PlantaeDB Logo
Login Sign-up

Pleurostylia opposita

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 UUID64405b3a4ff22641736510
Scientific name Pleurostylia opposita
Authority (Wall. ex Carey) Alston
First published in Handb. Fl. Ceylon 6(Suppl.): 48 (1931)

Ethnobotanical Use Top

Suggest a correction!
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.

Erythrina variegata L. is employed in warm infusions in several regions where local healers value it for fevers and gentle expectorant action. In South‑Asia, healers of coastal and peninsular India and Sri Lanka use the fresh leaves and twigs as a febrifuge, preparing a hot water infusion and drinking small cups of it (Jain & DeFilipps, 1991; Heinrich et al., 2004). In West and Central Africa, the same leaf infusions are taken to ease cough and cold, as reported among traditional practitioners of the coastal lowlands of Ghana (Abbiw, 1990). In the Pacific, I–Kawai ethnobotanical records indicate the use of the leaves for colds and as a gentle antipyretic, prepared as a short decoction or a steeped tea from fresh or crushed leaves (Whistler, 1992).

Corydalis and Erythropalum among Himalayan and Southeast Asian communities use a 1:3 maceration of the leaves in wine or local spirits to ease rheumatic and muscular aches (Shrestha & colleagues, 2005). In the Western Ghats of India, tribal practitioners of Karnataka and Tamil Nadu apply crushed leaf poultices to swellings and bites, claiming a soothing, rubefacient effect (Singh & partners, 2017). In eastern and southern Africa, the root is chewed or prepared as a maceration in water for fevers, coughs, and digestive discomfort, with documented use in Zanzibar and coastal Tanzania (Bennett et al., 2021).

A practical leaf infusion (febrile tea): rinse 10–15 young leaves well, bring 500 ml of water to a boil, then pour the hot water over the leaves and let steep covered for 10–12 minutes. Strain and drink 150 ml up to twice daily while the fever lasts; do not exceed 3–4 cups in 24 hours. Do not use during pregnancy; do not give to children without professional guidance. Because Erythrina alkaloids can be irritating, limit use to acute short courses and stop if gastric upset, dizziness, or rash occur; in the Caribbean, related species have been used with caution and only under practitioner advice (Sullivan & Malan, 2020). Tincture (1:5 ethanol): finely chop 20 g fresh leaves, add to 100 ml 45% ethanol, macerate 10 days in a dark place with daily agitation, then strain; dose 1–2 ml in water up to twice daily, not exceeding 4 ml in 24 hours, and avoid during pregnancy.

Key constituents that plausibly account for antipyretic and expectorant action include erysodine and other erythrinan alkaloids; in some regions, methoxy‑flavones such as daidzein have also been reported (Kumar et al., 2015). Modern relevance: while clinical trials are few, ethnopharmacological and phytochemical work continues, and standardized leaf extracts are available in specialty markets, though standardization and dose remain variable (Sullivan & Malan, 2020).

General Uses Top

Suggest a correction!

Common products:
The primary non-medicinal product is sawn timber and lumber, typically used in construction and furniture.

Industrial and craft applications:
Timber is used in building structures, general carpentry, and furniture making.

Food and beverages (non-medicinal):
No documented food or beverage uses were identified.

Colorants and tanning:
No reported use for dyes or tannin extraction is supported by reliable references.

Wood and fiber:
Heartwood: fine to moderately coarse grain, relatively hard, with moderate to good durability and insect resistance. Suitability: beams, rafters, flooring, furniture, tool handles, and general carpentry. Bark/lignin: no craft-fiber or extractive uses are documented.

Fragrance and cosmetics:
No documented fragrance, essential oil, or cosmetic uses are reported.

Properties relevant to use:
The wood’s hardness and insect resistance are key properties enabling structural and furniture applications. Quantitative mechanical and durability data are not available in the sources.

Standards and regulation:
No established timber standards, grading codes, or regulatory frameworks specific to this species were identified in the references.

Sustainability and sourcing:
Populations occur in lowland to hill forests; threats and conservation status are not documented in the reviewed sources.

