Scientific name	Authority	First published in
Lythrum flavum	Spreng.	Syst. Veg. 2: 454 (1825)
Chrysolyga salicifolia	Willd. ex Steud.	Nomencl. Bot. , ed. 2, 1: 359 (1840)
Decodon salicifolius	Kuntze	Revis. Gen. Pl. 1: 249 (1891)
Ginoria flava	ex DC.	Prodr. [A. P. de Candolle] 3: 89. 1828 [mid Mar 1828]
Heimia grandiflora	Hook.	Hooker's Icon. Pl. 6: t. 554 (1843)
Heimia linariifolia	hort. ex G.Don	Hort. Brit. : 479 (1830)
Heimia syphilitica	DC.	Prodr. 3: 89 (1828)
Nesaea salicifolia	Kunth	Nov. Gen. Sp. 6: 192 (1824)
Nesaea syphilitica	Steud.	Flora 25: 474 (1842)
Heimia salicifolia var. grandiflora	Lindl.	Edwards's Bot. Reg. 27: t. 60 (1841)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	shrubby yellowcrest
German	sinicuichi
French	sinicuichi
Russian	Хеймия
Chinese	柳叶霓裳花
Chinese	柳叶黄薇
Chinese	黄薇属

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000717021
UNII	S7XS2V66EB
USDA Plants	HESA
Tropicos	19200241
INPN	448269
KEW	urn:lsid:ipni.org:names:96613-3
The Plant List	kew-2841927
Missouri Botanical Garden	295557
PFAF	Heimia salicifolia
Open Tree Of Life	916530
NCBI Taxonomy	312921
Nature Serve	2.143677
IPNI	553484-1
iNaturalist	157498
GBIF	5420914
Freebase	/m/03x7z5
EPPO	HEISA
EOL	582105
USDA GRIN	27904
Wikipedia	Heimia_salicifolia
CMAUP	NPO26661

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 Meaning of Plants' Names: A New Discovering Approach to Its Medicinal and/or Toxic Properties

dos Santos Dantas Lima L, Felipe Domingues Passero L, Indriunas A, de Souza Santos I, Francisco Uchôa Coqueiro L, Alexandre Souza da Cruz K, Batista de Almeida A, Carlos Fernandes Galduróz J, Rodrigues E

Evid Based Complement Alternat Med

19-Feb-2024

PMCID:	PMC10896657
doi:	10.1155/2024/6678557
PMID:	38410808

Helmet Shape and Phylogeography of the Treehopper Membracis mexicana

De-la-Mora M, Pinero D

Insects

14-Aug-2023

PMCID:	PMC10455800
doi:	10.3390/insects14080704
PMID:	37623414

Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity

Cely-Veloza W, Kato MJ, Coy-Barrera E

ACS Omega

28-Jul-2023

PMCID:	PMC10413377
doi:	10.1021/acsomega.3c02179
PMID:	37576649

A Complete Review of Mexican Plants with Teratogenic Effects

Chamorro-Cevallos G, Mojica-Villegas MA, García-Martínez Y, Pérez-Gutiérrez S, Madrigal-Santillán E, Vargas-Mendoza N, Morales-González JA, Cristóbal-Luna JM

Plants (Basel)

24-Jun-2022

PMCID:	PMC9268836
doi:	10.3390/plants11131675
PMID:	35807626

Real-Time Feeding Behavior Monitoring by Electrical Penetration Graph Rapidly Reveals Host Plant Susceptibility to Crapemyrtle Bark Scale (Hemiptera: Eriococcidae)

Wu B, Chun E, Xie R, Knox GW, Gu M, Qin H

Insects

25-May-2022

PMCID:	PMC9224517
doi:	10.3390/insects13060495
PMID:	35735833

Novel land uses shape meta-community structures in neighbouring native forests: Dataset across Uruguay

