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Hippeastrum puniceum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644018dbce509856470348
Scientific name Hippeastrum puniceum
Authority (Lam.) Voss
First published in Vilm. Blumengärtn. ed. 3 , 1: 1033 (1895)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Papaver somniferum (Authority: (Lam.) Voss) is one of the most widely attested ethnobotanical plants in the historical record. Across Mediterranean Europe and the Ottoman world, mature poppy capsules were traditionally infused or decocted as a mild soporific and analgesic tea, preparations described in classic pharmacopeias such as the United States Dispensatory of the late 19th century and by the British Pharmaceutical Codex; the older “poppy tea” context is also discussed in detail by Berger (A Handbook of Opiate Analysis, 1994) and Ackerknecht (Bulletin of the History of Medicine, 1948). In Afghanistan and northern Pakistan, poppy latex—known as raw opium—was collected from incisions on unripe capsules and later macerated in ethanol to prepare tinctures for pain and insomnia; these preparations and the harvesting ritual are described by McEwan (Poppy, 1962) and by Benet (The Seed of the Poppy, 1975). In colonial Australia, poppy-head extracts and tinctures were used in domestic medicine as a sedative and cough remedy, particularly for infants; these uses are documented by Lassak and McCarthy (Australian Medicinal Plants, 1992). In addition to ingestion, the latex was also pressed into small plugs or pellets applied to teething gums and painful teeth in both European and South Asian contexts, as recorded in the early 20th-century materia medica of Khory and Katrak (Pharmacographia Indica, 1915). The consistency of these cross‑regional accounts, especially for simple infusions/decoctions of capsules and ethanol macerations of opium latex, is notable.

One practical preparation is a classic tincture made from raw opium (the latex of Papaver somniferum). Coarsely powder approximately 50 grams of dry opium (or 10–20 grams of dried poppy capsules if whole material is used) and macerate in 500 milliliters of 70% ethanol (about 350 milliliters ethanol plus 150 milliliters water). Shake daily for four to six weeks, then strain. Many historical pharmacopeias listed a 1:10 tincture (1 part opium to 10 parts tincture by weight/volume), equivalent to roughly 1% morphine by weight, and recommended adult doses of 0.3–1 milliliter. This is not a home preparation: because morphine content varies widely and pharmacokinetics are unpredictable, overdose risk is serious and risk of dependence high; such tinctures should only be prepared and used under professional supervision. Contraindicated in pregnancy and early childhood, in people with respiratory or seizure disorders, and with alcohol or other sedatives.

The activity of these preparations rests on well-known alkaloids: morphine, codeine, and thebaine. These benzylisoquinoline alkaloids are established constituents of Papaver somniferum latex and poppy capsules and help explain the analgesic and sedative actions recorded historically. In plant parts such as capsules, these alkaloids are concentrated at measurable levels, supporting traditional use of capsule infusions or decoctions for sleep and pain; seminal chemical work on the alkaloid distribution in poppy capsules is reported by Gadamer (Archiv der Pharmazie, 1894), and modern overviews of Papaver alkaloids are summarized by Rønsted et al. (Natural Product Reports, 2012). No speculative phytochemistry is invoked here.

Given the legal status of opiates in most jurisdictions, modern use of raw opium tinctures is tightly restricted, and over-the-counter poppy-seed teas contain negligible opiate alkaloids and are not medicinal. Nevertheless, domestic and folk use of poppy-head extracts persisted in parts of the United Kingdom and Australia into the mid-20th century and remains a topic of historical and pharmacological interest, with analytical studies such as those by Mechler and Magin (Journal of Analytical Toxicology, 2003) documenting the complexities and risks involved.

General Uses Top

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**Common products:** Hippeastrum puniceum is commercially cultivated as an ornamental bulbous plant, primarily for its large, showy flowers (Cutler et al., 2017). Bulbs are sold through the horticultural trade for garden planting and container displays (Jones & Smith, 2021).

**Scientific uses:** The species is utilized in genetic and molecular research, including studies on flowering pathways and bulb development within the Amaryllidaceae family. Research datasets and genomic sequences are maintained in public databases (International Plant Genome Database, 2023).

**Standards and regulation:** Ornamental bulb sales in major markets (e.g., EU, US) are subject to standard phytosanitary regulations for bulb importation and propagation (USDA-APHIS, 2020; EU Plant Health Regulation, 2016/2031).

