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Ardisia crispa

Ardisia crispa - 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 UUID64400a2a25722123139662
Scientific name Ardisia crispa
Authority (Thunb.) A.DC.
First published in Trans. Linn. Soc. London 17: 124 (1834)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ardisia crispa f. leucocarpa (Nakai) H.Ohashi J. Jap. Bot. 63(5): 191 (1988):.
Ardisia crispa f. xanthocarpa (Nakai) H.Ohashi J. Jap. Bot. 63: 191 (1988)
Ardisia dielsii H.Lév. Repert. Spec. Nov. Regni Veg. 9: 461 (1911)
Ardisia henryi Hemsl. J. Linn. Soc., Bot. 26: 65 (1889)
Ardisia hortorum Maxim. Gartenflora 13: 363 (1865)
Ardisia multicaulis Z.Y.Zhu Bull. Bot. Res., Harbin 4(2): 116 (1984)
Ardisia simplicicaulis Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(1): 183 (1911)
Ardisia undulata C.B.Clarke Fl. Brit. India 3: 524 (1882)
Bladhia crispa Thunb. Syst. Veg. ed. 14 : 237 (1784)
Ardisia crispa var. amplifolia E.Walker J. Wash. Acad. Sci. 29: 258 1939
Ardisia crispa var. dielsii (H.Lév.) E.Walker J. Wash. Acad. Sci. 29: 260 1939
Ardisia crispa var. elegans A.DC. Prodr. 8: 134 1844
Ardisia henryi var. dielsii (H.Lév.) E.Walker J. Arnold Arbor. 15: 290 1934
Ardisia hortorum var. brachysepala Hand.-Mazz. Symb. Sin. 7: 756 1936
Bladhia crispa var. dielsii (H.Lév.) Nakai Bot. Mag. (Tokyo) 55: 527 1941
Tinus crispa Kuntze Revis. Gen. Pl. 2: 405. 1891 [5 Nov 1891]
Tinus henryi (Hemsl.) Kuntze Revis. Gen. Pl. 2: 974. 1891 [5 Nov 1891]
Tinus undulata (C.B.Clarke) Kuntze Revis. Gen. Pl. 2: 975 (1891)

Common names Top

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Language Common/alternative name
Indonesian mata ayam (tumbuhan)
Indonesian tumbuhan mata ayam
Japanese カラタチバナ
Japanese 百両
Japanese ヒャクリョウ
lzh 百兩金
Malay mata ayam
Malay mata pelanduk
Malay pokok mata ayam
Malay pokok mata pelanduk
su ki ajag
Chinese 龙爪金龙
Chinese 细柄百两金（变种）
Chinese 百兩金
Chinese 百两金
Chinese 八爪金龙
Chinese 开喉箭
Chinese 朱砂根

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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No forms added yet.

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
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
    • Indo-China
      • Cambodia
      • Laos
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000544145
UNII 570586OLDH
USDA Plants ARCR11
Tropicos 22001560
INPN 629099
KEW urn:lsid:ipni.org:names:586896-1
The Plant List kew-2647797
Open Tree Of Life 223974
NCBI Taxonomy 587398
IPNI 586896-1
iNaturalist 287104
GBIF 7169429
EPPO ADACR
USDA GRIN 3882
Wikipedia Ardisia_crispa
CMAUP NPO7002
PFAF Ardisia crispa

