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Uvaria grandiflora

Uvaria grandiflora - 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 UUID643ffa291246b368397708
Scientific name Uvaria grandiflora
Authority Roxb. ex Hornem.
First published in Hort. Bot. Hafn. , Suppl.: 141 (1819)

Description Top

Suggest a correction or write a new one!
Uvaria grandiflora is an Asian liana species in the family Annonaceae and tribe Uvarieae. It is native to China, Indochina, Malesia and New Guinea. It has a variety of external links related to it, such as Wikimedia Commons, Wikispecies, Catalogue of Life, and more.

Synonyms Top

Scientific name Authority First published in
Uva grandiflora Kuntze Revis. Gen. Pl. 1: 7 (1891)
Uvaria cardinalis Elmer Leafl. Philipp. Bot. 5: 1748 (1913)
Unona grandiflora Lesch. ex DC. Prodr. 1: 90 (1824)
Uvaria rubra C.B.Rob. Bull. Torrey Bot. Club 35: 68 (1908)
Uvaria rhodantha Hance Ann. Bot. Syst. 2: 19 (1851)
Uvaria purpurea Blume Bijdr. Fl. Ned. Ind. : 11 (1825)
Uvaria platypetala Champ. ex Benth. Hooker's J. Bot. Kew Gard. Misc. 3: 257 (1851)
Uvaria flava Teijsm. & Binn. Natuurk. Tijdschr. Ned.-Indië 25: 419 (1863)
Guatteria macrantha C.Presl Reliq. Haenk. 2: 78 (1835)
Uvaria purpurea var. tuberculata King J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 61: 18 1893
Uvaria purpurea var. subbiflora Miq. Fl. Ned. Ind., Eerste Bijv. 368 1861
Uvaria purpurea var. flava (Teijsm. & Binn.) Scheff. Natuurk. Tijdschr. Ned.-Indië 31: 4 1869
Uvaria purpurea var. alba Scheff. Natuurk. Tijdschr. Ned.-Indië 31: 4 1869
Uvaria grandiflora var. tuberculata (King) Sinclair Gard. Bull. Singapore 14: 203 1955

Common names Top

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Language Common/alternative name
Indonesian akar layak
Chinese 大花紫玉盘
Chinese 麦奴
Chinese 各骆子藤
Chinese 山椒子
Chinese 山芭蕉罗
Chinese 川血乌
Chinese 红肉梨
Chinese 葡萄木

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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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-tropical
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000416394
Tropicos 100374451
KEW urn:lsid:ipni.org:names:927670-1
The Plant List kew-2448240
Open Tree Of Life 340654
NCBI Taxonomy 174973
IPNI 927670-1
iNaturalist 425818
GBIF 3154445
EOL 1054185
USDA GRIN 40962
Wikipedia Uvaria_grandiflora
CMAUP NPO10791

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
Anti-diabetic compounds from Uvaria dulcis Dunal Teerapongpisan P, Praparatana R, Noppradit B, Laphookhieo S, Puttarak P Heliyon 28-Feb-2024
PMCID:PMC10920384
doi:10.1016/j.heliyon.2024.e26962
PMID:38463830
The Role of Natural and Semi-Synthetic Compounds in Ovarian Cancer: Updates on Mechanisms of Action, Current Trends and Perspectives Islam MR, Rahman MM, Dhar PS, Nowrin FT, Sultana N, Akter M, Rauf A, Khalil AA, Gianoncelli A, Ribaudo G Molecules 22-Feb-2023