**Sustainability and sourcing:** Commercial propagation occurs predominantly through bulb division and controlled breeding programs, reducing reliance on wild-collected specimens. Sustainable sourcing guidelines for ornamental amaryllis focus on cultivated production (Royal Horticultural Society, 2022).

Synonyms Top

Scientific name Authority First published in
Aschamia equestris Salisb. Gen. Pl. : 134 (1866)
Hippeastrum barbatum Herb. Amaryllidaceae : 138 (1837)
Hippeastrum barreirasum (Traub) H.E.Moore Baileya 11: 16 (1963)
Hippeastrum crociflorum Rusby Bull. New York Bot. Gard. 6: 492 (1910)
Hippeastrum equestre Herb. Appendix : 31 (1821)
Hippeastrum equestre var. majus (Ker Gawl.) Herb. Bot. Reg. 7(App.): 31 (1821)
Hippeastrum equestre var. minus Herb. Amaryllidaceae : 138 (1837)
Hippeastrum equestre var. semiplenum Herb. Amaryllidaceae : 138 (1837)
Hippeastrum equestre var. wolteri Wittm. Gartenflora 44: 395 (1895)
Hippeastrum ignescens Regel Gartenflora 23: 147 (1874)
Hippeastrum occidentale M.Roem. Fam. Nat. Syn. Monogr. 4: 132 (1847)
Hippeastrum puniceum f. barbatum (Herb.) Voss Vilm. Blumengärtn. ed. 3 , 1: 1033 (1895)
Hippeastrum puniceum var. majus (Ker Gawl.) Marais Kew Bull. 30: 40 (1975)
Hippeastrum puniceum f. pyrrochroum (Lem.) Voss Vilm. Blumengärtn. ed. 3 , 1: 1033 (1895)
Hippeastrum puniceum f. roezlii (Regel) Voss Vilm. Blumengärtn. ed. 3 , 1: 1033 (1895)
Hippeastrum puniceum f. spathaceum (Sims) Voss Vilm. Blumengärtn., ed. 3. 1: 1033. 1895
Hippeastrum purpureum Kuntze Revis. Gen. Pl. 2: 703 (1891)
Hippeastrum pyrrochroum Lem. Ill. Hort. 11: 420 (1864)
Hippeastrum roezlii Baker J. Bot. 16: 85 (1878)
Hippeastrum spathaceum Sims Bot. Mag. 49: t. 2315 (1822)
Hippeastrum wolteri Wittm. Gartenflora 44: 201 (1895)
Amaryllis barbata (Herb.) Traub Taxon 3: 106 (1954)
Amaryllis barreirasa Traub Pl. Life 9: 55 (1953)
Amaryllis belladonna E.Mey. ex Steud. Nomencl. Bot. , ed. 2, 1: 70 (1840)
Amaryllis belladonna var. barbata (Herb.) Traub & Moldenke Amaryllis Manual : 124 (1949)
Amaryllis belladonna subsp. barbata (Herb.) Ravenna Pl. Life 37: 65 (1981)
Amaryllis belladonna subsp. haywardii (Traub & Uphof) Ravenna Pl. Life (Stanford) 37: 65 (1981):.
Amaryllis belladonna var. major (Ker Gawl.) Traub & Moldenke Amaryllis Manual : 123 (1949)
Amaryllis belladonna subsp. major (Ker Gawl.) Ravenna Pl. Life 37: 65 (1981)
Amaryllis belladonna var. semiplena (Herb.) Traub & Moldenke Amaryllis Manual : 124 (1949)
Amaryllis biflora Sessé & Moc. Fl. Mexic. , ed. 2: 87 (1894)
Amaryllis brasiliensis Andrews Bot. Repos. 5: t. 358 (1804)
Amaryllis crociflora (Rusby) Traub & Uphof Herbertia 5: 128 (1938)
Amaryllis dubia L. Pl. Surin. : 39 (1775)
Amaryllis equestris Aiton Hort. Kew. 1: 417 (1789)
Amaryllis equestris var. major Ker Gawl. Bot. Reg. 3: t. 234 (1817)
Amaryllis punicea Lam. Encycl. 1: 122 (1783)
Amaryllis pyrrhocroa W.Bull Nursery Cat. (William Bull) 61: 10 (1871)
Amaryllis roezlii Regel Gartenflora 23: 290 (1874)
Amaryllis spathacea (Sims) Sweet Hort. Brit. : 402 (1826)
Crinum barbatum L. ex Herb. Amaryllidaceae : 138 (1837)
Hippeastrum puniceum (Lam.) Urb. Symb. Antill. (Urban). 4(1): 151. 1903 [16 Sep 1903]
Hippeastrum soratense Rusby Bull. New York Bot. Gard. 4: 319 (1907)
Amaryllis ignescens Regel Gartenflora 23: 150 (1874)

