Alangium chinense - Unknown
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Internal ID UUID6440376d0a6ff257005989
Scientific name Alangium chinense
Authority (Lour.) Harms
First published in Ber. Deutsch. Bot. Ges. xv. 24 (1897), in obs.

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Synonyms Top

Scientific name Authority First published in
Karangolum chinense Kuntze Revis. Gen. Pl. 1: 272 (1891)
Marlea affinis Decne. Voy. Inde 4: 74 (1841)
Marlea begoniifolia Roxb. Hort. Bengal. [28]. 1814
Marlea chinensis Druce Rep. Bot. Soc. Exch. Club Brit. Isles 1916: 634 (1917)
Marlea virgata Zoll. Natuurk. Tijdschr. Ned.-Indië 14: 157 (1857)
Stelanthes solitarius Stokes Bot. Mat. Med. 2: 339 (1812)
Stylidium bauthas Lour. ex Gomes Mem. Acad. Sc. Lisb. Cl. Sc. Pol. Mor. Bel.-Let. n. s. iv. (1), 28 (1868); Merrill in Trans. Am. Phil. Soc. n. s. xxiv. II. 16, 296 (1935), in syn.
Stylidium chinense Lour. Fl. Cochinch. 1: 221. 1790 [Sep 1790]
Stylis chinensis Poir. Encycl. , Suppl. 5: 260 (1817)
Alangium begoniifolium (Roxb.) Baill. Hist. Pl. 6: 270 (1877)
Alangium chinense subsp. pauciflorum W.P.Fang J. Sichuan Univ., Nat. Sci. Ed. 2: 94 (1979)
Alangium chinense var. pauciflorum W.P.Fang ex Y.C.Ho Fl. Tsinling. 1(3): 455 (1981)
Alangium chinense subsp. strigosum W.P.Fang J. Sichuan Univ., Nat. Sci. Ed. 2: 93 (1979)
Alangium chinense subsp. triangulare (Wangerin) W.P.Fang J. Sichuan Univ., Nat. Sci. Ed. 2: 95 (1979)
Alangium kenyense Chiov. Racc. Bot. : 47 (1935)
Alangium octopetalum Hanes ex Blanco Fl. Filip., ed. 2 : 310 (1845)
Alangium platanifolium f. triangulare Wangerin Pflanzenr. IV, 220b: 24 1910
Guettarda jasminiflora Blanco Fl. Filip. : 722 (1837)

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Language Common/alternative name
Arabic علنج صيني
Czech alángium čínské
su ki careuh
Thai ผีเสื้อ
za gogingz
Chinese 八月炸
Chinese 白龙须
Chinese 八角枫
Chinese 华瓜木
Chinese 華八角楓
Chinese 櫙木
Chinese 八角楓

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Varieties (abbr. var.) Top

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Germination/Propagation Top

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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-0000936752
UNII 1PI50RE3BW
Tropicos 8700102
KEW urn:lsid:ipni.org:names:58133-1
The Plant List kew-5545
PaleoBotany 113267
Open Tree Of Life 899878
NCBI Taxonomy 16897
IPNI 58134-1
iNaturalist 133644
GBIF 7326263
Freebase /m/03mh0db
EPPO ALNCH
USDA GRIN 2108
Wikipedia Alangium_chinense
CMAUP NPO15986
PFAF Alangium chinense

