Scientific name	Authority	First published in
Ruta frutescens	Siev. ex Fisch.	Enum. Pl. Nov. 1: 90 (1841)
Haplophyllum flexuosum	Boiss.	Diagn. Pl. Orient. , ser. 2, 1: 118 (1854)
Haplophyllum perforatum	Kar. & Kir.	Bull. Soc. Imp. Naturalistes Moscou 14: 397. 1841
Haplophyllum sieversii	Fisch.	Enum. Pl. Nov. 1: 89 (1841)
Ruta perforata	M.Bieb.	Tabl. Prov. Mer Casp. , German ed.: 172 (1800)
Ruta acutifolia	DC.	Prodr. 1: 711 (1824)
Ruta flexuosa	Engl.	Nat. Pflanzenfam. 3(4): 131 (1896)
Ruta sieversii	B.Fedtsch.	Rastitel'n. Turkestana : 555 (1915)
Haplophyllum perforatum	Kar. & Kir.	Bull. Soc. Imp. Naturalistes Moscou 14: 397 (1841)

Common names Top

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Language	Common/alternative name
Chinese	大叶芸香

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
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Mongolia
  - Mongolia
- Western Asia
  - Afghanistan
  - Iran

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000715467
Tropicos	28101465
KEW	urn:lsid:ipni.org:names:771245-1
Open Tree Of Life	239196
Observations.org	118370
NCBI Taxonomy	452768
IPNI	771245-1
iNaturalist	905154
GBIF	5834553
Elurikkus	641912
USDA GRIN	455157

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

Furoquinoline Alkaloids: Insights into Chemistry, Occurrence, and Biological Properties

Szewczyk A, Pęczek F

Int J Mol Sci

15-Aug-2023

PMCID:	PMC10454094
doi:	10.3390/ijms241612811
PMID:	37628986

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

Metabolomics in the Context of Plant Natural Products Research: From Sample Preparation to Metabolite Analysis

Salem MA, Perez de Souza L, Serag A, Fernie AR, Farag MA, Ezzat SM, Alseekh S

Metabolites

15-Jan-2020

PMCID:	PMC7023240
doi:	10.3390/metabo10010037
PMID:	31952212

Biologically Active Quinoline and Quinazoline Alkaloids Part II

Shang XF, Morris-Natschke SL, Yang GZ, Liu YQ, Guo X, Xu XS, Goto M, Li JC, Zhang JY, Lee KH

Med Res Rev

27-Feb-2018

PMCID:	PMC6105521
doi:	10.1002/med.21492
PMID:	29485730

The genus Cladosporium

Bensch K, Braun U, Groenewald JZ, Crous PW

Stud Mycol

06-Jun-2012

PMCID:	PMC3390897
doi:	10.3114/sim0003
PMID:	22815589

Accelerated dereplication of crude extracts using HPLC-PDA-MS-SPE-NMR: quinolinone alkaloids of Haplophyllum acutifolium.

Staerk D, Kesting JR, Sairafianpour M, Witt M, Asili J, Emami SA, Jaroszewski JW

Phytochemistry

01-May-2009

doi:	10.1016/J.PHYTOCHEM.2009.05.004
PMID:	19540540

Cytotoxic effects of haplamine and its major metabolites on human cancer cell lines.

Ea S, Giacometti S, Ciccolini J, Akhmedjanova V, Aubert C

Planta Med

01-Aug-2008

doi:	10.1055/S-2008-1081298
PMID:	18666046

The structure of perfamine

D. M. Razakova, I. A. Bessonova, S. Yu. Yunusov

Springer Science and Business Media LLC

09-Jul-2008

doi:	10.1007/BF00564966

Methylevoxine - a new alkaloid from Haplophyllum perforatum

V. I. Akhmedzhanova, I. A. Bessonova, S. Yu. Yunusov

Springer Science and Business Media LLC

09-Jul-2008

doi:	10.1007/BF00570710

Furoquinoline Alkaloids of Ertela (Monnieria) trifolia (L.) Kuntze from the Suriname Rainforest

