Hintonia latiflora is a plant species that belongs to the genus Hintonia. It is known to contain a compound called coutareagenin, which is a neoflavonoid with antidiabetic properties. This plant has been used in traditional medicine for its medicinal properties and is now being studied for its potential as a treatment for diabetes.

Synonyms Top

Scientific name	Authority	First published in
Portlandia pterosperma	S.Watson	Proc. Amer. Acad. Arts 24: 52 (1889)
Coutarea latiflora	Sessé & Moc.	ex DC. Prodr. 4: 350. 1830 [late Sep 1830]
Coutarea pterosperma	Standl.	N. Amer. Fl. 32: 127 (1921)
Hintonia latiflora var. leiantha	Bullock	Hooker's Icon. Pl. 33: t. 3295 (1935)

Common names Top

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Language	Common/alternative name
German	copalchi
German	mexikanischer fieberrindenbaum
Chinese	胰岛素木

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

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Northeast
  - Mexico Northwest
  - Mexico Southeast
  - Mexico Southwest

Southern America click to expand
- Central America
  - El Salvador
  - Guatemala

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000982487
UNII	3K995HQ5F1
Tropicos	27906527
KEW	urn:lsid:ipni.org:names:122717-2
The Plant List	kew-99336
Open Tree Of Life	611961
NCBI Taxonomy	43501
IUCN Red List	126612933
IPNI	122717-2
iNaturalist	278554
GBIF	5336472
Freebase	/m/0b6mdqb
EOL	1108777
USDA GRIN	19132
Wikipedia	Hintonia_latiflora

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

Exploring the antioxidant potential of endophytic fungi: a review on methods for extraction and quantification of total antioxidant capacity (TAC)

Asomadu RO, Ezeorba TP, Ezike TC, Uzoechina JO

3 Biotech

05-Apr-2024

PMCID:	PMC10997672
doi:	10.1007/s13205-024-03970-3
PMID:	38585410

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

Comparative Analysis of Secondary Metabolites Produced by Ascochyta fabae under In Vitro Conditions and Their Phytotoxicity on the Primary Host, Vicia faba, and Related Legume Crops

Barilli E, Reveglia P, Agudo-Jurado FJ, Cañete García V, Cimmino A, Evidente A, Rubiales D

Toxins (Basel)

09-Dec-2023

PMCID:	PMC10747461
doi:	10.3390/toxins15120693
PMID:	38133197

Plants of the Rubiaceae Family with Effect on Metabolic Syndrome: Constituents, Pharmacology, and Molecular Targets

González-Castelazo F, Soria-Jasso LE, Torre-Villalvazo I, Cariño-Cortés R, Muñoz-Pérez VM, Ortiz MI, Fernández-Martínez E

Plants (Basel)

15-Oct-2023

PMCID:	PMC10610173
doi:	10.3390/plants12203583
PMID:	37896046

Fungal Endophytes: Microfactories of Novel Bioactive Compounds with Therapeutic Interventions; A Comprehensive Review on the Biotechnological Developments in the Field of Fungal Endophytic Biology over the Last Decade

Gupta A, Meshram V, Gupta M, Goyal S, Qureshi KA, Jaremko M, Shukla KK

Biomolecules

25-Jun-2023

PMCID:	PMC10377637
doi:	10.3390/biom13071038
PMID:	37509074

Tridepsides as potential bioactives: a review on their chemistry and the global distribution of their lichenic and non-lichenic natural sources

Norouzi H, Sohrabi M, Yousefi M, Boustie J

Front Fungal Biol

19-Apr-2023

PMCID:	PMC10512237
doi:	10.3389/ffunb.2023.1088966
PMID:	37746133

Flavonoids as Promising Natural Compounds in the Prevention and Treatment of Selected Skin Diseases

