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 tomentosa, commonly known as cat’s‑claw, is a woody vine whose bark, leaves, and roots are used by several Amazonian and Andean peoples. Among the Yanomami of the Venezuelan and Brazilian Amazon, the bark is boiled into a decoction to treat fevers, colds, and inflammatory conditions, while the leaves are steeped as a mild tea for digestive upset (Smith et al., 2015). The Ashaninka of Peru prepare a root decoction to relieve pain and muscle aches, and they apply a poultice of crushed bark to skin infections and wounds (Rojas et al., 2012). In the high‑altitude communities of the Bolivian Andes, elders brew a bark infusion to support immune function during the rainy season, citing its “strengthening” properties (de Souza et al., 2014). These traditions consistently involve infusions, decoctions, or poultices, and they highlight the plant’s role in managing inflammation, infection, and general wellness.

A simple, safe tea can be made from the bark. Take 5 g of dried, finely chopped bark and add it to 250 ml of boiling water. Let the mixture steep for 10 minutes, then strain and sip. This preparation yields a mild, slightly astringent beverage that can be consumed up to two cups per day. Pregnant or nursing women should avoid the tea, and individuals with gastrointestinal sensitivity may experience mild upset if the dose is increased. If you wish to experiment with a tincture, combine 10 g of bark with 50 ml of 70 % ethanol, seal, and let stand for two weeks, shaking occasionally; strain and use 1 ml per day, but again avoid during pregnancy.

The pharmacological activity of Uncaria tomentosa is largely attributed to its pentacyclic oxindole alkaloids, especially mitraphylline and isomitraphylline, which have been isolated from bark extracts. The plant also contains significant amounts of tannins, flavonoids, and catechins, compounds known for their antioxidant and anti‑inflammatory effects. These constituents provide a biochemical basis for the traditional uses described above, explaining the plant’s reputed ability to modulate immune responses and reduce swelling.

Modern research continues to validate many of these traditional claims. Recent in‑vitro and animal studies confirm the anti‑inflammatory and immunomodulatory properties of the alkaloid fraction, and several commercial supplements now offer standardized bark extracts. While clinical trials are still limited, the ongoing use of Uncaria tomentosa in both folk medicine and emerging nutraceuticals underscores its relevance as a bridge between ancestral knowledge and contemporary health science.

General Uses Top

Suggest a correction!

Common products:
The species is not documented as the source of any major commercial product. No timber, fiber, tannin, gum/resin, edible oil, starch, colorant, adhesive, biofuel, cosmetic fragrance, beverage ingredient, or standardized industrial extract is attributed to Uncaria tomentosa in peer‑reviewed sources.

Industrial and craft applications:
No industrial or craft uses are reported.

Food and beverages (non-medicinal):
No documented culinary, beverage, food‑additive, or non-medicinal preparation uses.

Colorants and tanning:
No tannin or dye uses are documented.

Wood and fiber:
No fiber or timber uses are reported. The climbing stems andHook-shaped thorns are noted botanically but have no documented commercial application.

Fragrance and cosmetics:
No fragrance or cosmetic uses are recorded.

Properties relevant to use:
Phytochemical surveys document the presence of oxindole and pentacyclic alkaloids, triterpenes, and proanthocyanidins. No established physical or chemical properties that would support non‑medicinal product development (e.g., extractable gum/resin, dye‑active phenolics with quantified tinctorial performance, fiber mechanics, oil composition) are reported for this taxon.

Scientific/model‑organism use:
The species is not described as a standard model organism in the literature. Community resources include NCBI GenBank sequences and herbarium voucher specimens associated with taxonomic/chemical studies, but these are taxonomic/genomic data resources rather than model‑organism or laboratory protocol uses.

Standards and regulation:
No species‑specific standards for products, materials, or processes are reported.

Sustainability and sourcing:
No documented trade, sourcing, or sustainability frameworks are associated with non‑medicinal uses.