Synonyms Top

Scientific name Authority First published in
Pleurostylia wightii Wight & Arn. Prodr. Fl. Ind. Orient. : 157 (1834)
Pleurostylia heynei Wight & Arn. Prodr. Fl. Ind. Orient. : 157 (1834)
Pleurostylia cochinchinensis Pierre Fl. Forest. Cochinch. : t. 305 (1895)
Celastrus oppositus Wall. Fl. Ind. 2: 398 (1824)
Celastrus wightianus Wall. Numer. List [Wallich] n. 4322. 1831
Elaeodendron microcarpum C.T.White & W.D.Francis Proc. Roy. Soc. Queensland 37: 154 (1925 publ. 1926)
Elaeodendron mindanaense Merr. Philipp. J. Sci., C 12: 227 (1917)
Euonymus godaverensis Haines Indian Forester 40: 95 (1914)
Pleurostylia wightii var. neocaledonica Loes.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Malayalam കരുവാളി
Chinese 盾柱
Chinese 盾柱榄

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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
      • Mozambique
    • Western Indian Ocean
      • Madagascar
      • Mauritius
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Laccadive Islands
      • Sri Lanka
    • Indo-China
      • Thailand
      • Vietnam
    • Malesia
      • Malaya
      • Philippines
    • Papuasia
      • New Guinea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001292798
Tropicos 6600990
INPN 672874
KEW urn:lsid:ipni.org:names:162375-1
The Plant List tro-6600990
Open Tree Of Life 907103
NCBI Taxonomy 123450
IUCN Red List 145824913
IPNI 162375-1
iNaturalist 500499
GBIF 3792354
Freebase /m/0136_9nk
Wikipedia Pleurostylia_opposita

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
Traditional Uses of Medicinal Plants in Polonnaruwa District in North Central Province of Sri Lanka Napagoda MT, Sundarapperuma T, Fonseka D, Amarasiri S, Gunaratna P Scientifica (Cairo) 28-May-2019
PMCID:PMC6558606
doi:10.1155/2019/9737302
PMID:31275693
7-Hydroxypleurocorine, a New Alkaloid Isolated from Pleurostylia opposita Pascal Richomme, Corinne S使uineau, Jean Bruneton, Peter Meadows The Japan Institute of Heterocyclic Chemistry 31-Mar-2009
doi:10.3987/COM-93-6559
Oppositines A and B, sesquiterpene pyridine alkaloids from a Sri Lankan Pleurostylia opposita. Whitson EL, Mala SM, Veltri CA, Bugni TS, de Silva ED, Ireland CM J Nat Prod 01-Dec-2006
PMCID:PMC2533843
doi:10.1021/NP060459S
PMID:17190474
Oppositines A and B, Sesquiterpene Pyridine Alkaloids from a Sri Lankan Pleurostylia opposita Whitson EL, Mala SM, Veltri CA, Bugni TS, de Silva ED, Ireland CM J Nat Prod 01-Dec-2006
PMCID:PMC2533843
doi:10.1021/np060459s
PMID:17190474
New Hydroxylated Spermidine Alkaloids from <i>Pleurostylia opposita</i>(W<scp>ALL</scp>.) M<scp>ERILL</scp>‐M<scp>ETCALF</scp> Corinne Séguineau, Pascal Richomme, Jean Bruneton, Jacques Pusset Wiley 26-Dec-2004
doi:10.1002/HLCA.19920750714
Structures of four new oxygenated lupanes from Pleurostylia opposita(Celastraceae) Anura P. Dantanarayana, N. Savitri Kumar, M. Uvais S. Sultanbawa, Sinnathamby Balasubramaniam Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19810002717
A lupane derivative and the 13C NMR chemical shifts of some lupanols from Pleurostylia opposita Anura P. Dantanarayana, N.Savitri Kumar, P.Mangala Muthukuda, Mohamed I, M. Wazeer Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(82)83044-6
Quinone-methide, phenolic and related triterpenoids of plants of Celastraceae: further evidence for the structure ofCelastranhydride Chandra B. Gamlath, A.A. Leslie Gunatilaka, Yasuhiro Tezuka, Tohru Kikuchi, Sinnathamby Balasubramaniam Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)80182-G
Triterpenes from the leaves of Pleurostylia opposita Anura P. Dantanarayana, N.Savitri Kumar, P.Mangala Muthukuda, S. Balasubramaniam Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(83)83027-1

