Orixa japonica, also known as East Asian orixa or Japanese orixa, is a deciduous shrub native to Japan and South Korea. It can grow up to 3 metres in height and is typically found on sunny slopes in forested areas at elevations between 500 and 1300 metres. A recent study has discovered that this plant contains previously unknown alkaloids that may be effective against Plasmodium falciparum, a species of protozoan that causes human malaria. In addition to its potential medicinal properties, Orixa japonica also has a unique leaf pattern where the angles of subsequent leaves follow a distinct pattern of 180 degrees, 90 degrees, 180 degrees, and 270 degrees, which then repeats.

Synonyms Top

Scientific name	Authority	First published in
Celastrus dilatatus	Thunb.	Trans. Linn. Soc. London 2: 332 (1794)
Celastrus japonicus	K.Koch	Dendrologie 1: 625 (1869)
Celastrus orixa	Siebold & Zucc.	Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(2): 150 (1845)
Sabia feddei	H.Lév.	Repert. Spec. Nov. Regni Veg. 9: 456 (1911)
Sabia cavaleriei	H.Lév.	Repert. Spec. Nov. Regni Veg. 9: 456 (1911)
Othera orixa	Lam.	Tabl. Encycl. i. 310.
Ilex orixa	Spreng.	Syst. Veg. 1: 496 (1824)
Orixa subcoriacea	Z.M.Tan	Bull. Bot. Res., Harbin 9(2): 45 (1989)
Orixa racemosa	Z.M.Tan	Bull. Bot. Res., Harbin 9(2): 44 (1989)
Euodia ramiflora	A.Gray	Mem. Amer. Acad. Arts , n.s., 6: 383 (1859)

Common names Top

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Filter by language:

Language	Common/alternative name
English	japanese orixa
English	east asian orixa
Arabic	عقفاء يابانية
Arabic	عقف ياباني
Japanese	コクサギ
Korean	상산나무
Polish	oriksa japońska
Chinese	臭药
Chinese	臭山羊
Chinese	臭苗
Chinese	白胡椒
Chinese	拔马瘟
Chinese	大素药
Chinese	大山羊
Chinese	和常山
Chinese	臭常山

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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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 North-central
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan
  - Korea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001133214
Tropicos	28101582
KEW	urn:lsid:ipni.org:names:162301-1
The Plant List	tro-28101582
PFAF	Orixa japonica
Open Tree Of Life	710085
NCBI Taxonomy	354507
IUCN Red List	147620777
IPNI	162301-1
iNaturalist	448041
GBIF	5594331
Freebase	/m/0r4xxqn
EPPO	ORXJA
EOL	2888536
Elurikkus	209838
USDA GRIN	460209
Wikipedia	Orixa_japonica
CMAUP	NPO340

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

Behavioral and Electrophysiological Study on Eight Japanese Papilio Species with Five Hostplant Volatiles and Linalool

Inoue TA, Suetake M, Nishidzu N, Yokohari F, Niihara K, Fukuda T

J Chem Ecol

28-Jun-2023

PMCID:	PMC10611675
doi:	10.1007/s10886-023-01433-2
PMID:	37378686

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

Insights from the Endophytic Fungi in Amphisphaeria (Sordariomycetes): A. orixae sp. nov. from Orixa japonica and Its Secondary Metabolites

Wang X, Wanasinghe DN, Zhang J, Ma J, Zhou P, Zhang L, Lu Y, Zhang Z

Microorganisms

11-May-2023

PMCID:	PMC10221786
doi:	10.3390/microorganisms11051268
PMID:	37317242

Phylogeny and systematics of the genus Clonostachys

Wang Y, Tang DX, Luo R, Wang YB, Thanarut C, Dao VM, Yu H

Front Microbiol

03-Mar-2023

PMCID:	PMC10020229
doi:	10.3389/fmicb.2023.1117753
PMID:	36937310

Plastome evolution and phylogeny of the tribe Ruteae (Rutaceae)

Liu Q, Gao Y, Dong W, Zhao L

Ecol Evol

09-Feb-2023

PMCID:	PMC9911629
doi:	10.1002/ece3.9821
PMID:	36789335

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

Anti-Diabesity Middle Eastern Medicinal Plants and Their Action Mechanisms

Saad B, Kmail A, Haq SZ

Evid Based Complement Alternat Med

18-Jul-2022

PMCID:	PMC9313926
doi:	10.1155/2022/2276094
PMID:	35899227

The complete chloroplast genome sequence of Dictamnus albus L.