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
Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T J Ethnobiol Ethnomed 18-Mar-2024
PMCID:PMC10946099
doi:10.1186/s13002-024-00676-x
PMID:38500123
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
An Overview of Therapeutic Targeting of Nrf2 Signaling Pathway in Rheumatoid Arthritis Saha S ACS Omega 20-Feb-2024
PMCID:PMC10918843
doi:10.1021/acsomega.4c00163
PMID:38463248
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
Integrated Network Pharmacology and Experimental Approach to Investigate the Protective Effect of Jin Gu Lian Capsule on Rheumatoid Arthritis by Inhibiting Inflammation via IL-17/NF-κB Pathway Chen T, Li S, Lian D, Hu Q, Hou H, Niu D, Li H, Song L, Gao Y, Chen Y, Hu X, Li J, Ye Z, Peng B, Zhang G Drug Des Devel Ther 13-Dec-2023
PMCID:PMC10725692
doi:10.2147/DDDT.S423022
PMID:38107658
Anti-cervical cancer mechanism of bioactive compounds from Alangium platanifolium based on the ‘compound-target-disease’ network Zhang H, Zhang R, Su Y, Zheng J, Li H, Han Z, Kong Y, Liu H, Zhang Z, Sai C Heliyon 06-Oct-2023
PMCID:PMC10582369
doi:10.1016/j.heliyon.2023.e20747
PMID:37860565
Woody plant functional traits and phylogenetic signals correlate with urbanization in remnant forest patches Yang J, Wang Z, Pan Y, Zheng Y Ecol Evol 31-Jul-2023
PMCID:PMC10388403
doi:10.1002/ece3.10366
PMID:37529580
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Variation of soil physicochemical properties of different vegetation restoration types on subtropical karst area in southern China Xiao C, You R, Zhu N, Mi X, Gao L, Zhou X, Zhou G PLoS One 16-Mar-2023
PMCID:PMC10019609
doi:10.1371/journal.pone.0282620
PMID:36928208
Tree species composition along environmental and disturbance gradients in tropical sub-montane forests, Tanzania Lolila NJ, Shirima DD, Mauya EW PLoS One 08-Mar-2023
PMCID:PMC9994703
doi:10.1371/journal.pone.0282528
PMID:36888683
Role of Plant-Derived Compounds in the Molecular Pathways Related to Inflammation Olędzka AJ, Czerwińska ME Int J Mol Sci 28-Feb-2023
PMCID:PMC10003729
doi:10.3390/ijms24054666
PMID:36902097
Changes in homegardens in relocation villages, a case study in the Baiku Yao area in Southern China Hu R, Xu C, Nong Y, Luo B J Ethnobiol Ethnomed 27-Feb-2023
PMCID:PMC9972620
doi:10.1186/s13002-023-00578-4
PMID:36849896
Protective effect of compatible herbs in Jin-Gu-Lian formula against Alangium chinense-induced neurotoxicity via oxidative stress, neurotransmitter metabolisms, and pharmacokinetics Lian D, Chen T, Yan L, Hou H, Gao S, Hu Q, Zhang G, Li H, Song L, Gao Y, Pu Y, Chen Y, Peng B Front Pharmacol 16-Feb-2023
PMCID:PMC9977795
doi:10.3389/fphar.2023.1133982
PMID:36874008
Role of reactive oxygen species and mitochondrial damage in rheumatoid arthritis and targeted drugs Jing W, Liu C, Su C, Liu L, Chen P, Li X, Zhang X, Yuan B, Wang H, Du X Front Immunol 09-Feb-2023
PMCID:PMC9948260
doi:10.3389/fimmu.2023.1107670
PMID:36845127
Bioactive substances inhibiting COX-2 and cancer cells isolated from the fibrous roots of Alangium chinense (Lour.) Harms Xiao T, Cheng X, Huang J, Guo Z, Tao L, Shen X RSC Adv 26-Jan-2023
PMCID:PMC9891086
doi:10.1039/d2ra06931h
PMID:36756416

