Scientific name	Authority	First published in
Larix deodara	K.Koch	Wochenschr. Vereines Beförd. Gartenbaues Königl. Preuss. Staaten 10: 308 (1867)
Pinus deodara	Roxb. ex D.Don	Descr. Pinus 2: 8 (1824)
Abies deodara	Lindl.	Penny Cyclop. 1: 34 (1833)
Cedrus indica	Chambr.	Traité Prat. Arbr. Résin. Conif. : 341 (1845)
Cedrus libani subsp. deodora	(Roxb. ex D.Don) P.D.Sell	Watsonia 18: 92 (1990)
Cedrus libani var. deodara	(Roxb. ex D.Don) Hook.f.	Himal. J. 1: 257 1854
Cedrus deodara var. variegata	Carrière	Traité Gén. Conif. ed. 2: 368. 1867
Cedrus deodara var. argentea	J.Nelson	Pinaceae 56. 1866
Cedrus deodara var. fastigiata	Carrière	Traité Gén. Conif. ed. 2: 368. 1867
Cedrus deodara var. compacta	Carrière	Traité Gén. Conif. ed. 2: 369. 1867
Cedrus deodara var. tristis	Carrière	Traité Gén. Conif. ed. 2: 369. 1867
Cedrus deodara var. flava	Carrière	Traité Gén. Conif. ed. 2: 369. 1867
Cedrus deodara f. pendula	Beissn.	Mitt. Deutsch. Dendrol. Ges. 9: 100 1900
Cedrus deodara f. aurea	(J.Nelson) Rehder	Bibl. Cult. Trees : 32 (1949)
Cedrus deodara f. argentea	(J.Nelson) Beissn.	Handb. Conif. 32 1887
Cedrus deodara var. aurea	J.Nelson	Pinaceae : 56 (1855)
Pinus deodara var. robusta	C.Lawson	Abietineae- List Pl. Fir Tribe 23. 1851
Cedrus deodara f. robusta	(C.Lawson) Beissn.	Handb. Conif. 32 1887
Pinus deodara	Roxb.	Hort. Bengal. 69. 1814

Common names Top

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Filter by language:

Language	Common/alternative name
English	deodar cedar
English	himalayan cedar
Spanish	cedro del himalaya
Spanish	cedro de la india
Spanish	cedro deodar
Arabic	أرز هيملايا
Arabic	أرز دوداري
Arabic	أبهل هندي
Arabic	ابهل هندي
Arabic	شجرة الجن
Arabic	صنوبر هندي
Azerbaijani	himalay sidri
azb	هیمالیا سیدری
Belarusian	Гімалайскі кедр
Belarusian	Кедр гімалайскі
Bulgarian	хималайски кедър
Catalan	cedre de l'himàlaia
Czech	cedr himálajský
Czech	cedr himalájský
Welsh	cedrwydden ddeodar
Danish	himalaya-ceder
German	himalaya-zeder
German	deodar
German	himalaja-zeder
German	himalajazeder
German	himalayazeder
Esperanto	deodaro
Esperanto	himalaja cedro
Basque	himalaiako zedro
Persian	سدر هیمالیا
Finnish	himalajansetri
French	cèdre de l'himalaya
French	cedre de l'himalaya
French	cèdre déodar
French	cèdre sacré
Galician	cedro do himalaia
Hebrew	ארז ההימלאיה
Hebrew	ארז הימלאי
Hindi	सीडर
Hindi	देवदार
Croatian	himalajski cedar
Upper Sorbian	himalajaska cedra
Hungarian	himalájai cédrus
Armenian	մայրի հիմալայան
Icelandic	himalajasedrus
Italian	cedro dell'himalaya
Italian	cedri dell'himalaya
Italian	cedri deodara
Italian	cedro deodara
Japanese	ヒマラヤスギ
Japanese	ヒマラヤシーダー
Japanese	ヒマラヤ杉
Georgian	ჰიმალაიური კედარი
Georgian	ჰიმალაის კედარი
Kannada	ದೇವದಾರು
Korean	개잎갈나무
Korean	히말라야시다
koi	Гималаись сыспу
Lithuanian	himalajinis kedras
Latvian	himalaju ciedrs
Macedonian	хималајски кедар
Malayalam	deodar
Malayalam	ദേവതാരം
Malayalam	ദേവദാരം
Malayalam	ദേവദാരു
Marathi	देवदार
Norwegian Bokmål	himalaiaseder
Norwegian Bokmål	himalayaseder
Nepali	देवदार
Dutch	deodar
Dutch	himalayaceder
Dutch	deodarceder
Punjabi	ਦਿਓਦਾਰ
Polish	cedr himalajski
Punjab	دیودار
Portuguese	cedro-do-himalaia
Portuguese	cedro deodara
Portuguese	cedro do himalaia
Portuguese	cedro-deodara
Portuguese	cedro-dos-himalaias
Portuguese	deodara
Russian	Кедр гималайский
Russian	Гималайский кедр
Slovenian	himalajska cedra
Serbian	Хималајски кедар
Tamil	தேவதாரம்
Telugu	దేవదారు
Telugu	దేవదారు పత్రి
Telugu	దేవదారుపత్రం
Telugu	దేవదారువు
Turkish	himalaya sediri
Ukrainian	Кедр гімалайський
Urdu	دیودار
Urdu	cedar
Urdu	سرو
Vietnamese	tuyết tùng himalaya
Chinese	香柏
Chinese	雪松
Chinese	喜马拉雅雪松
Chinese	喜馬拉雅雪松