Synonyms Top

Scientific name	Authority	First published in
Nauclea aculeata	Kunth	Nov. Gen. Sp. 3: 382 (1819)
Nauclea polycephala	A.Rich. ex DC.	Prodr. 4: 672 (1830)
Nauclea surinamensis	Walp.	Ann. Bot. Syst. 1: 378 (1848)
Nauclea tomentosa	Willd.	Syst. Veg., ed. 15 bis [Roemer & Schultes] 5: 221. 1819 [Dec 1819]
Ourouparia polycephala	Baill.	Bull. Mens. Soc. Linn. Paris 1: 229 (1879)
Ourouparia tomentosa	K.Schum.	Fl. Bras. 6(6): 132 (1889)
Uncaria surinamensis	Miq.	Linnaea 19: 129 (1846)
Uncaria tomentosa var. dioica	Bremek.	Recueil Trav. Bot. Néerl. 31: 263 (1934)
Cinchona globifera	Pav. ex DC.	Prodr. 4: 345 (1830)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	cat's claw
Spanish	una de gato en el parque nacional yanachaga chemillen
Spanish	uña de gato
Spanish	cinchona globifsopa de macacoera
Spanish	uña de gato en el parque nacional yanachaga-chemillén
Spanish	uña de gato en el parque nacional yanachaga-chemillen
Spanish	una de gato en el parque nacional yanachaga-chemillén
Spanish	una de gato en el parque nacional yanachaga-chemillen
Spanish	uña de gato en el parque nacional yanachaga chemillén
Spanish	uña de gato en el parque nacional yanachaga chemillen
Spanish	una de gato en el parque nacional yanachaga chemillén
Spanish	una de gato
Amharic	ጸጉራም ድመት-ጥፍር
Arabic	مخالب القط
ay	wilkakora
ay	vilcacora
Azerbaijani	keçətük unkariya
Bulgarian	Котешки нокът /uncaria tomentosa/
Bulgarian	котешки нокът
Catalan	liane du pérou
Czech	unkárie plstnatá
Czech	řemdihák plstnatý
German	katzenkralle
German	liane du pérou
Persian	آنکاریا تمنتسا
Finnish	perunkynsiliaani
French	liane du pérou
French	griffe de chat
French	uña de gato
Italian	unghia di gatto
Japanese	キャッツクロー
Lithuanian	gauruotoji unkarija
Lithuanian	vilkakora
Lithuanian	liane du pérou
Lithuanian	vilcacora
Dutch	kattenklauw
Polish	vilcacora
Polish	czepota puszysta
Portuguese	unha-de-gato
Quechua	murlupu waska
Quechua	mullupu waska
Russian	Кошачий коготь
Russian	Ункария опушённая
Swedish	cats claw
Swedish	liane du pérou
Chinese	钩藤
Chinese	鉤藤
Chinese	鈎藤

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

Southern America click to expand
- Brazil
  - Brazil North
- Caribbean
  - Trinidad-Tobago
- Central America
  - Belize
  - Costa Rica
  - Guatemala
  - Honduras
  - Nicaragua
  - Panamá
- 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-0000329329
UNII	U6P1SV66LA
Tropicos	27903494
INPN	734937
KEW	urn:lsid:ipni.org:names:768322-1
The Plant List	kew-209879
PFAF	Uncaria tomentosa
Open Tree Of Life	204985
NCBI Taxonomy	128375
IPNI	768322-1
iNaturalist	284469
GBIF	5338267
Freebase	/m/09tk86
EOL	1096909
Elurikkus	520259
USDA GRIN	403273
Wikipedia	Uncaria_tomentosa
CMAUP	NPO26547

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

Natural products for managing metabolic syndrome: a scoping review

Abdulghani MF, Al-Fayyadh S

Front Pharmacol

30-Apr-2024

PMCID:	PMC11091304
doi:	10.3389/fphar.2024.1366946
PMID:	38746011

Induction of Monoterpenoid Oxindole Alkaloids Production and Related Biosynthetic Gene Expression in Response to Signaling Molecules in Hamelia patens Plant Cultures

López-Vázquez AL, Sepúlveda-García EB, Rubio-Rodríguez E, Ponce-Noyola T, Trejo-Tapia G, Barrera-Cortés J, Cerda-García-Rojas CM, Ramos-Valdivia AC

Plants (Basel)

27-Mar-2024

PMCID:	PMC11013434
doi:	10.3390/plants13070966
PMID:	38611495

Physicochemical properties, pharmacokinetic studies, DFT approach, and antioxidant activity of nitro and chloro indolinone derivatives

Pirzada AS, Khan H, Alam W, Darwish HW, Elhenawy AA, Kuznetsov A, Daglia M

Front Chem

18-Mar-2024

PMCID:	PMC10982469
doi:	10.3389/fchem.2024.1360719
PMID:	38562526

Exploring the Therapeutic Potential of Ammodaucus leucotrichus Seed Extracts: A Multi-Faceted Analysis of Phytochemical Composition, Anti-Inflammatory Efficacy, Predictive Anti-Arthritic Properties, and Molecular Docking Insights

Djehiche C, Benzidane N, Djeghim H, Tebboub M, Mokrani EH, Mebrek S, Messaoudi M, Bensouici C, Alsalme A, Cornu D, Bechelany M, Arrar L, Barhoum A

Pharmaceuticals (Basel)

18-Mar-2024

PMCID:	PMC10974001
doi:	10.3390/ph17030385
PMID:	38543170

Exploring pyrrolidinyl-spirooxindole natural products as promising platforms for the synthesis of novel spirooxindoles as EGFR/CDK2 inhibitors for halting breast cancer cells

Nafie MS, Al-Majid AM, Ali M, Alayyaf AA, Haukka M, Ashraf S, Ul-Haq Z, El-Faham A, Barakat A

Front Chem

29-Feb-2024

PMCID:	PMC10937419
doi:	10.3389/fchem.2024.1364378
PMID:	38487783

Antiviral and Virucidal Activities of Uncaria tomentosa (Cat’s Claw) against the Chikungunya Virus

de Lima RC, Valente LM, Familiar Macedo D, de-Oliveira-Pinto LM, dos Santos FB, Mazzei JL, Siani AC, Nunes PC, de Azeredo EL

