Scientific name	Authority	First published in
Nageia ovata	Gordon	Pinetum , Suppl.: 42 (1862)
Nageia nankoensis	(Hayata) R.R.Mill	Novon 9: 77 (1999)
Nageia caesia	Kuntze	Revis. Gen. Pl. 2: 800 (1891)
Nageia japonica	Gaertn.	Fruct. Sem. Pl. 1: 191 (1788)
Nageia nagi var. koshuensis	(Kaneh.) D.Z.Fu	Acta Phytotax. Sin. 30: 524 (1992)
Nageia nagi var. formosensis	(Dümmer) Silba	Phytologia 68: 38 (1990)
Nageia cuspidata	Gordon	Pinetum : 136 (1858)
Nageia grandifolia	Gordon	Pinetum : 137 (1858)
Podocarpus formosensis	Dümmer	Gard. Chron. , ser. 3, 52: 295 (1912)
Podocarpus koshunensis	(Kaneh.) Kaneh.	Formos. Trees , ed. rev.: 36 (1936)
Podocarpus caesius	Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 15: 379 (1870)
Podocarpus cuspidatus	Endl.	Syn. Conif. : 207 (1847)
Podocarpus ovata	(Gordon) Henkel & W.Hochst.	Syn. Nadelhölz. : 381 (1865)
Podocarpus nageia	R.Br. ex Endl.	Mém. Mus. Hist. Nat. 13: 75 1825
Podocarpus nagi	(Thunb.) Pilg.	Pflanzenr. IV, 5: 60 1903
Podocarpus grandifolius	Endl.	Syn. Conif. : 208 (1847)
Decussocarpus nagi	(Thunb.) de Laub.	J. Arnold Arbor. 50: 357 (1969)
Decussocarpus nagi var. formosensis	(Dümmer) Silba	Phytologia 58: 366 (1985)
Podocarpus nagi var. ovatus	(Gordon) Makino	Bot. Mag. (Tokyo) 17: 114. 1903
Podocarpus japonicus	J.Nelson	Pinaceae 155. 1866 (1866)
Podocarpus nagi var. caesius	(Maxim.) Makino	Bot. Mag. (Tokyo) 17: 115. 1903
Agathis veitchii	(Henkel & W.Hochst.) Seward & S.O.Ford	Philos. Trans., Ser. B 198: 317 (1906)
Podocarpus nageia var. angustifolius	Maxim.	Gartenflora 13: 37. 1864
Podocarpus nageia var. rotundifolius	Maxim.	Gartenflora 13: 37. 1864
Podocarpus nagi var. angustifolius	(Maxim.) Makino	Bot. Mag. (Tokyo) 17: 114 1903
Podocarpus nagi var. rotundifolius	(Maxim.) Makino	Bot. Mag. (Tokyo) 17: 114 1903
Dammara veitchii	Henkel & W.Hochst.	Syn. Nadelholz. 216. 1865
Podocarpus nagi	(Thunb.) Pilg.	Pflanzenr. , IV, 5: 60 (1903)
Podocarpus nageia	R.Br. ex Mirb.	Mém. Mus. Hist. Nat. 13: 75. 1825
Podocarpus nagi	(Thunb.) Zoll. & Moritzi ex Makino	Bot. Mag. (Tokyo) 17: 113. 1903 [Jul 1903]
Podocarpus ovatus	Henk. & Hochst.	Syn. Nadelhölz. : 381 (1865)

Common names Top

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Filter by language:

Language	Common/alternative name
English	asian bayberry
English	nagi
Arabic	ناغية يابانية
Japanese	梛
Japanese	竹柏
Japanese	ナギ
Malayalam	നഗിയ നാഗി
Chinese	小叶罗汉松
Chinese	山杉
Chinese	竹柏
Chinese	竹柏根

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

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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 Southeast
  - Hainan
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000380933
UNII	KAH483MJMH
Tropicos	31200091
KEW	urn:lsid:ipni.org:names:262544-1
The Plant List	kew-2382061
Missouri Botanical Garden	287311
PFAF	Nageia nagi
Open Tree Of Life	983645
NCBI Taxonomy	36012
IUCN Red List	46347417
IPNI	262544-1
iNaturalist	135904
GBIF	2687779
Freebase	/m/02vtzt2
EPPO	PODNA
EOL	1034966
USDA GRIN	25009
Wikipedia	Nageia_nagi

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

Pest categorisation of Pyrrhoderma noxium

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL

EFSA J

19-Mar-2024

PMCID:	PMC10949325
doi:	10.2903/j.efsa.2024.8667
PMID:	38505477

From immune checkpoints to therapies: understanding immune checkpoint regulation and the influence of natural products and traditional medicine on immune checkpoint and immunotherapy in lung cancer

