Scientific name	Authority	First published in
Uva chamae	Kuntze	Revis. Gen. Pl. 1: 7 (1891)
Uva cylindrica	Kuntze	Revis. Gen. Pl. 1: 7 (1891)
Uva cristata	Kuntze	Revis. Gen. Pl. 1: 7 (1891)
Uvaria cristata	R.Br. ex Oliv.	Fl. Trop. Afr. 1: 23 (1868)
Uvaria cylindrica	Schumach. & Thonn.	Beskr. Guin. Pl. : 256 (1827)
Unona macrocarpa	DC.	Syst. Nat. [Candolle] 1: 489. 1817 [1818 publ. 1-15 Nov 1817]
Uvaria nigrescens	Engl. & Diels	Monogr. Afrik. Pflanzen-Fam. 6: 15 (1901)
Uvaria macrocarpa	(DC.) Hook.f. & Benth.	Niger Fl. [W. J. Hooker]. 211. 1849 [Nov-Dec 1849]
Xylopiastrum macrocarpum	(Vahl) Roberty	Bull. Inst. Franç. Afrique Noire 15: 1398 (1953)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
fon	hoovi kwékwè

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 click to expand
- Northeast Tropical Africa
  - Chad
  - Sudan
- West Tropical Africa
  - Benin
  - Burkina
  - Gambia
  - Ghana
  - Guinea
  - Guinea-Bissau
  - Ivory Coast
  - Liberia
  - Mali
  - Nigeria
  - Senegal
  - Sierra Leone
  - Togo
- West-central Tropical Africa
  - Cameroon
  - Central African Republic
  - Zaïre

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000415872
Tropicos	1601215
KEW	urn:lsid:ipni.org:names:75615-1
The Plant List	kew-2447564
Open Tree Of Life	340656
NCBI Taxonomy	174970
IUCN Red List	156107113
IPNI	75615-1
iNaturalist	507034
GBIF	3154319
Freebase	/m/047sfc7
EOL	1053997
USDA GRIN	40961
Wikipedia	Uvaria_chamae
CMAUP	NPO17534

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

Seasonal fluctuation and alternative host plants of vegetable crop-infesting tephritids in non-vegetable growing areas in South Sudanese zone of Burkina Faso

Zida I, Sawadogo A, Nacro S

J Insect Sci

04-May-2024

PMCID:	PMC11069279
doi:	10.1093/jisesa/ieae047
PMID:	38703099

Phenolic Content, Antioxidant Potential, and Antimicrobial Activity of Uvaria chamae (Annonaceae), a Food Plant from Burkina Faso

Kaboré K, Dibala CI, Sama H, Diao M, Somda MK, Dicko MH

Biochem Res Int

26-Mar-2024

PMCID:	PMC10987249
doi:	10.1155/2024/1289859
PMID:	38567288

Anti-diabetic compounds from Uvaria dulcis Dunal

Teerapongpisan P, Praparatana R, Noppradit B, Laphookhieo S, Puttarak P

Heliyon

28-Feb-2024

PMCID:	PMC10920384
doi:	10.1016/j.heliyon.2024.e26962
PMID:	38463830

Polyherbal Combinations Used by Traditional Health Practitioners against Mental Illnesses in Bamako, Mali, West Africa

Moussavi N, Mounkoro PP, Dembele SM, Ballo NN, Togola A, Diallo D, Sanogo R, Wangensteen H, Paulsen BS

Plants (Basel)

04-Feb-2024

PMCID:	PMC10857219
doi:	10.3390/plants13030454
PMID:	38337987

Exploring the Therapeutic Potential of Traditional Antimalarial and Antidengue Plants: A Mechanistic Perspective

Kamaraj C, Ragavendran C, Prem P, Naveen Kumar S, Ali A, Kazmi A, Ullah A, Chandra Satish Kumar R, Khan SU, Luna-Arias JP, Mashwani ZU, Balasubramani G, Rehman SU