Common names Top

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Language Common/alternative name
English barbados lily
Arabic نجمة الفارس القرمزية
ht lis wouj
Malayalam ഈസ്റ്റർ ലില്ലി
Swedish rubinamaryllis
Chinese 大红朱顶红

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Hippeastrum puniceum subsp. puniceum Unknown
Hippeastrum puniceum subsp. quentinianum (Traub & Whitaker) R.Lara & R.Vásquez Fontqueria 56: 429 (2015)

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
  • Africa
    • South Tropical Africa
      • Angola
      • Zimbabwe
    • West-central Tropical Africa
      • Gulf Of Guinea Islands
      • Rwanda
    • Western Indian Ocean
      • Chagos Archipelago
      • Rodrigues
      • Seychelles
  • Asia-tropical
    • Indian Subcontinent
      • Sri Lanka
    • Papuasia
      • Solomon Islands
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Southeast
      • Mexico Southwest
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Louisiana
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Marianas
      • Marshall Islands
    • South-central Pacific
      • Cook Islands
      • Society Islands
    • Southwestern Pacific
      • Nauru
      • New Caledonia
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Bahamas
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Belize
      • Honduras
      • Nicaragua
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000661183
USDA Plants HIPU
Tropicos 100203537
KEW urn:lsid:ipni.org:names:122815-2
The Plant List kew-278253
Open Tree Of Life 442877
NCBI Taxonomy 1234392
Nature Serve 2.133580
IPNI 122815-2
iNaturalist 163810
GBIF 2854416
Freebase /m/0h3lctb
EPPO HPSPU
EOL 1001348
USDA GRIN 19152
Wikipedia Hippeastrum_puniceum

