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Syzygium nervosum

Syzygium nervosum - 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 UUID643fee48755a5728699679
Scientific name Syzygium nervosum
Authority DC.
First published in Prodr. 3: 260 (1828)

Description Top

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Synonyms Top

Scientific name Authority First published in
Syzygium cerasoides (Roxb.) Chatterjee & Kanjilal J. Bombay Nat. Hist. Soc. 55: 755 (1967)
Syzygium nervosum var. obovatum (Kurz) An.Kumar J. Econ. Taxon. Bot. 7: 664 (1985 publ. 1986)
Syzygium nodosum Miq. Fl. Ned. Ind. 1(1): 447 (1855)
Syzygium operculatum (Roxb.) Nied. Nat. Pflanzenfam. 3(7): 85 (1893)
Syzygium wallichianum C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 500 (1845)
Eugenia operculata var. obovata Kurz Forest Fl. Burma 1: 482 1877
Calyptranthes costata Buch.-Ham. Numer. List [Wallich] n. 3556. 1831
Calyptranthes cuneata Buch.-Ham. ex Wall. Numer. List : n.º 3557 (1831)
Calyptranthes grandis Buch.-Ham. ex Wall. Numer. List : n.º 3554 (1831)
Calyptranthes makul Blanco Fl. Filip. : 419 (1837)
Calyptranthes mangiferifolia Hance ex Walp. Ann. Bot. Syst. 2: 629 (1852)
Calyptranthes tatna Buch.-Ham. ex Wall. Numer. List : n.º 3555 (1831)
Cleistocalyx cerasoides (Roxb.) I.M.Turner Gard. Bull. Singapore 57: 26 (2005)
Cleistocalyx cerasoides var. paniala (Roxb.) I.M.Turner Gard. Bull. Singapore 57: 26 (2005)
Syzygium nervosum var. paniala (Roxb.) Craven & Biffin Blumea 51: 138 (2006)
Eugenia operculata var. paniala (Roxb.) King J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 70: 130. 1901
Cleistocalyx nervosus var. paniala (Roxb.) J.Parn. & Chantaranothai Novon 6: 201 (1996)
Cleistocalyx operculatus (Roxb.) Merr. & L.M.Perry J. Arnold Arbor. 18: 337 (1937)
Cleistocalyx operculatus var. paniala (Roxb.) Chantar. & J.Parn. Kew Bull. 48: 591 (1993)
Eugenia cerasoides Roxb. Fl. Ind. ed. 1832 , 2: 488 (1832)
Eugenia clausa C.B.Rob. Philipp. J. Sci., C 4: 380 (1909)
Eugenia divaricato-cymosa Hayata Icon. Pl. Formosan. 3: 118 (1913)
Eugenia gigantea Ridl. J. Straits Branch Roy. Asiat. Soc. 45: 192 (1906)
Eugenia holtzei F.Muell. Australas. J. Pharm. 1: 199 (1886)
Eugenia holtziana F.Muell. Sec. Cens. Austral. Pl. (1889) 101, sphalm.
Eugenia operculata Roxb. Hort. Bengal. 37. 1814
Eugenia paniala Roxb. Fl. Ind. ed. 1832 , 2: 489 (1832)
Eugenia suavis Ridl. J. Fed. Malay States Mus. 5: 160 (1915)
Cleistocalyx nervosum var. paniala (Roxb.) J.Parn. & Chantar. Novon 6: 201 (1996)
Syzygium suave (Ridl.) Widodo Reinwardtia 13: 237 (2012)
Syzygium operculatum var. obovatum (Duthie) Gamble Fl. Madras 1: 481 (1919)
Eugenia holtzeana F.Muell. Syst. Census Austral. Pl. Suppl. 4: 3. 1889 (1889)
Eugenia operculata var. cerasoides (Roxb.) Craib Fl. Siam. 1: 654. 1931
Syzygium cerasoides Raizada

Common names Top

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Language Common/alternative name
Assamese কোটাহি জামু
Japanese ヴォイの木
Nepali क्यामुना
Chinese 水翁叶
Chinese 水翁根
Chinese 水翁皮
Chinese 水翁花
Chinese 水翁蒲桃
Chinese 水翁蒲桃（水榕、水翁花）
Chinese 水榕
Chinese 水翁

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
      • Tibet
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Christmas Island
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000319069
Tropicos 22107486
KEW urn:lsid:ipni.org:names:601984-1
The Plant List kew-199981
Open Tree Of Life 466450
NCBI Taxonomy 219895
IUCN Red List 130887438
IPNI 601984-1
iNaturalist 134219
GBIF 3184115
Freebase /m/04q2bjx
USDA GRIN 452516
Wikipedia Syzygium_nervosum
CMAUP NPO4734