Zhou Y, Wang F, Li G, Xu J, Zhang J, Gullen E, Yang J, Wang J

Front Immunol

15-Feb-2024

PMCID:	PMC10902058
doi:	10.3389/fimmu.2024.1340307
PMID:	38426097

A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes

Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B

Molecules

21-Dec-2023

PMCID:	PMC10780140
doi:	10.3390/molecules29010060
PMID:	38202643

Phytochemical and metabolic profiling of the different Podocarpus species in Egypt: Potential antimicrobial and antiproliferative activities

Mohamed NZ, Shaaban L, Safan S, El-Sayed AS

Heliyon

09-Sep-2023

PMCID:	PMC10559778
doi:	10.1016/j.heliyon.2023.e20034
PMID:	37810029

A systematic review of the research progress of traditional Chinese medicine against pulmonary fibrosis: from a pharmacological perspective

Qin S, Tan P, Xie J, Zhou Y, Zhao J

Chin Med

03-Aug-2023

PMCID:	PMC10398979
doi:	10.1186/s13020-023-00797-7
PMID:	37537605

Projecting Podocarpaceae response to climate change: we are not out of the woods yet

Twala TC, Fisher JT, Glennon KL

AoB Plants

08-Jun-2023

PMCID:	PMC10321399
doi:	10.1093/aobpla/plad034
PMID:	37415722

Tanshinone-I for the treatment of uterine fibroids: Molecular docking, simulation, and density functional theory investigations

Tiwari A, Tiwari V, Sharma A, Singh D, Singh Rawat M, Virmani T, Virmani R, Kumar G, Kumar M, Alhalmi A, Noman OM, Mothana RA, Alali M

Saudi Pharm J

08-May-2023

PMCID:	PMC10209546
doi:	10.1016/j.jsps.2023.05.002
PMID:	37250358

Recent Advances (2015–2020) in Drug Discovery for Attenuation of Pulmonary Fibrosis and COPD

Dorababu A, Maraswami M

Molecules

24-Apr-2023

PMCID:	PMC10179756
doi:	10.3390/molecules28093674
PMID:	37175084

Diversity, Distribution, Systematics and Conservation Status of Podocarpaceae

Khan R, Hill RS, Liu J, Biffin E

Plants (Basel)

03-Mar-2023

PMCID:	PMC10005643
doi:	10.3390/plants12051171
PMID:	36904033

Biochemical and antioxidant activity of wild edible fruits of the eastern Himalaya, India

Rymbai H, Verma VK, Talang H, Assumi SR, Devi MB, Vanlalruati, Sangma RH, Biam KP, Chanu LJ, Makdoh B, Singh AR, Mawleiñ J, Hazarika S, Mishra VK

Front Nutr

01-Mar-2023

PMCID:	PMC10014916
doi:	10.3389/fnut.2023.1039965
PMID:	36937364

Submerged leaves of live indoor foliage plants adsorb H1N1 influenza virus from suspension

Song HJ, Yang SW, Jo JW, Choi YK, Lee IS, Lee BU, Lee SH, Kim HH, Kim KJ, Kim HJ

Plant Signal Behav

12-Jan-2023

PMCID:	PMC9851199
doi:	10.1080/15592324.2022.2163869
PMID:	36635991

Natural Products as Outstanding Alternatives in Diabetes Mellitus: A Patent Review

Rodríguez IA, Serafini M, Alves IA, Lang KL, Silva FR, Aragón DM

Pharmaceutics

27-Dec-2022

PMCID:	PMC9867152
doi:	10.3390/pharmaceutics15010085
PMID:	36678714

Natural Products/Bioactive Compounds as a Source of Anticancer Drugs

Asma ST, Acaroz U, Imre K, Morar A, Shah SR, Hussain SZ, Arslan-Acaroz D, Demirbas H, Hajrulai-Musliu Z, Istanbullugil FR, Soleimanzadeh A, Morozov D, Zhu K, Herman V, Ayad A, Athanassiou C, Ince S

Cancers (Basel)

15-Dec-2022

PMCID:	PMC9777303
doi:	10.3390/cancers14246203
PMID:	36551687

Research Progress on Small Molecular Inhibitors of the Type 3 Secretion System

Lv C, Li Y, Wei Y, Wang J, Yu H, Gao F, Zhu C, Jia X, Tong M, Dong P, Gao Q, Geng L

Molecules

30-Nov-2022

PMCID:	PMC9740592
doi:	10.3390/molecules27238348
PMID:	36500441

Antimicrobial potentials of natural products against multidrug resistance pathogens: a comprehensive review

Elmaidomy AH, Shady NH, Abdeljawad KM, Elzamkan MB, Helmy HH, Tarshan EA, Adly AN, Hussien YH, Sayed NG, Zayed A, Abdelmohsen UR

