhept-6-en-2-yl)-9-ethyl-4,4,13,14-tetramethyl-1,2,5,6,7,8,10,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 5316255 Click to see CCC12CCC3(C(CCC3(C1CCC4C2CCC(=O)C4(C)C)C)C(C)CCC(C)C(=C)C)C 454.80 unknown https://doi.org/10.1002/CHIN.200436206
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,12S,15R,16R)-15-[(5S)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 162944137 Click to see CC(CCC(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 438.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.026
(1S,3R,8S,11S,12S,15R,16R)-15-[(2S,5R)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 162944141 Click to see CC(CCC(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 438.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.026
15-(5,6-Dimethylhept-6-en-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 13918176 Click to see CC(CCC(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 438.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.026
24-Methylenecycloartanone 14635659 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 438.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.026
24-Methylidene-9,19-cyclolanostan-3-one 3083719 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 438.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.026
CID 634880 634880 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 438.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.026
Cyclolaudenone 21592246 Click to see CC(CCC(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 438.70 unknown https://doi.org/10.1002/CHIN.200436206
https://doi.org/10.1016/J.PHYTOCHEM.2004.02.026

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