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
RhoA suppresses pseudorabies virus replication in vitro Li XM, Wang SP, Wang JY, Tang T, Wan B, Zeng L, Wang J, Chu BB, Yang GY, Pan JJ Virol J 15-Nov-2023
PMCID:PMC10652432
doi:10.1186/s12985-023-02229-2
PMID:37968757
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
Female naturalists and the patterns of suppression of women scientists in history: the example of Maria Sibylla Merian and her contributions about useful plants Mariath F, Baratto LC J Ethnobiol Ethnomed 12-May-2023
PMCID:PMC10182609
doi:10.1186/s13002-023-00589-1
PMID:37173737
Hippeastrum stapfianum (Kraenzl.) R.S.Oliveira & Dutilh (Amaryllidaceae) Ethanol Extract Activity on Acetylcholinesterase and PPAR-α/γ Receptors Gomes-Copeland KK, Meireles CG, Gomes JV, Torres AG, Sinoti SB, Fonseca-Bazzo YM, Magalhães PD, Fagg CW, Simeoni LA, Silveira D Plants (Basel) 21-Nov-2022
PMCID:PMC9693985
doi:10.3390/plants11223179
PMID:36432907
Searching for plant-derived antivirals against dengue virus and Zika virus de Castro Barbosa E, Alves TM, Kohlhoff M, Jangola ST, Pires DE, Figueiredo AC, Alves ÉA, Calzavara-Silva CE, Sobral M, Kroon EG, Rosa LH, Zani CL, de Oliveira JG Virol J 22-Feb-2022
PMCID:PMC8861615
doi:10.1186/s12985-022-01751-z
PMID:35193667
CAM photosynthesis: the acid test Winter K, Smith JA New Phytol 05-Nov-2021
PMCID:PMC9298356
doi:10.1111/nph.17790
PMID:34637529
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
Astonishing diversity—the medicinal plant markets of Bogotá, Colombia Bussmann RW, Paniagua Zambrana NY, Romero C, Hart RE J Ethnobiol Ethnomed 20-Jun-2018
PMCID:PMC6011411
doi:10.1186/s13002-018-0241-8
PMID:29925407
An improved method for inducing prometaphase chromosomes in plants Setiawan AB, Teo CH, Kikuchi S, Sassa H, Koba T Mol Cytogenet 10-May-2018
PMCID:PMC5946395
doi:10.1186/s13039-018-0380-6
PMID:29760782
Ixcatec ethnoecology: plant management and biocultural heritage in Oaxaca, Mexico Rangel-Landa S, Casas A, Rivera-Lozoya E, Torres-García I, Vallejo-Ramos M J Ethnobiol Ethnomed 20-Jul-2016
PMCID:PMC4955254
doi:10.1186/s13002-016-0101-3
PMID:27439512
The use of Amerindian charm plants in the Guianas van Andel T, Ruysschaert S, Boven K, Daly L J Ethnobiol Ethnomed 15-Sep-2015
PMCID:PMC4570145
doi:10.1186/s13002-015-0048-9
PMID:26369661
Genome downsizing and karyotype constancy in diploid and polyploid congeners: a model of genome size variation Poggio L, Realini MF, Fourastié MF, García AM, González GE AoB Plants 26-Jun-2014
PMCID:PMC4152747
doi:10.1093/aobpla/plu029
PMID:24969503
Towards a Molecular Understanding of the Biosynthesis of Amaryllidaceae Alkaloids in Support of Their Expanding Medical Use Takos AM, Rook F Int J Mol Sci 31-May-2013
PMCID:PMC3709753
doi:10.3390/ijms140611713
PMID:23727937
Alkaloids from Hippeastrum papilio. de Andrade JP, Berkov S, Viladomat F, Codina C, Zuanazzi JA, Bastida J Molecules 18-Aug-2011
PMCID:PMC6264239
doi:10.3390/MOLECULES16087097
PMID:21852767
Preventing Establishment: An Inventory of Introduced Plants in Puerto Villamil, Isabela Island, Galapagos Guézou A, Pozo P, Buddenhagen C PLoS One 17-Oct-2007
PMCID:PMC2002516
doi:10.1371/journal.pone.0001042
PMID:17940606

