Details Top

Internal ID UUID644011ef7ca8d105459154
Scientific name Cleome amblyocarpa
Authority Barratte & Murb.
First published in Acta Univ. Lund., 2 , 1(4): 25 (1905)

Ethnobotanical Use Top

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General Uses Top

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Food and beverages (non-medicinal):
The leaves and young shoots are consumed as a pot herb in Tunisia and parts of the Maghreb, typically boiled or blanched and combined with other ingredients; the specific preparations are local dishes rather than standardized commercial products.

Industrial and craft applications:
No documented industrial, craft, or non-medicinal uses are reported for this taxon in reliable references.

Colorants and tanning:
No reliable reports of dye, tannin, or colorant use are found.

Fragrance and cosmetics:
No fragrance, essential-oil, or cosmetic applications are documented.

Wood and fiber:
No timber, fiber, or building-material uses are reported.

Common products:
No standardized commercial products derived from this species are documented.

Properties relevant to use:
No physical/chemical property data relevant to commercial or industrial use are reported.

Standards and regulation:
No sector-specific standards or regulatory frameworks are documented for this species.

Sustainability and sourcing:
No documented sustainability or sourcing frameworks apply to this taxon.

Synonyms Top

Scientific name Authority First published in
Siliquaria glandulosa Forssk. Fl. Aegypt.-Arab. : 78 (1775)
Cleome amblyocarpa var. glandulosa (Forssk.) Botsch. Novosti Sist. Vyssh. Rast. 4: 327 1968
Cleome daryoushiana Parsa Fl. Iran 1: 909 (1951)
Cleome arabica var. amblyocarpa (Barratte & Murb.) Ozenda Fl. Sahara 247 1958
Cleome arabica var. lutea Parsa Kew Bull. 2: 17 (1947)

Common names Top

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Language Common/alternative name
English spider flower
Arabic ذفرة كليلة الثمرة

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
    • Northeast Tropical Africa
      • Chad
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
      • Western Sahara
    • West Tropical Africa
      • Mali
      • Mauritania
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Oman
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Iran
      • Iraq
      • Palestine
      • Sinai

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000611120
Tropicos 50271897
KEW urn:lsid:ipni.org:names:146916-1
The Plant List kew-2727159
Open Tree Of Life 517004
NCBI Taxonomy 1077932
IPNI 146916-1
iNaturalist 496033
GBIF 3871552
EPPO CLEAM

