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Uncaria elliptica

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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 UUID643ff005a5913851593059
Scientific name Uncaria elliptica
Authority R.Br. ex G.Don
First published in Gen. Hist. 3: 471 (1834)

Description Top

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Uncaria elliptica, also known as Uncaria thwaitesii, is a plant species in the Rubiaceae family. It is found in Sri Lanka, Indo-China, and west Malesia. Its distribution includes Borneo, Cambodia, Java, the Malay Peninsula, Myanmar, Sri Lanka, Sumatra, and Thailand. In the 1998 IUCN Red List, it was classified as "critically endangered" and was thought to only be native to Sri Lanka. However, it is now considered a synonym of Uncaria thwaitesii, which has a wider distribution.

Synonyms Top

Scientific name Authority First published in
Nauclea dasyoneura Walp. Repert. Bot. Syst. 2: 513 (1843)
Nauclea elliptica Walp. Repert. Bot. Syst. 2: 512 (1843)
Uncaria brevispina Maingay ex Hook.f. Fl. Brit. India 3: 31 (1880)
Uncaria dasyoneura Korth. Verh. Nat. Gesch. Ned. Bezitt., Bot. : 169 (1842)
Uncaria dasyoneura var. thwaitesii Hook.f. Fl. Brit. India 3: 31. 1880
Uncaria rostrata Pierre ex Pit. Fl. Indo-Chine 3: 53 (1922)
Uncaria thwaitesii Alston Ann. Roy. Bot. Gard. (Peradeniya) 11: 208 (1929)
Uruparia dasyoneura Kuntze Revis. Gen. Pl. 1: 301 (1891)

Common names Top

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No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
  • Asia-tropical
    • Indian Subcontinent
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Myanmar
      • Thailand
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000329223
Tropicos 100271340
KEW urn:lsid:ipni.org:names:768231-1
The Plant List kew-209780
Open Tree Of Life 3881129
NCBI Taxonomy 1891678
IPNI 768231-1
GBIF 5338248
EOL 1108216
USDA GRIN 417584
Wikipedia Uncaria_elliptica
CMAUP NPO4763

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
The influence of extraction methods on rutin yield of cassava leaves (Manihot esculenta Crantz) Chahyadi A, Elfahmi Saudi Pharm J 22-Sep-2020
PMCID:PMC7679431
doi:10.1016/j.jsps.2020.09.012
PMID:33250654
Secondary Metabolites from Rubiaceae Species Martins D, Nunez CV Molecules 22-Jul-2015
PMCID:PMC6331836
doi:10.3390/molecules200713422
PMID:26205062
Rauniticine-allo-Oxindole B and Rauniticinic-allo Acid B, New Heteroyohimbine-Type Oxindole Alkaloids from the Stems of Malaysian Uncaria longiflora var. pteropoda Salim F, Ismail NH, Awang K, Ahmad R Molecules 04-Aug-2011
PMCID:PMC6264538
doi:10.3390/molecules16086541
PMID:21818057
Macrophyllionium and macrophyllines A and B, oxindole alkaloids from Uncaria macrophylla. Wang K, Zhou XY, Wang YY, Li MM, Li YS, Peng LY, Cheng X, Li Y, Wang YP, Zhao QS J Nat Prod 28-Jan-2011
doi:10.1021/NP1004938
PMID:21070010
Rigorous Biogenetic Network for a Group of Indole Alkaloids Derived from Strictosidine Szabó LF Molecules 27-Aug-2008
PMCID:PMC6245392
doi:10.3390/molecules13081875
PMID:18794791
Studies on the Formation and Growth of Uncaria elliptica Tissue Culture Khoon Huat Law, Nagaratnam P. Das American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50067A016
Ursene carboxylic acids of Uncaria elliptica Thushara K.K. Diyabalanage, G. Percy Wannigama, Aruna Weerasuriya, Lalith Jayasinghe, Peta Simmonds Elsevier BV 01-May-2003
doi:10.1016/0031-9422(95)00428-A
Alkaloids of Uncaria elliptica Thushara K.K. Diyabalanage, B.M.Mallika Kumarihamy, G.Percy Wannigama, Lalith Jayasinghe, Lucio Merlini, Leonardo Scaglioni Elsevier BV 04-Mar-2003
doi:10.1016/S0031-9422(97)00204-5
Alkaloidal and other constituents of Uncaria elliptica and canthium dicoccum W.H.M.W. Herath, M.U.S. Sultanbawa, G.P. Wannigama, André Cavé Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(79)83028-9
Three new ursene carboxylic acids from Uncaria thwaitesii W.H.M.Wimalaseela Herath, M.Uvais S. Sultanbawa, G.Percy Wannigama Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)88746-4
Alkaloids of uncaria elliptica J.David Phillipson, Narong Supavita Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80276-9
Production of (−)-epicatechin by Uncaria elliptica callus cultures Khoon-Huat Law, Nagaratnam P. Das Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80191-8

