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Avicennia marina

Avicennia marina - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Avicennia marina - 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 UUID643fec09dd500349252021
Scientific name Avicennia marina
Authority (Forssk.) Vierh.
First published in Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 71: 435 (1907)

Description Top

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Synonyms Top

Scientific name Authority First published in
Avicennia marina var. intermedia (Griff.) Bakh. Bull. Jard. Bot. Buitenzorg III, 3: 104 1921
Sceura marina Forssk. Fl. Aegypt.-Arab. : 37 (1775)
Avicennia tomentosa var. arabica Walp. Repert. Bot. Syst. 4: 133. 1845

Common names Top

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Language Common/alternative name
English gray mangrove
Afrikaans witseebasboom
Arabic قرم بحري
ban api-api
Bulgarian морска авицения
Bengali পেয়ারা বাইন
Bengali সাদা বায়েন
Bengali বড়ো বায়েন
Bengali পেয়ারা বান
Czech kolíkovník mořský
Persian حرا
Hebrew אביצניה ימית
Indonesian api-api
Italian mangrovia grigia.
Japanese ヒルギダマシ
Malayalam ചെറൂപ്പട്ടി
Malayalam ചെറിയ ഉപ്പട്ടി
Malay pokok api-api merah
Malay pokok api-api jambu
Russian Чёрный мангр
Russian Авиценния морская
Vietnamese mắm ổi
Chinese 海欖雌
Chinese 海豆
Chinese 咸水矮让木
Chinese 白骨壤
Chinese 海茄冬
Chinese 海榄雌
Chinese 阳桃叶

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Avicennia marina subsp. australasica (Walp.) J.Everett Telopea 5: 628 (1994)
Avicennia marina subsp. eucalyptifolia (Valeton) J.Everett Telopea 5: 629 (1994)
Avicennia marina subsp. marina Denkschriften der Kaiserlichen Akademie der Wissenchaften. Mathematisch-Naturwissenschaftliche Classe 71 1907

Varieties (abbr. var.) Top

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Name Authority First published in
Avicennia marina var. marina Denkschriften der Kaiserlichen Akademie der Wissenchaften. Mathematisch-Naturwissenschaftliche Classe 71 1907
Avicennia marina var. rumphiana (Hallier f.) Bakh. Bull. Jard. Bot. Buitenzorg , sér. 3, 3: 104 (1921)

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
    • Northeast Tropical Africa
      • Djibouti
      • Eritrea
      • Socotra
      • Somalia
      • Sudan
    • Northern Africa
      • Egypt
    • South Tropical Africa
      • Mozambique
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
    • Western Indian Ocean
      • Aldabra
      • Comoros
      • Madagascar
      • Mozambique Channel Islands
      • Seychelles
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Oman
      • Saudi Arabia
      • Yemen
    • China
      • China Southeast
      • Hainan
    • Eastern Asia
      • Nansei-shoto
      • Taiwan
    • Western Asia
      • Iran
      • Sinai
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
      • Pakistan
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Christmas Island
      • Cocos (keeling) Islands
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands
  • Australasia
    • Australia
      • New South Wales
      • Norfolk Island
      • Northern Territory
      • Queensland
      • South Australia
      • Victoria
      • Western Australia
    • New Zealand
      • New Zealand North

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000303022
USDA Plants AVMA3
Tropicos 33700757
INPN 672495
KEW urn:lsid:ipni.org:names:861130-1
The Plant List kew-18454
PaleoBotany 51163
Open Tree Of Life 77591
NCBI Taxonomy 82927
Nature Serve 2.136884
IUCN Red List 178828
IPNI 861130-1
iNaturalist 75723
GBIF 2925403
Freebase /m/08hnfk
EOL 483341
Calflora (Californian flora) 9725
USDA GRIN 417483
Wikipedia Avicennia_marina

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_019155195.1 amgenome_v1.0 Chromosome SRM University 2021-07-07 248.0x 435.46 Mb