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!

Start at 4°C for 3 months, then warm to 20°C for another 3 months.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - Tibet
- Western Asia
  - Afghanistan

Asia-tropical click to expand
- Indian Subcontinent
  - India
  - Nepal
  - Pakistan
  - West Himalaya

Europe click to expand
- Northern Europe
  - Great Britain
- Southeastern Europe
  - Greece
  - Italy
- Southwestern Europe
  - France
  - Portugal

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000592532
UNII	T72K3W0X0I
USDA Plants	CEDE2
Tropicos	24900655
INPN	89454
Flora of Italy	8335
KEW	urn:lsid:ipni.org:names:676701-1
The Plant List	kew-2707322
Missouri Botanical Garden	245529
PaleoBotany	73855
Open Tree Of Life	924430
Observations.org	116094
NCBI Taxonomy	3322
NBN Atlas	NHMSYS0000457002
Nature Serve	2.136824
IUCN Red List	42304
IPNI	676701-1
iNaturalist	69820
GBIF	5284698
Freebase	/m/049qtn
EPPO	CEUDE
EOL	1033603
Elurikkus	3519
Calflora (Californian flora)	9302
USDA GRIN	9692
Wikipedia	Cedrus_deodara

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

Ectomycorrhiza and ethylenediurea reduced the impact of high nitrogen and ozone stresses and increased the growth of Cedrus deodara

Jamil HM, Gatasheh MK, Ahmad R, Ibrahim KE, Khan SA, Irshad U, Shahzad M, Abbasi AM

Heliyon

27-Mar-2024

PMCID:	PMC10998246
doi:	10.1016/j.heliyon.2024.e28635
PMID:	38586366

Confronting the complexities of antimicrobial management for Staphylococcus aureus causing bovine mastitis: an innovative paradigm

Saeed SI, Kamaruzzaman NF, Gahamanyi N, Nguyen TT, Hossain D, Kahwa I

Ir Vet J

28-Feb-2024

PMCID:	PMC10900600
doi:	10.1186/s13620-024-00264-1
PMID:	38418988

Antioxidant Activity of Essential Oils from Pinaceae Species

Ancuceanu R, Anghel AI, Hovaneț MV, Ciobanu AM, Lascu BE, Dinu M

Antioxidants (Basel)