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 / Corynanthean-type alkaloids
Isocorynantheidine 10948612 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=CC=CC=C34 368.50 unknown via CMAUP database
methyl (1S,2S,17S,19R)-2-methyl-4,14,21,31-tetrazaoctacyclo[15.15.0.02,14.03,11.05,10.019,31.020,28.022,27]dotriaconta-3(11),5,7,9,15,20(28),22,24,26-nonaene-16-carboxylate 162888766 Click to see CC12C3CN4CCC5=C(C4CC3C(=CN1CCC6=C2NC7=CC=CC=C67)C(=O)OC)NC8=CC=CC=C58 492.60 unknown https://doi.org/10.1016/0031-9422(79)83028-9
Roxburghine 324225 Click to see CC12C3CN4CCC5=C(C4CC3C(=CN1CCC6=C2NC7=CC=CC=C67)C(=O)OC)NC8=CC=CC=C58 492.60 unknown https://doi.org/10.1016/0031-9422(79)83028-9
> Alkaloids and derivatives / Harmala alkaloids
Harman 5281404 Click to see CC1=NC=CC2=C1NC3=CC=CC=C23 182.22 unknown via CMAUP database
> Alkaloids and derivatives / Yohimbine alkaloids
19-epi-3-Isoajmalicine 179461 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
19-epi-Ajmalicine 179460 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
3-Isoajmalicine 11416867 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
Ajmalicine 441975 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
https://doi.org/10.1016/S0031-9422(97)00204-5
Lamuran 251561 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
https://doi.org/10.1016/S0031-9422(97)00204-5
methyl (1R,14S,15R,16R,20S)-14-hydroxy-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,18-pentaene-19-carboxylate 163185221 Click to see CC1C2C(CC3C4=C(CCN3C2O)C5=CC=CC=C5N4)C(=CO1)C(=O)OC 368.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
methyl (1R,15S,16R,20S)-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,18-pentaene-19-carboxylate 15558583 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
methyl (1S,13R,15S,16S,20S)-16-methyl-13-oxido-17-oxa-3-aza-13-azoniapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,18-pentaene-19-carboxylate 163186436 Click to see CC1C2C[N+]3(CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45)[O-] 368.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
Methyl 14-hydroxy-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,18-pentaene-19-carboxylate 162980538 Click to see CC1C2C(CC3C4=C(CCN3C2O)C5=CC=CC=C5N4)C(=CO1)C(=O)OC 368.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
Rauniticine 72338 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
Tetrahydroalstonine 72340 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
Tetrahydroalstonine N-oxide 163184423 Click to see CC1C2C[N+]3(CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45)[O-] 368.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerone 92785 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Alnincanone 12305742 Click to see CC(C)C1(CCC(O1)(C)C2CCC3(C2CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4aS,6aR,6aS,6bR,8aR,12aR,14bS)-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-8,10-dioxo-2,3,4,5,6,6a,7,8a,11,12,13,14b-dodecahydropicene-4a-carboxylic acid 15226720 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(=O)C5C4(CCC(=O)C5(C)C)C)C)C2C1(C)O)C)C(=O)O 484.70 unknown https://doi.org/10.1016/0031-9422(95)00428-A
(1R,2R,4aS,6aR,6aS,6bR,8R,8aR,10S,12aR,14bS)-8,10-diacetyloxy-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 15226721 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)C)OC(=O)C)C)OC(=O)C)C)C2C1(C)O)C)C(=O)O 572.80 unknown https://doi.org/10.1016/0031-9422(95)00428-A