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 endophytic fungi: a review on methods for extraction and quantification of total antioxidant capacity (TAC) Asomadu RO, Ezeorba TP, Ezike TC, Uzoechina JO 3 Biotech 05-Apr-2024
PMCID:PMC10997672
doi:10.1007/s13205-024-03970-3
PMID:38585410
The tale of an endemic shrimp’s exceptional osmoregulation and the ancient Athalassic mangrove oasis Giraldes BW, Boughattas S, Benslimane FM, Althani AA, Schubart CD, Huber CS, Utz LR, Al-Khayat JA, Sadooni FN, Amado EM Sci Rep 20-Mar-2024
PMCID:PMC10954768
doi:10.1038/s41598-024-56907-4
PMID:38509217
Optimizing tomato seedling growth with indigenous mangrove bacterial inoculants and reduced NPK fertilization Tounsi-Hammami S, Khan MA, Zeb A, Anwar AR, Arora N, Naseem M, Mundra S Front Plant Sci 14-Mar-2024
PMCID:PMC10973150
doi:10.3389/fpls.2024.1356545
PMID:38550289
Isolation and characterization of a newly discovered plant growth-promoting endophytic fungal strain from the genus Talaromyces Kharkwal AC, Joshi H, Shandilya C, Dabral S, Kumar N, Varma A Sci Rep 12-Mar-2024
PMCID:PMC10933278
doi:10.1038/s41598-024-54687-5
PMID:38472228
Marine-Derived Bioactive Metabolites as a Potential Therapeutic Intervention in Managing Viral Diseases: Insights from the SARS-CoV-2 In Silico and Pre-Clinical Studies Okechukwu QN, Adepoju FO, Kanwugu ON, Adadi P, Serrano-Aroca Á, Uversky VN, Okpala CO Pharmaceuticals (Basel) 01-Mar-2024
PMCID:PMC10975954
doi:10.3390/ph17030328
PMID:38543114
Efficacy of Various Herbal Preparations Against Oral Candida: A Lab-Based Study Karni PA, Muraleedharan A, Bhandary S, Mujoo S, Maini AP, Chaturvedi M J Pharm Bioallied Sci 29-Feb-2024
PMCID:PMC11000960
doi:10.4103/jpbs.jpbs_486_23
PMID:38595550
Quantifying mangrove carbon assimilation rates using UAV imagery Blanco-Sacristán J, Johansen K, Elías-Lara M, Tu YH, Duarte CM, McCabe MF Sci Rep 26-Feb-2024
PMCID:PMC10897312
doi:10.1038/s41598-024-55090-w
PMID:38409194
Genetic diversity and population structure of natural provenances of Sonneratia caseolaris in Vietnam Le S, Le TV J Genet Eng Biotechnol 23-Feb-2024
PMCID:PMC10903747
doi:10.1016/j.jgeb.2024.100356
PMID:38494260
The Role of Autophagy in Human Uveal Melanoma and the Development of Potential Disease Biomarkers and Novel Therapeutic Paradigms Wang JZ, Paulus P, Niu Y, Zhu L, Morisseau C, Rawling T, Murray M, Hammock BD, Zhou F Biomedicines 19-Feb-2024
PMCID:PMC10886749
doi:10.3390/biomedicines12020462
PMID:38398064
The reproductive biology of Ellochelon vaigiensis from the Vietnamese Mekong Delta Dinh QM, Truong NT, Nguyen TH, Lam TT, Nguyen TT, Jaafar Z Ecol Evol 14-Feb-2024
PMCID:PMC10867543
doi:10.1002/ece3.11033
PMID:38362163
Use of Aureobasidium in a sustainable economy Rensink S, van Nieuwenhuijzen EJ, Sailer MF, Struck C, Wösten HA Appl Microbiol Biotechnol 13-Feb-2024
PMCID:PMC10864419
doi:10.1007/s00253-024-13025-5
PMID:38349550
The Hypersaline Soils of the Odiel Saltmarshes Natural Area as a Source for Uncovering a New Taxon: Pseudidiomarina terrestris sp. nov Galisteo C, de la Haba RR, Ventosa A, Sánchez-Porro C Microorganisms 11-Feb-2024
PMCID:PMC10893183
doi:10.3390/microorganisms12020375
PMID:38399779
Characterization and transformation of TtMYB1 transcription factor from Tritipyrum to improve salt tolerance in wheat Mu Y, Shi L, Tian H, Tian H, Zhang J, Zhao F, Zhang Q, Zhang S, Geng G BMC Genomics 09-Feb-2024
PMCID:PMC10854188
doi:10.1186/s12864-024-10051-5
PMID:38336658
Organophosphate Triesters and Their Transformation Products in Sediments of Mangrove Wetlands in the Beibu Gulf, South China Sea Zhang L, Xing Y, Zhang P, Luo X, Niu Z Molecules 05-Feb-2024
PMCID:PMC10856239
doi:10.3390/molecules29030736
PMID:38338479
Special Issue Editorial: “Antibacterial Agents from Natural Sources” Martins CH Molecules 30-Jan-2024
PMCID:PMC10856429
doi:10.3390/molecules29030644
PMID:38338388

