Calocedrus macrolepis, also known as Chinese incense-cedar, is a medium-sized conifer tree native to southwest China, northern Vietnam, northern Laos, extreme northern Thailand, and northeastern Myanmar. It can reach heights of 25-35 meters and has a trunk diameter of up to 2 meters. The bark starts off orange-brown and becomes greyish and fissured as the tree ages. The foliage is made up of flattened sprays with scale-like leaves that are arranged in pairs, giving the appearance of whorls. The upper side of the foliage is glossy green while the underside is white with dense stomata. The tree produces seed cones that are pale purple with a whitish wax coating and have four scales arranged in pairs. The cones turn brown after about 8 months and the pollen cones are 4-8 mm long. This species is closely related to Calocedrus formosana, with the main difference being the shorter cone stem of C. formosana. While still fairly widespread in the wild, C. macrolepis is threatened by over-harvesting for its valuable wood and is categorized as Vulnerable by the IUCN. It is also commonly planted for wood production within its native range.

Synonyms Top

Scientific name	Authority	First published in
Libocedrus macrolepis	(Kurz) Benth. & Hook.f.	Gen. Pl. 3: 426 (1880)
Thuja macrolepis	Voss	Mitt. Deutsch. Dendrol. Ges. 16: 88 (1907)
Heyderia macrolepis	(Kurz) H.L.Li	J. Arnold Arbor. 34: 23 (1953)

Common names Top

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Filter by language:

Language	Common/alternative name
English	chinese incense-cedar
Persian	سرو عود چینی
Russian	Калоцедрус крупночешуйчатый
Vietnamese	pơ mu giả
Vietnamese	tô hạp bách
Vietnamese	bách xanh
Chinese	翠柏
Chinese	大鳞肖楠
Chinese	长柄翠柏

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan

Asia-tropical click to expand
- Indo-China
  - Laos
  - Myanmar
  - Thailand
  - Vietnam

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000580855
Tropicos	9400426
KEW	urn:lsid:ipni.org:names:261793-1
The Plant List	kew-2692990
Open Tree Of Life	216741
NCBI Taxonomy	103965
IUCN Red List	32384
IPNI	261793-1
iNaturalist	136236
GBIF	2683942
Freebase	/m/027zjm8
EPPO	CCDMA
EOL	1034911
USDA GRIN	451762
Wikipedia	Calocedrus_macrolepis
CMAUP	NPO14832

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

Identification and variation analysis of the composition and content of essential oil and fragrance compounds in Phoebe zhennan wood at different tree ages

Yang H, Zhang S, Gu Y, Peng J, Huang X, Guo H, Chen L, Jiang Y, Liu M, Luo X, Xie J, Wan X

Front Plant Sci

26-Mar-2024

PMCID:	PMC11002133
doi:	10.3389/fpls.2024.1368894
PMID:	38595765

Antifungal Activity of Cedrol from Cunninghamia lanceolate var. konishii against Phellinus noxius and Its Mechanism

Hsiao WW, Lau KM, Chien SC, Chu FH, Chung WH, Wang SY

Plants (Basel)

21-Jan-2024

PMCID:	PMC10821468
doi:	10.3390/plants13020321
PMID:	38276778

Leaf variegation caused by plastome structural variation: an example from Dianella tasmanica

Zhou S, Ma K, Mower JP, Liu Y, Zhou R

Hortic Res

10-Jan-2024

PMCID:	PMC10923649
doi:	10.1093/hr/uhae009
PMID:	38464478

Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China

Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C

J Ethnobiol Ethnomed

30-May-2023

PMCID:	PMC10230803
doi:	10.1186/s13002-023-00594-4
PMID:	37254191

Biological activities of meroterpenoids isolated from different sources

Fuloria NK, Raheja RK, Shah KH, Oza MJ, Kulkarni YA, Subramaniyan V, Sekar M, Fuloria S

Front Pharmacol

19-Sep-2022

PMCID:	PMC9527340
doi:	10.3389/fphar.2022.830103
PMID:	36199687

Antioxidant, antifungal, and aphicidal activity of the triterpenoids spinasterol and 22,23-dihydrospinasterol from leaves of Citrullus colocynthis L.