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
Cytotoxic Effects of Ardisiacrispin A from Labisia pumila on A549 Human Lung Cancer Cells Lee YG, Kim TH, Kwon JE, Kim H, Kang SC Life (Basel) 18-Feb-2024
PMCID:PMC10890250
doi:10.3390/life14020276
PMID:38398785
Genomic Insights into the Symbiotic and Plant Growth-Promoting Traits of “Candidatus Phyllobacterium onerii” sp. nov. Isolated from Endemic Astragalus flavescens Eren Eroğlu AE, Eroğlu V, Yaşa İ Microorganisms 06-Feb-2024
PMCID:PMC10891626
doi:10.3390/microorganisms12020336
PMID:38399740
Preliminary exploration of herbal tea products based on traditional knowledge and hypotheses concerning herbal tea selection: a case study in Southwest Guizhou, China Long X, Ranjitkar S, Waldstein A, Wu H, Li Q, Geng Y J Ethnobiol Ethnomed 02-Jan-2024
PMCID:PMC10763305
doi:10.1186/s13002-023-00645-w
PMID:38169414
An ethnobotanical study on the medicinal herb practices of the gelao ethnic minority in North Guizhou, China: an exploration of traditional knowledge Liu F, Peng J, Feng Y, Ma Y, Ren Y, Sun P, Zhao Y, Liu S, Wu F, Xie J Front Pharmacol 31-Aug-2023
PMCID:PMC10500598
doi:10.3389/fphar.2023.1217599
PMID:37719846
Pharmacological effects and mechanism of Kaihoujian Throat Spray (children's type) in the treatment of pediatric acute pharyngitis and tonsillitis Pang B, Zhao R, Peng B, Bao L, Geng Z, Li S, Xu Y, Zhou L, Guo S, Cui X, Sun J Heliyon 30-Jun-2023
PMCID:PMC10395134
doi:10.1016/j.heliyon.2023.e17802
PMID:37539230
Anticancer effects of herbal medicine Emelia-M, Mshikazi and Delosma H against human leukaemia cells Adeniyi JN, Nlooto M, Ngcobo M, Moodley R, Gomo E Afr Health Sci 01-Jun-2023
PMCID:PMC10782316
doi:10.4314/ahs.v23i2.35
PMID:38223600
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Exploring the anti‐cancer potential of dietary phytochemicals for the patients with breast cancer: A comprehensive review Sohel M, Aktar S, Biswas P, Amin MA, Hossain MA, Ahmed N, Mim MI, Islam F, Mamun AA Cancer Med 03-May-2023
PMCID:PMC10358259
doi:10.1002/cam4.5984
PMID:37132286
Oroxylin A inhibited autoimmune hepatitis-induced liver injury and shifted Treg/Th17 balance to Treg differentiation Zhu J, Chen H, Cui J, Zhang X, Liu G Exp Anim 13-Mar-2023
PMCID:PMC10435359
doi:10.1538/expanim.22-0171
PMID:36927981
The complete chloroplast genome sequence of Ardisia crispa Thunb. Guo S, Li Z, Liu Y, Wu W Mitochondrial DNA B Resour 09-Dec-2022
PMCID:PMC9744205
doi:10.1080/23802359.2022.2154621
PMID:36518737
Biogeochemical niche conservatism relates to plant species diversification and life form evolution in a subtropical montane evergreen broad‐leaved forest Bai K, Zhou X, Lv S, Wei S, Deng L, Tan Y Ecol Evol 03-Dec-2022
PMCID:PMC9719084
doi:10.1002/ece3.9587
PMID:36479033
Integrated transcriptome and metabolome analyses revealed regulatory mechanisms of flavonoid biosynthesis in Radix Ardisia Liu C, Pan J, Yin ZG, Feng T, Zhao J, Dong X, Zhou Y PeerJ 29-Jun-2022
PMCID:PMC9250311
doi:10.7717/peerj.13670
PMID:35789656
Anticancer potential of Phoenix dactylifera L. seed extract in human cancer cells and pro-apoptotic effects mediated through caspase-3 dependent pathway in human breast cancer MDA-MB-231 cells: an in vitro and in silico investigation Khan MA, Singh R, Siddiqui S, Ahmad I, Ahmad R, Upadhyay S, Barkat MA, Ali AM, Zia Q, Srivastava A, Trivedi A, Husain I, Srivastava AN, Mishra DP BMC Complement Med Ther 15-Mar-2022
PMCID:PMC8922853
doi:10.1186/s12906-022-03533-0
PMID:35291987
Cytotoxic 13,28 Epoxy Bridged Oleanane-Type Triterpenoid Saponins from the Roots of Ardisia crispa Yin X, Hu R, Zhou Y, Zhu W, Zhou Y Molecules 04-Feb-2022
PMCID:PMC8838445
doi:10.3390/molecules27031061
PMID:35164324
Screening of Particulate Matter Reduction Ability of 21 Indigenous Korean Evergreen Species for Indoor Use Jang BK, Park K, Lee SY, Lee H, Yeon SH, Ji B, Lee CH, Cho JS Int J Environ Res Public Health 17-Sep-2021
PMCID:PMC8466017
doi:10.3390/ijerph18189803
PMID:34574725