RSC Adv

13-Oct-2022

PMCID:	PMC9558262
doi:	10.1039/d2ra04884a
PMID:	36320761

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
> Lipids and lipid-like molecules / Endocannabinoids
1,3-Dihydroxypropan-2-yl 3,8-diacetyloxyicosanoate	163021367	Click to see CCCCCCCCCCCCC(CCCCC(CC(=O)OC(CO)CO)OC(=O)C)OC(=O)C	502.70	unknown	https://doi.org/10.1007/S10600-016-1573-Z
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosa-5,11,14-trienoic acid	152108	Click to see CCCCCC=CCC=CCCCCC=CCCCC(=O)O	306.50	unknown	https://doi.org/10.1246/NIKKASHI1948.78.1223
Sciadonic acid	445084	Click to see CCCCCC=CCC=CCCCCC=CCCCC(=O)O	306.50	unknown	https://doi.org/10.1246/NIKKASHI1948.78.1223
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(+)-Totarol	326995	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1055/S-2006-957655 https://doi.org/10.1016/0031-9422(91)85049-6
(1S,4aS,10aS)-7-hydroxy-1,4a-dimethyl-8-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde	40469620	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C=O)C)O	300.40	unknown	https://doi.org/10.1055/S-2006-957655
(1S,4aS,10aS)-7-hydroxy-1,4a-dimethyl-8-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	162861820	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C(=O)O)C)O	316.40	unknown	https://doi.org/10.1055/S-2006-957655
(2S,4aS,10aS)-1,1,4a-trimethyl-8-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,7-diol	163005909	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCC(C3(C)C)O)C)O	302.50	unknown	https://doi.org/10.1055/S-2006-957655
(4bS,8S,8aS)-8-(hydroxymethyl)-4b,8-dimethyl-1-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-2-ol	36688275	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)CO)C)O	302.50	unknown	https://doi.org/10.1055/S-2006-957655
14-Isopropylpodocarpa-8,11,13-triene-3,13-diol	622898	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCC(C3(C)C)O)C)O	302.50	unknown	https://doi.org/10.1016/0031-9422(91)85049-6 https://doi.org/10.1055/S-2006-957655
16-Hydroxytotarol	15694357	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)CO)C)O	302.50	unknown	https://doi.org/10.1016/0031-9422(91)85049-6
4beta-Carboxy-19-nortotarol	15694359	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C(=O)O)C)O	316.40	unknown	https://doi.org/10.1016/0031-9422(91)85049-6
6-Hydroxy-1,1,4A-trimethyl-7-(propan-2-YL)-1,2,3,4,4A,9,10,10A-octahydrophenanthren-9-one	275529	Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O	300.40	unknown	https://doi.org/10.1055/S-2006-957655 https://doi.org/10.1016/0031-9422(91)85049-6
7-Hydroxy-1,4a-dimethyl-8-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde	3478376	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C=O)C)O	300.40	unknown	https://doi.org/10.1016/0031-9422(91)85049-6 https://doi.org/10.1055/S-2006-957655
7-Hydroxy-1,4a-dimethyl-8-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	5315694	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C(=O)O)C)O	316.40	unknown	https://doi.org/10.1016/0031-9422(91)85049-6 https://doi.org/10.1055/S-2006-957655
8-(Hydroxymethyl)-4b,8-dimethyl-1-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-2-ol	317837	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)CO)C)O	302.50	unknown	https://doi.org/10.1016/0031-9422(91)85049-6 https://doi.org/10.1055/S-2006-957655
Sugiol	94162	Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O	300.40	unknown	https://doi.org/10.1055/S-2006-957655 https://doi.org/10.1016/0031-9422(91)85049-6
