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Internal ID UUID64405038bcbd3511414775
Scientific name Anastrophyllum auritum
Authority (Lehm.) Stephani
First published in Sp. Hepat. 2: 120 1901

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Synonyms Top

Scientific name Authority First published in
Anastrophyllum calcaratum Stephani Wiss. Erg. Deut. Zentr.-Afr. Exped., Bot. 2: 113 1910
Anastrophyllum gambaragarae Gola Ann. Bot. (Rome) 6: 274 1907
Anastrophyllum grossitextum Stephani Wiss. Erg. Deut. Zentr.-Afr. Exped., Bot. 2: 114 1910
Anastrophyllum hintzeanum Stephani Sp. Hepat. 6: 106 1917
Sphenolobus savioi Gola Mem. Reale Accad. Sci. Torino, ser. 2, 65: 4 1914

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Database ID/link to page
World Flora Online wfo-0001197651
Tropicos 35187239
INPN 727947
The Plant List tro-35187239
Open Tree Of Life 20969
NCBI Taxonomy 402098
iNaturalist 579806
GBIF 8212730

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Strategies to access the [5-8] bicyclic core encountered in the sesquiterpene, diterpene and sesterterpene series Alleman C, Gadais C, Legentil L, Porée FH Beilstein J Org Chem 03-Mar-2023
PMCID:PMC9989678
doi:10.3762/bjoc.19.23
PMID:36895430
Navigating the Chiral Pool in the Total Synthesis of Complex Terpene Natural Products Brill ZG, Condakes ML, Ting CP, Maimone TJ Chem Rev 15-Mar-2017
PMCID:PMC5638449
doi:10.1021/acs.chemrev.6b00834
PMID:28293944
Sphenolobane and fusicoccane diterpenoids from the liverwort Anastrophyllum auritum Josef Zapp, Gunther Burkhardt, Hans Becker Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90359-5

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(+)-alpha-Barbatene 14037349 Click to see CC1=CCC2(CC1C3(C2(CCC3)C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)90359-5
Fusicocca-2,10(14)-diene 10659816 Click to see CC1CCC2=C(CCC2(CC3=C(CCC13)C)C)C(C)C 272.50 unknown https://doi.org/10.1016/S0031-9422(00)90359-5
Fusicoccadiene 91747810 Click to see CC1CCC2=C(CCC2(CC3=C(CCC13)C)C)C(C)C 272.50 unknown https://doi.org/10.1016/S0031-9422(00)90359-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Fusicoccane diterpenoids
Fusicoauritone 16059571 Click to see CC1CCC2C(CCC2(CC3=C(C(=O)CC13O)C)C)C(C)C 304.50 unknown https://doi.org/10.1016/S0031-9422(00)90359-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Curcumene 92139 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(00)90359-5
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)- 89316 Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)90359-5
delta-Elemene 12309449 Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)90359-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Ent-Spathulenol 13854255 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)90359-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)90359-5
> Organoheterocyclic compounds / Oxanes
(1R,3R,6R,7S,10S,11R,14S)-3,10,14-trimethyl-6-propan-2-yl-15-oxatetracyclo[9.3.1.01,11.03,7]pentadecan-13-one 11098758 Click to see CC1CCC2C(CCC2(CC34C1(O3)CC(=O)C4C)C)C(C)C 304.50 unknown https://doi.org/10.1016/S0031-9422(00)90359-5
(2aR,3S,5aS,6R,8aR,9aR,10aS)-Dodecahydro-3,8a,10a-trimethyl-6-(1-methylethyl)-2H-cyclopenta[6 inverted exclamation marka,7 inverted exclamation marka]cycloocta[1 inverted exclamation marka,2 inverted exclamation marka:1,5]cyclopent[1,2-b]oxiren-2-one 14707341 Click to see CC1CCC2C(CCC2(CC34C1C(=O)CC3(O4)C)C)C(C)C 304.50 unknown https://doi.org/10.1016/S0031-9422(00)90359-5

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