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Vitex madiensis

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643ff099ac9fb235543173
Scientific name Vitex madiensis
Authority Oliv.
First published in Trans. Linn. Soc. London 29: 134 (1875)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Vitex madiensis subsp. madiensis Unknown
Vitex madiensis subsp. milanjiensis (Britten) F.White Forest Fl. N. Rhodes. : 455 (1962)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Somalia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Mali
      • Niger
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cabinda
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000333251
Tropicos 33702640
KEW urn:lsid:ipni.org:names:865856-1
The Plant List kew-213602
Open Tree Of Life 5793059
NCBI Taxonomy 1899206
IUCN Red List 146206777
IPNI 865856-1
iNaturalist 469597
GBIF 7309412
CMAUP NPO25699

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
Antiprotozoal Activity of Plants Used in the Management of Sleeping Sickness in Angola and Bioactivity-Guided Fractionation of Brasenia schreberi J.F.Gmel and Nymphaea lotus L. Active against T. b. rhodesiense Vahekeni N, Brillatz T, Rahmaty M, Cal M, Keller-Maerki S, Rocchetti R, Kaiser M, Sax S, Mattli K, Wolfram E, Marcourt L, Queiroz EF, Wolfender JL, Mäser P Molecules 03-Apr-2024
PMCID:PMC11013945
doi:10.3390/molecules29071611
PMID:38611890
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
Medicinal plants of the upper Aswa River catchment of northern Uganda - a cultural crossroads Masters ET J Ethnobiol Ethnomed 27-Oct-2023
PMCID:PMC10605377
doi:10.1186/s13002-023-00620-5
PMID:37884931
Smallholders’ knowledge about healing goat gastrointestinal parasite infections with wild plants in southern DR Congo Mavungu GN, Mutombo CS, Numbi DM, Nsenga SN, Muyumba WN, Pongombo CS, Bakari SA, Nachtergael A, Vandenput S, Okombe VE, Duez P Front Pharmacol 01-Mar-2023
PMCID:PMC10016610
doi:10.3389/fphar.2023.1124267
PMID:36937835
Chemical Profile, Antioxidant and Anti-Inflammatory Potency of Extracts of Vitex madiensis Oliv. and Crossopteryx febrifuga (Afzel ex G. Don) Boungou-Tsona G, Gainche M, Decombat C, Ripoche I, Bikindou K, Delort L, Caldefie-Chézet F, Loumouamou A, Chalard P Plants (Basel) 13-Jan-2023
PMCID:PMC9864984
doi:10.3390/plants12020386
PMID:36679099
Ethnopharmacological Study of Medicinal Plants Used for the Treatment of Cardiovascular Diseases and Their Associated Risk Factors in sub-Saharan Africa Odukoya JO, Odukoya JO, Mmutlane EM, Ndinteh DT Plants (Basel) 23-May-2022
PMCID:PMC9143319
doi:10.3390/plants11101387
PMID:35631812
Antidiabetic Medicinal Plants Used in Democratic Republic of Congo: A Critical Review of Ethnopharmacology and Bioactivity Data Kasali FM, Kadima JN, Peter EL, Mtewa AG, Ajayi CO, Tusiimire J, Tolo CU, Ogwang PE, Weisheit A, Agaba AG Front Pharmacol 27-Oct-2021
PMCID:PMC8579071
doi:10.3389/fphar.2021.757090
PMID:34776975
Ethnobotanical and phytotherapeutic study from Kouni community of the sub-prefecture of Kayes (Bouenza – Congo) Kimpouni V, Mamboueni JC, Tsoungould FG, Mikoko EN Heliyon 02-Aug-2019
PMCID:PMC6690559
doi:10.1016/j.heliyon.2019.e02007
PMID:31417965
Wild edible plants used by communities in and around selected forest reserves of Teso-Karamoja region, Uganda Ojelel S, Mucunguzi P, Katuura E, Kakudidi EK, Namaganda M, Kalema J J Ethnobiol Ethnomed 09-Jan-2019
PMCID:PMC6327394
doi:10.1186/s13002-018-0278-8
PMID:30626418
First large-scale ethnobotanical survey in the province of Uíge, northern Angola Lautenschläger T, Monizi M, Pedro M, Mandombe JL, Bránquima MF, Heinze C, Neinhuis C J Ethnobiol Ethnomed 25-Jul-2018
PMCID:PMC6060550
doi:10.1186/s13002-018-0238-3
PMID:30045744
Ethnobotanical survey of herbs used in the management of diabetes mellitus in Southern Katanga Area/DR Congo Amuri B, Maseho M, Simbi L, Duez P, Byanga K Pan Afr Med J 18-Jul-2018
PMCID:PMC6294981
doi:10.11604/pamj.2018.30.218.11718
PMID:30574237
Plants from disturbed savannah vegetation and their usage by Bakongo tribes in Uíge, Northern Angola Göhre A, Toto-Nienguesse ÁB, Futuro M, Neinhuis C, Lautenschläger T J Ethnobiol Ethnomed 20-Sep-2016
