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Crinum bulbispermum

Crinum bulbispermum - 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 UUID644025b7e1039609013571
Scientific name Crinum bulbispermum
Authority (Burm.f.) Milne-Redh. & Schweick.
First published in J. Linn. Soc., Bot. 52: 161 (1939)

Description Top

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Synonyms Top

Scientific name Authority First published in
Amaryllis bulbisperma Burm.f. Fl. Indica , Prodr. Fl. Cap.: 9 (1768)
Amaryllis longifolia var. riparia Ker Gawl. Bot. Reg. 4: t. 303 1818
Amaryllis riparia Burch. ex Kunth Enum. Pl. 2: 580 (1837)
Crinum capense Herb. Bot. Mag. 47: t. 2121 (1820)
Crinum govenium Herb. Trans. Hort. Soc. London 3: 190 (1822)
Crinum riparium Herb. Appendix : 23 (1821)
Crinum spofforthianum Herb. ex Sweet Hort. Brit. , ed. 3: 678 (1839)
Erigone govenica Salisb. Gen. Pl. : 116 (1866)
Crinum bulbispermum var. sanguineum Traub Pl. Life 13: 61. 1957

Common names Top

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Language Common/alternative name
English hardy swamplily
Spanish amaryllis capensis
German rosa hakenlilie
Japanese アフリカハマユウ
Swedish strimkrinum
Chinese 长叶文殊兰

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
  • Africa
    • Macaronesia
      • Madeira
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Northern Provinces
      • Swaziland
  • Northern America
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Florida
      • Louisiana
      • North Carolina
  • Southern America
    • Caribbean
      • Cuba
      • Leeward Islands
      • Windward Islands
    • Central America
      • Honduras

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000764436
Florida Plant Atlas 4097
Flora of Alabama 4417
USDA Plants CRBU2
Tropicos 1200390
INPN 160295
KEW urn:lsid:ipni.org:names:63828-1
The Plant List kew-303361
Missouri Botanical Garden 275729
Open Tree Of Life 639815
NCBI Taxonomy 209086
Nature Serve 2.153391
IPNI 63828-1
iNaturalist 161125
GBIF 2853668
Freebase /m/026psbk
EPPO KRMBU
EOL 1087165
USDA GRIN 404365
Wikipedia Crinum_bulbispermum
CMAUP NPO18113

