Harpullia pendula - Unknown
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Internal ID UUID64404dea675b0236111624
Scientific name Harpullia pendula
Authority Planch. ex F.Muell.
First published in Trans. & Proc. Philos. Inst. Victoria 3: 26 (1859)

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Language Common/alternative name
English tulipwood
English black tulipwood
English queensland tulipwood
Estonian tulbi-harpulipuu
Hebrew הרפוליה נטויה
Chinese 垂枝假山罗

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

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Database ID/link to page
World Flora Online wfo-0001135002
Tropicos 28600888
KEW urn:lsid:ipni.org:names:783341-1
The Plant List tro-28600888
Open Tree Of Life 232572
NCBI Taxonomy 884417
IUCN Red List 192227460
IPNI 783341-1
iNaturalist 369494
GBIF 3786672
Freebase /m/0b767vx
EOL 2869568
USDA GRIN 18258
Wikipedia Harpullia_pendula

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
C-Phycocyanin and Lycium barbarum Polysaccharides Protect against Aspirin-Induced Inflammation and Apoptosis in Gastric RGM-1 Cells Liu YC, Chang CC, Matsui H, Chao JC Nutrients 01-Dec-2022
PMCID:PMC9736128
doi:10.3390/nu14235113
PMID:36501143
Natural and Historical Heritage of the Lisbon Botanical Gardens: An Integrative Approach with Tree Collections Cunha AR, Soares AL, Brilhante M, Arsénio P, Vasconcelos T, Espírito-Santo D, Duarte MC, Romeiras MM Plants (Basel) 04-Jul-2021
PMCID:PMC8309379
doi:10.3390/plants10071367
PMID:34371570
Novel Green Biosynthesis of 5-Fluorouracil Chromium Nanoparticles Using Harpullia pendula Extract for Treatment of Colorectal Cancer Saddik MS, Elsayed MM, Abdelkader MS, El-Mokhtar MA, Abdel-Aleem JA, Abu-Dief AM, Al-Hakkani MF, Farghaly HS, Abou-Taleb HA Pharmaceutics 06-Feb-2021
PMCID:PMC7915530
doi:10.3390/pharmaceutics13020226
PMID:33562032
A Simple Method for Simulating Drought Effects on Plants Marchin RM, Ossola A, Leishman MR, Ellsworth DS Front Plant Sci 21-Jan-2020
PMCID:PMC6985571
doi:10.3389/fpls.2019.01715
PMID:32038685
Species delimitation in asexual insects of economic importance: The case of black scale (Parasaissetia nigra), a cosmopolitan parthenogenetic pest scale insect Lin YP, Edwards RD, Kondo T, Semple TL, Cook LG PLoS One 01-May-2017
PMCID:PMC5411049
doi:10.1371/journal.pone.0175889
PMID:28459805
Cytotoxic Barrigenol-like Triterpenoids from an Extract of Cyrilla racemiflora Housed in a Repository Ren Y, VanSchoiack A, Chai HB, Goetz M, Kinghorn AD J Nat Prod 30-Sep-2015
PMCID:PMC4619146
doi:10.1021/acs.jnatprod.5b00532
PMID:26422131
Chemical constituents of Harpullia pendula. II. Further constituents of the bark and leaves RF Cherry, PW Khong, KG Lewis CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9771397
Occurrence of Physical Dormancy in Seeds of Australian Sapindaceae: A Survey of 14 Species in Nine Genera Cook A, Turner SR, Baskin JM, Baskin CC, Steadman KJ, Dixon KW Ann Bot 27-Mar-2008
PMCID:PMC2710253
doi:10.1093/aob/mcn043
PMID:18369237
Chemical constituents of Harpullia pendula PW Khong, KG Lewis CSIRO Publishing 20-Dec-2006
doi:10.1071/CH9761351