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
Pyridine, 3-(2-piperidinyl)- 2181 Click to see C1CCNC(C1)C2=CN=CC=C2 162.23 unknown via CMAUP database
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
4,5-Dimethoxycanthin-6-one 638215 Click to see COC1=C(C(=O)N2C3=CC=CC=C3C4=C2C1=NC=C4)OC 280.28 unknown https://doi.org/10.1021/NP4000747
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
(4S,6S,8R,9Z,11E)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.06,8]nonadeca-1(15),9,11,16,18-pentaene-2,13-dione 51535441 Click to see CC1CC2C(O2)C=CC=CC(=O)CC3=C(C(=CC(=C3Cl)O)O)C(=O)O1 364.80 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
(4S)-6-hydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13)-tetraene-10,11-dione 73353443 Click to see CC1COC2=C(C(=O)C(=O)C3=C2C1=C(C=C3C)O)C 258.27 unknown https://doi.org/10.1021/NP4000747
Mansonone E 94303 Click to see CC1COC2=C(C(=O)C(=O)C3=C(C=CC1=C32)C)C 242.27 unknown https://doi.org/10.1021/NP4000747
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(6R,9R)-Roseoside 44570408 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown https://doi.org/10.1021/NP990391Z
4-Hydroxy-3,5,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one 73815023 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown https://doi.org/10.1021/NP990391Z
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R)-7,8-Dihydroxycalamenene 14864211 Click to see CC1CCC(C2=C1C(=C(C(=C2)C)O)O)C(C)C 234.33 unknown https://doi.org/10.1021/NP4000747
1alpha-Methoxy-1beta,6-dimethyl-4-isopropyl-7-hydroxynaphthalene-2(1H)-one 71726174 Click to see CC1=CC2=C(C=C1O)C(C(=O)C=C2C(C)C)(C)OC 260.33 unknown https://doi.org/10.1021/NP4000747
2,7-Dihydroxy-4-isopropyl-6-methylnaphthalene-1-carbaldehyde 71726175 Click to see CC1=CC2=C(C=C1O)C(=C(C=C2C(C)C)O)C=O 244.28 unknown https://doi.org/10.1021/NP4000747
2,7-Dihydroxy-4-isopropyl-6-methylnaphthalene-1-carboxylic acid methyl ester 71726176 Click to see CC1=CC2=C(C=C1O)C(=C(C=C2C(C)C)O)C(=O)OC 274.31 unknown https://doi.org/10.1021/NP4000747
2,7-Dihydroxycadalene 157057 Click to see CC1=CC2=C(C=C1O)C(=C(C=C2C(C)C)O)C 230.30 unknown https://doi.org/10.1021/NP4000747
7-Hydroxycadalene 608115 Click to see CC1=C2C=C(C(=CC2=C(C=C1)C(C)C)C)O 214.30 unknown https://doi.org/10.1021/NP4000747
Lacinilene C 170551 Click to see CC1=CC2=C(C=C1O)C(C(=O)C=C2C(C)C)(C)O 246.30 unknown https://doi.org/10.1021/NP4000747
Mansonone C 21742 Click to see CC1=C2C(=C(C=C1)C(C)C)C=C(C(=O)C2=O)C 228.29 unknown https://doi.org/10.1021/NP4000747
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1R,4aR,6R,7S,7aR)-6-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 154730823 Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown https://doi.org/10.1021/NP990391Z
6-Hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 4430509 Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown https://doi.org/10.1021/NP990391Z
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(11R,12R,12aS,13aR)-12-ethenyl-2,3-dihydroxy-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,10,11,12,12a,13,13a-octahydroisoquinolino[2,1-b]isoquinolin-8-one 162923707 Click to see C=CC1C(CC=C2C1CC3C4=CC(=C(C=C4CCN3C2=O)O)O)OC5C(C(C(C(O5)CO)O)O)O 489.50 unknown https://doi.org/10.1021/NP990391Z
12-Ethenyl-2,3-dihydroxy-11-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,10,11,12,12a,13,13a-octahydroisoquinolino[2,1-b]isoquinolin-8-one 162923706 Click to see C=CC1C(CC=C2C1CC3C4=CC(=C(C=C4CCN3C2=O)O)O)OC5C(C(C(C(O5)CO)O)O)O 489.50 unknown https://doi.org/10.1021/NP990391Z
2-Phenylethyl beta-primeveroside 131129 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=CC=C3)O)O)O)O)O)O 416.40 unknown https://doi.org/10.1021/NP990391Z
Benzyl alcohol xylopyranosyl-(1-6)-glucopyranoside 14730864 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O 402.40 unknown https://doi.org/10.1021/NP990391Z
https://doi.org/10.1248/CPB.49.1343
