Scientific name	Authority	First published in
Cudrania tricuspidata	Bureau ex Lavallée	Énum. Arbres : 243 (1877)
Cudrania triloba	Hance	J. Bot. 6: 49 (1868)
Cudranus triloba	Hance	J. Bot. 6(62): 49–50 1868
Vanieria tricuspidata	Hu	J. Arnold Arbor. 5: 228 (1924)
Vanieria triloba	(Hance) Satake	J. Fac. Sci. Univ. Tokyo, Sect. 3, Bot. 3: 497 (1931)
Morus integrifolia	H.Lév. & Vaniot	Bull. Acad. Int. Géogr. Bot. 17(210-211): iii (1907)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Azerbaijani	Üçdişli kudraniya
German	seidenraupenbaum
Persian	ماکلورا تریکوسپیداتا
Croatian	kineski dud
Armenian	կուդրանիա եռատամնավոր
lzh	柘
Russian	Кудрания триостренная
Vietnamese	dâu gai
Vietnamese	chá
Vietnamese	cây bớm
Vietnamese	gai mang
Vietnamese	hoàng lồ ba mũi
Vietnamese	mỏ quạ ba mũi
Vietnamese	sọng vàng
Vietnamese	vàng lồ ba mũi
Vietnamese	xuyên phá thạch
za	gooenciq
Chinese	一种维管植物
Chinese	穿破石
Chinese	柘樹
Chinese	黄桑
Chinese	灰桑
Chinese	如柘
Chinese	柘树茎叶
Chinese	柘树果实
Chinese	柘树
Chinese	柘木白皮
Chinese	柘木
Chinese	柘(拓）
Chinese	拓树
Chinese	奴柘刺
Chinese	山荔枝果
Chinese	奴拓刺
Chinese	柘

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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
  - Korea

Asia-tropical click to expand
- Indo-China
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001085025
UNII	QOE5U8M2TG
Tropicos	21302135
KEW	urn:lsid:ipni.org:names:854453-1
The Plant List	tro-21302135
Open Tree Of Life	828247
NCBI Taxonomy	210328
IUCN Red List	135925696
IPNI	854453-1
iNaturalist	743229
GBIF	3764024
Freebase	/m/06dtzf
EPPO	MACTR
EOL	488084
USDA GRIN	23062
Wikipedia	Maclura_tricuspidata
CMAUP	NPO30804

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

Prenylated Flavonoids of the Moraceae Family: A Comprehensive Review of Their Biological Activities

Morante-Carriel J, Živković S, Nájera H, Sellés-Marchart S, Martínez-Márquez A, Martínez-Esteso MJ, Obrebska A, Samper-Herrero A, Bru-Martínez R

Plants (Basel)

27-Apr-2024

PMCID:	PMC11085352
doi:	10.3390/plants13091211
PMID:	38732426

Microbiome and cancer: from mechanistic implications in disease progression and treatment to development of novel antitumoral strategies

Constantin M, Chifiriuc MC, Mihaescu G, Corcionivoschi N, Burlibasa L, Bleotu C, Tudorache S, Mitache MM, Filip R, Munteanu SG, Gradisteanu Pircalabioru G

Front Immunol

23-Apr-2024

PMCID:	PMC11074409
doi:	10.3389/fimmu.2024.1373504
PMID:	38715617

A Review of the Use of Native and Engineered Probiotics for Colorectal Cancer Therapy

Han H, Zhang Y, Tang H, Zhou T, Khan A

Int J Mol Sci

31-Mar-2024

PMCID:	PMC11011422
doi:	10.3390/ijms25073896
PMID:	38612706

Quadrat soil pollen signal reflects plant important values in forests and shrublands from subtropical China

Li K, Tan B, Liao M, Ni J

Front Plant Sci

20-Mar-2024

PMCID:	PMC10987713
doi:	10.3389/fpls.2024.1348182
PMID:	38571712

Structures and Biological Activities of Secondary Metabolites from Xylaria spp.

Chen W, Yu M, Chen S, Gong T, Xie L, Liu J, Bian C, Huang G, Zheng C

J Fungi (Basel)

29-Feb-2024

PMCID:	PMC10971283
doi:	10.3390/jof10030190
PMID:	38535199

Long-Term Tracking of the Effects of Colostrum-Derived Lacticaseibacillus rhamnosus Probio-M9 on Gut Microbiota in Mice with Colitis-Associated Tumorigenesis

Zhao F, Hiraishi K, Li X, Hu Y, Kojima D, Sun Z, Zhang H, Kurahara LH

Biomedicines

27-Feb-2024

PMCID:	PMC10967742
doi:	10.3390/biomedicines12030531
PMID:	38540144

Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China

Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X

J Ethnobiol Ethnomed

23-Feb-2024

PMCID:	PMC10893717
doi:	10.1186/s13002-024-00656-1
PMID:	38395900

Interactions Between the Ubiquitin–Proteasome System, Nrf2, and the Cannabinoidome as Protective Strategies to Combat Neurodegeneration: Review on Experimental Evidence

Monsalvo-Maraver LA, Ovalle-Noguez EA, Nava-Osorio J, Maya-López M, Rangel-López E, Túnez I, Tinkov AA, Tizabi Y, Aschner M, Santamaría A