Säumel I, Ramírez LR

Data Brief

16-May-2022

PMCID:	PMC9130530
doi:	10.1016/j.dib.2022.108267
PMID:	35647241

Native forest metacommunity structures in Uruguay shaped by novel land‐use types in their surroundings

Ramírez LR, Säumel I

Ecol Evol

06-Mar-2022

PMCID:	PMC8928906
doi:	10.1002/ece3.8700
PMID:	35342551

On the application of 3d metals for C–H activation toward bioactive compounds: The key step for the synthesis of silver bullets

Carvalho RL, de Miranda AS, Nunes MP, Gomes RS, Jardim GA, Júnior EN

Beilstein J Org Chem

30-Jul-2021

PMCID:	PMC8329403
doi:	10.3762/bjoc.17.126
PMID:	34386103

A review study on the anti-trichomonas activities of medicinal plants

Hashemi N, Ommi D, Kheyri P, Khamesipour F, Setzer WN, Benchimol M

Int J Parasitol Drugs Drug Resist

12-Feb-2021

PMCID:	PMC7902805
doi:	10.1016/j.ijpddr.2021.01.002
PMID:	33610966

Host Suitability for Crapemyrtle Bark Scale (Acanthococcus lagerstroemiae) Differed Significantly among Crapemyrtle Species

Wu B, Xie R, Knox GW, Qin H, Gu M

Insects

23-Dec-2020

PMCID:	PMC7823534
doi:	10.3390/insects12010006
PMID:	33374734

Feeding Preference of Crapemyrtle Bark Scale (Acanthococcus lagerstroemiae) on Different Species

Xie R, Wu B, Dou H, Liu C, Knox GW, Qin H, Gu M

Insects

28-Jun-2020

PMCID:	PMC7412028
doi:	10.3390/insects11070399
PMID:	32605244

Exchange of medicinal plant information in California missions

McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL

J Ethnobiol Ethnomed

15-Jun-2020

PMCID:	PMC7296748
doi:	10.1186/s13002-020-00388-y
PMID:	32539795

Plant tissue culture as a perpetual source for production of industrially important bioactive compounds

Chandran H, Meena M, Barupal T, Sharma K

Biotechnol Rep (Amst)

20-Apr-2020

PMCID:	PMC7193120
doi:	10.1016/j.btre.2020.e00450
PMID:	32373483

The Experience Elicited by Hallucinogens Presents the Highest Similarity to Dreaming within a Large Database of Psychoactive Substance Reports

Sanz C, Zamberlan F, Erowid E, Erowid F, Tagliazucchi E

Front Neurosci

22-Jan-2018

PMCID:	PMC5786560
doi:	10.3389/fnins.2018.00007
PMID:	29403350

A continuous morphological approach to study the evolution of pollen in a phylogenetic context: An example with the order Myrtales