Liu J, Wang Z, Ren W, Liu C, Li X, Han J, Ma W

Mitochondrial DNA B Resour

14-Jun-2022

PMCID:	PMC9225780
doi:	10.1080/23802359.2022.2081097
PMID:	35756457

UHPLC-ESI-QqTOF Analysis and In Vitro Rumen Fermentation for Exploiting Fagus sylvatica Leaf in Ruminant Diet

Formato M, Piccolella S, Zidorn C, Vastolo A, Calabrò S, Cutrignelli MI, Pacifico S

Molecules

29-Mar-2022

PMCID:	PMC9000816
doi:	10.3390/molecules27072217
PMID:	35408616

In Silico Approaches to Identify Polyphenol Compounds as α-Glucosidase and α-Amylase Inhibitors against Type-II Diabetes

Riyaphan J, Pham DC, Leong MK, Weng CF

Biomolecules

14-Dec-2021

PMCID:	PMC8699780
doi:	10.3390/biom11121877
PMID:	34944521

Coexpression of Three Odorant-Binding Protein Genes in the Foreleg Gustatory Sensilla of Swallowtail Butterfly Visualized by Multicolor FISH Analysis

Ugajin A, Ozaki K

Front Insect Sci

30-Jul-2021

PMCID:	PMC10926539
doi:	10.3389/finsc.2021.696179
PMID:	38468877

Metabolic and Epigenetics Action Mechanisms of Antiobesity Medicinal Plants and Phytochemicals

Saad B, Ghareeb B, Kmail A

Evid Based Complement Alternat Med

09-Jun-2021

PMCID:	PMC8208872
doi:	10.1155/2021/9995903
PMID:	34211580

Characterization of the complete chloroplast genome of the medicinal plant Orixa japonica (Rutaceae) in Zhejiang Province and its phylogenetic analysis within family Rutaceae

Ying Z, Yan M, Zhou M, He X, Cheng R

Mitochondrial DNA B Resour

24-May-2021

PMCID:	PMC8158279
doi:	10.1080/23802359.2021.1931511
PMID:	34104754

Ampelomyces strains isolated from diverse powdery mildew hosts in Japan: Their phylogeny and mycoparasitic activity, including timing and quantifying mycoparasitism of Pseudoidium neolycopersici on tomato

Németh MZ, Mizuno Y, Kobayashi H, Seress D, Shishido N, Kimura Y, Takamatsu S, Suzuki T, Takikawa Y, Kakutani K, Matsuda Y, Kiss L, Nonomura T

