Scientific name	Authority	First published in
Retinispora pisifera	Siebold & Zucc.	Fl. Jap. 2: 39 (1844)
Retinispora plumosa	hort. ex Carrière	Traité Gén. Conif., ed. 2. 791; Veitch, ex C. Koch, Dendrol. 2(2): 170. 1867
Retinispora squarrosa	Siebold & Zucc.	Fl. Jap. 2: 40 (1844)
Retinispora stricta	hort. ex Gordon	Pinetum , ed. 2: 428 (1875)
Retinispora filifera	Fowler	Gard. Chron. 1872: 1490 (1872)
Retinispora leptoclada	Zucc. ex Gordon	Pinetum , Suppl.: 91 (1862)
Thuja pisifera	Mast.	J. Linn. Soc., Bot. 18: 489 (1881)
Chamaecyparis leptoclada	Henk. & Hochst.	Syn. Nadelhölz. : 257 (1865)
Chamaecyparis obtusa var. plumosa	Carrière	Traité Gén. Conif. , ed. 2: 791 (1867)
Chamaecyparis plumosa	hort. ex Beissn.	Handb. Nadelholzk. (1891) 87.
Chamaecyparis squarrosa	Siebold & Zucc.	in Endl. Conif. 65.
Cupressus leptoclada	hort. ex Lavallée	Énum. Arbres : 282 (1877)
Cupressus pisifera	(Siebold & Zucc.) F.Muell.	Dendrologie 2(2): 170 (1873)
Cupressus squarrosa	Siebold & Zucc.	P. Lawson & Son, Abietineae- List Pl. Fir Tribe No. 10, 64 (1851); ListsSeeds, Pl., etc. 266 (1851).
Cupressus squarrosa	Laws. ex Gordon	Pinetum 296. 1858
Chamaecyparis pisifera f. squarrosa	(Siebold & Zucc.) Beissn. & Hochst.	Handb. Conif. 13 1887
Chamaecyparis pisifera var. filifera	(Veitch ex Sénécl.) Hartw. & Rümpler	Bäume Sträucher 661. 1875
Chamaecyparis pisifera var. plumosa	(Carrière) Ed.Otto	Neue Allg. Deutsche Garten- Blumenzeitung 24: 141. 1868
Cupressus pisifera var. filiera	(Veitch ex Sénécl.) Lavallée	Énum. Arbres 280 1877
Cupressus pisifera var. plumosa	(Carrière) Lavallée	Énum. Arbres 280 1877
Retinispora pisifera var. aurea	Gordon	Pinetum Suppl.: 94. 1862
Chamaecyparis pisifera f. aurea	(Gordon) Rehder	Bibl. Cult. Trees 55 1949
Retinispora aurea	(Gordon) de Vos	Bered. Woordenboek 183. 1867 (1867)
Cupressus pisifera var. sulphurea	A.H.Kent	Man. Conif. 225 1900
Chamaecyparis pisifera f. sulphurea	(A.H.Kent) Rehder	Bibl. Cult. Trees 55 1949
Chamaecyparis pisifera f. filifera	(Veitch ex Sénécl.) Voss	Vilm. Blumengärtn. ed. 3 1: 1228 1896
Chamaecyparis filifera	Veitch ex Sénécl.	Conifères 54. 1868 (1868)
Retinispora pisifera var. filiformis	R.Sm.	Pl. Fir Tribe 39. 1874
Thuja pisifera var. filifera	(Veitch ex Sénécl.) Mast.	J. Linn. Soc., Bot. 18: 491 `88`
Chamaecyparis pisifera var. filicoides	Regel	Russ. Dendrol. ed. 2: 27. 1883
Chamaecyparis pisifera var. filiformis	(R.Sm.) Beissn.	Ziergehloze Gart. Park. ed. 2: 454 1884
Cupressus pisifera f. pendula	Mast.	J. Linn. Soc., Bot. 31: 356 1893
Chamaecyparis pisifera var. pendula	(Mast.) Zederb.	Sitzungsber. Kaiserl. Akad. Wiss., Math.-Naturwiss. Cl. 116: 1942 1907
Chamaecyparis pisifera var. filifera-pendula	Nash	J. New York Bot. Gard. 18: 167. 1817
Chamaecyparis pisifera f. filifera-aurea	Beissn.	Handb. Nadelholzk. 91 1891
Chamaecyparis pisifera f. standishii	Beissn.	Handb. Nadelholzk. 91 1891
Chamaecyparis pisifera f. aurea-nana	Beissn.	Handb. Nadelholzk. 91 1891
Chamaecyparis pisifera f. filifera-aureovariegata	Beissn.	Handb. Nadelholzk. ed. 2: 572 1909
Chamaecyparis pisifera f. plumosa	(Carrière) Beissn.	Handb. Conif. 13 1887
Chamaecyparis plumosa var. argentea	Sénécl.	Conifères 57. 1868
Retinispora plumosa var. aurea	R.Sm.	Pl. Fir Tribe 39. 1874
Cupressus obtusa var. plumosa-aurea	Lavallée	Énum. Arbres 281 1877
Cupressus obtusa var. plumosa-argentea	Lavallée	Énum. Arbres 281 1877
Chamaecyparis squarrosa var. leptoclada	Endl.	Syn. Conif. 65. 1847
Chamaecyparis pisifera f. leptoclada	(Endl.) Rehder	Bibl. Cult. Trees 56 1949
Chamaecyparis squarrosa var. sulphurea	G.Nicholson	Ill. Dict. Gard. Suppl.: 222. 1900
Chamaecyparis pisifera f. minima	Hornibr.	Dwarf Conifers 49 1923
Cupressus pisifera var. plumosa	(Carrière) Geerinck	Taxonomania 12: 13. 2004 [29 March 2004]