Neurotox Res

23-Feb-2024

PMCID:	PMC10891226
doi:	10.1007/s12640-024-00694-3
PMID:	38393521

Morin ameliorates myocardial injury in diabetic rats via modulation of inflammatory pathways

Verma VK, Malik S, Mutneja E, Sahu AK, Prajapati V, Mishra P, Bhatia J, Arya DS

Lab Anim Res

09-Feb-2024

PMCID:	PMC10854036
doi:	10.1186/s42826-024-00190-x
PMID:	38331877

Molecular Mechanism of Natural Food Antioxidants to Regulate ROS in Treating Cancer: A Review

Muchtaridi M, Az-Zahra F, Wongso H, Setyawati LU, Novitasari D, Ikram EH

Antioxidants (Basel)

06-Feb-2024

PMCID:	PMC10885946
doi:	10.3390/antiox13020207
PMID:	38397805

Proteolytic Activity of Silkworm Thorn (Cudrania tricuspidata) Fruit for Enzymatic Hydrolysis of Food Proteins

Yang NE, Lee DH, Hwang J, Son WY, Kim KS, Kim GY, Kim HW

Molecules

02-Feb-2024

PMCID:	PMC10856028
doi:	10.3390/molecules29030693
PMID:	38338437

Molecular Characterization of an Isolate of Bean Common Mosaic Virus First Identified in Gardenia Using Metatranscriptome and Small RNA Sequencing

Xu ZT, Weng HT, Chen JP, Zhang CX, Li JM, Li YY

Plant Pathol J

01-Feb-2024

PMCID:	PMC10850531
doi:	10.5423/PPJ.OA.11.2023.0163
PMID:	38326960

Integration of Physiological, Transcriptomic, and Metabolomic Analyses Reveal Molecular Mechanisms of Salt Stress in Maclura tricuspidata

Sui D, Wang B, El-Kassaby YA, Wang L

Plants (Basel)

29-Jan-2024

PMCID:	PMC10857159
doi:	10.3390/plants13030397
PMID:	38337930

Overcoming cancer risk in inflammatory bowel disease: new insights into preventive strategies and pathogenesis mechanisms including interactions of immune cells, cancer signaling pathways, and gut microbiota

Zhang H, Shi Y, Lin C, He C, Wang S, Li Q, Sun Y, Li M

Front Immunol

15-Jan-2024

PMCID:	PMC10822953
doi:	10.3389/fimmu.2023.1338918
PMID:	38288125

Ferroptosis, a Regulated Form of Cell Death, as a Target for the Development of Novel Drugs Preventing Ischemia/Reperfusion of Cardiac Injury, Cardiomyopathy and Stress-Induced Cardiac Injury

Ryabov VV, Maslov LN, Vyshlov EV, Mukhomedzyanov AV, Kilin M, Gusakova SV, Gombozhapova AE, Panteleev OO