PLoS One

11-May-2021

PMCID:	PMC8112701
doi:	10.1371/journal.pone.0251444
PMID:	33974648

Content Snapshots

N/A

Ann Bot

07-May-2021

PMCID:	PMC8103799
doi:	10.1093/aob/mcab049

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Carvone, (+)-	16724	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	via CMAUP database
Cyclohexanol, 2-methyl-5-(1-methylethyl)-, (1alpha,2beta,5alpha)-	6432473	Click to see CC1CCC(CC1O)C(C)C	156.26	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
[(4S,4aR,8aR)-4,4a-dimethyl-7-oxo-6-propan-2-ylidene-2,3,4,5,8,8a-hexahydro-1H-naphthalen-2-yl] (Z)-3-methylsulfanylprop-2-enoate	5318694	Click to see CC1CC(CC2C1(CC(=C(C)C)C(=O)C2)C)OC(=O)C=CSC	336.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Orizabin	5281491	Click to see CC1=CC2C(C(CC3(C(CC1(O3)O)O)C)OC(=O)C(C)C)C(=C)C(=O)O2	366.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelan-3-one	244297	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)97421-1
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)97421-1
Isoarborinol	12305182	Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C	426.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3R,4R)-3,4-Dihydroxy-3-methyloxolan-2-one	11126294	Click to see CC1(C(COC1=O)O)O	132.11	unknown	https://doi.org/10.1271/BBB.64.1970
3,4-Dihydroxy-3-methyloxolan-2-one	11469098	Click to see CC1(C(COC1=O)O)O	132.11	unknown	https://doi.org/10.1271/BBB.64.1970
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Norpluviine	12313583	Click to see COC1=C(C=C2CN3CCC4=CCC(C(C43)C2=C1)O)O	273.33	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Dihydrofuranoquinolines
2-(10-Methoxy-3,5,14-trioxa-16-azatetracyclo[7.7.0.02,6.011,15]hexadeca-1(9),2(6),7,10,15-pentaen-13-yl)propan-2-ol	14845308	Click to see CC(C)(C1CC2=C(C3=C(C4=C(C=C3)OCO4)N=C2O1)OC)O	303.31	unknown	https://doi.org/10.1271/BBB.65.710
2-(10-Methoxy-3,5,14-trioxa-16-azatetracyclo[7.7.0.02,6.011,15]hexadeca-1(9),2(6),7,10,15-pentaen-13-yl)propan-2-yl acetate	15287474	Click to see CC(=O)OC(C)(C)C1CC2=C(C3=C(C4=C(C=C3)OCO4)N=C2O1)OC	345.30	unknown	https://doi.org/10.1021/NP0401462
2-[(13R)-10-methoxy-3,5,14-trioxa-16-azatetracyclo[7.7.0.02,6.011,15]hexadeca-1(9),2(6),7,10,15-pentaen-13-yl]propan-2-yl acetate	163018902	Click to see CC(=O)OC(C)(C)C1CC2=C(C3=C(C4=C(C=C3)OCO4)N=C2O1)OC	345.30	unknown	https://doi.org/10.1021/NP0401462
2-[(13S)-10-methoxy-3,5,14-trioxa-16-azatetracyclo[7.7.0.02,6.011,15]hexadeca-1(9),2(6),7,10,15-pentaen-13-yl]propan-2-ol	44138157	Click to see CC(C)(C1CC2=C(C3=C(C4=C(C=C3)OCO4)N=C2O1)OC)O	303.31	unknown	https://doi.org/10.1271/BBB.65.710
Isoplatydesmine	11219133	Click to see CC(C)(C1CC2=C(O1)N(C3=CC=CC=C3C2=O)C)O	259.30	unknown	via CMAUP database
Isopteleflorine	197708	Click to see CC(C)(C1CC2=C(C3=C(C4=C(C=C3)OCO4)N=C2O1)OC)O	303.31	unknown	https://doi.org/10.1271/BBB.65.710
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
(R)-1-((4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy)-3-methylbutane-2,3-diol	636924	Click to see CC(C)(C(COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)O)O	347.40	unknown	https://doi.org/10.1271/BBB1961.41.1263
Evoxine	73416	Click to see CC(C)(C(COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)O)O	347.40	unknown	https://doi.org/10.1271/BBB1961.41.1263