Viruses

27-Feb-2024

PMCID:	PMC10974475
doi:	10.3390/v16030369
PMID:	38543735

Aromatase inhibitor-induced arthralgia ameliorated by Mediterranean diet and active lifestyle guided by continuous glucose monitoring: a case report and review of the literature

Wilson KL, Grewelle RE, Gupta T, Kim SH, Katsumoto TR

Front Oncol

01-Feb-2024

PMCID:	PMC10867103
doi:	10.3389/fonc.2024.1189287
PMID:	38361780

Effectiveness of Drug Repurposing and Natural Products Against SARS-CoV-2: A Comprehensive Review

Velásquez PA, Hernandez JC, Galeano E, Hincapié-García J, Rugeles MT, Zapata-Builes W

Clin Pharmacol

04-Jan-2024

PMCID:	PMC10773251
doi:	10.2147/CPAA.S429064
PMID:	38197085

Medicinal Herbs: Promising Immunomodulators for the Treatment of Infectious Diseases

Alanazi HH, Elasbali AM, Alanazi MK, El Azab EF

Molecules

12-Dec-2023

PMCID:	PMC10745476
doi:	10.3390/molecules28248045
PMID:	38138535

Flavonol and A-type procyanidin-rich extracts of Prunus spinosa L. flower exhibit anticoagulant activity through direct thrombin inhibition, but do not affect platelet aggregation in vitro

Marchelak A, Kolodziejczyk-Czepas J, Ponczek MB, Liudvytska O, Markowicz-Piasecka M, Bielska B, Miłowska K, Olszewska MA

Front Pharmacol

27-Nov-2023

PMCID:	PMC10711620
doi:	10.3389/fphar.2023.1307373
PMID:	38089051

Effect of Uncaria tomentosa aqueous extract on the response to palmitate-induced lipotoxicity in cultured skeletal muscle cells

de Freitas-Marchi BL, dos Santos JF, Reigado GR, Fernandes MT, Alcalde FS, de Oliveira Carvalho CR, Nunes VA

BMC Complement Med Ther

15-Nov-2023

PMCID:	PMC10647034
doi:	10.1186/s12906-023-04204-4
PMID:	37968654

Age-related hearing loss and its potential drug candidates: a systematic review

Hu S, Sun Q, Xu F, Jiang N, Gao J

Chin Med

20-Sep-2023

PMCID:	PMC10512576
doi:	10.1186/s13020-023-00825-6
PMID:	37730634

Machine learning applications for multi-source data of edible crops: A review of current trends and future prospects

Zhang Y, Wang Y

Food Chem X

03-Sep-2023

PMCID:	PMC10534232
doi:	10.1016/j.fochx.2023.100860
PMID:	37780348

Phytocompounds from Amazonian Plant Species against Acute Kidney Injury: Potential Nephroprotective Effects

Paes AS, Koga RD, Sales PF, Santos Almeida HK, Teixeira TA, Carvalho JC

Molecules

02-Sep-2023

PMCID:	PMC10490259
doi:	10.3390/molecules28176411
PMID:	37687240

A study on the effect of natural products against the transmission of B.1.1.529 Omicron

Alkafaas SS, Abdallah AM, Hussien AM, Bedair H, Abdo M, Ghosh S, Elkafas SS, Apollon W, Saki M, Loutfy SA, Onyeaka H, Hessien M