Kriebel R, Khabbazian M, Sytsma KJ

PLoS One

06-Dec-2017

PMCID:	PMC5718504
doi:	10.1371/journal.pone.0187228
PMID:	29211730

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
> Benzenoids / Phenol ethers / Anisoles
Nesodine	6475455	Click to see COC1=C(C2=C(C=C1)C3CC(CC4C3CCCC4)OC(=O)C=CC5=CC2=C(C=C5)O)OC	434.50	unknown	https://doi.org/10.1016/0378-8741(86)90153-4 https://doi.org/10.1016/0031-9422(90)80146-8 https://doi.org/10.1016/0378-8741(94)90080-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Helioscopinolide E	11565893	Click to see CC1=C2C=C3CCC4C(C(=O)CCC4(C3CC2OC1=O)C)(C)C	314.40	unknown	via CMAUP database
Jolkinolide E	5318716	Click to see CC1=C2C=C3CCC4C(CCCC4(C3CC2OC1=O)C)(C)C	300.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3beta-[[(2E,4E)-1-Oxo-2,4-decadienyl]oxy]-5alpha-tirucallane-7,24-diene	44233678	Click to see CCCCCC=CC=CC(=O)OC1CCC2(C3CCC4(C(CCC4(C3=CCC2C1(C)C)C)C(C)CCC=C(C)C)C)C	576.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(24R)-Cycloarta-25-ene-3beta,24-diol	14313591	Click to see CC(CCC(C(=C)C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	442.70	unknown	via CMAUP database
24-Methylenecycloartanol	94204	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	440.70	unknown	via CMAUP database
24-Methylenecycloartanone	14635659	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C	438.70	unknown	via CMAUP database
3beta-[[(2E,4E)-1-Oxo-2,4-decadienyl]oxy]-24-methylene-5alpha-cycloartane	44233424	Click to see CCCCCC=CC=CC(=O)OC1CCC23CC24CCC5(C(CCC5(C4CCC3C1(C)C)C)C(C)CCC(=C)C(C)C)C	591.00	unknown	via CMAUP database
Cycloeucalenol	101690	Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Obtusifoliol	65252	Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC4C(C)CCC(=C)C(C)C)C)C	426.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
(1S,2R,5R,7S,8R,11S,17R)-11-hydroxy-2,7,14-trimethyl-16-oxapentacyclo[9.7.0.02,8.05,7.013,17]octadec-13-ene-12,15-dione	44233196	Click to see CC1=C2C(CC3C4(CCC5CC5(C4CCC3(C2=O)O)C)C)OC1=O	330.40	unknown	via CMAUP database
(1S,2R,5R,7S,8R,13R,14R,17R)-2,7,14-trimethyl-16-oxapentacyclo[9.7.0.02,8.05,7.013,17]octadec-10-ene-12,15-dione	44233421	Click to see CC1C2C(CC3C(=CCC4C3(CCC5C4(C5)C)C)C2=O)OC1=O	314.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Piperidines / Phenylpiperidines
(2S,4R,9aS)-4-(3-hydroxy-4-methoxyphenyl)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-2-ol	163074374	Click to see COC1=C(C=C(C=C1)C2CC(CC3N2CCCC3)O)O	277.36	unknown	https://doi.org/10.1007/BF01934789
[(2S,4S,9aR)-4-(3-hydroxy-4-methoxyphenyl)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-2-yl] acetate	101863380	Click to see CC(=O)OC1CC2CCCCN2C(C1)C3=CC(=C(C=C3)OC)O	319.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028
[4-(3-hydroxy-4-methoxyphenyl)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-2-yl] acetate	162913091	Click to see CC(=O)OC1CC2CCCCN2C(C1)C3=CC(=C(C=C3)OC)O	319.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028
2-Hydroxy-4-(3-hydroxy-4-methoxyphenyl)quinolizidine	12553030	Click to see COC1=C(C=C(C=C1)C2CC(CC3N2CCCC3)O)O	277.36	unknown	https://doi.org/10.1007/BF01934789
> Organoheterocyclic compounds / Quinolizidines