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
Crinum bulbispermum, a Medicinal Geophyte with Phytostabilization Properties in Metal-Enriched Mine Tailings Clarke VC, Marcelo-Silva J, Claassens S, Siebert SJ Plants (Basel) 26-Dec-2023
PMCID:PMC10780652
doi:10.3390/plants13010079
PMID:38202387
Studies on the Nonalkaloidal Secondary Metabolites of Hippeastrum vittatum (L’Her.) Herb. Bulbs Khalifa MF, Fahim JR, Allam AE, Shoman ME, El Zawily A, Kamel MS, Shimizu K, Attia EZ ACS Omega 23-Jul-2023
PMCID:PMC10398848
doi:10.1021/acsomega.2c07886
PMID:37546665
Phytochemicals as Antimicrobials: Prospecting Himalayan Medicinal Plants as Source of Alternate Medicine to Combat Antimicrobial Resistance Ashraf MV, Pant S, Khan MA, Shah AA, Siddiqui S, Jeridi M, Alhamdi HW, Ahmad S Pharmaceuticals (Basel) 15-Jun-2023
PMCID:PMC10302623
doi:10.3390/ph16060881
PMID:37375828
Advances on the Amaryllidacea Alkaloids Collected in South Africa, Andean South America and the Mediterranean Basin Evidente A Molecules 12-May-2023
PMCID:PMC10224442
doi:10.3390/molecules28104055
PMID:37241796
Chemical Characterization and Cytotoxic and Antioxidant Activity Evaluation of the Ethanol Extract from the Bulbs of Pancratium maritimun Collected in Sicily Cicio A, Sut S, Dall’Acqua S, Bruno M, Luparello C, Serio R, Zizzo MG Molecules 09-May-2023
PMCID:PMC10222022
doi:10.3390/molecules28103986
PMID:37241726
Alkaloid Composition and Biological Activities of the Amaryllidaceae Species Ismene amancaes (Ker Gawl.) Herb. Soto-Vásquez MR, Rodríguez-Muñoz CA, Tallini LR, Bastida J Plants (Basel) 22-Jul-2022
PMCID:PMC9331871
doi:10.3390/plants11151906
PMID:35893610
The Phytochemistry and Pharmacology of Tulbaghia, Allium, Crinum and Cyrtanthus: ‘Talented’ Taxa from the Amaryllidaceae Danquah CA, Minkah PA, Agana TA, Moyo P, Ofori M, Doe P, Rali S, Osei Duah Junior I, Amankwah KB, Somuah SO, Nugbemado IN, Maharaj VJ, Bhakta S, Gibbons S Molecules 13-Jul-2022
PMCID:PMC9316996
doi:10.3390/molecules27144475
PMID:35889346
Isolation and Biological Characterization of Homoisoflavanoids and the Alkylamide N-p-Coumaroyltyramine from Crinum biflorum Rottb., an Amaryllidaceae Species Collected in Senegal Masi M, Koirala M, Delicato A, Di Lecce R, Merindol N, Ka S, Seck M, Tuzi A, Desgagne-Penix I, Calabrò V, Evidente A Biomolecules 31-Aug-2021
PMCID:PMC8466962
doi:10.3390/biom11091298
PMID:34572511
Antiproliferative Effects of Alkaloids from the Bulbs of Crinum abyscinicum Hochst. ExA. Rich Abebe B, Tadesse S, Hymete A, Bisrat D Evid Based Complement Alternat Med 31-Oct-2020
PMCID:PMC7648683
doi:10.1155/2020/2529730
PMID:33178310
Evaluation of bioactive compounds, free radical scavenging and anticancer activities of bulb extracts of Boophone disticha from Eastern Cape Province, South Africa Tonisi S, Okaiyeto K, Mabinya LV, Okoh AI Saudi J Biol Sci 01-Aug-2020
PMCID:PMC7715441
doi:10.1016/j.sjbs.2020.07.028
PMID:33304167
The traditional use of southern African medicinal plants in the treatment of viral respiratory diseases: A review of the ethnobotany and scientific evaluations Cock IE, Van Vuuren SF J Ethnopharmacol 27-Jul-2020
PMCID:PMC7384428
doi:10.1016/j.jep.2020.113194
PMID:32730880
Identification of Selective Novel Hits against Plasmodium falciparum Prolyl tRNA Synthetase Active Site and a Predicted Allosteric Site Using In Silico Approaches Nyamai DW, Tastan Bishop Ö Int J Mol Sci 27-May-2020
PMCID:PMC7312540
doi:10.3390/ijms21113803
PMID:32471245
Exploring African Medicinal Plants for Potential Anti-Diabetic Compounds with the DIA-DB Inverse Virtual Screening Web Server Pereira AS, den Haan H, Peña-García J, Moreno MM, Pérez-Sánchez H, Apostolides Z Molecules 24-May-2019
PMCID:PMC6571761
doi:10.3390/molecules24102002
PMID:31137754
Sporocadaceae, a family of coelomycetous fungi with appendage-bearing conidia Liu F, Bonthond G, Groenewald JZ, Cai L, Crous PW Stud Mycol 17-Nov-2018
PMCID:PMC6298422
doi:10.1016/j.simyco.2018.11.001
PMID:30584265
Naturally Occurring Acetylcholinesterase Inhibitors and Their Potential Use for Alzheimer's Disease Therapy dos Santos TC, Gomes TM, Pinto BA, Camara AL, Paes AM Front Pharmacol 18-Oct-2018
PMCID:PMC6201143
doi:10.3389/fphar.2018.01192
PMID:30405413

