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.

Uncaria elliptica, a tropical liana also known as katong-katong, is used widely across Southeast Asia for internal fevers, aches, and digestive upset. In Indonesia, people prepare decoctions of the inner bark or young shoots to break fever, while the leaves are sometimes infused as a mild tea for dyspepsia and to “cool the stomach” (Atta-ur-Rahman et al., 1994). Across the Philippines, root or bark decoctions are taken for fever and body aches, and in Thailand and Vietnam leaf infusions are common remedies for stomach pain and to “settle the gut” (Harley & Kritsonis, 2009). On the Malay Peninsula, communities combine inner bark or young shoots with other herbs in decoctions for colic, gas, and low-grade fevers (Ong & Norhanom, 2001). These accounts consistently emphasize the bark or young shoots for stronger fever-relieving decoctions and the leaves for gentler stomach-calming infusions.

A practical leaf tea is the simplest way to start. Rinse 1–2 teaspoons of fresh young leaves (about 2–3 g), add to 250 ml of just-boiled water, and let steep 10–15 minutes before straining. Take 1 cup 2–3 times daily as needed for mild dyspepsia or to “cool” a feverish stomach; discontinue if stomach discomfort increases (Harley & Kritsonis, 2009). Safety: do not use this plant if you are pregnant or nursing; avoid in people with known hypotension or bleeding disorders, or when taking blood thinners or antihypertensive medications. Do not give to infants or young children. Stop if you experience dizziness or excessive sweating.

Several alkaloids have been isolated from U. elliptica and are well documented for related Uncaria species, providing plausible mechanisms for its traditional effects. These include oxindole alkaloids like mitraphylline, rhynchophylline, isorhynchophylline, and corynoxeine, along with hirsuteine and hirsutine, which are known to occur in U. elliptica and in related Uncaria taxa (Aimi et al., 1992; Oshima et al., 1990). These compounds have smooth-muscle relaxing and mild antihypertensive activity in pharmacological studies, which aligns with the observed relief from gastrointestinal cramps and feverish discomfort.

Current relevance remains modest. While most commercial attention still focuses on the better-known Uncaria tomentosa (cat’s claw), Uncaria elliptica is still wild‑harvested locally as a fever and stomach tea in parts of Indonesia, Malaysia, and the Philippines, and small field studies continue to confirm its alkaloid profile. The plant is not widely sold outside Southeast Asia, but conservation concern for U. elliptica is low and its traditional uses continue in the region’s home gardens and market stalls (Philippines Forest Products Research and Development Institute, 2014).

General Uses Top

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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)
Uncaria gambier	Thwaites	Enum. Pl. Zeyl. : 138 (1859)

Common names Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

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

Links to other databases Top

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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	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-Epiajmalicine	179460	Click to see	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	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	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	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	368.40	unknown	https://doi.org/10.1016/S0031-9422(00)80276-9
Rauniticine	72338	Click to see	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	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	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	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	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	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	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	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	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
Uncaric acid	10838721	Click to see	488.70	unknown	https://doi.org/10.1016/0031-9422(95)00428-A
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)-	220774	Click to see	456.70	unknown	https://doi.org/10.1016/S0031-9422(00)88746-4
> 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	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/10.1016/0031-9422(95)00428-A https://doi.org/10.1016/S0031-9422(00)88746-4
Stigmast-5-en-3-ol	22012	Click to see	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	368.40	unknown	https://doi.org/10.1016/S0031-9422(00)80276-9
Isomitraphylline	11726520	Click to see	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 (1'R,3S,4'aS,5'aS,10'aR)-1,2,5',5'a,7',8',10',10'a-octahydro-1'-methyl-2-oxospiro(3H-indole-3,6'(4'aH)-(1H)pyrano(3,4-f)indolizine)-4'-carboxylate	188999	Click to see	368.40	unknown	https://doi.org/10.1016/S0031-9422(00)80276-9
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	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	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	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	368.40	unknown	https://doi.org/10.1016/S0031-9422(97)00204-5 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	290.27	unknown	https://doi.org/10.1016/0031-9422(89)80191-8 https://doi.org/10.1021/NP50067A016
> 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	448.40	unknown	via CMAUP database

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Uncaria elliptica

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