Scientific name	Authority	First published in
Juniperus virginiana var. prostrata	Torr.	Fl. New York 2: 235 (1843)
Juniperus repens	Nutt.	Gen. N. Amer. Pl. 2: 245 (1818)
Juniperus racemosa	Risso	Hist. Nat. Prod. Eur. Mérid. 2: 459 (1826)
Juniperus horizontalis subsp. hamptonensis	Silba	J. Int. Conifer Preserv. Soc. 11: 28 (2004)
Juniperus horizontalis subsp. neopangaea	Silba	J. Int. Conifer Preserv. Soc. 11: 28 (2004)
Juniperus prostrata	Pers.	Syn. Pl. 2: 632 (1807)
Juniperus hudsonica	F.B.Forbes	Pinet. Woburn. : 208 (1839)
Juniperus horizontalis var. alpina	Rehder	Man. Cult. Trees : 15 (1927)
Juniperus horizontalis f. alpina	(Loudon) Rehder	J. Arnold Arbor. 6: 203 (1925)
Juniperus horizontalis f. glomerata	Rehder	J. Arnold Arbor. 6: 202 (1925)
Juniperus horizontalis var. glomerata	Rehder	Man. Cult. Trees : 15 (1927)
Juniperus horizontalis f. lobata	O.W.Knight	Rhodora 9: 202 (1907)
Juniperus sabina var. prostrata	(Pers.) Loudon	Arbor. Frutic. Brit. 4: 2499 (1838)
Juniperus sabina var. procumbens	Pursh	Fl. Amer. Sept. 2: 647 (1813)
Juniperus sabina var. humilis	Hook.	Fl. Bor.-Amer. 2: 166 (1838)
Sabina prostrata	Antoine	Cupress.-Gatt. : 57 (1857)
Sabina racemosa	Antoine	Cupress.-Gatt. : 71 (1857)
Sabina horizontalis	Rydb.	Bull. Torrey Bot. Club 39: 100 (1912)
Sabina horizontalis f. douglasii	(Rehder) Moldenke	Phytologia 4: 128 (1952)
Juniperus sabina var. alpina	Loudon	Arbor. Frutic. Brit. 4: 2499 (1838)
Juniperus sabina f. prostrata	(Pers.) Voss	Vilm. Blumengärtn. ed. 3 , 1: 1228 (1895)
Juniperus horizontalis var. variegata	Beissn.
Juniperus horizontalis var. douglasii	Rehder in L.H.Bailey	Stand. Cycl. Hort. 3: 1722 (1915)

Common names Top

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Filter by language:

Language	Common/alternative name
English	american savin
English	creeping juniper
English	shrubby red cedar
English	waukegan juniper
Czech	jalovec polehlý
German	kriech-wacholder
Basque	ipuru herrestari
Persian	ارس خزنده
Finnish	laakakataja
French	genévrier rampant
French	sevigné
French	savignier
Hungarian	henye boróka
Icelandic	skriðeinir
Japanese	アメリカハイビャクシン
Kazakh	Жайыла өсетін арша
Polish	jałowiec płożący
Punjab	رڑدا صنوبر
Russian	Можжевельник распростёртый
Slovenian	polegli brin
Swedish	amerikansk krypen
Chinese	匍匐雪松
Chinese	平枝圆柏

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Suggest a correction or add new data!

Alternate between 4°C and 20°C for 3 months each, over several cycles, with an extended germination period.

Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

soak seeds a few seconds in boiling water

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Northern America click to expand
- Eastern Canada
  - Labrador
  - Newfoundland
  - Nova Scotia
  - Ontario
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Minnesota
  - North Dakota
  - South Dakota
  - Wisconsin
- Northeastern U.S.A.
  - Massachusetts
  - Michigan
  - New York
  - Vermont
- Northwestern U.S.A.
  - Colorado
  - Montana
  - Wyoming
- Subarctic America
  - Alaska
  - Northwest Territorie
  - Nunavut
  - Yukon
- Western Canada
  - Alberta
  - British Columbia
  - Manitoba
  - Saskatchewan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000355700
Cornell Woody Plants	124
Canadensys	4705
USDA Plants	JUHO2
UConn	229
Tropicos	9400150
INPN	610894
KEW	urn:lsid:ipni.org:names:262244-1
The Plant List	kew-2332743
Missouri Botanical Garden	279603
PFAF	Juniperus horizontalis
Open Tree Of Life	142117
Observations.org	195439
NCBI Taxonomy	669713
Nature Serve	2.144512
IUCN Red List	42237
IPNI	262244-1
iNaturalist	47573
GBIF	2684410
Freebase	/m/08njst
WisFlora	3982
FEIS	plants/shrub/junhor
EPPO	IUPHO
EOL	1034922
Elurikkus	281766
USDA GRIN	20836
Wikipedia	Juniperus_horizontalis
CMAUP	NPO12487