26-Feb-2024

PMCID:	PMC10967544
doi:	10.3390/antiox13030286
PMID:	38539820

The genus Fomitopsis (Polyporales, Basidiomycota) reconsidered

Spirin V, Runnel K, Vlasák J, Viner I, Barrett MD, Ryvarden L, Bernicchia A, Rivoire B, Ainsworth AM, Grebenc T, Cartabia M, Niemelä T, Larsson KH, Miettinen O

Stud Mycol

22-Feb-2024

PMCID:	PMC11003443
doi:	10.3114/sim.2024.107.03
PMID:	38600960

Evaluation of the anti-arthritic activity of Rhuflex-F – A proprietary Ayurvedic herbomineral formulation in albino rats

Gupta V, Panigrahi B, De S, Nariya MB

Ayu

21-Feb-2024

PMCID:	PMC10946666
doi:	10.4103/ayu.ayu_327_21
PMID:	38505109

Integrative management of insomnia during cancer chemotherapy: A case report

Arathi P, Sreejith K, Pavithran K, Soman D

J Ayurveda Integr Med

19-Feb-2024

PMCID:	PMC10885578
doi:	10.1016/j.jaim.2024.100899
PMID:	38377655

Reactive oxygen species may be involved in the distinctive biological effects of different doses of 12C6+ ion beams on Arabidopsis

Yin Y, Cui D, Chi Q, Xu H, Guan P, Zhang H, Jiao T, Wang X, Wang L, Sun H

Front Plant Sci

19-Jan-2024

PMCID:	PMC10835405
doi:	10.3389/fpls.2023.1337640
PMID:	38312361

Ayurvedic clinical decision-making methods to predict, prevent and manage childhood allergic disorders

Karthik KP, Dileep A, Rajagopala S, Arun Kumar M, Dharmarajan P, Vellela J

J Ayurveda Integr Med

18-Jan-2024

PMCID:	PMC10828817
doi:	10.1016/j.jaim.2023.100857
PMID:	38237455

Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants

Kirker GT, Hassan B, Mankowski ME, Eller FJ

Insects

18-Jan-2024

PMCID:	PMC10816604
doi:	10.3390/insects15010069
PMID:	38249075

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

Structural and Functional Strategies in Cenchrus Species to Combat Environmental Extremities Imposed by Multiple Abiotic Stresses

Basharat S, Ahmad F, Hameed M, Ahmad MS, Asghar A, Fatima S, Ahmad KS, Shah SM, Hashem A, Avila-Quezada GD, Abd_Allah EF, Abbas Z

Plants (Basel)

11-Jan-2024

PMCID:	PMC10818359
doi:	10.3390/plants13020203
PMID:	38256756

Early onset of aridity in the past millennium: Insights from vegetation dynamics and climate change in the alpine, cold-desert region of Trans Himalaya, India

Mohanty RB, Mishra AK, Mishra K, Yadava AK, Quamar MF, Barua IC, Kar R

PLoS One

10-Jan-2024

PMCID:	PMC10781162
doi:	10.1371/journal.pone.0295785
PMID:	38198444

Effect of Crown Layers on Reproductive Effort and Success in Andromonoecious Aesculus indica (Wall. ex Camb.) Hook (Sapindaceae) in a Temperate Forest of Garhwal Himalaya

Pradhan P, Sukumaran A, Khanduri VP, Singh B, Rawat D, Riyal MK, Kumar M, Pinto MM

Plants (Basel)

10-Jan-2024

PMCID:	PMC10818387
doi:	10.3390/plants13020183
PMID:	38256737

First Report of Diplodia quercivora and Neofusicoccum vitifusiforme Associated with Cankers and Necrosis of Holm Oak (Quercus ilex) in Declining Stands in Southern Italy

Del Grosso C, Palmieri D, Marchese L, Melissano L, Lima G

J Fungi (Basel)

03-Jan-2024

PMCID:	PMC10820903
doi:	10.3390/jof10010035
PMID:	38248945

Multi-century (635-year) spring season precipitation reconstruction from northern Pakistan revealed increasing extremes

