Scientific name	Authority	First published in
Azalea elliptica	(Maxim.) Kuntze	Revis. Gen. Pl. 2: 387 (1891)
Rhododendron amamiense	Ohwi	Acta Phytotax. Geobot. 6: 49 (1937)
Rhododendron tanakae	Hayata	Icon. Pl. Formosan. 4: 15 (1914)
Rhododendron wilsoniae	Hemsl. & E.H.Wilson	Bull. Misc. Inform. Kew 1910: 116 (1910)
Rhododendron wilsoniae var. ionanthum	W.P.Fang	Acta Phytotax. Sin. 21(4): 463. 1983 [18 Nov 1983]
Rhododendron leiopodum	Hayata	Icon. Pl. Formosan. 3: 136 (1913)
Rhododendron leptosanthum	Hayata	Icon. Pl. Formosan. 3: 137 (1913)
Rhododendron latoucheae var. ionanthum	(W.P.Fang) G.Z.Li	Guihaia 15(3): 205. 1995
Rhododendron ellipticum var. leptosanthum	(Hayata) S.S.Ying	Quart. J. Chin. Forest. 9(4): 122 (1976)
Rhododendron latoucheae var. amamiense	(Ohwi) T.Yamaz.	Revis. Gen. Rhododendron Japan, Taiwan, Korea & Sakhalin : 25 (1996)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Japanese	聖紫花
Japanese	セイシカ
Korean	성자화
Chinese	云锦杜鹃
Chinese	西施花
Chinese	鹿角杜鹃
Chinese	光脚杜鹃
Chinese	岩杜鹃
Chinese	鹿角杜鵑

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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 click to expand
- China
  - China South-central
  - China Southeast
- Eastern Asia
  - Nansei-shoto
  - Taiwan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001229749
Tropicos	50060696
KEW	urn:lsid:ipni.org:names:332730-1
The Plant List	tro-50060696
Open Tree Of Life	695238
NCBI Taxonomy	184576
IPNI	332730-1
iNaturalist	348980
GBIF	7328541
EOL	2891318
USDA GRIN	459050
CMAUP	NPO9925

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

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

Bioactive Steroids Bearing Oxirane Ring

Dembitsky VM

Biomedicines

09-Aug-2023

PMCID:	PMC10452232
doi:	10.3390/biomedicines11082237
PMID:	37626733

Insight into the Molecular Mechanism of Flower Color Regulation in Rhododendron latoucheae Franch: A Multi-Omics Approach

Xiao P, Zhang H, Liao Q, Zhu N, Chen J, Ma L, Zhang M, Shen S

Plants (Basel)

08-Aug-2023

PMCID:	PMC10458524
doi:	10.3390/plants12162897
PMID:	37631109

Characterization Variation of the Differential Coloring Substances in Rapeseed Petals with Different Colors Using UPLC-HESI-MS/MS

Zeng H, Zheng T, Li Y, Chen Q, Xue Y, Tang Q, Xu H, Chen M

Molecules

26-Jul-2023

PMCID:	PMC10419860
doi:	10.3390/molecules28155670
PMID:	37570640

Phytolith Assemblages as a Promising Tool for Quantitative Canopy Coverage Reconstruction in Subtropical Forests, China

Li N, Yu F, Sack D, Huang Z, Tian G, Liu S

Front Plant Sci

20-Jun-2022

PMCID:	PMC9251495
doi:	10.3389/fpls.2022.912627
PMID:	35795347

Anti-viral triterpenes: a review

Darshani P, Sen Sarma S, Srivastava AK, Baishya R, Kumar D

Phytochem Rev

05-Mar-2022

PMCID:	PMC8896976
doi:	10.1007/s11101-022-09808-1
PMID:	35283698

De novo transcriptomic analysis and identification of EST-SSR markers in Stephanandra incisa

Zhang C, Wu Z, Jiang X, Li W, Lu Y, Wang K

Sci Rep

13-Jan-2021

PMCID:	PMC7806653
doi:	10.1038/s41598-020-80329-7
PMID:	33441871

Full-length transcriptome sequencing analysis and development of EST-SSR markers for the endangered species Populus wulianensis

Wu Q, Zang F, Xie X, Ma Y, Zheng Y, Zang D

Sci Rep

01-Oct-2020

PMCID:	PMC7530656
doi:	10.1038/s41598-020-73289-5
PMID:	33004908

Natural Products-Derived Chemicals: Breaking Barriers to Novel Anti-HSV Drug Development

Treml J, Gazdová M, Šmejkal K, Šudomová M, Kubatka P, Hassan ST

Viruses

29-Jan-2020

PMCID:	PMC7077281
doi:	10.3390/v12020154
PMID:	32013134

Rhodoterpenoids A‒C, Three New Rearranged Triterpenoids from Rhododendron latoucheae by HPLC‒MS‒SPE‒NMR

Liu F, Wang YN, Li Y, Ma SG, Qu J, Liu YB, Niu CS, Tang ZH, Zhang TT, Li YH, Li L, Yu SS