PMCID:PMC10004182
doi:10.3390/molecules28052070
PMID:36903316
Natural Products as Anticancer Agents: Current Status and Future Perspectives Naeem A, Hu P, Yang M, Zhang J, Liu Y, Zhu W, Zheng Q Molecules 30-Nov-2022
PMCID:PMC9737905
doi:10.3390/molecules27238367
PMID:36500466
Development of S4A–BSA–Au NPs for enhanced anti-tumor therapy of canine breast cancer Chen Q, Xu C, Sun Z, Yang J, Chen F, Lin Z, Lin D, Jiang Y, Lin J Nanoscale Adv 21-Oct-2021
PMCID:PMC9419510
doi:10.1039/d1na00640a
PMID:36132165
Mechanisms and Advances in Anti-Ovarian Cancer with Natural Plants Component Wu J, Zhou T, Wang Y, Jiang Y, Wang Y Molecules 30-Sep-2021
PMCID:PMC8512305
doi:10.3390/molecules26195949
PMID:34641493
Insights into the Bioprospecting of the Endophytic Fungi of the Medicinal Plant Palicourea rigida Kunth (Rubiaceae): Detailed Biological Activities dos Santos IR, Abdel-Azeem AM, Mohesien MT, Piekutowska M, Sheir DH, da Silva LL, da Silva Castro C, Carvalho DD, Bezerra JD, Saad HA, Borges LL, Xavier-Santos S J Fungi (Basel) 25-Aug-2021
PMCID:PMC8468907
doi:10.3390/jof7090689
PMID:34575727
Potential of the natural products against leishmaniasis in Old World - a review of in-vitro studies Cortes S, Bruno de Sousa C, Morais T, Lago J, Campino L Pathog Glob Health 27-Apr-2020
PMCID:PMC7448914
doi:10.1080/20477724.2020.1754655
PMID:32339079
Miyabeacin: A new cyclodimer presents a potential role for willow in cancer therapy Ward JL, Wu Y, Harflett C, Onafuye H, Corol D, Lomax C, Macalpine WJ, Cinatl J Jr, Wass MN, Michaelis M, Beale MH Sci Rep 15-Apr-2020
PMCID:PMC7160102
doi:10.1038/s41598-020-63349-1
PMID:32296088
Antitumoral Properties of Natural Products Fabiani R Molecules 03-Feb-2020
PMCID:PMC7037154
doi:10.3390/molecules25030650
PMID:32028725
Sidechain Diversification of Grandifloracin Allows Identification of Analogues with Enhanced Anti‐Austerity Activity against Human PANC‐1 Pancreatic Cancer Cells Alexander BE, Sun S, Palframan MJ, Kociok‐Köhn G, Dibwe DF, Watanabe S, Caggiano L, Awale S, Lewis SE ChemMedChem 10-Dec-2019
PMCID:PMC7003952
doi:10.1002/cmdc.201900549
PMID:31821731
Metal-Free C–H Functionalization of Allenamides: An Access to Branched Allylic Esters Luo G, Liu Y, Ding N, Li X, Zhao Z ACS Omega 09-Sep-2019
PMCID:PMC6751998
doi:10.1021/acsomega.9b02712
PMID:31552378
Zeylenone represses the progress of human prostate cancer by downregulating the Wnt/β-catenin pathway Zeng S, Zhu B, Zeng J, Wu W, Jiang C Mol Med Rep 17-Oct-2018
PMCID:PMC6236222
doi:10.3892/mmr.2018.9564
PMID:30365080
Zeylenone Induces Mitochondrial Apoptosis and Inhibits Migration and Invasion in Gastric Cancer Yang S, Liao Y, Li L, Xu X, Cao L Molecules 27-Aug-2018
PMCID:PMC6225419
doi:10.3390/molecules23092149
PMID:30150551
Stigmatic exudate in the Annonaceae: Pollinator reward, pollen germination medium or extragynoecial compitum? Lau JY, Pang C, Ramsden L, Saunders RM J Integr Plant Biol 31-Oct-2017