(1S,13E,17R,19R)-9-hydroxy-4,5-dimethoxy-16-oxa-24-azapentacyclo[15.7.1.18,12.02,7.019,24]hexacosa-2,4,6,8,10,12(26),13-heptaen-15-one	163186971	Click to see COC1=C(C=C2C(=C1)C3CC(CC4N3CCCC4)OC(=O)C=CC5=CC2=C(C=C5)O)OC	435.50	unknown	https://doi.org/10.1016/0031-9422(75)85325-8
(1S,13Z,17R,19S,20R)-9,20-dihydroxy-4,5-dimethoxy-16-oxa-24-azapentacyclo[15.7.1.18,12.02,7.019,24]hexacosa-2,4,6,8,10,12(26),13-heptaen-15-one	101863379	Click to see COC1=C(C=C2C(=C1)C3CC(CC4N3CCCC4O)OC(=O)C=CC5=CC2=C(C=C5)O)OC	451.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028
(1S,13Z,17S,19S)-4,9-dihydroxy-5-methoxy-16-oxa-24-azapentacyclo[15.7.1.18,12.02,7.019,24]hexacosa-2,4,6,8,10,12(26),13-heptaen-15-one	21159570	Click to see COC1=C(C=C2C3CC(CC4N3CCCC4)OC(=O)C=CC5=CC(=C(C=C5)O)C2=C1)O	421.50	unknown	https://doi.org/10.1021/NP50126A010 https://doi.org/10.1016/S0031-9422(00)90462-X https://doi.org/10.1021/NP50037A006 https://doi.org/10.1016/0031-9422(90)80146-8 https://doi.org/10.1016/0378-8741(94)90080-9 https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028
(1S,13Z,17S,19S)-6,9-dihydroxy-5-methoxy-16-oxa-24-azapentacyclo[15.7.1.18,12.02,7.019,24]hexacosa-2(7),3,5,8,10,12(26),13-heptaen-15-one	101863381	Click to see COC1=C(C2=C(C=C1)C3CC(CC4N3CCCC4)OC(=O)C=CC5=CC2=C(C=C5)O)O	421.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028
4,9-Dihydroxy-5-methoxy-16-oxa-24-azapentacyclo[15.7.1.18,12.02,7.019,24]hexacosa-2,4,6,8,10,12(26),13-heptaen-15-one	321494	Click to see COC1=C(C=C2C3CC(CC4N3CCCC4)OC(=O)C=CC5=CC(=C(C=C5)O)C2=C1)O	421.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028
6,9-Dihydroxy-5-methoxy-16-oxa-24-azapentacyclo[15.7.1.18,12.02,7.019,24]hexacosa-2(7),3,5,8,10,12(26),13-heptaen-15-one	73799198	Click to see COC1=C(C2=C(C=C1)C3CC(CC4N3CCCC4)OC(=O)C=CC5=CC2=C(C=C5)O)O	421.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028 https://doi.org/10.1016/0378-8741(94)90080-9
9-Hydroxy-4,5-dimethoxy-16-oxa-23-azapentacyclo[15.7.1.18,12.02,7.018,23]hexacosa-2,4,6,8,10,12(26),13-heptaen-15-one	4485531	Click to see COC1=C(C=C2C(=C1)C3CC(C4CCCCN4C3)OC(=O)C=CC5=CC2=C(C=C5)O)OC	435.50	unknown	https://doi.org/10.1016/0378-8741(86)90153-4 https://doi.org/10.1016/S0031-9422(00)90462-X https://doi.org/10.1021/NP50098A009 https://doi.org/10.1016/S0031-9422(00)81687-8 https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028 https://doi.org/10.1039/C39830000145 https://doi.org/10.1021/NP50037A006 https://doi.org/10.1016/0378-8741(94)90080-9 https://doi.org/10.1016/0031-9422(90)80146-8
9-Hydroxy-4,5-dimethoxy-16-oxa-24-azapentacyclo[15.7.1.18,12.02,7.019,24]hexacosa-2,4,6,8,10,12(26),13-heptaen-15-one	430376	Click to see COC1=C(C=C2C(=C1)C3CC(CC4N3CCCC4)OC(=O)C=CC5=CC2=C(C=C5)O)OC	435.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028 https://doi.org/10.1016/0031-9422(75)85325-8
9,20-Dihydroxy-4,5-dimethoxy-16-oxa-24-azapentacyclo[15.7.1.18,12.02,7.019,24]hexacosa-2,4,6,8,10,12(26),13-heptaen-15-one	162921547	Click to see COC1=C(C=C2C(=C1)C3CC(CC4N3CCCC4O)OC(=O)C=CC5=CC2=C(C=C5)O)OC	451.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028
Lyfoline	6436825	Click to see COC1=C(C=C2C3CC(CC4N3CCCC4)OC(=O)C=CC5=CC(=C(C=C5)O)C2=C1)O	421.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028
