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Mandevilla pentlandiana

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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 UUID643fe278486b1114330890
Scientific name Mandevilla pentlandiana
Authority Woodson
First published in Ann. Missouri Bot. Gard. 19: 63 (1932)

Description Top

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Synonyms Top

Scientific name Authority First published in
Laseguea bracteata K.Schum. Nat. Pflanzenfam. 4(2): 171 (1895)
Laseguea hookeri Müll.Arg. Fl. Bras. 6(1): 136 (1860)
Laseguea mandonii Britton Mem. Torrey Bot. Club 4: 220. 1895
Laseguea pentlandiana DC. Ann. Sci. Nat., Bot. , sér. 3, 1: 262 (1844)
Parsonsia bracteata Hook. & Arn. J. Bot. (Hooker) 1: 287 (1834)
Echites hookeri A.DC. Prodr. 8: 476 (1844)
Echites tweedieanus Hieron. Bol. Acad. Nac. Ci. Republ. Argent. 4: 370 (1881)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil South
      • Brazil Southeast
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
    • Western South America
      • Bolivia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000234999
Tropicos 1801913
KEW urn:lsid:ipni.org:names:152033-2
The Plant List kew-119329
Open Tree Of Life 727480
NCBI Taxonomy 387715
IPNI 152033-2
iNaturalist 527639
GBIF 3616744

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
The diversity and evolution of pollination systems in large plant clades: Apocynaceae as a case study Ollerton J, Liede-Schumann S, Endress ME, Meve U, Rech AR, Shuttleworth A, Keller HA, Fishbein M, Alvarado-Cárdenas LO, Amorim FW, Bernhardt P, Celep F, Chirango Y, Chiriboga-Arroyo F, Civeyrel L, Cocucci A, Cranmer L, da Silva-Batista IC, de Jager L, Deprá MS, Domingos-Melo A, Dvorsky C, Agostini K, Freitas L, Gaglianone MC, Galetto L, Gilbert M, González-Ramírez I, Gorostiague P, Goyder D, Hachuy-Filho L, Heiduk A, Howard A, Ionta G, Islas-Hernández SC, Johnson SD, Joubert L, Kaiser-Bunbury CN, Kephart S, Kidyoo A, Koptur S, Koschnitzke C, Lamborn E, Livshultz T, Machado IC, Marino S, Mema L, Mochizuki K, Morellato LP, Mrisha CK, Muiruri EW, Nakahama N, Nascimento VT, Nuttman C, Oliveira PE, Peter CI, Punekar S, Rafferty N, Rapini A, Ren ZX, Rodríguez-Flores CI, Rosero L, Sakai S, Sazima M, Steenhuisen SL, Tan CW, Torres C, Trøjelsgaard K, Ushimaru A, Vieira MF, Wiemer AP, Yamashiro T, Nadia T, Queiroz J, Quirino Z Ann Bot 07-Aug-2018
PMCID:PMC6344220
doi:10.1093/aob/mcy127
PMID:30099492
Cytotoxic Activity of Extracts from Plants of Central Argentina on Sensitive and Multidrug-Resistant Leukemia Cells: Isolation of an Active Principle from Gaillardia megapotamica González ML, Joray MB, Laiolo J, Crespo MI, Palacios SM, Ruiz GM, Carpinella MC Evid Based Complement Alternat Med 10-May-2018
PMCID:PMC5971282
doi:10.1155/2018/9185935
PMID:29861776
Medicinal plants and natural products in amelioration of arsenic toxicity: a short review Bhattacharya S Pharm Biol 08-Dec-2016
PMCID:PMC6130623
doi:10.1080/13880209.2016.1235207
PMID:27931138
Alterations in flowering strategies and sexual allocation of Caragana stenophylla along a climatic aridity gradient Xie L, Guo H, Ma C Sci Rep 15-Sep-2016
PMCID:PMC5024338
doi:10.1038/srep33602
PMID:27628093
Floral Longevity and Nectar Secretion of Platanthera chlorantha (Custer) Rchb. (Orchidaceae) STPICZYŃSKA M Ann Bot 01-Aug-2003
PMCID:PMC4243647
doi:10.1093/aob/mcg124
PMID:12805083
Cardenolide glycosides from the roots of mandevilla pentlandiana Gabriela M. Cabrera, Mónica E. Deluca, Alicia M. Seldes, Eduardo G. Gros, Juan C. Oberti, Janeen Crockett, Michael L. Gross Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)95101-X
Steroidal derivatives from the roots of mandevilla pentlandiana Gabriela Cabrera, Jorge A. Palermo, Alicia M. Seldes, Eduardo G. Gros, Juan Carlos Oberti Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)95209-9