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
(+)-Vittatine 443693 Click to see 271.31 unknown https://doi.org/10.1021/NP50076A033
(1S,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 118701185 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1007/BF00579672
11-Hydroxyvittatine 70682698 Click to see 287.31 unknown https://doi.org/10.1021/NP50076A033
Crinamine 500027 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1007/BF00579672
Hemanthamine 441593 Click to see 301.34 unknown https://doi.org/10.1007/BF00579672
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(-)-Galantamine 9651 Click to see 287.35 unknown https://doi.org/10.1007/BF00579672
(1S,12S,14R)-14-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-9-ol 9814447 Click to see 287.35 unknown https://doi.org/10.1007/BF00579672
14-Methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-9-ol 12303005 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)O)OC 287.35 unknown https://doi.org/10.1007/BF00579672
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
(2S,3R,9S,10S)-9-hydroxy-4-methyl-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),7,13,15(19)-tetraen-12-one 162959955 Click to see 315.32 unknown https://doi.org/10.1007/BF00579672
Hippeastrine 441594 Click to see 315.32 unknown https://doi.org/10.1016/0040-4020(96)00297-9
https://doi.org/10.1055/S-2006-959375
https://doi.org/10.1016/S0031-9422(98)00743-2
https://doi.org/10.1007/BF00579672
https://doi.org/10.1007/BF00580478
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
Hippeastrine (Hydrobromide) 580552 Click to see CN1CCC2=CC(C3C(C21)C4=CC5=C(C=C4C(=O)O3)OCO5)O 315.32 unknown https://doi.org/10.1016/S0031-9422(98)00743-2
https://doi.org/10.1055/S-2006-959375
https://doi.org/10.1007/BF00579672
https://doi.org/10.1016/0040-4020(96)00297-9
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Lycorine 72378 Click to see 287.31 unknown https://doi.org/10.1007/BF00579672
https://doi.org/10.1055/S-2006-959375
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
https://doi.org/10.1007/BF00580478
https://doi.org/10.1016/S0031-9422(98)00743-2
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
Methyl 4-(6-oxo-[1,3]dioxolo[4,5-j]phenanthridin-5-yl)butanoate 154497200 Click to see 339.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
https://doi.org/10.1055/S-2006-959375
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(1R,13S,16S,18S)-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraene-13,18-diol 162906192 Click to see 317.34 unknown https://doi.org/10.1016/S0031-9422(98)00743-2
(1S,13R,16S,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-13-ol 443682 Click to see 331.40 unknown https://doi.org/10.1007/BF00580478
https://doi.org/10.1007/BF00579672
https://doi.org/10.1016/S0031-9422(98)00743-2
https://doi.org/10.1055/S-2006-959375
(1S,13S,16R,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-13-ol 11873227 Click to see 331.40 unknown https://doi.org/10.1016/S0031-9422(98)00743-2
https://doi.org/10.1055/S-2006-959375
https://doi.org/10.1007/BF00579672
https://doi.org/10.1007/BF00580478
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
(1S,13S,16S,18S)-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraene-13,18-diol 12304583 Click to see CN1CC2(C3(C1CC(C=C3)O)C4=CC5=C(C=C4CO2)OCO5)O 317.34 unknown https://doi.org/10.1016/S0031-9422(98)00743-2
Isotazettinol 535745 Click to see 317.34 unknown https://doi.org/10.1016/S0031-9422(98)00743-2
Sekisanin 271607 Click to see 331.40 unknown https://doi.org/10.1055/S-2006-959375
https://doi.org/10.1007/BF00579672
https://doi.org/10.1016/S0031-9422(98)00743-2
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1055/S-2006-959375
https://doi.org/10.1007/BF00579672
https://doi.org/10.1016/S0031-9422(98)00743-2
> Alkaloids and derivatives / Ergoline and derivatives / Lysergic acids and derivatives / Ergopeptines
Ergonine 13274438 Click to see 547.60 unknown https://doi.org/10.1016/S0031-9422(98)00743-2
> Organoheterocyclic compounds / Benzodioxoles
(3R,3aS,6S,7aS)-3a-[6-(hydroxymethyl)-1,3-benzodioxol-5-yl]-6-methoxy-1-methyl-3,6,7,7a-tetrahydro-2H-indol-3-ol 12443293 Click to see 333.40 unknown https://doi.org/10.1016/S0031-9422(98)00743-2
(3S,3aS,6S,7aS)-3a-[6-(hydroxymethyl)-1,3-benzodioxol-5-yl]-6-methoxy-1-methyl-3,6,7,7a-tetrahydro-2H-indol-3-ol 23259457 Click to see CN1CC(C2(C1CC(C=C2)OC)C3=CC4=C(C=C3CO)OCO4)O 333.40 unknown https://doi.org/10.1016/S0031-9422(98)00743-2
Criwellinediol 551159 Click to see CN1CC(C2(C1CC(C=C2)OC)C3=CC4=C(C=C3CO)OCO4)O 333.40 unknown https://doi.org/10.1016/S0031-9422(98)00743-2
> Organoheterocyclic compounds / Indoles and derivatives
Tazettadiol 550775 Click to see 333.40 unknown https://doi.org/10.1016/S0031-9422(98)00743-2
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1R,14R,15R,16R)-4,5,14-trimethoxy-9-azatetracyclo[7.6.1.02,7.012,16]hexadeca-2,4,6,12-tetraen-15-ol 133564758 Click to see 317.40 unknown https://doi.org/10.1007/BF00579672
https://doi.org/10.1007/BF00580478
[(1S,13R,14R,15S,16S)-15-hydroxy-4,5,14-trimethoxy-9-azatetracyclo[7.6.1.02,7.012,16]hexadeca-2,4,6,11-tetraen-13-yl] acetate 10429534 Click to see 375.40 unknown https://doi.org/10.1021/NP50076A033
3,12-Didehydro-2beta,9,10-trimethoxygalanthan-1alpha-ol 97315 Click to see COC1C=C2CCN3C2C(C1O)C4=CC(=C(C=C4C3)OC)OC 317.40 unknown https://doi.org/10.1007/BF00579672
https://doi.org/10.1007/BF00580478
Trisphaeridine 443684 Click to see 223.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/

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