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Rhaphidophora decursiva

Rhaphidophora decursiva - Unknown
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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 UUID643feae04c8df076951053
Scientific name Rhaphidophora decursiva
Authority (Roxb.) Schott
First published in Bonplandia (Hannover) 5: 45 (1857)

Description Top

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Synonyms Top

Scientific name Authority First published in
Monstera decursiva Schott Wiener Z. Kunst 4: 1028 (1830)
Monstera multijuga K.Koch ex Ender Index Aroid. : 75 (1864)
Pothos decursivus Roxb. Fl. Ind. 1: 456 (1820)
Rhaphidophora affinis Schott Prodr. Syst. Aroid. : 385 (1860)
Rhaphidophora eximia Schott Bonplandia (Hannover) 5: 45 (1857)
Rhaphidophora grandis Schott Oesterr. Bot. Z. 8: 349 (1858)
Rhaphidophora insignis Schott Gen. Aroid. : t. 77 (1858)
Scindapsus decursivus Schott Melet. Bot. : 21 (1832)
Raphidophora decursiva (Roxb.) A.Schott

Common names Top

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Language Common/alternative name
Chinese 大青蛇
Chinese 鸭绿江
Chinese 青竹标
Chinese 过岗龙
Chinese 过山龙
Chinese 老蛇藤
Chinese 石蛇
Chinese 石莲藕
Chinese 当年见
Chinese 山包谷
Chinese 大青龙
Chinese 爬树龙
Chinese 大青竹标
Chinese 大戆毒
Chinese 上木蜈蚣
Chinese 万丈洁
Chinese 裂叶崖角藤
Chinese 爬樹龍
Chinese 崖角藤/过山龙
Chinese 大过山龙
Chinese 爬山虎
Chinese 过江龙

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
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
      • Tibet
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000295939
Tropicos 2103921
KEW urn:lsid:ipni.org:names:88471-1
The Plant List kew-177736
Open Tree Of Life 474105
NCBI Taxonomy 258281
IPNI 88471-1
iNaturalist 431536
GBIF 5329707
Freebase /m/065yc7f
EOL 1131879
USDA GRIN 31070
Wikipedia Rhaphidophora_decursiva

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
Naturally occurring phenylethanoids and phenylpropanoids: antimalarial potential Abdelmohsen UR, Bayoumi SA, Mohamed NM, Mostafa YA, Ngwa CJ, Pradel G, Farag SF RSC Adv 07-Sep-2023
PMCID:PMC10483269
doi:10.1039/d3ra04242a
PMID:37692342
Structures of the xyloglucans in the monocotyledon family Araceae (aroids) Hsiung SY, Li J, Imre B, Kao MR, Liao HC, Wang D, Chen CH, Liang PH, Harris PJ, Hsieh YS Planta 17-Jan-2023
PMCID:PMC9845173
doi:10.1007/s00425-023-04071-w
PMID:36650257
Evolution of the Colocasiomyia gigantea Species Group (Diptera: Drosophilidae): Phylogeny, Biogeography and Shift of Host Use Xiao L, Li NN, Yang LK, Li JL, Gao JJ Insects 18-Jul-2022
PMCID:PMC9319340
doi:10.3390/insects13070647
PMID:35886823
Plants as Sources of Natural and Recombinant Antimalaria Agents Habibi P, Shi Y, Fatima Grossi-de-Sa M, Khan I Mol Biotechnol 29-Apr-2022
PMCID:PMC9053566
doi:10.1007/s12033-022-00499-9
PMID:35488142
Vegetation Classification and Distribution Patterns in the South Slope of Yarlung Zangbo Grand Canyon National Nature Reserve, Eastern Himalayas Wu PP, Wang Z, Jia NX, Dong SQ, Qu XY, Qiao XG, Liu CC, Guo K Plants (Basel) 28-Apr-2022
PMCID:PMC9105001
doi:10.3390/plants11091194
PMID:35567195
New Trichothecenes Isolated from the Marine Algicolous Fungus Trichoderma brevicompactum Safwan S, Wang SW, Hsiao G, Hsiao SW, Hsu SJ, Lee TH, Lee CK Mar Drugs 18-Jan-2022
PMCID:PMC8875558
doi:10.3390/md20020080
PMID:35200610
Total synthesis of (±)-decursivine via BINOL-phosphoric acid catalyzed tandem oxidative cyclization Parvatkar PT, Smotkin ES, Manetsch R Sci Rep 07-Oct-2021
PMCID:PMC8497573
doi:10.1038/s41598-021-99064-8
PMID:34620892
Botanical candidates from Saudi Arabian flora as potential therapeutics for Plasmodium infection Al-Quraishy S, Abdel-Maksoud MA, Al-Shaebi EM, Dkhil MA Saudi J Biol Sci 27-Nov-2020
PMCID:PMC7878689
doi:10.1016/j.sjbs.2020.11.069
PMID:33613066
Ethnobotany and diversity of medicinal plants used by the Buyi in eastern Yunnan, China Xiong Y, Sui X, Ahmed S, Wang Z, Long C Plant Divers 07-Oct-2020
PMCID:PMC7936110
doi:10.1016/j.pld.2020.09.004
PMID:33733008
An ethnoveterinary study on medicinal plants used by the Buyi people in Southwest Guizhou, China Xiong Y, Long C J Ethnobiol Ethnomed 17-Aug-2020
PMCID:PMC7433110
doi:10.1186/s13002-020-00396-y
PMID:32807192
Synthesis of Benzo[b]azocin‐2‐ones by Aryl Amination and Ring‐Expansion of α‐(Iodophenyl)‐β‐oxoesters Dierks A, Tönjes J, Schmidtmann M, Christoffers J Chemistry 28-Oct-2019
PMCID:PMC6899745
doi:10.1002/chem.201903139
PMID:31433088
Antimalarial Activity of Plant Metabolites Pan WH, Xu XY, Shi N, Tsang SW, Zhang HJ Int J Mol Sci 06-May-2018
PMCID:PMC5983777
doi:10.3390/ijms19051382
PMID:29734792
Sub-chronic toxicopathological study of lantadenes of Lantana camara weed in Guinea pigs Kumar R, Sharma R, Patil RD, Mal G, Kumar A, Patial V, Kumar P, Singh B BMC Vet Res 13-Apr-2018
PMCID:PMC5899389
doi:10.1186/s12917-018-1444-x
PMID:29653586
Bright Side of Lignin Depolymerization: Toward New Platform Chemicals Sun Z, Fridrich B, de Santi A, Elangovan S, Barta K Chem Rev 16-Jan-2018
PMCID:PMC5785760
doi:10.1021/acs.chemrev.7b00588
PMID:29337543
Discovery of Bioactive Compounds by the UIC-ICBG Drug Discovery Program in the 18 Years Since 1998 Zhang HJ, Li WF, Fong HH, Soejarto DD Molecules 31-Oct-2016
PMCID:PMC6273581
doi:10.3390/molecules21111448
PMID:27809237