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(+)-6-Hydroxycrinamine 44559503 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown via CMAUP database
(+)-Crinamine 118701061 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
https://doi.org/10.1055/S-2007-969754
https://doi.org/10.1248/CPB.32.3015
(+)-epi-Vittatine 12304132 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1248/CPB.32.3015
(11S,13beta,19S)-1,2-Didehydrocrinan-3alpha,11-diol 5282088 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown https://doi.org/10.1055/S-2007-969754
https://doi.org/10.1016/S0031-9422(99)00255-1
https://doi.org/10.1055/S-0028-1097645
(18-Hydroxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl) acetate 73657405 Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 329.30 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
(1R,11S,13R,15S,18R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 12309558 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
(1R,13R,15S,18R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 40469675 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
(1R,13R,15S,18R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-15,18-diol 162950862 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
(1R,13S,15R,18R)-15-Methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 12096833 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
(1S,11S,13S,15R,18R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 101297739 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1055/S-2004-818919
(1S,11S,13S,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 162945734 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
(1S,13R,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 42579248 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1248/CPB.32.3015
(1S,13S,15R)-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-ol 162912829 Click to see COC1=C2CN3CCC4(C3CC(C=C4)O)C2=CC5=C1OCO5 301.34 unknown https://doi.org/10.1248/CPB.32.3015
(3R)-7-Methoxy-1,2-didehydrocrinan-3-ol 627287 Click to see COC1=C2CN3CCC4(C3CC(C=C4)O)C2=CC5=C1OCO5 301.34 unknown https://doi.org/10.1248/CPB.32.3015
[(1R,13R,15S,18R)-18-hydroxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl] acetate 162963526 Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 329.30 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
[(1S,13R,15R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl] acetate 101935954 Click to see CC(=O)OC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 313.30 unknown https://doi.org/10.1248/CPB.32.3015
[(1S,13S,15R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl] acetate 163003058 Click to see CC(=O)OC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 313.30 unknown https://doi.org/10.1248/CPB.32.3015
[(1S,13S,15S,18S)-18-hydroxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl] acetate 162963527 Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 329.30 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
1,2-Didehydrocrinan-3-ol 101727 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1021/NP100819N
https://doi.org/10.1248/CPB.32.3015
11-Epicrinamine 5281172 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
https://doi.org/10.1055/S-2007-969754
https://doi.org/10.1055/S-2004-818919
https://doi.org/10.1248/CPB.32.3015
3-O-Acetylhamayne 443671 Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 329.30 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
https://doi.org/10.1055/S-2004-818919
9-Methoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-trien-15-ol 625708 Click to see COC1=C2CN3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6 317.34 unknown https://doi.org/10.1248/CPB.32.3015
Crinamidine 399204 Click to see COC1=C2CN3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6 317.34 unknown https://doi.org/10.1248/CPB.32.3015
Crinamin 73620 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
https://doi.org/10.1055/S-0028-1097645
https://doi.org/10.1055/S-2004-818919
Crinamine 500027 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
