Scientific name	Authority	First published in
Mussaenda parviflora var. formosana	Matsum.	Bot. Mag. (Tokyo) 24: 147. 1900
Mussaenda parviflora var. yaeyamensis	(Masam.) T.Yamaz.	J. Jap. Bot. 39: 320 1964
Mussaenda pubescens var. yaeyamensis	Masam.	Trans. Nat. Hist. Soc. Formosa 29: 831. 1939
Mussaenda taihokuensis	Masam.	Trans. Nat. Hist. Soc. Formosa 29: 179 (1939)
Mussaenda yaeyamensis	(Masam.) Masam.	Trans. Nat. Hist. Soc. Formosa 29: 216 (1939)

Common names Top

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Language	Common/alternative name
Japanese	コンロンカ
Chinese	玉葉金花
Chinese	小玉叶金花
Chinese	小玉葉金花

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 click to expand
- China
  - China Southeast
- Eastern Asia
  - Japan
  - Nansei-shoto
  - Taiwan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000246713
Tropicos	50087444
KEW	urn:lsid:ipni.org:names:756761-1
The Plant List	kew-130539
Open Tree Of Life	3877288
NCBI Taxonomy	2100675
IPNI	756761-1
iNaturalist	607635
GBIF	2892619
EPPO	MDAPA
EOL	1103337
USDA GRIN	24779
CMAUP	NPO26078
Wikipedia	Mussaenda_parviflora

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

Stem cambial variants of Taiwan lianas

Yang SZ, Chen PH, Chen JJ

Bot Stud

24-Sep-2022

PMCID:	PMC9509506
doi:	10.1186/s40529-022-00358-5
PMID:	36153445

Shift of Host Range for the Immature Stages of the Lanternfly, Pyrops watanabei (Matsumura) (Hemiptera, Fulgoridae) Native to Taiwan

Hsu MH, Yang YL, Wu ML, Wang LJ

Insects

12-Sep-2022

PMCID:	PMC9500622
doi:	10.3390/insects13090826
PMID:	36135527

Iridoid Glycosides Isolated from Bellardia trixago Identified as Inhibitors of Orobanche cumana Radicle Growth

Soriano G, Siciliano A, Fernández-Aparicio M, Cala Peralta A, Masi M, Moreno-Robles A, Guida M, Cimmino A

Toxins (Basel)

17-Aug-2022

PMCID:	PMC9414233
doi:	10.3390/toxins14080559
PMID:	36006221

Is heterostyly rare on oceanic islands?

Watanabe K, Sugawara T

AoB Plants

21-Jul-2015

PMCID:	PMC4570599
doi:	10.1093/aobpla/plv087
PMID:	26199401

Two new iridoid glucosides from Mussaenda parviflora and Mussaenda shikokiana

Yoshio Takeda, Hiroshi Nishimura, Hiroyuki Inouye

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)88791-9

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 / Phenol ethers / Anisoles
1,2,3-Trimethoxybenzene	12462	Click to see COC1=C(C(=CC=C1)OC)OC	168.19	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
5-chloro-2-(4-(2-(2-hydroxyethoxy)ethyl)piperazin-1-yl)-N-(6-(3-methoxybenzamido)pyridin-3-yl)isonicotinamide	13848072	Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O	390.40	unknown	https://doi.org/10.1016/S0031-9422(00)88791-9
methyl (1S,4aS,7S,7aS)-7-hydroxy-7-methyl-1-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate	163191389	Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O	390.40	unknown	https://doi.org/10.1016/S0031-9422(00)88791-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
3beta-(2-O-beta-D-Galactopyranosyl-beta-D-glucurono pyranosyloxy)olean-12-en-28-oic acid	101923141	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)O)C	795.00	unknown	via CMAUP database
Araloside A	10079497	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C	927.10	unknown	via CMAUP database
Calenduloside E	176079	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)O)C	632.80	unknown	via CMAUP database
Calenduloside F	13909684	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C	795.00	unknown	via CMAUP database
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylate	21669007	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)OC)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C	971.10	unknown	via CMAUP database
Narcissiflorine	162878	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C	764.90	unknown	via CMAUP database
Papyrioside LE	11803947	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CCC7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O	941.10	unknown	via CMAUP database
Papyrioside LF	10819773	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CCC7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)COC(=O)C)O)O)O	983.10	unknown	via CMAUP database
Scheffleraside II	101720880	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(C(O9)C(=O)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O	1103.20	unknown	via CMAUP database
Udosaponin B	21635582	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C	957.10	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	13878127	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)O)C	588.80	unknown	via CMAUP database
3-Epipapyriogenin C	16112782	Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)O)C)C	468.70	unknown	via CMAUP database
3-O-alpha-L-Arabinopyranosylechinocystic acid	15379012	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(CO6)O)O)O)C)C(=O)O)C	604.80	unknown	via CMAUP database
3alpha,21beta,22alpha-Trihydroxyoleana-11,13(18)-diene-28-oic acid	16112781	Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1O)O)C(=O)O)C)C)(C)C)O)C)C	486.70	unknown	via CMAUP database
Guaianin N	10395290	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C	751.00	unknown	via CMAUP database
Papyriogenin A	3081523	Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)C)C	466.70	unknown	via CMAUP database
Papyriogenin C	3081568	Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)O)C)C	468.70	unknown	via CMAUP database
Papyriogenin D	101277260	Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)C)C	468.70	unknown	via CMAUP database
Papyriogenin E	101277261	Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)O)C)C	470.70	unknown	via CMAUP database
Papyriogenin F	102239749	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)O)C)C	470.70	unknown	via CMAUP database
Papyrioside LG	10605857	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CC=C7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O	939.10	unknown	via CMAUP database
Papyrioside LH	10748397	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CC=C7C6(CCC8C7(CCC(=O)C8(C)C)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O	937.10	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
28-Noroleana-11,13(18),17(22)-triene-3,21-dione	102588576	Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2=CC1=O)C)C)(C)C)C)C	420.60	unknown	via CMAUP database
3alpha-Hydroxy-28-noroleana-11,13(18),17(22)-triene-21-one	102588575	Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2=CC1=O)C)C)(C)C)O)C)C	422.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
1-Benzofuran-5-carbaldehyde	2773875	Click to see C1=CC2=C(C=CO2)C=C1C=O	146.14	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Beta propiolactones
Papyriogenin G	101967008	Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC26C(C1O)OC6=O)C)C)(C)C)O)C)C	468.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
3,4-Dihydrocoumarin	660	Click to see C1CC(=O)OC2=CC=CC=C21	148.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Phenylallyl alcohol	308	Click to see C1=CC=C(C=C1)C=CCO	134.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin	323	Click to see C1=CC=C2C(=C1)C=CC(=O)O2	146.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Kaempferol 3,4',7-triacetate	44584293	Click to see CC(=O)OC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC(=O)C)O)OC(=O)C	412.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin	5316673	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	432.40	unknown	via CMAUP database
Astragalin	5282102	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-7-O-glycosides
kaempferol 7-O-(2-E-p-coumaroyl-alpha-L-rhamnopyranoside)	11678667	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)O)O	578.50	unknown	via CMAUP database
kaempferol 7-O-(2,3-di-E-p-coumaroyl-alpha-L-rhamnopyranoside)	11607311	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O)O	724.70	unknown	via CMAUP database

Biological Material Top

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Mussaenda parviflora

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