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

Temporal variation of allergenic potential in urban parks during the vegetation period: a case study from Bratislava, Slovakia

Zahradníková E, Rendeková A, Ščevková J

Environ Sci Pollut Res Int

05-Dec-2023

PMCID:	PMC10791852
doi:	10.1007/s11356-023-31137-9
PMID:	38052730

Plant Essential Oils as Biopesticides: Applications, Mechanisms, Innovations, and Constraints

Gupta I, Singh R, Muthusamy S, Sharma M, Grewal K, Singh HP, Batish DR

Plants (Basel)

10-Aug-2023

PMCID:	PMC10458566
doi:	10.3390/plants12162916
PMID:	37631128

Survival, growth, and biogenic amine production of Enterococcus faecium FC12 in response to extracts and essential oils of Rubus fruticosus and Juniperus oxycedrus

Montanari C, Barbieri F, Lorenzini S, Gottardi D, Šimat V, Özogul F, Gardini F, Tabanelli G

Front Nutr

13-Jan-2023

PMCID:	PMC9880475
doi:	10.3389/fnut.2022.1092172
PMID:	36712524

Juniperus horizontalis Moench: Chemical Composition, Herbicidal and Insecticidal Activities of Its Essential Oil and of Its Main Component, Sabinene

Gruľová D, Baranová B, Sedlák V, De Martino L, Zheljazkov VD, Konečná M, Poráčová J, Caputo L, De Feo V

Molecules

01-Dec-2022

PMCID:	PMC9739652
doi:	10.3390/molecules27238408
PMID:	36500500

Juniperus sabina L. as a Source of Podophyllotoxins: Extraction Optimization and Anticholinesterase Activities

Xu S, Li X, Liu S, Tian P, Li D

Int J Mol Sci

06-Sep-2022

PMCID:	PMC9499582
doi:	10.3390/ijms231810205
PMID:	36142118

New Reports of Phytophthora Species in Plant Nurseries in Spain

Mora-Sala B, León M, Pérez-Sierra A, Abad-Campos P

Pathogens

23-Jul-2022

PMCID:	PMC9394253
doi:	10.3390/pathogens11080826
PMID:	35894049

Mass propagation of Juniperus procera Hoechst. Ex Endl. From seedling and screening of bioactive compounds in shoot and callus extract

Salih AM, Al-Qurainy F, Khan S, Tarroum M, Nadeem M, Shaikhaldein HO, Alabdallah NM, Alansi S, Alshameri A

BMC Plant Biol

21-Apr-2021

PMCID:	PMC8059214
doi:	10.1186/s12870-021-02946-2
PMID:	33882830

GIS-based mapping and assessment of noise pollution in Safranbolu, Karabuk, Turkey

Esmeray E, Eren S

Environ Dev Sustain

27-Feb-2021

PMCID:	PMC7970821
doi:	10.1007/s10668-021-01303-5
PMID:	33758575

Examining the molecular mechanisms contributing to the success of an invasive species across different ecosystems

Lamar SK, Beddows I, Partridge CG

Ecol Evol

31-Aug-2020

PMCID:	PMC7520182
doi:	10.1002/ece3.6688
PMID:	33005380

Phytophthora Diversity in Pennsylvania Nurseries and Greenhouses Inferred from Clinical Samples Collected over Four Decades

Molnar C, Nikolaeva E, Kim S, Olson T, Bily D, Kim JE, Kang S

Microorganisms

16-Jul-2020

PMCID:	PMC7409235
doi:	10.3390/microorganisms8071056
PMID:	32708553

Gymnosporangium species on Malus: species delineation, diversity and host alternation

Zhao P, Qi XH, Crous PW, Duan WJ, Cai L

Persoonia

10-Jan-2020

PMCID:	PMC8375348
doi:	10.3767/persoonia.2020.45.03
PMID:	34456372

Evolutionary history predicts high‐impact invasions by herbivorous insects

Mech AM, Thomas KA, Marsico TD, Herms DA, Allen CR, Ayres MP, Gandhi KJ, Gurevitch J, Havill NP, Hufbauer RA, Liebhold AM, Raffa KF, Schulz AN, Uden DR, Tobin PC

