Dendrophthoe falcata - Unknown
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Internal ID UUID6440164a5e0f5131383427
Scientific name Dendrophthoe falcata
Authority (L.f.) Ettingsh.
First published in Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 32: 52 (1872)

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Synonyms Top

Scientific name Authority First published in
Lonicera zeylanica Gaertn. Fruct. Sem. Pl. 1: 137 (1788)
Loranthus clavigerus Wall. Numer. List : n.º 6873 (1832)
Loranthus amplexifolius DC. Prodr. 4: 305 (1830)
Loranthus bicolor Roxb. Pl. Coromandel 2: 19 (1800)
Loranthus indicus Desr. Encycl. 3: 601 (1792)
Loranthus imbricatus Edgew. Trans. Linn. Soc. London 20: 59 (1846)
Loranthus falcatus L.f. Suppl. Pl. : 211 (1782)
Loranthus lineatus Edgew. Trans. Linn. Soc. London 20: 59 (1846)
Loranthus wightianus Wall. Numer. List : n.º 6872 (1832)
Loranthus koenigianus Agardh. ex Schult.f. Syst. Veg., ed. 15 bis 7: 108 (1829)
Loranthus sarcophyllus Wall. Numer. List : n.º 6863 (1832)
Treubella indica Tiegh. Bull. Soc. Bot. France 41: 267 (1894)
Scurrula bicolor G.Don Gen. Hist. 3: 424 (1834)
Scurrula amplexifolia G.Don Gen. Hist. 3: 424 (1834)
Scurrula longiflora G.Don Gen. Hist. 3: 423 (1834)
Scurrula koenigiana G.Don Gen. Hist. 3: 425 (1834)
Scurrula elegans G.Don Gen. Hist. 3: 424 (1834)
Scurrula indica G.Don Gen. Hist. 3: 424 (1834)
Scurrula falcata G.Don Gen. Hist. 3: 424 (1834)
Dendrophthoe falcata var. amplexifolia (DC.) Rajasek. J. Econ. Taxon. Bot. 31: 182 (2007)
Dendrophthoe bicolor Mart. Flora 13(1): 109 (1830)
Dendrophthoe discolor Barlow Proc. Linn. Soc. New South Wales 87: 55 (1962)
Dendrophthoe elegans Mart. Flora 13(1): 109 (1830)
Dendrophthoe falcata var. pubescens (Hook.f.) V.Chandras. Fl. Tamil Nadu 2: 215 (1987)
Dendrophthoe indica (Desr.) Miq. Fl. Ned. Ind. 1(1): 820 (1856)
Dendrophthoe koenigiana Blume Syst. Veg., ed. 15 bis 7: 1730 (1830)
Dendrophthoe longiflora Blume Syst. Veg., ed. 15 bis [Roemer & Schultes] 7(2): 1730. 1830 [Oct-Dec 1830]
Etubila longiflora Raf. Sylva Tellur. : 125 (1838)

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Language Common/alternative name
English honey suckled mistletoe
Bengali মধুপায়ী ধাইরা
Malayalam ഇത്തിൾക്കണ്ണി

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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

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Database ID/link to page
World Flora Online wfo-0000641204
KEW urn:lsid:ipni.org:names:112395-3
The Plant List kew-2760884
Open Tree Of Life 1031064
NCBI Taxonomy 160049
IPNI 548263-1
iNaturalist 427493
GBIF 7288062
Freebase /m/0cc5tk9
EPPO DNDFA
USDA GRIN 423381
Wikipedia Dendrophthoe_falcata
CMAUP NPO10444