Sci Rep

11-Aug-2017

PMCID:	PMC5554136
doi:	10.1038/s41598-017-06320-x
PMID:	28801631

Similarity of plant functional traits and aggregation pattern in a subtropical forest

Zhang B, Lu X, Jiang J, DeAngelis DL, Fu Z, Zhang J

Ecol Evol

26-Apr-2017

PMCID:	PMC5478052
doi:	10.1002/ece3.2973
PMID:	28649322

Tree Species Traits but Not Diversity Mitigate Stem Breakage in a Subtropical Forest following a Rare and Extreme Ice Storm

Nadrowski K, Pietsch K, Baruffol M, Both S, Gutknecht J, Bruelheide H, Heklau H, Kahl A, Kahl T, Niklaus P, Kröber W, Liu X, Mi X, Michalski S, von Oheimb G, Purschke O, Schmid B, Fang T, Welk E, Wirth C

PLoS One

30-May-2014

PMCID:	PMC4039427
doi:	10.1371/journal.pone.0096022
PMID:	24879434

Spatial Heterogeneity of Soil Chemical Properties in a Subtropical Karst Forest, Southwest China

Zhang Z, Hu B, Hu G

ScientificWorldJournal

12-Feb-2014

PMCID:	PMC3943189
doi:	10.1155/2014/473651
PMID:	24715813

Topographic Variation in Aboveground Biomass in a Subtropical Evergreen Broad-Leaved Forest in China

Lin D, Lai J, Muller-Landau HC, Mi X, Ma K

PLoS One

30-Oct-2012

PMCID:	PMC3484055
doi:	10.1371/journal.pone.0048244
PMID:	23118961

Constituents from the leaves of Rhododendron latoucheae.

Fan CQ, Zhao WM, Ding BY, Qin GW

Fitoterapia

01-May-2001

doi:	10.1016/S0367-326X(00)00316-6
PMID:	11395277

Phytochemical Profile Top

Add a new one!

