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Garcinia morella

Garcinia morella - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64401d32e2405128553147
Scientific name Garcinia morella
Authority (Gaertn.) Desr.
First published in Encycl. 3: 701 (1792)

Description Top

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Garcinia morella is a tree species in the Clusiaceae family, native to India and Sri Lanka. It is known by various names in different languages and has a smooth, dark brown bark and simple, opposite leaves. The flowers are dioecious and the fruit, although edible, is very acidic. The fruit can be preserved by drying and used in pickles, chutneys, and curries. In traditional medicine, the fruit is used to treat dysentery and gastritis, and the bark produces a yellow resin called gamboge, which is used in food, paints, and medicines. The tree is also used as a rootstock for the mangosteen. Chemical compounds found in Garcinia morella include xanthonoids and forbesione. In some regions of India, the fruit is boiled to produce a thick black liquid called "odduli" which is used in cooking and can be stored for years without preservatives.

Synonyms Top

Scientific name Authority First published in
Mangostana morella Gaertn. Fruct. Sem. Pl. 2: 106 (1790)
Stalagmitis cambogioides Murray Commentat. Soc. Regiae Sci. Gott. 9: 173 (1789)
Garcinia cambogioides (Murray) Headland Mat. Med. Ind. , ed. 3: 839 (1837)
Garcinia gutta Wight Ill. Ind. Bot. 1: 126 (1840)
Hebradendron cambogioides (Murray) Graham Compan. Bot. Mag. 2: 109 (1836)
Cambogia gutta L. Syst. Nat., ed. 10. 2: 1073. 1759

Common names Top

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Language Common/alternative name
Japanese インドガンボジ
Kannada ಅರಿಸಿನ ಗುರುಗಿ
Malayalam ചികിരി
Malayalam പുളിഞ്ചിക്കായ്
Malayalam മക്കി
Malayalam ഇരവി
Russian Гарциния морелла
tcy ಜಾರಿಗೆ
Chinese 桑藤黄
Chinese 莫雷拉藤黄
Chinese 巴圖安

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000694490
Tropicos 50066433
KEW urn:lsid:ipni.org:names:428102-1
The Plant List kew-2817012
Open Tree Of Life 5763401
NCBI Taxonomy 1585849
IUCN Red List 169574690
IPNI 428102-1
GBIF 3713627
Freebase /m/03h4jmb
EPPO GANMO
USDA GRIN 71014
Wikipedia Garcinia_morella
CMAUP NPO3806