Totaradiol	9995105	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCC(C3(C)C)O)C)O	302.50	unknown	https://doi.org/10.1016/0031-9422(91)85049-6
Totaral	15694358	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C=O)C)O	300.40	unknown	https://doi.org/10.1016/0031-9422(91)85049-6
Totarol	92783	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1021/NP50088A008 https://doi.org/10.1055/S-2006-957655 https://doi.org/10.1007/BF01969731 https://doi.org/10.1016/0031-9422(91)85049-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Corchoionol C	137705650	Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C	224.30	unknown	https://doi.org/10.1016/0031-9422(91)85049-6 https://doi.org/10.1016/0031-9422(91)83237-F
Vomifoliol	5280462	Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C	224.30	unknown	https://doi.org/10.1016/0031-9422(91)85049-6 https://doi.org/10.1016/0031-9422(91)83237-F
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[15-(Acetyloxymethyl)-8-ethyl-7-hydroxy-4,11-dimethyl-9,16-dioxo-3,10,17-trioxatetracyclo[12.3.0.02,4.07,11]heptadec-14-en-13-yl] 2-(hydroxymethyl)prop-2-enoate	85123464	Click to see CCC1C(=O)OC2(C1(CCC3(C(O3)C4C(=C(C(=O)O4)COC(=O)C)C(C2)OC(=O)C(=C)CO)C)O)C	508.50	unknown	https://doi.org/10.1016/0031-9422(91)83237-F https://doi.org/10.1021/NP50086A004 https://doi.org/10.1021/ACS.JNATPROD.7B00347 https://doi.org/10.1007/BF02033650
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(91)85049-6
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(91)85049-6
> Organoheterocyclic compounds / Naphthopyrans
(1S,2R,4R,5R,10S,14S,17R)-5-[(2R)-1-hydroxypropan-2-yl]-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.02,4.04,9.014,17]heptadeca-8,12-diene-7,15-dione	162971316	Click to see CC(CO)C1C23C(O2)C4C5C(C3=CC(=O)O1)(CC=CC5(C(=O)O4)C)C	346.40	unknown	https://doi.org/10.1021/JO00139A007
(1S,2S,4R,5S,6R,9S,10R,17R)-5,10-dihydroxy-1,6-dimethyl-12-propan-2-yl-3,8,13-trioxapentacyclo[7.7.1.02,4.06,17.011,16]heptadeca-11,15-diene-7,14-dione	12313081	Click to see CC(C)C1=C2C(C3C4C(C(C5C(C4(C2=CC(=O)O1)C)O5)O)(C(=O)O3)C)O	362.40	unknown	https://doi.org/10.1016/0031-9422(91)85049-6
(1S,6R,9R,12R,13S,16R)-13-hydroxy-1,12-dimethyl-6-propan-2-yl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,7-diene-4,11-dione	21637844	Click to see CC(C)C1C2=CC3C4C(C2=CC(=O)O1)(CCC(C4(C(=O)O3)C)O)C	332.40	unknown	https://doi.org/10.3987/S-1978-01-0123
(1S,6R,9R,12S,16R)-6-[(2R)-1-hydroxypropan-2-yl]-1,12-dimethyl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,7,13-triene-4,11-dione	163048680	Click to see CC(CO)C1C2=CC3C4C(C2=CC(=O)O1)(CC=CC4(C(=O)O3)C)C	330.40	unknown	https://doi.org/10.1016/0031-9422(90)85374-O
(1S,6R,9R,17R)-5-hydroxy-12-(1-hydroxyethyl)-1,6-dimethyl-3,8,13-trioxapentacyclo[7.7.1.02,4.06,17.011,16]heptadeca-11,15-diene-7,14-dione	162856281	Click to see CC(C1=C2CC3C4C(C(C5C(C4(C2=CC(=O)O1)C)O5)O)(C(=O)O3)C)O	348.30	unknown	https://doi.org/10.1021/ACS.JNATPROD.7B00347
(1S,6R,9S,17R)-12-ethyl-5,10-dihydroxy-1,6-dimethyl-3,8,13-trioxapentacyclo[7.7.1.02,4.06,17.011,16]heptadeca-11,15-diene-7,14-dione	162995811	Click to see CCC1=C2C(C3C4C(C(C5C(C4(C2=CC(=O)O1)C)O5)O)(C(=O)O3)C)O	348.30	unknown	https://doi.org/10.1021/ACS.JNATPROD.7B00347
(1S,6R,9S,17R)-5,10-dihydroxy-1,6-dimethyl-12-propan-2-yl-3,8,13-trioxapentacyclo[7.7.1.02,4.06,17.011,16]heptadeca-11,15-diene-7,14-dione	138113851	Click to see CC(C)C1=C2C(C3C4C(C(C5C(C4(C2=CC(=O)O1)C)O5)O)(C(=O)O3)C)O	362.40	unknown	https://doi.org/10.1007/S10600-016-1573-Z https://doi.org/10.1271/BBB.56.1302 https://doi.org/10.1016/0031-9422(91)83237-F https://doi.org/10.1016/0031-9422(91)85049-6 https://doi.org/10.1021/NP50086A004 https://doi.org/10.1007/BF02033650