Can J Infect Dis Med Microbiol

28-Oct-2023

PMCID:	PMC10625492
doi:	10.1155/2023/1860084
PMID:	37927532

A Novel Tri-Hydroxy-Methylated Chalcone Isolated from Chromolaena tacotana with Anti-Cancer Potential Targeting Pro-Survival Proteins

Mendez-Callejas G, Piñeros-Avila M, Yosa-Reyes J, Pestana-Nobles R, Torrenegra R, Camargo-Ubate MF, Bello-Castro AE, Celis CA

Int J Mol Sci

14-Oct-2023

PMCID:	PMC10607159
doi:	10.3390/ijms242015185
PMID:	37894866

Anticancer Potential of Natural Chalcones: In Vitro and In Vivo Evidence

Michalkova R, Mirossay L, Kello M, Mojzisova G, Baloghova J, Podracka A, Mojzis J

Int J Mol Sci

19-Jun-2023

PMCID:	PMC10299153
doi:	10.3390/ijms241210354
PMID:	37373500

Medical Ethnobotany of the Bissau-Guinean Community of Migrants Living in Northern Italy and Comparison with the Ethnopharmacology of Guinea-Bissau

Sambù A, Cornara L, Catarino L, Indjai B, Biagi M, Giordani P

Plants (Basel)

08-May-2023

PMCID:	PMC10181441
doi:	10.3390/plants12091909
PMID:	37176967

Filamentous temperature sensitive mutant Z: a putative target to combat antibacterial resistance

Kifayat S, Yele V, Ashames A, Sigalapalli DK, Bhandare RR, Shaik AB, Nasipireddy V, Sanapalli BK

RSC Adv

11-Apr-2023

PMCID:	PMC10089256
doi:	10.1039/d3ra00013c
PMID:	37057268

Modeling current and future distribution patterns of Uvaria chamae in Benin (West Africa): Challenges and opportunities for its sustainable management

Daï EH, Hermann Houndonougbo JS, Idohou R, Ouédraogo A, Kakaï RG, Hotes S, Assogbadjo AE

Heliyon

11-Feb-2023

PMCID:	PMC9984439
doi:	10.1016/j.heliyon.2023.e13658
PMID:	36879756

Anti-inflammatory, Antinociceptive, and Toxicological Properties of Uvaria comperei Stem Crude Extract and Fractions

Simo MK, Siwe GT, Taboula Kayo M, Chen Z, Mangoua Kouamo M, Dize D, Jazet PD, Sameza ML, Fekam FB, Froldi G

Biomed Res Int

23-Jan-2023

PMCID:	PMC9886488
doi:	10.1155/2023/2754725
PMID:	36726837

Antibacterial potential of chalcones and its derivatives against Staphylococcus aureus

da Silva L, Donato IA, Gonçalves CA, Scherf JR, dos Santos HS, Mori E, Coutinho HD, da Cunha FA

3 Biotech

01-Dec-2022

PMCID:	PMC9712905
doi:	10.1007/s13205-022-03398-7
PMID:	36466769

An insight into the potent medicinal plant Phyllanthus amarus Schum. and Thonn.

Bose Mazumdar Ghosh A, Banerjee A, Chattopadhyay S

Nucleus (Calcutta)

12-Nov-2022

PMCID:	PMC9660160
doi:	10.1007/s13237-022-00409-z
PMID:	36407559

Ethnobotanical Survey of Medicinal Plants Used in the Treatment of COVID-19 and Related Respiratory Infections in Ogbomosho South and North Local Government Areas, Oyo State, Nigeria

Odebunmi CA, Adetunji TL, Adetunji AE, Olatunde A, Oluwole OE, Adewale IA, Ejiwumi AO, Iheme CE, Aremu TO

Plants (Basel)

10-Oct-2022

PMCID:	PMC9573491
doi:	10.3390/plants11192667
PMID:	36235532

Identification of Potential Allosteric Site Binders of Indoleamine 2,3-Dioxygenase 1 from Plants: A Virtual and Molecular Dynamics Investigation

de Almeida VM, Santos-Filho OA

Pharmaceuticals (Basel)