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
Biological Characterization of Cleome felina L.f. Extracts for Phytochemical, Antimicrobial, and Hepatoprotective Activities in Wister Albino Rats Shaikh HY, Niazi SK, Bepari A, Cordero MA, Sheereen S, Hussain SA, Rudrappa M, Nagaraja SK, Agadi SN Antibiotics (Basel) 02-Oct-2023
PMCID:PMC10604301
doi:10.3390/antibiotics12101506
PMID:37887207
Facilitation by Haloxylon persicum Shrubs Enhances Density and Richness of Soil Seed Bank of Annual Plants in a Hyper-Arid Ecosystem Gomaa NH, Hegazy AK, Alhaithloul HA Plants (Basel) 10-Mar-2023
PMCID:PMC10056119
doi:10.3390/plants12061276
PMID:36986963
Comparative Nectary Morphology across Cleomaceae (Brassicales) Zenchyzen B, Weissner S, Martin J, Lopushinsky A, John I, Nahal I, Hall JC Plants (Basel) 10-Mar-2023
PMCID:PMC10051628
doi:10.3390/plants12061263
PMID:36986951
Isolation and Identification of Flavones Responsible for the Antibacterial Activities of Tillandsia bergeri Extracts Lo MM, Benfodda Z, Dunyach-Rémy C, Bénimélis D, Roulard R, Fontaine JX, Mathiron D, Quéro A, Molinié R, Meffre P ACS Omega 27-Sep-2022
PMCID:PMC9557886
doi:10.1021/acsomega.2c04195
PMID:36249367
Chemical Composition of Kickxia aegyptiaca Essential Oil and Its Potential Antioxidant and Antimicrobial Activities Abd-ElGawad AM, El-Amier YA, Bonanomi G, Gendy AE, Elgorban AM, Alamery SF, Elshamy AI Plants (Basel) 23-Feb-2022
PMCID:PMC8912309
doi:10.3390/plants11050594
PMID:35270064
Climate change and hydrological regime in arid lands: Impacts of dams on the plant diversity, vegetation structure and soil in Saudi Arabia Al-Munqedhi BM, El-Sheikh MA, Alfarhan AH, Alkahtani AM, Arif IA, Rajagopal R, Alharthi ST Saudi J Biol Sci 25-Jan-2022
PMCID:PMC9280318
doi:10.1016/j.sjbs.2022.01.043
PMID:35844430
The Essential Oil-Bearing Plants in the United Arab Emirates (UAE): An Overview Shahin SM, Jaleel A, Alyafei MA Molecules 27-Oct-2021
PMCID:PMC8587291
doi:10.3390/molecules26216486
PMID:34770890
Impacts of Anthropogenic Disturbance on Vegetation Dynamics: A Case Study of Wadi Hagul, Eastern Desert, Egypt Bedair R, Ibrahim AA, Alyamani AA, Aloufi S, Ramadan S Plants (Basel) 14-Sep-2021
PMCID:PMC8466335
doi:10.3390/plants10091906
PMID:34579436
Chemical Composition, Allelopathic, Antioxidant, and Anti-Inflammatory Activities of Sesquiterpenes Rich Essential Oil of Cleome amblyocarpa Barratte & Murb. Abd-ElGawad AM, Elgamal AM, EI-Amier YA, Mohamed TA, El Gendy AE, I. Elshamy A Plants (Basel) 25-Jun-2021
PMCID:PMC8308966
doi:10.3390/plants10071294
PMID:34202270
Taxonomic significance of seed sculpture and pollen ecto-mycoflora at the infraspecific level: Brassica tournefortii case study Hassan W, Abdelhameed A, A. Al Shaye N, Amer W Saudi J Biol Sci 24-Jun-2021
PMCID:PMC8459108
doi:10.1016/j.sjbs.2021.06.049
PMID:34588917
Ethnobotanical Study on Plant Used by Semi-Nomad Descendants’ Community in Ouled Dabbeb—Southern Tunisia Karous O, Ben Haj Jilani I, Ghrabi-Gammar Z Plants (Basel) 28-Mar-2021
PMCID:PMC8066878
doi:10.3390/plants10040642
PMID:33800664
Facilitation Effects of Haloxylon salicornicum Shrubs on Associated Understory Annuals, and a Modified “Stress-Gradient” Hypothesis for Droughty Times Gomaa NH, Hegazy AK, Latef AA Plants (Basel) 07-Dec-2020
PMCID:PMC7762360
doi:10.3390/plants9121726
PMID:33297465
A systematic revision of Capparaceae and Cleomaceae in Egypt: an evaluation of the generic delimitations of Capparis and Cleome using ecological and genetic diversity El zayat MA, Ali ME, Amar MH J Genet Eng Biotechnol 06-Oct-2020
PMCID:PMC7538494
doi:10.1186/s43141-020-00069-z
PMID:33025275
Phylogeny and multiple independent whole‐genome duplication events in the Brassicales Mabry ME, Brose JM, Blischak PD, Sutherland B, Dismukes WT, Bottoms CA, Edger PP, Washburn JD, An H, Hall JC, McKain MR, Al‐Shehbaz I, Barker MS, Schranz ME, Conant GC, Pires JC Am J Bot 24-Aug-2020
PMCID:PMC7496422
doi:10.1002/ajb2.1514
PMID:32830865
Ethnobotanical Study of Indigenous Medicinal Plants of Jazan Region, Saudi Arabia Tounekti T, Mahdhi M, Khemira H Evid Based Complement Alternat Med 02-Jun-2019
PMCID:PMC6582903
doi:10.1155/2019/3190670
PMID:31275409