Ahmed M, Sajid AR, Javeed A, Aslam M, Ahsan T, Hussain D, Mateen A, Li X, Qin P, Ji M

Sci Rep

22-Mar-2022

PMCID:	PMC8940894
doi:	10.1038/s41598-022-08999-z
PMID:	35318417

Anti-lymphangiogenic diterpenes from the bark of Calocedrus macrolepis var. formosana

Lee TH, Hsieh CL, Wu HC, Wang SW, Yu CL, Hsiao G, Cheng MJ, Hsieh WT, Kuo YH

J Food Drug Anal

15-Dec-2021

PMCID:	PMC9931016
doi:	10.38212/2224-6614.3375
PMID:	35649142

Distinct Genetic Structure Reflects Ploidy Level Differentiation in Newly Discovered, Extremely Small Populations of Xanthocyparis vietnamensis from Southwestern China

Jiang Y, Ju T, Neaves LE, Li J, Tan W, Huang Y, Liu Y, Mao K

Front Genet

01-Nov-2021

PMCID:	PMC8591046
doi:	10.3389/fgene.2021.733576
PMID:	34790221

Recent Approaches towards Control of Fungal Diseases in Plants: An Updated Review

El-Baky NA, Amara AA

J Fungi (Basel)

25-Oct-2021

PMCID:	PMC8621679
doi:	10.3390/jof7110900
PMID:	34829188

A computer-aided method for identifying the presence of softwood growth ring boundaries

Lin Q, He T, Sun Y, He X, Qiu J

PLoS One

18-Sep-2020

PMCID:	PMC7500654
doi:	10.1371/journal.pone.0235727
PMID:	32946443

Essential Oils and Health

Ramsey JT, Shropshire BC, Nagy TR, Chambers KD, Li Y, Korach KS

Yale J Biol Med

29-Jun-2020

PMCID:	PMC7309671
PMID:	32607090

Terpenoids as Potential Geroprotectors

Proshkina E, Plyusnin S, Babak T, Lashmanova E, Maganova F, Koval L, Platonova E, Shaposhnikov M, Moskalev A

Antioxidants (Basel)

17-Jun-2020

PMCID:	PMC7346221
doi:	10.3390/antiox9060529
PMID:	32560451

Plastome Structural Conservation and Evolution in the Clusioid Clade of Malpighiales

Jin DM, Jin JJ, Yi TS

Sci Rep

04-Jun-2020

PMCID:	PMC7272398
doi:	10.1038/s41598-020-66024-7
PMID:	32499506

Natural Products as Fungicide and Their Role in Crop Protection

Santra HK, Banerjee D

Natural Bioactive Products in Sustainable Agriculture

12-May-2020

PMCID:	PMC7212785
doi:	10.1007/978-981-15-3024-1_9

The complete chloroplast genome sequence of Thuja koraiensis from Changbai Mountain in China