02-Sep-2022

PMCID:	PMC9502501
doi:	10.3390/ph15091099
PMID:	36145319

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
1,2-Benzenedi(carboxylic-14C)acid, dibutyl ester	171810	Click to see CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC	282.33	unknown	via CMAUP database
Benzenemethanol, 2-methoxy-, benzoate	3085295	Click to see COC1=CC=CC=C1COC(=O)C2=CC=CC=C2	242.27	unknown	https://doi.org/10.1016/S0031-9422(00)88802-0
Benzenemethanol, alpha-methoxy-, benzoate	578269	Click to see COC(C1=CC=CC=C1)OC(=O)C2=CC=CC=C2	242.27	unknown	https://doi.org/10.1055/S-2006-962016
Benzyl Benzoate	2345	Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2	212.24	unknown	https://doi.org/10.1055/S-2006-962016
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
4-Hydroxybenzoate	54675830	Click to see C1=CC(=CC=C1C(=O)O)[O-]	137.11	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzylethers
1-Methoxy-2-(phenylmethoxymethyl)benzene	57052255	Click to see COC1=CC=CC=C1COCC2=CC=CC=C2	228.29	unknown	https://doi.org/10.1016/S0031-9422(00)88802-0
Benzyl methyl ether	10869	Click to see COCC1=CC=CC=C1	122.16	unknown	https://doi.org/10.1055/S-2006-962016
Bis(2-methoxybenzyl) ether	12084155	Click to see COC1=CC=CC=C1COCC2=CC=CC=C2OC	258.31	unknown	https://doi.org/10.1016/S0031-9422(00)88802-0
Dibenzyl ether	7657	Click to see C1=CC=C(C=C1)COCC2=CC=CC=C2	198.26	unknown	https://doi.org/10.1055/S-2006-962016
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
2-[(4-Methoxy-2-methyl-5-propan-2-ylphenyl)methyl]phenol	85914556	Click to see CC1=CC(=C(C=C1CC2=CC=CC=C2O)C(C)C)OC	270.40	unknown	https://doi.org/10.1016/S0031-9422(00)88802-0
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
Benzethonium	2335	Click to see CC(C)(C)CC(C)(C)C1=CC=C(C=C1)OCCOCC[N+](C)(C)CC2=CC=CC=C2	412.60	unknown	https://doi.org/10.1080/10575630290026437
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol	8103	Click to see CCCCCCO	102.17	unknown	https://doi.org/10.1055/S-2006-962016
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Annonaceous acetogenins
(2R)-2-methyl-4-[12-[(2R,3S)-3-[2-[(2R,3S)-3-[(Z)-tetradec-3-enyl]oxiran-2-yl]ethyl]oxiran-2-yl]dodecyl]-2H-furan-5-one	162876346	Click to see CCCCCCCCCCC=CCCC1C(O1)CCC2C(O2)CCCCCCCCCCCCC3=CC(OC3=O)C	572.90	unknown	https://doi.org/10.1055/S-2006-941542
(2R)-4-[12-[(2S,3R)-3-[2-[(2S,3R)-3-[2-[(2S,3R)-3-decyloxiran-2-yl]ethyl]oxiran-2-yl]ethyl]oxiran-2-yl]dodecyl]-2-methyl-2H-furan-5-one	162895038	Click to see CCCCCCCCCCC1C(O1)CCC2C(O2)CCC3C(O3)CCCCCCCCCCCCC4=CC(OC4=O)C	588.90	unknown	https://doi.org/10.1055/S-2006-941542
(2S)-4-[(13R)-13-[(2R,5R)-5-[(2S,5R)-5-[(2R,6R)-6-hexyloxan-2-yl]oxolan-2-yl]oxolan-2-yl]-13-hydroxytridecyl]-2-methyl-2H-furan-5-one	163193119	Click to see CCCCCCC1CCCC(O1)C2CCC(O2)C3CCC(O3)C(CCCCCCCCCCCCC4=CC(OC4=O)C)O	604.90	unknown	https://doi.org/10.1055/S-2006-941542
(2S)-4-[(13R)-13-[(2S,5R)-5-[(2R,5S)-5-[(1S,5R)-1,5-dihydroxyundecyl]oxolan-2-yl]oxolan-2-yl]-13-hydroxytridecyl]-2-methyl-2H-furan-5-one	162924287	Click to see CCCCCCC(CCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCCCCC3=CC(OC3=O)C)O)O)O	622.90	unknown	https://doi.org/10.1021/NP030521A
(2S)-4-[(13R)-13-[(2S,5R)-5-[(2S,5R)-5-[(2R,6R)-6-hexyloxan-2-yl]oxolan-2-yl]oxolan-2-yl]-13-hydroxytridecyl]-2-methyl-2H-furan-5-one	162884356	Click to see CCCCCCC1CCCC(O1)C2CCC(O2)C3CCC(O3)C(CCCCCCCCCCCCC4=CC(OC4=O)C)O	604.90	unknown	https://doi.org/10.1021/NP030521A