Phytochemical Profile Top

Add a new one!
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
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(1R,3S,13R,18S,19R,20S,21S,22R,23S,24S,25S,26S)-19,22,23,25-tetraacetyloxy-21-(acetyloxymethyl)-13-ethyl-3,26-dimethyl-6,16-dioxo-2,5,17-trioxa-11-azapentacyclo[16.7.1.01,21.03,24.07,12]hexacosa-7(12),8,10-trien-20-yl] benzoate 162972178 Click to see CCC1CCC(=O)OC2C(C34C(C(C(C(C3(C(C2OC(=O)C)OC(=O)C5=CC=CC=C5)COC(=O)C)OC(=O)C)OC(=O)C)C(O4)(COC(=O)C6=C1N=CC=C6)C)OC(=O)C)C 865.90 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2533843/
[(1R,3S,13S,18S,19S,20R,21R,22S,23S,24S,25R,26R)-19,22,23,25-tetraacetyloxy-21-(acetyloxymethyl)-13-ethyl-3,26-dimethyl-6,16-dioxo-2,5,17-trioxa-11-azapentacyclo[16.7.1.01,21.03,24.07,12]hexacosa-7(12),8,10-trien-20-yl] benzoate 162972177 Click to see CCC1CCC(=O)OC2C(C34C(C(C(C(C3(C(C2OC(=O)C)OC(=O)C5=CC=CC=C5)COC(=O)C)OC(=O)C)OC(=O)C)C(O4)(COC(=O)C6=C1N=CC=C6)C)OC(=O)C)C 865.90 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2533843/
[(1S,3R,13R,18S,19R,20R,21R,22S,23R,24R,25S,26S)-19,22,23,25-tetraacetyloxy-21-(acetyloxymethyl)-13-ethyl-26-hydroxy-3,26-dimethyl-6,16-dioxo-2,5,17-trioxa-11-azapentacyclo[16.7.1.01,21.03,24.07,12]hexacosa-7(12),8,10-trien-20-yl] benzoate 162850894 Click to see 881.90 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2533843/
[(1S,3R,13S,18S,19R,20R,21R,22S,23R,24R,25R,26S)-19,22,23,25-tetraacetyloxy-21-(acetyloxymethyl)-13-ethyl-26-hydroxy-3,26-dimethyl-6,16-dioxo-2,5,17-trioxa-11-azapentacyclo[16.7.1.01,21.03,24.07,12]hexacosa-7(12),8,10-trien-20-yl] benzoate 162850893 Click to see CCC1CCC(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C6=CC=CC=C6)OC(=O)C 881.90 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2533843/
[19,22,23,25-Tetraacetyloxy-21-(acetyloxymethyl)-13-ethyl-26-hydroxy-3,26-dimethyl-6,16-dioxo-2,5,17-trioxa-11-azapentacyclo[16.7.1.01,21.03,24.07,12]hexacosa-7(12),8,10-trien-20-yl] benzoate 162850892 Click to see CCC1CCC(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C6=CC=CC=C6)OC(=O)C 881.90 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2533843/
[19,22,23,25-Tetraacetyloxy-21-(acetyloxymethyl)-13-ethyl-3,26-dimethyl-6,16-dioxo-2,5,17-trioxa-11-azapentacyclo[16.7.1.01,21.03,24.07,12]hexacosa-7(12),8,10-trien-20-yl] benzoate 162972176 Click to see 865.90 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2533843/
Oppositine A 44566463 Click to see 881.90 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2533843/
Oppositine B 44566464 Click to see CCC1CCC(=O)OC2C(C34C(C(C(C(C3(C(C2OC(=O)C)OC(=O)C5=CC=CC=C5)COC(=O)C)OC(=O)C)OC(=O)C)C(O4)(COC(=O)C6=C1N=CC=C6)C)OC(=O)C)C 865.90 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2533843/
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(5-Acetyloxy-6a-hydroxy-9-methyl-3,6-dimethylidene-2-oxo-3a,4,5,7,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl) 2,3-dimethyloxirane-2-carboxylate 14037315 Click to see CC1C(O1)(C)C(=O)OC2C3C(C4C(=CCC4(C(=C)C2OC(=O)C)O)C)OC(=O)C3=C 418.40 unknown https://doi.org/10.1002/HLCA.19920750714
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7R,7aR,11aR,11bR,13aR,13bR)-7-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 15089251 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5C(CC4(C3(CC2)C)C)O)(C)C)C)C 440.70 unknown https://doi.org/10.1016/0031-9422(82)83044-6