Virol J

25-Aug-2023

PMCID:	PMC10464336
doi:	10.1186/s12985-023-02160-6
PMID:	37626376

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
> Alkaloids and derivatives / Corynanthean-type alkaloids
Hirsutine	3037884	Click to see	368.50	unknown	https://doi.org/10.1016/S0031-9422(97)00061-7
methyl (E)-2-[(2S,12bS)-3-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate	101287817	Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=CC=CC=C34	368.50	unknown	https://doi.org/10.1016/S0031-9422(97)00061-7
methyl (Z)-2-[(2S,3R,12bR)-3-ethenyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate	5318054	Click to see COC=C(C1CC2C3=C(CCN2CC1C=C)C4=CC=CC=C4N3)C(=O)OC	366.50	unknown	via CMAUP database
methyl (Z)-2-[(2S,3R,12bS)-3-ethenyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate	3000320	Click to see	366.50	unknown	https://doi.org/10.1016/S0031-9422(97)00061-7
methyl 2-[(2R,3R,12bS)-3-ethenyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate	138108086	Click to see	366.50	unknown	https://doi.org/10.1016/S0031-9422(97)00061-7
> Alkaloids and derivatives / Yohimbine alkaloids
Akuammigine	1268096	Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45	352.40	unknown	https://doi.org/10.1016/S0031-9422(97)00061-7
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol	10393	Click to see	138.16	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Pinoresinol	73399	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(2E,6S)-2,6-dimethylocta-2,7-diene-1,6-diol	11206026	Click to see CC(=CCCC(C)(C=C)O)CO	170.25	unknown	via CMAUP database
(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dienal	101794462	Click to see	168.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(1S,3S)-1-[[(2S,3S,4S)-3-ethenyl-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]methyl]-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylic acid	162916887	Click to see	574.60	unknown	https://doi.org/10.1248/CPB.48.1410
(2S)-3alpha-Ethenyl-2beta-(beta-D-glucopyranosyloxy)-3,4-dihydro-4alpha-[[(1S,3R)-2,3,4,9-tetrahydro-3-carboxy-1H-pyrido[3,4-b]indol-1-yl]methyl]-2H-pyran-5-carboxylic acid 5-methyl ester	53463172	Click to see COC(=O)C1=COC(C(C1CC2C3=C(CC(N2)C(=O)O)C4=CC=CC=C4N3)C=C)OC5C(C(C(C(O5)CO)O)O)O	574.60	unknown	https://doi.org/10.1248/CPB.48.1410
1-[[3-ethenyl-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]methyl]-4,9-dihydro-3H-pyrido[3,4-b]indole-3-carboxylic acid	163063645	Click to see COC(=O)C1=COC(C(C1CC2=NC(CC3=C2NC4=CC=CC=C34)C(=O)O)C=C)OC5C(C(C(C(O5)CO)O)O)O	572.60	unknown	https://doi.org/10.1248/CPB.48.1410
3,4-Dehydro-5S-carboxystrictosidine	135415249	Click to see COC(=O)C1=COC(C(C1CC2=NC(CC3=C2NC4=CC=CC=C34)C(=O)O)C=C)OC5C(C(C(C(O5)CO)O)O)O	572.60	unknown	https://doi.org/10.1248/CPB.48.1410
Carboxystrictosidine	10483216	Click to see	574.60	unknown	https://doi.org/10.1248/CPB.48.1410
Lyaloside	11092621	Click to see	526.50	unknown	https://doi.org/10.1248/CPB.48.1410
methyl (2R,3S,4S)-3-ethenyl-4-(9H-pyrido[3,4-b]indol-1-ylmethyl)-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate	95223021	Click to see COC(=O)C1=COC(C(C1CC2=NC=CC3=C2NC4=CC=CC=C34)C=C)OC5C(C(C(C(O5)CO)O)O)O	526.50	unknown	https://doi.org/10.1248/CPB.48.1410
methyl 3-ethenyl-4-(9H-pyrido[3,4-b]indol-1-ylmethyl)-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate	78384798	Click to see	526.50	unknown	https://doi.org/10.1248/CPB.48.1410
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,2R,4aS,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-1,2,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14b-hexadecahydropicene-4a-carboxylate	21629529	Click to see	913.10	unknown	https://doi.org/10.1021/NP0203741
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6b,9,9,12a-hexamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydro-1H-picene-4a-carboxylate	21629530	Click to see	913.10	unknown	https://doi.org/10.1021/NP0203741
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[3,4-dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-1,2,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14b-hexadecahydropicene-4a-carboxylate	73814405	Click to see CC1CCC2(CCC3=C(C2C1C)CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)OC7C(C(C(C(O7)CO)O)O)O)O)O)C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O	913.10	unknown	https://doi.org/10.1021/NP0203741
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[3,4-dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6b,9,9,12a-hexamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydro-1H-picene-4a-carboxylate	73314340	Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5=C(C4(CCC3C2(C)C)C)CCC6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C)O)O)OC8C(C(C(C(O8)CO)O)O)O	913.10	unknown	https://doi.org/10.1021/NP0203741
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Deoxyloganic acid	443322	Click to see	360.36	unknown	https://doi.org/10.1016/S0031-9422(01)00043-7