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
Avicennone A 44423351 Click to see CC(C)(C1CC(=C(C2=CC=CC=C2C(=O)OC)OC)C(=O)O1)O 320.30 unknown https://doi.org/10.1021/NP060587G
methyl 2-[(E)-[(4S,5S)-4-hydroxy-5-(2-hydroxypropan-2-yl)-2-oxooxolan-3-ylidene]-methoxymethyl]benzoate 16737079 Click to see CC(C)(C1C(C(=C(C2=CC=CC=C2C(=O)OC)OC)C(=O)O1)O)O 336.30 unknown https://doi.org/10.1021/NP060587G
Methyl 2-[[4-hydroxy-5-(2-hydroxypropan-2-yl)-2-oxooxolan-3-ylidene]-methoxymethyl]benzoate 73316552 Click to see CC(C)(C1C(C(=C(C2=CC=CC=C2C(=O)OC)OC)C(=O)O1)O)O 336.30 unknown https://doi.org/10.1021/NP060587G
Methyl 2-[[5-(2-hydroxypropan-2-yl)-2-oxooxolan-3-ylidene]-methoxymethyl]benzoate 73316555 Click to see CC(C)(C1CC(=C(C2=CC=CC=C2C(=O)OC)OC)C(=O)O1)O 320.30 unknown https://doi.org/10.1021/NP060587G
> Benzenoids / Tetralins
7-Hydroxy-1a-(3-methylbut-2-enyl)-7,7a-dihydronaphtho[2,3-b]oxiren-2-one 73316553 Click to see CC(=CCC12C(O1)C(C3=CC=CC=C3C2=O)O)C 244.28 unknown https://doi.org/10.1021/NP060587G
Avicennone C 16737080 Click to see CC(=CCC12C(O1)C(C3=CC=CC=C3C2=O)O)C 244.28 unknown https://doi.org/10.1021/NP060587G
> Lignans, neolignans and related compounds / Aryltetralin lignans
(3S,4R)-6-hydroxy-4-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5,7-dimethoxy-3,4-dihydronaphthalene-2-carbaldehyde 163034289 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(=CC3=CC(=C(C(=C23)OC)O)OC)C=O)CO 416.40 unknown https://doi.org/10.1055/S-2008-1034318
6-Hydroxy-4-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5,7-dimethoxy-3,4-dihydronaphthalene-2-carbaldehyde 75163497 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(=CC3=CC(=C(C(=C23)OC)O)OC)C=O)CO 416.40 unknown https://doi.org/10.1055/S-2008-1034318
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(+)-Lyoniresinol 11711453 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown https://doi.org/10.1055/S-2008-1034318
Lyoniresinol 317840 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown https://doi.org/10.1055/S-2008-1034318
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-lyoniresinol-3-alpha-O-beta-D-glucopyranoside 10483388 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(C(O4)CO)O)O)O 582.60 unknown https://doi.org/10.1055/S-2008-1034318
2-[[7-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14521083 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(C(O4)CO)O)O)O 582.60 unknown https://doi.org/10.1055/S-2008-1034318
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aR)-5,6,10-trihydroxy-7-[(2S)-1-hydroxypropan-2-yl]-1,1,4a-trimethyl-3,4-dihydro-2H-phenanthren-9-one 162896079 Click to see CC(CO)C1=C(C(=C2C(=C1)C(=O)C(=C3C2(CCCC3(C)C)C)O)O)O 346.40 unknown https://doi.org/10.1055/S-2008-1034318
5,6,10-trihydroxy-7-(1-hydroxypropan-2-yl)-1,1,4a-trimethyl-3,4-dihydro-2H-phenanthren-9-one 162896078 Click to see CC(CO)C1=C(C(=C2C(=C1)C(=O)C(=C3C2(CCCC3(C)C)C)O)O)O 346.40 unknown https://doi.org/10.1055/S-2008-1034318
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Epitaraxerol 344467 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1071/CH9610662
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1071/CH9610662
