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Terminalia tetraphylla

Terminalia tetraphylla - 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 UUID6440686423af3842626315
Scientific name Terminalia tetraphylla
Authority (Aubl.) Gere & Boatwr.
First published in Bot. J. Linn. Soc. 184(3): 322. 2017 [22 Jun 2017] [epublished]

Description Top

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Synonyms Top

Scientific name Authority First published in
Lithocardium tetraphyllum (Aubl.) Kuntze Revis. Gen. Pl. 2: 977. 1891 [5 Nov 1891]
Terminalia capitata C.Wright Anales Acad. Ci. Méd. Habana 5: 409 (1869)
Terminalia obovata Cambess. Fl. Bras. Merid. 2: 241 (1830)
Buchenavia capitata (Vahl) Eichler Flora 49: 165 (1866)
Buchenavia ptariensis Steyerm. Fieldiana, Bot. 28: 423 (1952)
Buchenavia tetraphylla (Aubl.) R.A.Howard J. Arnold Arbor. 64: 266 (1983)
Buchenavia vaupesana Cuatrec. Fieldiana, Bot. 27: 108 (1950)
Bucida capitata Vahl Eclog. Amer. 1: 50 (1797)
Cordia tetraphylla Aubl. Hist. Pl. Guiane 1: 224 (1775)
Gimbernatea obovata Ruiz & Pav. Syst. Veg. Fl. Peruv. Chil. 274 1798
Hudsonia arborea Lunan Hort. Jamaic. ii. 310 (1814).
Pseudolmedia bucidifolia Bello Anales Soc. Esp. Hist. Nat. 12: 109 (1883)

Common names Top

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Language Common/alternative name
Arabic بوشنوية رباعية الأوراق
Swedish buchenavia tetraphylla

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Costa Rica
      • Panamá
    • Northern South America
      • French Guiana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001421877
Tropicos 100457283
INPN 889284
KEW urn:lsid:ipni.org:names:77164595-1
NCBI Taxonomy 470568
IPNI 77164595-1
iNaturalist 1048743
GBIF 9307101
CMAUP NPO25550

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
Exploring the Antioxidant Potential of Talisia esculenta Using In Vitro and In Vivo Approaches da Silva Cordeiro ML, de Queiroz Aquino-Martins VG, da Silva AP, Naliato GF, Silveira ER, Theodoro RC, da Santos DY, Rocha HA, Scortecci KC Nutrients 04-Sep-2023
PMCID:PMC10490396
doi:10.3390/nu15173855
PMID:37686887
Role of phytocompounds as the potential anti-viral agent: an overview Mohanty SS, Sahoo CR, Paidesetty SK, Padhy RN Naunyn Schmiedebergs Arch Pharmacol 09-May-2023
PMCID:PMC10169142
doi:10.1007/s00210-023-02517-2
PMID:37160482
Prospecting Plant Extracts and Bioactive Molecules with Antimicrobial Activity in Brazilian Biomes: A Review de Queiroz JC, Leite JR, Vasconcelos AG Antibiotics (Basel) 21-Feb-2023
PMCID:PMC10044579
doi:10.3390/antibiotics12030427
PMID:36978294
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
Amazonian fruits with potential effects on COVID‐19 by inflammaging modulation: A narrative review Manica‐Cattani MF, Hoefel AL, Azzolin VF, Montano MA, da Cruz Jung IE, Ribeiro EE, Azzolin VF, da Cruz IB J Food Biochem 14-Oct-2022
PMCID:PMC9874877
doi:10.1111/jfbc.14472
PMID:36240164
Diversity in Chemical Structures and Biological Properties of Plant Alkaloids Bhambhani S, Kondhare KR, Giri AP Molecules 03-Jun-2021
PMCID:PMC8199754
doi:10.3390/molecules26113374
PMID:34204857