Khan N, Gaire NP, Rahmonov O, Ullah R

Sci Rep

02-Jan-2024

PMCID:	PMC10761852
doi:	10.1038/s41598-023-50819-5
PMID:	38168593

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 / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol	244	Click to see C1=CC=C(C=C1)CO	108.14	unknown	https://doi.org/10.1080/10412905.1990.9697826
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
6-(2-Hydroxy-5-methylphenyl)-6-methylheptan-2-one	13855300	Click to see CC1=CC(=C(C=C1)O)C(C)(C)CCCC(=O)C	234.33	unknown	https://doi.org/10.1016/0031-9422(81)80031-3
> Benzenoids / Perylenequinones
3,6a,7,10-Tetrahydroxy-4,9-dioxo-4,5,6,6a,6b,7,8,9-octahydroperylene	14767801	Click to see C1CC2(C3C(CC(=O)C4=C(C=CC(=C34)C5=C2C(=C(C=C5)O)C1=O)O)O)O	352.30	unknown	https://doi.org/10.1016/0031-9422(80)83107-4
> Benzenoids / Phenols / Methoxyphenols
4-[3-Hydroxy-1-[4-(3-hydroxypropyl)-2-methoxyphenoxy]prop-1-enyl]-2-methoxyphenol	162901846	Click to see COC1=C(C=CC(=C1)CCCO)OC(=CCO)C2=CC(=C(C=C2)O)OC	360.40	unknown	https://doi.org/10.1016/0031-9422(80)83107-4
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(5S,6R,7R)-5-(4-hydroxy-3-methoxyphenyl)-6,7-bis(hydroxymethyl)-3-methoxy-5,6,7,8-tetrahydronaphthalen-2-ol	163034338	Click to see COC1=C(C=CC(=C1)C2C(C(CC3=CC(=C(C=C23)OC)O)CO)CO)O	360.40	unknown	https://doi.org/10.1016/0031-9422(80)83107-4
(6R,7R,8S)-8-(3,4-dimethoxyphenyl)-6,7-bis(hydroxymethyl)-3-methoxy-5,6,7,8-tetrahydronaphthalen-2-ol	21722949	Click to see COC1=C(C=C(C=C1)C2C(C(CC3=CC(=C(C=C23)O)OC)CO)CO)OC	374.40	unknown	https://doi.org/10.1016/0031-9422(82)80172-6
5-(4-Hydroxy-3-methoxyphenyl)-6,7-bis(hydroxymethyl)-3-methoxy-5,6,7,8-tetrahydronaphthalen-2-ol	129181947	Click to see COC1=C(C=CC(=C1)C2C(C(CC3=CC(=C(C=C23)OC)O)CO)CO)O	360.40	unknown	https://doi.org/10.1016/0031-9422(80)83107-4
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
2,3-bis(4-Hydroxy-3-methoxybenzyl)butane-1,4-diol	586372	Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O	362.40	unknown	https://doi.org/10.1016/0031-9422(82)80172-6
meso-Secoisolariciresinol	11552274	Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O	362.40	unknown	https://doi.org/10.1016/0031-9422(82)80172-6
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Lariciresinol	332427	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1016/0031-9422(80)83107-4
Tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-((4-hydroxy-3-methoxyphenyl)methyl)-3-furanmethanol	134203	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1016/0031-9422(80)83107-4
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactols
(-)-Lactol	10316469	Click to see COC1=C(C=CC(=C1)CC2COC(C2CC3=CC(=C(C=C3)O)OC)O)O	360.40	unknown	https://doi.org/10.1021/JF010573A
(2R,3S,4S)-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-ol	162915278	Click to see COC1=C(C=CC(=C1)CC2COC(C2CC3=CC(=C(C=C3)O)OC)O)O	360.40	unknown	https://doi.org/10.1021/JF010573A
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(+)-Nortrachelogenin	479756	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O	374.40	unknown	https://doi.org/10.1021/JF010573A
(3R,4S)-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one	36688829	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)O	358.40	unknown	https://doi.org/10.1021/JF010573A
3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one	345761	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)O	358.40	unknown	https://doi.org/10.1021/JF010573A
Matairesinol	119205	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)O	358.40	unknown	https://doi.org/10.1021/JF010573A