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
Natural-derived acetophenones: chemistry and pharmacological activities Ahmadpourmir H, Attar H, Asili J, Soheili V, Taghizadeh SF, Shakeri A Nat Prod Bioprospect 10-May-2024
PMCID:PMC11087454
doi:10.1007/s13659-024-00447-x
PMID:38727781
Research Progress on Extraction and Detection Technologies of Flavonoid Compounds in Foods Li W, Zhang X, Wang S, Gao X, Zhang X Foods 19-Feb-2024
PMCID:PMC10887530
doi:10.3390/foods13040628
PMID:38397605
Correction: He et al. Biology, Ecology and Management of Tephritid Fruit Flies in China: A Review. Insects 2023, 14, 196 He Y, Xu Y, Chen X Insects 31-Jan-2024
PMCID:PMC10889426
doi:10.3390/insects15020093
PMID:38392559
Recent Highlights in Sustainable Bio-Based Edible Films and Coatings for Fruit and Vegetable Applications Martins VF, Pintado ME, Morais RM, Morais AM Foods 19-Jan-2024
PMCID:PMC10814993
doi:10.3390/foods13020318
PMID:38275685
Selenium Nanoparticles: Green Synthesis and Biomedical Application Mikhailova EO Molecules 15-Dec-2023
PMCID:PMC10745377
doi:10.3390/molecules28248125
PMID:38138613
Intra- and interspecific ecophysiological responses to waterlogging stress in two contrasting waterlogging-tolerant arbor species Tian M, Li D, Cisse EH, Miao L, Zhou J, Yang W, Chen B, Li L, Tian H, Ye B, Yang F Front Plant Sci 13-Nov-2023
PMCID:PMC10679334
doi:10.3389/fpls.2023.1257730
PMID:38023841
Advances in the Preparation, Stability, Metabolism, and Physiological Roles of Anthocyanins: A Review Li Q, Zhang F, Wang Z, Feng Y, Han Y Foods 30-Oct-2023
PMCID:PMC10647620
doi:10.3390/foods12213969
PMID:37959087
Metabolomics and molecular networking approach for exploring the anti-diabetic activity of medicinal plants Timilsina AP, Raut BK, Huo C, Khadayat K, Budhathoki P, Ghimire M, Budhathoki R, Aryal N, Kim KH, Parajuli N RSC Adv 19-Oct-2023
PMCID:PMC10585453
doi:10.1039/d3ra04037b
PMID:37869390
Flavonoids: Overview of Biosynthesis, Biological Activity, and Current Extraction Techniques Liga S, Paul C, Péter F Plants (Basel) 23-Jul-2023
PMCID:PMC10384615
doi:10.3390/plants12142732
PMID:37514347
Stable biogenic silver nanoparticles from Syzygium nervosum bud extract for enhanced catalytic, antibacterial and antifungal properties Lan Pham T, Dat Doan V, Le Dang Q, Anh Nguyen T, Huong Nguyen TL, Thuy Tran TD, Lan Nguyen TP, Anh Vo TK, Huy Nguyen T, Lam Tran D RSC Adv 12-Jul-2023
PMCID:PMC10336774
doi:10.1039/d3ra02754f
PMID:37448638
Antibacterial effect of essential oils and their components against Xanthomonas arboricola pv. pruni revealed by microdilution and direct bioautographic assays Kolozsváriné Nagy J, Móricz ÁM, Böszörményi A, Ambrus Á, Schwarczinger I Front Cell Infect Microbiol 14-Jun-2023
PMCID:PMC10303133
doi:10.3389/fcimb.2023.1204027
PMID:37389207
A Review of the In Vitro Inhibition of α-Amylase and α-Glucosidase by Chalcone Derivatives Tran TD, Tu VL, Hoang TM, Dat TV, Tam DN, Phat NT, Hung DT, Huynh HH, Do TC, Le HH, Minh LH Cureus 07-Apr-2023
PMCID:PMC10164439
doi:10.7759/cureus.37267
PMID:37162770
Ethnobotanical study on herbal tea drinks in Guangxi, China Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C J Ethnobiol Ethnomed 31-Mar-2023
PMCID:PMC10064729
doi:10.1186/s13002-023-00579-3
PMID:37004116
The role of selenium and nano selenium on physiological responses in plant: a review Khan Z, Thounaojam TC, Chowdhury D, Upadhyaya H Plant Growth Regul 24-Mar-2023
PMCID:PMC10036987
doi:10.1007/s10725-023-00988-0
PMID:37197287
Fabrication of Antibacterial Ag/Graphene-Integrated Non-woven Polypropylene Textile for Air Pollutant Filtering La DD, Pham KT, Lai HT, Tran DL, Van Bui C, Nguyen PH, Chang SW, Um MJ, Nguyen DD Waste Biomass Valorization 23-Mar-2023
PMCID:PMC10034908
doi:10.1007/s12649-023-02101-y
PMID:37363338