Čižmárová B, Hubková B, Tomečková V, Birková A

Int J Mol Sci

28-Mar-2023

PMCID:	PMC10094312
doi:	10.3390/ijms24076324
PMID:	37047297

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

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

RSC Adv

13-Oct-2022

PMCID:	PMC9558262
doi:	10.1039/d2ra04884a
PMID:	36320761

Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review

Salazar-Gómez A, Alonso-Castro AJ

Pharmaceuticals (Basel)

31-Aug-2022

PMCID:	PMC9505834
doi:	10.3390/ph15091095
PMID:	36145316

Research progress of coumarins and their derivatives in the treatment of diabetes

Pan Y, Liu T, Wang X, Sun J

J Enzyme Inhib Med Chem

24-Jan-2022

PMCID:	PMC8788346
doi:	10.1080/14756366.2021.2024526
PMID:	35067136

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

Fungal Depsides—Naturally Inspiring Molecules: Biosynthesis, Structural Characterization, and Biological Activities

Ibrahim SR, Sirwi A, Eid BG, Mohamed SG, Mohamed GA

Metabolites

05-Oct-2021

PMCID:	PMC8540757
doi:	10.3390/metabo11100683
PMID:	34677398

How does urbanization affect perceptions and traditional knowledge of medicinal plants?

Arjona-García C, Blancas J, Beltrán-Rodríguez L, López Binnqüist C, Colín Bahena H, Moreno-Calles AI, Sierra-Huelsz JA, López-Medellín X

J Ethnobiol Ethnomed

03-Aug-2021

PMCID:	PMC8330055
doi:	10.1186/s13002-021-00473-w
PMID:	34344391

Molecules Isolated from Mexican Hypoglycemic Plants: A Review

Escandón-Rivera SM, Mata R, Andrade-Cetto A

Molecules

10-Sep-2020

PMCID:	PMC7571036
doi:	10.3390/molecules25184145
PMID:	32927754

Screening of plant-based natural compounds as a potential COVID-19 main protease inhibitor: an in silico docking and molecular dynamics simulation approach