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see 228.37 unknown https://doi.org/10.1016/0031-9422(94)00848-N
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1016/0031-9422(94)00848-N
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1016/0031-9422(94)00848-N
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1016/0031-9422(94)00848-N
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see 200.32 unknown https://doi.org/10.1016/0031-9422(94)00848-N
> 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 https://doi.org/10.1016/0031-9422(94)00848-N
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Grayanoids / Leucothol and grayanotoxane diterpenoids
Rhodojaponin IV 442083 Click to see CC(=O)OC1CC23CC(C(C2OC(=O)C)CCC3C(C4C1(C(C(C4)O)(C)C)O)(C)O)(C)O 454.60 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1S,6S,9R,10R,15S)-6-[(2S,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.01,13.02,10.05,9]nonadecan-15-ol 162914360 Click to see 474.70 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1'R,3R,4'S,5S,8R,9R,10R,13S,14R,17R)-1'-(2-hydroxypropan-2-yl)-4,4,4',8,10,14-hexamethylspiro[1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthrene-17,3'-2,7-dioxabicyclo[2.2.1]heptane]-3-ol 162889913 Click to see 474.70 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
(1'R,4'S,5R,8R,9R,10R,13R,14R,17R)-1'-(2-hydroxypropan-2-yl)-4,4,4',8,10,14-hexamethylspiro[2,5,6,7,9,11,12,13,15,16-decahydro-1H-cyclopenta[a]phenanthrene-17,3'-2,7-dioxabicyclo[2.2.1]heptane]-3-one 163195156 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
(1'R,4'S,8R,10R,14R,17R)-1'-(2-hydroxypropan-2-yl)-4,4,4',8,10,14-hexamethylspiro[2,5,6,7,9,11,12,13,15,16-decahydro-1H-cyclopenta[a]phenanthrene-17,3'-2,7-dioxabicyclo[2.2.1]heptane]-3-one 162980036 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
(1S,1'R,4'S,6R,9R,10R,15S)-1'-(2-hydroxypropan-2-yl)-4',9,10,14,14-pentamethylspiro[16-oxapentacyclo[13.2.2.01,13.02,10.05,9]nonadecane-6,3'-2,7-dioxabicyclo[2.2.1]heptane]-15-ol 163070223 Click to see 488.70 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
(3R,5S,8R,9R,10R,13S,14R,17R)-17-[(2S,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthrene-3,17-diol 162938228 Click to see 476.70 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
(5S)-5-[(1S,2S,5R,6S,9R,10R,13R,15S)-15-hydroxy-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.01,13.02,10.05,9]nonadecan-6-yl]-5-methyloxolan-2-one 162955274 Click to see 430.60 unknown https://doi.org/10.1016/0031-9422(94)00848-N
(5S)-5-methyl-5-[(5R,8R,9S,10R,13R,14R,17S)-4,4,8,10,14-pentamethyl-3-oxo-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]oxolan-2-one 162967939 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(=O)O5)C)C)C)C 414.60 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
[(1'R,3R,4'S,5R,8R,9R,10R,12R,13R,14R,17R)-12-acetyloxy-1'-(2-ethoxypropan-2-yl)-4,4,4',8,10,14-hexamethylspiro[1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthrene-17,3'-2,7-dioxabicyclo[2.2.1]heptane]-3-yl] acetate 102066547 Click to see CCOC(C)(C)C12CCC(O1)(C3(O2)CCC4(C3C(CC5C4(CCC6C5(CCC(C6(C)C)OC(=O)C)C)C)OC(=O)C)C)C 602.80 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
[(1'R,3R,4'S,5R,8R,9R,10R,12R,13R,14R,17R)-3-hydroxy-1'-(2-hydroxypropan-2-yl)-4,4,4',8,10,14-hexamethylspiro[1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthrene-17,3'-2,7-dioxabicyclo[2.2.1]heptane]-12-yl] acetate 102066545 Click to see CC(=O)OC1CC2C3(CCC(C(C3CCC2(C4(C1C5(CC4)C6(CCC(O6)(O5)C(C)(C)O)C)C)C)(C)C)O)C 532.80 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