(1R,2S,4aR,6aR,6aS,6bR,8aR,10R,12aR,14bR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 162948455 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)88746-4
(1R,4aS,6aS,6aS,6bR,8aS,12aR,14bR)-1,8,10-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 129316997 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)C)O)C)O)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/0031-9422(95)00428-A
(1S,2R,4aR,6aR,6aS,6bR,8aR,12aR,14bS)-14b-hydroxy-1,4a,6a,6b,9,9,12a-heptamethyl-8,10-dioxo-1,2,3,4,5,6,6a,7,8a,11,12,13-dodecahydropicene-2-carboxylic acid 101316929 Click to see CC1C(CCC2(C1(C3=CCC4C5(CCC(=O)C(C5C(=O)CC4(C3(CC2)C)C)(C)C)C)O)C)C(=O)O 484.70 unknown https://doi.org/10.1016/S0031-9422(00)88746-4
(1S,2R,4aR,6aR,6aS,6bR,8R,8aR,10S,12aR,14bS)-8,10-diacetyloxy-14b-hydroxy-1,4a,6a,6b,9,9,12a-heptamethyl-1,2,3,4,5,6,6a,7,8,8a,10,11,12,13-tetradecahydropicene-2-carboxylic acid 162972728 Click to see CC1C(CCC2(C1(C3=CCC4C5(CCC(C(C5C(CC4(C3(CC2)C)C)OC(=O)C)(C)C)OC(=O)C)C)O)C)C(=O)O 572.80 unknown https://doi.org/10.1016/S0031-9422(00)88746-4
(1S,2R,4aR,6aR,6aS,6bR,8R,8aR,10S,12aR,14bS)-8,10,14b-trihydroxy-1,4a,6a,6b,9,9,12a-heptamethyl-1,2,3,4,5,6,6a,7,8,8a,10,11,12,13-tetradecahydropicene-2-carboxylic acid 101324876 Click to see CC1C(CCC2(C1(C3=CCC4C5(CCC(C(C5C(CC4(C3(CC2)C)C)O)(C)C)O)C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/S0031-9422(00)88746-4
(3beta,6alpha,19alpha)-3,6,19-Trihydroxy-12-ursen-28-oic acid 14355557 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)C)O)C)O)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/0031-9422(95)00428-A
1-Hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-8,10-dioxo-2,3,4,5,6,6a,7,8a,11,12,13,14b-dodecahydropicene-4a-carboxylic acid 163006447 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(=O)C5C4(CCC(=O)C5(C)C)C)C)C2C1(C)O)C)C(=O)O 484.70 unknown https://doi.org/10.1016/0031-9422(95)00428-A
14b-Hydroxy-1,4a,6a,6b,9,9,12a-heptamethyl-8,10-dioxo-1,2,3,4,5,6,6a,7,8a,11,12,13-dodecahydropicene-2-carboxylic acid 162907669 Click to see CC1C(CCC2(C1(C3=CCC4C5(CCC(=O)C(C5C(=O)CC4(C3(CC2)C)C)(C)C)C)O)C)C(=O)O 484.70 unknown https://doi.org/10.1016/S0031-9422(00)88746-4
8,10-Diacetyloxy-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162987858 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)C)OC(=O)C)C)OC(=O)C)C)C2C1(C)O)C)C(=O)O 572.80 unknown https://doi.org/10.1016/0031-9422(95)00428-A
8,10-Diacetyloxy-14b-hydroxy-1,4a,6a,6b,9,9,12a-heptamethyl-1,2,3,4,5,6,6a,7,8,8a,10,11,12,13-tetradecahydropicene-2-carboxylic acid 162972727 Click to see CC1C(CCC2(C1(C3=CCC4C5(CCC(C(C5C(CC4(C3(CC2)C)C)OC(=O)C)(C)C)OC(=O)C)C)O)C)C(=O)O 572.80 unknown https://doi.org/10.1016/S0031-9422(00)88746-4
8,10,14b-Trihydroxy-1,4a,6a,6b,9,9,12a-heptamethyl-1,2,3,4,5,6,6a,7,8,8a,10,11,12,13-tetradecahydropicene-2-carboxylic acid 163018147 Click to see CC1C(CCC2(C1(C3=CCC4C5(CCC(C(C5C(CC4(C3(CC2)C)C)O)(C)C)O)C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/S0031-9422(00)88746-4
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)88746-4
Uncaric acid 10838721 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)C)O)C)O)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/0031-9422(95)00428-A
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17S)-17-[(2R,5R)-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 162965363 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)88746-4