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2S,3R,4S,5R)-2-[[(4bS,8aS)-4-hydroxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-yl]oxy]oxane-3,4,5-triol 163049870 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C)O)OC4C(C(C(CO4)O)O)O 434.60 unknown https://doi.org/10.1055/S-2008-1034318
2-[(4-Hydroxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-yl)oxy]oxane-3,4,5-triol 163049869 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C)O)OC4C(C(C(CO4)O)O)O 434.60 unknown https://doi.org/10.1055/S-2008-1034318
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,7aS)-7-[[(E,3R)-3-hydroxy-5-phenylpent-4-enoyl]oxymethyl]-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid 162944404 Click to see C1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)COC(=O)CC(C=CC4=CC=CC=C4)O 548.50 unknown https://doi.org/10.1002/MRC.2224
(1S,4aS,7R,7aS)-1-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 163022016 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)O)O 522.50 unknown https://doi.org/10.1002/MRC.2224
(1S,4aS,7R,7aS)-1-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(E)-3-(4-methoxyphenyl)prop-2-enoyl]oxyoxan-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 162908307 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)OC)O 536.50 unknown https://doi.org/10.1002/MRC.2224
(1S,4aS,7R,7aS)-1-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(E)-3-phenylprop-2-enoyl]oxyoxan-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 162998484 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=CC=C4)O 506.50 unknown https://doi.org/10.1002/MRC.2224
(1S,4aS,7S,7aS)-1-[(2S,3R,4S,5S,6R)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 101919824 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O 538.50 unknown https://doi.org/10.1016/S0305-1978(98)00060-X
(1S,4aS,7S,7aS)-1-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 163185261 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)O)O 522.50 unknown https://doi.org/10.1002/MRC.2224
(1S,4aS,7S,7aS)-1-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(E)-3-(4-methoxyphenyl)prop-2-enoyl]oxyoxan-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 162908306 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)OC)O 536.50 unknown https://doi.org/10.1002/MRC.2224
(1S,4aS,7S,7aS)-1-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(E)-3-phenylprop-2-enoyl]oxyoxan-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 101919823 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=CC=C4)O 506.50 unknown https://doi.org/10.1016/S0031-9422(00)81110-3
https://doi.org/10.1002/MRC.2224
1-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3-phenylprop-2-enoyloxy)oxan-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 162998482 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=CC=C4)O 506.50 unknown https://doi.org/10.1002/MRC.2224
1-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3-(4-hydroxyphenyl)prop-2-enoyloxy]oxan-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 76401241 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)O)O 522.50 unknown https://doi.org/10.1002/MRC.2224
