Scientific name	Authority	First published in
Juniperus virginiana var. scopulorum	(Sarg.) Lemmon	Cone-bear. Trees Pacif. Slope , ed. 4: 114 (1900)
Juniperus virginiana subsp. scopulorum	(Lemm.) A.E.Murray	Kalmia 13: 8 (1983)
Juniperus excelsa	Pursh	Fl. Amer. Sept. 2: 647 (1813)
Juniperus occidentalis var. pleiosperma	Engelm.	Trans. Acad. Sci. St. Louis 3: 590 (1877)
Juniperus scopulorum var. columnaris	Fassett	Bull. Torrey Bot. Club 72: 482 (1945)
Juniperus scopulorum f. columnaris	(Fassett) Rehder	Bibl. Cult. Trees : 63 (1949)
Sabina scopulorum	Rydb.	Bull. Torrey Bot. Club 32: 598 (1905)
Juniperus maritima	R.P.Adams	Phytologia 89: 278 (2007)
Juniperus virginiana var. montana	Vasey	Dept. Agric. Bot. Div. Bull. 1875: 47. 1876

Common names Top

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Filter by language:

Language	Common/alternative name
English	river juniper
English	rocky mountain red-cedar
English	rocky mountain juniper
English	red-cedar
Spanish	cedro rojo
Bulgarian	скална хвойна
chy	vé'evêšéstótó'e
Czech	jalovec skalní
German	rocky-mountain-wacholder
German	zypressen-wacholder
Persian	ارس کوههای راکی
French	genévrier des rocheuses
Hebrew	ערער המצוקים
Hungarian	oregoni boróka
Icelandic	klettaeinir
Japanese	コロラドビャクシン
nv	gad niʼeełí
Punjab	راکی پہاڑ صنوبر
Russian	Можжевельник скальный
Swedish	röden
Chinese	落基山圆柏
Chinese	岩生圆柏

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!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Northern America click to expand
- Mexico
  - Mexico Northeast
  - Mexico Northwest
- North-central U.S.A.
  - Nebraska
  - North Dakota
  - South Dakota
- Northwestern U.S.A.
  - Colorado
  - Idaho
  - Montana
  - Oregon
  - Washington
  - Wyoming
- South-central U.S.A.
  - New Mexico
- Southwestern U.S.A.
  - Arizona
  - Nevada
  - Utah
- Western Canada
  - Alberta
  - British Columbia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000354991
UNII	U8G3433UI7
Cornell Woody Plants	127
Canadensys	4707
USDA Plants	JUSC2
UConn	232
Tropicos	9400155
INPN	610896
KEW	urn:lsid:ipni.org:names:132535-2
The Plant List	kew-2331680
PFAF	Juniperus scopulorum
Open Tree Of Life	287287
Observations.org	195438
NCBI Taxonomy	466205
Nature Serve	2.142742
IUCN Red List	42252
IPNI	132535-2
iNaturalist	135883
GBIF	2684773
Freebase	/m/08nhd_
FEIS	plants/tree/junsco
EPPO	IUPSC
EOL	1034924
Elurikkus	281801
Calflora (Californian flora)	9350
USDA GRIN	20863
Wikipedia	Juniperus_scopulorum
CMAUP	NPO18765

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 Precious Potential of the Sacred Tree Chamaecyparis obtusa (Siebold & Zucc.) Endl. as a Source of Secondary Metabolites with Broad Biological Applications

Górski KM, Kowalczyk T, Picot L, Rijo P, Ghorbanpour M, Sitarek P

Int J Mol Sci

27-Feb-2024

PMCID:	PMC10932367
doi:	10.3390/ijms25052723
PMID:	38473970

Commodity risk assessment of Corylus avellana plants from the UK

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P

EFSA J

12-Jan-2024

PMCID:	PMC10784871
doi:	10.2903/j.efsa.2024.8495
PMID:	38222930

Mule deer fawn recruitment dynamics in an energy disturbed landscape

Murphy KJ, Roberts DR, Jensen WF, Nielsen SE, Johnson SK, Hosek BM, Stillings B, Kolar J, Boyce MS, Ciuti S

Ecol Evol

19-Apr-2023

PMCID:	PMC10116077
doi:	10.1002/ece3.9976
PMID:	37091564

Western Spruce Budworm Effects on Forest Resilience

Polinko AD, Rapp MA, Sánchez Meador AJ, Graves AD, Ryerson DE, Waring KM

Plants (Basel)