PMCID:PMC5725718
doi:10.1111/jipb.12598
PMID:28880427
Annonaceae: Breaking the Wall of Inflammation Attiq A, Jalil J, Husain K Front Pharmacol 20-Oct-2017
PMCID:PMC5654839
doi:10.3389/fphar.2017.00752
PMID:29104539

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
((1S,5R,6S)-5-(Benzoyloxy)-1,6-dihydroxy-2-oxocyclohex-3-en-1-yl)methyl benzoate 10571940 Click to see C1=CC=C(C=C1)C(=O)OCC2(C(C(C=CC2=O)OC(=O)C3=CC=CC=C3)O)O 382.40 unknown https://doi.org/10.1016/S0031-9422(97)00026-5
https://doi.org/10.1271/BBB.66.537
https://doi.org/10.1271/BBB.65.1395
(+)-Grandifloracin 53362276 Click to see C1=CC=C(C=C1)C(=O)OCC2(C3C=CC(C2=O)C4C3C(C(=O)C=C4)(COC(=O)C5=CC=CC=C5)O)O 488.50 unknown https://doi.org/10.1016/S0031-9422(97)00026-5
(+)-Zeylenol 14283260 Click to see C1=CC=C(C=C1)C(=O)OCC2(C(C=CC(C2O)OC(=O)C3=CC=CC=C3)O)O 384.40 unknown https://doi.org/10.1271/BBB.66.537
https://doi.org/10.1016/0031-9422(95)00500-7
https://doi.org/10.1271/BBB.65.1395
(1,5,6-Trihydroxy-2-oxocyclohex-3-en-1-yl)methyl benzoate 163036323 Click to see C1=CC=C(C=C1)C(=O)OCC2(C(C(C=CC2=O)O)O)O 278.26 unknown https://doi.org/10.1271/BBB.66.537
(2-Benzoyloxy-1,5,6-trihydroxycyclohex-3-en-1-yl)methyl benzoate 162876178 Click to see C1=CC=C(C=C1)C(=O)OCC2(C(C=CC(C2O)O)OC(=O)C3=CC=CC=C3)O 384.40 unknown https://doi.org/10.1016/0031-9422(95)00500-7
(2-Benzoyloxy-3-hydroxy-7-oxabicyclo[4.1.0]hept-4-en-1-yl)methyl benzoate 163010689 Click to see C1=CC=C(C=C1)C(=O)OCC23C(O2)C=CC(C3OC(=O)C4=CC=CC=C4)O 366.40 unknown https://doi.org/10.1016/0031-9422(84)83114-3
(2-Hydroxy-6-methoxyphenyl)methyl benzoate 127260385 Click to see COC1=CC=CC(=C1COC(=O)C2=CC=CC=C2)O 258.27 unknown https://doi.org/10.1016/0031-9422(84)83114-3
(4-acetyloxy-5-oxo-4H-oxepin-3-yl)methyl benzoate 72988482 Click to see CC(=O)OC1C(=O)C=COC=C1COC(=O)C2=CC=CC=C2 302.28 unknown https://doi.org/10.1021/NP050500B
(4,6-Dihydroxy-8-oxo-2-oxabicyclo[2.2.2]octan-5-yl) benzoate 162937230 Click to see C1C2C(C(C(C1=O)(CO2)O)OC(=O)C3=CC=CC=C3)O 278.26 unknown https://doi.org/10.1271/BBB.66.537
(5-Benzoyloxy-1,6-dihydroxy-2-methoxycyclohex-3-en-1-yl)methyl benzoate 44715732 Click to see COC1C=CC(C(C1(COC(=O)C2=CC=CC=C2)O)O)OC(=O)C3=CC=CC=C3 398.40 unknown https://doi.org/10.1271/BBB.65.1395
(5-Benzoyloxy-2-ethoxy-1,6-dihydroxycyclohex-3-en-1-yl)methyl benzoate 74315890 Click to see CCOC1C=CC(C(C1(COC(=O)C2=CC=CC=C2)O)O)OC(=O)C3=CC=CC=C3 412.40 unknown https://doi.org/10.1016/0031-9422(95)00500-7
(5-Benzoyloxy-4-hydroxy-8-oxo-2-oxabicyclo[2.2.2]octan-6-yl) benzoate 162873190 Click to see C1C2C(C(C(C1=O)(CO2)O)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4 382.40 unknown https://doi.org/10.1016/S0031-9422(97)00026-5
https://doi.org/10.1271/BBB.66.537
(5-Benzoyloxy-6-hydroxycyclohexa-1,3-dien-1-yl)methyl benzoate 85453426 Click to see C1=CC=C(C=C1)C(=O)OCC2=CC=CC(C2O)OC(=O)C3=CC=CC=C3 350.40 unknown https://doi.org/10.1016/S0040-4039(00)86811-2