Benzyl beta-primeveroside 131248 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O 402.40 unknown https://doi.org/10.1021/NP990391Z
https://doi.org/10.1248/CPB.49.1343
Hex(?1-2)[Pen(?1-6)]Hex-O-Bn 85347750 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1248/CPB.49.1343
NCGC00386010-01_C24H36O15_Benzyl beta-D-glucopyranosyl-(1->2)-[beta-D-xylopyranosyl-(1->6)]-beta-D-glucopyranoside 10962780 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1248/CPB.49.1343
Phenylethyl primeveroside 14704521 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=CC=C3)O)O)O)O)O)O 416.40 unknown https://doi.org/10.1021/NP990391Z
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[3,4,5-Trihydroxy-6-[2-(hydroxymethyl)phenoxy]oxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 162874541 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP990391Z
[3,4,5-Trihydroxy-6-[2-(hydroxymethyl)phenoxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 85251879 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O 438.40 unknown https://doi.org/10.1021/NP990391Z
2-(2-Hydroxyphenoxy)-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxane-3,4,5-triol 85267749 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC=CC=C3O)O)O)O)O)O)O 404.40 unknown https://doi.org/10.1021/NP990391Z
2-[[[2-(beta-D-Glucopyranosyloxy)-6-hydroxybenzoyl]oxy]methyl]phenyl beta-D-glucopyranoside 14311134 Click to see C1=CC=C(C(=C1)COC(=O)C2=C(C=CC=C2OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 584.50 unknown https://doi.org/10.1021/NP990391Z
2-[2-(Hydroxymethyl)phenoxy]-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxane-3,4,5-triol 162951313 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC=CC=C3CO)O)O)O)O)O)O 418.40 unknown https://doi.org/10.1021/NP990391Z
https://doi.org/10.1248/CPB.49.1343
beta-D-Glucopyranoside, 2-(hydroxymethyl)phenyl 5145 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown https://doi.org/10.1248/CPB.49.1343
https://doi.org/10.1021/NP990391Z
coumaroyl(3-OH)(-6)Glc(b)-O-Ph(2-CH2OH) 101702500 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP990391Z
galloyl(-6)Glc(b)-O-Ph(2-CH2OH) 10741653 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O 438.40 unknown https://doi.org/10.1021/NP990391Z
Glc(b1-2)[Xyl(b1-6)]Glc(b)-O-Ph(2-CH2OH) 10907998 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC=CC=C3CO)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O)O 580.50 unknown https://doi.org/10.1248/CPB.49.1343
Glc(b1-2)Glc(b)-O-Ph(2-CH2OH) 10884825 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)CO)O)O)OC3C(C(C(C(O3)CO)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.49.1343
Henryoside 14311135 Click to see C1=CC=C(C(=C1)COC(=O)C2=C(C=CC=C2OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 584.50 unknown https://doi.org/10.1080/14786419.2012.691496
https://doi.org/10.1248/CPB.49.1343
https://doi.org/10.1021/NP990391Z
Hex(?1-2)[Pen(?1-6)]Hex-O-Ph(2-CH2OH) 85311288 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC=CC=C3CO)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O)O 580.50 unknown https://doi.org/10.1248/CPB.49.1343
Hex(?1-2)Hex-O-Ph(2-CH2OH) 85301922 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)CO)O)O)OC3C(C(C(C(O3)CO)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.49.1343
Salicin 439503 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown https://doi.org/10.1248/CPB.49.1343
https://doi.org/10.1021/NP990391Z
https://doi.org/10.1080/14786419.2012.691496
Xyl(b1-6)Glc(b)-O-Ph(2-CH2OH) 101702499 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC=CC=C3CO)O)O)O)O)O)O 418.40 unknown https://doi.org/10.1021/NP990391Z
https://doi.org/10.1248/CPB.49.1343
Xyl(b1-6)Glc(b)-O-Ph(2-OH) 10787388 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC=CC=C3O)O)O)O)O)O)O 404.40 unknown https://doi.org/10.1021/NP990391Z