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
Interaction of energy and sulfur microbial diet and smoking status with polygenic variants associated with lipoprotein metabolism Hur HJ, Yang HJ, Kim MJ, Lee K, Jang DJ, Kim MS, Park S Front Nutr 04-Oct-2023
PMCID:PMC10582641
doi:10.3389/fnut.2023.1244185
PMID:37860035
A Narrative Review of the Herbal Preparation of Ayurvedic, Traditional Chinese, and Kampō Medicines Applied as Radioprotectors Ibáñez B, Melero A, Montoro A, Merino-Torres JF, Soriano JM, San Onofre N Antioxidants (Basel) 17-Jul-2023
PMCID:PMC10376155
doi:10.3390/antiox12071437
PMID:37507975
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
Neuroprotective Effects of Agri-Food By-Products Rich in Phenolic Compounds Rojas-García A, Fernández-Ochoa Á, Cádiz-Gurrea MD, Arráez-Román D, Segura-Carretero A Nutrients 14-Jan-2023
PMCID:PMC9865516
doi:10.3390/nu15020449
PMID:36678322
A Review of Herbal Medicine-Based Phytochemical of Garcinia as Molecular Therapy for Breast Cancer Triyasa KS, Diantini A, Barliana MI Drug Des Devel Ther 12-Oct-2022
PMCID:PMC9554952
doi:10.2147/DDDT.S358229
PMID:36248245
The Main Protease of SARS-CoV-2 as a Target for Phytochemicals against Coronavirus Issa SS, Sokornova SV, Zhidkin RR, Matveeva TV Plants (Basel) 17-Jul-2022
PMCID:PMC9319234
doi:10.3390/plants11141862
PMID:35890496
Erratum: Murthy et al. Phytochemicals and Biological Activities of Garcinia morella (Gaertn.) Desr.: A Review. Molecules 2020, 25, 5690 Murthy HN, Dalawai D, Dewir YH, Ibrahim A Molecules 21-Jul-2021
PMCID:PMC8348941
doi:10.3390/molecules26154398
PMID:34361860
Phytochemicals and Biological Activities of Garcinia morella (Gaertn.) Desr.: A Review Murthy HN, Dalawai D, Dewir YH, Ibrahim A Molecules 02-Dec-2020
PMCID:PMC7730552
doi:10.3390/molecules25235690
PMID:33276654
Culturable diversity of bacterial endophytes associated with medicinal plants of the Western Ghats, India Webster G, Mullins AJ, Cunningham-Oakes E, Renganathan A, Aswathanarayan JB, Mahenthiralingam E, Vittal RR FEMS Microbiol Ecol 25-Jul-2020
PMCID:PMC7422900
doi:10.1093/femsec/fiaa147
PMID:32710748
Efficacy and Mechanism of Traditional Medicinal Plants and Bioactive Compounds against Clinically Important Pathogens Mickymaray S Antibiotics (Basel) 09-Dec-2019
PMCID:PMC6963422
doi:10.3390/antibiotics8040257
PMID:31835403
Methicillin-resistant Staphylococcus aureus (MRSA) and anti-MRSA activities of extracts of some medicinal plants: A brief review Okwu MU, Olley M, Akpoka AO, Izevbuwa OE AIMS Microbiol 15-Apr-2019
PMCID:PMC6642907
doi:10.3934/microbiol.2019.2.117
PMID:31384707
Potential Anticancer Agents Characterized from Selected Tropical Plants Ren Y, Carcache de Blanco EJ, Fuchs JR, Soejarto DD, Burdette JE, Swanson SM, Kinghorn AD J Nat Prod 04-Mar-2019
PMCID:PMC6441492
doi:10.1021/acs.jnatprod.9b00018
PMID:30830783
Carboxyxanthones: Bioactive Agents and Molecular Scaffold for Synthesis of Analogues and Derivatives Ribeiro J, Veloso C, Fernandes C, Tiritan ME, Pinto MM Molecules 05-Jan-2019
PMCID:PMC6337274
doi:10.3390/molecules24010180
PMID:30621303
Changes in MIDAS, Perceived Stress, Frontalis Muscle Activity and Non-Steroidal Anti-Inflammatory Drugs Usage in Patients with Migraine Headache without Aura following Ayurveda and Yoga Compared to Controls: An Open Labeled Non-Randomized Study Vasudha MS, Manjunath NK, Nagendra HR Ann Neurosci 11-Sep-2018
PMCID:PMC6470355
doi:10.1159/000492269
PMID:31000965
Gambogic acid inhibits LPS-induced macrophage pro-inflammatory cytokine production mainly through suppression of the p38 pathway Ma J, Huang K, Ma Y, Chen S, Liu C, Shan Z, Fang X Iran J Basic Med Sci 01-Jul-2018
PMCID:PMC6098961
doi:10.22038/IJBMS.2018.23897.5995
PMID:30140411