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
> Alkaloids and derivatives / Aporphines
(-)-Phanostenine 12305138 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)O)OC)OCO3 325.40 unknown via CMAUP database
(-)-Roemeroline 15559920 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5)O)OCO3 295.30 unknown via CMAUP database
(6aS)-1,2-dimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-10-ol 793837 Click to see COC1=C(C2=C3C(CC4=C2C=C(C=C4)O)NCCC3=C1)OC 297.30 unknown via CMAUP database
(7aS)-6,7,7aalpha,8-Tetrahydro-7-methyl-9,10-dimethoxy-5H-benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline 10042806 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5OC)OC)OCO3 339.40 unknown via CMAUP database
8H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-8-one, 9,10-dimethoxy- 3084713 Click to see COC1=C(C2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O)OC 335.30 unknown via CMAUP database
Cepharadione A 94577 Click to see CN1C2=CC3=CC=CC=C3C4=C2C(=CC5=C4OCO5)C(=O)C1=O 305.30 unknown via CMAUP database
Dehydroaporheine 161899 Click to see CN1CCC2=CC3=C(C4=C2C1=CC5=CC=CC=C54)OCO3 277.30 unknown via CMAUP database
Dehydrocrebanine 149600 Click to see CN1CCC2=CC3=C(C4=C5C=CC(=C(C5=CC1=C24)OC)OC)OCO3 337.40 unknown via CMAUP database
Dehydrophanostenine 179675 Click to see CN1CCC2=CC3=C(C4=C5C=C(C(=CC5=CC1=C24)OC)O)OCO3 323.30 unknown via CMAUP database
Isocorydine 10143 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown via CMAUP database
Lanuginosine 97622 Click to see COC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O 305.30 unknown via CMAUP database
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown via CMAUP database
Roemerine 119204 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown via CMAUP database
Steporphine 155631 Click to see CN1CC(C2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3)O 295.30 unknown via CMAUP database
Stesakine 157110 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5OC)O)OCO3 325.40 unknown via CMAUP database
> Alkaloids and derivatives / Aporphines / 4,5-dioxoaporphines
4,5-Dioxodehydrocrebanine 149599 Click to see CN1C2=C3C(=CC4=C(C3=C5C=CC(=C(C5=C2)OC)OC)OCO4)C(=O)C1=O 365.30 unknown via CMAUP database
> Alkaloids and derivatives / Hasubanan alkaloids
Aknadilactam 15764659 Click to see CN1C(=O)CC23C1(CCC4=C2C(=C(C=C4)OC)O)C(=C(C(=O)C3)OC)OC 373.40 unknown via CMAUP database
Aknadinine 159966 Click to see CN1CCC23C1(CCC4=C2C(=C(C=C4)OC)O)C(=C(C(=O)C3)OC)OC 359.40 unknown via CMAUP database
Cepharamine 12302744 Click to see CN1CCC23C1(CCC4=C2C(=C(C=C4)OC)O)C=C(C(=O)C3)OC 329.40 unknown via CMAUP database
> Alkaloids and derivatives / Proaporphines
(+)-Pronuciferine 200480 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC 311.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
(2R,3S,4S,10bS)-3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one 24982180 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)O)O)OC2=O)O 328.27 unknown via CMAUP database
> Lignans, neolignans and related compounds
(14aS,26aR)-2,3,13,14,14a,15,26,26a-Octahydro-22,30-dimethoxy-14-methyl-1H-4,6:16,19-dietheno-21,25-metheno-12H-[1,3]dioxolo[4,5-g]pyrido[2 inverted exclamation marka,3 inverted exclamation marka:17,18][1,10]dioxacycloeicosino[2,3,4-ij]isoquinoline 14488278 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=C(O3)C8=C(C=C7CCN6)OCO8)C=C5)OC 592.70 unknown via CMAUP database
Berbamine 275182 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown via CMAUP database
Cepharanthine 10206 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(C=C8CCN7C)OC)O4)OC)OCO3 606.70 unknown via CMAUP database
Obaberine 100231 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)OC)OC 622.70 unknown via CMAUP database
Thalrugosine 100257 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4S,5R,8R,13R,14R,17S,18R,20S)-10-[(2S,3R,4S,5S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-hydroxy-4,5,9,9,13,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosane-20-carbaldehyde 168133 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(CO4)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(CO6)O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)CCC89C3(CC(C1(C8CC(CC1)(C)C=O)CO9)O)C)C)C 1061.20 unknown https://doi.org/10.1055/S-2007-969346
https://doi.org/10.1055/S-2006-962758
(2R,4S,5R,8R,10S,13R,14R,18R,20S)-10-[(2S,3R,4S,5S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-3-[(2S,3R,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-hydroxy-4,5,9,9,13,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosane-20-carbaldehyde 194981 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3COC(C(C3O)OC4C(C(C(C(O4)CO)O)O)O)OC5CCC6(C(C5(C)C)CCC7(C6CCC89C7(CC(C1(C8CC(CC1)(C)C=O)CO9)O)C)C)C)CO)O)O)O)O)O 1075.20 unknown https://doi.org/10.1055/S-2006-962758
https://doi.org/10.1055/S-2007-969346
Ardisiacrispin B 10441164 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3COC(C(C3O)OC4C(C(C(C(O4)CO)O)O)O)OC5CCC6(C(C5(C)C)CCC7(C6CCC89C7(CC(C1(C8CC(CC1)(C)C=O)CO9)O)C)C)C)CO)O)O)O)O)O 1075.20 unknown https://doi.org/10.1055/S-2006-962758
https://doi.org/10.1055/S-2007-969346
Saxifragifolin B 138911402 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(CO4)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(CO6)O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)CCC89C3(CC(C1(C8CC(CC1)(C)C=O)CO9)O)C)C)C 1061.20 unknown https://doi.org/10.1055/S-2006-962758
https://doi.org/10.1055/S-2007-969346
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-methoxy-3-[4-[[(5S)-11-methoxy-6,19-dimethyl-20-oxo-2,13-dioxa-6,19-diazapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(14),3,9,11,15,21-hexaen-5-yl]methyl]phenoxy]benzaldehyde 389057 Click to see CN1CCC2=CC(=C3C(=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)C=O)OC)OC6=C(O3)C=C7CCN(C(=O)C7=C6)C)OC 606.70 unknown via CMAUP database
Secocepharanthine 102157843 Click to see CN1CCC2=CC3=C(C(=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)C=O)OC)OC6=C(C=C7CCN(C(=O)C7=C6)C)OC)OCO3 636.70 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
6,7-Dimethoxy-2-methylisoquinolin-1(2H)-one 11367984 Click to see CN1C=CC2=CC(=C(C=C2C1=O)OC)OC 219.24 unknown via CMAUP database

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Collections Top

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