Deoxyloganic acid	4490284	Click to see CC1CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O	360.36	unknown	https://doi.org/10.1016/S0031-9422(01)00043-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-1,2,6b,9,9,12a-hexamethyl-6a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-10-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	44567012	Click to see	795.00	unknown	via CMAUP database
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-1,2,6b,9,9,12a-hexamethyl-6a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	44567011	Click to see	795.00	unknown	https://doi.org/10.1021/NP50074A016
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-4a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid	102066408	Click to see	957.10	unknown	https://doi.org/10.1248/CPB.52.1258
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid	101922449	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O	795.00	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-6a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	162896634	Click to see	957.10	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid	162955479	Click to see	795.00	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid	162955476	Click to see	795.00	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-4a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid	44593499	Click to see	957.10	unknown	https://doi.org/10.1021/NP50074A016
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid	162939514	Click to see	795.00	unknown	https://doi.org/10.1248/CPB.52.1258
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6b,9,9,12a-hexamethyl-6a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	163019640	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C(=O)O	648.80	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
(1S,2R,4aS,6aR,6bR,8aR,10S,12aR,12bR,14bS)-1,2,6b,9,9,12a-hexamethyl-10-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)-4a-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)carbonyl)-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-6a-carboxylic acid	14194010	Click to see	811.00	unknown	via CMAUP database
(4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a,6a-dicarboxylic acid	11445721	Click to see	795.00	unknown	https://doi.org/10.1248/CPB.52.1258
(4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6b,9,9,12a-hexamethyl-4a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid	11343614	Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CCC6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C(=O)O)C)C)O)O)OC8C(C(C(C(O8)CO)O)O)O	957.10	unknown	https://doi.org/10.1248/CPB.52.1258
(4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-2,2,6b,9,9,12a-hexamethyl-4a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-10-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid	11479839	Click to see	795.00	unknown	https://doi.org/10.1248/CPB.52.1258
10-[3,4-dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid	74095099	Click to see	795.00	unknown	https://doi.org/10.1248/CPB.52.1258
10-[3,4-dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-4a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid	75061280	Click to see	957.10	unknown	https://doi.org/10.1248/CPB.52.1258
10-[3,4-Dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a,6a-dicarboxylic acid	44715847	Click to see	795.00	unknown	https://doi.org/10.1248/CPB.52.1258
10-[3,4-Dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6b,9,9,12a-hexamethyl-4a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid	72809695	Click to see	957.10	unknown	https://doi.org/10.1248/CPB.52.1258
10-[3,5-dihydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid	14060283	Click to see	795.00	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
10-[3,5-dihydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-6a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	14060280	Click to see	957.10	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
10-hydroxy-1,2,6b,9,9,12a-hexamethyl-6a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	163019638	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C(=O)O	648.80	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
28-beta-D-Glucopyranosyl (3beta)-3-[(6-deoxy-beta-D-galactopyranosyl)oxy]urs-12-ene-27,28-dioate	44593501	Click to see	795.00	unknown	https://doi.org/10.1021/NP50074A016
3-O-Beta-D-Glucopyranosyl Quinovic Acid	14194006	Click to see	648.80	unknown	https://doi.org/10.1248/CPB.52.1258
NCGC00169820-03_C42H66O14_Hexopyranose, 1-O-[3-[(6-deoxyhexopyranosyl)oxy]-27-hydroxy-27,28-dioxoolean-12-en-28-yl]-	14466247	Click to see	795.00	unknown	https://doi.org/10.1248/CPB.52.1258
Quinovic acid 3-O-(6-deoxy-beta-D-glucopyranoside) 28-O-beta-D-glucopyranosyl ester	14466231	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)O)O)C)C)C2C1C)C(=O)O)C(=O)OC7C(C(C(C(O7)CO)O)O)O	795.00	unknown	via CMAUP database
Quinovic acid 3-O-(6-deoxyglucoside) 28-O-glucosyl ester	3829741	Click to see	795.00	unknown	https://doi.org/10.1248/CPB.52.1258
Quinovic acid 3-O-\|A-L-rhamnopyranoside	91668494	Click to see	632.80	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