A review study on the anti-trichomonas activities of medicinal plants Hashemi N, Ommi D, Kheyri P, Khamesipour F, Setzer WN, Benchimol M Int J Parasitol Drugs Drug Resist 12-Feb-2021
PMCID:PMC7902805
doi:10.1016/j.ijpddr.2021.01.002
PMID:33610966
Emerging paradigms of viral diseases and paramount role of natural resources as antiviral agents Sagaya Jansi R, Khusro A, Agastian P, Alfarhan A, Al-Dhabi NA, Arasu MV, Rajagopal R, Barcelo D, Al-Tamimi A Sci Total Environ 07-Nov-2020
PMCID:PMC7833357
doi:10.1016/j.scitotenv.2020.143539
PMID:33234268
Total Synthesis of Novel Skeleton Flavan-Alkaloids Zhen J, Simon JE, Wu Q Molecules 30-Sep-2020
PMCID:PMC7582810
doi:10.3390/molecules25194491
PMID:33007965
Phytosociological Study, Diversity and Conservation Status of the Cloud Forest in the Dominican Republic Cano Ortiz A, Musarella CM, Pinto Gomes CJ, Quinto Canas R, Piñar Fuentes JC, Cano E Plants (Basel) 12-Jun-2020
PMCID:PMC7356210
doi:10.3390/plants9060741
PMID:32545541
Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products Kaur R, Sharma P, Gupta GK, Ntie-Kang F, Kumar D Molecules 29-Apr-2020
PMCID:PMC7249135
doi:10.3390/molecules25092070
PMID:32365518
Products Derived from Buchenavia tetraphylla Leaves Have In Vitro Antioxidant Activity and Protect Tenebrio molitor Larvae against Escherichia coli-Induced Injury Silva TF, Cavalcanti Filho JR, Barreto Fonsêca MM, dos Santos NM, Barbosa da Silva AC, Zagmignan A, Abreu AG, Sant’Anna da Silva AP, Lima VL, da Silva NH, Dutra LM, Almeida JR, da Silva MV, Correia MT, Nascimento da Silva LC Pharmaceuticals (Basel) 16-Mar-2020
PMCID:PMC7151707
doi:10.3390/ph13030046
PMID:32188166
The potential of plant systems to break the HIV‐TB link Habibi P, Daniell H, Soccol CR, Grossi‐de‐Sa MF Plant Biotechnol J 18-Jul-2019
PMCID:PMC6737023
doi:10.1111/pbi.13110
PMID:30908823
Antiviral Evaluation of Herbal Drugs Mukherjee PK Quality Control and Evaluation of Herbal Drugs 21-Jun-2019
PMCID:PMC7149824
doi:10.1016/B978-0-12-813374-3.00016-8
Candida Infections and Therapeutic Strategies: Mechanisms of Action for Traditional and Alternative Agents de Oliveira Santos GC, Vasconcelos CC, Lopes AJ, de Sousa Cartágenes MD, Filho AK, do Nascimento FR, Ramos RM, Pires ER, de Andrade MS, Rocha FM, de Andrade Monteiro C Front Microbiol 03-Jul-2018
PMCID:PMC6038711
doi:10.3389/fmicb.2018.01351
PMID:30018595

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 / Diphenylethers
2-Hydroxy-6-[2-hydroxy-6-(hydroxymethyl)-4-methyl-phenoxy]-3-(3-methylbut-2-enyl)benzoic acid 23843930 Click to see CC1=CC(=C(C(=C1)O)OC2=C(C(=C(C=C2)CC=C(C)C)O)C(=O)O)CO 358.40 unknown via CMAUP database
6-[2-hydroxy-6-(hydroxymethyl)-4-methylphenoxy]-2-methoxy-3-[(1S)-1-methoxy-3-methylbutyl]benzoic acid 38351229 Click to see CC1=CC(=C(C(=C1)O)OC2=C(C(=C(C=C2)C(CC(C)C)OC)OC)C(=O)O)CO 404.50 unknown via CMAUP database
6-[2-hydroxy-6-(hydroxymethyl)-4-methylphenoxy]-3-[(1S)-1-hydroxy-3-methylbutyl]-2-methoxybenzoic acid 71608329 Click to see CC1=CC(=C(C(=C1)O)OC2=C(C(=C(C=C2)C(CC(C)C)O)OC)C(=O)O)CO 390.40 unknown via CMAUP database