Cao S, Al-Rehaily AJ, Brodie P, Wisse JH, Moniz E, Malone S, Kingston DG

Phytochemistry

21-Sep-2007

PMCID:	PMC2245804
doi:	10.1016/j.phytochem.2007.08.009
PMID:	17889047

Acetylhaplophyllidine, a new alkaloid fromHaplophyllum perforatum

I. A. Bessonova

Springer Science and Business Media LLC

11-Feb-2006

doi:	10.1007/BF02323307

New alkaloids fromHaplophyllum

V. I. Akhmedzhanova

Springer Science and Business Media LLC

11-Feb-2006

doi:	10.1007/BF02323293

Alkaloids ofHaplophyllum perforatum. II

Kh. A. Abdullaeva, I. A. Bessonova, S. Yu. Yunusov

Springer Science and Business Media LLC

06-Feb-2005

doi:	10.1007/BF01134623

Haplaphine — A new alkaloid ofHaplophyllum perforatum

I. A. Bessonova, S. Yu. Yunusov

Springer Science and Business Media LLC

10-Dec-2004

doi:	10.1007/BF00599289

Obtusifolin ? A new coumarin from roots of Haplophyllum obtusifolium

I. A. Bessonova, �. Kh. Batirov, M. R. Yagudaev

Springer Science and Business Media LLC

10-Dec-2004

doi:	10.1007/BF00596740

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
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Hexahydrobenzophenanthridine alkaloids
Chelidonine	197810	Click to see CN1CC2=C(C=CC3=C2OCO3)C4C1C5=CC6=C(C=C5CC4O)OCO6	353.40	unknown	https://doi.org/10.1007/BF00596694
Chelidonine (+)	10147	Click to see CN1CC2=C(C=CC3=C2OCO3)C4C1C5=CC6=C(C=C5CC4O)OCO6	353.40	unknown	https://doi.org/10.1007/BF00596694
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
Diphyllin	100492	Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2O)COC3=O)C4=CC5=C(C=C4)OCO5)OC	380.30	unknown	https://doi.org/10.1007/BF00596694
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Epieudesmin	7000209	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC	386.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004
(+)-Eudesmin	73117	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC	386.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004 https://doi.org/10.1007/BF00714932
(3aS,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan	137795855	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC	386.40	unknown	https://doi.org/10.1007/BF00568495 https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004 https://doi.org/10.1007/BF00630180 https://doi.org/10.1007/BF00579795 https://doi.org/10.1007/BF00567798 https://doi.org/10.1007/BF00568641
1,4-Bis(3,4-dimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan	234823	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC	386.40	unknown	https://doi.org/10.1007/BF00630180 https://doi.org/10.1007/BF00579795 https://doi.org/10.1007/BF00568495 https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004 https://doi.org/10.1007/BF00599289 https://doi.org/10.1007/BF00714932 https://doi.org/10.1007/BF00568641
Eudesmine	325601	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC	386.40	unknown	https://doi.org/10.1007/BF00599289
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3S,4S)-3-(1,3-benzodioxol-5-ylmethyl)-4-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one	92154432	Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC4=C(C=C3)OCO4)OC	370.40	unknown	https://doi.org/10.1016/S0031-9422(01)00188-1
3-(1,3-Benzodioxol-5-ylmethyl)-4-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one	495973	Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC4=C(C=C3)OCO4)OC	370.40	unknown	https://doi.org/10.1016/S0031-9422(01)00188-1
Kusunokinin	384876	Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC4=C(C=C3)OCO4)OC	370.40	unknown	https://doi.org/10.1016/S0031-9422(01)00188-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	https://doi.org/10.1016/S0031-9422(01)00188-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