PMCID:PMC5030725
doi:10.1186/s13002-016-0116-9
PMID:27650466
The symbolic efficacy of medicinal plants: practices, knowledge, and religious beliefs amongst the Nalu healers of Guinea-Bissau Frazão-Moreira A J Ethnobiol Ethnomed 17-Jun-2016
PMCID:PMC4912713
doi:10.1186/s13002-016-0095-x
PMID:27316468
Efficient Isolation of a Large Amount of 20-Hydroxyecdysone from<i>Vitex madiensis</i>(Verbenaceae) by Droplet Counter-Current Chromatography Isao Kubo, Akiko Matsumoto, Johnson F. Ayafor Oxford University Press (OUP) 13-Apr-2016
doi:10.1080/00021369.1984.10866383
Ecological data in support of an analysis of Guinea-Bissau׳s medicinal flora Catarino L, Havik PJ, Indjai B, Romeiras MM Data Brief 30-Mar-2016
PMCID:PMC5063803
doi:10.1016/j.dib.2016.03.077
PMID:27761498

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Dimethyl anthranilate 6826 Click to see CNC1=CC=CC=C1C(=O)OC 165.19 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see C1=CC=C(C=C1)CO 108.14 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol 14529 Click to see CC1=CC=C(C=C1)C(C)(C)O 150.22 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropenes
1-Methyl-4-(prop-1-en-2-yl)benzene 62385 Click to see CC1=CC=C(C=C1)C(=C)C 132.20 unknown via CMAUP database
alpha,3-Dimethylstyrene 70759 Click to see CC1=CC(=CC=C1)C(=C)C 132.20 unknown via CMAUP database
o-Isopropenyltoluene 81886 Click to see CC1=CC=CC=C1C(=C)C 132.20 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(-)-Synephrine 854067 Click to see CNCC(C1=CC=C(C=C1)O)O 167.20 unknown via CMAUP database
> Benzenoids / Phenols / 4-alkoxyphenols
4-(3-Methyl-2-butenoxy)phenol 11435274 Click to see CC(=CCOC1=CC=C(C=C1)O)C 178.23 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
6-Hexadecen-4-yne, (E)- 5367338 Click to see CCCCCCCCCC=CC#CCCC 220.39 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkatetraenes
12-Methyl-1,5,9,11-tridecatetraene 564371 Click to see CC(=CC=CCCC=CCCC=C)C 190.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Hexacosanoic acid 10469 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 396.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Decyl acetate 8167 Click to see CCCCCCCCCCOC(=O)C 200.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(3R,3aS,4S,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysene-4,9-diol 101281371 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CC(C5C4(CCC5C(C)(C)O)C)O)C)C)C 460.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
(Z)-alpha-ocimene 5463455 Click to see CC(=C)CCC=C(C)C=C 136.23 unknown via CMAUP database
beta-CITRONELLOL, (R)- 101977 Click to see CC(CCC=C(C)C)CCO 156.26 unknown via CMAUP database
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown via CMAUP database
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown via CMAUP database
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
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
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
(-)-alpha-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(+)-2-Carene 78249 Click to see CC1=CC2C(C2(C)C)CC1 136.23 unknown via CMAUP database
(+)-trans-Sabinene hydrate 11228920 Click to see CC(C)C12CCC(C1C2)(C)O 154.25 unknown via CMAUP database
(1S,2R,5R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hexan-2-ol 11744854 Click to see CC(C)C12CCC(C1C2)(C)O 154.25 unknown via CMAUP database
(1S,2S,3R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-diol 21626089 Click to see CC1(C2CCC1(C(C2O)O)C)C 170.25 unknown via CMAUP database
alpha-THUJENE, (+/-)- 12444324 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown via CMAUP database
(+)-alpha-Phellandrene 443160 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown via CMAUP database
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
(+)-Perillaldehyde 1548901 Click to see CC(=C)C1CCC(=CC1)C=O 150.22 unknown via CMAUP database
(5R)-5-isopropyl-2-methyl-2-cyclohexen-1-one 10888107 Click to see CC1=CCC(CC1=O)C(C)C 152.23 unknown via CMAUP database