Ecol Evol

17-Oct-2019

PMCID:	PMC6854116
doi:	10.1002/ece3.5709
PMID:	31832155

Decoupled recovery of ecological communities after reclamation

Sylvain ZA, Branson DH, Rand TA, West NM, Espeland EK

PeerJ

21-Jun-2019

PMCID:	PMC6590388
doi:	10.7717/peerj.7038
PMID:	31275739

Expanding and testing fluorescent amplified fragment length polymorphisms for identifying roots of boreal forest plant species

Metzler P, La Flèche M, Karst J

Appl Plant Sci

08-Apr-2019

PMCID:	PMC6476169
doi:	10.1002/aps3.1236
PMID:	31024780

In vitro mineral nutrition of Curcuma longa L. affects production of volatile compounds in rhizomes after transfer to the greenhouse

El-Hawaz RF, Grace MH, Janbey A, Lila MA, Adelberg JW

BMC Plant Biol

18-Jun-2018

PMCID:	PMC6006571
doi:	10.1186/s12870-018-1345-y
PMID:	29914391

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 / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
Dihydrochelerythrine	485077	Click to see CN1CC2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5	349.40	unknown	via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
Formamide, N-(6-(2-hydroxy-3,4-dimethoxyphenyl)naphtho(2,3-d)-1,3-dioxol-5-yl)-N-methyl-	3085181	Click to see CN(C=O)C1=C(C=CC2=CC3=C(C=C21)OCO3)C4=C(C(=C(C=C4)OC)OC)O	381.40	unknown	via CMAUP database
> Alkaloids and derivatives / Harmala alkaloids
methyl 9H-pyrido[3,4-b]indole-1-carboxylate	597266	Click to see COC(=O)C1=NC=CC2=C1NC3=CC=CC=C23	226.23	unknown	via CMAUP database
> Alkaloids and derivatives / Strychnos alkaloids
C-Alkaloid G	6391813	Click to see CC=C1C[N+]2(CCC34C2CC1C5=CN6C7=CC=CC=C7C89C61C(=CN(C53O1)C1=CC=CC=C41)C1CC8[N+](CC9)(CC1=CC)C)C	596.80	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	154.12	unknown	via CMAUP database
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Methyl 4-hydroxy-3,5-dimethoxybenzoate	70164	Click to see COC1=CC(=CC(=C1O)OC)C(=O)OC	212.20	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate	7428	Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O	184.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl vanillate	19844	Click to see COC1=C(C=CC(=C1)C(=O)OC)O	182.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben	7456	Click to see COC(=O)C1=CC=C(C=C1)O	152.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
3,4,5-Trimethoxybenzyl alcohol	77449	Click to see COC1=CC(=CC(=C1OC)OC)CO	198.22	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
4-Hydroxy-3-methoxycinnamaldehyde	5280536	Click to see COC1=C(C=CC(=C1)C=CC=O)O	178.18	unknown	via CMAUP database
N-Trans-feruloyltramine	5280537	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O	313.30	unknown	via CMAUP database
Syringaldehyde	8655	Click to see COC1=CC(=CC(=C1O)OC)C=O	182.17	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
4-(1,3-Benzodioxol-5-ylmethyl)-3-(1,3-benzodioxol-5-ylmethylidene)oxolan-2-one	98946	Click to see C1C(C(=CC2=CC3=C(C=C2)OCO3)C(=O)O1)CC4=CC5=C(C=C4)OCO5	352.30	unknown	https://doi.org/10.1139/V61-339
Savinin	5281867	Click to see C1C(C(=CC2=CC3=C(C=C2)OCO3)C(=O)O1)CC4=CC5=C(C=C4)OCO5	352.30	unknown	https://doi.org/10.1139/V61-339
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
1,4a-dimethyl-6-methylidene-5-(3-methylpenta-2,4-dienyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid	72957164	Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C	302.50	unknown	https://doi.org/10.1139/V61-339
Communic Acid	637125	Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C	302.50	unknown	https://doi.org/10.1139/V61-339
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(3S)-3-methyl-6-propan-2-ylidenecyclohexene	71385764	Click to see CC1CCC(=C(C)C)C=C1	136.23	unknown	https://doi.org/10.1139/V65-138
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1-Methyl-4-(1,2,2-trimethylcyclopentyl)benzene	519346	Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C	202.33	unknown	https://doi.org/10.1139/V61-339
Cuparene	86895	Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C	202.33	unknown	https://doi.org/10.1139/V61-339
Thujopsen	97829	Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C	204.35	unknown	https://doi.org/10.1139/V61-339
Thujopsene	442402	Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C	204.35	unknown	https://doi.org/10.1139/V61-339
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
alpha-Cedrene	6431015	Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C	204.35	unknown	https://doi.org/10.1139/V61-339
Cedran-8-ol	522667	Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O	222.37	unknown	https://doi.org/10.1139/V61-339
Cedrene	521207	Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C	204.35	unknown	https://doi.org/10.1139/V61-339
Cedrol	65575	Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O	222.37	unknown	https://doi.org/10.1139/V61-339
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
CID 12443227	12443227	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	via CMAUP database
Taraxerol	92097	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	via CMAUP database
Taraxerone	92785	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C	424.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Amyrin acetate	92156	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	via CMAUP database