(2S)-4-[(13R)-13-hydroxy-13-[(2S,5R)-5-[(2R,5S)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]-3-oxotridecyl]-2-methyl-2H-furan-5-one	163041965	Click to see CCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCC(=O)CCC3=CC(OC3=O)C)O)O	620.90	unknown	https://doi.org/10.1055/S-2006-941542
(5S)-3-((11R)-11-Hydroxy-11-((2R,2'R,5R,5'R)-octahydro-5'-((1S)-1-hydroxytridecyl)(2,2'-bifuran)-5-yl)undecyl)-5-methyl-2(5H)-furanone	118726382	Click to see CCCCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCCC3=CC(OC3=O)C)O)O	606.90	unknown	https://doi.org/10.1021/NP030521A
4-[(13S)-13-hydroxy-13-[(2S,5S)-5-[(1S)-1-hydroxyhexadecyl]oxolan-2-yl]tridecyl]-2-methyl-2H-furan-5-one	101392148	Click to see CCCCCCCCCCCCCCCC(C1CCC(O1)C(CCCCCCCCCCCCC2=CC(OC2=O)C)O)O	607.00	unknown	https://doi.org/10.1080/10575630290026437
4-[(15S)-15-hydroxy-15-[(2S,5S)-5-[(1S)-1-hydroxytetradecyl]oxolan-2-yl]pentadecyl]-2-methyl-2H-furan-5-one	101392149	Click to see CCCCCCCCCCCCCC(C1CCC(O1)C(CCCCCCCCCCCCCCC2=CC(OC2=O)C)O)O	607.00	unknown	https://doi.org/10.1080/10575630290026437
4-[13-[5-[5-(6-hexyloxan-2-yl)oxolan-2-yl]oxolan-2-yl]-13-hydroxytridecyl]-2-methyl-2H-furan-5-one	72808938	Click to see CCCCCCC1CCCC(O1)C2CCC(O2)C3CCC(O3)C(CCCCCCCCCCCCC4=CC(OC4=O)C)O	604.90	unknown	https://doi.org/10.1055/S-2006-941542 https://doi.org/10.1021/NP030521A
4-[13-hydroxy-13-[5-[5-(1-hydroxyundecyl)oxolan-2-yl]oxolan-2-yl]-3-oxotridecyl]-2-methyl-2H-furan-5-one	73155226	Click to see CCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCC(=O)CCC3=CC(OC3=O)C)O)O	620.90	unknown	https://doi.org/10.1055/S-2006-941542
4-[17-hydroxy-17-[5-(1-hydroxyundecyl)oxolan-2-yl]heptadecyl]-2-methyl-2H-furan-5-one	14759339	Click to see CCCCCCCCCCC(C1CCC(O1)C(CCCCCCCCCCCCCCCCC2=CC(OC2=O)C)O)O	592.90	unknown	https://doi.org/10.1080/10575630290026437
Asitribin	363980	Click to see CCCCCCC(CCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCCCCC3=CC(OC3=O)C)O)O)O	622.90	unknown	https://doi.org/10.1021/NP030521A https://doi.org/10.1055/S-2006-941542
Chamuvarinin	11342455	Click to see CCCCCCC1CCCC(O1)C2CCC(O2)C3CCC(O3)C(CCCCCCCCCCCCC4=CC(OC4=O)C)O	604.90	unknown	https://doi.org/10.1021/NP030521A
cis-Uvariamicin IB	14759336	Click to see CCCCCCCCCCCCCCC(C1CCC(O1)C(CCCCCCCCCCCCC2=CC(OC2=O)C)O)O	592.90	unknown	https://doi.org/10.1080/10575630290026437
Deacetyluvaricin	44138071	Click to see CCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCCCCC3=CC(OC3=O)C)O)O	606.90	unknown	https://doi.org/10.1021/NP030521A
Desacetyluvaricin	127149	Click to see CCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCCCCC3=CC(OC3=O)C)O)O	606.90	unknown	https://doi.org/10.1055/S-2006-941542 https://doi.org/10.1021/NP030521A
Neoannonin B	75229600	Click to see CCCCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCCC3=CC(OC3=O)C)O)O	606.90	unknown	https://doi.org/10.1021/NP030521A
rel-5-Methyl-3-[12-[(2R,3S)-3-[2-[(2S,3R)-3-[(3Z)-3-tetradecen-1-yl]-2-oxiranyl]ethyl]-2-oxiranyl]dodecyl]-2(5H)-furanone	162876345	Click to see CCCCCCCCCCC=CCCC1C(O1)CCC2C(O2)CCCCCCCCCCCCC3=CC(OC3=O)C	572.90	unknown	https://doi.org/10.1055/S-2006-941542
Rel-Squamocin-J	76315048	Click to see CCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCCC3=CC(OC3=O)C)O)O	578.90	unknown	https://doi.org/10.1021/NP030521A
Squamocin	441612	Click to see CCCCCCC(CCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCCCCC3=CC(OC3=O)C)O)O)O	622.90	unknown	https://doi.org/10.1021/NP030521A https://doi.org/10.1055/S-2006-941542