(1S,8R,9S,12R,13R,15S,17R)-8-hydroxy-1,12-dimethyl-6-propan-2-yl-5,10,14-trioxapentacyclo[7.7.1.02,7.012,17.013,15]heptadeca-2,6-diene-4,11-dione	14507389	Click to see CC(C)C1=C2C(C3C4C(C2=CC(=O)O1)(CC5C(C4(C(=O)O3)C)O5)C)O	346.40	unknown	https://doi.org/10.3987/S-1978-01-0123
(1S,8R,9S,12S,14R,15S,16R)-8,14,15-trihydroxy-1,12-dimethyl-6-propan-2-yl-5,10-dioxatetracyclo[7.6.1.0^{2,7.0^{12,16]hexadeca-2,6-diene-4,11-dione	12313078	Click to see CC(C)C1=C2C(C3C4C(CC(C(C4(C2=CC(=O)O1)C)O)O)(C(=O)O3)C)O	364.40	unknown	https://doi.org/10.1021/JO00139A007
(1S,8R,9S,12S,15R,16R)-8-hydroxy-1,12-dimethyl-6-propan-2-yl-15-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione	10484616	Click to see CC(C)C1=C2C(C3C4C(CCC(C4(C2=CC(=O)O1)C)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)(C(=O)O3)C)O	672.70	unknown	https://doi.org/10.1016/0031-9422(95)94785-L
(1S,8R,9S,12S,15R,16R)-8,15-dihydroxy-1,12-dimethyl-6-propan-2-yl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6,13-triene-4,11-dione	163021460	Click to see CC(C)C1=C2C(C3C4C(C=CC(C4(C2=CC(=O)O1)C)O)(C(=O)O3)C)O	346.40	unknown	https://doi.org/10.1016/S0031-9422(00)90725-8
(1S,8R,9S,12S,15S,16R)-8,15-dihydroxy-1,12-dimethyl-6-propan-2-yl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11,14-trione	145966023	Click to see CC(C)C1=C2C(C3C4C(CC(=O)C(C4(C2=CC(=O)O1)C)O)(C(=O)O3)C)O	362.40	unknown	https://doi.org/10.1021/ACS.JNATPROD.7B00347
(1S,8R,9S,12S,16R)-8-hydroxy-1,12-dimethyl-6-propan-2-yl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione	162890396	Click to see CC(C)C1=C2C(C3C4C(C2=CC(=O)O1)(CCCC4(C(=O)O3)C)C)O	332.40	unknown	https://doi.org/10.1016/S0031-9422(00)90725-8
(1S,8R,9S,12S,16R)-8-hydroxy-1,12-dimethyl-6-propan-2-yl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6,13-triene-4,11-dione	162977560	Click to see CC(C)C1=C2C(C3C4C(C2=CC(=O)O1)(CC=CC4(C(=O)O3)C)C)O	330.40	unknown	https://doi.org/10.1016/S0031-9422(00)90725-8
(1S,9R,12R,15R,16S)-8-hydroxy-1,12-dimethyl-6-propan-2-yl-15-[(2R,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione	101927624	Click to see CC(C)C1=C2C(C3C4C(CCC(C4(C2=CC(=O)O1)C)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)(C(=O)O3)C)O	672.70	unknown	https://doi.org/10.1016/0031-9422(95)94785-L
(1S,9R,12R,16R)-6-ethyl-13,14,15-trihydroxy-1,12-dimethyl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione	162818720	Click to see CCC1=C2CC3C4C(C2=CC(=O)O1)(C(C(C(C4(C(=O)O3)C)O)O)O)C	350.40	unknown	https://doi.org/10.1021/ACS.JNATPROD.7B00347
(1S,9R,12R,16R)-6-ethyl-13,15-dihydroxy-1,12-dimethyl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione	162818724	Click to see CCC1=C2CC3C4C(C2=CC(=O)O1)(C(CC(C4(C(=O)O3)C)O)O)C	334.40	unknown	https://doi.org/10.1021/ACS.JNATPROD.7B00347
(1S,9R,12R,16S)-15-chloro-13,14-dihydroxy-6-(1-hydroxyethyl)-1,12-dimethyl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione	162818726	Click to see CC(C1=C2CC3C4C(C(C(C(C4(C2=CC(=O)O1)C)Cl)O)O)(C(=O)O3)C)O	384.80	unknown	https://doi.org/10.1021/ACS.JNATPROD.7B00347
(1S,9R,12S,16R)-15-hydroxy-6-(1-hydroxyethyl)-1,12-dimethyl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione	162818722	Click to see CC(C1=C2CC3C4C(CCC(C4(C2=CC(=O)O1)C)O)(C(=O)O3)C)O	334.40	unknown	https://doi.org/10.1021/ACS.JNATPROD.7B00347