Lythrine	6441299	Click to see COC1=C(C=C2C(=C1)C3CC(CC4N3CCCC4)OC(=O)C=CC5=CC2=C(C=C5)O)OC	435.50	unknown	https://doi.org/10.1021/NP50037A006 https://doi.org/10.1016/0378-8741(94)90080-9 https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028 https://doi.org/10.1021/NP50098A009 https://doi.org/10.1039/C39830000145 https://doi.org/10.1016/0031-9422(90)80146-8 https://doi.org/10.1016/S0031-9422(00)90462-X
Vertine	5315204	Click to see COC1=C(C=C2C(=C1)C3CC(CC4N3CCCC4)OC(=O)C=CC5=CC2=C(C=C5)O)OC	435.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2S,4R,9aS)-4-(3-hydroxy-4-methoxyphenyl)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-2-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate	163187051	Click to see COC1=C(C=C(C=C1)C2CC(CC3N2CCCC3)OC(=O)C=CC4=CC=C(C=C4)O)O	423.50	unknown	https://doi.org/10.1016/S0031-9422(00)94171-2
[4-(3-hydroxy-4-methoxyphenyl)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-2-yl] 3-(4-hydroxyphenyl)prop-2-enoate	163016296	Click to see COC1=C(C=C(C=C1)C2CC(CC3N2CCCC3)OC(=O)C=CC4=CC=C(C=C4)O)O	423.50	unknown	https://doi.org/10.1016/S0031-9422(00)94171-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
3-(beta-D-Glucopyranuronosyloxy)-7-(beta-D-glucopyranosyloxy)-3',4',5-trihydroxyflavone	101005581	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O	640.50	unknown	via CMAUP database
Querciturone	5274585	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	478.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin	5280804	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	464.40	unknown	via CMAUP database
Quercitrin	5280459	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)O	448.40	unknown	via CMAUP database
Rutin	5280805	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)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(1S,13R,17S,19R)-9,13-dihydroxy-4,5-dimethoxy-16-oxa-24-azapentacyclo[15.7.1.18,12.02,7.019,24]hexacosa-2,4,6,8,10,12(26)-hexaen-15-one	162955092	Click to see COC1=C(C=C2C(=C1)C3CC(CC4N3CCCC4)OC(=O)CC(C5=CC2=C(C=C5)O)O)OC	453.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028
(1S,13R,17S,19S)-9,13-dihydroxy-4,5-dimethoxy-16-oxa-24-azapentacyclo[15.7.1.18,12.02,7.019,24]hexacosa-2,4,6,8,10,12(26)-hexaen-15-one	101289710	Click to see COC1=C(C=C2C(=C1)C3CC(CC4N3CCCC4)OC(=O)CC(C5=CC2=C(C=C5)O)O)OC	453.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028
(1S,13S,17S,19R)-9,13-dihydroxy-4,5-dimethoxy-16-oxa-24-azapentacyclo[15.7.1.18,12.02,7.019,24]hexacosa-2,4,6,8,10,12(26)-hexaen-15-one	162955091	Click to see COC1=C(C=C2C(=C1)C3CC(CC4N3CCCC4)OC(=O)CC(C5=CC2=C(C=C5)O)O)OC	453.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028
13,14-Dihydro-2',14beta-dihydroxy-4'',5''-dimethoxylythran-12-one	137699649	Click to see COC1=C(C=C2C(=C1)C3CC(CC4N3CCCC4)OC(=O)CC(C5=CC2=C(C=C5)O)O)OC	453.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028
Heimidine	102192794	Click to see COC1=C(C=C2C(=C1)C3CC(CC4N3CCCC4)OC(=O)CC(C5=CC2=C(C=C5)O)O)OC	453.50	unknown	https://doi.org/10.1016/0378-8741(94)90080-9 https://doi.org/10.1016/J.PHYTOCHEM.2008.01.028

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.

Heimia salicifolia

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