allo-Murolic acid	101047266	Click to see CC(CCCCCCCCCCCCCC1C(C(=C)C(=O)O1)C(=O)O)O	368.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(25R)-5alpha-Spirostan-3beta-yl acetate	102278	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC(=O)C)C)C)C)OC1	458.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/S0031-9422(01)00188-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol	5997	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	386.70	unknown	https://doi.org/10.1016/S0031-9422(01)00188-1
> 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/10.1007/BF00568641 https://doi.org/10.1016/S0031-9422(01)00188-1
24-Ethylcholest-5-en-3beta-ol	22012	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/S0031-9422(01)00188-1 https://doi.org/10.1007/BF00568641
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/S0031-9422(01)00188-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol	13918927	Click to see COC1=C2C=COC2=NC3=C1C=CC(=C3OC)OC4C(C(C(C(O4)CO)O)O)O	407.40	unknown	https://doi.org/10.1007/BF00565611
(2S,3R,4S,5S,6R)-2-[(2S,3R,4R,5S,6S)-2-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-3,5-dihydroxy-6-methyloxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	13918930	Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)O)OC5C(C(C(C(O5)CO)O)O)O)O	553.50	unknown	https://doi.org/10.1007/BF00596655
(2S,3S,4R,5R,6S)-2-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-6-methyloxane-3,4,5-triol	163090930	Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)O)O)O	391.40	unknown	https://doi.org/10.1007/BF00567897
[(2R,3R,4S,5R,6S)-4,5-diacetyloxy-6-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-2-methyloxan-3-yl] acetate	163194445	Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)OC(=O)C)OC(=O)C)OC(=O)C	517.50	unknown	https://doi.org/10.1007/BF00573574
[(2S,3S,4R,5R,6S)-4,5-diacetyloxy-6-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-2-methyloxan-3-yl] acetate	99975890	Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)OC(=O)C)OC(=O)C)OC(=O)C	517.50	unknown	https://doi.org/10.1007/BF00573574
[2-(4,8-Dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-5-hydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl] acetate	15599716	Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)OC(=O)C)OC5C(C(C(C(O5)CO)O)O)O)O	595.50	unknown	https://doi.org/10.1007/BF00596740
[4,5-Diacetyloxy-6-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-2-methyloxan-3-yl] acetate	3776116	Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)OC(=O)C)OC(=O)C)OC(=O)C	517.50	unknown	https://doi.org/10.1007/BF00573574
2-({4,8-Dimethoxyfuro[2,3-B]quinolin-7-YL}oxy)-6-methyloxane-3,4,5-triol	3518320	Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)O)O)O	391.40	unknown	https://doi.org/10.1007/BF00567798 https://doi.org/10.1007/BF00567897
2-(4,8-Dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol	13918926	Click to see COC1=C2C=COC2=NC3=C1C=CC(=C3OC)OC4C(C(C(C(O4)CO)O)O)O	407.40	unknown	https://doi.org/10.1007/BF00565611
2-[2-(4,8-Dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-3,5-dihydroxy-6-methyloxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	13918928	Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)O)OC5C(C(C(C(O5)CO)O)O)O)O	553.50	unknown	https://doi.org/10.1007/BF00596655
Glycoperine	442906	Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)O)O)O	391.40	unknown	https://doi.org/10.1007/BF00597580 https://doi.org/10.1007/BF00630180 https://doi.org/10.1007/BF00567798 https://doi.org/10.1007/BF00567897
Haplosidine	15599717	Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)OC(=O)C)OC5C(C(C(C(O5)CO)O)O)O)O	595.50	unknown	https://doi.org/10.1007/BF00597580 https://doi.org/10.1007/BF00596740
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Haploperoside E	21607628	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C4C=CC(=O)OC4=C3)OC)OC5C(C(C(C(O5)C)O)O)O)O)O)O)O)O	646.60	unknown	https://doi.org/10.1007/BF00574243