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1R,4S,7R,11S,12R)-12-hydroxy-3,3,7,11-tetramethyl-2-oxatricyclo[6.3.1.04,12]dodec-8-en-10-one 71726173 Click to see CC1CCC2C(OC3C2(C1=CC(=O)C3C)O)(C)C 250.33 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives
8-Hydroxy-3,6,9-trimethylbenzo[de]quinolin-7-one 136239438 Click to see CC1=C2C3=C(C=C1)C(=CN=C3C(=C(C2=O)O)C)C 239.27 unknown https://doi.org/10.1021/NP4000747
> Organoheterocyclic compounds / Piperidines / Benzylpiperidines / N-benzylpiperidines
(2R)-1-[(2-hydroxyphenyl)methyl]-2-pyridin-3-ylpiperidin-2-ol 71726245 Click to see C1CCN(C(C1)(C2=CN=CC=C2)O)CC3=CC=CC=C3O 284.35 unknown via CMAUP database
(2R)-N-Hydroxybenzylanabasine 29955676 Click to see C1CCN(C(C1)C2=CN=CC=C2)CC3=CC=CC=C3O 268.35 unknown https://doi.org/10.1021/NP4000747
(2S)-2-Hydroxy-N-hydroxybenzylanabasine 71726244 Click to see C1CCN(C(C1)(C2=CN=CC=C2)O)CC3=CC=CC=C3O 284.35 unknown via CMAUP database
(2S)-N-Hydroxybenzylanabasine 29955678 Click to see C1CCN(C(C1)C2=CN=CC=C2)CC3=CC=CC=C3O 268.35 unknown https://doi.org/10.1021/NP4000747
1-[(2-Hydroxyphenyl)methyl]-2-pyridin-3-ylpiperidin-2-ol 73356513 Click to see C1CCN(C(C1)(C2=CN=CC=C2)O)CC3=CC=CC=C3O 284.35 unknown https://doi.org/10.1021/NP4000747
2-[(2-Pyridin-3-ylpiperidin-1-yl)methyl]phenol 45928083 Click to see C1CCN(C(C1)C2=CN=CC=C2)CC3=CC=CC=C3O 268.35 unknown https://doi.org/10.1021/NP4000747
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
Phomalactone 6475274 Click to see CC=CC1C(C=CC(=O)O1)O 154.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1021/NP990391Z
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 14825575 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 596.50 unknown https://doi.org/10.1021/NP990391Z
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 14185727 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1021/NP990391Z
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 13647412 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)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown https://doi.org/10.1021/NP990391Z
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2-O-beta-D-xylopyranosyl-beta-D-galactopyranosyl)oxy]- 5274586 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 596.50 unknown https://doi.org/10.1021/NP990391Z
4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2-O-beta-D-xylopyranosyl-beta-D-galactopyranosyl)oxy]- 10438202 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 580.50 unknown https://doi.org/10.1021/NP990391Z
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1021/NP990391Z
Panasenoside 9986191 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)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown https://doi.org/10.1021/NP990391Z
quercetin 3-O-beta-D-glucosylgalactoside 14185728 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1021/NP990391Z
Rustoside 74977996 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 580.50 unknown https://doi.org/10.1021/NP990391Z
> Phenylpropanoids and polyketides / Tannins
galloyl(-4)[galloyl(-6)]Glc(b)-O-Ph(2-CH2OH) 10817209 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 590.50 unknown https://doi.org/10.1021/NP990391Z
galloyl(-4)[galloyl(-6)]Hex-O-Ph(2-CH2OH) 85278055 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 590.50 unknown https://doi.org/10.1021/NP990391Z
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3,4,5,11,12,21,22,23-Octahydroxy-13-[2-(hydroxymethyl)phenoxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaene-8,18-dione 85202157 Click to see C1C2C(C(C(C(O2)OC3=CC=CC=C3CO)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O 588.50 unknown https://doi.org/10.1021/NP990391Z
4',6'-O-Hexahydroxydibenzoylsalicin 10603452 Click to see C1C2C(C(C(C(O2)OC3=CC=CC=C3CO)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O 588.50 unknown https://doi.org/10.1021/NP990391Z

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