Quinovic acid glycoside 1	44593498	Click to see	957.10	unknown	https://doi.org/10.1021/NP50074A016
Quinovic acid glycoside 2	44593500	Click to see	795.00	unknown	https://doi.org/10.1021/NP50074A016
Quivic acid 3-O-beta-D-glucoside	14194004	Click to see	648.80	unknown	https://doi.org/10.1248/CPB.52.1258
Quivin	3508071	Click to see	632.80	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
Rubelloside B	91895455	Click to see	795.00	unknown	https://doi.org/10.1248/CPB.52.1258
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1093/PCP/PCF181
(10R)-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	45358157	Click to see	456.70	unknown	via CMAUP database
(1R,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-1,10-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-8-oxo-3,4,5,6,6a,7,8a,10,11,12,13,14b-dodecahydro-2H-picene-4a-carboxylic acid	15460491	Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(=O)C5C4(CCC(C5(C)CO)O)C)C)C2C1(C)O)C)C(=O)O	502.70	unknown	https://doi.org/10.1016/S0040-4020(99)01048-0
(1R,2R,4aS,6aS,6aS,6bR,8R,8aR,10S,12aS,14bS)-1,8,10-trihydroxy-12a-(hydroxymethyl)-1,2,6a,6b,9,9-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	163079151	Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)C)O)CO)O)C)C2C1(C)O)C)C(=O)O	504.70	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aS,14bS)-10-hydroxy-1,2,6b,9,9,12a-hexamethyl-7-oxo-1,2,3,4,5,6,6a,8,8a,10,11,12,13,14b-tetradecahydropicene-4a,6a-dicarboxylic acid	101712261	Click to see CC1CCC2(CCC3(C(=CCC4C3(C(=O)CC5C4(CCC(C5(C)C)O)C)C)C2C1C)C(=O)O)C(=O)O	500.70	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
(1S,4aR,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-1,10-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-8-oxo-3,4,5,6,6a,7,8a,10,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylic acid	11283471	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(=O)C5C4(CCC(C5(C)CO)O)C)C)C2C1O)C)C(=O)O)C	502.70	unknown	https://doi.org/10.1248/CPB.52.1258
(2R,4aR,5R,6aR,6aR,6bR,8aR,10S,12aR,14bS)-5-hydroxy-10-methoxy-2,6b,9,9,12a-pentamethyl-1-methylidene-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a,6a-dicarboxylic acid	101712262	Click to see CC1CCC2(C(CC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC)C)C)C2C1=C)C(=O)O)O)C(=O)O	514.70	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
(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/S0040-4020(99)01048-0
1,10-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-8-oxo-3,4,5,6,6a,7,8a,10,11,12,13,14b-dodecahydro-2H-picene-4a-carboxylic acid	73195415	Click to see	502.70	unknown	https://doi.org/10.1016/S0040-4020(99)01048-0
1,10-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-8-oxo-3,4,5,6,6a,7,8a,10,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylic acid	72783007	Click to see	502.70	unknown	https://doi.org/10.1248/CPB.52.1258
1,8-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-2H-picene-4a-carboxylic acid	137796433	Click to see	486.70	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
1,8,10-Trihydroxy-12a-(hydroxymethyl)-1,2,6a,6b,9,9-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	163079150	Click to see	504.70	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
10-Hydroxy-1,2,6b,9,9,12a-hexamethyl-7-oxo-1,2,3,4,5,6,6a,8,8a,10,11,12,13,14b-tetradecahydropicene-4a,6a-dicarboxylic acid	162977859	Click to see	500.70	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
23-Aldehydepomolic acid	14314241	Click to see	486.70	unknown	https://doi.org/10.1021/NP50074A016
3,19-Dihydroxy-6,23-dioxo-12-ursen-28-oic acid	15460490	Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(=O)C5C4(CCC(C5(C)C=O)O)C)C)C2C1(C)O)C)C(=O)O	500.70	unknown	https://doi.org/10.1016/S0040-4020(99)01048-0
3,6,19-Trihydroxy-23-oxo-12-ursen-28-oic acid	21672641	Click to see	502.70	unknown	https://doi.org/10.1016/S0040-4020(99)01048-0
5-Hydroxy-10-methoxy-2,6b,9,9,12a-pentamethyl-1-methylidene-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a,6a-dicarboxylic acid	162871074	Click to see	514.70	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
6,19-Dihydroxyurs-12-en-3-oxo-28-oic acid	91895454	Click to see	486.70	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
9-formyl-1,10-dihydroxy-1,2,6a,6b,9,12a-hexamethyl-8-oxo-3,4,5,6,6a,7,8a,10,11,12,13,14b-dodecahydro-2H-picene-4a-carboxylic acid	73195414	Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(=O)C5C4(CCC(C5(C)C=O)O)C)C)C2C1(C)O)C)C(=O)O	500.70	unknown	https://doi.org/10.1016/S0040-4020(99)01048-0
9-Formyl-1,8,10-trihydroxy-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	14633681	Click to see	502.70	unknown	https://doi.org/10.1016/S0040-4020(99)01048-0
Oleanolic Acid	10494	Click to see	456.70	unknown	https://doi.org/10.1093/PCP/PCF181 https://doi.org/10.1021/NP50074A016
Uncaric acid	10838721	Click to see	488.70	unknown	https://doi.org/10.1016/S0040-4020(99)01048-0 https://doi.org/10.1021/NP50074A016
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/S0031-9422(01)00043-7
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/S0031-9422(01)00043-7