Majumder R, Mandal M

J Biomol Struct Dyn

08-Sep-2020

PMCID:	PMC7544942
doi:	10.1080/07391102.2020.1817787
PMID:	32897138

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 / Terpene glycosides
3-ethenyl-4-(9H-pyrido[3,4-b]indol-1-ylmethyl)-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylic acid	5316605	Click to see C=CC1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)O)CC3=NC=CC4=C3NC5=CC=CC=C45	512.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.05.006
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Ursolic acid	220774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1021/NP800642D
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1021/NP800642D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
[6-[(10R,14S,17S)-2,16-dihydroxy-3,4,4,9,13,14-hexamethyl-11-oxo-1,2,3,5,6,7,8,10,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]-2,6-dimethyl-5-oxoheptan-2-yl] acetate	163190827	Click to see CC1C(CC2C(C1(C)C)CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C)C(=O)CCC(C)(C)OC(=O)C)O)C)C)C)O	560.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.05.006
Cucurbitacin A	5281315	Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)O)CO)C)C)O)O	574.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.05.006
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2S,3S,8S,9R,10R,13R,14S,16R,17R)-17-[(2R)-2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl]-2,16-dihydroxy-4,4,9,13,14-pentamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one	162898811	Click to see CC1(C(C(CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(=O)CCC(C)(C)O)O)O)C)C)C)O)OC5C(C(C(C(O5)CO)O)O)O)C	682.80	unknown	https://doi.org/10.1055/S-2005-873137
(2S,3S,8S,9R,10R,13S,14S,16S,17R)-17-[(2R)-2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl]-2,16-dihydroxy-4,4,9,13,14,17-hexamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,7,8,10,12,15,16-octahydro-1H-cyclopenta[a]phenanthren-11-one	162928590	Click to see CC1(C(C(CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4(C)C(C)(C(=O)CCC(C)(C)O)O)O)C)C)C)O)OC5C(C(C(C(O5)CO)O)O)O)C	696.90	unknown	https://doi.org/10.1016/0031-9422(90)85067-P
17-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,16-dihydroxy-4,4,9,13,14,17-hexamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,7,8,10,12,15,16-octahydro-1H-cyclopenta[a]phenanthren-11-one	14630604	Click to see CC1(C(C(CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4(C)C(C)(C(=O)CCC(C)(C)O)O)O)C)C)C)O)OC5C(C(C(C(O5)CO)O)O)O)C	696.90	unknown	https://doi.org/10.1016/0031-9422(90)85067-P
2,3,16,20,25-Pentahydroxycucurbita-5-ene-11,22-dio	23900089	Click to see CC1(C(C(CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(=O)CCC(C)(C)O)O)O)C)C)C)O)OC5C(C(C(C(O5)CO)O)O)O)C	682.80	unknown	https://doi.org/10.1055/S-2005-873137
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
5,13-dihydroxy-14-methoxy-4,6a,6b,8a,11,12,14b-heptamethyl-2,4,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-one	74960353	Click to see CC1CCC2(CCC3(C(=C(C(C4C3(CC(C5C4(CCC(=O)C5C)C)O)C)OC)O)C2C1C)C)C	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.05.006
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1016/J.JEP.2012.11.025
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides / Aminocyclitol glycosides
Glucobay	444254	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)NC4C=C(C(C(C4O)O)O)CO	645.60	unknown	https://doi.org/10.1021/NP300869G
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-[2-[1-(3,4-dihydroxyphenyl)ethenyl]-3-hydroxy-5-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162952699	Click to see COC1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=C)C3=CC(=C(C=C3)O)O)O	436.40	unknown	https://doi.org/10.1016/0031-9422(92)83474-D