(6-Acetyloxy-5-benzoyloxy-1-hydroxy-2-methoxycyclohex-3-en-1-yl)methyl benzoate 162867210 Click to see CC(=O)OC1C(C=CC(C1(COC(=O)C2=CC=CC=C2)O)OC)OC(=O)C3=CC=CC=C3 440.40 unknown https://doi.org/10.1271/BBB.66.537
(6-Acetyloxy-5-benzoyloxy-1-hydroxy-2-oxocyclohex-3-en-1-yl)methyl benzoate 139600691 Click to see CC(=O)OC1C(C=CC(=O)C1(COC(=O)C2=CC=CC=C2)O)OC(=O)C3=CC=CC=C3 424.40 unknown https://doi.org/10.1271/BBB.65.1395
(6-Acetyloxy-5-benzoyloxy-2-ethoxy-1-hydroxycyclohex-3-en-1-yl)methyl benzoate 163025919 Click to see CCOC1C=CC(C(C1(COC(=O)C2=CC=CC=C2)O)OC(=O)C)OC(=O)C3=CC=CC=C3 454.50 unknown https://doi.org/10.1016/0031-9422(95)00500-7
(6-Benzoyloxy-1,5-dihydroxy-2-oxocyclohex-3-en-1-yl)methyl benzoate 162942634 Click to see C1=CC=C(C=C1)C(=O)OCC2(C(C(C=CC2=O)O)OC(=O)C3=CC=CC=C3)O 382.40 unknown https://doi.org/10.1271/BBB.66.537
(6-Benzoyloxy-5-hydroxycyclohex-3-en-1-yl)methyl benzoate 163049505 Click to see C1C=CC(C(C1COC(=O)C2=CC=CC=C2)OC(=O)C3=CC=CC=C3)O 352.40 unknown https://doi.org/10.1016/0031-9422(84)83114-3
[(1R,2S,5R,6S)-6-acetyloxy-5-benzoyloxy-1-hydroxy-2-methoxycyclohex-3-en-1-yl]methyl benzoate 101165033 Click to see CC(=O)OC1C(C=CC(C1(COC(=O)C2=CC=CC=C2)O)OC)OC(=O)C3=CC=CC=C3 440.40 unknown https://doi.org/10.1271/BBB.66.537
[(1R,2S,5R,6S)-6-acetyloxy-5-benzoyloxy-2-ethoxy-1-hydroxycyclohex-3-en-1-yl]methyl benzoate 101683474 Click to see CCOC1C=CC(C(C1(COC(=O)C2=CC=CC=C2)O)OC(=O)C)OC(=O)C3=CC=CC=C3 454.50 unknown https://doi.org/10.1016/0031-9422(95)00500-7
[(1R,4S,5S,6R)-4,6-dihydroxy-8-oxo-2-oxabicyclo[2.2.2]octan-5-yl] benzoate 101165038 Click to see C1C2C(C(C(C1=O)(CO2)O)OC(=O)C3=CC=CC=C3)O 278.26 unknown https://doi.org/10.1271/BBB.66.537
[(1R,4S,5S,6R)-5-benzoyloxy-4-hydroxy-8-oxo-2-oxabicyclo[2.2.2]octan-6-yl] benzoate 101707997 Click to see C1C2C(C(C(C1=O)(CO2)O)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4 382.40 unknown https://doi.org/10.1271/BBB.66.537
[(1R,5S,6R)-1,5,6-trihydroxy-2-oxocyclohex-3-en-1-yl]methyl benzoate 101165036 Click to see C1=CC=C(C=C1)C(=O)OCC2(C(C(C=CC2=O)O)O)O 278.26 unknown https://doi.org/10.1271/BBB.66.537
[(1R,5S,6R)-6-benzoyloxy-1,5-dihydroxy-2-oxocyclohex-3-en-1-yl]methyl benzoate 101165035 Click to see C1=CC=C(C=C1)C(=O)OCC2(C(C(C=CC2=O)O)OC(=O)C3=CC=CC=C3)O 382.40 unknown https://doi.org/10.1271/BBB.66.537
[(1S,2S,3R,6S)-2-benzoyloxy-3-hydroxy-7-oxabicyclo[4.1.0]hept-4-en-1-yl]methyl benzoate 163010691 Click to see C1=CC=C(C=C1)C(=O)OCC23C(O2)C=CC(C3OC(=O)C4=CC=CC=C4)O 366.40 unknown https://doi.org/10.1016/0031-9422(84)83114-3
[(1S,2S,5R,6S)-2-benzoyloxy-1,5,6-trihydroxycyclohex-3-en-1-yl]methyl benzoate 162876179 Click to see C1=CC=C(C=C1)C(=O)OCC2(C(C=CC(C2O)O)OC(=O)C3=CC=CC=C3)O 384.40 unknown https://doi.org/10.1016/0031-9422(95)00500-7