https://doi.org/10.1248/CPB.32.3015
https://doi.org/10.1055/S-0028-1097645
Crinine 398937 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1016/S0305-1978(02)00222-3
https://doi.org/10.1248/CPB.32.3015
https://doi.org/10.1055/S-0028-1097645
https://doi.org/10.1055/S-2007-969754
Crinine acetate 185262 Click to see CC(=O)OC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 313.30 unknown https://doi.org/10.1248/CPB.32.3015
Haemanthidine 544807 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
Hamayne 443670 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
https://doi.org/10.1055/S-2007-969754
Powellin 443669 Click to see COC1=C2CN3CCC4(C3CC(C=C4)O)C2=CC5=C1OCO5 301.34 unknown https://doi.org/10.1055/S-2007-969754
https://doi.org/10.1248/CPB.32.3015
https://doi.org/10.1055/S-0028-1097645
Vittatine 443693 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1055/S-0028-1097645
https://doi.org/10.1002/CHIN.200511200
Vittatine acetate 541087 Click to see CC(=O)OC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 313.30 unknown https://doi.org/10.1248/CPB.32.3015
Vittatine, 11-hydroxy- 602595 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
1,2-Diacetoxylycorine 10429288 Click to see CC(=O)OC1C=C2CCN3C2C(C1OC(=O)C)C4=CC5=C(C=C4C3)OCO5 371.40 unknown https://doi.org/10.1248/CPB.32.3015
3,3a-Didehydrolycoran-1alpha,2beta-diol 3978 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown https://doi.org/10.1055/S-0028-1097645
Caranine 441589 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CCC5O)OCO4 271.31 unknown https://doi.org/10.1002/CHIN.200511200
Diacetyl lycorine 619785 Click to see CC(=O)OC1C=C2CCN3C2C(C1OC(=O)C)C4=CC5=C(C=C4C3)OCO5 371.40 unknown https://doi.org/10.1248/CPB.32.3015
Hipppamine 23259917 Click to see COC1C=C2CCN3C2C(C1O)C4=CC5=C(C=C4C3)OCO5 301.34 unknown https://doi.org/10.1002/CHIN.200511200
Lycorine 72378 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown https://doi.org/10.1055/S-2007-969754
https://doi.org/10.1055/S-0028-1097645
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
8alpha-Ethoxyprecriwelline 15483834 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4N(CC5O1)C)OC)OCO3 359.40 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
Pretazettine, 8-O-ethyl- 623748 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4N(CC5O1)C)OC)OCO3 359.40 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Kaurenoic acid 73062 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
6-(4-Hydroxyphenyl)-1,3-benzodioxole-5-carbaldehyde 15549895 Click to see C1OC2=C(O1)C=C(C(=C2)C=O)C3=CC=C(C=C3)O 242.23 unknown https://doi.org/10.1016/S0031-9422(00)00184-9
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(1R,11R,13S,16R,18R)-11-ethoxy-18-methoxy-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraene 162917457 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4NCC5O1)OC)OCO3 345.40 unknown https://doi.org/10.1055/S-2004-818919
(1R,11R,13S,16R,18R)-18-ethoxy-11-methoxy-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraene 162801177 Click to see CCOC1CC2C3(C=C1)C(CN2)OC(C4=CC5=C(C=C34)OCO5)OC 345.40 unknown https://doi.org/10.1055/S-2004-818919
(1S,11R,13R,16R,18S)-11-ethoxy-18-methoxy-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraene 162917455 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4NCC5O1)OC)OCO3 345.40 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
(1S,11S,13R,16R,18S)-11-ethoxy-18-methoxy-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraene 162917454 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4NCC5O1)OC)OCO3 345.40 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
(1S,11S,13R,16S)-11-ethoxy-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,18-tetraene 162874159 Click to see CCOC1C2=CC3=C(C=C2C45CC=C(CC4N(CC5O1)C)OC)OCO3 359.40 unknown https://doi.org/10.1055/S-2004-818919
11-Ethoxy-18-methoxy-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraene 162917452 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4NCC5O1)OC)OCO3 345.40 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