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
Geometric entropy of plant leaves: A measure of morphological complexity Muraleedharan V, Rajan SC, R J PLoS One 02-Jan-2024
PMCID:PMC10760904
doi:10.1371/journal.pone.0293596
PMID:38166118
Editorial: New drugs, approaches, and strategies to combat antimicrobial resistance Singh CK, Sodhi KK, Mubarak MS Front Pharmacol 06-Nov-2023
PMCID:PMC10657978
doi:10.3389/fphar.2023.1295623
PMID:38026960
The Antioxidant Activity of Mistletoes (Viscum album and Other Species) Nicoletti M Plants (Basel) 20-Jul-2023
PMCID:PMC10384781
doi:10.3390/plants12142707
PMID:37514321
Mapping of traditional healthcare providers and their healing approaches in a tribal community of district Sirohi, Rajasthan Dwivedi R, Goyal P, Yadav SS, Dwivedi P, Singh P, Singh K J Family Med Prim Care 30-Jun-2023
PMCID:PMC10451593
doi:10.4103/jfmpc.jfmpc_1610_22
PMID:37636156
Single botanical drugs in the Ayurvedic Pharmacopoeia of India—A quantitative ethnobotanical analysis Yao R, Heinrich M, Zhang B, Wei X, Qi Y, Gao W Front Pharmacol 11-May-2023
PMCID:PMC10213908
doi:10.3389/fphar.2023.1136446
PMID:37251315
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
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831
Dendrophthoe falcata (L.f.) Ettingsh. and Dendrophthoe pentandra (L.) Miq.: A review of traditional medical uses, phytochemistry, pharmacology, toxicity, and applications Kong D, Wang L, Niu Y, Cheng L, Sang B, Wang D, Tian J, Zhao W, Liu X, Chen Y, Wang F, Zhou H, Jia R Front Pharmacol 02-Feb-2023
PMCID:PMC9934394
doi:10.3389/fphar.2023.1096379
PMID:36817117
Biosynthesized Silver Nanoparticles Using Morus alba (White Mulberry) Leaf Extract as Potential Antibacterial and Anticancer Agents Kumkoon T, Srisaisap M, Boonserm P Molecules 26-Jan-2023
PMCID:PMC9920803
doi:10.3390/molecules28031213
PMID:36770881
Bibliometric analysis on exploitation of biogenic gold and silver nanoparticles in breast, ovarian and cervical cancer therapy Bhandari M, Raj S, Kumar A, Kaur DP Front Pharmacol 22-Dec-2022
PMCID:PMC9818348
doi:10.3389/fphar.2022.1035769
PMID:36618941
Mitigating the Mistletoe Menace: Biotechnological and Smart Management Approaches Mudgal G, Kaur J, Chand K, Parashar M, Dhar SK, Singh GB, Gururani MA Biology (Basel) 10-Nov-2022
PMCID:PMC9687506
doi:10.3390/biology11111645
PMID:36358346
Applications of Gold and Silver Nanoparticles in Theranostics Sakthi Devi R, Girigoswami A, Siddharth M, Girigoswami K Appl Biochem Biotechnol 13-May-2022
PMCID:PMC9099041
doi:10.1007/s12010-022-03963-z
PMID:35551613
Inventorization and Consensus Analysis of Ethnoveterinary Medicinal Knowledge Among the Local People in Eastern India: Perception, Cultural Significance, and Resilience Mandal SK, Rahaman CH Front Pharmacol 29-Apr-2022
PMCID:PMC9099233
doi:10.3389/fphar.2022.861577
PMID:35571138
Synthesis, Characterization and Biomedical Application of Silver Nanoparticles Naganthran A, Verasoundarapandian G, Khalid FE, Masarudin MJ, Zulkharnain A, Nawawi NM, Karim M, Che Abdullah CA, Ahmad SA Materials (Basel) 06-Jan-2022
PMCID:PMC8779869
doi:10.3390/ma15020427
PMID:35057145
Potential Anti-Mycobacterium tuberculosis Activity of Plant Secondary Metabolites: Insight with Molecular Docking Interactions Kumar M, Singh SK, Singh PP, Singh VK, Rai AC, Srivastava AK, Shukla L, Kesawat MS, Kumar Jaiswal A, Chung SM, Kumar A Antioxidants (Basel) 14-Dec-2021
PMCID:PMC8750514
doi:10.3390/antiox10121990
PMID:34943093