(R)-(+)-4-Isopropylcyclohex-1-ene-1-carboxaldehyde 12305140 Click to see CC(C)C1CCC(=CC1)C=O 152.23 unknown via CMAUP database
2-[(1R)-4-methylcyclohex-3-en-1-yl]prop-2-enyl acetate 11333027 Click to see CC1=CCC(CC1)C(=C)COC(=O)C 194.27 unknown via CMAUP database
2-Cyclohexen-1-ol, 1-methyl-4-(1-methylethenyl)-, trans- 12618691 Click to see CC(=C)C1CCC(C=C1)(C)O 152.23 unknown via CMAUP database
2-Cyclohexen-1-ol, 2-methyl-5-(1-methylethenyl)-, acetate, (1R-trans)- 6951358 Click to see CC1=CCC(CC1OC(=O)C)C(=C)C 194.27 unknown via CMAUP database
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown via CMAUP database
Carvone, (-)- 439570 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
trans-1(7),8-p-Menthadien-2-ol 6428442 Click to see CC(=C)C1CCC(=C)C(C1)O 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(Z,Z)-alpha-Farnesene 5317320 Click to see CC(=CCCC(=CCC=C(C)C=C)C)C 204.35 unknown via CMAUP database
alpha-Sinensal 5281534 Click to see CC(=CCC=C(C)C=C)CCC=C(C)C=O 218.33 unknown via CMAUP database
trans,trans-Farnesol 445070 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Selinene 10856614 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
alpha-Carotene 6419725 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C 536.90 unknown via CMAUP database
Asymmetrical zeta-carotene/Asym. zeta-carotene/7,8,11,12-Tetrahydrolycopene 16061252 Click to see CC(=CCCC(=CCCC(=CCCC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C)C)C 540.90 unknown via CMAUP database
Beta-Carotene 5280489 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C 536.90 unknown via CMAUP database
epsilon,psi-Carotene, (6R)- 5281230 Click to see CC1=CCCC(C1C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C)(C)C 536.90 unknown via CMAUP database
Lycopene 446925 Click to see CC(=CCCC(=CC=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C)C)C 536.90 unknown via CMAUP database
Phytofluene 6436722 Click to see CC(=CCCC(=CCCC(=CCCC(=CC=CC=C(C)C=CC=C(C)CCC=C(C)CCC=C(C)C)C)C)C)C 542.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(1S,2R,4S)-1-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-2,6,6-trimethylcyclohexane-1,2,4-triol 23258402 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2(C(CC(CC2(C)O)O)(C)C)O)C)C 602.90 unknown via CMAUP database
(1S,3S,6R)-6-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(1R,4S,6S)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol 101341894 Click to see CC(=CC=CC=C(C)C=CC=C(C)C=CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=CC34C(CC(CC3(O4)C)O)(C)C 600.90 unknown via CMAUP database
(3S,5R,6S)-beta-cryptoxanthin 5,6-epoxide 23256985 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC23C(CC(CC2(O3)C)O)(C)C)C)C 568.90 unknown via CMAUP database
(3S,5R,8R,3'R)-mutatoxanthin 21765300 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C2C=C3C(CC(CC3(O2)C)O)(C)C)C)C 584.90 unknown via CMAUP database
(8a(2)R)-Neochrome 14034169 Click to see CC(=CC=CC=C(C)C=CC=C(C)C1C=C2C(CC(CC2(O1)C)O)(C)C)C=CC=C(C)C=C=C3C(CC(CC3(C)O)O)(C)C 600.90 unknown via CMAUP database
all-trans-Neoxanthin 5281247 Click to see CC(=CC=CC=C(C)C=CC=C(C)C=C=C1C(CC(CC1(C)O)O)(C)C)C=CC=C(C)C=CC23C(CC(CC2(O3)C)O)(C)C 600.90 unknown via CMAUP database
beta-Cryptoxathin-5',6'-epoxide 21587177 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC23C(CCCC2(O3)C)(C)C)C)C 568.90 unknown via CMAUP database
Cryptoxanthin 5281235 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C 552.90 unknown via CMAUP database
Rubixanthin 5281252 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C 552.90 unknown via CMAUP database
Violaxanthin 448438 Click to see CC(=CC=CC=C(C)C=CC=C(C)C=CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=CC34C(CC(CC3(O4)C)O)(C)C 600.90 unknown via CMAUP database
Zeaxanthin 5280899 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C 568.90 unknown via CMAUP database
Zeinoxanthin 5281234 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C 552.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3E,5E,7E,9E,11E,13E,15E,17E,19E)-20-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-5,9,14,18-tetramethylicosa-3,5,7,9,11,13,15,17,19-nonaen-2-one 101306769 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)C)C)C 472.70 unknown via CMAUP database