Gamma-Fagarine	107936	Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3	229.23	unknown	https://doi.org/10.1021/NP0401462
Kokusagine	5318829	Click to see COC1=C2C=COC2=NC3=C1C=CC4=C3OCO4	243.21	unknown	https://doi.org/10.1248/YAKUSHI1947.73.7_773 https://doi.org/10.1039/P19720002116 https://doi.org/10.1016/S0031-9422(00)97107-3 https://doi.org/10.1021/NP0401462 https://doi.org/10.1248/CPB1953.2.159 https://doi.org/10.1271/BBB1961.41.1263
Kokusaginine	10227	Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC	259.26	unknown	via CMAUP database
Skimmianine	6760	Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC	259.26	unknown	https://doi.org/10.1021/NP0401462 https://doi.org/10.1016/S0031-9422(00)97107-3 https://doi.org/10.1248/YAKUSHI1947.73.7_773
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
Eduline	622180	Click to see CN1C2=C(C=C(C=C2)OC)C(=O)C=C1C3=CC=CC=C3	265.31	unknown	https://doi.org/10.1248/BPB.24.100
Japonine	442915	Click to see CN1C2=C(C=C(C=C2)OC)C(=O)C(=C1C3=CC=CC=C3)OC	295.30	unknown	https://doi.org/10.1016/S0031-9422(00)85386-8 https://doi.org/10.1039/P19720002116 https://doi.org/10.1248/BPB.24.100 https://doi.org/10.1271/BBB1961.41.1263
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives
(-)-Preorixine	176904	Click to see CC1(C(O1)CC2=C(C3=C(C4=C(C=C3)OCO4)N=C2OC)OC)C	317.34	unknown	https://doi.org/10.1016/0031-9422(95)00742-3 https://doi.org/10.1021/NP0401462 https://doi.org/10.1016/S0031-9422(00)97107-3 https://doi.org/10.3987/COM-92-S(T)78
(2R)-1-(6,8-dimethoxy-[1,3]dioxolo[4,5-h]quinolin-7-yl)-3-methoxy-3-methylbutan-2-ol	10497975	Click to see CC(C)(C(CC1=C(C2=C(C3=C(C=C2)OCO3)N=C1OC)OC)O)OC	349.40	unknown	https://doi.org/10.1016/0031-9422(95)00742-3 https://doi.org/10.1271/BBB.65.710
(2R)-1-(6,8-dimethoxy-[1,3]dioxolo[4,5-h]quinolin-7-yl)-3-methylbut-3-en-2-ol	15815868	Click to see CC(=C)C(CC1=C(C2=C(C3=C(C=C2)OCO3)N=C1OC)OC)O	317.34	unknown	https://doi.org/10.1016/0031-9422(95)00742-3 https://doi.org/10.1021/NP0401462 https://doi.org/10.1016/S0031-9422(00)97107-3
(2R)-1-(6,8-dimethoxy-[1,3]dioxolo[4,5-h]quinolin-7-yl)-3-methylbutane-2,3-diol	176905	Click to see CC(C)(C(CC1=C(C2=C(C3=C(C=C2)OCO3)N=C1OC)OC)O)O	335.40	unknown	https://doi.org/10.1248/CPB.44.1885 https://doi.org/10.1016/0031-9422(95)00742-3 https://doi.org/10.1021/NP0401462 https://doi.org/10.3987/COM-92-S(T)78 https://doi.org/10.1016/S0031-9422(00)97107-3
(2S)-1-(6,8-dimethoxy-[1,3]dioxolo[4,5-h]quinolin-7-yl)-3-methylbutane-2,3-diol	101289701	Click to see CC(C)(C(CC1=C(C2=C(C3=C(C=C2)OCO3)N=C1OC)OC)O)O	335.40	unknown	https://doi.org/10.1021/NP0401462 https://doi.org/10.1248/CPB.8.523 https://doi.org/10.1016/S0031-9422(00)97107-3 https://doi.org/10.3987/COM-92-S(T)78 https://doi.org/10.1248/YAKUSHI1881.51.9_707
1-(6,8-Dimethoxy-[1,3]dioxolo[4,5-h]quinolin-7-yl)-3-methoxy-3-methylbutan-2-ol	85160690	Click to see CC(C)(C(CC1=C(C2=C(C3=C(C=C2)OCO3)N=C1OC)OC)O)OC	349.40	unknown	https://doi.org/10.1016/0031-9422(95)00742-3 https://doi.org/10.1271/BBB.65.710
