Cnidoscolus vitifolius - Unknown
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Internal ID UUID644032a351f3a365366545
Scientific name Cnidoscolus vitifolius
Authority Pohl
First published in Pl. Bras. Icon. Descr. 1: 61 (1827)

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Synonyms Top

Scientific name Authority First published in
Jatropha vitifolia Mill. Gard. Dict. ed. 8 : n.º 5 (1768)
Jatropha vitifolia var. obtusifolia Müll.Arg. Prodr. 15(2): 1097 (1866)
Manihot spinosissima Steud. Nomencl. Bot. , ed. 2, 2: 99 (1841)
Jatropha vitifolia var. genuina Müll.Arg. Prodr. 15(2): 1097 (1866)

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Varieties (abbr. var.) Top

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Name Authority First published in
Cnidoscolus vitifolius var. cnicodendrum (Griseb.) Lourteig & O'Donnell Lilloa 9: 116 1943

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000899474
Tropicos 12806499
KEW urn:lsid:ipni.org:names:341797-1
The Plant List kew-44263
Open Tree Of Life 3914555
NCBI Taxonomy 2358363
IPNI 341797-1
iNaturalist 705172
GBIF 3073633

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)!
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Title Authors Publication Released IDs
A Global Overview of Diversity and Phylogeny of the Rust Genus Uromyces Gautam AK, Avasthi S, Verma RK, Sushma, Niranjan M, Devadatha B, Jayawardena RS, Suwannarach N, Karunarathna SC J Fungi (Basel) 14-Jun-2022
PMCID:PMC9224716
doi:10.3390/jof8060633
PMID:35736116
Mycosphaerellaceae – Chaos or clarity? Videira SI, Groenewald JZ, Nakashima C, Braun U, Barreto RW, de Wit PJ, Crous PW Stud Mycol 28-Sep-2017
PMCID:PMC5693839
doi:10.1016/j.simyco.2017.09.003
PMID:29180830
All that glitters is not Ramularia Videira SI, Groenewald JZ, Braun U, Shin HD, Crous PW Stud Mycol 29-Jun-2016
PMCID:PMC4986539
doi:10.1016/j.simyco.2016.06.001
PMID:27570325
Plant Identification Based on Leaf Midrib Cross-Section Images Using Fractal Descriptors da Silva NR, Florindo JB, Gómez MC, Rossatto DR, Kolb RM, Bruno OM PLoS One 19-Jun-2015
PMCID:PMC4475074
doi:10.1371/journal.pone.0130014
PMID:26091501
Acyl lupeols from cnidoscolus vitifolius Rosenei L Brum, Neli K Honda, Sonia C Hess, Alberto J Cavalheiro, Franco Delle Monache Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00069-7

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 / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Acetyl aleuritolic acid 161616 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/S0031-9422(98)00069-7
Acetylaleuritolic acid 429885 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/S0031-9422(98)00069-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) 3-phenylpropanoate 53463243 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)CCC6=CC=CC=C6)C)C 558.90 unknown https://doi.org/10.1016/S0031-9422(98)00069-7
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) hexanoate 78171771 Click to see CCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 524.90 unknown https://doi.org/10.1016/S0031-9422(98)00069-7
Cynanester A 132563 Click to see CCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 524.90 unknown https://doi.org/10.1016/S0031-9422(98)00069-7
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(98)00069-7
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(98)00069-7
Lupeol dihydrocinnamate 185302 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)CCC6=CC=CC=C6)C)C 558.90 unknown https://doi.org/10.1016/S0031-9422(98)00069-7
Lupeol trans-cinnamate 5471662 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC=CC=C6)C)C 556.90 unknown https://doi.org/10.1016/S0031-9422(98)00069-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
[8,8-Dimethyl-10-(3-methylbutanoyloxy)-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] 2-methylbut-2-enoate 75596126 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)CC(C)C 428.50 unknown https://doi.org/10.1016/S0031-9422(98)00069-7

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