Nortrachelogenin	394846	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O	374.40	unknown	https://doi.org/10.1021/JF010573A
Wikstromol	99938	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O	374.40	unknown	https://doi.org/10.1021/JF010573A
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
[(7R)-1,16-dihydroxyhexadecan-7-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	163189173	Click to see C1=CC(=C(C=C1C=CC(=O)OC(CCCCCCCCCO)CCCCCCO)O)O	436.60	unknown	https://doi.org/10.1248/CPB.35.229
[(8R)-16-hydroxyhexadecan-8-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	163193118	Click to see CCCCCCCC(CCCCCCCCO)OC(=O)C=CC1=CC(=C(C=C1)O)O	420.60	unknown	https://doi.org/10.1248/CPB.35.2443
1,16-Dihydroxyhexadecan-7-yl 3-(3,4-dihydroxyphenyl)prop-2-enoate	73813187	Click to see C1=CC(=C(C=C1C=CC(=O)OC(CCCCCCCCCO)CCCCCCO)O)O	436.60	unknown	https://doi.org/10.1248/CPB.35.229
16-Hydroxyhexadecan-8-yl 3-(3,4-dihydroxyphenyl)prop-2-enoate	73818342	Click to see CCCCCCCC(CCCCCCCCO)OC(=O)C=CC1=CC(=C(C=C1)O)O	420.60	unknown	https://doi.org/10.1248/CPB.35.2443
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aR,4bR,10aR)-7-(2-methoxypropan-2-yl)-1,4a-dimethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	21637792	Click to see CC12CCCC(C1CC=C3C2CCC(=C3)C(C)(C)OC)(C)C(=O)O	332.50	unknown	https://doi.org/10.1248/CPB.35.2443
(1R,4aS,10aR)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid	10017708	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C	300.40	unknown	https://doi.org/10.1248/CPB.35.229
1-(Hydroxymethyl)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol	23786420	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)CO)C	302.50	unknown	https://doi.org/10.1248/CPB.35.229 https://doi.org/10.1248/CPB.35.2443
1,4a-Dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	15618	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C	300.40	unknown	https://doi.org/10.1248/CPB.35.229
15-Hydroxyabieta-7,13-dien-18-oic acid	643004	Click to see CC12CCCC(C1CC=C3C2CCC(=C3)C(C)(C)O)(C)C(=O)O	318.40	unknown	https://doi.org/10.1248/CPB.35.2443
15-Hydroxydehydroabietic acid	14487943	Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O	316.40	unknown	https://doi.org/10.1248/CPB.35.229
7-(2-Hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	14779864	Click to see CC12CCCC(C1CC=C3C2CCC(=C3)C(C)(C)O)(C)C(=O)O	318.40	unknown	https://doi.org/10.1248/CPB.35.2443
7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic Acid	9944781	Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O	316.40	unknown	https://doi.org/10.1248/CPB.35.229
7-(2-Methoxypropan-2-yl)-1,4a-dimethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	73818341	Click to see CC12CCCC(C1CC=C3C2CCC(=C3)C(C)(C)OC)(C)C(=O)O	332.50	unknown	https://doi.org/10.1248/CPB.35.2443
7alpha-Hydroxydehydroabietinol	21626425	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)CO)C	302.50	unknown	https://doi.org/10.1248/CPB.35.229
7beta-Hydroxydehydroabietic acid	13370052	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C(=O)O)C	316.40	unknown	https://doi.org/10.1248/CPB.35.2443
7beta,15-Dihydroxydehydroabietic acid	21626423	Click to see CC12CCCC(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)(C)C(=O)O	332.40	unknown	https://doi.org/10.1248/CPB.35.229
7beta,18-Dihydroxydehydroabietanol	21632835	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)CO)C	302.50	unknown	https://doi.org/10.1248/CPB.35.2443