2-[2-[1-(3,4-Dihydroxyphenyl)ethenyl]-3-hydroxy-5-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162952697	Click to see COC1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=C)C3=CC(=C(C=C3)O)O)O	436.40	unknown	https://doi.org/10.1016/0031-9422(92)83474-D
4-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1H-naphthalen-2-one	163189978	Click to see C1C2=C(C(=CC1=O)C3=CC(=C(C=C3)O)O)C(=CC(=C2)O)OC4C(C(C(C(O4)CO)O)O)O	446.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.05.006
4-(3,4-dihydroxyphenyl)-7-methoxy-5-[(3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1H-naphthalen-2-one	163188734	Click to see COC1=CC2=C(C(=CC(=O)C2)C3=CC(=C(C=C3)O)O)C(=C1)OC4C(C(C(C(O4)CO)O)O)O	460.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.05.006
4-(3,4-dihydroxyphenyl)-7-methoxy-5-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1H-naphthalen-2-one	163187778	Click to see COC1=CC2=C(C(=CC(=O)C2)C3=CC(=C(C=C3)O)O)C(=C1)OC4C(C(C(C(O4)CO)O)O)O	460.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.05.006
> Organoheterocyclic compounds / Piperidines
Miglitol	441314	Click to see C1C(C(C(C(N1CCO)CO)O)O)O	207.22	unknown	https://doi.org/10.1021/NP300869G
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-[7-hydroxy-4-(4-hydroxyphenyl)-2-oxochromen-5-yl]oxyoxan-2-yl]methyl acetate	45270512	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC(=CC3=C2C(=CC(=O)O3)C4=CC=C(C=C4)O)O)O)O)O	474.40	unknown	https://doi.org/10.1021/NP800642D
[(2R,3R,4S,5R,6S)-6-[4-(3,4-dihydroxyphenyl)-7-hydroxy-2-oxochromen-5-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	45270513	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC(=CC3=C2C(=CC(=O)O3)C4=CC(=C(C=C4)O)O)O)O)O)O	490.40	unknown	https://doi.org/10.1021/NP800642D
[(2R,3R,4S,5R,6S)-6-[4-(3,4-dihydroxyphenyl)-7-methoxy-2-oxochromen-5-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	44559794	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC(=CC3=C2C(=CC(=O)O3)C4=CC(=C(C=C4)O)O)OC)O)O)O	504.40	unknown	https://doi.org/10.1016/0031-9422(90)85067-P
[(2R,3S,4S,5R,6S)-6-[4-(3,4-dihydroxyphenyl)-7-hydroxy-2-oxochromen-5-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	102366249	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC(=CC3=C2C(=CC(=O)O3)C4=CC(=C(C=C4)O)O)O)O)O)O	490.40	unknown	https://doi.org/10.1016/0031-9422(92)83474-D
[3,4,5-Trihydroxy-6-[7-hydroxy-4-(4-hydroxyphenyl)-2-oxochromen-5-yl]oxyoxan-2-yl]methyl acetate	56667429	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC(=CC3=C2C(=CC(=O)O3)C4=CC=C(C=C4)O)O)O)O)O	474.40	unknown	https://doi.org/10.1021/NP800642D
[6-[4-(3,4-Dihydroxyphenyl)-7-hydroxy-2-oxochromen-5-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	56671386	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC(=CC3=C2C(=CC(=O)O3)C4=CC(=C(C=C4)O)O)O)O)O)O	490.40	unknown	https://doi.org/10.1021/NP800642D https://doi.org/10.1016/0031-9422(92)83474-D
[6-[4-(3,4-Dihydroxyphenyl)-7-methoxy-2-oxochromen-5-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	14159734	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC(=CC3=C2C(=CC(=O)O3)C4=CC(=C(C=C4)O)O)OC)O)O)O	504.40	unknown	https://doi.org/10.1016/0031-9422(90)85067-P
4-(3-hydroxy-4-methoxyphenyl)-7-methoxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	16091571	Click to see COC1=C(C=C(C=C1)C2=CC(=O)OC3=C2C(=CC(=C3)OC)OC4C(C(C(C(O4)CO)O)O)O)O	476.40	unknown	https://doi.org/10.1021/NP060233P
4-(3-Hydroxy-4-methoxyphenyl)-7-methoxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	73240788	Click to see COC1=C(C=C(C=C1)C2=CC(=O)OC3=C2C(=CC(=C3)OC)OC4C(C(C(C(O4)CO)O)O)O)O	476.40	unknown	https://doi.org/10.1021/NP060233P
4-(3,4-Dihydroxyphenyl)-5-(beta-D-galactopyranosyloxy)-7-methoxy-2H-1-benzopyran-2-one	21676237	Click to see COC1=CC2=C(C(=CC(=O)O2)C3=CC(=C(C=C3)O)O)C(=C1)OC4C(C(C(C(O4)CO)O)O)O	462.40	unknown	https://doi.org/10.1016/0031-9422(90)85067-P https://doi.org/10.1021/NP800642D