Common names Top

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Filter by language:

Language	Common/alternative name
English	sawara cypress
Spanish	cipres de guisantes
Spanish	cipres pisifero
Spanish	ciprés de guisantes
Spanish	cipres de hondo
Spanish	ciprés de hondo
Spanish	ciprés pisífero
Spanish	falso cipres sawara
Spanish	falso ciprés sawara
Spanish	cameciparis sawara
Spanish	camecíparis sawara
Azerbaijani	noxudmeyvəli sərvpəri
azb	نوخودمئیوهلی سروپری
ba	Борсаҡ емешле кипарис
Czech	cypřišek hrachonosný
Welsh	cypreswydden sawara
Danish	Ærtecypres
German	sawara-scheinzypresse
German	faden-scheinzypresse
German	erbsenfrüchtige scheinzypresse
Persian	سرو ریسمان سبز
Finnish	hernesypressi
Upper Sorbian	Štapata cypresa
Hungarian	szavara hamisciprus
Icelandic	ertusýprus
Japanese	檜榁
Japanese	ヒムロ杉
Japanese	椹
Japanese	サワラ
Lithuanian	Žirniavaisis puskiparisis
Lithuanian	Žirniasėklis puskiparisis
Malayalam	ചമേസിപാരിസ് പിസിഫെറ
Norwegian Bokmål	ertesypress
Norwegian Bokmål	sawarasypress
Norwegian Bokmål	sawara
Polish	cyprysik groszkowy
Portuguese	cipreste-sawara
Portuguese	tuia macarrão
Portuguese	tuia azul
Portuguese	cipreste sawara
Russian	Кипарисовик горохоплодный
Swedish	Ärtcypress
Chinese	日本花柏
Chinese	五彩松
Chinese	羽叶花柏

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!

Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Eastern Asia
  - Japan
  - Korea

Europe click to expand
- Northern Europe
  - Great Britain
  - Ireland

Northern America click to expand
- Northeastern U.S.A.
  - New York

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000599479
Cornell Woody Plants	304
USDA Plants	CHPI12
UConn	108
Tropicos	9400439
INPN	90413
KEW	urn:lsid:ipni.org:names:261847-1
The Plant List	kew-2715306
Plantarium	10010
Missouri Botanical Garden	279623
PaleoBotany	31393
Open Tree Of Life	883814
Observations.org	138808
NCBI Taxonomy	99808
NBN Atlas	NBNSYS0000034351
Nature Serve	2.131411
IUCN Red List	42213
IPNI	261847-1
iNaturalist	123925
GBIF	2683880
Freebase	/m/048mb9
EPPO	CHCPI
EOL	323366
USDA GRIN	10096
Wikipedia	Chamaecyparis_pisifera
CMAUP	NPO6272

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

Current status of the cryopreservation of embryogenic material of woody species

Ballesteros D, Martínez MT, Sánchez-Romero C, Montalbán IA, Sales E, Moncaleán P, Arrillaga I, Corredoira E

Front Plant Sci

17-Jan-2024

PMCID:	PMC10828030
doi:	10.3389/fpls.2023.1337152
PMID:	38298606

Somatic Embryogenesis in Conifers: One Clade to Rule Them All?