1-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3-(4-methoxyphenyl)prop-2-enoyloxy]oxan-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 162908304 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)OC)O 536.50 unknown https://doi.org/10.1002/MRC.2224
5-chloro-2-(4-(2-(2-hydroxyethoxy)ethyl)piperazin-1-yl)-N-(6-(3-methoxybenzamido)pyridin-3-yl)isonicotinamide 13848072 Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)81110-3
7-[(3-Hydroxy-5-phenylpent-4-enoyl)oxymethyl]-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid 162944402 Click to see C1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)COC(=O)CC(C=CC4=CC=CC=C4)O 548.50 unknown https://doi.org/10.1002/MRC.2224
Geniposide 107848 Click to see COC(=O)C1=COC(C2C1CC=C2CO)OC3C(C(C(C(O3)CO)O)O)O 388.40 unknown https://doi.org/10.1016/S0031-9422(00)81110-3
Geniposidic acid 443354 Click to see C1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO 374.34 unknown https://doi.org/10.1515/ZNC-2001-11-1209
methyl (1S,4aS,6S,7S,7aS)-7-methyl-6-[(2E,4E)-5-phenylpenta-2,4-dienoyl]oxy-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-carboxylate 163193467 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C=CC=CC4=CC=CC=C4 546.60 unknown https://doi.org/10.1016/S0031-9422(00)81110-3
methyl (1S,4aS,7aS)-7-[[(2E,4E)-5-phenylpenta-2,4-dienoyl]oxymethyl]-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 163190640 Click to see COC(=O)C1=COC(C2C1CC=C2COC(=O)C=CC=CC3=CC=CC=C3)OC4C(C(C(C(O4)CO)O)O)O 544.50 unknown https://doi.org/10.1016/S0031-9422(00)81110-3
methyl (4aR,7aS)-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 137706142 Click to see COC(=O)C1=COC(C2C1CC=C2CO)OC3C(C(C(C(O3)CO)O)O)O 388.40 unknown https://doi.org/10.1016/S0031-9422(00)81110-3
methyl 1-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3-phenylprop-2-enoyloxy)oxan-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 162865531 Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=CC=C4)O 520.50 unknown https://doi.org/10.1016/S0031-9422(00)81110-3
Methyl 7-(5-phenylpenta-2,4-dienoyloxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 163001026 Click to see COC(=O)C1=COC(C2C1CC=C2COC(=O)C=CC=CC3=CC=CC=C3)OC4C(C(C(C(O4)CO)O)O)O 544.50 unknown https://doi.org/10.1016/S0031-9422(00)81110-3
Methyl 7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 3515873 Click to see COC(=O)C1=COC(C2C1CC=C2CO)OC3C(C(C(C(O3)CO)O)O)O 388.40 unknown https://doi.org/10.1016/S0031-9422(00)81110-3
Methyl 7-methyl-6-(5-phenylpenta-2,4-dienoyloxy)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 163037982 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C=CC=CC4=CC=CC=C4 546.60 unknown https://doi.org/10.1016/S0031-9422(00)81110-3
Mussaenoside 182423 Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)81110-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Bupleuroside XI 46905101 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)CO)C)C)C)COC8C(C(C(C(O8)CO)O)O)O)O)O)O 913.10 unknown https://doi.org/10.1016/S0031-9422(00)81110-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