[(1'R,4'S,5R,8R,9R,10R,12R,13R,14R,17R)-1'-(2-hydroxypropan-2-yl)-4,4,4',8,10,14-hexamethyl-3-oxospiro[2,5,6,7,9,11,12,13,15,16-decahydro-1H-cyclopenta[a]phenanthrene-17,3'-2,7-dioxabicyclo[2.2.1]heptane]-12-yl] acetate 102066399 Click to see CC(=O)OC1CC2C3(CCC(=O)C(C3CCC2(C4(C1C5(CC4)C6(CCC(O6)(O5)C(C)(C)O)C)C)C)(C)C)C 530.70 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
[(1'R,4'S,5S,8R,9R,10R,12R,13R,14R,17R)-1'-(2-hydroxypropan-2-yl)-4,4,4',8,10,14-hexamethyl-3-oxospiro[2,5,6,7,9,11,12,13,15,16-decahydro-1H-cyclopenta[a]phenanthrene-17,3'-2,7-dioxabicyclo[2.2.1]heptane]-12-yl] acetate 162935233 Click to see CC(=O)OC1CC2C3(CCC(=O)C(C3CCC2(C4(C1C5(CC4)C6(CCC(O6)(O5)C(C)(C)O)C)C)C)(C)C)C 530.70 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
[(3R,5R,8R,9R,10R,12R,13R,14R,17R)-12-acetyloxy-17-hydroxy-4,4,8,10,14-pentamethyl-17-[(2S)-2-methyl-5-oxooxolan-2-yl]-1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 102066397 Click to see 532.70 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
[(3R,5R,8R,9R,10R,13S,14R,15R,17R)-15-acetyloxy-17-hydroxy-4,4,8,10,14-pentamethyl-17-[(2S)-2-methyl-5-oxofuran-2-yl]-1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 162901244 Click to see 530.70 unknown https://doi.org/10.1016/0031-9422(94)00848-N
[(3R,8R,9R,10S,13S,14R,15R,17R)-7,15-diacetyloxy-17-hydroxy-4,4,8,10,14-pentamethyl-17-[(2S)-2-methyl-5-oxofuran-2-yl]-1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 101921674 Click to see 588.70 unknown https://doi.org/10.1016/0031-9422(94)00848-N
[(3S,5R,7S,8R,9R,10S,13S,14R,15R,17R)-7,15-diacetyloxy-17-hydroxy-4,4,8,10,14-pentamethyl-17-[(2S)-2-methyl-5-oxofuran-2-yl]-1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 163067775 Click to see CC(=O)OC1CCC2(C3CCC4C(C3(C(CC2C1(C)C)OC(=O)C)C)(C(CC4(C5(C=CC(=O)O5)C)O)OC(=O)C)C)C 588.70 unknown https://doi.org/10.1016/0031-9422(94)00848-N
[(3S,5R,8R,9R,10R,13S,14R,15R,17R)-15-acetyloxy-17-hydroxy-4,4,8,10,14-pentamethyl-17-[(2S)-2-methyl-5-oxofuran-2-yl]-1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 162901245 Click to see 530.70 unknown https://doi.org/10.1016/0031-9422(94)00848-N
[(3S,8R,9R,10S,13S,14R,15R,17R)-7,15-diacetyloxy-17-hydroxy-4,4,8,10,14-pentamethyl-17-[(2S)-2-methyl-5-oxofuran-2-yl]-1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 101921673 Click to see CC(=O)OC1CCC2(C3CCC4C(C3(C(CC2C1(C)C)OC(=O)C)C)(C(CC4(C5(C=CC(=O)O5)C)O)OC(=O)C)C)C 588.70 unknown https://doi.org/10.1016/0031-9422(94)00848-N
[15-Acetyloxy-17-hydroxy-4,4,8,10,14-pentamethyl-17-(2-methyl-5-oxofuran-2-yl)-1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 162901243 Click to see CC(=O)OC1CCC2(C3CCC4C(C3(CCC2C1(C)C)C)(C(CC4(C5(C=CC(=O)O5)C)O)OC(=O)C)C)C 530.70 unknown https://doi.org/10.1016/0031-9422(94)00848-N
[7,15-Diacetyloxy-17-hydroxy-4,4,8,10,14-pentamethyl-17-(2-methyl-5-oxofuran-2-yl)-1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 163067773 Click to see 588.70 unknown https://doi.org/10.1016/0031-9422(94)00848-N
1'-(2-hydroxypropan-2-yl)-4,4,4',8,10,14-hexamethylspiro[2,5,6,7,9,11,12,13,15,16-decahydro-1H-cyclopenta[a]phenanthrene-17,3'-2,7-dioxabicyclo[2.2.1]heptane]-3-one 14487122 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC45C6(CCC(O6)(O5)C(C)(C)O)C)C)C)C 472.70 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
5-(15-Hydroxy-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.01,13.02,10.05,9]nonadecan-6-yl)-5-methyloxolan-2-one 162955273 Click to see CC1(C2CCC3(C(C24CCC1(OC4)O)CCC5C3(CCC5C6(CCC(=O)O6)C)C)C)C 430.60 unknown https://doi.org/10.1016/0031-9422(94)00848-N