7-O-Acetylsecopenicillide C 71460590 Click to see CC1=CC(=C(C(=C1)O)OC2=C(C(=C(C=C2)CC=C(C)C)O)C(=O)O)COC(=O)C 400.40 unknown via CMAUP database
> Benzenoids / Tetralins
(1R,3R)-spiro[2,3-dihydro-1H-naphthalene-4,3'-2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene]-1,3,8-triol 51354124 Click to see C1C(C2=C(C=CC=C2O)C3(C1O)OC4=CC=CC5=C4C(=CC=C5)O3)O 336.30 unknown via CMAUP database
(1S,2R,3S)-2-chlorospiro[2,3-dihydro-1H-naphthalene-4,3'-2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene]-1,3,8-triol 51354126 Click to see C1=CC2=C3C(=C1)OC4(C(C(C(C5=C4C=CC=C5O)O)Cl)O)OC3=CC=C2 370.80 unknown via CMAUP database
(1S,3R)-spiro[2,3-dihydro-1H-naphthalene-4,3'-2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene]-1,3,8-triol 51354123 Click to see C1C(C2=C(C=CC=C2O)C3(C1O)OC4=CC=CC5=C4C(=CC=C5)O3)O 336.30 unknown via CMAUP database
(2S)-1,1-[Naphthalene-1,8-diylbis(oxy)]-3beta-chlorotetralin-2alpha,4alpha,5-triol 51354127 Click to see C1=CC2=C3C(=C1)OC4(C(C(C(C5=C4C=CC=C5O)O)Cl)O)OC3=CC=C2 370.80 unknown via CMAUP database
Palmarumycin BG-1 51354122 Click to see C1C(C2(C3=C(C1=O)C(=CC=C3)O)OC4=CC=CC5=C4C(=CC=C5)O2)O 334.30 unknown via CMAUP database
Sulfuric acid (2R)-1,1-[naphthalene-1,8-diylbis(oxy)]-2alpha,4beta-dihydroxytetralin-5-yl ester 51354125 Click to see C1C(C2=C(C=CC=C2OS(=O)(=O)O)C3(C1O)OC4=CC=CC5=C4C(=CC=C5)O3)O 416.40 unknown via CMAUP database
Sulfuric acid (2S)-1,1-[naphthalene-1,8-diylbis(oxy)]-2alpha,4beta-dihydroxy-3alpha-chlorotetralin-5-yl ester 51354407 Click to see C1=CC2=C3C(=C1)OC4(C(C(C(C5=C4C=CC=C5OS(=O)(=O)O)O)Cl)O)OC3=CC=C2 450.80 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dotriacontane 11008 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 450.90 unknown via CMAUP database
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown via CMAUP database
Heptacosane 11636 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC 380.70 unknown via CMAUP database
Hexacosane 12407 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC 366.70 unknown via CMAUP database
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown via CMAUP database
Pentacosane 12406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC 352.70 unknown via CMAUP database
Pentatriacontane 12413 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 492.90 unknown via CMAUP database
Triacontane 12535 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 422.80 unknown via CMAUP database
Tritriacontane 12411 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 464.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ustusolate A 23843911 Click to see CC=CC=CC=CC(=O)OC1C=C(C(C2(C1C(CCC2)(C)C)C)(CO)O)CO 390.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
3-Hexadecenoic acid 5312418 Click to see CCCCCCCCCCCCC=CCC(=O)O 254.41 unknown via CMAUP database
7-Hexadecenoic acid 543268 Click to see CCCCCCCCC=CCCCCCC(=O)O 254.41 unknown via CMAUP database
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
c9-Heptadecenoic acid acid 3014063 Click to see CCCCCCCC=CCCCCCCCC(=O)O 268.40 unknown via CMAUP database
Heptadecanoic acid 10465 Click to see CCCCCCCCCCCCCCCCC(=O)O 270.50 unknown via CMAUP database