Fraga HP, Moraes PE, Vieira LD, Guerra MP

Plants (Basel)

14-Jul-2023

PMCID:	PMC10385530
doi:	10.3390/plants12142648
PMID:	37514262

Development of Native Essential Oils from Forestry Resources in South Korea

Park C, Woo H

Life (Basel)

29-Nov-2022

PMCID:	PMC9785413
doi:	10.3390/life12121995
PMID:	36556360

High-throughput discovery of plastid genes causing albino phenotypes in ornamental chimeric plants

Park HS, Jeon JH, Cho W, Lee Y, Park JY, Kim J, Park YS, Koo HJ, Kang JH, Lee TJ, Kim SH, Kim JB, Kwon HY, Kim SH, Paek NC, Jang G, Suh JY, Yang TJ

Hortic Res

03-Nov-2022

PMCID:	PMC9832966
doi:	10.1093/hr/uhac246
PMID:	36643742

Secondary plant metabolites as potent drug candidates against antimicrobial-resistant pathogens

Keita K, Darkoh C, Okafor F

SN Appl Sci

08-Jul-2022

PMCID:	PMC9264742
doi:	10.1007/s42452-022-05084-y
PMID:	35821909

Present scenarios and future prospects of herbal nanomedicine for antifungal therapy

Yadav R, Pradhan M, Yadav K, Mahalvar A, Yadav H

J Drug Deliv Sci Technol

13-May-2022

PMCID:	PMC9101776
doi:	10.1016/j.jddst.2022.103430
PMID:	35582019

Serological survey of antibodies to four pathogens in wild boars in Nagano Prefecture, Japan

KANEKO F, KITAMURA N, SUZUKI K, KATO M

J Vet Med Sci

25-Apr-2022

PMCID:	PMC9246675
doi:	10.1292/jvms.22-0035
PMID:	35466116

Physiological and Psychological Relaxation Effects of Fir Essential Oil on University Students

Kim C, Song C

Int J Environ Res Public Health

21-Apr-2022

PMCID:	PMC9103969
doi:	10.3390/ijerph19095063
PMID:	35564457

Hedycaryol – Central Intermediates in Sesquiterpene Biosynthesis, Part II

Xu H, Dickschat JS

Chemistry

21-Mar-2022

PMCID:	PMC9310801
doi:	10.1002/chem.202200405
PMID:	35239190

Identifying and extracting bark key features of 42 tree species using convolutional neural networks and class activation mapping

Kim TK, Hong J, Ryu D, Kim S, Byeon SY, Huh W, Kim K, Baek GH, Kim HS

Sci Rep

19-Mar-2022

PMCID:	PMC8934343
doi:	10.1038/s41598-022-08571-9
PMID:	35306532

Geosmithia Species Associated With Bark Beetles From China, With the Description of Nine New Species

Zhang X, Li Y, Si H, Zhao G, Kolařík M, Hulcr J, Jiang X, Dai M, Chang R

Front Microbiol

14-Mar-2022

PMCID:	PMC8964297
doi:	10.3389/fmicb.2022.820402
PMID:	35369427

RhizoVision Explorer: open-source software for root image analysis and measurement standardization

Seethepalli A, Dhakal K, Griffiths M, Guo H, Freschet GT, York LM

AoB Plants

13-Sep-2021

PMCID:	PMC8598384
doi:	10.1093/aobpla/plab056
PMID:	34804466

Forest Therapy Alone or with a Guide: Is There a Difference between Self-Guided Forest Therapy and Guided Forest Therapy Programs?