1-(6,8-Dimethoxy-[1,3]dioxolo[4,5-h]quinolin-7-yl)-3-methylbutane-2,3-diol	5320308	Click to see CC(C)(C(CC1=C(C2=C(C3=C(C=C2)OCO3)N=C1OC)OC)O)O	335.40	unknown	https://doi.org/10.1016/0031-9422(95)00742-3 https://doi.org/10.1021/NP0401462 https://doi.org/10.3987/COM-92-S(T)78 https://doi.org/10.1016/S0031-9422(00)97107-3 https://doi.org/10.1248/CPB.8.523 https://doi.org/10.1248/YAKUSHI1881.51.9_707
6,8-Dimethoxy-7-(3-methylbut-2-enyl)-[1,3]dioxolo[4,5-h]quinoline	14845306	Click to see CC(=CCC1=C(C2=C(C3=C(C=C2)OCO3)N=C1OC)OC)C	301.34	unknown	https://doi.org/10.1016/S0031-9422(00)97107-3
6,8-Dimethoxy-7-[(3,3-dimethyloxiran-2alpha-yl)methyl]-1,3-dioxolo[4,5-h]quinoline	15815867	Click to see CC1(C(O1)CC2=C(C3=C(C4=C(C=C3)OCO4)N=C2OC)OC)C	317.34	unknown	https://doi.org/10.1248/CPB.44.1885 https://doi.org/10.1016/0031-9422(95)00742-3 https://doi.org/10.1021/NP0401462 https://doi.org/10.3987/COM-92-S(T)78 https://doi.org/10.1016/S0031-9422(00)97107-3
7-[[(2S)-3,3-dimethyloxiran-2-yl]methyl]-6,8-dimethoxy-[1,3]dioxolo[4,5-h]quinoline	102002697	Click to see CC1(C(O1)CC2=C(C3=C(C4=C(C=C3)OCO4)N=C2OC)OC)C	317.34	unknown	https://doi.org/10.1016/S0031-9422(00)97107-3 https://doi.org/10.3987/COM-92-S(T)78
Isoptelefolidine	101663727	Click to see CC(=C)C(CC1=C(C2=C(C3=C(C=C2)OCO3)N=C1OC)OC)O	317.34	unknown	https://doi.org/10.1248/CPB.44.1885 https://doi.org/10.1016/0031-9422(95)00742-3 https://doi.org/10.1021/NP0401462 https://doi.org/10.1016/S0031-9422(00)97107-3
Orixinone	5320309	Click to see CC(C)C(=O)CC1=C(C2=C(C3=C(C=C2)OCO3)N=C1OC)OC	317.34	unknown	https://doi.org/10.1248/CPB.44.1885 https://doi.org/10.1016/0031-9422(95)00742-3 https://doi.org/10.1021/NP0401462 https://doi.org/10.1039/P19720002116 https://doi.org/10.3987/COM-92-S(T)78 https://doi.org/10.1016/S0031-9422(00)97107-3
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methyl-3-(3-methylbut-2-enyl)quinolin-2-one	15460082	Click to see CC(=CCC1=C(C2=CC=CC=C2N(C1=O)C)OC)C	257.33	unknown	https://doi.org/10.1016/S0031-9422(00)97107-3
4,8-dimethoxy-3-(3-methyl-2-oxobut-3-enyl)-1H-quinolin-2-one	11426211	Click to see CC(=C)C(=O)CC1=C(C2=C(C(=CC=C2)OC)NC1=O)OC	287.31	unknown	https://doi.org/10.1021/NP0401462
6-methoxy-7-(3-methyl-2-oxobutyl)-9H-[1,3]dioxolo[4,5-h]quinolin-8-one	101664023	Click to see CC(C)C(=O)CC1=C(C2=C(C3=C(C=C2)OCO3)NC1=O)OC	303.31	unknown	https://doi.org/10.1016/S0031-9422(00)97107-3 https://doi.org/10.1271/BBB.65.710
6-Methoxy-9-methyl-7-(3-methyl-2-oxobutyl)-[1,3]dioxolo[4,5-h]quinolin-8-one	12305090	Click to see CC(C)C(=O)CC1=C(C2=C(C3=C(C=C2)OCO3)N(C1=O)C)OC	317.34	unknown	https://doi.org/10.1016/S0031-9422(00)97107-3
7-(2,3-dihydroxy-3-methylbutyl)-6-methoxy-9H-[1,3]dioxolo[4,5-h]quinolin-8-one	6325747	Click to see CC(C)(C(CC1=C(C2=C(C3=C(C=C2)OCO3)NC1=O)OC)O)O	321.32	unknown	via CMAUP database
Bmcqlkyntfqtrn-uhfffaoysa-	11243539	Click to see CC(=C)C(=O)CC1=C(C2=C(C(=CC=C2)OC)N(C1=O)C)OC	301.34	unknown	https://doi.org/10.1021/NP0401462
Orijanone	10778640	Click to see CC(C)C(=O)CC1=C(C2=CC=CC=C2N(C1=O)C)OC	273.33	unknown	https://doi.org/10.1271/BBB.65.710
orixalone A	11278088	Click to see CC(C)C(=O)CC1=C(C2=C(C(=CC=C2)OC)N(C1=O)C)OC	303.35	unknown	https://doi.org/10.1021/NP0401462
Preskimmianine	12305721	Click to see CC(=CCC1=C(C2=C(C(=C(C=C2)OC)OC)NC1=O)OC)C	303.35	unknown	via CMAUP database