28-Nov-2022

PMCID:	PMC9736256
doi:	10.3390/plants11233266
PMID:	36501306

Analysis of the annual pollen integral in Albuquerque, New Mexico, shows a negative trend with temperatures for Juniper, Cottonwood, Elm, and Mulberry

Aprea CM, Torres DJ, Cordova MM

Aerobiologia (Bologna)

26-Sep-2022

PMCID:	PMC10104481
doi:	10.1007/s10453-022-09756-5
PMID:	37065185

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

Thinning increases forest resiliency during unprecedented drought

Sankey T, Tatum J

Sci Rep

31-May-2022

PMCID:	PMC9156747
doi:	10.1038/s41598-022-12982-z
PMID:	35641556

Daily torpor reduces the energetic consequences of microhabitat selection for a widespread bat

Alston JM, Dillon ME, Keinath DA, Abernethy IM, Goheen JR

Ecology

11-Apr-2022

PMCID:	PMC9286574
doi:	10.1002/ecy.3677
PMID:	35262926

Phylogenetic Position of a New Trisetacus Mite Species (Nalepellidae) Destroying Seeds of North American Junipers and New Hypotheses on Basal Divergence of Eriophyoidea

Chetverikov PE, Rector BG, Tonkel K, Dimitri L, Cheglakov DS, Romanovich AE, Amrine J

Insects

15-Feb-2022

PMCID:	PMC8876007
doi:	10.3390/insects13020201
PMID:	35206774

Changes in Antioxidative, Oxidoreductive and Detoxification Enzymes during Development of Aphids and Temperature Increase

Durak R, Dampc J, Kula-Maximenko M, Mołoń M, Durak T

Antioxidants (Basel)

25-Jul-2021

PMCID:	PMC8388978
doi:	10.3390/antiox10081181
PMID:	34439429

Influence of three times weekly alfalfa supplementation on the behavior of beef cows grazing dormant Montana rangeland

Davis NG, Wyffels SA, Sanford C, DelCurto T

Transl Anim Sci

22-Dec-2020

PMCID:	PMC7754230
doi:	10.1093/tas/txaa098
PMID:	33381722

Sex-Specific Elk Resource Selection during the Anthrax Risk Period

YANG A, PROFFITT KM, ASHER V, RYAN SJ, BLACKBURN JK

J Wildl Manage

01-Oct-2020

PMCID:	PMC8356676
doi:	10.1002/jwmg.21952
PMID:	34393269

“It made me feel brighter in myself”- The health and well-being impacts of a residential front garden horticultural intervention

Chalmin-Pui LS, Roe J, Griffiths A, Smyth N, Heaton T, Clayden A, Cameron R

Landsc Urban Plan

30-Sep-2020

PMCID:	PMC7525452
doi:	10.1016/j.landurbplan.2020.103958
PMID:	33012932

Urban resources limit pair coordination over offspring provisioning

Baldan D, Ouyang JQ

Sci Rep

28-Sep-2020

PMCID:	PMC7522258
doi:	10.1038/s41598-020-72951-2
PMID:	32985594

Ultra-Micro-Scale-Fractionation (UMSF) as a Powerful Tool for Bioactive Molecules Discovery