Kim JG, Shin WS

Int J Environ Res Public Health

29-Jun-2021

PMCID:	PMC8296901
doi:	10.3390/ijerph18136957
PMID:	34209647

Factors Influencing Somatic Embryo Maturation in Sugi (Japanese Cedar, Cryptomeria japonica (Thunb. ex L.f.) D. Don)

Maruyama TE, Ueno S, Mori H, Kaneeda T, Moriguchi Y

Plants (Basel)

26-Apr-2021

PMCID:	PMC8145757
doi:	10.3390/plants10050874
PMID:	33926083

The Influence of Forest Activities in a University Campus Forest on Student’s Psychological Effects

Kim JG, Jeon J, Shin WS

Int J Environ Res Public Health

02-Mar-2021

PMCID:	PMC7967591
doi:	10.3390/ijerph18052457
PMID:	33801534

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 / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol	14529	Click to see CC1=CC=C(C=C1)C(C)(C)O	150.22	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(4S,5R)-4-(4-hydroxyphenyl)-5-[(2R,3R,4S)-2,3,4-trihydroxyoxolan-2-yl]oxolan-2-one	162887321	Click to see C1C(C(OC1=O)C2(C(C(CO2)O)O)O)C3=CC=C(C=C3)O	296.27	unknown	https://doi.org/10.1016/0031-9422(88)87047-X
4-(4-Hydroxyphenyl)-5-(2,3,4-trihydroxyoxolan-2-yl)oxolan-2-one	14160575	Click to see C1C(C(OC1=O)C2(C(C(CO2)O)O)O)C3=CC=C(C=C3)O	296.27	unknown	https://doi.org/10.1016/0031-9422(90)89046-C https://doi.org/10.1016/0031-9422(88)87047-X
6,7,8-Trihydroxy-4-(4-hydroxyphenyl)-1,10-dioxaspiro[4.5]decan-2-one	14463063	Click to see C1C(C2(C(C(C(CO2)O)O)O)OC1=O)C3=CC=C(C=C3)O	296.27	unknown	https://doi.org/10.1016/0031-9422(90)89046-C
> Benzenoids / Phenols / Methoxyphenols
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	via CMAUP database
> Benzenoids / Tetralins
(6aS)-7,7-dimethyl-3-propan-2-yl-5,6,6a,8,9,10-hexahydrocyclohepta[a]naphthalen-2-ol	162873341	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2=CCCCC3(C)C)O	284.40	unknown	https://doi.org/10.1016/0031-9422(80)83073-1
7,7-Dimethyl-3-propan-2-yl-5,6,6a,8,9,10-hexahydrocyclohepta[a]naphthalen-2-ol	162873340	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2=CCCCC3(C)C)O	284.40	unknown	https://doi.org/10.1016/0031-9422(80)83073-1
> Lignans, neolignans and related compounds
Agatharesinol	15558522	Click to see C1=CC(=CC=C1C=CC(C2=CC=C(C=C2)O)C(CO)O)O	286.32	unknown	https://doi.org/10.1016/0031-9422(90)89046-C
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(2R)-2alpha-(3-Hydroxy-5-methoxyphenyl)-3-(hydroxymethyl)-4beta-(3-methoxy-4-hydroxybenzyl)tetrahydrofuran-3alpha-ol	46830376	Click to see COC1=CC(=CC(=C1)O)C2C(C(CO2)CC3=CC(=C(C=C3)O)OC)(CO)O	376.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(Z)-hex-3-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	5318045	Click to see CCC=CCCOC1C(C(C(C(O1)CO)O)O)O	262.30	unknown	via CMAUP database
(E)-8-Decene-4,6-diynyl 6-O-D-apio-beta-D-furanosyl beta-D-glucopyranoside	46830373	Click to see CC=CC#CC#CCCCOC1C(C(C(C(O1)COC2C(C(CO2)(CO)O)O)O)O)O	442.50	unknown	via CMAUP database
[(8E)-8-Decene-4,6-diynyl]6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside	46830375	Click to see CC=CC#CC#CCCCOC1C(C(C(C(O1)COC2C(C(C(C(O2)C)O)O)O)O)O)O	456.50	unknown	via CMAUP database
[(8Z)-8-Decene-4,6-diynyl]6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranoside	101506974	Click to see CC=CC#CC#CCCCOC1C(C(C(C(O1)COC2C(C(CO2)(CO)O)O)O)O)O	442.50	unknown	via CMAUP database
[(S)-1,5-Dimethyl-1-ethenyl-6-hydroxy-4-hexenyl]beta-D-glucopyranoside	44559174	Click to see CC(=CCCC(C)(C=C)OC1C(C(C(C(O1)CO)O)O)O)CO	332.39	unknown	via CMAUP database
4,6-Decadiynyl 6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside	46830374	Click to see CCCC#CC#CCCCOC1C(C(C(C(O1)COC2C(C(C(C(O2)C)O)O)O)O)O)O	458.50	unknown	via CMAUP database
4,6-Decadiynyl 6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranoside	46830349	Click to see CCCC#CC#CCCCOC1C(C(C(C(O1)COC2C(C(CO2)(CO)O)O)O)O)O	444.50	unknown	via CMAUP database
> 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/S0031-9422(00)81063-8
Nonacosan-10-ol	25240035	Click to see CCCCCCCCCCCCCCCCCCCC(CCCCCCCCC)O	424.80	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(+)-Pisiferal	13785026	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C=O)O	300.40	unknown	https://doi.org/10.1016/0031-9422(80)83073-1 https://doi.org/10.1016/S0031-9422(00)81063-8 https://doi.org/10.1248/CPB.49.1479