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
Nonadecanoic acid 12591 Click to see CCCCCCCCCCCCCCCCCCC(=O)O 298.50 unknown via CMAUP database
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Palmitolinoleic acid 4668 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Pentadecanoic acid 13849 Click to see CCCCCCCCCCCCCCC(=O)O 242.40 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
Vaccenic acid 122325 Click to see CCCCCCC=CCCCCCCCCCC(=O)O 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see CCCCCCCCCCCC(=O)O 200.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1S)-1-[(2S,4aR,4bR,5R,8aR)-5-hydroxy-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl]ethane-1,2-diol 11602232 Click to see CC1(CCC(C2(C1CCC3=CC(CCC32)(C)C(CO)O)C)O)C 322.50 unknown via CMAUP database
(1S)-1-[(2S,4aR,4bR,8aR)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl]ethane-1,2-diol 11551288 Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C(CO)O)C)C 306.50 unknown via CMAUP database
(4aR,4bR,7S,10aR)-7-[(1S)-1,2-dihydroxyethyl]-1,1,4a,7-tetramethyl-2,3,4b,5,6,9,10,10a-octahydrophenanthren-4-one 11702511 Click to see CC1(CCC(=O)C2(C1CCC3=CC(CCC32)(C)C(CO)O)C)C 320.50 unknown via CMAUP database
(5S,8R,9R,10S,13S)-17-Hydroxy-16-oxobeyerane-18-al 11392987 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)(C(=O)C4)CO)C)C=O 318.40 unknown via CMAUP database
Ceriopsin C 101202346 Click to see CC1(CCC(C2(C1CC=C3C2CCC(C3)(C)C(CO)O)C)O)C 322.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
13-Hydroxykaur-16-en-18-al 100967712 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)(C(=C)C4)O)C)C=O 302.50 unknown via CMAUP database
13,16alpha,17-Trihydroxy-ent-9(11)-kauren-19-oic acid 11428064 Click to see CC12CCCC(C1CCC34C2=CCC(C3)(C(C4)(CO)O)O)(C)C(=O)O 350.40 unknown via CMAUP database
16,17-Dihydroxykaura-18-one 44575992 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)C=O 320.50 unknown via CMAUP database
16alpha,17-Dihydroxy-ent-9(11)-kauren-19-al 11324617 Click to see CC1(CCCC2(C1CCC34C2=CCC(C3)C(C4)(CO)O)C)C=O 318.40 unknown via CMAUP database
16alphaH-17,19-ent-kauranediol 102594837 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)CO)C)CO 306.50 unknown via CMAUP database
17-Chloro-13,16beta-dihydroxy-ent-kauran-19-al 21589750 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)(C(C4)(CCl)O)O)C)C=O 354.90 unknown via CMAUP database
17-Hydroxykaura-18-oic acid 46210307 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)CO)(C)C(=O)O 320.50 unknown via CMAUP database
ent-16beta,17-Dihydroxy-9(11)-kauren-19-oic acid 23249404 Click to see CC12CCCC(C1CCC34C2=CCC(C3)C(C4)(CO)O)(C)C(=O)O 334.40 unknown via CMAUP database
ent-Kaur-16-en-19-ol 443465 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO 288.50 unknown via CMAUP database
Kaur-16-ene-13,18-diol 100967711 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)(C(=C)C4)O)C)CO 304.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
bruguierins A 11513260 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CC(C2(C3CCC4C(CCC4(C3(CCC2C1(C)C)C)C)C(C)(CCC=C(C)C)O)C)O 727.20 unknown via CMAUP database