McCallum JL, Vacon JN, Kirby CW

Molecules

12-Aug-2020

PMCID:	PMC7464926
doi:	10.3390/molecules25163677
PMID:	32806767

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 / Aporphines
Anolobine	164710	Click to see C1CNC2CC3=C(C=CC(=C3)O)C4=C2C1=CC5=C4OCO5	281.30	unknown	via CMAUP database
Anonaine	160597	Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5	265.31	unknown	via CMAUP database
Asimilobine	160875	Click to see COC1=C(C=C2CCNC3C2=C1C4=CC=CC=C4C3)O	267.32	unknown	via CMAUP database
Atherospermidine	77514	Click to see COC1=C2C(=C3C4=CC=CC=C4C(=O)C5=NC=CC1=C35)OCO2	305.30	unknown	via CMAUP database
Boldine 2-methyl ether	16573	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC	341.40	unknown	via CMAUP database
Dicentrinone	177744	Click to see COC1=C(C=C2C(=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O)OC	335.30	unknown	via CMAUP database
Isocorydine	10143	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC	341.40	unknown	via CMAUP database
Lanuginosine	97622	Click to see COC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O	305.30	unknown	via CMAUP database
Laurotetanine	31415	Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC	327.40	unknown	via CMAUP database
Liriodenine	10144	Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53	275.26	unknown	via CMAUP database
Lysicamine	122691	Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC=CC=C42)OC	291.30	unknown	via CMAUP database
Norisocorydine	12313549	Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O	327.40	unknown	via CMAUP database
Norstephalagine	133381	Click to see COC1=C2C(=C3C4=CC=CC=C4CC5C3=C1CCN5)OCO2	295.30	unknown	via CMAUP database
O-Nornuciferine	197017	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=CC=C43)OC)O	281.30	unknown	via CMAUP database
Oxoglaucine	97662	Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC(=C(C=C42)OC)OC)OC	351.40	unknown	via CMAUP database
Romucosine	10734687	Click to see COC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3	323.30	unknown	via CMAUP database
Romucosine H	5320994	Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3C(=O)OC)OC)OC)C=C1)O	385.40	unknown	via CMAUP database
Xylopine	160503	Click to see COC1=CC2=C(C=C1)C3=C4C(C2)NCCC4=CC5=C3OCO5	295.30	unknown	via CMAUP database
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
Michelalbine	10378981	Click to see C1CNC2C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)O	281.30	unknown	via CMAUP database
Ushinsunine	197018	Click to see CN1CCC2=CC3=C(C4=C2C1C(C5=CC=CC=C54)O)OCO3	295.30	unknown	via CMAUP database
> Alkaloids and derivatives / Proaporphines
(4S)-10,11-dimethoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohexa-2,5-diene]-1'-one	830726	Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)OC	297.30	unknown	via CMAUP database
Pronuciferine, (-)-	793841	Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC	311.40	unknown	via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Corydalmine	161665	Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)OC)OC	341.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Halobenzoic acids and derivatives / Halobenzoic acids
3-Chlorobenzoic acid	447	Click to see C1=CC(=CC(=C1)Cl)C(=O)O	156.56	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
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
3,4,5-Trimethoxybenzoic acid	8357	Click to see COC1=CC(=CC(=C1OC)OC)C(=O)O	212.20	unknown	via CMAUP database
Syringic acid	10742	Click to see COC1=CC(=CC(=C1O)OC)C(=O)O	198.17	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
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3-Hydroxy-4-methoxybenzoic acid	12575	Click to see COC1=C(C=C(C=C1)C(=O)O)O	168.15	unknown	via CMAUP database
Methyl 3-hydroxy-4-methoxybenzoate	4056967	Click to see COC1=C(C=C(C=C1)C(=O)OC)O	182.17	unknown	via CMAUP database
Methyl 4-methoxybenzoate	8499	Click to see COC1=CC=C(C=C1)C(=O)OC	166.17	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 / Phenols / Methoxyphenols
(2S)-3-(4-hydroxy-3,5-dimethoxyphenyl)propane-1,2-diol	86330909	Click to see COC1=CC(=CC(=C1O)OC)CC(CO)O	228.24	unknown	via CMAUP database
Isoeugenol	853433	Click to see CC=CC1=CC(=C(C=C1)O)OC	164.20	unknown	via CMAUP database
Isovanillin	12127	Click to see COC1=C(C=C(C=C1)C=O)O	152.15	unknown	via CMAUP database
n-Dihydroferuloyltyramine	16119667	Click to see COC1=C(C=CC(=C1)CCC(=O)NCCC2=CC=C(C=C2)O)O	315.40	unknown	via CMAUP database
Syringaldehyde	8655	Click to see COC1=CC(=CC(=C1O)OC)C=O	182.17	unknown	via CMAUP database
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Lirioresinol C	11796268	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
Episyringaresinol	12309694	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
Syringaresinol, (+)-	443023	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