Haploperozide	20105835	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C4C=CC(=O)OC4=C3)OC)OC5C(C(C(C(O5)C)O)O)O)O)O)O)O)O	646.60	unknown	https://doi.org/10.1007/BF00574243
> Organoheterocyclic compounds / Furopyridines
(2S,7R)-2,11-dimethoxy-5,5-dimethyl-6,15-dioxa-17-azatetracyclo[8.7.0.02,7.012,16]heptadeca-1(10),11,13,16-tetraene	162940063	Click to see CC1(CCC2(C(O1)CCC3=C2N=C4C(=C3OC)C=CO4)OC)C	317.40	unknown	https://doi.org/10.1007/BF00567899
(7R)-4,7-dimethoxy-7-(3-methylbut-2-enyl)furo[2,3-b]quinolin-8-one	163048557	Click to see CC(=CCC1(C=CC2=C(C1=O)N=C3C(=C2OC)C=CO3)OC)C	313.30	unknown	https://doi.org/10.1007/BF00568495
(7S,8S)-8-(3-hydroxy-3-methylbutyl)-4,8-dimethoxy-6,7-dihydro-5H-furo[2,3-b]quinolin-7-ol	750664	Click to see CC(C)(CCC1(C(CCC2=C1N=C3C(=C2OC)C=CO3)O)OC)O	335.40	unknown	https://doi.org/10.1007/BF00566989
(8S)-4,8-dimethoxy-8-[(2R)-3-methylbutan-2-yl]furo[2,3-b]quinolin-7-one	162886540	Click to see CC(C)C(C)C1(C(=O)C=CC2=C1N=C3C(=C2OC)C=CO3)OC	315.40	unknown	https://doi.org/10.1007/BF00714932
[(7R,8R)-4,8-dimethoxy-8-(3-methylbut-2-enyl)-6,7-dihydro-5H-furo[2,3-b]quinolin-7-yl] acetate	7274570	Click to see CC(=CCC1(C(CCC2=C1N=C3C(=C2OC)C=CO3)OC(=O)C)OC)C	359.40	unknown	https://doi.org/10.1007/BF02323307
2,11-Dimethoxy-5,5-dimethyl-6,15-dioxa-17-azatetracyclo[8.7.0.02,7.012,16]heptadeca-1(10),11,13,16-tetraene	73813820	Click to see CC1(CCC2(C(O1)CCC3=C2N=C4C(=C3OC)C=CO4)OC)C	317.40	unknown	https://doi.org/10.1007/BF02323307 https://doi.org/10.1007/BF00567899
4,7-Dimethoxy-7-(3-methylbut-2-enyl)furo[2,3-b]quinolin-8-one	90473784	Click to see CC(=CCC1(C=CC2=C(C1=O)N=C3C(=C2OC)C=CO3)OC)C	313.30	unknown	https://doi.org/10.1007/BF00568495
4,8-Dimethoxy-8-(3-methyl-but-2-enyl)-5,6,7,8-tetrahydro-furo[2,3-b]quinolin-7-ol	2837665	Click to see CC(=CCC1(C(CCC2=C1N=C3C(=C2OC)C=CO3)O)OC)C	317.40	unknown	https://doi.org/10.1007/BF00566989 https://doi.org/10.1007/BF02323307
4,8-Dimethoxy-8-(3-methylbutan-2-yl)furo[2,3-b]quinolin-7-one	162886539	Click to see CC(C)C(C)C1(C(=O)C=CC2=C1N=C3C(=C2OC)C=CO3)OC	315.40	unknown	https://doi.org/10.1007/BF00714932
Acetic acid 4,8-dimethoxy-8-(3-methyl-but-2-enyl)-5,6,7,8-tetrahydro-furo[2,3-b]quinolin-7-yl ester	3151987	Click to see CC(=CCC1(C(CCC2=C1N=C3C(=C2OC)C=CO3)OC(=O)C)OC)C	359.40	unknown	https://doi.org/10.1007/BF02323307
Haplophyllidine	442910	Click to see CC(=CCC1(C(CCC2=C1N=C3C(=C2OC)C=CO3)O)OC)C	317.40	unknown	https://doi.org/10.1007/BF00566989 https://doi.org/10.1007/BF02323307
Perfamine	3110227	Click to see CC(=CCC1(C(=O)C=CC2=C1N=C3C(=C2OC)C=CO3)OC)C	313.30	unknown	https://doi.org/10.1007/BF00630180 https://doi.org/10.1007/BF00568495 https://doi.org/10.1007/BF00579795 https://doi.org/10.1007/BF00564966 https://doi.org/10.1007/BF00568641
Perforine	644731	Click to see CC(C)(CCC1(C(CCC2=C1N=C3C(=C2OC)C=CO3)O)OC)O	335.40	unknown	https://doi.org/10.1007/BF00566989
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
(2R)-1-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-3-methylbut-3-en-2-ol	92443142	Click to see CC(=C)C(COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)O	329.30	unknown	https://doi.org/10.1007/BF00563975
(2S)-1-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-3-methoxy-3-methylbutan-2-ol	162906325	Click to see CC(C)(C(COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)O)OC	361.40	unknown	https://doi.org/10.1007/BF00567798 https://doi.org/10.1007/BF00714932 https://doi.org/10.1007/BF00570710
(2S)-1-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-3-methylbut-3-en-2-ol	23629252	Click to see CC(=C)C(COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)O	329.30	unknown	https://doi.org/10.1007/BF00563975 https://doi.org/10.1007/BF01134623
(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/10.1007/BF00714932 https://doi.org/10.1016/S0031-9422(01)00188-1 https://doi.org/10.1007/BF00596694 https://doi.org/10.1007/BF01134623