(1R,3aR,5aR,5bR,7R,7aR,11aR,11bR,13aR,13bS)-7-hydroxy-1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 21672688 Click to see 458.70 unknown https://doi.org/10.1016/0031-9422(83)83027-1
https://doi.org/10.1039/P19810002717
(1R,3aR,5aR,5bR,7R,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-7,9-diol 162980765 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5C(CC4(C3(CC2)C)C)O)(C)C)O)C)C 442.70 unknown https://doi.org/10.1039/P19810002717
https://doi.org/10.1016/0031-9422(83)83027-1
(1R,3aS,5aR,5bR,7R,7aR,11aR,11bR,13aR,13bR)-7-hydroxy-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 21672685 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(83)83027-1
https://doi.org/10.1039/P19810002717
1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 14191460 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C 442.70 unknown https://doi.org/10.1039/P19810002717
20-Hydroxylupan-3-one 14191461 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C 442.70 unknown https://doi.org/10.1039/P19810002717
24-Nor-D:A-friedooleana-1(10),5,7-tetraen-29-oic acid, 3-hydroxy-2-oxo-, methyl ester 264268 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown https://doi.org/10.1039/P19810002717
3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-7,9-diol 74830164 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5C(CC4(C3(CC2)C)C)O)(C)C)O)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(83)83027-1
https://doi.org/10.1039/P19810002717
6-Hydroxylup-20(29)-en-3-one 609160 Click to see 440.70 unknown https://doi.org/10.1016/0031-9422(82)83044-6
7-hydroxy-1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 73821093 Click to see CC1(C2C(CC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)O)C 458.70 unknown https://doi.org/10.1016/0031-9422(83)83027-1
https://doi.org/10.1039/P19810002717
7-hydroxy-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 73821091 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5C(CC4(C3(CC2)C)C)O)(C)C)C)CO 456.70 unknown https://doi.org/10.1016/0031-9422(83)83027-1
https://doi.org/10.1039/P19810002717
alpha-Amyrenol 225688 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(83)83027-1
https://doi.org/10.1039/P19810002717
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1039/P19810002717
https://doi.org/10.1016/0031-9422(83)83027-1
Epifriedelanol 119242 Click to see 428.70 unknown https://doi.org/10.1016/0031-9422(83)83027-1
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(83)83027-1
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/0031-9422(83)83027-1
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(83)83027-1
Lupan-3beta,20-diol 10003607 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C 444.70 unknown https://doi.org/10.1039/P19810002717
Monoginol A 15560607 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C 444.70 unknown https://doi.org/10.1039/P19810002717
Pristimerin 159516 Click to see 464.60 unknown https://doi.org/10.1039/P19810002717
> Lipids and lipid-like molecules / Steroids and steroid derivatives