9-hydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic Acid	10448477	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C(=O)O)C	316.40	unknown	https://doi.org/10.1248/CPB.35.2443
9-Hydroxy-7-(2-hydroxypropan-2-YL)-1,4A-dimethyl-2,3,4,9,10,10A-hexahydrophenanthrene-1-carboxylic acid	45782962	Click to see CC12CCCC(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)(C)C(=O)O	332.40	unknown	https://doi.org/10.1248/CPB.35.229
Dehydroabietic acid	94391	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C	300.40	unknown	https://doi.org/10.1248/CPB.35.229
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
1-O-(16-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenyl) 4-O-methyl 2-methylbut-2-enedioate	163023455	Click to see CC(=CCCC(=CCOC(=O)C(=CC(=O)OC)C)C)CCC=C(C)CCC=C(C)CO	432.60	unknown	https://doi.org/10.1016/0031-9422(80)85133-8 https://doi.org/10.1007/S10600-011-0040-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
(3R,4aR,5S,9aR)-2,5,9,9-tetramethyl-4,4a,6,7,8,9a-hexahydro-3H-benzo[7]annulene-3,5-diol	162900619	Click to see CC1=CC2C(CC1O)C(CCCC2(C)C)(C)O	238.37	unknown	https://doi.org/10.1016/S0031-9422(00)88974-8
(3R,4aR,5S,9aS)-2,5,9,9-tetramethyl-4,4a,6,7,8,9a-hexahydro-3H-benzo[7]annulene-3,5-diol	101820944	Click to see CC1=CC2C(CC1O)C(CCCC2(C)C)(C)O	238.37	unknown	https://doi.org/10.1016/S0031-9422(00)88974-8
2,5,9,9-tetramethyl-4,4a,6,7,8,9a-hexahydro-1H-benzo[7]annulene-1,5-diol	3496773	Click to see CC1=CCC2C(C1O)C(CCCC2(C)O)(C)C	238.37	unknown	https://doi.org/10.1016/S0031-9422(00)88974-8
2,5,9,9-tetramethyl-4,4a,6,7,8,9a-hexahydro-3H-benzo[7]annulene-3,5-diol	23265059	Click to see CC1=CC2C(CC1O)C(CCCC2(C)C)(C)O	238.37	unknown	https://doi.org/10.1016/S0031-9422(00)88974-8
Centarol	442349	Click to see CC1=CCC2C(C1O)C(CCCC2(C)O)(C)C	238.37	unknown	https://doi.org/10.1016/S0031-9422(00)88974-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	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	https://doi.org/10.1248/CPB.35.229
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	https://doi.org/10.1248/CPB.35.229
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(4aR,9aR)-3,5,5,9a-tetramethyl-1,2,4a,6,7,8-hexahydrobenzo[7]annulen-9-one	101417506	Click to see CC1=CC2C(CCCC(=O)C2(CC1)C)(C)C	220.35	unknown	https://doi.org/10.1002/CHIN.197733304
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
7-hydroxy-2,3,4,5-tetramethoxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyxanthen-9-one	163063925	Click to see COC1=CC(=CC2=C1OC3=C(C2=O)C(=C(C(=C3OC)OC)OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O	642.60	unknown	https://doi.org/10.1248/CPB.35.2443
> Organoheterocyclic compounds / Oxanes
(1S,8R)-3,7,11,11-tetramethyl-12-oxatricyclo[6.3.1.01,6]dodeca-2,6-diene	101966999	Click to see CC1=CC23C(=C(C(O2)CCC3(C)C)C)CC1	218.33	unknown	https://doi.org/10.1002/CHIN.197733304
(6S)-2,2,6-trimethyl-6-[(1R)-4-methylcyclohex-3-en-1-yl]oxan-4-one	101162778	Click to see CC1=CCC(CC1)C2(CC(=O)CC(O2)(C)C)C	236.35	unknown	https://doi.org/10.1002/CHIN.197733304
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R)-2beta-[3-Methoxy-4-(beta-D-glucopyranosyloxy)phenyl]-5-(3-hydroxypropyl)-7-hydroxy-2,3-dihydrobenzofuran-3alpha-methanol	101165148	Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)CCCO)O)CO)OC4C(C(C(C(O4)CO)O)O)O	508.50	unknown	https://doi.org/10.1016/0031-9422(80)83107-4
2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-(3-hydroxypropyl)-2,3-dihydro-1-benzofuran-7-ol	187915	Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)CCCO)O)CO)O	346.40	unknown	https://doi.org/10.1016/0031-9422(80)83107-4