Apocarotenal 5478003 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=O)C)C 416.60 unknown via CMAUP database
beta-Citraurin 9845703 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=O)C)C 432.60 unknown via CMAUP database
beta-Citraurinene 90429320 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C)C)C 418.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,7S,10R,13R,14R,16S,19R,20S)-19-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 98050000 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=CC(=O)OC7O)C)C)C 502.50 unknown via CMAUP database
(1R,2R,7S,10S,13R,14R,16S,19S,20S)-19-(furan-3-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 92966492 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown via CMAUP database
(2'R,5aR,7aR,8R,9S,11aR,11bR)-9-[(S)-furan-3-yl-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-5,5,7a,9,11b-pentamethyl-3,7-dioxospiro[6,10,11,11a-tetrahydro-5aH-benzo[g][2]benzoxepine-8,3'-oxirane]-2'-carboxylic acid 53363753 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC(C34C(O4)C(=O)O)(C)C(C5=COC=C5)OC6C(C(C(C(O6)CO)O)O)O)C)C 634.70 unknown via CMAUP database
Limonin 179651 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown via CMAUP database
Nomilin 72320 Click to see CC(=O)OC1CC(=O)OC(C2C1(C3CCC4(C(OC(=O)C5C4(C3(C(=O)C2)C)O5)C6=COC=C6)C)C)(C)C 514.60 unknown via CMAUP database
Obacunone 119041 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 454.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
17-(2,3-dihydroxy-6-methylheptan-2-yl)-2,3,11,14-tetrahydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 4482423 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)O)O 480.60 unknown https://doi.org/10.1080/00021369.1984.10866383
2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 271605 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown https://doi.org/10.1080/00021369.1984.10866383
20-Hydroxyecdysone 5459840 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown https://doi.org/10.1271/BBB1961.48.1683
https://doi.org/10.1080/00021369.1984.10866383
Ajugasterone C 441826 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)O)O 480.60 unknown https://doi.org/10.1271/BBB1961.48.1683
https://doi.org/10.1080/00021369.1984.10866383
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5,5'-Oxybis(5-methylene-2-furaldehyde) 12366272 Click to see C1=C(OC(=C1)C=O)COCC2=CC=C(O2)C=O 234.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
(R)-alpha-Citronellal 72941638 Click to see CC(CCCC(=C)C)CC=O 154.25 unknown via CMAUP database
Decanal 8175 Click to see CCCCCCCCCC=O 156.26 unknown via CMAUP database
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown via CMAUP database
Octanal 454 Click to see CCCCCCCC=O 128.21 unknown via CMAUP database
Undecanal 8186 Click to see CCCCCCCCCCC=O 170.29 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 via CMAUP database
> Organoheterocyclic compounds / Oxepanes
(1R,4R,6S)-1-methyl-4-(prop-1-en-2-yl)-7-oxabicyclo[4.1.0]heptane 6857487 Click to see CC(=C)C1CCC2(C(C1)O2)C 152.23 unknown via CMAUP database
Carvone oxide 11030188 Click to see CC(=C)C1CC2C(O2)(C(=O)C1)C 166.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
2-(4-Hydroxyphenyl)ethyl 3-(4-hydroxyphenyl)prop-2-enoate 86163337 Click to see C1=CC(=CC=C1CCOC(=O)C=CC2=CC=C(C=C2)O)O 284.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthoxyletin 66548 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C 258.27 unknown via CMAUP database
Xanthyletin 65188 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3-Hydroxy-5,6,7,4'-tetramethoxyflavone 24752965 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)O 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Hesperidin 10621 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown via CMAUP database
Naringin 442428 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Takakin 44258588 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7-Dihydroxy-3,6-dimethoxyflavone 5481646 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC=CC=C3)O 314.29 unknown via CMAUP database