Acanthoside D	21603207	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC	742.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(4R,10S)-nonacosane-4,10-diol	162915875	Click to see CCCCCCCCCCCCCCCCCCCC(CCCCCC(CCC)O)O	440.80	unknown	https://doi.org/10.1016/0031-9422(81)85274-0
4,10-Nonacosanediol	85977331	Click to see CCCCCCCCCCCCCCCCCCCC(CCCCCC(CCC)O)O	440.80	unknown	https://doi.org/10.1016/0031-9422(81)85274-0
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(R)-nonacosan-10-ol	342803	Click to see CCCCCCCCCCCCCCCCCCCC(CCCCCCCCC)O	424.80	unknown	https://doi.org/10.1016/0031-9422(81)85274-0
Nonacosan-10-ol	25240035	Click to see CCCCCCCCCCCCCCCCCCCC(CCCCCCCCC)O	424.80	unknown	https://doi.org/10.1016/0031-9422(81)85274-0
Safynol	6442707	Click to see CC=CC#CC#CC#CC=CC(CO)O	200.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Isocupressic acid	6438138	Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C	320.50	unknown	https://doi.org/10.1002/(SICI)1099-1565(199905/06)10:3<132::AID-PCA444>3.0.CO;2-B
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(16R)-17-Hydroxykaura-18-oic acid	44575990	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)CO)(C)C(=O)O	320.50	unknown	via CMAUP database
(1S,4R,9R,10R,13R,14S)-14-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-14-ol	12112093	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)C	306.50	unknown	via CMAUP database
(1S,4S,5R,9S,10R,13R,14R)-14-(dimethoxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	46210308	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)C(OC)OC)(C)C(=O)O	364.50	unknown	via CMAUP database
(4R)-17-Acetoxykauran-18-oic acid	102425890	Click to see CC(=O)OCC1CC23CCC4C(C2CCC1C3)(CCCC4(C)C(=O)O)C	362.50	unknown	via CMAUP database
[(1S,4S,5R,9S,10R,13R,14R)-5-(hydroxymethyl)-5,9-dimethyl-14-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methanol	46210166	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)CO)C)CO	306.50	unknown	via CMAUP database
16alphaH-17,19-ent-kauranediol	102594837	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)CO)C)CO	306.50	unknown	via CMAUP database
16beta,17-Dihydroxy-ent-kaurane-19-oic acid	469209	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(CO)O)(C)C(=O)O	336.50	unknown	via CMAUP database
17-Hydroxykaura-18-oic acid	46210307	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)CO)(C)C(=O)O	320.50	unknown	via CMAUP database
Diterpenoid SP-II	442023	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(CO)O)(C)C(=O)O	336.50	unknown	via CMAUP database
ent-Kauran-16-beta-ol	21593607	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)C	290.50	unknown	via CMAUP database
Kaurane-16alpha,17-diol	13816761	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)C	306.50	unknown	via CMAUP database
Kaurenoic acid	73062	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O	302.50	unknown	via CMAUP database
Methyl 16alpha,17-dihydroxy-ent-kauran-19-oate	46233487	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(CO)O)(C)C(=O)OC	350.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(5beta,8alpha,9beta,10alpha,12alpha,16R)-16,17-Dihydroxyatisane-18-oic acid methyl ester	25006930	Click to see CC12CCCC(C1CCC34C2CC(CC3)C(C4)(CO)O)(C)C(=O)OC	350.50	unknown	via CMAUP database
methyl (1S,4S,5R,9S,10R,12S,13R)-13-(acetyloxymethyl)-13-hydroxy-5,9-dimethyltetracyclo[10.2.2.01,10.04,9]hexadecane-5-carboxylate	25006927	Click to see CC(=O)OCC1(CC23CCC1CC2C4(CCCC(C4CC3)(C)C(=O)OC)C)O	392.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol	443162	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1002/JPS.3080191008
(+)-alpha-Terpineol	442501	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1002/JPS.3080191008
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1002/JPS.3080191008
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1002/JPS.3080191008
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(5aS,11aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,12,13,13b-tetradecahydrocyclopenta[a]chrysene	5318564	Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4=C3CCC5C4(CCCC5(C)C)C)C)C)C	410.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
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
Sitoindoside I	9832350	Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O	815.30	unknown	via CMAUP database
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
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	via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
9-beta-d-Arabinofuranosylade-nine	12358320	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine	6029	Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O	244.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Cysteic Acid	25701	Click to see C(C(C(=O)O)N)S(=O)(=O)O	169.16	unknown	https://doi.org/10.1016/S0021-9673(01)97854-9
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Methionine and derivatives
Methionine	6137	Click to see CSCCC(C(=O)O)N	149.21	unknown	https://doi.org/10.1016/S0021-9673(01)97854-9
