Amphipterygium adstringens - Unknown
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Internal ID UUID644008e69ec84167087390
Scientific name Amphipterygium adstringens
Authority (Schltdl.) Schiede ex Standl.
First published in Contr. U.S. Natl. Herb. 23: 673 (1923)

Description Top

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Amphipterygium adstringens, also known as cuachalalate, is a medicinal plant that has been used in Mexico for centuries. Its bark is the most sought after part of the plant and is believed to have curative effects for various ailments such as malaria, stomach cancer, and ulcers. Due to its popularity, the plant has become endangered and is mainly found in central and southern Mexico. It grows in hot temperatures in deciduous jungles or Quercus and Ilex forests and blooms in the summer. The plant is dioecious, with male and female flowers on separate individuals. Its bark is wrinkled, grayish in color, and has corky protuberances. The leaves are imparipinnate with 3-7 leaflets and have a cuneate base and an obtuse or rounded apex. The plant is also used for dental purposes, as it is believed to harden gums.

Synonyms Top

Scientific name Authority First published in
Juliania adstringens Schltdl. Linnaea 17: 636 (1844)
Hypopterygium adstringens Schltdl. Linnaea 17: 635 (1844)

Common names Top

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Language Common/alternative name
Spanish chalalate
Spanish coachalalate
Spanish cuachalala
Spanish cuachalalate
Spanish juliania adstringens

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southwest

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000531841
Tropicos 16800004
KEW urn:lsid:ipni.org:names:442506-1
The Plant List kew-2634734
Open Tree Of Life 983814
NCBI Taxonomy 124857
IUCN Red List 136749685
IPNI 442506-1
iNaturalist 209860
GBIF 3661100
Freebase /m/0jl0tv4
USDA GRIN 312558
Wikipedia Amphipterygium_adstringens