[(2S,3S,5S,6S,10R,13R,17R)-10,13-dimethyl-2,3-disulfooxy-17-[(1R)-1,4,5,5-tetramethylheptyl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl] hydrogen sulfate 455339 Click to see CCC(C)(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC(C4C3(CC(C(C4)OS(=O)(=O)O)OS(=O)(=O)O)C)OS(=O)(=O)O)C 702.90 unknown https://doi.org/10.1016/S0367-326X(99)00169-0
> Organoheterocyclic compounds / Naphthofurans
(2S,3aR,9R,9aS)-3a,9-dihydroxy-2-(2-hydroxypropan-2-yl)-2,3,9,9a-tetrahydrobenzo[f][1]benzofuran-4-one 16737081 Click to see CC(C)(C1CC2(C(O1)C(C3=CC=CC=C3C2=O)O)O)O 278.30 unknown https://doi.org/10.1021/NP060587G
(2S,3aS,9R,9aR)-9-hydroxy-2-(2-hydroxypropan-2-yl)-3,3a,9,9a-tetrahydro-2H-benzo[f][1]benzofuran-4-one 16737083 Click to see CC(C)(C1CC2C(O1)C(C3=CC=CC=C3C2=O)O)O 262.30 unknown https://doi.org/10.1021/NP060587G
(2S,3R)-2-(2-hydroxypropan-2-yl)-4,9-dimethoxy-2,3-dihydrobenzo[f][1]benzofuran-3-ol 11335710 Click to see CC(C)(C1C(C2=C(C3=CC=CC=C3C(=C2O1)OC)OC)O)O 304.34 unknown https://doi.org/10.1021/NP060587G
2-(2-Hydroxypropan-2-yl)-4,9-dimethoxy-2,3-dihydrobenzo[f][1]benzofuran-3-ol 24840461 Click to see CC(C)(C1C(C2=C(C3=CC=CC=C3C(=C2O1)OC)OC)O)O 304.34 unknown https://doi.org/10.1021/NP060587G
2-(2-Hydroxypropan-2-yl)benzo[g][1]benzofuran-4,5-dione 10538978 Click to see CC(C)(C1=CC2=C(O1)C3=CC=CC=C3C(=O)C2=O)O 256.25 unknown https://doi.org/10.1016/0031-9422(85)80018-2
2-(4,9-Dimethoxy-2,3-dihydrobenzo[f][1]benzofuran-2-yl)propan-2-ol 10732088 Click to see CC(C)(C1CC2=C(C3=CC=CC=C3C(=C2O1)OC)OC)O 288.34 unknown https://doi.org/10.1021/NP060587G
2-[(2R)-4,9-dimethoxy-2,3-dihydrobenzo[f][1]benzofuran-2-yl]propan-2-ol 162881787 Click to see CC(C)(C1CC2=C(C3=CC=CC=C3C(=C2O1)OC)OC)O 288.34 unknown https://doi.org/10.1021/NP060587G
3-Hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydrobenzo[f][1]benzofuran-4,9-dione 73324230 Click to see CC(C)(C1C(C2=C(O1)C(=O)C3=CC=CC=C3C2=O)O)O 274.27 unknown https://doi.org/10.1021/NP060587G
3-Hydroxynaphtho[1,2-b]furan-4,5-dione 85521316 Click to see C1=CC=C2C(=C1)C3=C(C(=CO3)O)C(=O)C2=O 214.17 unknown https://doi.org/10.1016/0031-9422(85)80018-2
3a,9-Dihydroxy-2-(2-hydroxypropan-2-yl)-2,3,9,9a-tetrahydrobenzo[f][1]benzofuran-4-one 73316554 Click to see CC(C)(C1CC2(C(O1)C(C3=CC=CC=C3C2=O)O)O)O 278.30 unknown https://doi.org/10.1021/NP060587G
6-Hydroxybenzo[f][1]benzofuran-4,9-dione 44423352 Click to see C1=CC2=C(C=C1O)C(=O)C3=C(C2=O)OC=C3 214.17 unknown https://doi.org/10.1021/NP060587G
7-Hydroxybenzo[f][1]benzofuran-4,9-dione 44423353 Click to see C1=CC2=C(C=C1O)C(=O)C3=C(C2=O)C=CO3 214.17 unknown https://doi.org/10.1021/NP060587G
9-hydroxy-2-(2-hydroxypropan-2-yl)-3,3a,9,9a-tetrahydro-2H-benzo[f][1]benzofuran-4-one 53702747 Click to see CC(C)(C1CC2C(O1)C(C3=CC=CC=C3C2=O)O)O 262.30 unknown https://doi.org/10.1021/NP060587G
Avicenol A 11208912 Click to see CC(C)(C1C(C2=C(C3=CC=CC=C3C(=C2O1)OC)OC)O)O 304.34 unknown https://doi.org/10.1021/NP060587G
Avicenol C 44423356 Click to see CC(C)(C1CC2=C(C3=CC=CC=C3C(=C2O1)OC)OC)O 288.34 unknown https://doi.org/10.1021/NP060587G
Avicequinone A 16757531 Click to see CC(C)(C1C(C2=C(O1)C(=O)C3=CC=CC=C3C2=O)O)O 274.27 unknown https://doi.org/10.1021/NP060587G
Avicequinone C 10563004 Click to see CC(C)(C1=CC2=C(O1)C(=O)C3=CC=CC=C3C2=O)O 256.25 unknown https://doi.org/10.1021/NP060587G