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-Tetracosanol 10472 Click to see CCCCCCCCCCCCCCCCCCCCCCCCO 354.70 unknown https://doi.org/10.1071/CH9771397
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aR,6bS,8aR,9S,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol 21594154 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)CO)C)C)(C)C)O)C)C 458.70 unknown https://doi.org/10.1071/CH9761351
(4aR,6aR,6bS,7R,8S,8aS,9S,12aS,14aR,14bR)-7,8,9-trihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one 145958942 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(C(C(C2(C(C1)O)CO)O)O)C)C)(C)C)C)C 488.70 unknown https://doi.org/10.1071/CH9771397
[(4S,4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-5,10-dihydroxy-4a-(hydroxymethyl)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-4-yl] (Z)-2-methylbut-2-enoate 102003237 Click to see CC=C(C)C(=O)OC1CC(CC2C1(C(CC3(C2=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)O)CO)(C)C 556.80 unknown https://doi.org/10.1071/CH9761351
[(4S,4aR,5S,6R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-5,6,10-trihydroxy-4a-(hydroxymethyl)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-4-yl] (Z)-2-methylbut-2-enoate 101600045 Click to see CC=C(C)C(=O)OC1CC(CC2C1(C(C(C3(C2=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)O)O)CO)(C)C 572.80 unknown https://doi.org/10.1071/CH9761351
[(4S,4aS,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-4,10-dihydroxy-4a-(hydroxymethyl)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-5-yl] (Z)-2-methylbut-2-enoate 162867713 Click to see CC=C(C)C(=O)OC1CC2(C(=CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C5C1(C(CC(C5)(C)C)O)CO)C 556.80 unknown https://doi.org/10.1071/CH9761351
[4,10-Dihydroxy-4a-(hydroxymethyl)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-5-yl] 2-methylbut-2-enoate 162867712 Click to see CC=C(C)C(=O)OC1CC2(C(=CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C5C1(C(CC(C5)(C)C)O)CO)C 556.80 unknown https://doi.org/10.1071/CH9761351
[5,10-Dihydroxy-4a-(hydroxymethyl)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-4-yl] 2-methylbut-2-enoate 85174080 Click to see CC=C(C)C(=O)OC1CC(CC2C1(C(CC3(C2=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)O)CO)(C)C 556.80 unknown https://doi.org/10.1071/CH9761351
[5,6,10-Trihydroxy-4a-(hydroxymethyl)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-4-yl] 2-methylbut-2-enoate 162906544 Click to see CC=C(C)C(=O)OC1CC(CC2C1(C(C(C3(C2=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)O)O)CO)(C)C 572.80 unknown https://doi.org/10.1071/CH9761351
16beta-Deuterobarringenol A1 435279 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(C(C(C2(C(C1)O)CO)O)O)C)C)(C)C)O)C)C 490.70 unknown https://doi.org/10.1071/CH9761351
22alpha-Hydroxyerythrodiol 73810233 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)CO)C)C)(C)C)O)C)C 458.70 unknown https://doi.org/10.1071/CH9761351
7,8,9-trihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one 162879465 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(C(C(C2(C(C1)O)CO)O)O)C)C)(C)C)C)C 488.70 unknown https://doi.org/10.1071/CH9771397
A1-Barrigenol 12299984 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(C(C(C2(C(C1)O)CO)O)O)C)C)(C)C)O)C)C 490.70 unknown https://doi.org/10.1071/CH9761351
Camelliagenin A 612548 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1)O)CO)O)C)C)(C)C)O)C)C 474.70 unknown https://doi.org/10.1071/CH9761351
Camelliagenin A 12302281 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1)O)CO)O)C)C)(C)C)O)C)C 474.70 unknown https://doi.org/10.1071/CH9761351
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1071/CH9771397
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1071/CH9771397
> 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/10.1071/CH9771397
> Organoheterocyclic compounds / Pyridines and derivatives / Bipyridines and oligopyridines
(NZ)-N-[(4-methoxy-3-methylsulfinyl-6-pyridin-2-ylpyridin-2-yl)methylidene]hydroxylamine 136675100 Click to see COC1=CC(=NC(=C1S(=O)C)C=NO)C2=CC=CC=N2 291.33 unknown https://doi.org/10.1071/CH9771397
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
2-Propenoic acid, 3-(4-hydroxyphenyl)-, methyl ester 92203 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown https://doi.org/10.1071/CH9761351
Methyl 4-hydroxycinnamate 5319562 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown https://doi.org/10.1071/CH9761351

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