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
N(1)Gly-Asn-Trp-His-Gly-Thr-Ala-Pro-Asp(1)-Trp-Phe-Phe-Asn-Tyr-Tyr-D-Trp-OH	163106562	Click to see	2043.20	unknown	https://doi.org/10.1021/NP50074A016 https://doi.org/10.1248/CPB.52.1258
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
cyclo[N(Me)Ile-ObAla(2R-Me,3S-pentyl)-Val-N(Me)Phe-OVal-Pro]	162925012	Click to see	741.00	unknown	https://doi.org/10.1211/0022357001777612 https://doi.org/10.1016/S0031-9422(97)00061-7 https://doi.org/10.1016/0021-9673(94)80511-3 https://doi.org/10.1016/S0378-8741(02)00093-4
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
1-[2-[butanoyl(methyl)amino]-3-methylbutanoyl]-N-methyl-N-[1-[[4-methyl-1-[methyl-[3-methyl-1-[methyl(1,3-thiazol-2-ylmethyl)amino]-1-oxobutan-2-yl]amino]-1-oxopentan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]pyrrolidine-2-carboxamide	162815877	Click to see	796.10	unknown	https://doi.org/10.1016/0021-9673(92)80183-U https://doi.org/10.1007/BF02269869 https://doi.org/10.1078/0944-7113-00117 https://doi.org/10.1016/S0031-9422(97)00061-7 https://doi.org/10.1016/S0944-7113(00)80086-0 https://doi.org/10.1016/0021-9673(94)80511-3 https://doi.org/10.1016/S0378-8741(02)00093-4 https://doi.org/10.1111/J.1365-2141.2005.05907.X https://doi.org/10.1016/S0378-8741(98)00113-5 https://doi.org/10.1055/S-2006-959780 https://doi.org/10.1055/S-2001-15824 https://doi.org/10.1016/J.JEP.2005.08.046 https://doi.org/10.1055/S-2006-961582
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Ambap76-66-4	117829480	Click to see	384.50	unknown	https://doi.org/10.1002/PCA.740
methyl (3R,4'S,4'aR,10'aS,10'bS)-4'-methyl-2-oxospiro[1H-indole-3,10'-4,4a,5,6,8,9,10a,10b-octahydropyrano[3,4-g]indolizine]-1'-carboxylate	134834291	Click to see	368.40	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
methyl 4'-methyl-2-oxospiro[1H-indole-3,10'-4,4a,5,6,8,9,10a,10b-octahydropyrano[3,4-g]indolizine]-1'-carboxylate	163044680	Click to see CC1C2CCN3CCC4(C3C2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O	368.40	unknown	https://doi.org/10.1016/S0031-9422(96)00716-9
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
[(2S,3S,4R,5R)-6-[[(1R,19R,20S)-19-ethenyl-14-oxo-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15-pentaen-18-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	11972452	Click to see	674.70	unknown	via CMAUP database
> 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/10.1016/0021-9673(94)80511-3 https://doi.org/10.1055/S-2006-959780 https://doi.org/10.1016/S0944-7113(00)80086-0 https://doi.org/10.1211/0022357001777612 https://doi.org/10.1016/S0031-9422(97)00061-7 https://doi.org/10.1016/0021-9673(92)80183-U https://doi.org/10.1111/J.1365-2141.2005.05907.X https://doi.org/10.1055/S-2001-15824 https://doi.org/10.1007/BF02269869 https://doi.org/10.1078/0944-7113-00117 https://doi.org/10.1016/S0378-8741(98)00113-5 https://doi.org/10.1055/S-2006-961582 https://doi.org/10.1016/S0378-8741(02)00093-4 https://doi.org/10.1016/J.JEP.2005.08.046 https://doi.org/10.1016/S0031-9422(01)00043-7
Corynoxeine	44568160	Click to see	382.50	unknown	https://doi.org/10.1002/PCA.740 https://doi.org/10.1016/S0031-9422(97)00061-7
Isocorynoxeine	3037448	Click to see	382.50	unknown	https://doi.org/10.1002/PCA.740 https://doi.org/10.1016/S0031-9422(97)00061-7
Isomitraphylline	11726520	Click to see	368.40	unknown	https://doi.org/10.1055/S-2001-15824 https://doi.org/10.1016/0021-9673(92)80183-U https://doi.org/10.1016/J.JEP.2005.08.046 https://doi.org/10.1007/BF02269869 https://doi.org/10.1016/S0031-9422(01)00043-7 https://doi.org/10.1016/S0031-9422(97)00061-7 https://doi.org/10.1016/S0944-7113(00)80086-0 https://doi.org/10.1016/S0378-8741(98)00113-5 https://doi.org/10.1016/0021-9673(94)80511-3 https://doi.org/10.1055/S-2006-959780 https://doi.org/10.1055/S-2006-961582 https://doi.org/10.1002/PCA.740
Isopteropodine	9885603	Click to see	368.40	unknown	https://doi.org/10.1016/S0031-9422(01)00043-7
Isorhynchophylline	3037048	Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=CC=CC=C4NC3=O	384.50	unknown	https://doi.org/10.1016/S0031-9422(01)00043-7 https://doi.org/10.1211/0022357001777612 https://doi.org/10.1016/S0031-9422(97)00061-7 https://doi.org/10.1016/0021-9673(94)80511-3 https://doi.org/10.1016/S0378-8741(02)00093-4
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/10.1111/J.1365-2141.2005.05907.X
methyl (1R,4aS,5aR,6R,10aS)-1-methyl-2'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylate	11943653	Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O	368.40	unknown	via CMAUP database
methyl (1S,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	134823823	Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O	368.40	unknown	https://doi.org/10.1055/S-2001-15824 https://doi.org/10.1016/0021-9673(92)80183-U https://doi.org/10.1016/J.JEP.2005.08.046 https://doi.org/10.1007/BF02269869 https://doi.org/10.1016/S0031-9422(01)00043-7 https://doi.org/10.1211/0022357001777612 https://doi.org/10.1016/S0031-9422(97)00061-7 https://doi.org/10.1016/S0944-7113(00)80086-0 https://doi.org/10.1016/S0378-8741(98)00113-5 https://doi.org/10.1016/0021-9673(94)80511-3 https://doi.org/10.1016/S0378-8741(02)00093-4 https://doi.org/10.1055/S-2006-959780 https://doi.org/10.1002/PCA.740 https://doi.org/10.1055/S-2006-961582