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Cherimolacyclopeptide A	11205172	Click to see CCC(C)C1C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NCC(=O)NC(C(=O)NC(C(=O)N3CCCC3C(=O)N1)CC(C)C)CCSC)C(C)O)CCC(=O)N	838.00	unknown	via CMAUP database
Cherimolacyclopeptide C	11216146	Click to see CCC(C)C1C(=O)N2CCCC2C(=O)N3CCCC3C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CC4=CNC5=CC=CC=C54)C)C	692.80	unknown	via CMAUP database
Cherimolacyclopeptide D	11599937	Click to see CC1C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NCC(=O)NC(C(=O)NC(C(=O)N1)CC(=O)N)CC(C)C)C(C)O)C(C)C	652.70	unknown	via CMAUP database
Cherimolacyclopeptide F	101773878	Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)N3CCCC3C(=O)NCC(=O)NC(C(=O)NCC(=O)N1)CCSC)CCSC)CC(C)C)CC4=CC=C(C=C4)O	960.20	unknown	via CMAUP database
cyclo[Ala-Pro-Gly-Ala-Val-Pro-Ile-Tyr]	11585828	Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NCC(=O)NC(C(=O)NC(C(=O)N3CCCC3C(=O)N1)C(C)C)C)C)CC4=CC=C(C=C4)O	768.90	unknown	via CMAUP database
cyclo[Gly-Leu-Gly-Phe-Tyr-Pro]	71608845	Click to see CC(C)CC1C(=O)NCC(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NCC(=O)N1)CC3=CC=C(C=C3)O)CC4=CC=CC=C4	634.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Koaburaside monomethyl ether	636454	Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)CO)O)O)O	346.33	unknown	via CMAUP database
Thalictoside	21629843	Click to see C1=CC(=CC=C1CC[N+](=O)[O-])OC2C(C(C(C(O2)CO)O)O)O	329.30	unknown	via CMAUP database
> 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 / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone	68262	Click to see COC1=CC(=O)C=C(C1=O)OC	168.15	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
CID 10487440	10487440	Click to see C=CCC1=CC2=C(C=C1)OCO2	174.14	unknown	via CMAUP database
Safrole	5144	Click to see C=CCC1=CC2=C(C=C1)OCO2	162.18	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Cheritamine	101428698	Click to see CCCCC=CCCCCCCCCCCCCCCCCCCCCCCCC(=O)NCCC1=CNC2=CC=CC=C21	593.00	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(R)-1-[(4-Hydroxyphenyl)methyl]-5,6-dimethoxy-1,2,3,4-tetrahydroisoquinolin-7-ol	101687011	Click to see COC1=C2CCNC(C2=CC(=C1OC)O)CC3=CC=C(C=C3)O	315.40	unknown	via CMAUP database
1-[Hydroxy(4-hydroxyphenyl)methyl]-6-methoxyisoquinolin-7-ol	637078	Click to see COC1=C(C=C2C(=C1)C=CN=C2C(C3=CC=C(C=C3)O)O)O	297.30	unknown	via CMAUP database
1alpha-(3-Methoxy-4-hydroxybenzyl)-2-methyl-1,2,3,4-tetrahydro-6-methoxyisoquinoline-7-ol	14357385	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)O)OC)O)OC	329.40	unknown	via CMAUP database
Annocherine B	5319094	Click to see COC1=C(C=C2C(=C1)C=CN=C2C(C3=CC=C(C=C3)O)OC)O	311.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
7-Hydroxy-6-methoxy-2-methylisoquinolin-1-one	59620302	Click to see CN1C=CC2=CC(=C(C=C2C1=O)O)OC	205.21	unknown	via CMAUP database
Cherianoine	5315819	Click to see CN1C=CC2=CC(=C(C(=C2C1=O)OC)O)OC	235.24	unknown	via CMAUP database
Thalifoline	89048	Click to see CN1CCC2=CC(=C(C=C2C1=O)O)OC	207.23	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Nicotinic acid	938	Click to see C1=CC(=CN=C1)C(=O)O	123.11	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / Pyrrolidine carboxylic acids and derivatives / Pyrrolidinecarboxamides
2-Oxopyrrolidine-1-carboxamide	326996	Click to see C1CC(=O)N(C1)C(=O)N	128.13	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
4H-pyrano[3,4-c]quinolin-4-one	638628	Click to see C1=CC=C2C(=C1)C3=C(C=N2)C(=O)OC=C3	197.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
3-(3,4-Dihydroxyphenyl)-N-phenethylpropenamide, (E)-	11391937	Click to see C1=CC=C(C=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)O	283.32	unknown	via CMAUP database
cis-Caffeoyltyramine	16119508	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC(=C(C=C2)O)O)O	299.32	unknown	via CMAUP database
FERULOYL-beta-PHENETHYLAMINE	11162295	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=CC=C2)O	297.30	unknown	via CMAUP database
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
N-Feruloyl-3-methoxytyramine, (Z)-	5322166	Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O	343.40	unknown	via CMAUP database
N-trans-feruloylmethoxytyramine	5352115	Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O	343.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
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 (2Z)-3-(4-hydroxyphenyl)acrylate	12343877	Click to see COC(=O)C=CC1=CC=C(C=C1)O	178.18	unknown	via CMAUP database
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 / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(4-Hydroxyphenyl)propionic acid	10394	Click to see C1=CC(=CC=C1CCC(=O)O)O	166.17	unknown	via CMAUP database

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Juniperus scopulorum

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