Scientific name	Authority	First published in
Luculia intermedia	Hutch.	Pl. Wilson. 3: 408 (1916)
Luculia intermedia var. pubescens	W.C.Chen	Acta Phytotax. Sin. 22: 139 (1984)
Luculia pinceana var. pubescens	(W.C.Chen) W.C.Chen	Fl. Reipubl. Popularis Sin. 71(1): 241 (1999)

Common names Top

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Filter by language:

Language	Common/alternative name
Chinese	滇丁香
Chinese	滇丁香（滇丁草）

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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 click to expand
- China
  - China South-central
  - China Southeast
  - Tibet

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - East Himalaya
  - Nepal
- Indo-China
  - Myanmar
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000230741
Tropicos	50158742
KEW	urn:lsid:ipni.org:names:755399-1
The Plant List	kew-115285
Open Tree Of Life	746793
NCBI Taxonomy	170349
IUCN Red List	146526628
IPNI	755399-1
iNaturalist	410764
GBIF	2900018
EPPO	LULPI
EOL	1095234
USDA GRIN	22762
CMAUP	NPO23930

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 Nighttime Fragrance of Guettarda scabra (Rubiaceae): Flower Scent and Its Implications for Moth Pollination

Pimienta MC, Salazar D, Koptur S

Molecules

29-Aug-2023

PMCID:	PMC10489014
doi:	10.3390/molecules28176312
PMID:	37687140

Features of floral odor and nectar in the distylous Luculia pinceana (Rubiaceae) promote compatible pollination by hawkmoths

Wang X, Chen Y, Yi Y

Ecol Evol

21-Mar-2023

PMCID:	PMC10030271
doi:	10.1002/ece3.9920
PMID:	36969924

Basic Characteristics of Flower Transcriptome Data and Derived Novel EST-SSR Markers of Luculia yunnanensis, an Endangered Species Endemic to Yunnan, Southwestern China

Zhang Y, Liu X, Li Y, Liu X, Ma H, Qu S, Li Z

Plants (Basel)

29-Apr-2022

PMCID:	PMC9104135
doi:	10.3390/plants11091204
PMID:	35567204

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

Metabolite and Transcriptome Profiling Analysis Revealed That Melatonin Positively Regulates Floral Scent Production in Hedychium coronarium

Abbas F, Zhou Y, He J, Ke Y, Qin W, Yu R, Fan Y

Front Plant Sci

17-Dec-2021

PMCID:	PMC8719004
doi:	10.3389/fpls.2021.808899
PMID:	34975998

Evolution of Autonomous Selfing in Marginal Habitats: Spatiotemporal Variation in the Floral Traits of the Distylous Primula wannanensis

Zhang W, Hu YF, He X, Zhou W, Shao JW

Front Plant Sci

16-Dec-2021

PMCID:	PMC8716950
doi:	10.3389/fpls.2021.781281
PMID:	34975966

Headspace Volatiles and Endogenous Extracts of Prunus mume Cultivars with Different Aroma Types

Wang X, Wu Y, Zhu H, Zhang H, Xu J, Fu Q, Bao M, Zhang J

Molecules

30-Nov-2021

PMCID:	PMC8658796
doi:	10.3390/molecules26237256
PMID:	34885838

HS–SPME–GC–MS and Electronic Nose Reveal Differences in the Volatile Profiles of Hedychium Flowers

Zhou Y, Abbas F, Wang Z, Yu Y, Yue Y, Li X, Yu R, Fan Y

Molecules

06-Sep-2021

PMCID:	PMC8433901
doi:	10.3390/molecules26175425
PMID:	34500858

Self‐incompatibility limits sexual reproduction rather than environmental conditions in an invasive water primrose

Portillo Lemus LO, Bozec M, Harang M, Coudreuse J, Haury J, Stoeckel S, Barloy D

Plant Environ Interact

29-Mar-2021

PMCID:	PMC10168087
doi:	10.1002/pei3.10042
PMID:	37284282

Ethnomedicine study on traditional medicinal plants in the Wuliang Mountains of Jingdong, Yunnan, China

Gao L, Wei N, Yang G, Zhang Z, Liu G, Cai C

J Ethnobiol Ethnomed

19-Aug-2019

PMCID:	PMC6699132
doi:	10.1186/s13002-019-0316-1
PMID:	31426826

Identification of Floral Scent Profiles in Bearded Irises

Yuan Y, Sun Y, Zhao Y, Liu C, Chen X, Li F, Bao J

Molecules

07-May-2019

PMCID:	PMC6540295
doi:	10.3390/molecules24091773
PMID:	31067789

Discrimination of Malus Taxa with Different Scent Intensities Using Electronic Nose and Gas Chromatography–Mass Spectrometry

Fan J, Zhang W, Zhou T, Zhang D, Zhang D, Zhang L, Wang G, Cao F

Sensors (Basel)

12-Oct-2018

PMCID:	PMC6210091
doi:	10.3390/s18103429
PMID:	30322071

Comparative Proteomic and Physiological Analysis Reveals the Variation Mechanisms of Leaf Coloration and Carbon Fixation in a Xantha Mutant of Ginkgo biloba L.