(1S,9R,12S,16R)-6-ethyl-14,15-dihydroxy-1,12-dimethyl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione	162960623	Click to see CCC1=C2CC3C4C(CC(C(C4(C2=CC(=O)O1)C)O)O)(C(=O)O3)C	334.40	unknown	https://doi.org/10.1021/ACS.JNATPROD.7B00347
(1S,9R,12S,16R)-6-ethyl-15-hydroxy-1,12-dimethyl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione	162974175	Click to see CCC1=C2CC3C4C(CCC(C4(C2=CC(=O)O1)C)O)(C(=O)O3)C	318.40	unknown	https://doi.org/10.1021/ACS.JNATPROD.7B00347
1-Deoxy-2beta,3beta-epoxynagilactone A	155554	Click to see CC(C)C1=C2C(C3C4C(C2=CC(=O)O1)(CC5C(C4(C(=O)O3)C)O5)C)O	346.40	unknown	https://doi.org/10.3987/S-1978-01-0123
13-Hydroxy-1,12-dimethyl-6-propan-2-yl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,7-diene-4,11-dione	73818364	Click to see CC(C)C1C2=CC3C4C(C2=CC(=O)O1)(CCC(C4(C(=O)O3)C)O)C	332.40	unknown	https://doi.org/10.3987/S-1978-01-0123
14-[3,5-Dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-8-hydroxy-1,12-dimethyl-6-propan-2-yl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione	85131079	Click to see CC(C)C1=C2C(C3C4C(C2=CC(=O)O1)(CC(CC4(C(=O)O3)C)OC5C(C(C(C(O5)CO)O)OC6C(C(C(C(O6)CO)O)O)O)O)C)O	672.70	unknown	https://doi.org/10.1016/0031-9422(95)94785-L
14-Hydroxy-1,12-dimethyl-6-propan-2-yl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,7-diene-4,11-dione	14507407	Click to see CC(C)C1C2=CC3C4C(C2=CC(=O)O1)(CC(CC4(C(=O)O3)C)O)C	332.40	unknown	https://doi.org/10.1016/0031-9422(91)84188-X
2-alpha-Hydroxynagilactone	14507409	Click to see CC(C)C1C2=CC3C4C(C2=CC(=O)O1)(CC(CC4(C(=O)O3)C)O)C	332.40	unknown	https://doi.org/10.1016/0031-9422(91)84188-X
3a,10b-Dimethyl-7-(propan-2-yl)-1,2,3,3a,5a,7,10b,10c-octahydro-4H,9H-furo[2',3',4':4,5]naphtho[2,1-c]pyran-4,9-dione	317836	Click to see CC(C)C1C2=CC3C4C(C2=CC(=O)O1)(CCCC4(C(=O)O3)C)C	316.40	unknown	https://doi.org/10.1007/BF02033650
5-(1-Hydroxypropan-2-yl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.02,4.04,9.014,17]heptadeca-8,12-diene-7,15-dione	332524	Click to see CC(CO)C1C23C(O2)C4C5C(C3=CC(=O)O1)(CC=CC5(C(=O)O4)C)C	346.40	unknown	https://doi.org/10.1021/JO00139A007
6-(1-Hydroxypropan-2-yl)-1,12-dimethyl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,7,13-triene-4,11-dione	163048679	Click to see CC(CO)C1C2=CC3C4C(C2=CC(=O)O1)(CC=CC4(C(=O)O3)C)C	330.40	unknown	https://doi.org/10.1016/0031-9422(90)85374-O
8-Hydroxy-1,12-dimethyl-6-propan-2-yl-14-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione	85143504	Click to see CC(C)C1=C2C(C3C4C(C2=CC(=O)O1)(CC(CC4(C(=O)O3)C)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)C)O	672.70	unknown	https://doi.org/10.1016/0031-9422(95)94785-L
8-Hydroxy-1,12-dimethyl-6-propan-2-yl-15-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione	85155907	Click to see CC(C)C1=C2C(C3C4C(CCC(C4(C2=CC(=O)O1)C)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)(C(=O)O3)C)O	672.70	unknown	https://doi.org/10.1016/0031-9422(95)94785-L
8-Hydroxy-1,12-dimethyl-6-propan-2-yl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione	162890395	Click to see CC(C)C1=C2C(C3C4C(C2=CC(=O)O1)(CCCC4(C(=O)O3)C)C)O	332.40	unknown	https://doi.org/10.1016/S0031-9422(00)90725-8
8-Hydroxy-1,12-dimethyl-6-propan-2-yl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6,13-triene-4,11-dione	162977559	Click to see CC(C)C1=C2C(C3C4C(C2=CC(=O)O1)(CC=CC4(C(=O)O3)C)C)O	330.40	unknown	https://doi.org/10.1016/S0031-9422(00)90725-8