Eupatilin 5273755 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3,4',6,7-Tetramethoxyflavone 14887080 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=CC(=C(C=C3O2)OC)OC)OC 342.30 unknown via CMAUP database
3',4',5',5,7-Pentamethoxyflavone 493376 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC(=C(C(=C3)OC)OC)OC 372.40 unknown via CMAUP database
5-Hydroxy-3',4',6,7-tetramethoxyflavone 152430 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC 358.30 unknown via CMAUP database
8-Hydroxy-4',5,7-trimethoxyflavone 5318368 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3OC)OC)O 328.30 unknown via CMAUP database
Apigenin trimethyl ether 79730 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC 312.30 unknown via CMAUP database
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown via CMAUP database
Fastigenin 162464 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown via CMAUP database
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown via CMAUP database
Sinensetin 145659 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
2-(3,4-Dimethoxyphenyl)-7-hydroxy-5,6,8-trimethoxy-4H-1-benzopyran-4-one 10452846 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)O)OC)OC 388.40 unknown via CMAUP database
3,5,6,7,8,3',4'-Heptamethphoxyflavone 150893 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)OC)OC 432.40 unknown via CMAUP database
3'-Demethylnobiletin 183466 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)O 388.40 unknown via CMAUP database
3',4'-Didemethylnobiletin 5318041 Click to see COC1=C(C(=C(C2=C1C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)OC 374.30 unknown via CMAUP database
4'-Hydroxy-3',5,6,7,8-pentamethoxyflavone 21593928 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)O 388.40 unknown via CMAUP database
4'-Hydroxy-5,6,7,8-tetramethoxyflavone 3010100 Click to see COC1=C(C(=C(C2=C1C(=O)C=C(O2)C3=CC=C(C=C3)O)OC)OC)OC 358.30 unknown via CMAUP database
4',5-Dihydroxy-7,8-dimethoxyflavone 14585506 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC 314.29 unknown via CMAUP database
4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-6,7,8-trimethoxy- 44584772 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=CC(=C(C(=C3O2)OC)OC)OC)OC 372.40 unknown via CMAUP database
5-Hydroxy-7,8,4'-trimethoxyflavone 14353376 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)OC 328.30 unknown via CMAUP database
5-o-Desmethylnobiletin 358832 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 388.40 unknown via CMAUP database
6-Demethoxytangeretin 629964 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3OC)OC)OC 342.30 unknown via CMAUP database
7-Hydroxy-4',5,6,8-tetramethoxyflavone 5318356 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)O)OC 358.30 unknown via CMAUP database
8-Methoxycirsilineol 181092 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O 374.30 unknown via CMAUP database
Acerosin 177696 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)O 360.30 unknown via CMAUP database
Gardenin B 96539 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O 358.30 unknown via CMAUP database
Gardenin D 3080750 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O 374.30 unknown via CMAUP database
Isosinensetin 632135 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3OC)OC)OC)OC 372.40 unknown via CMAUP database
Linderoflavone B 97151 Click to see COC1=C(C(=C(C2=C1C(=O)C=C(O2)C3=CC4=C(C=C3)OCO4)OC)OC)OC 386.40 unknown via CMAUP database
Nobiletin 72344 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)OC 402.40 unknown via CMAUP database
Sudachitin 12443122 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)O 360.30 unknown via CMAUP database
Tangeretin 68077 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
4'-Hydroxy-3,6-dimethoxy-6'',6''-dimethylpyrano[2,3:7,8]flavone 44258693 Click to see CC1(C=CC2=C3C(=CC(=C2O1)OC)C(=O)C(=C(O3)C4=CC=C(C=C4)O)OC)C 380.40 unknown via CMAUP database

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