Int J Mol Sci

11-Jan-2024

PMCID:	PMC10815150
doi:	10.3390/ijms25020897
PMID:	38255971

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzophenones
(7,8-Dihydroxy-2,2-dimethylchromen-6-yl)-(3-hydroxyphenyl)methanone	118722303	Click to see CC1(C=CC2=CC(=C(C(=C2O1)O)O)C(=O)C3=CC(=CC=C3)O)C	312.30	unknown	https://doi.org/10.1021/NP5002797
[2,3-dihydroxy-4-methoxy-5-[(E)-3-methylbut-1-enyl]phenyl]-(3-hydroxyphenyl)methanone	118722302	Click to see CC(C)C=CC1=CC(=C(C(=C1OC)O)O)C(=O)C2=CC(=CC=C2)O	328.40	unknown	https://doi.org/10.1021/NP5002797
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl 14-oxooctadecanoate	13991164	Click to see CCCCC(=O)CCCCCCCCCCCCC(=O)OC	312.50	unknown	https://doi.org/10.1016/J.BMCL.2009.07.098 https://doi.org/10.1271/BBB.70.427
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxychromone	5281343	Click to see C1=COC2=CC(=CC(=C2C1=O)O)O	178.14	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
5-Hydroxy-2,2-dimethylpyrano[3,2-g]chromen-6-one	13545810	Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=CO3)C	244.24	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(2S)-4,8,9-trihydroxy-2,3,3-trimethyl-2H-furo[3,2-b]xanthen-5-one	163040074	Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)(C)C	328.30	unknown	https://doi.org/10.1016/J.BMC.2004.01.030
1-Hydroxy-3,6,7-trimethoxyxanthen-9-one	5318373	Click to see COC1=CC(=C2C(=C1)OC3=CC(=C(C=C3C2=O)OC)OC)O	302.28	unknown	https://doi.org/10.1016/J.BMC.2004.01.030
1,3-Dihydroxy-6,7-dimethoxyxanthen-9-one	69866203	Click to see COC1=C(C=C2C(=C1)C(=O)C3=C(C=C(C=C3O2)O)O)OC	288.25	unknown	https://doi.org/10.1021/NP5002797
2,6-Dihydroxyxanthone	14408256	Click to see C1=CC2=C(C=C1O)OC3=C(C2=O)C=C(C=C3)O	228.20	unknown	https://doi.org/10.1021/NP5002797
5,9,10-trihydroxy-1,1,2-trimethyl-2H-furo[2,3-c]xanthen-6-one	10336602	Click to see CC1C(C2=C(O1)C=C(C3=C2OC4=C(C3=O)C=CC(=C4O)O)O)(C)C	328.30	unknown	https://doi.org/10.1021/NP5002797
6,7-dihydroxy-3-methoxy-2-(2-methylbut-3-en-2-yl)-4-[(E)-3-methylbut-1-enyl]xanthen-9-one	118722298	Click to see CC(C)C=CC1=C2C(=CC(=C1OC)C(C)(C)C=C)C(=O)C3=CC(=C(C=C3O2)O)O	394.50	unknown	https://doi.org/10.1021/NP5002797
Cudratricusxanthone L	16757392	Click to see CC(C)(C=C)C1=C(C=C(C2=C1OC3=CC(=C(C=C3C2=O)O)O)O)O	328.30	unknown	https://doi.org/10.1021/NP070059K
isocudraniaxanthone A	10687703	Click to see CC(C)(C=C)C1=C(C=C(C2=C1OC3=C(C2=O)C=CC(=C3O)O)O)O	328.30	unknown	via CMAUP database
isocudraniaxanthone B	10831150	Click to see CC(C)(C=C)C1=C(C=C(C2=C1OC3=C(C2=O)C=CC(=C3O)O)O)OC	342.30	unknown	https://doi.org/10.1016/J.BMCL.2006.08.032 https://doi.org/10.1021/NP5002797 https://doi.org/10.1016/J.BMCL.2005.08.099
Toxyloxanthone C	5495919	Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)(C)C	328.30	unknown	https://doi.org/10.1016/J.BMC.2004.01.030
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
1,3,6-Trihydroxy-5-methoxy-2-(2-methylbut-3-en-2-yl)-7-(3-methylbut-2-enyl)xanthen-9-one	141497209	Click to see CC(=CCC1=CC2=C(C(=C1O)OC)OC3=C(C2=O)C(=C(C(=C3)O)C(C)(C)C=C)O)C	410.50	unknown	https://doi.org/10.1055/S-2006-960993
1,3,6-Trihydroxy-5-methoxy-2,7-bis(3-methylbut-2-enyl)xanthen-9-one	10024541	Click to see CC(=CCC1=CC2=C(C(=C1O)OC)OC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)C	410.50	unknown	https://doi.org/10.1055/S-2006-960993
1,5,6-trihydroxy-6',6'-dimethyl-2H-pyrano(2',3':3,4)-2-(3-methylbut-2-enyl)xanthone	16743994	Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(O3)C(=C(C=C4)O)O)C=CC(O2)(C)C)C	394.40	unknown	https://doi.org/10.1016/J.BMC.2004.01.030
Cudratricuxanthone	25028556	Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=CC(=C(C=C4O3)O)O)C=CC(O2)(C)C)C	394.40	unknown	https://doi.org/10.1016/J.BMC.2004.01.030
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
(2R)-7,8-dihydroxy-4-methoxy-2,3,3-trimethyl-5-(3-methylbut-2-enyl)-2H-furo[2,3-a]xanthen-11-one	118722300	Click to see CC1C(C2=C(C(=C3C(=C2O1)C(=O)C4=C(O3)C(=C(C=C4)O)O)CC=C(C)C)OC)(C)C	410.50	unknown	https://doi.org/10.1021/NP5002797
(2S)-4,7,8-trihydroxy-2,3,3-trimethyl-11-(3-methylbut-2-enyl)-2H-furo[3,2-b]xanthen-5-one	163040280	Click to see CC1C(C2=C(O1)C(=C3C(=C2O)C(=O)C4=CC(=C(C=C4O3)O)O)CC=C(C)C)(C)C	396.40	unknown	https://doi.org/10.1016/J.BMCL.2007.10.007 https://doi.org/10.1016/J.BMC.2004.01.030
(2S)-4,7,8-trihydroxy-2,3,3-trimethyl-9-(3-methylbut-2-enyl)-2H-furo[3,2-b]xanthen-5-one	162978302	Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=CC(=C(C(=C4O3)CC=C(C)C)O)O)(C)C	396.40	unknown	https://doi.org/10.1016/J.BMCL.2007.10.007 https://doi.org/10.1016/J.BMCL.2005.08.099 https://doi.org/10.1016/J.BMC.2004.01.030