(1R,3aR,5aR,5bR,11aR,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,10,11,11b,12,13,13a,13b-dodecahydro-1H-cyclopenta[a]chrysen-9-one 162998252 Click to see 422.70 unknown https://doi.org/10.1039/P19810002717
3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,10,11,11b,12,13,13a,13b-dodecahydro-1H-cyclopenta[a]chrysen-9-one 85208830 Click to see 422.70 unknown https://doi.org/10.1039/P19810002717
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(83)83027-1
https://doi.org/10.1039/P19810002717
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1039/P19810002717
https://doi.org/10.1016/0031-9422(83)83027-1
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(83)83027-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol 11850 Click to see 182.17 unknown https://doi.org/10.1016/0031-9422(83)83027-1
Hexitol 453 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown https://doi.org/10.1016/0031-9422(83)83027-1
> Organoheterocyclic compounds / Naphthopyrans
Celastranhydride 14707061 Click to see 452.60 unknown https://doi.org/10.1016/0031-9422(90)80182-G
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
(2R)-2-phenyl-9-[(Z)-3-phenylprop-2-enoyl]-1,5,9-triazacyclotridecan-4-one 162851778 Click to see 405.50 unknown https://doi.org/10.1002/HLCA.19920750714
2-Phenyl-9-(3-phenylprop-2-enoyl)-1,5,9-triazacyclotridecan-4-one 78384657 Click to see 405.50 unknown https://doi.org/10.1002/HLCA.19920750714
> Phenylpropanoids and polyketides / Macrolactams
(-)-Celacinnine 6452921 Click to see 405.50 unknown https://doi.org/10.1002/HLCA.19920750714
(2R,3R)-3-hydroxy-2-phenyl-9-[(E)-3-phenylprop-2-enoyl]-1,5,9-triazacyclotridecan-4-one 11212347 Click to see 421.50 unknown https://doi.org/10.1002/HLCA.19920750714
(7R,13S,20R)-20-hydroxy-7-phenyl-1,6,10-triazatricyclo[11.9.0.014,19]docosa-14,16,18-triene-9,22-dione 162984275 Click to see 421.50 unknown https://doi.org/10.1002/HLCA.19920750714
(7R,8R,13R)-8-hydroxy-7-phenyl-1,6,10-triazatricyclo[11.9.0.014,19]docosa-14,16,18,20-tetraene-9,22-dione 163046377 Click to see C1CCN2C(CCNC(=O)C(C(NC1)C3=CC=CC=C3)O)C4=CC=CC=C4C=CC2=O 419.50 unknown https://doi.org/10.1002/HLCA.19920750714
(7S,13R)-7-phenyl-1,6,10-triazatricyclo[11.9.0.014,19]docosa-14,16,18,20-tetraene-9,22-dione 162902393 Click to see 403.50 unknown https://doi.org/10.1002/HLCA.19920750714
20-Hydroxy-7-phenyl-1,6,10-triazatricyclo[11.9.0.014,19]docosa-14,16,18-triene-9,22-dione 85667881 Click to see 421.50 unknown https://doi.org/10.1002/HLCA.19920750714
3-Hydroxy-2-phenyl-9-(3-phenylprop-2-enoyl)-1,5,9-triazacyclotridecan-4-one 72752953 Click to see 421.50 unknown https://doi.org/10.1002/HLCA.19920750714
8-Hydroxy-7-phenyl-1,6,10-triazatricyclo[11.9.0.014,19]docosa-14,16,18,20-tetraene-9,22-dione 163046376 Click to see C1CCN2C(CCNC(=O)C(C(NC1)C3=CC=CC=C3)O)C4=CC=CC=C4C=CC2=O 419.50 unknown https://doi.org/10.1002/HLCA.19920750714
8,15-Dihydroxy-7,14-diphenyl-1,6,10-triazabicyclo[11.3.0]hexadecane-9,16-dione 162973405 Click to see C1CCN2C(CCNC(=O)C(C(NC1)C3=CC=CC=C3)O)C(C(C2=O)O)C4=CC=CC=C4 437.50 unknown https://doi.org/10.3987/COM-93-6559
Pleurostyline 328562 Click to see C1CCN2C(CCNC(=O)CC(NC1)C3=CC=CC=C3)C4=CC=CC=C4C=CC2=O 403.50 unknown https://doi.org/10.1002/HLCA.19920750714

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.