[(1S,2S,5R,6S)-5-benzoyloxy-2-ethoxy-1,6-dihydroxycyclohex-3-en-1-yl]methyl benzoate 101683473 Click to see CCOC1C=CC(C(C1(COC(=O)C2=CC=CC=C2)O)O)OC(=O)C3=CC=CC=C3 412.40 unknown https://doi.org/10.1016/0031-9422(95)00500-7
[(1S,4R,5S,6R)-5-benzoyloxy-4-hydroxy-8-oxo-2-oxabicyclo[2.2.2]octan-6-yl] benzoate 162873191 Click to see C1C2C(C(C(C1=O)(CO2)O)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4 382.40 unknown https://doi.org/10.1016/S0031-9422(97)00026-5
[(1S,5S,6R)-6-benzoyloxy-5-hydroxycyclohex-3-en-1-yl]methyl benzoate 163049506 Click to see C1C=CC(C(C1COC(=O)C2=CC=CC=C2)OC(=O)C3=CC=CC=C3)O 352.40 unknown https://doi.org/10.1016/0031-9422(84)83114-3
[(5R,6R)-5-benzoyloxy-6-hydroxycyclohexa-1,3-dien-1-yl]methyl benzoate 26113783 Click to see C1=CC=C(C=C1)C(=O)OCC2=CC=CC(C2O)OC(=O)C3=CC=CC=C3 350.40 unknown https://doi.org/10.1016/S0040-4039(00)86811-2
[(Z)-3-[(2S,3S)-3-(acetyloxymethyl)-3-(benzoyloxymethyl)oxiran-2-yl]prop-2-enyl] benzoate 163185664 Click to see CC(=O)OCC1(C(O1)C=CCOC(=O)C2=CC=CC=C2)COC(=O)C3=CC=CC=C3 410.40 unknown https://doi.org/10.1021/NP050500B
[5-(Acetyloxymethyl)-6-benzoyloxy-4,5-dihydroxyhex-2-enyl] benzoate 73050722 Click to see CC(=O)OCC(COC(=O)C1=CC=CC=C1)(C(C=CCOC(=O)C2=CC=CC=C2)O)O 428.40 unknown https://doi.org/10.1021/NP050500B
[5-(Acetyloxymethyl)-6-benzoyloxyhexa-2,4-dienyl] benzoate 73062974 Click to see CC(=O)OCC(=CC=CCOC(=O)C1=CC=CC=C1)COC(=O)C2=CC=CC=C2 394.40 unknown https://doi.org/10.1021/NP050500B
[6-(Benzoyloxymethyl)-6,9-dihydroxy-5,10-dioxo-9-tricyclo[6.2.2.02,7]dodeca-3,11-dienyl]methyl benzoate 73322603 Click to see C1=CC=C(C=C1)C(=O)OCC2(C3C=CC(C2=O)C4C3C(C(=O)C=C4)(COC(=O)C5=CC=CC=C5)O)O 488.50 unknown https://doi.org/10.1016/S0031-9422(97)00026-5
2-Hydroxybenzyl benzoate 12731045 Click to see C1=CC=C(C=C1)C(=O)OCC2=CC=CC=C2O 228.24 unknown https://doi.org/10.1016/0031-9422(84)83114-3
2-O-Acetylzeylenone 101110143 Click to see CC(=O)OC1C(C=CC(=O)C1(COC(=O)C2=CC=CC=C2)O)OC(=O)C3=CC=CC=C3 424.40 unknown https://doi.org/10.1271/BBB.65.1395
3-[3-(Acetyloxymethyl)-3-(benzoyloxymethyl)oxiran-2-yl]prop-2-enyl benzoate 72999568 Click to see CC(=O)OCC1(C(O1)C=CCOC(=O)C2=CC=CC=C2)COC(=O)C3=CC=CC=C3 410.40 unknown https://doi.org/10.1021/NP050500B
Benzenemethanol, 2-methoxy-, benzoate 3085295 Click to see COC1=CC=CC=C1COC(=O)C2=CC=CC=C2 242.27 unknown https://doi.org/10.1016/0031-9422(84)83114-3
Benzoic acid [(1S)-1,6alpha-dihydroxy-2beta-methoxy-5beta-(benzoyloxy)-3-cyclohexene-1beta-yl]methyl ester 101110142 Click to see COC1C=CC(C(C1(COC(=O)C2=CC=CC=C2)O)O)OC(=O)C3=CC=CC=C3 398.40 unknown https://doi.org/10.1271/BBB.65.1395
Benzyl Benzoate 2345 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2 212.24 unknown https://doi.org/10.1016/0031-9422(84)83114-3
Grandiuvarin A 163044035 Click to see CC(=O)OCC1(C(O1)C=CCOC(=O)C2=CC=CC=C2)COC(=O)C3=CC=CC=C3 410.40 unknown https://doi.org/10.1021/NP050500B