(2S)-8,9-dihydroxy-4-methoxy-2,3,3-trimethyl-5-(3-methylbut-2-enyl)-2H-furo[2,3-a]xanthen-11-one	118722301	Click to see CC1C(C2=C(C(=C3C(=C2O1)C(=O)C4=CC(=C(C=C4O3)O)O)CC=C(C)C)OC)(C)C	410.50	unknown	https://doi.org/10.1021/NP5002797
1,3,5-Trihydroxy-4-(3-methylbut-2-en-1-yl)-9H-xanthen-9-one	10335672	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C(=CC=C3)O)C	312.30	unknown	https://doi.org/10.1021/NP5002797
1,6,7-Trihydroxy-3-(3-methylbut-2-enoxy)-4-(3-methylbut-2-enyl)xanthen-9-one	10475843	Click to see CC(=CCC1=C(C=C(C2=C1OC3=CC(=C(C=C3C2=O)O)O)O)OCC=C(C)C)C	396.40	unknown	https://doi.org/10.1016/J.BMC.2004.01.030
4-(2,4-dimethylpent-3-en-2-yl)-1,6,7-trihydroxy-3-methyl-9H-xanthen-9-one	44419437	Click to see CC1=CC(=C2C(=C1C(C)(C)C=C(C)C)OC3=CC(=C(C=C3C2=O)O)O)O	354.40	unknown	https://doi.org/10.1016/J.BMCL.2006.08.032
4,7,8-trihydroxy-2,3,3-trimethyl-11-(3-methylbut-2-enyl)-2H-furo[3,2-b]xanthen-5-one	25028557	Click to see CC1C(C2=C(O1)C(=C3C(=C2O)C(=O)C4=CC(=C(C=C4O3)O)O)CC=C(C)C)(C)C	396.40	unknown	https://doi.org/10.1016/J.BMCL.2007.10.007 https://doi.org/10.1016/J.BMC.2004.01.030
8,10-Dihydroxy-2-(2-hydroxypropan-2-yl)-7-(3-methylbut-2-enyl)-1,2-dihydrofuro[3,2-a]xanthen-11-one	21591069	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C=CC4=C3CC(O4)C(C)(C)O)C	396.40	unknown	https://doi.org/10.1055/S-2006-961016
Cudratricusxanthone E	49799569	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)O)O)CC=C(C)C)O)C	396.40	unknown	https://doi.org/10.1016/J.BMC.2004.01.030
Cudratricusxanthone K	16757289	Click to see CC(=CCC1=C(C2=C(C(=C1OC)CC=C(C)C)OC3=CC(=C(C=C3C2=O)O)O)O)C	410.50	unknown	https://doi.org/10.1021/NP070059K https://doi.org/10.1021/NP5002797
Cudraxanthone G	42645953	Click to see CC(=CCC1=C(C2=C(C(=C1OC)CC=C(C)C)OC3=C(C2=O)C=CC=C3O)O)C	394.50	unknown	https://doi.org/10.1055/S-2006-960993
Cudraxanthone L	11486277	Click to see CC(=CCC1=C2C(=CC(=C1O)O)C(=O)C3=C(O2)C=C(C(=C3O)C(C)(C)C=C)O)C	396.40	unknown	https://doi.org/10.1055/S-2006-960059 https://doi.org/10.1016/J.BMCL.2006.08.032 https://doi.org/10.1021/NP070059K https://doi.org/10.1016/J.BMCL.2007.10.007 https://doi.org/10.1016/J.BMCL.2005.08.099 https://doi.org/10.1021/NP030481A
cudraxanthone M	11689770	Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=CC(=C(C(=C4O3)CC=C(C)C)O)O)(C)C	396.40	unknown	https://doi.org/10.1055/S-2006-960059 https://doi.org/10.1016/J.BMCL.2006.08.032 https://doi.org/10.1016/J.BMCL.2007.10.007 https://doi.org/10.1016/J.BMCL.2005.08.099 https://doi.org/10.1021/NP5002797 https://doi.org/10.1016/J.BMC.2004.01.030
Macluraxanthone B	5353737	Click to see CC(=CCC1=C(C(=C(C2=C1OC3=CC(=C(C=C3C2=O)O)O)O)C(C)(C)C=C)O)C	396.40	unknown	https://doi.org/10.1016/J.BMCL.2006.08.032 https://doi.org/10.1016/J.BMCL.2007.10.007 https://doi.org/10.1021/NP5002797 https://doi.org/10.1016/J.BMCL.2005.08.099 https://doi.org/10.1021/NP030481A
Xanthone V1a	10023643	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C(=C(C=C3)O)O)CC=C(C)C)O)C	396.40	unknown	https://doi.org/10.1016/J.BMC.2004.01.030
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
(2R)-5,8,9-trihydroxy-1,1,2-trimethyl-7-(3-methylbut-2-enyl)-2H-furo[2,3-c]xanthen-6-one	162912989	Click to see CC1C(C2=C(O1)C=C(C3=C2OC4=C(C3=O)C(=C(C(=C4)O)O)CC=C(C)C)O)(C)C	396.40	unknown	https://doi.org/10.1021/NP070059K
(2S)-5,8,9-trihydroxy-7-(3-hydroxy-3-methylbutyl)-1,1,2-trimethyl-2H-furo[2,3-c]xanthen-6-one	162906590	Click to see CC1C(C2=C(O1)C=C(C3=C2OC4=C(C3=O)C(=C(C(=C4)O)O)CCC(C)(C)O)O)(C)C	414.40	unknown	https://doi.org/10.1016/J.BMC.2004.01.030
1,3,6,7-Tetrahydroxy-2-(2-methylbut-3-en-2-yl)-8-(3-methylbut-2-enyl)xanthen-9-one	44156959	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)C(C)(C)C=C)O)O)O)C	396.40	unknown	https://doi.org/10.1016/J.BMCL.2007.10.007
5,8,9-trihydroxy-7-(3-hydroxy-3-methylbutyl)-1,1,2-trimethyl-2H-furo[2,3-c]xanthen-6-one	162906589	Click to see CC1C(C2=C(O1)C=C(C3=C2OC4=C(C3=O)C(=C(C(=C4)O)O)CCC(C)(C)O)O)(C)C	414.40	unknown	https://doi.org/10.1016/J.BMC.2004.01.030
6,9-Dihydroxy-3,3-dimethyl-8-(3-methylbut-2-enyl)pyrano[2,3-c]xanthen-7-one	86276176	Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(O2)C4=C(C=C3O)OC(C=C4)(C)C)O)C	378.40	unknown	https://doi.org/10.1055/S-2006-961016
8-(2,3-Dihydroxy-3-methylbutyl)-6,9-dihydroxy-3,3-dimethylpyrano[2,3-c]xanthen-7-one	101612265	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C(=C(C=C4)O)CC(C(C)(C)O)O)O)C	412.40	unknown	https://doi.org/10.1055/S-2006-960059