(+)-Pisiferol	13785024	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)CO)O	302.50	unknown	https://doi.org/10.1016/S0031-9422(00)90941-5 https://doi.org/10.1016/0031-9422(80)83073-1 https://doi.org/10.1248/CPB.49.1479 https://doi.org/10.1016/S0031-9422(00)81063-8
(+)-Verticillol	15119671	Click to see CC1=CCCC(=CCC2CCC(C(C2(C)C)CC1)(C)O)C	290.50	unknown	via CMAUP database
(11S)-12,12-dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1,3,5,7-tetraen-5-ol	14587210	Click to see CC(C)C1=C(C=C2C=C3CCCC(C3CCC2=C1)(C)C)O	284.40	unknown	https://doi.org/10.1246/CL.1984.1837 https://doi.org/10.1016/S0031-9422(00)81063-8
(12E)-labda-8(17),12,14-triene	23252995	Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C)C)C=C	272.50	unknown	via CMAUP database
(1S,11S)-12,12-dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-3(8),4,6-trien-1-ol	162903532	Click to see CC(C)C1=CC2=C(CC3(CCCC(C3CC2)(C)C)O)C=C1	286.50	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
(1S,2R,8S,11R)-1,2,8-trihydroxy-12,12-dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-3,6-dien-5-one	163028764	Click to see CC(C)C1=CC2(CCC3C(CCCC3(C(C2=CC1=O)O)O)(C)C)O	334.40	unknown	https://doi.org/10.1248/CPB.49.1479
(1S,4S,9S,10R,13R)-5,5,9,13-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene	101277372	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)(C=C4)C)C)C	272.50	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
(4aS,10aS)-6-hydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carbaldehyde	13785027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C=O)O	300.40	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
(4bR,8aS,10aS)-10a-hydroxy-4b-(hydroxymethyl)-8,8-dimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-one	163188381	Click to see CC(C)C1=CC2(CCC3C(CCCC3(C2=CC1=O)CO)(C)C)O	318.40	unknown	https://doi.org/10.1248/BPB.31.755
(4bS)-1-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-2-ol	460178	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C)C)O	286.50	unknown	via CMAUP database
(4R,8S)-7,7-dimethyl-13-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1(15),2,11,13-tetraene-4,14-diol	163020578	Click to see CC(C)C1=C(C=C2C=C3C(CCC2=C1)C(CCC3O)(C)C)O	300.40	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
(8aS)-8,8-dimethyl-2-propan-2-yl-9,10-dihydro-8aH-phenanthren-3-ol	162995963	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2=CC=CC3(C)C)O	268.40	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
1,2,8-Trihydroxy-12,12-dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-3,6-dien-5-one	85350149	Click to see CC(C)C1=CC2(CCC3C(CCCC3(C(C2=CC1=O)O)O)(C)C)O	334.40	unknown	https://doi.org/10.1248/CPB.49.1479
10a-Hydroxy-4b-(hydroxymethyl)-8,8-dimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-one	75069426	Click to see CC(C)C1=CC2(CCC3C(CCCC3(C2=CC1=O)CO)(C)C)O	318.40	unknown	https://doi.org/10.1248/BPB.31.755
12,12-Dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1,3,5,7-tetraen-5-ol	14587209	Click to see CC(C)C1=C(C=C2C=C3CCCC(C3CCC2=C1)(C)C)O	284.40	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
12,12-Dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7-tetraen-5-ol	11011523	Click to see CC(C)C1=C(C=C2CC3=CCCC(C3CCC2=C1)(C)C)O	284.40	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
12,12-Dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-3,5,7-triene-1,2,5-triol	5126500	Click to see CC(C)C1=C(C=C2C(C3(CCCC(C3CCC2=C1)(C)C)O)O)O	318.40	unknown	https://doi.org/10.1248/CPB.49.1479 https://doi.org/10.1016/S0031-9422(00)81063-8
12,12-Dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-3,5,7-triene-1,5-diol	4022498	Click to see CC(C)C1=C(C=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O	302.50	unknown	https://doi.org/10.1248/CPB.49.1479 https://doi.org/10.1016/S0031-9422(00)81063-8