1-(4,8-Dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-3-methylbutan-2-one	15559206	Click to see CC(C)C(=O)COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC	329.30	unknown	https://doi.org/10.1007/BF00563975
4-Methoxy-8-(3-methylbut-2-enoxy)furo[2,3-b]quinoline	85844455	Click to see CC(=CCOC1=CC=CC2=C1N=C3C(=C2OC)C=CO3)C	283.32	unknown	https://doi.org/10.1007/BF01134623 https://doi.org/10.1007/BF00567901
4,8-dimethoxy-9H-furo[2,3-b]quinolin-7-one	165368	Click to see COC1=C2C=CC(=O)C(=C2NC3=C1C=CO3)OC	245.23	unknown	https://doi.org/10.1007/BF00630180 https://doi.org/10.1007/BF02323307
7-[[(2R)-3,3-dimethyloxiran-2-yl]methoxy]-4,8-dimethoxyfuro[2,3-b]quinoline	23629251	Click to see CC1(C(O1)COC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)C	329.30	unknown	https://doi.org/10.1007/BF00714932
7-[[(2S)-3,3-dimethyloxiran-2-yl]methoxy]-4,8-dimethoxyfuro[2,3-b]quinoline	163035693	Click to see CC1(C(O1)COC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)C	329.30	unknown	https://doi.org/10.1007/BF00714932
7-Isopentenyloxy-gamma-fagarine	12110169	Click to see CC(=CCOC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)C	313.30	unknown	https://doi.org/10.1007/BF01134623 https://doi.org/10.1007/BF00567894
Anhydroevoxine	161441	Click to see CC1(C(O1)COC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)C	329.30	unknown	https://doi.org/10.1007/BF00630180 https://doi.org/10.1007/BF00714932
Dictamnine	68085	Click to see COC1=C2C=COC2=NC3=CC=CC=C31	199.20	unknown	https://doi.org/10.1007/BF00596694 https://doi.org/10.1007/BF00630180
Evodine	398789	Click to see CC(=C)C(COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)O	329.30	unknown	https://doi.org/10.1007/BF01134623 https://doi.org/10.1007/BF00630180 https://doi.org/10.1007/BF00563975
Evolitrine	196980	Click to see COC1=CC2=C(C=C1)C(=C3C=COC3=N2)OC	229.23	unknown	https://doi.org/10.1007/BF00630180
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/10.1007/BF00630180 https://doi.org/10.1007/BF00714932 https://doi.org/10.1016/S0031-9422(01)00188-1 https://doi.org/10.1007/BF00579795 https://doi.org/10.1007/BF00567798 https://doi.org/10.1007/BF00568641 https://doi.org/10.1007/BF00596694 https://doi.org/10.1007/BF01134623
Haplopine	5281846	Click to see COC1=C2C=COC2=NC3=C1C=CC(=C3OC)O	245.23	unknown	https://doi.org/10.1007/BF00566989 https://doi.org/10.1007/BF00630180 https://doi.org/10.1007/BF02323307
Methylevoxine	3569287	Click to see CC(C)(C(COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)O)OC	361.40	unknown	https://doi.org/10.1007/BF00630180 https://doi.org/10.1007/BF00567798 https://doi.org/10.1007/BF00714932 https://doi.org/10.1007/BF00570710
Robustine	164950	Click to see COC1=C2C=COC2=NC3=C1C=CC=C3O	215.20	unknown	https://doi.org/10.1007/BF00630180
Skimmianine	6760	Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC	259.26	unknown	https://doi.org/10.1007/BF00567972 https://doi.org/10.1007/BF00579795 https://doi.org/10.1007/BF01134623 https://doi.org/10.1007/BF00597580 https://doi.org/10.1007/BF02323307 https://doi.org/10.1007/BF00596694 https://doi.org/10.1007/BF00563344 https://doi.org/10.1007/BF00630180 https://doi.org/10.1007/BF00714932 https://doi.org/10.1007/BF00567798
> Organoheterocyclic compounds / Quinolines and derivatives / Hydroquinolines
2-n-Nonadienyl-4-quinolone	129820298	Click to see CCCCCC=CC=CC1=NC2=CC=CC=C2C(=O)C1	267.40	unknown	https://doi.org/10.1007/BF00568641
2-Nonyl-4-quinolone	126421925	Click to see CCCCCCCCCC1=NC2=CC=CC=C2C(=O)C1	271.40	unknown	https://doi.org/10.1007/BF00568641
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
2-(7-hydroxynona-3,5-dienyl)-1H-quinolin-4-one	163021249	Click to see CCC(C=CC=CCCC1=CC(=O)C2=CC=CC=C2N1)O	283.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004