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1248/CPB.54.740
> Benzenoids / Benzene and substituted derivatives / Styrenes
4-Vinylphenol 62453 Click to see C=CC1=CC=C(C=C1)O 120.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Sutherlandin trans-p-coumarate 10526195 Click to see C1=CC(=CC=C1C=CC(=O)OCC(=CC#N)COC2C(C(C(C(O2)CO)O)O)O)O 421.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1-Hydroxy-14-methoxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 73036810 Click to see CC(=O)OC1CC(C2(C(C1(C)C)CCC3(C2C(C=C4C3(CCC5(C4CC(CC5)(C)C)C)C)OC)C)C)O 514.80 unknown https://doi.org/10.1248/CPB.54.740
(1,14-Dihydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 13918516 Click to see CC(=O)OC1CC(C2(C(C1(C)C)CCC3(C2C(C=C4C3(CCC5(C4CC(CC5)(C)C)C)C)O)C)C)O 500.80 unknown https://doi.org/10.1248/CPB.54.740
(1,14-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl) acetate 73819956 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(C(CC(C5(C)C)OC(=O)C)O)C)C)O)C2C1C)C)C 500.80 unknown https://doi.org/10.1248/CPB.54.740
(14-Ethoxy-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 73024722 Click to see CCOC1C=C2C3CC(CCC3(CCC2(C4(C1C5(C(CC4)C(C(CC5O)OC(=O)C)(C)C)C)C)C)C)(C)C 528.80 unknown https://doi.org/10.1248/CPB.54.740
(2S)-2-[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-acetyloxy-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-1-yl]propanoic acid 21588191 Click to see CC(C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C)C(=O)O 500.80 unknown https://doi.org/10.1248/CPB.54.740
[(1R,3S,4aS,6aR,6bS,8aR,11R,12S,12aR,14R,14aS,14bS)-1,14-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate 21670088 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(C(CC(C5(C)C)OC(=O)C)O)C)C)O)C2C1C)C)C 500.80 unknown https://doi.org/10.1248/CPB.54.740
[(1R,3S,4aS,6aR,6bS,8aR,12aR,14R,14aS,14bS)-1-hydroxy-14-methoxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 11634922 Click to see CC(=O)OC1CC(C2(C(C1(C)C)CCC3(C2C(C=C4C3(CCC5(C4CC(CC5)(C)C)C)C)OC)C)C)O 514.80 unknown https://doi.org/10.1248/CPB.54.740
[(1R,3S,4aS,6aR,6bS,8aR,12aR,14R,14aS,14bS)-1,14-dihydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 102179689 Click to see CC(=O)OC1CC(C2(C(C1(C)C)CCC3(C2C(C=C4C3(CCC5(C4CC(CC5)(C)C)C)C)O)C)C)O 500.80 unknown https://doi.org/10.1248/CPB.54.740
[(1R,3S,4aS,6aR,6bS,8aR,12aR,14R,14aS,14bS)-14-hydroxy-1-(2-hydroxypropan-2-yloxy)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 11541341 Click to see CC(=O)OC1CC(C2(C(C1(C)C)CCC3(C2C(C=C4C3(CCC5(C4CC(CC5)(C)C)C)C)O)C)C)OC(C)(C)O 558.80 unknown https://doi.org/10.1248/CPB.54.740
[14-Hydroxy-1-(2-hydroxypropan-2-yloxy)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 73000355 Click to see CC(=O)OC1CC(C2(C(C1(C)C)CCC3(C2C(C=C4C3(CCC5(C4CC(CC5)(C)C)C)C)O)C)C)OC(C)(C)O 558.80 unknown https://doi.org/10.1248/CPB.54.740
2-(9-Acetyloxy-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-1-yl)propanoic acid 73807406 Click to see CC(C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C)C(=O)O 500.80 unknown https://doi.org/10.1248/CPB.54.740
3|A-Acetoxyurs-12-en-11-one 10528813 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 482.70 unknown https://doi.org/10.1248/CPB.54.740
3beta-Acetoxy-11alpha-ethoxyoleana-12-ene-1beta-ol 11598975 Click to see CCOC1C=C2C3CC(CCC3(CCC2(C4(C1C5(C(CC4)C(C(CC5O)OC(=O)C)(C)C)C)C)C)C)(C)C 528.80 unknown https://doi.org/10.1248/CPB.54.740
Acetic acid, 4,4,6a,6b,8a,11,12,14b-octamethyl-14-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-eicosahydropicen-3-yl ester 623524 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 482.70 unknown https://doi.org/10.1248/CPB.54.740
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.54.740
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.54.740
> Lipids and lipid-like molecules / Steroids and steroid derivatives
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-1-acetyl-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate 490366 Click to see CC(=O)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 470.70 unknown https://doi.org/10.1248/CPB.54.740
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4R,5S,6R)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol 667463 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown via CMAUP database
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown via CMAUP database
> Organoheterocyclic compounds / Furopyrans
1,5-Dihydroxy-13-methyl-14-propan-2-yl-3,7,10-trioxapentacyclo[6.4.1.19,12.02,4.05,13]tetradecan-11-one 73834164 Click to see CC(C)C1C2C3C4(C(CO3)(C5C(C4(C1C(=O)O2)O)O5)O)C 296.31 unknown https://doi.org/10.1248/CPB.54.740
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2R,3R,4R,5S,6R)-6-[5,6-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 59991342 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
Scutellarin 185617 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.54.740
2-(4-Hydroxyphenyl)-3-[[(2R)-3alpha,4beta-dihydroxy-5alpha-(hydroxymethyl)tetrahydrofuran]-2alpha-yloxy]-5,7-dihydroxy-4H-1-benzopyran-4-one 102421333 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O 418.30 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 12047524 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1248/CPB.54.740
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1248/CPB.54.740
isorhamnetin 3-O-beta-L-glucopyranoside 72551443 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-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
Juglanin 5318717 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O 418.30 unknown via CMAUP database
kaempferol 3-O-beta-L-glucopyranoside 9911508 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Kaempferol-3-O-rhamnoside 5835713 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1248/CPB.54.740
Quercetin 3-O-beta-D-xylopyranoside 5320861 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.54.740
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5,6-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 69753795 Click to see CC1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O)O 432.40 unknown via CMAUP database
7-[(2S,3S,4R,5S,6R)-3,4-dihydroxy-6-methyl-5-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5,6-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 59991324 Click to see CC1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O)OC5C(C(C(CO5)O)O)O 564.50 unknown via CMAUP database
Sorbarin 9824100 Click to see CC1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O)O 432.40 unknown via CMAUP database

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