Liu X, Yu W, Wang G, Cao F, Cai J, Wang H

Int J Mol Sci

27-Oct-2016

PMCID:	PMC5133795
doi:	10.3390/ijms17111794
PMID:	27801782

Volatile Organic Compounds Emissions from Luculia pinceana Flower and Its Changes at Different Stages of Flower Development

Li Y, Ma H, Wan Y, Li T, Liu X, Sun Z, Li Z

Molecules

22-Apr-2016

PMCID:	PMC6273779
doi:	10.3390/molecules21040531
PMID:	27110758

Flavonoids in Luculia pinceana

W. Y. Kang, J. M. Wang, Z. Q. Ji

Springer Science and Business Media LLC

19-Dec-2008

doi:	10.1007/S10600-008-9165-1

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane	12410	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	436.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(1R,3R,4R,4aS,8S,8aR)-4-[2-(furan-3-yl)ethyl]-8-(hydroxymethyl)-3,4a,8-trimethyl-2,3,5,6,7,8a-hexahydro-1H-naphthalene-1,4-diol	38350347	Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)CO)O	336.50	unknown	via CMAUP database
Marrubenol	10449689	Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)CO)O	336.50	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Betonicine	164642	Click to see C[N+]1(CC(CC1C(=O)[O-])O)C	159.18	unknown	via CMAUP database
L-Turicine	1550239	Click to see C[N+]1(CC(CC1C(=O)[O-])O)C	159.18	unknown	via CMAUP database
Turicine	6560290	Click to see C[N+]1(CC(CC1C(=O)[O-])O)C	159.18	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Forsythoside B	23928102	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O	756.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,4S,8S,9R,10S,12R)-9-[2-(furan-3-yl)ethyl]-9-hydroxy-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecan-3-one	25728881	Click to see CC1CC2C3C(CCCC3(C1(CCC4=COC=C4)O)C)(C(=O)O2)C	332.40	unknown	via CMAUP database
Marrubiin	73401	Click to see CC1CC2C3C(CCCC3(C1(CCC4=COC=C4)O)C)(C(=O)O2)C	332.40	unknown	via CMAUP database
Premarrubiin	168199	Click to see CC1CC2C3C(CCCC3(C14CCC5(O4)COC=C5)C)(C(=O)O2)C	332.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Acetoside	44429837	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	via CMAUP database
Phaselic acid, (-)-	92299542	Click to see C1=CC(=C(C=C1C=CC(=O)OC(CC(=O)O)C(=O)O)O)O	296.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vicenin 2	442664	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O	594.50	unknown	via CMAUP database
Vitexin	5280441	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Luteolin 7-glucuronide	5280601	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	12313332	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1007/S10600-008-9165-1
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	https://doi.org/10.1007/S10600-008-9165-1
Kaempferol-3-O-rhamnoside	5835713	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	https://doi.org/10.1007/S10600-008-9165-1
Kaempferol-3-O-rutinoside	5318767	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1007/S10600-008-9165-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin	5280704	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	via CMAUP database
Echinacin	6439941	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O	578.50	unknown	via CMAUP database
kaempferol 3-O-beta-D-glucopyranosyl-7-O-alpha-L-rhamnopyranoside	21606527	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O	594.50	unknown	https://doi.org/10.1007/S10600-008-9165-1
Kaempferol 3-rutinoside 7-rhamnoside	21676297	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O	740.70	unknown	https://doi.org/10.1007/S10600-008-9165-1
Kaempferol-3-O-glucoside-7-O-rhamnoside	14035324	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O	594.50	unknown	https://doi.org/10.1007/S10600-008-9165-1
Kaempferol, robinoside	5351997	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O	740.70	unknown	https://doi.org/10.1007/S10600-008-9165-1
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Transilitin	44258702	Click to see COC1=C(OC2=C(C1=O)C=CC(=C2O)O)C3=CC(=C(C=C3)O)O	316.26	unknown	https://doi.org/10.1007/S10600-008-9165-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Ladanein	3084066	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O	314.29	unknown	via CMAUP database

Biological Material Top

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Luculia pinceana

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