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 / Benzyloxycarbonyls
[(1S)-2-benzamido-1-phenylethyl] acetate 14572463 Click to see CC(=O)OC(CNC(=O)C1=CC=CC=C1)C2=CC=CC=C2 283.32 unknown https://doi.org/10.1016/S0031-9422(00)95101-X
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
3-Acetylsesterstatin 1 21629517 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC(C4(C3CCC5=C4C(=O)OC5)C)O)C)C 444.60 unknown https://doi.org/10.1016/S0031-9422(00)95101-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown https://doi.org/10.1016/S0031-9422(00)95209-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives
16-(Acetyloxy)-3,14-dihydroxycard-20(22)-enolide 288101 Click to see CC(=O)OC1CC2(C3CCC4CC(CCC4(C3CCC2(C1C5=CC(=O)OC5)C)C)O)O 432.50 unknown https://doi.org/10.1016/S0031-9422(00)95101-X
Digitoxigenin 4369270 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CCC4C5=CC(=O)OC5)O)C)O 374.50 unknown https://doi.org/10.1016/S0031-9422(00)95101-X
Oleandrigenin 9802865 Click to see CC(=O)OC1CC2(C3CCC4CC(CCC4(C3CCC2(C1C5=CC(=O)OC5)C)C)O)O 432.50 unknown https://doi.org/10.1016/S0031-9422(00)95101-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
[(3S,5R,10S,13R,14S,16S)-3-[(2R,5S)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate 10055 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)OC(=O)C)O)C)C)O)OC)O 592.70 unknown https://doi.org/10.1016/S0031-9422(00)95101-X
Echugin 202243 Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)OC)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O 843.00 unknown https://doi.org/10.1016/S0031-9422(00)95101-X
Echujin 44566920 Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)OC)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O 843.00 unknown https://doi.org/10.1016/S0031-9422(00)95101-X
Odoroside A 44425145 Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)OC)O 518.70 unknown https://doi.org/10.1016/S0031-9422(00)95101-X
Somalin 12310598 Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)OC)O 518.70 unknown https://doi.org/10.1016/S0031-9422(00)95101-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
[4,10,13,14-Tetramethyl-17-(5-propan-2-ylhept-5-en-2-yl)-1,2,3,4,5,6,7,8,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 73106482 Click to see CC=C(CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4C)OC(=O)C)C)C)C)C(C)C 482.80 unknown https://doi.org/10.1016/S0031-9422(00)95101-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
Methyl 3-[24-hydroxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-2,5,8,11,14,30-hexaoxo-22-oxa-3,6,9,12,15,29-hexazatetracyclo[14.12.2.218,21.123,27]tritriaconta-18,20,23,25,27(31),32-hexaen-7-yl]propanoate 75580660 Click to see CC1C(=O)NC(C(=O)N(C(C(=O)NC(C(=O)N(C2CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC(C(=O)N1)N(C2=O)C)O)C)C)CC5=CC=C(C=C5)OC)C)CCC(=O)OC 828.90 unknown https://doi.org/10.1016/S0031-9422(00)95101-X

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