Grandiuvarins B 16717100 Click to see CC(=O)OCC(COC(=O)C1=CC=CC=C1)(C(C=CCOC(=O)C2=CC=CC=C2)O)O 428.40 unknown https://doi.org/10.1021/NP050500B
Grandiuvarins C 11689734 Click to see CC(=O)OCC(=CC=CCOC(=O)C1=CC=CC=C1)COC(=O)C2=CC=CC=C2 394.40 unknown https://doi.org/10.1021/NP050500B
Grandiuvarone A 11507728 Click to see CC(=O)OC1C(=O)C=COC=C1COC(=O)C2=CC=CC=C2 302.28 unknown https://doi.org/10.1021/NP050500B
Uvarigranol B 133561686 Click to see CC(=O)OC1C(C=CC(C1(COC(=O)C2=CC=CC=C2)O)O)OC(=O)C3=CC=CC=C3 426.40 unknown https://doi.org/10.1016/0031-9422(95)00500-7
Uvarigranol G 10883503 Click to see C1=CC=C(C=C1)C(=O)OCC2(C(C=CC(C2O)OC(=O)C3=CC=CC=C3)O)O 384.40 unknown https://doi.org/10.1016/S0031-9422(98)80073-3
UvarigranolB 131849334 Click to see CC(=O)OC1C(C=CC(C1(COC(=O)C2=CC=CC=C2)O)O)OC(=O)C3=CC=CC=C3 426.40 unknown https://doi.org/10.1016/0031-9422(95)00500-7
Zeylenol 10992619 Click to see C1=CC=C(C=C1)C(=O)OCC2(C(C=CC(C2O)OC(=O)C3=CC=CC=C3)O)O 384.40 unknown https://doi.org/10.1271/BBB.65.1395
https://doi.org/10.1016/0031-9422(95)00500-7
https://doi.org/10.1271/BBB.66.537
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Benzyl 2,6-dihydroxybenzoate 10586364 Click to see C1=CC=C(C=C1)COC(=O)C2=C(C=CC=C2O)O 244.24 unknown https://doi.org/10.1016/0031-9422(84)83114-3
Benzyl salicylate 8363 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2O 228.24 unknown https://doi.org/10.1016/0031-9422(84)83114-3
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Benzyl 2-hydroxy-5-methoxybenzoate 7430404 Click to see COC1=CC(=C(C=C1)O)C(=O)OCC2=CC=CC=C2 258.27 unknown https://doi.org/10.1016/0031-9422(84)83114-3
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
Benzyl 2-hydroxy-6-methoxybenzoate 6430728 Click to see COC1=CC=CC(=C1C(=O)OCC2=CC=CC=C2)O 258.27 unknown https://doi.org/10.1016/0031-9422(84)83114-3
Benzyl 2-methoxybenzoate 584904 Click to see COC1=CC=CC=C1C(=O)OCC2=CC=CC=C2 242.27 unknown https://doi.org/10.1016/0031-9422(84)83114-3
Benzyl 2,5-dimethoxybenzoate 71327489 Click to see COC1=CC(=C(C=C1)OC)C(=O)OCC2=CC=CC=C2 272.29 unknown https://doi.org/10.1016/0031-9422(84)83114-3
Benzyl 2,6-dimethoxybenzoate 370912 Click to see COC1=C(C(=CC=C1)OC)C(=O)OCC2=CC=CC=C2 272.29 unknown https://doi.org/10.1016/0031-9422(84)83114-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Annonaceous acetogenins
(2R)-4-[(13R)-13-hydroxy-13-[(2S,5R)-5-[(2R,5S)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]tridecyl]-2-methyl-2H-furan-5-one 163048063 Click to see CCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCCCCC3=CC(OC3=O)C)O)O 606.90 unknown https://doi.org/10.1016/0031-9422(91)83652-2
(2S)-4-[(13R,15R)-13,15-dihydroxy-15-[(2R,5R)-5-[(1R)-1-hydroxytridecyl]oxolan-2-yl]pentadecyl]-2-methyl-2H-furan-5-one 10008858 Click to see CCCCCCCCCCCCC(C1CCC(O1)C(CC(CCCCCCCCCCCCC2=CC(OC2=O)C)O)O)O 608.90 unknown via CMAUP database