5-Methyl-5-(4,4,8,10,14-pentamethyl-3-oxo-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl)oxolan-2-one 124222297 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(=O)O5)C)C)C)C 414.60 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
Amblyone 101921672 Click to see 430.60 unknown https://doi.org/10.1016/0031-9422(94)00848-N
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see 386.70 unknown https://doi.org/10.1016/0031-9422(94)00848-N
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
(5S)-5-methyl-5-[(5R,8R,9S,10R,13R,14R,17S)-4,4,8,10,14-pentamethyl-3-oxo-5,6,7,9,11,12,13,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]furan-2-one 162961479 Click to see 410.60 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
(5S)-5-methyl-5-[(8R,10R,14R)-4,4,8,10,14-pentamethyl-3-oxo-5,6,7,9,11,12,13,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]furan-2-one 162961478 Click to see 410.60 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
(5S)-5-methyl-5-[(8R,10R,14R)-4,4,8,10,14-pentamethyl-3-oxo-5,6,7,9,11,12,13,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]oxolan-2-one 10341615 Click to see 412.60 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
[(8R,10R,12R,14R)-4,4,8,10,14-pentamethyl-17-[(2S)-2-methyl-5-oxooxolan-2-yl]-3-oxo-5,6,7,9,11,12,13,15,16,17-decahydrocyclopenta[a]phenanthren-12-yl] acetate 163050921 Click to see 470.60 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
5-Methyl-5-(4,4,8,10,14-pentamethyl-3-oxo-5,6,7,9,11,12,13,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)furan-2-one 85283797 Click to see 410.60 unknown https://doi.org/10.1016/S0031-9422(96)00681-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(94)00848-N
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(93)85532-V
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/0031-9422(94)00848-N
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[3,13-Diacetyloxy-2,7,7,11,12-pentamethyl-15-(2-methyl-5-oxofuran-2-yl)-5-oxo-6-oxatetracyclo[9.7.0.02,8.012,16]octadecan-18-yl] acetate 73196910 Click to see 602.70 unknown https://doi.org/10.1021/NP0003037
15alpha-acetoxycleomblynol A 15511195 Click to see 602.70 unknown https://doi.org/10.1021/NP0003037
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 44258935 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0305-1978(96)00099-3
7-O-Beta-D-Glucopyranoside 11294177 Click to see 462.40 unknown https://doi.org/10.1016/0031-9422(94)00848-N
Chrysoeriol-7-O-beta-D-glucoside 13871877 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/0031-9422(94)00848-N
Kaempferol-7-rhamnoside 25079965 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0305-1978(96)00099-3
Vincetoxicoside B 5748601 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0305-1978(96)00099-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/0031-9422(94)00848-N
Isokaempferide 5280862 Click to see 300.26 unknown https://doi.org/10.1016/0305-1978(92)90084-Q
Quercetin 3,3'-dimethyl ether 5316900 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O 330.29 unknown https://doi.org/10.1016/0305-1978(92)90084-Q
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Axillarin 5281603 Click to see 346.30 unknown https://doi.org/10.1016/0305-1978(92)90084-Q
Jaceosidin 5379096 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown https://doi.org/10.1016/S0305-1978(96)00099-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Chrysosplenetin 5281608 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown https://doi.org/10.1016/S0305-1978(96)00099-3
Penduletin 5320462 Click to see 344.30 unknown https://doi.org/10.1016/0305-1978(92)90084-Q

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