cudratricusxanthone A	11153672	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C(=C(C=C3O)O)C(C)(C)C=C)O)O)C	396.40	unknown	https://doi.org/10.1248/BPB.30.805 https://doi.org/10.1021/NP070059K https://doi.org/10.1016/J.BMCL.2007.10.007 https://doi.org/10.1016/J.BMCL.2005.08.099 https://doi.org/10.1016/J.BMC.2004.01.030 https://doi.org/10.1021/NP030481A
Cudratricusxanthone B	25028799	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C=C(C(=C3CC=C(C)C)O)O)C	396.40	unknown	https://doi.org/10.1016/J.BMC.2004.01.030
Cudratricusxanthone J	16757393	Click to see CC1C(C2=C(O1)C=C(C3=C2OC4=C(C3=O)C(=C(C(=C4)O)O)CC=C(C)C)O)(C)C	396.40	unknown	https://doi.org/10.1021/NP070059K
Cudratricusxanthone M	16757394	Click to see CC(C)(CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C(=C(C=C3O)O)C(C)(C)C=C)O)O)O	414.40	unknown	https://doi.org/10.1021/NP070059K
Cudraxanthone C	44405862	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C(=C(C=C3O)O)C(C)(C)C=C)O)OC)C	410.50	unknown	https://doi.org/10.1016/J.BMCL.2006.08.032 https://doi.org/10.1021/NP070059K https://doi.org/10.1055/S-2007-969682 https://doi.org/10.1016/J.BMCL.2005.08.099 https://doi.org/10.1248/BPB.29.838 https://doi.org/10.3987/R-1983-02-0213
Cudraxanthone D	11611248	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C(=C(C=C3O)OC)C(C)(C)C=C)O)O)C	410.50	unknown	https://doi.org/10.1016/J.BMCL.2006.08.032 https://doi.org/10.1016/J.BMCL.2007.10.007 https://doi.org/10.1016/J.BMCL.2005.08.099 https://doi.org/10.1055/S-2007-969682
Gerontoxanthone H	11211194	Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)C	380.40	unknown	https://doi.org/10.1055/S-2006-961016 https://doi.org/10.1016/J.BMC.2004.01.030 https://doi.org/10.1021/NP5002797 https://doi.org/10.1248/BPB.29.838
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(7S)-10,21-dihydroxy-7,8,8,18,18-pentamethyl-2,6,19-trioxapentacyclo[11.8.0.03,11.05,9.015,20]henicosa-1(13),3,5(9),10,14,16,20-heptaen-12-one	163046372	Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C5C(=C4)C=CC(O5)(C)C)O)(C)C	394.40	unknown	https://doi.org/10.1248/BPB.29.838
(7S)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.03,11.05,9.014,19]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one	118722299	Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=CC(=C5C(=C4O3)C=CC(O5)(C)C)O)(C)C	394.40	unknown	https://doi.org/10.1021/NP5002797
11-Hydroxy-7,7,18,18-tetramethyl-2,8,19-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-1(14),3(12),4(9),5,10,15(20),16,21-octaen-13-one	14259061	Click to see CC1(C=CC2=C(O1)C=CC3=C2C(=O)C4=C(O3)C5=C(C=C4O)OC(C=C5)(C)C)C	376.40	unknown	https://doi.org/10.1055/S-2007-969682 https://doi.org/10.1021/NP5002797 https://doi.org/10.3987/R-1983-02-0213
21-Hydroxy-6-(2-hydroxypropan-2-yl)-17,17-dimethyl-7,12,18-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),3(11),4(8),9,14(19),15,20-heptaen-2-one	101616167	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=C(C=C4)OC(C5)C(C)(C)O)O)C	394.40	unknown	https://doi.org/10.1055/S-2006-960059
5,8,10-trihydroxy-3,3-dimethyl-11-(2-methylbut-3-en-2-yl)pyrano[2,3-c]xanthen-7(3H)-one	44405880	Click to see CC1(C=CC2=C3C(=CC(=C2O1)O)C(=O)C4=C(O3)C(=C(C=C4O)O)C(C)(C)C=C)C	394.40	unknown	https://doi.org/10.1016/J.BMCL.2006.08.032 https://doi.org/10.1016/J.BMCL.2007.10.007 https://doi.org/10.1016/J.BMCL.2005.08.099
5,9,11-Trihydroxy-3,3-dimethyl-10-(2-methylbut-3-en-2-yl)pyrano[3,2-a]xanthen-12-one	101589679	Click to see CC1(C=CC2=C(O1)C(=CC3=C2C(=O)C4=C(O3)C=C(C(=C4O)C(C)(C)C=C)O)O)C	394.40	unknown	https://doi.org/10.1055/S-2006-961016
Cudraxanthone B	91885224	Click to see CC1(C=CC2=C(O1)C(=CC3=C2C(=O)C4=C(O3)C(=C(C=C4O)O)C(C)(C)C=C)O)C	394.40	unknown	https://doi.org/10.1055/S-2007-969682 https://doi.org/10.1248/BPB.29.838 https://doi.org/10.3987/R-1983-02-0213
gerontoxanthone A	11948658	Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C5C(=C4)C=CC(O5)(C)C)O)(C)C	394.40	unknown	https://doi.org/10.1248/BPB.29.838
Isocudraxanthone K	44426653	Click to see CC1(C=CC2=C3C(=CC(=C2O1)O)C(=O)C4=C(O3)C=C(C(=C4O)C(C)(C)C=C)O)C	394.40	unknown	https://doi.org/10.1021/NP070059K https://doi.org/10.1248/BPB.29.838
Macluraxanthone	5281646	Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC4=C(C3=O)C=CC(=C4O)O)O)C	394.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	https://doi.org/10.3987/COM-90-5416
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2R,3R)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-8-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one	25209720	Click to see C1=CC(=CC=C1CC2=C3C(=C(C=C2O)O)C(=O)C(C(O3)C4=CC=C(C=C4)O)O)O	394.40	unknown	https://doi.org/10.1021/NP800418J