(5R)-Uvarigrandin A 11734818 Click to see CCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCC(CCC3=CC(OC3=O)C)O)O)O 622.90 unknown via CMAUP database
Isodesacetyluvaricin 44591854 Click to see CCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCCCCC3=CC(OC3=O)C)O)O 606.90 unknown via CMAUP database
Squamocin L 461667 Click to see CCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCCCCC3=CC(OC3=O)C)O)O 606.90 unknown https://doi.org/10.1016/0031-9422(91)83652-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
Erythrodiol 101761 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C 442.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives
3-[(3S,5S,8R,9R,10S,13R,14S,17R)-3,14-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 11875905 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CCC4C5=CC(=O)OC5)O)C)O 374.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[3,4,5-triacetyloxy-6-[[5-acetyloxy-7-(acetyloxymethyl)-4a-hydroxy-5,7a-dihydro-1H-cyclopenta[c]pyran-1-yl]oxy]oxan-2-yl]methyl acetate 163004514 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C3C(=CC(C3(C=CO2)O)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 614.50 unknown https://doi.org/10.1271/BBB.65.1395
https://doi.org/10.1271/BBB.66.537
https://doi.org/10.1016/S0031-9422(97)00026-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
(6-Acetyloxy-2,5-dibenzoyloxy-1-hydroxycyclohex-3-en-1-yl)methyl benzoate 14283272 Click to see CC(=O)OC1C(C=CC(C1(COC(=O)C2=CC=CC=C2)O)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4 530.50 unknown https://doi.org/10.1271/BBB.66.537
[(1R,2S,5R,6S)-6-acetyloxy-2,5-dibenzoyloxy-1-hydroxycyclohex-3-en-1-yl]methyl benzoate 101165034 Click to see CC(=O)OC1C(C=CC(C1(COC(=O)C2=CC=CC=C2)O)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4 530.50 unknown https://doi.org/10.1271/BBB.66.537
[(1R,4S,5R,6S)-4-acetyloxy-5-(acetyloxymethyl)-6-benzoyloxy-5-hydroxycyclohex-2-en-1-yl] benzoate 102121368 Click to see CC(=O)OCC1(C(C=CC(C1OC(=O)C2=CC=CC=C2)OC(=O)C3=CC=CC=C3)OC(=O)C)O 468.50 unknown https://doi.org/10.1016/S0031-9422(98)80073-3
[(1S,4R,5R,6S)-5,6-diacetyloxy-4-benzoyloxy-1-hydroxycyclohex-2-en-1-yl]methyl benzoate 102121369 Click to see CC(=O)OC1C(C=CC(C1OC(=O)C)(COC(=O)C2=CC=CC=C2)O)OC(=O)C3=CC=CC=C3 468.50 unknown https://doi.org/10.1016/S0031-9422(98)80073-3
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / M-benzoquinones
4-Cyclohexene-1,3-dione, 5-hydroxy-2,2,6,6-tetramethyl-4-(1-oxo-3-phenylpropyl)- 3014646 Click to see CC1(C(=C(C(=O)C(C1=O)(C)C)C(=O)CCC2=CC=CC=C2)O)C 314.40 unknown https://doi.org/10.1271/BBB.66.537
https://doi.org/10.1016/S0031-9422(97)00026-5
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Isodictamnine 442913 Click to see CN1C2=CC=CC=C2C(=O)C3=C1OC=C3 199.20 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

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