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 / Aristolactams
2-Hydroxy-1,5-dimethoxydibenzo[cd,f]indol-4(5H)-one	622222	Click to see COC1=C(C=C2C3=C1C4=CC=CC=C4C=C3N(C2=O)OC)O	295.29	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
2,4,5-Trimethoxybenzaldehyde	20525	Click to see COC1=CC(=C(C=C1C=O)OC)OC	196.20	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(1S,5R,6R,7R,8S)-7-(3,4-dimethoxyphenyl)-8-hydroxy-5-methoxy-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one	44470608	Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)O)C3=CC(=C(C=C3)OC)OC	358.40	unknown	via CMAUP database
Kadsurenin L	3083437	Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)OC(=O)C)C3=CC(=C(C=C3)OC)OC	400.50	unknown	via CMAUP database
Piperenone	36406703	Click to see CC1C(OC2(C1(C=C(C(=O)C2)CC=C)OC)OC)C3=CC(=C(C=C3)OC)OC	388.50	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Elemicin	10248	Click to see COC1=CC(=CC(=C1OC)OC)CC=C	208.25	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Galbacin	11175182	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C	340.40	unknown	via CMAUP database
(2S)-2alpha-(3,4-Dimethoxyphenyl)-3beta,4alpha-dimethyl-5alpha-(1,3-benzodioxole-5-yl)tetrahydrofuran	26113495	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C	356.40	unknown	via CMAUP database
4-[(2R,3S,4R,5R)-5-(1,3-Benzodioxol-5-yl)tetrahydro-3,4-dimethyl-2-furanyl]-2-methoxyphenol	11078392	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)O)OC)C	342.40	unknown	via CMAUP database
4-[(2S,3R,4R,5R)-5-(3,4-dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol	93061877	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)OC)OC)C	358.40	unknown	via CMAUP database
5-((2R,3R,4S,5R)-5-(3,4-Dimethoxyphenyl)-3,4-dimethyloxolan-2-yl)-1,3-benzodioxole	188429	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C	356.40	unknown	via CMAUP database
Futokadsurin A	9548904	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)OC)OC)C	358.40	unknown	via CMAUP database
futokadsurin B	9548905	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C	356.40	unknown	via CMAUP database
futokadsurin C	9548906	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C	356.40	unknown	via CMAUP database
Galbelgin	11975378	Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C	372.50	unknown	via CMAUP database
Galgravin	101749	Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C	372.50	unknown	via CMAUP database
Machillin F	10450045	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)O)OC)C	342.40	unknown	via CMAUP database
nectandrin A	156516	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)OC)OC)C	358.40	unknown	via CMAUP database
Veraguensin	443026	Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C	372.50	unknown	via CMAUP database
Zuihonin A	338287	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C	340.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Pellitorine	5318516	Click to see CCCCCC=CC=CC(=O)NCC(C)C	223.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E,7S,11R)-3,7,11,15-tetramethylhexadec-2-en-1-ol	6474938	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	via CMAUP database
Phytol	5280435	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(2S)-2-[(3E)-4,8-dimethylnona-3,7-dienyl]-2,8-dimethyl-3,4-dihydrochromen-6-ol	163194297	Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)C)O	328.50	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
(4S)-4-[(E)-1-(1,3-benzodioxol-5-yl)prop-1-en-2-yl]-4,5-dimethoxy-2-prop-2-enylcyclohexa-2,5-dien-1-one	101833872	Click to see CC(=CC1=CC2=C(C=C1)OCO2)C3(C=C(C(=O)C=C3OC)CC=C)OC	354.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(1S,3R,4R)-3,4-Dihydroxy-4-[(1E,3R)-3-hydroxy-1-buten-1-yl]-3,5,5-trimethylcyclohexyl beta-D-glucopyranoside	23757168	Click to see CC(C=CC1(C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C)O)O	406.50	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
2-[3,4-Dihydroxy-4-(3-hydroxybut-1-enyl)-3,5,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	74029755	Click to see CC(C=CC1(C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C)O)O	406.50	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
Kiwiionoside	131752431	Click to see CC(C=CC1(C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C)O)O	406.50	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,5R,7aS)-5-butoxy-5-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid	162924466	Click to see CCCCOC1(C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO)O	462.40	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
(1S,4aS,5S,7aS)-5-butoxy-5-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid	162924467	Click to see CCCCOC1(C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO)O	462.40	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
5-butoxy-5-hydroxy-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid	162924465	Click to see CCCCOC1(C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO)O	462.40	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
5-Butoxy-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid	163187674	Click to see CCCCOC1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO	446.40	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
6alpha-Hydroxygeniposide; Deacetylasperulosidic acid methyl ester	3515876	Click to see COC(=O)C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O	404.40	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
Galioside	185774	Click to see COC(=O)C1=COC(C2C1C=CC2(CO)O)OC3C(C(C(C(O3)CO)O)O)O	404.40	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
methyl 7-hydroxy-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylate	100058	Click to see COC(=O)C1=COC(C2C1C=CC2(CO)O)OC3C(C(C(C(O3)CO)O)O)O	404.40	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
Scandoside methyl ester	442433	Click to see COC(=O)C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O	404.40	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Ursolic acid	220774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/S0367-326X(00)00316-6
2-[[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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73072970	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	574.80	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
24-Ethylcholest-5-en-3beta-ol	22012	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/S0367-326X(00)00316-6
Beta-Sitosterol	222284	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/S0367-326X(00)00316-6
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	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	https://doi.org/10.1016/S0367-326X(00)00316-6
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	https://doi.org/10.1016/S0367-326X(00)00316-6
Stigmasterol glucoside	6602508	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	574.80	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-Hydroxytyrosol 3-O-glucoside	5315870	Click to see C1=CC(=C(C=C1CCO)OC2C(C(C(C(O2)CO)O)O)O)O	316.30	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
Cimidahurnine	23928092	Click to see C1=CC(=C(C=C1CCO)OC2C(C(C(C(O2)CO)O)O)O)O	316.30	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
Tachioside	11962143	Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)CO)O)O)O)O	302.28	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
Zingerone beta-D-glucopyranoside	90743708	Click to see CC(=O)CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC	356.40	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
Zingerone glucoside	74937233	Click to see CC(=O)CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC	356.40	unknown	https://doi.org/10.1016/S0367-326X(00)00316-6
> Organoheterocyclic compounds / Benzodioxoles
(2beta,4beta,5alpha,5abeta)-4-(1,3-Benzodioxol-5-yl)-2,3,4,5-tetrahydro-7-methoxy-5-methyl-8H-2,5a-methano-1-benzoxepin-8-one	101820916	Click to see CC1C(CC2CC13C=C(C(=O)C=C3O2)OC)C4=CC5=C(C=C4)OCO5	340.40	unknown	via CMAUP database
(E,E)-Futoamide	15596445	Click to see CC(C)CNC(=O)C=CCCC=CC1=CC2=C(C=C1)OCO2	301.40	unknown	via CMAUP database
Kadsurin A	442885	Click to see CC1C(OC2(C1(C=C(C(=O)C2)CC=C)OC)OC)C3=CC4=C(C=C3)OCO4	372.40	unknown	via CMAUP database
Kadsurin B	10022290	Click to see CC1C(OC2(C1(C=C(C(C2)O)CC=C)OC)OC)C3=CC4=C(C=C3)OCO4	374.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-azaniumyl-3-(1H-indol-3-yl)propanoate	6923516	Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)[O-])[NH3+]	204.22	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2beta-(3,4-Dimethoxyphenyl)-3alpha-methyl-3aalpha-methoxy-5-allyl-2,3,3a,6-tetrahydrobenzofuran-6-one	10915273	Click to see CC1C(OC2=CC(=O)C(=CC12OC)CC=C)C3=CC(=C(C=C3)OC)OC	356.40	unknown	via CMAUP database
Kadsurenin M	208856	Click to see CC1C(OC2=C1C=C(C=C2OC)C=O)C3=CC(=C(C=C3)OC)OC	328.40	unknown	via CMAUP database
Kadsurenone	122159	Click to see CC1C(OC2=CC(=O)C(=CC12OC)CC=C)C3=CC(=C(C=C3)OC)OC	356.40	unknown	via CMAUP database

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Rhododendron latoucheae

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top