Squamocin L	461667	Click to see CCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCCCCC3=CC(OC3=O)C)O)O	606.90	unknown	https://doi.org/10.1055/S-2006-941542 https://doi.org/10.1021/NP030521A
Tripoxyrollin	131753021	Click to see CCCCCCCCCCC1C(O1)CCC2C(O2)CCC3C(O3)CCCCCCCCCCCCC4=CC(OC4=O)C	588.90	unknown	https://doi.org/10.1055/S-2006-941542
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1055/S-2006-962016
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1055/S-2006-962016
Linalyl acetate, (-)-	442474	Click to see CC(=CCCC(C)(C=C)OC(=O)C)C	196.29	unknown	via CMAUP database
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1055/S-2006-962016
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-Isopropyl-5-methylanisole	14104	Click to see CC1=CC(=C(C=C1)C(C)C)OC	164.24	unknown	https://doi.org/10.1055/S-2006-962016
2,5-Dimethoxy-p-cymene	6427071	Click to see CC1=CC(=C(C=C1OC)C(C)C)OC	194.27	unknown	https://doi.org/10.1016/S0031-9422(00)88802-0 https://doi.org/10.1055/S-2006-962016
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	via CMAUP database
Carvacrol methyl ether	80790	Click to see CC1=C(C=C(C=C1)C(C)C)OC	164.24	unknown	https://doi.org/10.1055/S-2006-962016
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1055/S-2006-962016
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Thujone	6553876	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	via CMAUP database
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1055/S-2006-962016
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1055/S-2006-962016
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1055/S-2006-962016
Borneol, (-)-	1201518	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1055/S-2006-962016
Camphor (synthetic)	159055	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1055/S-2006-962016
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-Terpinen-4-ol	5325830	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
(+)-alpha-Terpineol	442501	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1055/S-2006-962016
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-beta-Bourbonene	324224	Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
(+)-Gamma-cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	via CMAUP database
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	92042749	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	5315594	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1055/S-2006-962016
(1R,4aR)-4,7-dimethyl-1-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalene	5315589	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	5315592	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1055/S-2006-962016
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene	134779875	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
(E,E)-1,4,4-Trimethyl-8-methylene-1,5-cycloundecadiene	5318102	Click to see CC1=CCC(C=CCC(=C)CCC1)(C)C	204.35	unknown	via CMAUP database
(S)-gamma-Calacorene	5315609	Click to see CC1CC=C(C2=C1C=CC(=C2)C)C(C)C	200.32	unknown	https://doi.org/10.1055/S-2006-962016
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene	101708	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
1,6-Dimethyl-4-isopropyltetralin	10224	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1055/S-2006-962016
3,4-Dihydrocadalene	528708	Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C	200.32	unknown	https://doi.org/10.1055/S-2006-962016
alpha-Cadinene, (+)-	12306048	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1055/S-2006-962016