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
Inflammation in Prostate Cancer: Exploring the Promising Role of Phenolic Compounds as an Innovative Therapeutic Approach Fernandes R, Costa C, Fernandes R, Barros AN Biomedicines 24-Nov-2023
PMCID:PMC10740737
doi:10.3390/biomedicines11123140
PMID:38137361
Virulence factors and quorum sensing as targets of new therapeutic options by plant-derived compounds against bacterial infections caused by human and animal pathogens Kitpipit W, Scholfield CN, Sangkanu S, Nissapatorn V, Pereira MD, Paul AK, Mitsuwan W Vet World 14-Jun-2023
PMCID:PMC10421536
doi:10.14202/vetworld.2023.1346-1355
PMID:37577190
Advances in Cytoprotective Drug Discovery Yurchenko EA, Aminin DL Molecules 02-Jun-2023
PMCID:PMC10254749
doi:10.3390/molecules28114510
PMID:37298986
Ethnobotany, Biological Activities and Phytochemical Compounds of Some Species of the Genus Eryngium (Apiaceae), from the Central-Western Region of Mexico Cárdenas-Valdovinos JG, García-Ruiz I, Angoa-Pérez MV, Mena-Violante HG Molecules 15-May-2023
PMCID:PMC10221068
doi:10.3390/molecules28104094
PMID:37241835
Green Alternatives as Antimicrobial Agents in Mitigating Periodontal Diseases: A Narrative Review Mosaddad SA, Hussain A, Tebyaniyan H Microorganisms 11-May-2023
PMCID:PMC10220622
doi:10.3390/microorganisms11051269
PMID:37317243
Applications of Green Synthesized Metal Nanoparticles — a Review Vijayaram S, Razafindralambo H, Sun YZ, Vasantharaj S, Ghafarifarsani H, Hoseinifar SH, Raeeszadeh M Biol Trace Elem Res 13-Apr-2023
PMCID:PMC10097525
doi:10.1007/s12011-023-03645-9
PMID:37046039
In Vitro Biological Activity and Lymphoma Cell Growth Inhibition by Selected Mexican Medicinal Plants Rodríguez-Garza NE, Quintanilla-Licea R, Romo-Sáenz CI, Elizondo-Luevano JH, Tamez-Guerra P, Rodríguez-Padilla C, Gomez-Flores R Life (Basel) 06-Apr-2023
PMCID:PMC10143981
doi:10.3390/life13040958
PMID:37109486
Green Synthesis and Antiproliferative Activity of Gold Nanoparticles of a Controlled Size and Shape Obtained Using Shock Wave Extracts from Amphipterygium adstringens Torres-Ortiz D, García-Alcocer G, Loske AM, Fernández F, Becerra-Becerra E, Esparza R, Gonzalez-Reyna MA, Estevez M Bioengineering (Basel) 30-Mar-2023
PMCID:PMC10136038
doi:10.3390/bioengineering10040437
PMID:37106624
Antioxidants in Traditional Mexican Medicine and Their Applications as Antitumor Treatments Soto KM, Pérez Bueno JD, Mendoza López ML, Apátiga-Castro M, López-Romero JM, Mendoza S, Manzano-Ramírez A Pharmaceuticals (Basel) 23-Mar-2023
PMCID:PMC10145960
doi:10.3390/ph16040482
PMID:37111239
In Vitro Cytotoxic Activity of Methanol Extracts of Selected Medicinal Plants Traditionally Used in Mexico against Human Hepatocellular Carcinoma Elizondo-Luévano JH, Gomez-Flores R, Verde-Star MJ, Tamez-Guerra P, Romo-Sáenz CI, Chávez-Montes A, Rodríguez-Garza NE, Quintanilla-Licea R Plants (Basel) 27-Oct-2022
PMCID:PMC9659118
doi:10.3390/plants11212862
PMID:36365315
Anti-quorum sensing and biofilm inhibitory effect of some medicinal plants against gram-negative bacterial pathogens: in vitro and in silico investigations Samreen, Qais FA, Ahmad I Heliyon 17-Oct-2022
PMCID:PMC9614860
doi:10.1016/j.heliyon.2022.e11113
PMID:36311355
Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review Salazar-Gómez A, Alonso-Castro AJ Pharmaceuticals (Basel) 31-Aug-2022
PMCID:PMC9505834
doi:10.3390/ph15091095
PMID:36145316
Amphipterygium adstringens (Schltdl.) Schiede ex Standl (Anacardiaceae): An Endemic Plant with Relevant Pharmacological Properties Sotelo-Barrera M, Cília-García M, Luna-Cavazos M, Díaz-Núñez JL, Romero-Manzanares A, Soto-Hernández RM, Castillo-Juárez I Plants (Basel) 02-Jul-2022
PMCID:PMC9268796
doi:10.3390/plants11131766
PMID:35807718
Sustainable multifunctional phenolic lipids as potential therapeutics in Dentistry Dame-Teixeira N, El-Gendy R, Monici Silva I, Holanda CA, de Oliveira AS, Romeiro LA, Do T Sci Rep 03-Jun-2022
PMCID:PMC9166758
doi:10.1038/s41598-022-13292-0
PMID:35662265
Antimicrobial Properties of Compounds Isolated from Syzygium malaccense (L.) Merr. and L.M. Perry and Medicinal Plants Used in French Polynesia Quenon C, Hennebelle T, Butaud JF, Ho R, Samaillie J, Neut C, Lehartel T, Rivière C, Siah A, Bonneau N, Sahpaz S, Anthérieu S, Lebegue N, Raharivelomanana P, Roumy V Life (Basel) 14-May-2022
PMCID:PMC9147835
doi:10.3390/life12050733
PMID:35629400