(2R,3S)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-8-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one	162886502	Click to see C1=CC(=CC=C1CC2=C3C(=C(C=C2O)O)C(=O)C(C(O3)C4=CC=C(C=C4)O)O)O	394.40	unknown	https://doi.org/10.1021/NP800418J
(2S,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one	162929005	Click to see C1=CC(=CC=C1CC2=C(C3=C(C=C2O)OC(C(C3=O)O)C4=CC(=C(C=C4)O)O)O)O	410.40	unknown	https://doi.org/10.1016/0031-9422(95)00609-5
(2S,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-8-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one	163031736	Click to see C1=CC(=CC=C1CC2=C3C(=C(C=C2O)O)C(=O)C(C(O3)C4=CC(=C(C=C4)O)O)O)O	410.40	unknown	https://doi.org/10.1016/0031-9422(95)00609-5
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-6-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one	10069197	Click to see C1=CC(=CC=C1CC2=C(C3=C(C=C2O)OC(C(C3=O)O)C4=CC=C(C=C4)O)O)O	394.40	unknown	https://doi.org/10.1021/NP800418J https://doi.org/10.1248/BPB.29.838
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-8-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one	56677660	Click to see C1=CC(=CC=C1CC2=C3C(=C(C=C2O)O)C(=O)C(C(O3)C4=CC=C(C=C4)O)O)O	394.40	unknown	https://doi.org/10.1021/NP800418J
Gericudranin E	44559902	Click to see C1=CC(=CC=C1CC2=C(C3=C(C=C2O)OC(C(C3=O)O)C4=CC=C(C=C4)O)O)O	394.40	unknown	https://doi.org/10.1021/NP800418J https://doi.org/10.1248/BPB.29.838
Gericudranins B	42608135	Click to see C1=CC(=CC=C1CC2=C3C(=C(C=C2O)O)C(=O)C(C(O3)C4=CC(=C(C=C4)O)O)O)O	410.40	unknown	https://doi.org/10.1016/0031-9422(95)00609-5
Gericudranins C	10364206	Click to see C1=CC(=CC=C1CC2=C(C3=C(C=C2O)OC(C(C3=O)O)C4=CC(=C(C=C4)O)O)O)O	410.40	unknown	https://doi.org/10.1016/0031-9422(95)00609-5
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(2S,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-6,8-bis[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one	10839588	Click to see C1=CC(=CC=C1CC2=C(C(=C3C(=C2O)C(=O)C(C(O3)C4=CC(=C(C=C4)O)O)O)CC5=CC=C(C=C5)O)O)O	516.50	unknown	https://doi.org/10.1016/0031-9422(95)00609-5
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one	10097497	Click to see C1=CC(=CC=C1CC2=C(C(=C3C(=C2O)C(=O)C(C(O3)C4=CC=C(C=C4)O)O)CC5=CC=C(C=C5)O)O)O	500.50	unknown	https://doi.org/10.1021/NP800418J
gericudranin D	44559901	Click to see C1=CC(=CC=C1CC2=C(C(=C3C(=C2O)C(=O)C(C(O3)C4=CC=C(C=C4)O)O)CC5=CC=C(C=C5)O)O)O	500.50	unknown	https://doi.org/10.1021/NP800418J https://doi.org/10.1021/NP50124A024
Gericudranins A	10436583	Click to see C1=CC(=CC=C1CC2=C(C(=C3C(=C2O)C(=O)C(C(O3)C4=CC(=C(C=C4)O)O)O)CC5=CC=C(C=C5)O)O)O	516.50	unknown	https://doi.org/10.1016/0031-9422(95)00609-5
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(S)-2-(2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)chroman-4-one	44419446	Click to see CC(=CCC1=CC(=C(C=C1O)O)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)C	424.50	unknown	https://doi.org/10.1016/J.BMCL.2006.08.032 https://doi.org/10.1016/J.BMCL.2015.07.017 https://doi.org/10.1016/J.BMCL.2009.07.098 https://doi.org/10.1271/BBB.70.427
(S)-2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-en-1-yl)chroman-4-one	102004723	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C	356.40	unknown	https://doi.org/10.1021/NP070059K
5,7-Dihydroxy-2-(7-hydroxy-2,2-dimethylchromen-6-yl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	14886039	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)O)C	422.50	unknown	https://doi.org/10.3987/COM-90-5416 https://doi.org/10.1016/J.BMCL.2009.07.098 https://doi.org/10.3987/R-1983-02-0213 https://doi.org/10.1271/BBB.70.427
cudraflavanone A	21721847	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)O)C	422.50	unknown	https://doi.org/10.3987/R-1983-02-0213 https://doi.org/10.1016/J.BMCL.2015.07.017 https://doi.org/10.3987/R-1984-05-0997 https://doi.org/10.3987/COM-90-5416 https://doi.org/10.1016/J.BMCL.2006.08.032 https://doi.org/10.1055/S-2007-969453 https://doi.org/10.1021/NP070059K https://doi.org/10.1016/J.BMCL.2009.07.098 https://doi.org/10.1271/BBB.70.427
Cudraflavanone B	509244	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C	356.40	unknown	https://doi.org/10.1021/NP070059K
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-5,7-dihydroxy-2-(7-hydroxy-2,2-dimethylchromen-6-yl)-8-(3-hydroxy-3-methylbutyl)-2,3-dihydrochromen-4-one	122187384	Click to see CC1(C=CC2=CC(=C(C=C2O1)O)C3CC(=O)C4=C(C=C(C(=C4O3)CCC(C)(C)O)O)O)C	440.50	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017
(2S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(4-hydroxyphenyl)methyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	122187385	Click to see CC(=CCC1=C(C(=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)CC4=CC=C(C=C4)O)O)C	446.50	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017