12,12-Dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-3(8),4,6-trien-1-ol	162903531	Click to see CC(C)C1=CC2=C(CC3(CCCC(C3CC2)(C)C)O)C=C1	286.50	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
13-Isopropylpodocarpen-12-ol-20-al	520086	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C=O)O	300.40	unknown	https://doi.org/10.1248/CPB.49.1479 https://doi.org/10.1016/0031-9422(80)83073-1 https://doi.org/10.1016/S0031-9422(00)81063-8
15-Hydroxyferruginol	24770303	Click to see CC1(CCCC2(C1CCC3=CC(=C(C=C32)O)C(C)(C)O)C)C	302.50	unknown	https://doi.org/10.1016/0031-9422(80)83073-1
6-Hydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid	5088769	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O	316.40	unknown	https://doi.org/10.1271/BBB1961.48.2167 https://doi.org/10.1016/S0031-9422(00)90941-5 https://doi.org/10.1248/CPB.49.1479 https://doi.org/10.1016/S0031-9422(00)81063-8 https://doi.org/10.1271/BBB1961.42.1419
6-Methoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid	13654834	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)OC	330.50	unknown	https://doi.org/10.1271/BBB1961.48.2167 https://doi.org/10.1248/BPB.31.755 https://doi.org/10.1016/0031-9422(80)83073-1 https://doi.org/10.1248/CPB.49.1479 https://doi.org/10.1016/S0031-9422(00)81063-8
7,7-Dimethyl-13-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1(15),2,11,13-tetraene-4,14-diol	25067103	Click to see CC(C)C1=C(C=C2C=C3C(CCC2=C1)C(CCC3O)(C)C)O	300.40	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
8,8-dimethyl-2-propan-2-yl-9,10-dihydro-8aH-phenanthren-3-ol	129686282	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2=CC=CC3(C)C)O	268.40	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Abieta-8,11,13-triene-12,15-diol	133561437	Click to see CC1(CCCC2(C1CCC3=CC(=C(C=C32)O)C(C)(C)O)C)C	302.50	unknown	https://doi.org/10.1016/0031-9422(80)83073-1
Abieta-9(11),8(14),12-trien-12-ol	521330	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Abietatriene	6432211	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C)C	270.50	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Cupressene	623311	Click to see CC(C)C1=CC2C=CC3C(CCCC3(C2CC1)C)(C)C	272.50	unknown	via CMAUP database
delta8(14)-Pimaric acid	10116	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C	302.50	unknown	https://doi.org/10.1248/CPB.49.1479
dimethylamino (4aR,10aS)-6-methoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylate	162942710	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)ON(C)C)OC	373.50	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Dimethylamino 6-methoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylate	162942709	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)ON(C)C)OC	373.50	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
From the seeds of Chamaecyparis pisifera	355228	Click to see CC(C)C1=C(C=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O	302.50	unknown	https://doi.org/10.1248/CPB.49.1479 https://doi.org/10.1016/S0031-9422(00)81063-8
Lanigerol	188496	Click to see CC(C)C1=C(C=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O	302.50	unknown	https://doi.org/10.1248/CPB.49.1479 https://doi.org/10.1016/S0031-9422(00)81063-8
Manool	3034394	Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C	290.50	unknown	via CMAUP database
O-methylpisiferic acid	13654835	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)OC	330.50	unknown	https://doi.org/10.1248/BPB.31.755 https://doi.org/10.1271/BBB1961.48.2167 https://doi.org/10.1271/BBB1961.50.2405 https://doi.org/10.1016/0031-9422(80)83073-1 https://doi.org/10.1016/S0031-9422(00)81063-8 https://doi.org/10.1248/CPB.49.1479
Phenanthrene, 1,2,3,4,4a,9,10,10a-octahydro-6-methoxy-1,1,4a-trimethyl-7-(1-methylethyl)-, (4aS-trans)-	627188	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)OC	300.50	unknown	via CMAUP database
Pimara-7,15-dien-3-one	625348	Click to see CC1(C2CC=C3CC(CCC3C2(CCC1=O)C)(C)C=C)C	286.50	unknown	via CMAUP database
Pimaric acid	220338	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C	302.50	unknown	https://doi.org/10.1248/CPB.49.1479