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2-Heptadecyl-6-hydroxybenzoic acid 14274508 Click to see CCCCCCCCCCCCCCCCCC1=C(C(=CC=C1)O)C(=O)O 376.60 unknown https://doi.org/10.1055/S-2006-962108
https://doi.org/10.1016/0378-8741(91)90032-9
2-hydroxy-6-[(Z)-nonadec-16-enyl]benzoic acid 163185057 Click to see CCC=CCCCCCCCCCCCCCCCC1=C(C(=CC=C1)O)C(=O)O 402.60 unknown https://doi.org/10.1080/14786419.2010.534996
6-Nonadecylsalcylic acid 67451843 Click to see CCCCCCCCCCCCCCCCCCCC1=C(C(=CC=C1)O)C(=O)O 404.60 unknown https://doi.org/10.1080/14786419.2010.534996
https://doi.org/10.1055/S-2006-962108
Anacardic acid 167551 Click to see CCCCCCCCCCCCCCCC1=C(C(=CC=C1)O)C(=O)O 348.50 unknown https://doi.org/10.1080/14786419.2010.534996
https://doi.org/10.1055/S-2006-962108
https://doi.org/10.1016/0378-8741(91)90032-9
Ginkgolic acid 5281858 Click to see CCCCCCC=CCCCCCCCC1=C(C(=CC=C1)O)C(=O)O 346.50 unknown https://doi.org/10.1080/14786419.2010.534996
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(Z,6S)-6-[(1S,2'S,3aS,3'aS,5R,7aS,7'aS)-2'-hydroxy-3a,3'a,7',7',7a-pentamethyl-4,6'-dioxospiro[2,3,6,7-tetrahydro-1H-indene-5,3'-2,4,5,7a-tetrahydro-1H-indene]-1-yl]-2-methylhept-2-enoic acid 162930886 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3(C2=O)C(CC4C3(CCC(=O)C4(C)C)C)O)C)C 486.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
(Z,6S)-6-[(1S,2'S,3aS,3'aS,5S,7aS,7'aR)-2'-hydroxy-3a,3'a,7',7',7a-pentamethyl-4,6'-dioxospiro[2,3,6,7-tetrahydro-1H-indene-5,3'-2,4,5,7a-tetrahydro-1H-indene]-1-yl]-2-methylhept-2-enoic acid 162930885 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3(C2=O)C(CC4C3(CCC(=O)C4(C)C)C)O)C)C 486.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
6-(2'-hydroxy-3a,3'a,7',7',7a-pentamethyl-4,6'-dioxospiro[2,3,6,7-tetrahydro-1H-indene-5,3'-2,4,5,7a-tetrahydro-1H-indene]-1-yl)-2-methylhept-2-enoic acid 72794084 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3(C2=O)C(CC4C3(CCC(=O)C4(C)C)C)O)C)C 486.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(20R,24S)-20,24-Epoxy-25-hydroxydammaran-3-one 4357290 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 458.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
(5R,8R,9S,10R,13R,14R,17S)-17-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 40884713 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 458.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
(8R,9R,10R,14S,17S)-17-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 91884737 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 458.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
Ocotillone 12313665 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 458.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4S,5R,6S,9R,11R,14R,15S,18S,23S)-9-hydroxy-6,10,10,14,15,21,21-heptamethyl-3-oxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 163069229 Click to see CC1(CCC23CCC4(C5(CCC6C(C(CCC6(C5C7C(C4(C2C1)CC3=O)O7)C)O)(C)C)C)C)C 468.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
(1R,2R,4S,5R,6S,9S,11R,14R,15S,18S,23S)-9-hydroxy-6,10,10,14,15,21,21-heptamethyl-3-oxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 163069228 Click to see CC1(CCC23CCC4(C5(CCC6C(C(CCC6(C5C7C(C4(C2C1)CC3=O)O7)C)O)(C)C)C)C)C 468.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
(1S,2S,4S,5R,6S,9R,11R,14R,15S,18S,23R)-9-hydroxy-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 101731365 Click to see CC1(CCC23CCC4(C5(CCC6C(C(CCC6(C5C7C(C4(C2C1)OC3=O)O7)C)O)(C)C)C)C)C 470.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
(24Z)-3alpha-Hydroxy-7,11-dioxo-8,24-tirucalladiene-26-oic acid 9956997 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CC(=O)C3=C2C(=O)CC4C3(CCC(C4(C)C)O)C)C)C 484.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
(5R,7S,8R,9S,10S,13R,14S,17R)-3,7-dihydroxy-4,4,10,13,14-pentamethyl-17-[(E,2R)-5-methylhept-5-en-2-yl]-1,2,3,5,6,7,8,9,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-11-one 101285951 Click to see CC=C(C)CCC(C)C1CCC2(C1(CC(=O)C3C2C(CC4C3(CCC(C4(C)C)O)C)O)C)C 458.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
(E,6S)-2-methyl-6-[(10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]hept-2-enoic acid 6481480 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1080/14786419.2010.534996
(E,6S)-6-[(3R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid 162964135 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1080/14786419.2010.534996
(E,6S)-6-[(3R,5R,9S,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid 162964136 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
(E)-Masticadienonic acid 15560138 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1055/S-2003-45098
https://doi.org/10.1016/J.PHYMED.2003.05.003
(Z,6R)-2-methyl-6-[(9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]hept-2-enoic acid 162966549 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1016/J.JEP.2010.11.057
(Z,6R)-6-[(3R,9R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid 162964138 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1016/J.JEP.2010.11.057