2-(Hept-4-enyl)-1,4-dihydroquinolin-4-one	54120998	Click to see CCC=CCCCC1=CC(=O)C2=CC=CC=C2N1	241.33	unknown	https://doi.org/10.1007/BF00563344 https://doi.org/10.1007/BF00567972 https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004 https://doi.org/10.1007/BF00568641
2-[(3S,4E,6E)-3-hydroxynona-4,6-dienyl]-1H-quinolin-4-one	163067728	Click to see CCC=CC=CC(CCC1=CC(=O)C2=CC=CC=C2N1)O	283.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004
2-[(3S,4E,6Z)-3-hydroxynona-4,6-dienyl]-1H-quinolin-4-one	163067727	Click to see CCC=CC=CC(CCC1=CC(=O)C2=CC=CC=C2N1)O	283.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004
2-[(3Z,5E,7R)-7-hydroxynona-3,5-dienyl]-1H-quinolin-4-one	163185871	Click to see CCC(C=CC=CCCC1=CC(=O)C2=CC=CC=C2N1)O	283.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004
2-[(3Z,5Z,7S)-7-hydroxynona-3,5-dienyl]-1H-quinolin-4-one	163021250	Click to see CCC(C=CC=CCCC1=CC(=O)C2=CC=CC=C2N1)O	283.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004
2-[(3Z,6Z)-nona-3,6-dienyl]-1H-quinolin-4-one	44205807	Click to see CCC=CCC=CCCC1=CC(=O)C2=CC=CC=C2N1	267.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004
2-[(4E,6Z)-3-oxonona-4,6-dienyl]-1H-quinolin-4-one	101480812	Click to see CCC=CC=CC(=O)CCC1=CC(=O)C2=CC=CC=C2N1	281.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004
2-[(E)-hept-4-enyl]-1H-quinolin-4-one	19774525	Click to see CCC=CCCCC1=CC(=O)C2=CC=CC=C2N1	241.33	unknown	https://doi.org/10.1007/BF00563344 https://doi.org/10.1007/BF00567972
2-[(Z)-non-3-enyl]-1H-quinolin-4-one	101480813	Click to see CCCCCC=CCCC1=CC(=O)C2=CC=CC=C2N1	269.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004
2-nona-3,6-dienyl-1H-quinolin-4-one	54488188	Click to see CCC=CCC=CCCC1=CC(=O)C2=CC=CC=C2N1	267.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004
2-Nonylquinolin-4(1h)-One	9856730	Click to see CCCCCCCCCC1=CC(=O)C2=CC=CC=C2N1	271.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004
3-(2',3'-dihydroxy-3'-hydroxymethylbutyl)-4-methoxy-N-methylquinolin-2-one	129819729	Click to see CC(CO)(C(CC1=C(C2=CC=CC=C2N(C1=O)C)OC)O)O	307.34	unknown	https://doi.org/10.1007/BF00597580 https://doi.org/10.1007/BF00630180
4-(3-Methylbut-2-enoxy)quinolin-2-ol	21770009	Click to see CC(=CCOC1=CC(=O)NC2=CC=CC=C21)C	229.27	unknown	https://doi.org/10.1007/BF00599289
Acutine	163184322	Click to see CCC=CCCCC1=CC(=O)C2=CC=CC=C2N1	241.33	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroxyquinolones
3-Ethyl-7-hydroxy-4,8-dimethoxyquinolin-2-one	20975239	Click to see CCC1=C(C2=C(C(=C(C=C2)O)OC)NC1=O)OC	249.26	unknown	https://doi.org/10.1007/BF00630180
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
2,2,9-trimethyl-6H-pyrano[3,2-c]quinolin-5-one	162938070	Click to see CC1=CC2=C(C=C1)NC(=O)C3=C2OC(C=C3)(C)C	241.28	unknown	https://doi.org/10.1007/BF00599289
9-methoxy-2,2-dimethyl-4,6-dihydro-3H-pyrano[3,2-c]quinolin-5-one	13680805	Click to see CC1(CCC2=C(O1)C3=C(C=CC(=C3)OC)NC2=O)C	259.30	unknown	https://doi.org/10.1007/BF02323293 https://doi.org/10.1016/0031-9422(88)80170-5
Flindersine	68230	Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3NC2=O)C	227.26	unknown	https://doi.org/10.1007/BF00563653 https://doi.org/10.1007/BF00630180 https://doi.org/10.1007/BF02323307 https://doi.org/10.1007/BF00714932 https://doi.org/10.1016/S0031-9422(01)00188-1 https://doi.org/10.1007/BF00579795 https://doi.org/10.1007/BF00567798
Haplamine	648601	Click to see CC1(C=CC2=C(O1)C3=C(C=CC(=C3)OC)NC2=O)C	257.28	unknown	https://doi.org/10.1007/BF00579795 https://doi.org/10.1007/BF00568641 https://doi.org/10.1016/0031-9422(88)80170-5 https://doi.org/10.1007/BF00714932 https://doi.org/10.1055/S-2008-1081298 https://doi.org/10.1007/BF00630180 https://doi.org/10.1007/BF00568265 https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004 https://doi.org/10.1007/BF00567798 https://doi.org/10.1007/BF00597580 https://doi.org/10.1007/BF02323307 https://doi.org/10.1007/BF00568495