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Tritriacontane 12411 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 464.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1994.9699366
Neryl acetate 1549025 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1994.9699366
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
2,6-Dimethyl-2,4,6-octatriene 5368821 Click to see CC=C(C)C=CC=C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9699366
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9699366
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9699366
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.1994.9699366
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9699366
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1080/10412905.1994.9699366
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9699366
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9699366
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1080/10412905.1994.9699366
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1080/10412905.1994.9699366
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9699366
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1080/10412905.1994.9699366
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
(+)-Gamma-cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene 101708 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1080/10412905.1994.9699366
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1994.9699366
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
Calamenene 6429077 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1080/10412905.1994.9699366
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1994.9699366
cis-Nerolidol 5320128 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9699366
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4S,4aR,7aS,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 137704583 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9699366
Alloaromadendren 91746537 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
alpha-Gurjunene 15560276 Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
Viridiflorene 10910653 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
beta-Selinene 442393 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699366
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Dehydrosoyasaponin I 656760 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8=O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 941.10 unknown via CMAUP database
Soyasaponin I 122097 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 943.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4R,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol 21119301 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C 458.70 unknown via CMAUP database
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/10.1016/J.PHYTOCHEM.2003.11.002
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Sophoradiol 9846221 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)C)O)C)C 442.70 unknown via CMAUP database
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/10.1016/J.PHYTOCHEM.2003.11.002
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(Z,2R)-6-hydroxy-6-methylhept-4-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 101690746 Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.11.002
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.11.002
> Organoheterocyclic compounds / Heteroaromatic compounds
Perillene 68316 Click to see CC(=CCCC1=COC=C1)C 150.22 unknown https://doi.org/10.1080/10412905.1994.9699366
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2s)-8-Formyl-6-methylnaringenin 25155520 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)C=O)O 314.29 unknown https://doi.org/10.1248/CPB.56.1725
(S)-2,3-Dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone 6453244 Click to see CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3 270.28 unknown https://doi.org/10.1021/NP1002753
2H-1-Benzopyran-8-carboxaldehyde, 3,4-dihydro-5,7-dihydroxy-6-methyl-4-oxo-2-phenyl- 597205 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)C=O)O 298.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.11.002
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-methyl-4-oxo-2,3-dihydrochromene-8-carbaldehyde 163100707 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)C=O)O 314.29 unknown https://doi.org/10.1248/CPB.56.1725
Cryptostrobin 15953986 Click to see CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3 270.28 unknown https://doi.org/10.1021/NP1002753
Demethoxymatteucinol 180550 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)C)O 284.31 unknown https://doi.org/10.1021/NP1002753