(S)-5,7-dihydroxy-2-(7-hydroxy-2,2-dimethyl-2H-chromen-6-yl)-8-(3-hydroxy-3-methylbutyl)chroman-4-one	44419447	Click to see CC1(C=CC2=CC(=C(C=C2O1)O)C3CC(=O)C4=C(C=C(C(=C4O3)CCC(C)(C)O)O)O)C	440.50	unknown	https://doi.org/10.1016/J.BMCL.2006.08.032 https://doi.org/10.1016/J.BMCL.2009.07.098 https://doi.org/10.1271/BBB.70.427
5,7-Dihydroxy-2-(7-hydroxy-2,2-dimethylchromen-6-yl)-8-(3-hydroxy-3-methylbutyl)-2,3-dihydrochromen-4-one	163103087	Click to see CC1(C=CC2=CC(=C(C=C2O1)O)C3CC(=O)C4=C(C=C(C(=C4O3)CCC(C)(C)O)O)O)C	440.50	unknown	https://doi.org/10.1016/J.BMCL.2009.07.098 https://doi.org/10.1271/BBB.70.427
Senegalensin	124035	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)CC=C(C)C)O)C	408.50	unknown	https://doi.org/10.1021/NP800418J
Sophoraflavanone B	509245	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C	340.40	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-5,7,2',4'-Tetrahydroxyflavanone	10356745	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=C(C=C(C=C3)O)O	288.25	unknown	via CMAUP database
(S)-2-(3,5-Dihydroxyphenyl)-5,7-dihydroxychroman-4-one	52945930	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=CC(=C3)O)O	288.25	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one	932	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017
Eriodictyol	440735	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	via CMAUP database
Naringenin	439246	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3R)-3,5,6,7-tetrahydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one	101353295	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C(=C3O)O)O)O)O	304.25	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one	662	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	288.25	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017
Aromadendrin	122850	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	288.25	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Norartocarpetin	5481970	Click to see C1=CC(=C(C=C1O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
Cudraflavone B	5319925	Click to see CC(=CCC1=C(OC2=CC3=C(C=CC(O3)(C)C)C(=C2C1=O)O)C4=C(C=C(C=C4)O)O)C	420.50	unknown	https://doi.org/10.1016/J.BMC.2004.01.030 https://doi.org/10.3987/COM-90-5416 https://doi.org/10.1016/J.BMCL.2006.08.032 https://doi.org/10.1055/S-2007-969660 https://doi.org/10.1021/NP070059K https://doi.org/10.1016/J.BMCL.2009.07.098 https://doi.org/10.1271/BBB.70.427 https://doi.org/10.1248/BPB.29.838
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
Artocarpesin	399491	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(=CC2=O)C3=C(C=C(C=C3)O)O)O)C	354.40	unknown	https://doi.org/10.1016/J.BMC.2004.01.030
Cudraflavone C	5319924	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(=C(C2=O)CC=C(C)C)C3=C(C=C(C=C3)O)O)O)C	422.50	unknown	https://doi.org/10.3987/COM-90-5416
Cudraflavone D	14886040	Click to see CC(=CCC1=CC(=C(C=C1O)O)C2=CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)C	422.50	unknown	https://doi.org/10.3987/COM-90-5416
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/J.BMC.2004.01.030 https://doi.org/10.1016/J.BMCL.2015.07.017 https://doi.org/10.3987/COM-90-5416
Morin	5281670	Click to see C1=CC(=C(C=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	302.23	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	44259225	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	464.40	unknown	https://doi.org/10.1055/S-2007-969453
kaempferol 7-O-glucoside	10095180	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1055/S-2007-969453
Quercetin 7-O-glucoside	5381351	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	464.40	unknown	https://doi.org/10.1055/S-2007-969453
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(11S)-7,15-dihydroxy-19,19-dimethyl-11-(2-methylprop-1-enyl)-2,10,20-trioxapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(22),3(12),4(9),5,7,14,16(21),17-octaen-13-one	92448824	Click to see CC(=CC1C2=C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=CC(O5)(C)C)C(=C4C2=O)O)C	418.40	unknown	https://doi.org/10.1021/NP070059K https://doi.org/10.1016/J.BMCL.2009.07.098
Cudraflavone A	5316261	Click to see CC(=CC1C2=C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=CC(O5)(C)C)C(=C4C2=O)O)C	418.40	unknown	https://doi.org/10.3987/COM-90-5416 https://doi.org/10.1055/S-2007-969660 https://doi.org/10.1021/NP070059K https://doi.org/10.1016/J.BMCL.2009.07.098
