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Geijera parviflora

Geijera parviflora - 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 UUID64401d7a51280677311678
Scientific name Geijera parviflora
Authority Lindl.
First published in J. Exped. Trop. Australia : 102 (1848)

Description Top

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Synonyms Top

Scientific name Authority First published in
Zanthoxylum australasicum A.Juss. Mém. Mus. Hist. Nat. 12: 503 (1825)
Geijera pendula Lindl. J. Exped. Trop. Australia : 251 (1848)

Common names Top

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Language Common/alternative name
Chinese 小花钩瓣常山
Chinese 蓋節拉木

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
  • Australasia
    • Australia
      • New South Wales
      • Queensland
      • South Australia
      • Victoria

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000695902
UNII LSS78Z09IA
Tropicos 28100010
KEW urn:lsid:ipni.org:names:773711-1
The Plant List kew-2818545
PFAF Geijera parviflora
Open Tree Of Life 5233075
NCBI Taxonomy 1226077
IUCN Red List 200148932
IPNI 773711-1
iNaturalist 185434
GBIF 7269149
Freebase /m/0gh86c2
EPPO GEJPA
USDA GRIN 385
Wikipedia Geijera_parviflora
CMAUP NPO8274

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
Trees in trees a report from remote Australia Pye J Plant Signal Behav 07-Dec-2023
PMCID:PMC10761035
doi:10.1080/15592324.2023.2286392
PMID:38059450
Lipid concentration and composition in xylem sap of woody angiosperms from a tropical savanna and a seasonal rainforest Huang LB, Guan X, Aritsara AN, Zhu JJ, Jansen S, Cao KF Plant Divers 05-Jul-2023
PMCID:PMC10851283
doi:10.1016/j.pld.2023.07.001
PMID:38343598
Lipid-Coated Nanobubbles in Plants Ingram S, Jansen S, Schenk HJ Nanomaterials (Basel) 31-May-2023
PMCID:PMC10254470
doi:10.3390/nano13111776
PMID:37299679
Essential Oils from Vietnamese Asteraceae for Environmentally Friendly Control of Aedes Mosquitoes Hoi TM, Satyal P, Huong LT, Hau DV, Binh TD, Duyen DT, Dai DN, Huy NG, Chinh HV, Hoa VV, Hung NH, Setzer WN Molecules 17-Nov-2022
PMCID:PMC9699393
doi:10.3390/molecules27227961
PMID:36432060
Natural Products Inhibitors of Monoamine Oxidases—Potential New Drug Leads for Neuroprotection, Neurological Disorders, and Neuroblastoma Chaurasiya ND, Leon F, Muhammad I, Tekwani BL Molecules 04-Jul-2022
PMCID:PMC9268457
doi:10.3390/molecules27134297
PMID:35807542
Geiparvarin Inhibits OS Metastasis through Upregulation of ANGPTL4 Expression by Inhibiting miRNA-3912-3p Expression Jiang F, Wang GJ, Huang P, Chen S, Xiao H, Zhang L, Zou H Evid Based Complement Alternat Med 12-Apr-2022
PMCID:PMC9019413
doi:10.1155/2022/4663684
PMID:35463073
Hedycaryol – Central Intermediates in Sesquiterpene Biosynthesis, Part II Xu H, Dickschat JS Chemistry 21-Mar-2022
PMCID:PMC9310801
doi:10.1002/chem.202200405
PMID:35239190
Fundamental Chemistry of Essential Oils and Volatile Organic Compounds, Methods of Analysis and Authentication Sadgrove NJ, Padilla-González GF, Phumthum M Plants (Basel) 16-Mar-2022
PMCID:PMC8955314
doi:10.3390/plants11060789
PMID:35336671
Structures, Occurrences and Biosynthesis of 11,12,13-Tri-nor-Sesquiterpenes, an Intriguing Class of Bioactive Metabolites Coca-Ruíz V, Suárez I, Aleu J, Collado IG Plants (Basel) 14-Mar-2022
PMCID:PMC8949605
doi:10.3390/plants11060769
PMID:35336651
Natural Enantiomers: Occurrence, Biogenesis and Biological Properties Yu JH, Yu ZP, Capon RJ, Zhang H Molecules 14-Feb-2022
PMCID:PMC8880303
doi:10.3390/molecules27041279
PMID:35209066
A 2-oxoglutarate-dependent dioxygenase converts dihydrofuran to furan in Salvia diterpenoids Song JJ, Fang X, Li CY, Jiang Y, Li JX, Wu S, Guo J, Liu Y, Fan H, Huang YB, Wei YK, Kong Y, Zhao Q, Xu JJ, Hu YH, Chen XY, Yang L Plant Physiol 06-Dec-2021
PMCID:PMC8896610
doi:10.1093/plphys/kiab567
PMID:34893909
Zanthosimuline and Related Pyranoquinolines as Antifungal Agents for Postharvest Fruit Disease Control Di Liberto MG, Caldo AJ, Quiroga AD, Riveira MJ, Derita MG ACS Omega 25-Mar-2020
PMCID:PMC7144156
doi:10.1021/acsomega.0c00225
PMID:32280891
The risk-takers and -avoiders: germination sensitivity to water stress in an arid zone with unpredictable rainfall Duncan C, Schultz NL, Good MK, Lewandrowski W, Cook S AoB Plants 10-Oct-2019
PMCID:PMC6863470
doi:10.1093/aobpla/plz066
PMID:31777652
Lower dormancy with rapid germination is an important strategy for seeds in an arid zone with unpredictable rainfall Duncan C, Schultz N, Lewandrowski W, Good MK, Cook S PLoS One 10-Sep-2019
PMCID:PMC6736279
doi:10.1371/journal.pone.0218421
PMID:31504045
Type III secretion inhibitors for the management of bacterial plant diseases Puigvert M, Solé M, López‐Garcia B, Coll NS, Beattie KD, Davis RA, Elofsson M, Valls M Mol Plant Pathol 19-Oct-2018
PMCID:PMC6430469
doi:10.1111/mpp.12736
PMID:30062690