8,15-Dihydroxy-1,12-dimethyl-6-propan-2-yl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione	319647	Click to see CC(C)C1=C2C(C3C4C(CCC(C4(C2=CC(=O)O1)C)O)(C(=O)O3)C)O	348.40	unknown	https://doi.org/10.1021/JO00139A007
8,15-Dihydroxy-1,12-dimethyl-6-propan-2-yl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6,13-triene-4,11-dione	163021459	Click to see CC(C)C1=C2C(C3C4C(C=CC(C4(C2=CC(=O)O1)C)O)(C(=O)O3)C)O	346.40	unknown	https://doi.org/10.1016/S0031-9422(00)90725-8
methyl (2R)-2-[(1S,6R,9R,12S,14R,16R)-14-hydroxy-1,12-dimethyl-4,11-dioxo-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,7-dien-6-yl]propanoate	162904600	Click to see CC(C1C2=CC3C4C(C2=CC(=O)O1)(CC(CC4(C(=O)O3)C)O)C)C(=O)OC	376.40	unknown	https://doi.org/10.1016/0031-9422(90)85374-O
Methyl 2-(14-hydroxy-1,12-dimethyl-4,11-dioxo-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,7-dien-6-yl)propanoate	162904599	Click to see CC(C1C2=CC3C4C(C2=CC(=O)O1)(CC(CC4(C(=O)O3)C)O)C)C(=O)OC	376.40	unknown	https://doi.org/10.1016/0031-9422(91)83237-F https://doi.org/10.1016/0031-9422(90)85374-O
Nagilactone	319648	Click to see CC(C)C1=C2C(C3C4C(C(C5C(C4(C2=CC(=O)O1)C)O5)O)(C(=O)O3)C)O	362.40	unknown	https://doi.org/10.1016/0031-9422(91)85049-6 https://doi.org/10.1021/JO00139A007
Nagilactone A	3084328	Click to see CC(C)C1=C2C(C3C4C(CCC(C4(C2=CC(=O)O1)C)O)(C(=O)O3)C)O	348.40	unknown	https://doi.org/10.1271/BBB.56.1302 https://doi.org/10.1016/0031-9422(91)85049-6 https://doi.org/10.1021/ACS.JNATPROD.7B00347 https://doi.org/10.1021/JO00139A007 https://doi.org/10.1007/BF02033650
Nagilactone B	3084329	Click to see CC(C)C1=C2C(C3C4C(CC(C(C4(C2=CC(=O)O1)C)O)O)(C(=O)O3)C)O	364.40	unknown	https://doi.org/10.1021/ACS.JNATPROD.7B00347 https://doi.org/10.1021/JO00139A007 https://doi.org/10.1007/BF02033650
Nagilactone C	72505	Click to see CC(C)C1=C2C(C3C4C(C(C5C(C4(C2=CC(=O)O1)C)O5)O)(C(=O)O3)C)O	362.40	unknown	https://doi.org/10.1021/JO00139A007 https://doi.org/10.1016/0031-9422(91)83237-F https://doi.org/10.1271/BBB.56.1302 https://doi.org/10.1021/ACS.JNATPROD.7B00347 https://doi.org/10.1016/0031-9422(91)85049-6 https://doi.org/10.1021/NP50086A004 https://doi.org/10.1007/BF02033650
Nagilactone D	3084330	Click to see CCC1=C2CC3C4C(C(C5C(C4(C2=CC(=O)O1)C)O5)O)(C(=O)O3)C	332.30	unknown	https://doi.org/10.1016/0031-9422(91)83237-F https://doi.org/10.1021/NP50086A004 https://doi.org/10.1021/ACS.JNATPROD.7B00347 https://doi.org/10.1007/BF02033650
Nagilactone F	181498	Click to see CC(C)C1C2=CC3C4C(C2=CC(=O)O1)(CCCC4(C(=O)O3)C)C	316.40	unknown	https://doi.org/10.1007/BF02033650
Nagilactone F,8-epoxy-	100002	Click to see CC(C)C1C23C(O2)C4C5C(C3=CC(=O)O1)(CCCC5(C(=O)O4)C)C	332.40	unknown	https://doi.org/10.1021/ACS.JNATPROD.7B00347
Nagilactone G	71300384	Click to see CC(C)C1C23C(O2)C4C5C(C3=CC(=O)O1)(CCCC5(C(=O)O4)C)C	332.40	unknown	https://doi.org/10.1021/ACS.JNATPROD.7B00347
Nagilactoside C	10394719	Click to see CC(C)C1=C2C(C3C4C(C2=CC(=O)O1)(CC(CC4(C(=O)O3)C)OC5C(C(C(C(O5)CO)O)OC6C(C(C(C(O6)CO)O)O)O)O)C)O	672.70	unknown	https://doi.org/10.1016/0031-9422(95)94785-L
Nagilactoside D	10439473	Click to see CC(C)C1=C2C(C3C4C(C2=CC(=O)O1)(CC(CC4(C(=O)O3)C)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)C)O	672.70	unknown	https://doi.org/10.1016/0031-9422(95)94785-L
Podolactone B,2-deepoxy-15,16-dideoxy-	54607199	Click to see CC(C)C1C23C(O2)C4C5C(C3=CC(=O)O1)(CCC(C5(C(=O)O4)C)O)C	348.40	unknown	https://doi.org/10.1016/S0031-9422(00)90725-8 https://doi.org/10.1007/BF01969731 https://doi.org/10.1016/0031-9422(91)84188-X https://doi.org/10.1007/BF02033650
> Organoheterocyclic compounds / Oxepanes