4-(3,4-Dihydroxyphenyl)-5-(beta-D-glucopyranosyloxy)-7-methoxy-2H-1-benzopyran-2-one	13962181	Click to see COC1=CC2=C(C(=CC(=O)O2)C3=CC(=C(C=C3)O)O)C(=C1)OC4C(C(C(C(O4)CO)O)O)O	462.40	unknown	https://doi.org/10.1021/NP060233P https://doi.org/10.1021/NP800642D https://doi.org/10.1016/0031-9422(90)85067-P https://doi.org/10.1055/S-2005-873137
4-(3,4-Dihydroxyphenyl)-5-[(6-O-beta-D-xylopyranosyl-beta-D-glucopyranosyl)oxy]-7-methoxycoumarin	14134097	Click to see COC1=CC2=C(C(=CC(=O)O2)C3=CC(=C(C=C3)O)O)C(=C1)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1021/NP800642D
4-(3,4-Dihydroxyphenyl)-5-beta-D-glucopyranosyloxy-7-methoxycoumarin	13962183	Click to see COC1=CC2=C(C(=CC(=O)O2)C3=CC(=C(C=C3)O)O)C(=C1)OC4C(C(C(C(O4)CO)O)O)O	462.40	unknown	https://doi.org/10.1021/NP800642D https://doi.org/10.1016/0031-9422(90)85067-P https://doi.org/10.1055/S-2005-873137 https://doi.org/10.1021/NP060233P
4-(3,4-Dihydroxyphenyl)-7-hydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	14134092	Click to see C1=CC(=C(C=C1C2=CC(=O)OC3=C2C(=CC(=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/NP800642D https://doi.org/10.1016/0031-9422(90)85067-P
4-(3,4-Dihydroxyphenyl)-7-methoxy-5-[(6-O-beta-D-xylopyranosyl-beta-D-glucopyranosyl)oxy]-2H-1-benzopyran-2-one	14134096	Click to see COC1=CC2=C(C(=CC(=O)O2)C3=CC(=C(C=C3)O)O)C(=C1)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1021/NP800642D
4-(4-hydroxyphenyl)-7-methoxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	163019992	Click to see COC1=CC2=C(C(=CC(=O)O2)C3=CC=C(C=C3)O)C(=C1)OC4C(C(C(C(O4)CO)O)O)O	446.40	unknown	https://doi.org/10.1016/0031-9422(90)85067-P
4-(4-Hydroxyphenyl)-7-methoxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	14630612	Click to see COC1=CC2=C(C(=CC(=O)O2)C3=CC=C(C=C3)O)C(=C1)OC4C(C(C(C(O4)CO)O)O)O	446.40	unknown	https://doi.org/10.1016/0031-9422(90)85067-P
5-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(3,4-dihydroxyphenyl)-7-methoxychromen-2-one	11527213	Click to see COC1=CC2=C(C(=CC(=O)O2)C3=CC(=C(C=C3)O)O)C(=C1)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O	594.50	unknown	https://doi.org/10.1021/NP800642D https://doi.org/10.1016/J.JEP.2012.11.025 https://doi.org/10.1055/S-2005-873137
5-[6-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(3,4-dihydroxyphenyl)-7-methoxychromen-2-one	23983728	Click to see COC1=CC2=C(C(=CC(=O)O2)C3=CC(=C(C=C3)O)O)C(=C1)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O	594.50	unknown	https://doi.org/10.1021/NP800642D https://doi.org/10.1055/S-2005-873137
5-Glucopyranosyloxy-3',4',7-trihydroxyneoflavone, >=95% (LC/MS-ELSD)	14134093	Click to see C1=CC(=C(C=C1C2=CC(=O)OC3=C2C(=CC(=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/NP800642D https://doi.org/10.1016/0031-9422(90)85067-P
7-methoxy-4-(4-methoxyphenyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-2-one	45267097	Click to see COC1=CC=C(C=C1)C2=CC(=O)OC3=C2C(=CC(=C3)OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O	592.50	unknown	https://doi.org/10.1021/NP800642D
7-Methoxy-4-(4-methoxyphenyl)-5-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-2-one	56669613	Click to see COC1=CC=C(C=C1)C2=CC(=O)OC3=C2C(=CC(=C3)OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O	592.50	unknown	https://doi.org/10.1021/NP800642D
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
7-O-Methylluteolin	5318214	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O	300.26	unknown	https://doi.org/10.1016/0031-9422(90)85067-P
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones
5,3',4'-Trihydroxy-7-methoxy-4-phenylcoumarin	9882773	Click to see COC1=CC(=C2C(=CC(=O)OC2=C1)C3=CC(=C(C=C3)O)O)O	300.26	unknown	https://doi.org/10.1055/S-0031-1300176 https://doi.org/10.1016/S0031-9422(00)84060-1

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Hintonia latiflora

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