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(1E,3Z,7E)-1,7-dimethylcyclodeca-1,3,7-triene 60142682 Click to see CC1=CCCC(=CC=CCC1)C 162.27 unknown https://doi.org/10.1071/CH9682255
1,7-Dimethylcyclodeca-1,3,7-triene 555328 Click to see CC1=CCCC(=CC=CCC1)C 162.27 unknown https://doi.org/10.1071/CH9682255
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
2H-1-Benzopyran-2-one, 7-[[(2E)-3,7-dimethyl-2,6-octadienyl]oxy]- 400073 Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C 298.40 unknown https://doi.org/10.1016/0031-9422(72)80045-1
Auraptene 1550607 Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C 298.40 unknown https://doi.org/10.1016/0031-9422(72)80045-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17S)-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 162965363 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(72)80045-1
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/10.1016/0031-9422(72)80045-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Indican 441564 Click to see C1=CC=C2C(=C1)C(=CN2)OC3C(C(C(C(O3)CO)O)O)O 295.29 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
(2E)-2-(3-oxo-1H-indol-2-ylidene)-1H-indol-3-one 5318432 Click to see C1=CC=C2C(=C1)C(=O)C(=C3C(=O)C4=CC=CC=C4N3)N2 262.26 unknown via CMAUP database
(3Z)-3-(3-oxo-1H-indol-2-ylidene)-1H-indol-2-one 5318433 Click to see C1=CC=C2C(=C1)C(=C3C(=O)C4=CC=CC=C4N3)C(=O)N2 262.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-(6,7-Dihydroxy-3,7-dimethyloct-2-enoxy)chromen-2-one 277399 Click to see CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)CCC(C(C)(C)O)O 332.40 unknown https://doi.org/10.1016/0031-9422(72)80045-1
7-(7-Hydroxy-3,7-dimethyl-6-oxooct-2-enoxy)chromen-2-one 323703 Click to see CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)CCC(=O)C(C)(C)O 330.40 unknown https://doi.org/10.1016/0031-9422(72)80045-1
7-[(3S)-3-(5,5-dimethyl-4-oxofuran-2-yl)butoxy]chromen-2-one 92278966 Click to see CC(CCOC1=CC2=C(C=C1)C=CC(=O)O2)C3=CC(=O)C(O3)(C)C 328.40 unknown https://doi.org/10.1016/0031-9422(72)80045-1
7-[(E,6S)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]chromen-2-one 15560114 Click to see CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)CCC(C(C)(C)O)O 332.40 unknown https://doi.org/10.1016/0031-9422(72)80045-1
7-[(E)-7-hydroxy-3,7-dimethyl-6-oxooct-2-enoxy]chromen-2-one 5358858 Click to see CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)CCC(=O)C(C)(C)O 330.40 unknown https://doi.org/10.1016/0031-9422(72)80045-1
7-[3-(5,5-Dimethyl-4-oxofuran-2-yl)butoxy]chromen-2-one 289493 Click to see CC(CCOC1=CC2=C(C=C1)C=CC(=O)O2)C3=CC(=O)C(O3)(C)C 328.40 unknown https://doi.org/10.1016/0031-9422(72)80045-1
Coumarin, 7-methoxy-6-(3-methylcrotonoyl)- 620900 Click to see CC(=CC(=O)C1=C(C=C2C(=C1)C=CC(=O)O2)OC)C 258.27 unknown https://doi.org/10.1071/CH9671943
Geiparvarin 5910585 Click to see CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C3=CC(=O)C(O3)(C)C 326.30 unknown https://doi.org/10.1016/0031-9422(72)80045-1
https://doi.org/10.1071/CH9671943
https://doi.org/10.1016/S0960-894X(02)00798-9
Geiparvin 73427 Click to see CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C3=CC(=O)C(O3)(C)C 326.30 unknown https://doi.org/10.1071/CH9671943
https://doi.org/10.1016/0031-9422(72)80045-1
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
Pseudosemiglabrin 156341 Click to see CC(=O)OC1C2C(OC3=C2C4=C(C=C3)C(=O)C=C(O4)C5=CC=CC=C5)OC1(C)C 392.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,5-dihydroxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]chromen-4-one 101422383 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C3=C(C(=O)C4=C(C=C(C=C4O3)OC5C(C(C(C(O5)C)O)O)O)O)O)O)O)O 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(1R,14S)-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 92211494 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C 394.40 unknown via CMAUP database
12aalpha-Deguelin 92296469 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C 410.40 unknown via CMAUP database
Deguelin 107935 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C 394.40 unknown via CMAUP database
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 via CMAUP database
Rotenone 6758 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown via CMAUP database
Sumatrol 442824 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O 410.40 unknown via CMAUP database

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