Rhododendron micranthum - Unknown
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Internal ID UUID6440769ce0fdb153385606
Scientific name Rhododendron micranthum
Authority Turcz.
First published in Bull. Soc. Imp. Naturalistes Moscou 21(I): 586 (1848)

Description Top

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Synonyms Top

Scientific name Authority First published in
Azalea micrantha (Turcz.) Kuntze Revis. Gen. Pl. 2: 387 (1891)
Rhododendron rosthornii Diels Bot. Jahrb. Syst. 29: 509 (1900)
Rhododendron pritzelianum Diels Bot. Jahrb. Syst. 29: 510 (1900)

Common names Top

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Language Common/alternative name
Azerbaijani xırdaçiçəkli rododendron
Korean 꼬리진달내
Korean 참꽃나무겨우살이
Korean 꼬리진달래
Chinese 冬青叶
Chinese 照山白
Chinese 白镜子
Chinese 照白杜鹃
Chinese 照白杜鵑

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
sprinkle seed on 10 cm damp sphagnum moss; cover with clear plastic pop bottle cut in half; transplant seedling to acidic mix in shade outdoors when 5 cm high; protect from rodents and give protection in cold frame first winter

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Manchuria
    • Eastern Asia
      • Korea

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001048103
Tropicos 12303850
KEW urn:lsid:ipni.org:names:332879-1
The Plant List tro-12303850
Open Tree Of Life 844316
NCBI Taxonomy 118363
IPNI 332879-1
iNaturalist 502261
GBIF 4170281
Freebase /m/0nc83c6
EPPO RHOMI
EOL 2891337
Elurikkus 479241
USDA GRIN 31454
Wikipedia Rhododendron_micranthum
CMAUP NPO26763

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
Re-identification of Colletotrichum gloeosporioides Species Complex Isolates in Korea and Their Host Plants Thao LD, Choi H, Choi Y, Mageswari A, Lee D, Kim DH, Shin HD, Choi H, Ju HJ, Hong SB Plant Pathol J 01-Feb-2024
PMCID:PMC10850535
doi:10.5423/PPJ.OA.09.2023.0133
PMID:38326955
The complete chloroplast genome sequence of Rhododendron farrerae Tate ex Sweet (Ericaceae) Shen J, Huang L Mitochondrial DNA B Resour 04-Jan-2024
PMCID:PMC10769518
doi:10.1080/23802359.2023.2294897
PMID:38187010
Genome Survey Sequencing and Genetic Background Characterization of Ilex chinensis Sims (Aquifoliaceae) Based on Next-Generation Sequencing Zhou P, Li J, Huang J, Li F, Zhang Q, Zhang M Plants (Basel) 01-Dec-2022
PMCID:PMC9740704
doi:10.3390/plants11233322
PMID:36501361
Distribution of Woody Plant Species Among Different Disturbance Regimes of Forests in a Temperate Deciduous Broad-Leaved Forest Xi J, Shao Y, Li Z, Zhao P, Ye Y, Li W, Chen Y, Yuan Z Front Plant Sci 06-Apr-2021
PMCID:PMC8056040
doi:10.3389/fpls.2021.618524
PMID:33889163
Genome Survey Sequencing of In Vivo Mother Plant and In Vitro Plantlets of Mikania cordata Hong Y, Huang X, Li C, Ruan X, Wang Z, Su Y, Wang T Plants (Basel) 27-Nov-2020
PMCID:PMC7759884
doi:10.3390/plants9121665
PMID:33261119
Research Progress of the Antiviral Bioactivities of Natural Flavonoids Wang L, Song J, Liu A, Xiao B, Li S, Wen Z, Lu Y, Du G Nat Prod Bioprospect 18-Sep-2020
PMCID:PMC7500501
doi:10.1007/s13659-020-00257-x
PMID:32948973
Genome survey sequencing and identification of genomic SSR markers for Rhododendron micranthum Zhou XJ, Liu MX, Lu XY, Sun SS, Cheng YW, Ya HY Biosci Rep 18-Jun-2020
PMCID:PMC7303352
doi:10.1042/BSR20200988
PMID:32495827
Pathway-specific enzymes from bamboo and crop leaves biosynthesize anti-nociceptive C-glycosylated flavones Sun Y, Chen Z, Yang J, Mutanda I, Li S, Zhang Q, Zhang Y, Zhang Y, Wang Y Commun Biol 06-Mar-2020
PMCID:PMC7060329
doi:10.1038/s42003-020-0834-3
PMID:32144397
Medicinal wild plants used by the Mongol herdsmen in Bairin Area of Inner Mongolia and its comparative study between TMM and TCM Wurchaih, Huar, Menggenqiqig, Khasbagan J Ethnobiol Ethnomed 03-Jul-2019
PMCID:PMC6609360
doi:10.1186/s13002-019-0300-9
PMID:31269968
Micranthanosides I and II, two novel 1,10-secograyanane diterpenoids and their antinociceptive analogues from the leaves and twigs of Rhododendron micranthum Zhu Y, Yan H, Wang X, Zhang Z, Zhang H, Chai L, Li L, Qu J, Li Y RSC Adv 11-Jun-2019
PMCID:PMC9064816
doi:10.1039/c9ra01736d
PMID:35515239
Prediction of Lime Tolerance in Rhododendron Based on Herbarium Specimen and Geochemical Data Wang S, Leus L, Van Labeke MC, Van Huylenbroeck J Front Plant Sci 23-Oct-2018
PMCID:PMC6206291
doi:10.3389/fpls.2018.01538
PMID:30405673
Extract of Nicotiana tabacum as a potential control agent of Grapholita molesta (Lepidoptera: Tortricidae) Sarker S, Lim UT PLoS One 23-Aug-2018
PMCID:PMC6107112
doi:10.1371/journal.pone.0198302
PMID:30138428
Reference gene selection for qRT-PCR analysis of flower development in Lagerstroemia indica and L. speciosa Zheng T, Chen Z, Ju Y, Zhang H, Cai M, Pan H, Zhang Q PLoS One 26-Mar-2018
PMCID:PMC5868847
doi:10.1371/journal.pone.0195004
PMID:29579116
Factors controlling throughfall in a Pinus tabulaeformis forest in North China Wei X, Bi H, Liang W Sci Rep 25-Oct-2017
PMCID:PMC5656610
doi:10.1038/s41598-017-14464-z
PMID:29070837
Synopsis of Phyllosticta in China Zhang K, Shivas RG, Cai L Mycology 17-Apr-2015
PMCID:PMC4409051
doi:10.1080/21501203.2015.1027507
PMID:26000199