Yang CJ, Zhang H, Bai YL, Yang TT

Mitochondrial DNA B Resour

31-Jan-2020

PMCID:	PMC7748546
doi:	10.1080/23802359.2020.1719918
PMID:	33366820

Phytochemical Profile Top

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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 / Naphthalenes / Naphthols and derivatives
(3S)-5-(7-hydroxy-2-methyl-6-propan-2-ylnaphthalen-1-yl)-2-methylpentane-2,3-diol	163019732	Click to see CC1=C(C2=CC(=C(C=C2C=C1)C(C)C)O)CCC(C(C)(C)O)O	316.40	unknown	https://doi.org/10.1002/CBDV.201000237
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[9-[(4b,8,8-Trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthren-3-yl)oxy]-10-(2-butoxyethoxy)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-yl] acetate	73061809	Click to see CCCCOCCOC1C(C2C(CCCC2(C3=CC(=C(C=C13)C(C)C)OC(=O)C)C)(C)C)OC4=C(C=C5C=CC6C(CCCC6(C5=C4)C)(C)C)C(C)C	727.10	unknown	https://doi.org/10.1248/CPB.53.1463
10-[(4b,8,8-Trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthren-3-yl)oxy]-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol	73008184	Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)OC4C(C5=CC(=C(C=C5C6(C4C(CCC6)(C)C)C)OC)C(C)C)O	598.90	unknown	https://doi.org/10.1248/CPB.53.1463
10-[6-(2-Hydroxypropan-2-yl)-8a-methyl-4-methylidene-1,2,3,4a,5,6,7,8-octahydronaphthalen-1-yl]-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol	73172592	Click to see CC(C)C1=C(C=C2C(=C1)C(CC3C2(CCCC3(C)C)C)C4CCC(=C)C5C4(CCC(C5)C(C)(C)O)C)O	506.80	unknown	https://doi.org/10.1021/NP0600550
9-[(4b,8,8-Trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthren-3-yl)oxy]-10-(2-butoxyethoxy)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol	72984973	Click to see CCCCOCCOC1C(C2C(CCCC2(C3=CC(=C(C=C13)C(C)C)O)C)(C)C)OC4=C(C=C5C=CC6C(CCCC6(C5=C4)C)(C)C)C(C)C	685.00	unknown	https://doi.org/10.1248/CPB.53.1463
9-[(4b,8,8-Trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthren-3-yl)oxy]-10-methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol	73802887	Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)OC4C(C5=CC(=C(C=C5C6(C4C(CCC6)(C)C)C)O)C(C)C)OC	598.90	unknown	https://doi.org/10.1248/CPB.53.1463
9-[(4b,8,8-Trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthren-3-yl)oxy]-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-3,10-diol	73037073	Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)OC4C(C5=CC(=C(C=C5C6(C4C(CCC6)(C)C)C)O)C(C)C)O	584.90	unknown	https://doi.org/10.1021/NP058090E
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/10.1021/NP058090E
DELTA6-Dehydroferruginol	14165048	Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)O	284.40	unknown	https://doi.org/10.1021/NP058090E
Ferrugieudesmol	11994700	Click to see CC(C)C1=C(C=C2C(=C1)C(CC3C2(CCCC3(C)C)C)C4CCC(=C)C5C4(CCC(C5)C(C)(C)O)C)O	506.80	unknown	https://doi.org/10.1021/NP0600550
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1021/NP058090E
Formosadimer A	11563385	Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)OC4C(C5=CC(=C(C=C5C6(C4C(CCC6)(C)C)C)OC)C(C)C)O	598.90	unknown	https://doi.org/10.1248/CPB.53.1463
Formosadimer B	11498485	Click to see CCCCOCCOC1C(C2C(CCCC2(C3=CC(=C(C=C13)C(C)C)O)C)(C)C)OC4=C(C=C5C=CC6C(CCCC6(C5=C4)C)(C)C)C(C)C	685.00	unknown	https://doi.org/10.1248/CPB.53.1463
Formosadimer C	11686328	Click to see CCCCOCCOC1C(C2C(CCCC2(C3=CC(=C(C=C13)C(C)C)OC(=O)C)C)(C)C)OC4=C(C=C5C=CC6C(CCCC6(C5=C4)C)(C)C)C(C)C	727.10	unknown	https://doi.org/10.1248/CPB.53.1463
Sugikurojin B	23250764	Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)OC4C(C5=CC(=C(C=C5C6(C4C(CCC6)(C)C)C)O)C(C)C)OC	598.90	unknown	https://doi.org/10.1248/CPB.53.1463
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,7,7-Trimethylbicyclo[2.2.1]heptane-2,6-diol	14431886	Click to see CC1(C2CC(C1(C(C2)O)C)O)C	170.25	unknown	https://doi.org/10.1021/NP058090E
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydro-1-naphthalenol	519662	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1021/NP058090E
T-Muurolol	3084331	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1016/J.BIORTECH.2007.12.005
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,5R,8R,9R,10R,13R,14R,17R)-17-[(4E)-6-hydroxy-6-methylhepta-1,4-dien-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	9955042	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C(=C)CC=CC(C)(C)O)C)C)C	442.70	unknown	via CMAUP database
Diosgenin	99474	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	via CMAUP database
Yamogenin	441900	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-6-[(1S,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S)-3'-hydroxy-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	102155845	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O	901.00	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol	21603983	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'S,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol	16204068	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
Asparasaponin I	441899	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1049.20	unknown	via CMAUP database
Borassoside B	102155844	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O	901.00	unknown	via CMAUP database
Borassoside D	16204180	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
Borassoside E	16204181	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
Borassoside F	16204183	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1	1015.20	unknown	via CMAUP database
Collettinside III	10653210	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
Dioscin	119245	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
Disogluside	11827970	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)OC1	576.80	unknown	via CMAUP database
Methylprotodioscin	11263254	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC	1063.20	unknown	via CMAUP database
Pennogenin Rahamnosyl Chacotrioside	21603986	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1	1015.20	unknown	via CMAUP database
Progenin II	44429638	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
Prosapogenin A	11061578	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
Protodioscin	441891	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1049.20	unknown	via CMAUP database
Pseudoprotodioscin	21637110	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC8C7C(=C(O8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O	1031.20	unknown	via CMAUP database
Yamogenin 3-O-neohesperidoside	441901	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	722.90	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 / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-O-beta-D-mannopyranosyl-alpha-D-mannopyranose	5288769	Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
Gal(a1-6)a-Man	11724912	Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O	342.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
beta-D-Manp-(1->4)-beta-D-Manp-(1->4)-beta-D-Manp	5287808	Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O	504.40	unknown	via CMAUP database

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Calocedrus macrolepis

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