bruguierins B 11657758 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2C(CC4C3(CCC4C(C)(CCC=C(C)C)O)C)O)C)C 727.20 unknown via CMAUP database
bruguierins C 11629176 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CC(C2(C3CCC4C(CCC4(C3(CCC2C1(C)C)C)C)C(C)(CC=CC(C)(C)OO)O)C)O 759.20 unknown via CMAUP database
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Fucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Ustusol C 44557563 Click to see CC1(CCCC2(C1C(C=C(C2(CO)O)CO)OC)C)C 284.39 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Ustusol A 44480213 Click to see CC1=CC(=O)C2C(C(CCC2(C1(CO)O)C)O)(C)C 268.35 unknown via CMAUP database
Ustusol B 44557562 Click to see CC1=CC(=O)C2C(CC(CC2(C1(CO)O)C)O)(C)C 268.35 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
3-[(R)-1-Hydroxy-3-methylbutyl]-4-methoxy-9-methyl-11-hydroxy-5H,7H-dibenzo[b,g][1,5]dioxocin-5-one 25273618 Click to see CC1=CC2=C(C(=C1)O)OC3=C(C(=C(C=C3)C(CC(C)C)O)OC)C(=O)OC2 372.40 unknown via CMAUP database
3'-O-Methyldehydroisopenicillide 9864866 Click to see CC1=CC2=C(C(=C1)O)OC3=C(C(=C(C=C3)C=CC(C)(C)OC)OC)C(=O)OC2 384.40 unknown via CMAUP database
NCGC00386098-01_C21H22O6_11-Hydroxy-3-[(1E)-3-hydroxy-3-methyl-1-buten-1-yl]-4-methoxy-9-methyl-5H,7H-dibenzo[b,g][1,5]dioxocin-5-one 9896819 Click to see CC1=CC2=C(C(=C1)O)OC3=C(C(=C(C=C3)C=CC(C)(C)O)OC)C(=O)OC2 370.40 unknown via CMAUP database
Neosarphenol B 71451577 Click to see CC1=CC2=C(C(=C1)O)OC3=C(C(=C(C=C3)C=CC(=C)C)OC)C(=O)OC2 352.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(+)-Bruguierol C 17752611 Click to see CC12CCC(O1)CC3=C2C(=CC(=C3)O)O 206.24 unknown via CMAUP database
(1S,9R)-1-methyl-12-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-5-ol 11148193 Click to see CC12CCC(O1)CC3=C2C=CC(=C3)O 190.24 unknown via CMAUP database
(2S,7R,9S)-9-methoxy-7-methyl-2-propan-2-yl-7,9-dihydro-6H-furo[3,2-h]isochromen-3-one 73356791 Click to see CC1CC2=C(C(O1)OC)C3=C(C=C2)C(=O)C(O3)C(C)C 276.33 unknown via CMAUP database
7H-Furo(3,2-h)(2)benzopyran-3(2H)-one, 6,9-dihydro-7-hydroxy-7-methyl-2-(1-methylethylidene)-, (7R)- 156523 Click to see CC(=C1C(=O)C2=C(O1)C3=C(CC(OC3)(C)O)C=C2)C 260.28 unknown via CMAUP database
9beta-Methyl-6alpha,9alpha-epoxy-6,7,8,9-tetrahydro-5H-benzocycloheptene-2,3-diol 11367742 Click to see CC12CCC(O1)CC3=CC(=C(C=C23)O)O 206.24 unknown via CMAUP database
Aspergillumarin A 38346998 Click to see CC(=O)CCCC1CC2=C(C(=CC=C2)O)C(=O)O1 248.27 unknown via CMAUP database
Aspergillumarin B 38347996 Click to see CC(CCCC1CC2=C(C(=CC=C2)O)C(=O)O1)O 250.29 unknown via CMAUP database
Ustusorane B 44557645 Click to see CC1=CC2=C(CO1)C3=C(C=C2)C(=O)C(=C(C)C)O3 242.27 unknown via CMAUP database
Ustusorane C 44557646 Click to see CC1CC2=C(C(O1)OC)C3=C(C=C2)C(=O)C(=C(C)C)O3 274.31 unknown via CMAUP database
> Organoheterocyclic compounds / Dithiolanes / 1,2-dithiolanes
Bruguiesulfurol 11513780 Click to see C1C(CS(=O)(=O)S1)O 154.21 unknown via CMAUP database
> Organoheterocyclic compounds / Furopyrans
4,25-Dehydro-22-deoxyminiolutelide B 71608261 Click to see CC1C2(C3(C4C(O1)OC(=O)C4(CC5C3(C(O2)C=C6C(=CC(=O)OC6(C)C)C5=C)C)C)C(=O)OC)O 486.50 unknown via CMAUP database