haplophytin A	12968471	Click to see CC1(C=CC2=C(O1)C3=C(C=CC=C3OC)NC2=O)C	257.28	unknown	https://doi.org/10.1016/S0031-9422(01)00188-1
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1007/BF00579795
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
[(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-methyl-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(6-methoxy-2-oxochromen-7-yl)oxyoxan-2-yl]methoxy]oxan-3-yl] acetate	162903603	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C4C=CC(=O)OC4=C3)OC)O)O)O)O)O)OC(=O)C	542.50	unknown	https://doi.org/10.1007/BF00574243
[(2S,3R,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(6-methoxy-2-oxochromen-7-yl)oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate	162989693	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C=C4C=CC(=O)OC4=C3)OC)CO)O)O)O)O)OC(=O)C	542.50	unknown	https://doi.org/10.1007/BF00574368
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-(6-methoxy-2-oxochromen-7-yl)oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] acetate	21607626	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C4C=CC(=O)OC4=C3)OC)OC(=O)C)O)O)O)O)O	542.50	unknown	https://doi.org/10.1007/BF00574243
[4,5-Dihydroxy-2-methyl-6-[[3,4,5-trihydroxy-6-(6-methoxy-2-oxochromen-7-yl)oxyoxan-2-yl]methoxy]oxan-3-yl] acetate	24208683	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C4C=CC(=O)OC4=C3)OC)O)O)O)O)O)OC(=O)C	542.50	unknown	https://doi.org/10.1007/BF00574243
[6-[4,5-Dihydroxy-6-(hydroxymethyl)-2-(6-methoxy-2-oxochromen-7-yl)oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate	162989692	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C=C4C=CC(=O)OC4=C3)OC)CO)O)O)O)O)OC(=O)C	542.50	unknown	https://doi.org/10.1007/BF00574368
6-methoxy-2-oxo-2H-chromen-7-yl 2-O-acetyl-6-O-(6-deoxyhexopyranosyl)hexopyranoside	5069226	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C4C=CC(=O)OC4=C3)OC)OC(=O)C)O)O)O)O)O	542.50	unknown	https://doi.org/10.1007/BF00574243
6-Methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	346340	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	354.31	unknown	https://doi.org/10.1007/BF00638768
6-Methoxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-2-one	20106091	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C4C=CC(=O)OC4=C3)OC)O)O)O)O)O)O	500.40	unknown	https://doi.org/10.1007/BF00574243
7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6-methoxychromen-2-one	21607627	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C=C4C=CC(=O)OC4=C3)OC)CO)O)O)O)O)O	500.40	unknown	https://doi.org/10.1007/BF00638768 https://doi.org/10.1007/BF00574243
7-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-6-methoxychromen-2-one	24208684	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C=C4C=CC(=O)OC4=C3)OC)CO)O)O)O)O)O	500.40	unknown	https://doi.org/10.1007/BF00638768 https://doi.org/10.1007/BF00574243
Haploperoside	21607625	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C4C=CC(=O)OC4=C3)OC)O)O)O)O)O)O	500.40	unknown	https://doi.org/10.1007/BF00574243
Haploperoside A	133562493	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C4C=CC(=O)OC4=C3)OC)O)O)O)O)O)O	500.40	unknown	https://doi.org/10.1007/BF00638768 https://doi.org/10.1007/BF00574243
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	https://doi.org/10.1007/BF00638768
> 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	https://doi.org/10.1007/BF00638768
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Seselin	68229	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC(=O)C=C3)C	228.24	unknown	https://doi.org/10.1007/BF00596694
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Haplogenin	15907673	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O	332.26	unknown	https://doi.org/10.1007/BF00600852
Limocitrin	5489485	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)O)O	346.30	unknown	https://doi.org/10.1007/BF00600852