Pisiferadinol	355229	Click to see CC(C)C1=C(C=C2C(C3(CCCC(C3CCC2=C1)(C)C)O)O)O	318.40	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Pisiferdiol	101317815	Click to see CC(C)C1=C(C=C2C(C3(CCCC(C3CCC2=C1)(C)C)O)O)O	318.40	unknown	https://doi.org/10.1271/BBB1961.48.3177 https://doi.org/10.1248/CPB.49.1479 https://doi.org/10.1016/S0031-9422(00)81063-8
Pisiferic acid	162209	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O	316.40	unknown	https://doi.org/10.1271/BBB1961.42.1419 https://doi.org/10.1271/BBB1961.48.2167 https://doi.org/10.1271/BBB1961.50.2405 https://doi.org/10.1016/S0031-9422(00)90941-5 https://doi.org/10.1016/S0031-9422(00)81063-8 https://doi.org/10.1248/CPB.49.1479
Pisiferin	14587207	Click to see CC(C)C1=C(C=C2CC3=CCCC(C3CCC2=C1)(C)C)O	284.40	unknown	https://doi.org/10.1246/CL.1984.1837 https://doi.org/10.1016/0031-9422(80)83073-1 https://doi.org/10.1016/S0031-9422(00)81063-8
Pisiferol	185553	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)CO)O	302.50	unknown	https://doi.org/10.1016/S0031-9422(00)90941-5 https://doi.org/10.1016/0031-9422(80)83073-1 https://doi.org/10.1016/S0031-9422(00)81063-8 https://doi.org/10.1248/CPB.49.1479
Sclareol	163263	Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C	308.50	unknown	via CMAUP database
Stachene ketol	101289551	Click to see CC1(C2CCC34CC(CCC3C2(CC(=O)C1O)C)(C=C4)C)C	302.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
Dolabradiene	12309316	Click to see CC1(CCC2(C(C1)CCC3(C2CCCC3=C)C)C)C=C	272.50	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Trachylobane	521405	Click to see CC1(CCCC2(C1CCC34C2CC5C(C3)C5(C4)C)C)C	272.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(6S)-2,6-Dimethylocta-2,7-diene-1,6-diol	71374944	Click to see CC(=CCCC(C)(C=C)O)CO	170.25	unknown	via CMAUP database
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene	440966	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
(+)-3-Carene	443156	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	via CMAUP database
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene	6451618	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	via CMAUP database
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane	6429260	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	via CMAUP database
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
L-Born-2-yl acetate	44630108	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Tricyclene	79035	Click to see CC1(C2CC3C1(C3C2)C)C	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
alpha-Terpinyl acetate	111037	Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C	196.29	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
p-Menth-3-en-1-ol	11468	Click to see CC(C)C1=CCC(CC1)(C)O	154.25	unknown	via CMAUP database
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-gamma-Cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
(1S,3aR,4R,7S,7aS)-1-Acetyl-7-isopropyl-4-methyloctahydro-1H-inden-4-yl acetate	73823555	Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)OC(=O)C	280.40	unknown	https://doi.org/10.1002/MRC.1260281207
(1Z,4E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene	45115091	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	via CMAUP database
[(1S,3aR,4R,7S,7aS)-1-acetyl-4-methyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-4-yl] acetate	21679492	Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)OC(=O)C	280.40	unknown	https://doi.org/10.1002/MRC.1260281207
7-Megastigmene-3,5,6,9-tetraol	637237	Click to see CC(C=CC1(C(CC(CC1(C)O)O)(C)C)O)O	244.33	unknown	via CMAUP database
alpha-Ionol	5363817	Click to see CC1=CCCC(C1C=CC(C)O)(C)C	194.31	unknown	via CMAUP database
beta-Cadinene	10657	Click to see CC1=CCC2C(C1)C(CC=C2C)C(C)C	204.35	unknown	via CMAUP database
beta-Ionone	638014	Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C	192.30	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Caryophyllene,alpha + beta mixt.	5354499	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
CID 16396350	16396350	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Cubenol	11770062	Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C	222.37	unknown	via CMAUP database