alpha-Calacorene	12302243	Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C	200.32	unknown	https://doi.org/10.1055/S-2006-962016
alpha-Cubebene	442359	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
alpha-Muurolene	12306047	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
Beta-Bisabolene	10104370	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	via CMAUP database
beta-Bourbonene	62566	Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1055/S-2006-962016
beta-Cubebene	93081	Click to see CC1CCC(C2C13C2C(=C)CC3)C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
beta-Farnesene	5281517	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
Calamenene	6429077	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1055/S-2006-962016
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
Caryophyllene epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1055/S-2006-962016
Cedrelanol	160799	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1055/S-2006-962016
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
Cubenol	11770062	Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C	222.37	unknown	https://doi.org/10.1055/S-2006-962016
delta-Cadinol	3084311	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1055/S-2006-962016
gamma-Calacorene	14038842	Click to see CC1CC=C(C2=C1C=CC(=C2)C)C(C)C	200.32	unknown	https://doi.org/10.1055/S-2006-962016
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
T-Muurolol	3084331	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1055/S-2006-962016
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	97032059	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1055/S-2006-962016
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	5321422	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1055/S-2006-962016
alpha-Gurjunene	15560276	Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene	91723653	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962016
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Chamazulene	10719	Click to see CCC1=CC2=C(C=CC2=C(C=C1)C)C	184.28	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
(3beta,5alpha,8alpha,22E)-5,8-epidioxyergosta-6,22-dien-3-ol	6475145	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C	428.60	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
[(4S)-3,3,6-trimethylhepta-1,5-dien-4-yl] acetate	14890510	Click to see CC(=CC(C(C)(C)C=C)OC(=O)C)C	196.29	unknown	via CMAUP database
Butyl Acetate	31272	Click to see CCCCOC(=O)C	116.16	unknown	https://doi.org/10.1055/S-2006-962016
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5S)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxycyclohexane-1-carboxylic acid	11870310	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(4S)-3,3,6-trimethylhepta-1,5-dien-4-ol	12308602	Click to see CC(=CC(C(C)(C)C=C)O)C	154.25	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
2-Methyl-3-buten-2-ol	8257	Click to see CC(C)(C=C)O	86.13	unknown	https://doi.org/10.1055/S-2006-962016
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol	53436347	Click to see C12C3C4C1C5(C2C3=C45)O	118.13	unknown	https://doi.org/10.1055/S-2006-962016
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Isovaleraldehyde	11552	Click to see CC(C)CC=O	86.13	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one	9862	Click to see CC(=CCCC(=O)C)C	126.20	unknown	https://doi.org/10.1055/S-2006-962016