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-3,4-dihydroxy-6-[3,5,8-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl acetate	23265669	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C(=C(O4)C5=CC(=C(C=C5)O)OC)O)O)COC(=O)C)O)O)O)O)O	682.60	unknown	https://doi.org/10.1007/BF00574368
[(2R,3S,4S,5R,6S)-6-[3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	163188978	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C(=C2)O)C(=O)C(=C(O3)C4=CC(=C(C=C4)O)OC)O)OC)O)O)O	550.50	unknown	https://doi.org/10.1007/BF00714907
[3,4-Dihydroxy-6-[3,5,8-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl acetate	20106108	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C(=C(O4)C5=CC(=C(C=C5)O)OC)O)O)COC(=O)C)O)O)O)O)O	682.60	unknown	https://doi.org/10.1007/BF00574368
[3,4,5-Trihydroxy-6-[3,5,8-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl acetate	13800328	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C(=C2)O)C(=O)C(=C(O3)C4=CC(=C(C=C4)O)OC)O)O)O)O)O	536.40	unknown	https://doi.org/10.1007/BF00567281
[6-[3,5-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-4-oxochromen-7-yl]oxy-3,4-dihydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl acetate	20106107	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C(=C(O4)C5=CC(=C(C=C5)O)OC)O)OC)COC(=O)C)O)O)O)O)O	696.60	unknown	https://doi.org/10.1007/BF00602459
7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxychromen-4-one	102402394	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C(=C(O4)C5=CC(=C(C=C5)O)OC)O)OC)CO)O)O)O)O)O	654.60	unknown	https://doi.org/10.1007/BF00714907
7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,5,8-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one	163024983	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C(=C(O4)C5=CC(=C(C=C5)O)OC)O)O)CO)O)O)O)O)O	640.50	unknown	https://doi.org/10.1007/BF00714927
7-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxychromen-4-one	74978554	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C(=C(O4)C5=CC(=C(C=C5)O)OC)O)OC)CO)O)O)O)O)O	654.60	unknown	https://doi.org/10.1007/BF00714907
7-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,5,8-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one	74978551	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C(=C(O4)C5=CC(=C(C=C5)O)OC)O)O)CO)O)O)O)O)O	640.50	unknown	https://doi.org/10.1007/BF00714927
Haploside A	44260012	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C(=C2)O)C(=O)C(=C(O3)C4=CC(=C(C=C4)O)OC)O)O)O)O)O	536.40	unknown	https://doi.org/10.1007/BF00567281
Haploside C	44260015	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C(=C(O4)C5=CC(=C(C=C5)O)OC)O)OC)COC(=O)C)O)O)O)O)O	696.60	unknown	https://doi.org/10.1007/BF00602459
Haploside D	44260013	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C(=C(O4)C5=CC(=C(C=C5)O)OC)O)O)COC(=O)C)O)O)O)O)O	682.60	unknown	https://doi.org/10.1007/BF00568508
Haploside F	44260005	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C(=C(O4)C5=CC(=C(C=C5)O)OC)O)O)CO)O)O)O)O)O	640.50	unknown	https://doi.org/10.1007/BF00714927
Jexckogbyylxkd-vzrbyoqmsa-	13800329	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C(=C2)O)C(=O)C(=C(O3)C4=CC(=C(C=C4)O)OC)O)O)O)O)O	536.40	unknown	https://doi.org/10.1007/BF00567281
Limocitrin 7-(6''-acetylglucoside)	44260014	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C(=C2)O)C(=O)C(=C(O3)C4=CC(=C(C=C4)O)OC)O)OC)O)O)O	550.50	unknown	https://doi.org/10.1007/BF00714907
> Phenylpropanoids and polyketides / Stilbenes
(4-Oxo-7-phenacyl-2-propan-2-ylchromen-5-yl) acetate	72702043	Click to see CC(C)C1=CC(=O)C2=C(O1)C=C(C=C2OC(=O)C)CC(=O)C3=CC=CC=C3	364.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.05.004

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Haplophyllum acutifolium

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