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives
Guvacine 3532 Click to see C1CNCC(=C1)C(=O)O 127.14 unknown via CMAUP database
Guvacine hydrochloride 11957555 Click to see C1CNCC(=C1)C(=O)O.Cl 163.60 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Homophthalic acid 66643 Click to see C1=CC=C(C(=C1)CC(=O)O)C(=O)O 180.16 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzophenones
Maclurin 68213 Click to see C1=CC(=C(C=C1C(=O)C2=C(C=C(C=C2O)O)O)O)O 262.21 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
2-((1-Oxooctadecyl)oxy)-1-(((1-oxooctadecyl)oxy)methyl)ethyl oleate 13183956 Click to see CCCCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCC=CCCCCCCCC 889.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
(8S)-4,8-dimethyl-8,9-dihydronaphtho[2,1-f][1]benzofuran-7,11-dione 11778300 Click to see CC1COC2=C1C(=O)C3=C(C2=O)C4=CC=CC(=C4C=C3)C 278.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Xanthochymol 9938674 Click to see CC(=CCC1CC2(C(=O)C(=C(C3=CC(=C(C=C3)O)O)O)C(=O)C(C2=O)(C1(C)C)CC=C(C)C)CC(CCC(=C)C)C(=C)C)C 602.80 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Allogambogic acid 6444544 Click to see CC(=CCCC1(C=CC2=C(C(=C3C(=C2O1)C(=O)C4=CC5CC6C4(O3)C(C5=O)(OC6(C)C)CC=C(C)C(=O)O)CC=C(C)C)O)C)C 628.70 unknown via CMAUP database
Norathyriol 5281656 Click to see C1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)O)O)O 260.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
1,5-Dihydroxy-3-methoxy-2-prenylxanthone 10449043 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C(=CC=C3)O)OC)C 326.30 unknown via CMAUP database
1,7-Dihydroxy-3-methoxy-2-prenylxanthone 509269 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=CC(=C3)O)OC)C 326.30 unknown via CMAUP database
garcinone B 5495928 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C(=C3)O)OC(C=C4)(C)C)O)C 394.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
8-Deoxygartanin 392450 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C(=CC=C3)O)CC=C(C)C)O)C 380.40 unknown via CMAUP database
Gartanin 5281633 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(C=CC(=C3O2)O)O)CC=C(C)C)O)C 396.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
1-Isomangostin 5281641 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C4=C3OC(CC4)(C)C)O)O)OC)C 410.50 unknown via CMAUP database
3-Isomangostin 13873655 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(CC4)(C)C)O)O)OC)C 410.50 unknown via CMAUP database
9-Hydroxycalabaxanthone 5495929 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)O)OC)C 408.40 unknown via CMAUP database
Demethylcalabaxanthone 509270 Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)O)C 378.40 unknown via CMAUP database
Garcinone D 5495926 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CCC(C)(C)O)O)C 428.50 unknown via CMAUP database
Garcinone E 10298511 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C(=C(C(=C3C2=O)CC=C(C)C)O)O)CC=C(C)C)O)C 464.50 unknown via CMAUP database
Mangostin 5281650 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CC=C(C)C)O)C 410.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(1S,2S,17S,19R)-12-hydroxy-8,8,21,21-tetramethyl-5,19-bis(3-methylbut-2-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione 11432549 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C)O)C=CC(O2)(C)C)C 530.60 unknown via CMAUP database
(2Z)-4-[(1R,3aS,5S,14aS)-8-hydroxy-3,3,11,11-tetramethyl-13-(3-methylbut-2-en-1-yl)-7,15-dioxo-3a,4,5,7-tetrahydro-3H,11H-1,5-methanofuro[3,4-g]pyrano[3,2-b]xanthen-1-yl]-2-methylbut-2-enal 71306322 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C=O)O)C=CC(O2)(C)C)C 544.60 unknown https://doi.org/10.1002/MRC.2011
(E)-4-[(1S,2S,17S,19R)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 101389907 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 560.60 unknown https://doi.org/10.1002/MRC.2011
(E)-4-[(2R,17R,19S)-12-Hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enal 16078249 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C=O)O)C=CC(O2)(C)C)C 544.60 unknown via CMAUP database
(Z)-4-[(1R,2R,17R,19S)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enal 162997133 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C=O)O)C=CC(O2)(C)C)C 544.60 unknown https://doi.org/10.1039/JR9370000853
(Z)-4-[(1R,2R,17R,19S)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 102533562 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 560.60 unknown via CMAUP database
(Z)-4-[(1S,2S,17S,19R)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 54580250 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 560.60 unknown https://doi.org/10.1002/MRC.2011
4-[12-Hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enal 543652 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C=O)O)C=CC(O2)(C)C)C 544.60 unknown https://doi.org/10.1039/JR9370000853
https://doi.org/10.1002/MRC.2011
Br-Xanthone A 13964005 Click to see CC1(CCC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C=C(C5=C4CCC(O5)(C)C)O)C 396.40 unknown via CMAUP database
Cambogic acid 5353639 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C)C 628.70 unknown via CMAUP database
CID 550587 550587 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 560.60 unknown https://doi.org/10.1002/MRC.2011
CID 94860750 94860750 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C)C 628.70 unknown via CMAUP database
Dihydroisomorellin 16078255 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C(C3=O)CC6CC4C(OC5(C6=O)CC=C(C)C=O)(C)C)O)C=CC(O2)(C)C)C 546.60 unknown via CMAUP database
Gambogic Acid 9852185 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C)C 628.70 unknown via CMAUP database
Guttic acid 16072310 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C)C 628.70 unknown via CMAUP database
Morellin 21348143 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C=O)O)C=CC(O2)(C)C)C 544.60 unknown via CMAUP database
Neo-gambogic acid 6438568 Click to see CC(=CCCC1(CC(C2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)O)C)C 646.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(+)-Morelloflavone 12110448 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)O)O 556.50 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 130556 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Morelloflavone 5464454 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)O)O 556.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.06.025
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 10367864 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown via CMAUP database
isorhamnetin 3-O-glucoside 5318645 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Isorhamnetin-3-O-neohesperidoside 24204448 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)OC)O)CO)O)O)O)O)O 624.50 unknown via CMAUP database

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