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
gamma-Elemene	94254	Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C	204.35	unknown	via CMAUP database
Longifolene	289151	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Rimuen	6432170	Click to see CC1(CCCC2C1=CCC3C2(CCC(C3)(C)C=C)C)C	272.50	unknown	via CMAUP database
T-Muurolol	3084331	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
Thujopsen	97829	Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
Thujopsene	442402	Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
trans-Muurola-4(14),5-diene	91747125	Click to see CC1CCC(C2=CC(=C)CCC12)C(C)C	204.35	unknown	via CMAUP database
Vomifoliol	5280462	Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C	224.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Isoaromadendrene epoxide	534398	Click to see CC1CCC2C1C3C(C3(C)C)CC4C2(O4)C	220.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(1S,2R,8S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undecan-8-ol	44123431	Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
[1R-[1alpha,3alpha,4beta]]-4-Ethenyl-alpha,alpha,4-trimethyl-3-[1-methylethenyl]cyclohexanemethanol	11064030	Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(E)-4-[(4R)-2,6,6-trimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexen-1-yl]but-3-en-2-one	10872343	Click to see CC1=C(C(CC(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)C=CC(=O)C	370.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	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
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1R,2S,5R,8S,9R)-4,4,8-trimethyltricyclo[6.3.1.02,5]dodecane-1,9-diol	21637404	Click to see CC1(CC2C1CCC3(CC2(CCC3O)O)C)C	238.37	unknown	via CMAUP database
alpha-Acorenol	11972555	Click to see CC1CCC(C12CCC(=CC2)C)C(C)(C)O	222.37	unknown	via CMAUP database
Myrcenol	10975	Click to see CC(C)(CCCC(=C)C=C)O	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)81063-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Icariside B2	10385469	Click to see CC(=O)C=CC12C(CC(CC1(O2)C)OC3C(C(C(C(O3)CO)O)O)O)(C)C	386.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eleutheroside B	5316860	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural	237332	Click to see C1=C(OC(=C1)C=O)CO	126.11	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 / Phenylketones / Alkyl-phenylketones
(2R)-2,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one	86311182	Click to see COC1=CC(=CC(=C1O)OC)C(=O)C(CO)O	242.22	unknown	via CMAUP database
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one	54353627	Click to see COC1=CC(=CC(=C1O)OC)C(=O)CCO	226.23	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
methyl (3R)-3-(5,7-dihydroxy-4-oxochromen-2-yl)-4-oxopentanoate	162934036	Click to see CC(=O)C(CC(=O)OC)C1=CC(=O)C2=C(C=C(C=C2O1)O)O	306.27	unknown	https://doi.org/10.1248/CPB.49.1479
Methyl 3-(5,7-dihydroxy-4-oxochromen-2-yl)-4-oxopentanoate	11833709	Click to see CC(=O)C(CC(=O)OC)C1=CC(=O)C2=C(C=C(C=C2O1)O)O	306.27	unknown	https://doi.org/10.1248/CPB.49.1479
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Scopolin	439514	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	354.31	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
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one	662	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	288.25	unknown	https://doi.org/10.1248/CPB.49.1479
Aromadendrin	122850	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	288.25	unknown	https://doi.org/10.1248/CPB.49.1479
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1248/CPB.49.1479
Apigenin-7-olate	25200950	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)[O-])O	269.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Isocryptomerin	5318537	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC4=CC=C(C=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O	552.50	unknown	via CMAUP database

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Chamaecyparis pisifera

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