Pteleprenine	167633	Click to see CC(=CCC1=C(C2=C(C3=C(C=C2)OCO3)N(C1=O)C)OC)C	301.34	unknown	https://doi.org/10.1016/S0031-9422(00)97107-3 https://doi.org/10.1111/J.2042-7158.1998.TB07143.X
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
3,4-Dihydroxy-2,2,6-trimethyl-3,4-dihydropyrano[3,2-c]quinolin-5-one	73796527	Click to see CC1(C(C(C2=C(O1)C3=CC=CC=C3N(C2=O)C)O)O)C	275.30	unknown	https://doi.org/10.1021/NP0401462
Heuvgodfdjkjtp-wcqyabfasa-	21573064	Click to see CC1(C(C(C2=C(O1)C3=CC=CC=C3N(C2=O)C)O)O)C	275.30	unknown	https://doi.org/10.1021/NP0401462
N-Methylflindersine	72819	Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3N(C2=O)C)C	241.28	unknown	https://doi.org/10.1021/NP0401462 https://doi.org/10.1016/S0031-9422(00)97107-3
Zanthobungeanine	5315422	Click to see CC1(C=CC2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)C	271.31	unknown	https://doi.org/10.1016/S0031-9422(00)97107-3
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
7-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	320361	Click to see C1=CC(=CC2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	324.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Heraclenin	458010	Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C	286.28	unknown	https://doi.org/10.1021/NP0401462
Oxyimperatorin	182251	Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C	286.28	unknown	https://doi.org/10.1021/NP0401462
Pentosalen	10212	Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C	270.28	unknown	https://doi.org/10.1021/NP0401462 https://doi.org/10.1039/P19720002116
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten	2355	Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3	216.19	unknown	https://doi.org/10.1016/S0031-9422(00)97421-1 https://doi.org/10.1021/NP0401462 https://doi.org/10.1271/BBB1961.41.1263
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin	68079	Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC	246.21	unknown	https://doi.org/10.1271/BBB1961.41.1263
Methoxsalen	4114	Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2	216.19	unknown	https://doi.org/10.1016/S0031-9422(00)97421-1 https://doi.org/10.1271/BBB1961.41.1263
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
8-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-3,5,7-trihydroxy-2-(3-hydroxy-4-methoxyphenyl)-2,3-dihydrochromen-4-one	3512640	Click to see COC1=C(C=C(C=C1)C2C(C(=O)C3=C(C=C(C(=C3O2)C4C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)O)O)O)O	588.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Flavonol base + 4O, O-Hex-dHex-Pen	5859848	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)OC6C(C(C(CO6)O)O)O)O)O)O)O)O	742.60	unknown	https://doi.org/10.1271/BBB1961.54.1265
Quercetin 3-(2G-xylosylrutinoside)	5281690	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)OC6C(C(C(CO6)O)O)O)O)O)O)O)O	742.60	unknown	https://doi.org/10.1271/BBB1961.54.1265
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,6-Dihydroxy-2-(4-hydroxy-2,5-dimethoxyphenyl)-7-methoxychromen-4-one	5318508	Click to see COC1=CC(=C(C=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O)OC)O	360.30	unknown	via CMAUP database

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Orixa japonica

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