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
2-Butylbenzamide 15468173 Click to see CCCCC1=CC=CC=C1C(=O)N 177.24 unknown https://doi.org/10.1021/NP010037C
N-Butylbenzamide 76024 Click to see CCCCNC(=O)C1=CC=CC=C1 177.24 unknown https://doi.org/10.1021/NP010037C
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(2R)-2-(2,6-dimethoxy-4-prop-2-enylphenoxy)-3-(3,4,5-trimethoxyphenyl)propan-1-ol 11101826 Click to see COC1=CC(=CC(=C1OC(CC2=CC(=C(C(=C2)OC)OC)OC)CO)OC)CC=C 418.50 unknown https://doi.org/10.1021/NP010037C
2-(2,6-Dimethoxy-4-prop-2-enylphenoxy)-3-(3,4,5-trimethoxyphenyl)propan-1-ol 10862660 Click to see COC1=CC(=CC(=C1OC(CC2=CC(=C(C(=C2)OC)OC)OC)CO)OC)CC=C 418.50 unknown https://doi.org/10.1021/NP010037C
Rhaphidecursinol A 44559996 Click to see CC=CC1=CC(=C(C(=C1)OC)OC(CC2=CC(=C(C(=C2)OC)OC)OC)CO)OC 418.50 unknown https://doi.org/10.1021/NP010037C
> Benzenoids / Phenol ethers / Anisoles
(5R,11E)-15-hydroxy-17-methoxy-5-methyl-3,4-dioxabicyclo[11.4.0]heptadeca-1(13),11,14,16-tetraen-2-one 162933351 Click to see CC1CCCCCC=CC2=C(C(=CC(=C2)O)OC)C(=O)OO1 306.40 unknown https://doi.org/10.1021/NP010037C
15-Hydroxy-17-methoxy-5-methyl-3,4-dioxabicyclo[11.4.0]heptadeca-1(13),11,14,16-tetraen-2-one 85079474 Click to see CC1CCCCCC=CC2=C(C(=CC(=C2)O)OC)C(=O)OO1 306.40 unknown https://doi.org/10.1021/NP010037C
Rhaphidecurperoxin 9972426 Click to see CC1CCCCCC=CC2=C(C(=CC(=C2)O)OC)C(=O)OO1 306.40 unknown https://doi.org/10.1021/NP010037C
> Lignans, neolignans and related compounds
(1R,2R)-2-[2,6-dimethoxy-4-[(E)-prop-1-enyl]phenoxy]-1-(3,4,5-trimethoxyphenyl)propan-1-ol 6439400 Click to see CC=CC1=CC(=C(C(=C1)OC)OC(C)C(C2=CC(=C(C(=C2)OC)OC)OC)O)OC 418.50 unknown https://doi.org/10.1021/NP010037C
(1S,2R)-1-(3,4,5-Trimethoxyphenyl)-2-[2,6-dimethoxy-4-(1-propenyl)phenoxy]propane-1-ol 44559993 Click to see CC=CC1=CC(=C(C(=C1)OC)OC(C)C(C2=CC(=C(C(=C2)OC)OC)OC)O)OC 418.50 unknown https://doi.org/10.1021/NP010037C
2-(2,6-Dimethoxy-4-prop-1-enylphenoxy)-1-(3,4,5-trimethoxyphenyl)propan-1-ol 73717465 Click to see CC=CC1=CC(=C(C(=C1)OC)OC(C)C(C2=CC(=C(C(=C2)OC)OC)OC)O)OC 418.50 unknown https://doi.org/10.1021/NP010037C
2-(4-Allyl-2,6-dimethoxyphenoxy)-1-(3,4,5-trimethoxyphenyl)-1-propanol 10477119 Click to see CC(C(C1=CC(=C(C(=C1)OC)OC)OC)O)OC2=C(C=C(C=C2OC)CC=C)OC 418.50 unknown https://doi.org/10.1021/NP010037C
Rhaphidecursinol B 14018327 Click to see CC(C(C1=CC(=C(C(=C1)OC)OC)OC)O)OC2=C(C=C(C=C2OC)CC=C)OC 418.50 unknown https://doi.org/10.1021/NP010037C
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Pinoresinol 12309636 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1021/NP010037C
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1021/NP010037C
4-[3-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol 4546425 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC 388.40 unknown https://doi.org/10.1021/NP010037C