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2S)-5,7-dihydroxy-6-[[2-hydroxy-5-[(2-hydroxyphenyl)methyl]phenyl]methyl]-8-[(2-hydroxyphenyl)methyl]-2-phenyl-2,3-dihydrochromen-4-one	102063064	Click to see C1C(OC2=C(C1=O)C(=C(C(=C2CC3=CC=CC=C3O)O)CC4=C(C=CC(=C4)CC5=CC=CC=C5O)O)O)C6=CC=CC=C6	574.60	unknown	https://doi.org/10.1021/JO00393A054
(2S)-5,7-dihydroxy-8-[(2-hydroxyphenyl)methyl]-2-phenyl-2,3-dihydrochromen-4-one	5315801	Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)CC3=CC=CC=C3O)C4=CC=CC=C4	362.40	unknown	https://doi.org/10.1016/0031-9422(85)80065-0 https://doi.org/10.1021/JO00428A006 https://doi.org/10.1021/JO00869A062
5,7-Dihydroxy-6-[(2-hydroxyphenyl)methyl]-2-phenyl-2,3-dihydrochromen-4-one	21721817	Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)CC3=CC=CC=C3O)O)C4=CC=CC=C4	362.40	unknown	https://doi.org/10.1021/JO00428A006 https://doi.org/10.1021/JO00869A062
5,7-Dihydroxy-6,8-bis[(2-hydroxyphenyl)methyl]-2-phenyl-2,3-dihydrochromen-4-one	11719701	Click to see C1C(OC2=C(C(=C(C(=C2C1=O)O)CC3=CC=CC=C3O)O)CC4=CC=CC=C4O)C5=CC=CC=C5	468.50	unknown	https://doi.org/10.1021/JO00428A006
Chamanetin	21721821	Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)CC3=CC=CC=C3O)C4=CC=CC=C4	362.40	unknown	https://doi.org/10.1021/JO00428A006 https://doi.org/10.1021/JO00869A062
Chamuvaritin	100418	Click to see C1C2=CC=CC=C2OC3=C(C(=C(C(=C31)O)C(=O)CCC4=CC=CC=C4)O)CC5=CC=CC=C5O	452.50	unknown	https://doi.org/10.1016/0031-9422(77)84030-2
Dichamanetin	181193	Click to see C1C(OC2=C(C(=C(C(=C2C1=O)O)CC3=CC=CC=C3O)O)CC4=CC=CC=C4O)C5=CC=CC=C5	468.50	unknown	https://doi.org/10.1021/JO00428A006
Diuvaretin	3085222	Click to see COC1=C(C(=C(C(=C1C(=O)CCC2=CC=CC=C2)O)CC3=CC=CC=C3O)O)CC4=CC=CC=C4O	484.50	unknown	https://doi.org/10.1021/JO00428A006
Isochamanetin	5318528	Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)CC3=CC=CC=C3O)O)C4=CC=CC=C4	362.40	unknown	https://doi.org/10.1021/JO00428A006 https://doi.org/10.1021/JO00869A062
Isouvaretin	151670	Click to see COC1=C(C(=CC(=C1C(=O)CCC2=CC=CC=C2)O)O)CC3=CC=CC=C3O	378.40	unknown	https://doi.org/10.1021/JO00428A006 https://doi.org/10.1021/JO00869A062 https://doi.org/10.1016/0031-9422(77)84030-2
Uvaretin	73447	Click to see COC1=C(C(=C(C(=C1)O)CC2=CC=CC=C2O)O)C(=O)CCC3=CC=CC=C3	378.40	unknown	https://doi.org/10.1080/10575630290020604 https://doi.org/10.1021/NP50021A016 https://doi.org/10.1021/JO00428A006 https://doi.org/10.1021/JO00869A062
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxyflavanone	238782	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1021/JO00428A006
Pinocembrin	68071	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1021/JO00428A006
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin	5280704	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7-methoxy-2-phenylchroman-4-one	73201	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1021/JO00428A006
5-Hydroxy-7-methoxyflavanone	4101463	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1021/JO00428A006
Pinostrobin	6950539	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1021/JO00428A006
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
Decarboxycitrinone	10775271	Click to see CC1=C(OC(=O)C2=C(C=C(C(=C12)C)O)O)C	220.22	unknown	via CMAUP database

Biological Material Top

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.

Uvaria chamae

Table of Contents

Details Top

Description 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

Biological Material Top

Contributors Top

Collections Top