Desmethoxymatteucinol 625031 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)C)O 284.31 unknown https://doi.org/10.1021/NP1002753
Lawinal 189152 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)C=O)O 298.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.11.002
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3R)-3,5,7-trihydroxy-6,8-dimethyl-2-phenyl-2,3-dihydrochromen-4-one 49831444 Click to see CC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=CC=CC=C3)O)C)O 300.30 unknown https://doi.org/10.1021/NP1002753
(2S,3R)-2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one 98049813 Click to see C1=CC(=C(C=C1O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 304.25 unknown via CMAUP database
3,5,7-Trihydroxy-6,8-dimethyl-2-phenyl-2,3-dihydrochromen-4-one 66761753 Click to see CC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=CC=CC=C3)O)C)O 300.30 unknown https://doi.org/10.1021/NP1002753
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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
> 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 via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
Isoscoparin 442611 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown via CMAUP database
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Isoschaftoside 3084995 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 564.50 unknown via CMAUP database
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Schaftoside 442658 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
4-hydroxy-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]-2-methoxy-5-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzaldehyde 25155517 Click to see CC1=C(C(=C(C(=C1OC2C(C(C(C(O2)CO)O)O)O)C=O)OC)C(=O)C=CC3=CC=C(C=C3)O)O 490.50 unknown https://doi.org/10.1248/CPB.56.1725
4-Hydroxy-3-[3-(4-hydroxyphenyl)prop-2-enoyl]-2-methoxy-5-methyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzaldehyde 162876110 Click to see CC1=C(C(=C(C(=C1OC2C(C(C(C(O2)CO)O)O)O)C=O)OC)C(=O)C=CC3=CC=C(C=C3)O)O 490.50 unknown https://doi.org/10.1248/CPB.56.1725
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 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
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-6-methyl-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromene-8-carbaldehyde 25155518 Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)CO)O)O)O)C=O)OC(CC2=O)C4=CC=C(C=C4)O)O 476.40 unknown https://doi.org/10.1248/CPB.56.1725
5-Hydroxy-2-(4-hydroxyphenyl)-6-methyl-4-oxo-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromene-8-carbaldehyde 162970139 Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)CO)O)O)O)C=O)OC(CC2=O)C4=CC=C(C=C4)O)O 476.40 unknown https://doi.org/10.1248/CPB.56.1725
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
(2S)-2,7-Dihydroxy-5-methoxy-6,8-dimethylflavanone 49831445 Click to see CC1=C(C(=C(C2=C1OC(CC2=O)(C3=CC=CC=C3)O)OC)C)O 314.30 unknown https://doi.org/10.1021/NP1002753
(2s)-7-Hydroxy-5-methoxy-6,8-dimethyl flavanone 101890693 Click to see CC1=C(C(=C(C2=C1OC(CC2=O)C3=CC=CC=C3)OC)C)O 298.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.11.002
(2S)-7-hydroxy-5-methoxy-8-methylflavanone 52943439 Click to see CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=CC=C3 284.31 unknown https://doi.org/10.1021/NP1002753
2,7-dihydroxy-5-methoxy-6,8-dimethyl-2-phenyl-3H-chromen-4-one 66762038 Click to see CC1=C(C(=C(C2=C1OC(CC2=O)(C3=CC=CC=C3)O)OC)C)O 314.30 unknown https://doi.org/10.1021/NP1002753
7-Hydroxy-5-methoxy-6,8-dimethylflavanone 15413154 Click to see CC1=C(C(=C(C2=C1OC(CC2=O)C3=CC=CC=C3)OC)C)O 298.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.11.002
7-Hydroxy-5-methoxy-6,8-dimethylflavone 14753671 Click to see CC1=C(C(=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)OC)C)O 296.30 unknown https://doi.org/10.1021/NP1002753
7-Hydroxy-5-methoxy-8-methyl-2-phenyl-2,3-dihydrochromen-4-one 21721819 Click to see CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=CC=C3 284.31 unknown https://doi.org/10.1021/NP1002753
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5-hydroxy-7-methoxy-6,8-dimethylflavanone 21142052 Click to see CC1=C(C2=C(C(=C1OC)C)OC(CC2=O)C3=CC=CC=C3)O 298.30 unknown https://doi.org/10.1021/NP1002753
(2S)-6-formyl-8-methyl-7-O-methylpinocembrin 52945746 Click to see CC1=C2C(=C(C(=C1OC)C=O)O)C(=O)CC(O2)C3=CC=CC=C3 312.30 unknown https://doi.org/10.1021/NP1002753
(2s)-8-Formyl-5-hydroxy-7-methoxy-6-methylflavanone 12132943 Click to see CC1=C(C2=C(C(=C1OC)C=O)OC(CC2=O)C3=CC=CC=C3)O 312.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.11.002
https://doi.org/10.1021/NP1002753