Cycloartocarpesin	15224382	Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=C(C=C(C=C4)O)O)C	352.30	unknown	https://doi.org/10.1016/J.BMC.2004.01.030 https://doi.org/10.3987/COM-90-5416 https://doi.org/10.1016/J.BMCL.2006.08.032 https://doi.org/10.1055/S-2007-969453 https://doi.org/10.1016/J.BMCL.2009.07.098 https://doi.org/10.1271/BBB.70.427
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
4-Hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)furo[3,2-g]chromen-5-one	25209719	Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)C=C(O2)C(C)(C)O)C	420.50	unknown	https://doi.org/10.1021/NP800418J
Genistein	5280961	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O	270.24	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017
Orobol	5281801	Click to see C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O	286.24	unknown	https://doi.org/10.1021/NP800418J
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(2S)-4-hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one	94856056	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)O	354.40	unknown	https://doi.org/10.3987/COM-90-5416
(8R,9R)-5-hydroxy-3-(4-hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-9-methoxy-6-(3-methylbut-2-enyl)-8,9-dihydrofuro[2,3-h]chromen-4-one	25195224	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C3OC)C(C)(C)O)OC=C(C2=O)C4=CC=C(C=C4)O)O)C	452.50	unknown	https://doi.org/10.1021/NP800418J
(8S,9R)-5-hydroxy-3-(4-hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-9-methoxy-6-(3-methylbut-2-enyl)-8,9-dihydrofuro[2,3-h]chromen-4-one	162878580	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C3OC)C(C)(C)O)OC=C(C2=O)C4=CC=C(C=C4)O)O)C	452.50	unknown	https://doi.org/10.1021/NP800418J
(8S,9S)-5-hydroxy-3-(4-hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-9-methoxy-6-(3-methylbut-2-enyl)-8,9-dihydrofuro[2,3-h]chromen-4-one	162878581	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C3OC)C(C)(C)O)OC=C(C2=O)C4=CC=C(C=C4)O)O)C	452.50	unknown	https://doi.org/10.1021/NP800418J
3'-Hydroxyalpinumisoflavone 4'-methyl ether	44257309	Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC(=C(C=C4)OC)O)C	366.40	unknown	https://doi.org/10.1021/NP800418J
5-Hydroxy-3-(4-hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-9-methoxy-6-(3-methylbut-2-enyl)-8,9-dihydrofuro[2,3-h]chromen-4-one	56670819	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C3OC)C(C)(C)O)OC=C(C2=O)C4=CC=C(C=C4)O)O)C	452.50	unknown	https://doi.org/10.1021/NP800418J
5,7-Dihydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-3-(4-methoxyphenyl)chromen-4-one	25209718	Click to see CC(=C)C(CC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)OC)O)O	368.40	unknown	https://doi.org/10.1021/NP800418J
5,7-dihydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one	124355947	Click to see CC(=CCC1=C(C(=C(C2=C1OC=C(C2=O)C3=CC=C(C=C3)O)O)CC(C(=C)C)O)O)C	422.50	unknown	https://doi.org/10.1021/NP800418J
5,7-dihydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-(4-methoxyphenyl)chromen-4-one	163062357	Click to see CC(=C)C(CC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)OC)O)O	368.40	unknown	https://doi.org/10.1021/NP800418J
5,7-dihydroxy-8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)chromen-4-one	124355949	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)CC(C(=C)C)O)O)C	422.50	unknown	https://doi.org/10.1021/NP800418J
6,8-Diprenylgenistein	480783	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)CC=C(C)C)O)C	406.50	unknown	https://doi.org/10.1021/NP800418J
Erysenegalensein E	15478903	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)CC(C(=C)C)O)O)C	422.50	unknown	https://doi.org/10.1021/NP800418J
Erythrinin C	44257283	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)O	354.40	unknown	https://doi.org/10.3987/COM-90-5416
Euchrenone b10	402594	Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=CC=C(C=C4)O)CC(O2)C(C)(C)O)C	422.50	unknown	https://doi.org/10.1021/NP800418J
Isoerysenegalensein E	5318561	Click to see CC(=CCC1=C(C(=C(C2=C1OC=C(C2=O)C3=CC=C(C=C3)O)O)CC(C(=C)C)O)O)C	422.50	unknown	https://doi.org/10.1021/NP800418J
Wighteone	5281814	Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O)C	338.40	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-O-Methylorobol	5319744	Click to see COC1=C(C=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O	300.26	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A	5280373	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O	284.26	unknown	https://doi.org/10.1016/J.BMCL.2015.07.017

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Maclura tricuspidata

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top