Naphtho[1,2-b]furan-4,5-dione 598522 Click to see C1=CC=C2C(=C1)C3=C(C=CO3)C(=O)C2=O 198.17 unknown https://doi.org/10.1016/0031-9422(85)80018-2
Naphtho[2,3-b]furan-4,9-dione, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)- 512958 Click to see CC(C)(C1CC2=C(O1)C(=O)C3=CC=CC=C3C2=O)O 258.27 unknown https://doi.org/10.1021/NP060587G
Stenocarpoquinone B 44423355 Click to see CC(C)(C1CC2=C(O1)C(=O)C3=CC=CC=C3C2=O)O 258.27 unknown https://doi.org/10.1021/NP060587G
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 73323377 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1055/S-2006-959711
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1055/S-2006-959711
Calceolarioside A 5273566 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1055/S-2006-959711
Clerodenoside A 91884991 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)OC(=O)C)OC(=O)C)O 736.70 unknown https://doi.org/10.1055/S-2008-1034318
Clerodeside A 124222302 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)OC(=O)C)OC(=O)C)O 736.70 unknown https://doi.org/10.1055/S-2008-1034318
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1055/S-2006-959711
> Phenylpropanoids and polyketides / Cinnamyl alcohols
(3R)-3-hydroxy-5-phenylpent-4-enoic acid 9990135 Click to see C1=CC=C(C=C1)C=CC(CC(=O)O)O 192.21 unknown https://doi.org/10.1002/MRC.2224
CID 53959807 53959807 Click to see C1=CC=C(C=C1)C=CC(CC(=O)O)O 192.21 unknown https://doi.org/10.1002/MRC.2224
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5-hydroxy-2-[4-hydroxy-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-methoxychromen-4-one 162818191 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O 462.40 unknown https://doi.org/10.1016/S0367-326X(99)00169-0
7-hydroxy-2-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-5-methoxychromen-4-one 162975613 Click to see COC1=CC(=CC2=C1C(=O)C=C(O2)C3=CC(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O 462.40 unknown https://doi.org/10.1016/S0367-326X(99)00169-0
7-hydroxy-2-[4-hydroxy-3-[(2S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-5-methoxychromen-4-one 163193741 Click to see COC1=CC(=CC2=C1C(=O)C=C(O2)C3=CC(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O 462.40 unknown https://doi.org/10.1016/S0367-326X(99)00169-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2R,3S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162980716 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/S0367-326X(99)00169-0
Thermopsoside 11294177 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/S0367-326X(99)00169-0
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(1S,4aS,7aS)-7-[(4-hydroxy-3,5-dimethoxybenzoyl)oxymethyl]-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid 162870717 Click to see COC1=CC(=CC(=C1O)OC)C(=O)OCC2=CCC3C2C(OC=C3C(=O)O)OC4C(C(C(C(O4)CO)O)O)O 554.50 unknown https://doi.org/10.1002/MRC.2224
7-[(4-Hydroxy-3,5-dimethoxybenzoyl)oxymethyl]-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid 162870716 Click to see COC1=CC(=CC(=C1O)OC)C(=O)OCC2=CCC3C2C(OC=C3C(=O)O)OC4C(C(C(C(O4)CO)O)O)O 554.50 unknown https://doi.org/10.1002/MRC.2224

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