4-[6-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 234817 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1021/NP010037C
Medioresinol 181681 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC 388.40 unknown https://doi.org/10.1021/NP010037C
Syringaresinol 100067 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1021/NP010037C
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(2R,3R,4R,5R)-3,4-Dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)tetrahydrofuran 10048436 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1021/NP010037C
(2R,3S,4R,5R)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane 98683123 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1021/NP010037C
(2S,3R,4R,5R)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)tetrahydrofuran 21603492 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1021/NP010037C
3,4-Dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane 4485701 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1021/NP010037C
Grandisin 442876 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1021/NP010037C
> Lignans, neolignans and related compounds / Lignan lactones
2-(3',5'-Dimethoxy-4'-hydroxyphenyl)-3,7-dioxabicyclo[3.3.0]octan-6-one 5315434 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(=O)C3CO2 280.27 unknown https://doi.org/10.1021/NP010037C
Zhebeiresinol 162969347 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(=O)C3CO2 280.27 unknown https://doi.org/10.1021/NP010037C
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4-Hydroxy-3,5,5-trimethyl-4-(3-oxo-1-butenyl)-2-cyclohexen-1-one 440265 Click to see CC1=CC(=O)CC(C1(C=CC(=O)C)O)(C)C 222.28 unknown https://doi.org/10.1021/NP010037C
Dehydrovomifoliol 688492 Click to see CC1=CC(=O)CC(C1(C=CC(=O)C)O)(C)C 222.28 unknown https://doi.org/10.1021/NP010037C
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
Azadirachtin O 11170007 Click to see CC(C)CC(=O)OC1CC(C2(COC3C2C14COC(C4C(C3O)(C)C56C7CC(C5(O6)C)C8(C=COC8O7)O)C(=O)OC)C(=O)OC)OC(=O)C 706.70 unknown https://doi.org/10.1021/NP010037C
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(s)-5-Hydroxy-3,4-dimethyl-5-pentylfuran-2(5h)-one 155551640 Click to see CCCCCC1(C(=C(C(=O)O1)C)C)O 198.26 unknown https://doi.org/10.1021/NP010037C
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(3R,4R)-3-(1,3-benzodioxol-5-yl)-2-oxa-6,11-diazatetracyclo[7.5.2.04,15.012,16]hexadeca-1(15),9,12(16),13-tetraen-5-one 71560220 Click to see C1CNC(=O)C2C(OC3=C2C4=C(C=C3)NC=C41)C5=CC6=C(C=C5)OCO6 348.40 unknown https://doi.org/10.1076/PHBI.40.3.221.5832
Serotobenine 11725426 Click to see COC1=C(C=CC(=C1)C2C3C4=C(O2)C=CC5=C4C(=CN5)CCNC3=O)O 350.40 unknown https://doi.org/10.1076/PHBI.40.3.221.5832

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