2-[4-[7-Hydroxy-3-(hydroxymethyl)-5-(3-hydroxypropyl)-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	45782907	Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)CCCO)O)CO)OC4C(C(C(C(O4)CO)O)O)O	508.50	unknown	https://doi.org/10.1016/0031-9422(80)83107-4
2,3-Dihydro-2beta-(4-hydroxy-3-methoxyphenyl)-3beta-(hydroxymethyl)-5-(3-hydroxypropyl)benzofuran-7-ol	101992982	Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)CCCO)O)CO)O	346.40	unknown	https://doi.org/10.1016/0031-9422(80)83107-4
4-[(2S,3R)-3-(hydroxymethyl)-5-(3-hydroxypropyl)-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenol	162872299	Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C=CC(=C3)CCCO)CO)O	330.40	unknown	https://doi.org/10.1016/0031-9422(82)80172-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate	163193056	Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O	326.30	unknown	https://doi.org/10.1007/S10600-011-9901-9
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3-(4-hydroxyphenyl)prop-2-enoate	72727649	Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O	326.30	unknown	https://doi.org/10.1007/S10600-011-9901-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)chroman-4-one	5153580	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O	320.25	unknown	https://doi.org/10.1016/0031-9422(80)85133-8 https://doi.org/10.1007/S10600-011-0040-0
Cedrin	21721881	Click to see CC1=C(C2=C(C=C1O)OC(C(C2=O)O)C3=CC(=C(C(=C3)O)O)O)O	334.28	unknown	https://doi.org/10.1007/S10600-011-0040-0 https://doi.org/10.1016/0031-9422(80)85133-8
Dihydromyricetin	161557	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O	320.25	unknown	https://doi.org/10.1016/0031-9422(80)85133-8 https://doi.org/10.1007/S10600-011-0040-0
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one	667495	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1248/CPB.35.229
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one	932	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1248/CPB.35.229
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin	471	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://doi.org/10.1016/0031-9422(80)85133-8
Taxifolin	439533	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://doi.org/10.1016/0031-9422(80)85133-8
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	https://doi.org/10.1007/S10600-011-0040-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R,3R)-2-[3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3,5,7-trihydroxy-6-methyl-2,3-dihydrochromen-4-one	162906549	Click to see CC1=C(C2=C(C=C1O)OC(C(C2=O)O)C3=CC(=C(C(=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	496.40	unknown	https://doi.org/10.1016/0031-9422(80)85133-8
2-[3,4-Dihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3,5,7-trihydroxy-6-methyl-2,3-dihydrochromen-4-one	162906547	Click to see CC1=C(C2=C(C=C1O)OC(C(C2=O)O)C3=CC(=C(C(=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	496.40	unknown	https://doi.org/10.1016/0031-9422(80)85133-8
3,5,7-Trihydroxy-2-[4-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one	14282773	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	466.40	unknown	https://doi.org/10.1016/0031-9422(80)83107-4
Taxifolin 3'-glucoside	14282774	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	466.40	unknown	https://doi.org/10.1016/0031-9422(80)83107-4

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Cedrus deodara

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