(Z,6S)-2-methyl-6-[(5R,10S,13S,14S,17S)-4,4,10,13,14-pentamethyl-3,7-dioxo-2,5,6,11,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]hept-2-enoic acid 101731362 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2C(=O)CC4C3(CCC(=O)C4(C)C)C)C)C 468.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
(Z,6S)-2-methyl-6-[(5S,10S,13S,14S,17S)-4,4,10,13,14-pentamethyl-3,7-dioxo-2,5,6,11,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]hept-2-enoic acid 162981499 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2C(=O)CC4C3(CCC(=O)C4(C)C)C)C)C 468.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
(Z,6S)-6-[(3R,5R,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-7-oxo-1,2,3,5,6,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid 101731363 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2C(=O)CC4C3(CCC(C4(C)C)O)C)C)C 470.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
(Z,6S)-6-[(3R,5R,9R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-6-oxo-1,2,3,5,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid 101731364 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CC(=O)C4C3(CCC(C4(C)C)O)C)C)C 470.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
(Z,6S)-6-[(3R,5S,9R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-6-oxo-1,2,3,5,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid 162980756 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CC(=O)C4C3(CCC(C4(C)C)O)C)C)C 470.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
(Z,6S)-6-[(3S,5R,9S,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid 162964140 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
11alpha, 12alpha-Epoxyoleanolic lactone 177092 Click to see CC1(CCC23CCC4(C5(CCC6C(C(CCC6(C5C7C(C4(C2C1)OC3=O)O7)C)O)(C)C)C)C)C 470.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
2-Methyl-6-(4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)hept-2-enoic acid 346346 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
3-Epioleanolic acid 11869658 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1055/S-2006-962108
https://doi.org/10.1055/S-2003-45098
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
3-Oxo-olean-12-en-28-oic acid 12313702 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)O)C 454.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
3-Oxolanosta-7,24Z-dien-26-oic acid 73242216 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1016/S0378-8741(99)00047-1
https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
3Alpha-Hydroxymasticadienonic Acid 70692334 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
6-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylhept-2-enoic acid 73719044 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
6-(3-Hydroxy-4,4,10,13,14-pentamethyl-6-oxo-1,2,3,5,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)-2-methylhept-2-enoic acid 72817526 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CC(=O)C4C3(CCC(C4(C)C)O)C)C)C 470.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
6-(3-Hydroxy-4,4,10,13,14-pentamethyl-7-oxo-1,2,3,5,6,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)-2-methylhept-2-enoic acid 78075323 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2C(=O)CC4C3(CCC(C4(C)C)O)C)C)C 470.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
6-(3-hydroxy-4,4,10,13,14-pentamethyl-7,11-dioxo-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylhept-2-enoic acid 72826715 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CC(=O)C3=C2C(=O)CC4C3(CCC(C4(C)C)O)C)C)C 484.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
9-Hydroxy-6,10,10,14,15,21,21-heptamethyl-3-oxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 163069227 Click to see CC1(CCC23CCC4(C5(CCC6C(C(CCC6(C5C7C(C4(C2C1)CC3=O)O7)C)O)(C)C)C)C)C 468.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
9-Hydroxy-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 15598275 Click to see CC1(CCC23CCC4(C5(CCC6C(C(CCC6(C5C7C(C4(C2C1)OC3=O)O7)C)O)(C)C)C)C)C 470.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
CID 11340012 11340012 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
Gaderic acid DM 72787537 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2C(=O)CC4C3(CCC(=O)C4(C)C)C)C)C 468.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
Isomasticadienoic acid 15559980 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1055/S-2006-962108
Masticadienolic acid 102004474 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
Oleanoic acid 485707 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1080/14786419.2010.534996
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
Oleanonic acid 12313704 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)O)C 454.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
> 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/10.1055/S-2006-962108
https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
https://doi.org/10.1055/S-2003-45098
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2003-45098
https://doi.org/10.1016/J.PHYTOCHEM.2003.12.012
https://doi.org/10.1055/S-2006-962108
Beta-Sitosterol 222284 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/J.PHYTOCHEM.2003.12.012

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