5-Hydroxy-7-methoxy-6-methyl-4-oxo-2-phenyl-2,3-dihydrochromene-8-carbaldehyde 85435141 Click to see CC1=C(C2=C(C(=C1OC)C=O)OC(CC2=O)C3=CC=CC=C3)O 312.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.11.002
https://doi.org/10.1021/NP1002753
5-Hydroxy-7-methoxy-6,8-di-C-methylflavanone 369596 Click to see CC1=C(C2=C(C(=C1OC)C)OC(CC2=O)C3=CC=CC=C3)O 298.30 unknown https://doi.org/10.1021/NP1002753
Leridal 42607880 Click to see CC1=C2C(=C(C(=C1OC)C=O)O)C(=O)CC(O2)C3=CC=CC=C3 312.30 unknown https://doi.org/10.1021/NP1002753
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
3,9-Dihydroxypterocarpan 162933 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=C2C=CC(=C4)O 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
1,3,8-Trihydroxy-9-methoxy-[1]benzofuro[2,3-b]chromen-11-one 15126297 Click to see COC1=C(C=C2C(=C1)C3=C(O2)OC4=CC(=CC(=C4C3=O)O)O)O 314.25 unknown via CMAUP database
2'-Hydroxygenistein 5282074 Click to see C1=CC(=C(C=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)O 286.24 unknown via CMAUP database
7-Hydroxy-5-Methoxy-6,8-Dimethylisoflavone 49831443 Click to see CC1=C(C(=C(C2=C1OC=C(C2=O)C3=CC=CC=C3)OC)C)O 296.30 unknown https://doi.org/10.1021/NP1002753
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown via CMAUP database
Lupinalbin A 5324349 Click to see C1=CC2=C(C=C1O)OC3=C2C(=O)C4=C(C=C(C=C4O3)O)O 284.22 unknown via CMAUP database
Orobol 5281801 Click to see C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Ambocin 5491738 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC=C(C4=O)C5=CC=C(C=C5)O)O)O)O)O)O)(CO)O 564.50 unknown via CMAUP database
Daidzein 7-O-apiosyl-(1->6)-glucoside 20055730 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C(=O)C(=CO4)C5=CC=C(C=C5)O)O)O)O)O)(CO)O 548.50 unknown via CMAUP database
Genistin 5281377 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-Methoxydaidzein 5319422 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(3S)-3-(2,4-dimethoxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 92143157 Click to see COC1=CC(=C(C=C1)C2COC3=CC(=CC(=C3C2=O)O)O)OC 316.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown via CMAUP database
Panchovillin 21676203 Click to see COC1=CC(=CC(=C1OC)OC)C2=COC3=CC(=CC(=C3C2=O)O)O 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-4,2',4'-trihydroxy-6'-methoxy-3',5'-dimethylchalcone 49831446 Click to see CC1=C(C(=C(C(=C1O)C(=O)C=CC2=CC=C(C=C2)O)OC)C)O 314.30 unknown https://doi.org/10.1021/NP1002753
1-(2,4-Dihydroxy-6-methoxy-3,5-dimethylphenyl)-3-(2-hydroxyphenyl)prop-2-en-1-one 73095154 Click to see CC1=C(C(=C(C(=C1O)C(=O)C=CC2=CC=CC=C2O)OC)C)O 314.30 unknown https://doi.org/10.1021/NP1002753
1-(2,4-Dihydroxy-6-methoxy-3,5-dimethylphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one 75297996 Click to see CC1=C(C(=C(C(=C1O)C(=O)C=CC2=CC=C(C=C2)O)OC)C)O 314.30 unknown https://doi.org/10.1021/NP1002753
1-(2,4-Dihydroxy-6-methoxy-3,5-dimethylphenyl)-3-phenylprop-2-en-1-one 54341383 Click to see CC1=C(C(=C(C(=C1O)C(=O)C=CC2=CC=CC=C2)OC)C)O 298.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.11.002
https://doi.org/10.1021/NP1002753
2,2',4'-Trihydroxy-6'-methoxy-3',5'-dimethylchalcone 11771403 Click to see CC1=C(C(=C(C(=C1O)C(=O)C=CC2=CC=CC=C2O)OC)C)O 314.30 unknown https://doi.org/10.1021/NP1002753
2,4-dihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]-6-methoxy-3-methylbenzaldehyde 25155519 Click to see CC1=C(C(=C(C(=C1O)C(=O)C=CC2=CC=C(C=C2)O)OC)C=O)O 328.30 unknown https://doi.org/10.1248/CPB.56.1725
2,4-dihydroxy-6-methoxy-3-methyl-5-[(E)-3-phenylprop-2-enoyl]benzaldehyde 12132942 Click to see CC1=C(C(=C(C(=C1O)C(=O)C=CC2=CC=CC=C2)OC)C=O)O 312.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.11.002
2',4'-Dihydroxy-6'-methoxy-3'-methylchalcone 73097563 Click to see CC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=CC=C2)O 284.31 unknown https://doi.org/10.1021/NP1002753
2',4'-Dihydroxy-6'-methoxy-3',5'-dimethylchalcone 10424762 Click to see CC1=C(C(=C(C(=C1O)C(=O)C=CC2=CC=CC=C2)OC)C)O 298.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.11.002
https://doi.org/10.1021/NP1002753
3'-Formyl-4',6'-dihydroxy-2'-methoxy-5'-methyl-chalcone 91005428 Click to see CC1=C(C(=C(C(=C1O)C(=O)C=CC2=CC=CC=C2)OC)C=O)O 312.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.11.002
3'-Formyl-4',6',4-trihydroxy-2'-methoxy-5'-methylchalcone 91403539 Click to see CC1=C(C(=C(C(=C1O)C(=O)C=CC2=CC=C(C=C2)O)OC)C=O)O 328.30 unknown https://doi.org/10.1248/CPB.56.1725
Stercurensin 11778601 Click to see CC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=CC=C2)O 284.31 unknown https://doi.org/10.1021/NP1002753

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