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Grayanoids / Leucothol and grayanotoxane diterpenoids
Grayanotoxin I 9548612 Click to see CC(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)CC(C4(C)C)O)O)O)CC2(C)O 412.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
L-Born-2-yl acetate 44630108 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Cadinol 6428423 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
Caryophyllene oxide 2 13240188 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
20-Hydroxyecdysone 5459840 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown via CMAUP database
24-epi-Pterosterone 11027254 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)O 480.60 unknown via CMAUP database
25S-Inokosterone 12358616 Click to see CC(CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)CO 480.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
Ponasterone A 115127 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O 464.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
22,23-Dihydrobrassicasterol 5283637 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
Ergosta-5-ene-3beta-yl 6-O-palmitoyl-beta-D-glucopyranoside 13051627 Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(C)C(C)C)C)C)O)O)O 801.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-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 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Sitoindoside I 9832350 Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 815.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Blechnic acid 10316325 Click to see C1=CC(=C(C=C1C2C(C3=C(C=CC(=C3O2)O)C=CC(=O)O)C(=O)O)O)O 358.30 unknown via CMAUP database
Brainic acid 10436502 Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C2C(OC3=C(C=CC(=C23)C=CC(=O)O)O)C4=CC(=C(C=C4)O)O 514.40 unknown via CMAUP database
Przewalskinic acid A 9975641 Click to see C1=CC(=C(C=C1C2C(C3=C(C=CC(=C3O2)O)C=CC(=O)O)C(=O)O)O)O 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydrochromen-2-one 11953803 Click to see COC1=C(C=C2C(=C1)CCC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 356.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Kaempferol oxoanion 25202062 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)[O-])O 285.23 unknown via CMAUP database
Quercetin-7-olate 46906036 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)[O-])O)O 301.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Gossypetin 5280647 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O)O 318.23 unknown via CMAUP database
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
4-[5,7-dihydroxy-4-oxo-3-[(3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-yl]-2-hydroxyphenolate 54758589 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)[O-] 463.40 unknown via CMAUP database
CID 44258797 44258797 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 11968523 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O 804.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Woodorien 192694 Click to see COC(=O)C1=CC(=C(C=C1)O)OC2C(C(C(C(O2)CO)O)O)O 330.29 unknown via CMAUP database

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