(1S,2S,4R,5R,6R,9S,10R,12S,16R)-5,10-dihydroxy-1,6-dimethyl-12-propan-2-yl-3,8,13-trioxapentacyclo[7.6.1.02,4.06,16.011,15]hexadec-11(15)-ene-7,14-dione	163024682	Click to see CC(C)C1C2=C(C(=O)O1)C3(C4C(C2O)OC(=O)C4(C(C5C3O5)O)C)C	350.40	unknown	https://doi.org/10.1016/0031-9422(91)83237-F
5,10-Dihydroxy-1,6-dimethyl-12-propan-2-yl-3,8,13-trioxapentacyclo[7.6.1.02,4.06,16.011,15]hexadec-11(15)-ene-7,14-dione	163024681	Click to see CC(C)C1C2=C(C(=O)O1)C3(C4C(C2O)OC(=O)C4(C(C5C3O5)O)C)C	350.40	unknown	https://doi.org/10.1016/0031-9422(91)83237-F
> Phenylpropanoids and polyketides / Diarylheptanoids / Cyclic diarylheptanoids / Meta,meta-bridged biphenyls
(+)-Ar,11S-Myricanol	11783303	Click to see COC1=C2C=C(CCCCC(CCC3=CC2=C(C=C3)O)O)C(=C1OC)O	358.40	unknown	https://doi.org/10.1016/0031-9422(80)87049-X
(9S)-3,9,15-trihydroxy-16,17-dimethoxytricyclo[12.3.1.12,6]nonadeca-1(17),2,4,6(19),14(18),15-hexaen-7-one	162884180	Click to see COC1=C2C=C(CCCCC(CC(=O)C3=CC2=C(C=C3)O)O)C(=C1OC)O	372.40	unknown	https://doi.org/10.1016/0031-9422(80)87049-X
16,17-Dimethoxytricyclo[12.3.1.12,6]nonadeca-1(17),2,4,6(19),14(18),15-hexaene-3,9,15-triol	5319978	Click to see COC1=C2C=C(CCCCC(CCC3=CC2=C(C=C3)O)O)C(=C1OC)O	358.40	unknown	https://doi.org/10.1016/0031-9422(80)87049-X https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3070757/ https://doi.org/10.1039/C29700001206
3,9,15-Trihydroxy-16,17-dimethoxytricyclo[12.3.1.12,6]nonadeca-1(17),2,4,6(19),14(18),15-hexaen-7-one	162884179	Click to see COC1=C2C=C(CCCCC(CC(=O)C3=CC2=C(C=C3)O)O)C(=C1OC)O	372.40	unknown	https://doi.org/10.1016/0031-9422(80)87049-X
Myricanol	161779	Click to see COC1=C2C=C(CCCCC(CCC3=CC2=C(C=C3)O)O)C(=C1OC)O	358.40	unknown	https://doi.org/10.1039/C29700001206
Myricanone	161748	Click to see COC1=C2C=C(CCCCC(=O)CCC3=CC2=C(C=C3)O)C(=C1OC)O	356.40	unknown	https://doi.org/10.1002/CBDV.201600247 https://doi.org/10.1039/C29700001206 https://doi.org/10.1016/S0968-0896(02)00314-0 https://doi.org/10.1248/CPB.50.208 https://doi.org/10.1016/J.PHYTOCHEM.2014.04.003 https://doi.org/10.1016/0031-9422(80)87049-X https://doi.org/10.1016/J.JAMS.2013.05.003 https://doi.org/10.1021/NP300212C https://doi.org/10.3736/JINTEGRMED2013057 https://doi.org/10.1159/000371738
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone	5281600	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O	538.50	unknown	https://doi.org/10.1016/S0031-9422(00)81743-4
Isoginkgetin	5318569	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)OC	566.50	unknown	https://doi.org/10.1016/S0031-9422(00)81743-4
Sciadopitysin	5281696	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)OC)O)OC	580.50	unknown	https://doi.org/10.1007/S10600-016-1573-Z
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol	1203	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1271/BBB.56.1302
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1271/BBB.56.1302
> 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/10.1039/CT8966901287 https://doi.org/10.1007/S12272-009-1408-6
> Phenylpropanoids and polyketides / Macrolides and analogues
(R)-Lasiodiplodin	11833217	Click to see CC1CCCCCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1	292.40	unknown	https://doi.org/10.1007/BF01969731 https://doi.org/10.1016/S0031-9422(00)90725-8 https://doi.org/10.1016/0031-9422(91)84188-X https://doi.org/10.1007/BF02033650

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Nageia nagi

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