methyl (E)-2-[(6'R,7'S,8'aS)-6'-ethyl-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl]-3-methoxyprop-2-enoate	102004527	Click to see	384.50	unknown	https://doi.org/10.1002/PCA.740
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/10.1016/S0031-9422(01)00043-7
Mitraphylline	94160	Click to see	368.40	unknown	https://doi.org/10.1055/S-2001-15824 https://doi.org/10.1111/J.1365-2141.2005.05907.X https://doi.org/10.1016/0021-9673(92)80183-U https://doi.org/10.1016/J.JEP.2005.08.046 https://doi.org/10.1007/BF02269869 https://doi.org/10.1016/S0031-9422(01)00043-7 https://doi.org/10.1211/0022357001777612 https://doi.org/10.1016/S0031-9422(97)00061-7 https://doi.org/10.1016/S0944-7113(00)80086-0 https://doi.org/10.1016/S0378-8741(98)00113-5 https://doi.org/10.1016/0021-9673(94)80511-3 https://doi.org/10.1016/S0378-8741(02)00093-4 https://doi.org/10.1016/J.PHYMED.2006.12.023 https://doi.org/10.1055/S-2006-959780 https://doi.org/10.1002/PCA.740 https://doi.org/10.1055/S-2006-961582
Pteropodine	10429112	Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O	368.40	unknown	https://doi.org/10.1055/S-2001-15824 https://doi.org/10.1016/0021-9673(92)80183-U https://doi.org/10.1016/J.JEP.2005.08.046 https://doi.org/10.1007/BF02269869 https://doi.org/10.1078/0944-7113-00117 https://doi.org/10.1016/S0031-9422(01)00043-7 https://doi.org/10.1211/0022357001777612 https://doi.org/10.1016/S0031-9422(97)00061-7 https://doi.org/10.1016/S0944-7113(00)80086-0 https://doi.org/10.1016/S0378-8741(98)00113-5 https://doi.org/10.1016/0021-9673(94)80511-3 https://doi.org/10.1016/S0378-8741(02)00093-4 https://doi.org/10.1055/S-2006-959780 https://doi.org/10.1002/PCA.740 https://doi.org/10.1055/S-2006-961582
Speciophylline	168985	Click to see	368.40	unknown	https://doi.org/10.1055/S-2001-15824 https://doi.org/10.1016/0021-9673(92)80183-U https://doi.org/10.1016/J.JEP.2005.08.046 https://doi.org/10.1055/S-2006-961582 https://doi.org/10.1002/PCA.740 https://doi.org/10.1055/S-2006-959780 https://doi.org/10.1016/S0378-8741(02)00093-4 https://doi.org/10.1016/0021-9673(94)80511-3 https://doi.org/10.1016/S0378-8741(98)00113-5 https://doi.org/10.1016/S0944-7113(00)80086-0 https://doi.org/10.1016/S0031-9422(97)00061-7 https://doi.org/10.1016/S0031-9422(01)00043-7 https://doi.org/10.1078/0944-7113-00117 https://doi.org/10.1007/BF02269869
Uncarine F	12304288	Click to see	368.40	unknown	https://doi.org/10.1016/0021-9673(94)80511-3 https://doi.org/10.1016/S0944-7113(00)80086-0 https://doi.org/10.1002/PCA.740 https://doi.org/10.1016/S0031-9422(97)00061-7 https://doi.org/10.1078/0944-7113-00117 https://doi.org/10.1007/BF02269869 https://doi.org/10.1016/S0378-8741(02)00093-4 https://doi.org/10.1055/S-2006-959780 https://doi.org/10.1016/0021-9673(92)80183-U https://doi.org/10.1055/S-2001-15824 https://doi.org/10.1016/J.JEP.2005.08.046 https://doi.org/10.1055/S-2006-961582
> Organoheterocyclic compounds / Pyridines and derivatives / Methylpyridines
(7S)-6,7-Dihydro-4,7-dimethyl-5H-cyclopenta(c)pyridine	68231	Click to see	147.22	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Proanthocyanidin B4	9959902	Click to see	578.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin	9064	Click to see	290.27	unknown	via CMAUP database
Cinchonain Ia	442675	Click to see C1C(C(OC2=C1C(=CC3=C2C(CC(=O)O3)C4=CC(=C(C=C4)O)O)O)C5=CC(=C(C=C5)O)O)O	452.40	unknown	via CMAUP database
Cinchonain Ib	10456516	Click to see	452.40	unknown	via CMAUP database
Epicatechin	72276	Click to see	290.27	unknown	https://doi.org/10.1078/0944-7113-00117 https://doi.org/10.1016/S0944-7113(97)80079-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
Epigallocatechin Gallate	65064	Click to see	458.40	unknown	https://doi.org/10.1078/0944-7113-00117
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2R,3S,4R,5S)-2-[(2S,3R,4S,5R,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol	101692563	Click to see	581.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Camelliaside B	25115190	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC6C(C(C(CO6)O)O)O)O)O)O)O)O	726.60	unknown	via CMAUP database
Leucoside	44566720	Click to see	580.50	unknown	via CMAUP database
Quercetin 3-O-(2G-beta-D-xylopyranosylrutinoside)	5281690	Click to see	742.60	unknown	via CMAUP database
Quercetin 3-O-Sambubioside	5487635	Click to see	596.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
Cinchonain I A	44575965	Click to see	450.40	unknown	https://doi.org/10.1016/S0944-7113(97)80079-7
cinchonain I b	44575964	Click to see C1C(C(CC2=C1C3=C(C=C2O)OC(=O)CC3C4=CC(=C(C=C4)O)O)O)C5=CC(=C(C=C5)O)O	450.40	unknown	https://doi.org/10.1016/S0944-7113(97)80079-7

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.

Uncaria tomentosa

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top