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/10.1016/S0031-9422(00)88746-4
https://doi.org/10.1016/0031-9422(95)00428-A
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(95)00428-A
> Organoheterocyclic compounds / Indolizidines
(3R,20S)-19alpha-Methyl-2-oxoformosanan-16-carboxylic acid methyl ester 98363 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
https://doi.org/10.1016/S0031-9422(97)00204-5
Akuammigine pseudoindoxyl 181921 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C(=O)C5=CC=CC=C5N4 368.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
Isomitraphylline 11726520 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
https://doi.org/10.1016/S0031-9422(97)00204-5
Isorhynchophylline 3037048 Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=CC=CC=C4NC3=O 384.50 unknown via CMAUP database
methyl (1R,4aS,5aR,6S,10aS)-1-methyl-3'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,2'-1H-indole]-4-carboxylate 162954019 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C(=O)C5=CC=CC=C5N4 368.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
methyl (1R,4aS,5aS,6S,10aS)-1-methyl-2'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylate 6553938 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
methyl (1R,4aS,5aS,6S,10aS)-1-methyl-3'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,2'-1H-indole]-4-carboxylate 162954017 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C(=O)C5=CC=CC=C5N4 368.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
methyl (1S,4aR,5aS,6S,10aR)-1-methyl-3'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,2'-1H-indole]-4-carboxylate 162954018 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C(=O)C5=CC=CC=C5N4 368.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
methyl (1S,4aS,5aR,6R,10aS)-1-methyl-3'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,2'-1H-indole]-4-carboxylate 162954016 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C(=O)C5=CC=CC=C5N4 368.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
methyl (Z)-2-[(6'R,7'S)-6'-ethyl-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl]-3-methoxyprop-2-enoate 5318653 Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=CC=CC=C4NC3=O 384.50 unknown via CMAUP database
methyl 2-(6'-ethyl-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl)-3-methoxyprop-2-enoate 409518 Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=CC=CC=C4NC3=O 384.50 unknown https://doi.org/10.1021/NP1004938
Mitraphylline 94160 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
https://doi.org/10.1016/S0031-9422(97)00204-5
Uncarine A 188999 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
Uncarine B 12304286 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown https://doi.org/10.1016/S0031-9422(00)80276-9
https://doi.org/10.1016/S0031-9422(97)00204-5
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1021/NP50067A016
https://doi.org/10.1016/0031-9422(89)80191-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(2,3-Dihydroxyphenyl)-5,7-dihydroxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 53399169 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=C(C(=CC=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database

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