4,25-Dehydrominiolutelide B 71608260 Click to see CC1C2(C3(C4(C(CC5(C3(C(O1)OC5=O)O)C)C(=C)C6=CC(=O)OC(C6=CC4O2)(C)C)C)C(=O)OC)O 502.50 unknown via CMAUP database
berkeleyacetal A 24179625 Click to see CC1C(=O)C2(C3C(O1)OC(=O)C3(CC4C2(CC=C5C(=C4C)CC(=O)OC5(C)C)C)C)C(=O)OC 472.50 unknown via CMAUP database
berkeleyacetal B 24179626 Click to see CC1C(=O)C2(C3C(O1)OC(=O)C3(CC4C2(CC=C5C(=CC(=O)OC5(C)C)C46CO6)C)C)C(=O)OC 486.50 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
(2E,4E)-2,4,6-Octatrienoic acid [(5R)-1,3,5,5aalpha,6,7,8,9,9a,9balpha-decahydro-9balpha-hydroxy-6,6,9abeta-trimethyl-1-oxonaphtho[1,2-c]furan]-5beta-yl ester 10407821 Click to see CC=CC=CC=CC(=O)OC1C=C2COC(=O)C2(C3(C1C(CCC3)(C)C)C)O 386.50 unknown via CMAUP database
[(5R,5aS,9aS,9bS)-9b-hydroxy-6,6,9a-trimethyl-1-oxo-3,5,5a,7,8,9-hexahydrobenzo[e][2]benzofuran-5-yl] (2E,4E,7S)-7-hydroxyocta-2,4-dienoate 51693297 Click to see CC(CC=CC=CC(=O)OC1C=C2COC(=O)C2(C3(C1C(CCC3)(C)C)C)O)O 404.50 unknown via CMAUP database
Ustusolate D 44557643 Click to see CC1(CCCC2(C1C(C=C3C2(C(=O)OC3)O)OC(=O)C=CC=CC(OC)OC)C)C 420.50 unknown via CMAUP database
Ustusolate E 44480472 Click to see CC1(CCCC2(C1C(C=C3C2(C(=O)OC3)O)OC(=O)C=CC=CC=O)C)C 374.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
octadecyl (2R,3S)-2-(3-hydroxy-5-methoxyphenyl)-7-methoxy-5-[(E)-3-octadecoxy-3-oxoprop-1-enyl]-2,3-dihydro-1-benzofuran-3-carboxylate 25105546 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC2=C(C(=C1)OC)OC(C2C(=O)OCCCCCCCCCCCCCCCCCC)C3=CC(=CC(=C3)OC)O 891.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
5,7-Dihydroxy-6-(1-methylpiperidin-2-yl)-2-phenylchromen-4-one 57343252 Click to see CN1CCCCC1C2=C(C3=C(C=C2O)OC(=CC3=O)C4=CC=CC=C4)O 351.40 unknown https://doi.org/10.1002/CHIN.198425313
O-Demethylbuchenavianine 5352072 Click to see CN1CCCCC1C2=C(C=C(C3=C2OC(=CC3=O)C4=CC=CC=C4)O)O 351.40 unknown https://doi.org/10.1021/NP50080A008
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
Buchenavianine 393062 Click to see CN1CCCCC1C2=C3C(=C(C=C2O)OC)C(=O)C=C(O3)C4=CC=CC=C4 365.40 unknown https://doi.org/10.1021/NP50080A008
> Phenylpropanoids and polyketides / Macrolactams
(1S,4R,5E,7S,10Z,20S,21S)-4-ethyl-17-hydroxy-7-[(1S)-1-hydroxy-3-methylbut-2-enyl]-10,21-dimethyl-8,24,26-trioxa-14-azatetracyclo[13.8.2.11,20.019,25]hexacosa-5,10,15,17,19(25)-pentaene-9,13,22-trione 53235715 Click to see CCC1CCC23CC(=O)C(C(O2)C4=C(O3)C(=CC(=C4)O)NC(=O)CC=C(C(=O)OC(C=C1)C(C=C(C)C)O)C)C 553.60 unknown via CMAUP database
(9R,10E,12S,15Z,17S,24R)-9-ethyl-4,24-dihydroxy-12-[(1S)-1-hydroxy-3-methylbut-2-enyl]-3,15-dimethyl-13-oxa-19-azatetracyclo[15.6.1.05,23.020,24]tetracosa-1(23),2,4,10,15,20-hexaene-6,14,18,22-tetrone 72715428 Click to see CCC1CCC(=O)C2=C(C(=CC3=C2C(=O)C=C4C3(C(C=C(C(=O)OC(C=C1)C(C=C(C)C)O)C)C(=O)N4)O)C)O 549.60 unknown via CMAUP database
Divergolide B 53235716 Click to see CCC1CCC(=O)C=C2C(=CC3=C(O2)C(=CC(=C3)O)NC(=O)CC=C(C(=O)OC(C(C=C1)O)C=C(C)C)C)C 535.60 unknown via CMAUP database

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