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
Squalene	638072	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C	410.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
Limonin	179651	Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C	470.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
CID 9848259	9848259	Click to see CC1(C2C(=O)C(C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)O)C	486.50	unknown	via CMAUP database
Evodol	185481	Click to see CC1(C2=C(C(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)O)C	484.50	unknown	via CMAUP database
> 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/10.1139/V61-339
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/10.1139/V61-339
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
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine	60961	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Methyl chlorogenate	6476139	Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O	368.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
1,1,4a,7-Tetramethyl-2,3,4,4a,5,6,7,8-octahydro-1H-benzo[a]cyclohepten-7-ol	522326	Click to see CC1(CCCC2(C1=CCC(CC2)(C)O)C)C	222.37	unknown	https://doi.org/10.1139/V61-339
Widdrol	94334	Click to see CC1(CCCC2(C1=CCC(CC2)(C)O)C)C	222.37	unknown	https://doi.org/10.1139/V61-339
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see C1=CC(=CC=C1C=O)O	122.12	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(S)-alpha,4'-Dihydroxy-3'-methoxypropiophenone	12181418	Click to see CC(C(=O)C1=CC(=C(C=C1)O)OC)O	196.20	unknown	via CMAUP database
Paeonol	11092	Click to see CC(=O)C1=C(C=C(C=C1)OC)O	166.17	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
1H-Pyrido(3,4-b)indol-1-one, 2,3,4,9-tetrahydro-2-methyl-	162871	Click to see CN1CCC2=C(C1=O)NC3=CC=CC=C23	200.24	unknown	via CMAUP database
Hortiacine	378227	Click to see COC1=CC2=C(C=C1)NC3=C2CCN4C3=NC5=CC=CC=C5C4=O	317.30	unknown	via CMAUP database
Rutaecarpine	65752	Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C4=C1C5=CC=CC=C5N4	287.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Decarine	179640	Click to see COC1=C(C=CC2=C3C=CC4=CC5=C(C=C4C3=NC=C21)OCO5)O	319.30	unknown	via CMAUP database
Norchelerythrine	443719	Click to see COC1=C(C2=CN=C3C(=C2C=C1)C=CC4=CC5=C(C=C43)OCO5)OC	333.30	unknown	via CMAUP database
Oxychelerythrine	147279	Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=C(C1=O)C(=C(C=C5)OC)OC	363.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine	68085	Click to see COC1=C2C=COC2=NC3=CC=CC=C31	199.20	unknown	via CMAUP database
gamma-Fagarine	107936	Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3	229.23	unknown	via CMAUP database
Robustine	164950	Click to see COC1=C2C=COC2=NC3=C1C=CC=C3O	215.20	unknown	via CMAUP database
Skimmianine	6760	Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC	259.26	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methylquinolin-2-one	182073	Click to see CN1C2=CC=CC=C2C(=CC1=O)OC	189.21	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
n-cis-Feruloyltyramine	6440659	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O	313.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
cis-N-p-coumaroyltyramine	13939145	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O	283.32	unknown	via CMAUP database
Paprazine	5372945	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O	283.32	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Methyl 4-hydroxycinnamate	5319562	Click to see COC(=O)C=CC1=CC=C(C=C1)O	178.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Evofolin C	44445795	Click to see CC(=CCOC1=CC=C(C=C1)C=CCO)C	218.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Fraxin	5273568	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O	370.31	unknown	via CMAUP database
Isofraxoside	11508953	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC3C(C(C(C(O3)CO)O)O)O	370.31	unknown	via CMAUP database
Skimmin	99693	Click to see C1=CC(=CC2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	324.28	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
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Sophoraflavone B	5491513	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O	416.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
4',5,7-Trihydroxy-3-(alpha-D-arabinopyranosyloxy)flavone	11625890	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	418.30	unknown	via CMAUP database
kaempferol 3-O-beta-D-xyloside	21310440	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	418.30	unknown	via CMAUP database
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	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 / Stilbenes
(-)-Evofolin B	46229015	Click to see COC1=C(C=CC(=C1)C(CO)C(=O)C2=CC(=C(C=C2)O)OC)O	318.32	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins
beta-Glucogallin	124021	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O	332.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	via CMAUP database

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Juniperus horizontalis

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