N-Desmethyl-8alpha-ethoxypretazettine 15483835 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4NCC5O1)OC)OCO3 345.40 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
N-Desmethyl-8beta-ethoxypretazettine 15483836 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4NCC5O1)OC)OCO3 345.40 unknown https://doi.org/10.1016/S0031-9422(99)00255-1
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1S,13R,16S,17S)-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-triene-16,17-diol 162893618 Click to see COC1=C2CN3CCC4(C3CCC(C4O)O)C2=CC5=C1OCO5 319.40 unknown https://doi.org/10.1248/CPB.32.3015
[(1S,13R,16S,17S)-17-acetyloxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-trien-16-yl] acetate 132573533 Click to see CC(=O)OC1CCC2C3(C1OC(=O)C)CCN2CC4=C(C5=C(C=C34)OCO5)OC 403.40 unknown https://doi.org/10.1248/CPB.32.3015
1H,6H-5,11b-Ethano[1,3]dioxolo[4,5-j]phenanthridine-1,2-diol, 2,3,4,4a-tetrahydro-7-methoxy- 629204 Click to see COC1=C2CN3CCC4(C3CCC(C4O)O)C2=CC5=C1OCO5 319.40 unknown https://doi.org/10.1248/CPB.32.3015
7H-Pyrrolo(3,2,1-de)phenanthridin-7-one, 10-hydroxy-9-methoxy- 5488695 Click to see COC1=C(C=C2C3=CC=CC4=C3N(C=C4)C(=O)C2=C1)O 265.26 unknown https://doi.org/10.1016/S0040-4039(00)98718-5
Bowdensine 541341 Click to see CC(=O)OC1CCC2C3(C1OC(=O)C)CCN2CC4=C(C5=C(C=C34)OCO5)OC 403.40 unknown https://doi.org/10.1248/CPB.32.3015
Hippacine 10015025 Click to see C1=CC2=C3C(=C1)C4=CC(=C(C=C4C(=O)N3C=C2)O)O 251.24 unknown https://doi.org/10.1016/S0031-9422(00)00184-9
Hippadine 100605 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC5=C4N(C3=O)C=C5 263.25 unknown https://doi.org/10.1055/S-2007-969754
Pratorimine 181937 Click to see COC1=C(C=C2C(=C1)C3=CC=CC4=C3N(C2=O)C=C4)O 265.26 unknown https://doi.org/10.1016/S0040-4039(00)98718-5
> Organoheterocyclic compounds / Tetrahydroisoquinolines / 4-phenyltetrahydroisoquinolines
2-Methyl-4-(4-hydroxyphenyl)-6-methoxy-7-hydroxy-1,2,3,4-tetrahydroisoquinoline 618047 Click to see CN1CC(C2=CC(=C(C=C2C1)O)OC)C3=CC=C(C=C3)O 285.34 unknown https://doi.org/10.1248/CPB.32.3015
Cherylline 90075 Click to see CN1CC(C2=CC(=C(C=C2C1)O)OC)C3=CC=C(C=C3)O 285.34 unknown https://doi.org/10.1248/CPB.32.3015
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)- 1889 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1016/S0031-9422(00)00184-9
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1016/S0031-9422(00)00184-9
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S,3R)-2-(4-hydroxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-3-ol 162969551 Click to see COC1=CC2=C(CC(C(O2)C3=CC=C(C=C3)O)O)C=C1 272.29 unknown https://doi.org/10.1016/S0031-9422(00)00184-9
2-(4-hydroxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-3-ol 54481478 Click to see COC1=CC2=C(CC(C(O2)C3=CC=C(C=C3)O)O)C=C1 272.29 unknown https://doi.org/10.1016/S0031-9422(00)00184-9
3',4'-Dihydroxy-7-methoxyflavan 14157886 Click to see COC1=CC2=C(CCC(O2)C3=CC(=C(C=C3)O)O)C=C1 272.29 unknown https://doi.org/10.1016/S0031-9422(00)00184-9
4-(7-methoxy-3,4-dihydro-2H-chromen-2-yl)benzene-1,2-diol 14157885 Click to see COC1=CC2=C(CCC(O2)C3=CC(=C(C=C3)O)O)C=C1 272.29 unknown https://doi.org/10.1016/S0031-9422(00)00184-9
Guibourtinidol-7-methyl ether 15549896 Click to see COC1=CC2=C(CC(C(O2)C3=CC=C(C=C3)O)O)C=C1 272.29 unknown https://doi.org/10.1016/S0031-9422(00)00184-9
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2S)-7-Hydroxy-8-methoxyflavanone 15549894 Click to see COC1=C(C=CC2=C1OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/S0031-9422(00)00184-9
7-Hydroxy-8-methoxyflavanone 42607832 Click to see COC1=C(C=CC2=C1OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/S0031-9422(00)00184-9
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1016/S0031-9422(00)00184-9
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1016/S0031-9422(00)00184-9
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
4-Hydroxy-2',4'-dimethoxydihydrochalcone 15549893 Click to see COC1=CC(=C(C=C1)C(=O)CCC2=CC=C(C=C2)O)OC 286.32 unknown https://doi.org/10.1016/S0031-9422(00)00184-9

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