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Marsypianthes chamaedrys

Marsypianthes chamaedrys - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fe2a8bcb77945481863
Scientific name Marsypianthes chamaedrys
Authority (Vahl) Kuntze
First published in Revis. Gen. Pl. 2: 524 (1891)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hyptis chamaedrys Willd. Sp. Pl., ed. 4 , 3: 85 (1800)
Hyptis inflata Spreng. Syst. Veg. 2: 731 (1825)
Hyptis lurida Spreng. Syst. Veg. 2: 731 (1825)
Hyptis pseudochamaedrys Poit. Ann. Mus. Hist. Nat. 7: 469 (1806)
Marsypianthes arenosa Brandegee Univ. Calif. Publ. Bot. 10: 418 (1924)
Marsypianthes hyptoides Mart. ex Benth. Labiat. Gen. Spec. : 64 (1833)
Marsypianthes hyptoides var. arenosa Benth. Prodr. 12: 85 (1848)
Marsypianthes hyptoides var. bracteosa Benth. Prodr. 12: 85 (1848)
Marsypianthes hyptoides var. calycina Benth. Prodr. 12: 85 (1848)
Marsypianthes hyptoides var. elatior Benth. Prodr. 12: 85 (1848)
Marsypianthes hyptoides var. eriocephala Benth. Prodr. 12: 85 (1848)
Marsypianthes hyptoides var. umbrosa Benth. Prodr. 12: 85 (1848)
Marsypianthes secundiflora M.Martens & Galeotti Bull. Acad. Roy. Sci. Bruxelles 11(2): 185 (1844)
Marsypianthes sessiliflora C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 531 (1845)
Marsypianthes viscosa Klotzsch Reis. Guiana & Orinoko : 1148 (1841)
Clinopodium chamaedrys Vahl Symb. Bot. 3: 77 (1794)

Common names Top

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Language Common/alternative name
English ortela

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 North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Aruba
      • Cuba
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000236725
USDA Plants MACH3
Tropicos 17601496
INPN 630117
KEW urn:lsid:ipni.org:names:449997-1
The Plant List kew-120967
Open Tree Of Life 1062459
Observations.org 198779
NCBI Taxonomy 986255
IPNI 449997-1
iNaturalist 118916
GBIF 2926970
EPPO MAXCH
EOL 579213
Elurikkus 335747

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
Potential clinical applications of phytopharmaceuticals for the in‐patient management of coagulopathies in COVID‐19 Mukherjee AK, Chattopadhyay DJ Phytother Res 11-Feb-2022
PMCID:PMC9111032
doi:10.1002/ptr.7408
PMID:35147268
Phytotherapies in motion: French Guiana as a case study for cross-cultural ethnobotanical hybridization Tareau MA, Bonnefond A, Palisse M, Odonne G J Ethnobiol Ethnomed 16-Sep-2020
PMCID:PMC7493365
doi:10.1186/s13002-020-00404-1
PMID:32938478
Subtribe Hyptidinae (Lamiaceae): A promising source of bioactive metabolites Bridi H, de Carvalho Meirelles G, Lino von Poser G J Ethnopharmacol 05-Aug-2020
PMCID:PMC7403033
doi:10.1016/j.jep.2020.113225
PMID:32763419
Perspective on the Therapeutics of Anti-Snake Venom Gómez-Betancur I, Gogineni V, Salazar-Ospina A, León F Molecules 09-Sep-2019
PMCID:PMC6767026
doi:10.3390/molecules24183276
PMID:31505752
Brazilian medicinal plants with corroborated anti-inflammatory activities: a review Ribeiro VP, Arruda C, Abd El-Salam M, Bastos JK Pharm Biol 12-Apr-2018
PMCID:PMC6130656
doi:10.1080/13880209.2018.1454480
PMID:29648503
Medicinal Plants for the Treatment of Local Tissue Damage Induced by Snake Venoms: An Overview from Traditional Use to Pharmacological Evidence Félix-Silva J, Silva-Junior AA, Zucolotto SM, Fernandes-Pedrosa MD Evid Based Complement Alternat Med 21-Aug-2017
PMCID:PMC5585606
doi:10.1155/2017/5748256
PMID:28904556
Inhibitory potential of important phytochemicals from Pergularia daemia (Forsk.) chiov., on snake venom (Naja naja) Raghavamma ST, Rama Rao N, Devala Rao G J Genet Eng Biotechnol 25-Nov-2015
PMCID:PMC6299870
doi:10.1016/j.jgeb.2015.11.002
PMID:30647617
Phylogenetic lineages in Pseudocercospora Crous PW, Braun U, Hunter GC, Wingfield MJ, Verkley GJ, Shin HD, Nakashima C, Groenewald JZ Stud Mycol 06-Jun-2012
PMCID:PMC3713886
doi:10.3114/sim0005
PMID:24014898
Essential Oil Composition of<i>Marsypianthes chamaedrys</i>(Vahl) Kuntze Grown in Northeast Brazil Francisco José de Abreu Matos, Maria Iracema Lacerda Machado, Afrânio Aragão Craveiro, José Wilson Alencar, Fábio de Sousa Meneses Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.2001.9699601
Ethnopharmacology of Medicinal Plants of the Pantanal Region (Mato Grosso, Brazil) Bieski IG, Rios Santos F, de Oliveira RM, Espinosa MM, Macedo M, Albuquerque UP, de Oliveira Martins DT Evid Based Complement Alternat Med 26-Feb-2012
PMCID:PMC3303862
doi:10.1155/2012/272749
PMID:22474496
Database Survey of Anti-Inflammatory Plants in South America: A Review de Morais Lima GR, de Albuquerque Montenegro C, de Almeida CL, de Athayde-Filho PF, Barbosa-Filho JM, Batista LM Int J Mol Sci 21-Apr-2011
PMCID:PMC3127143
doi:10.3390/ijms12042692
PMID:21731467
Counteracting effect of glycyrrhizin on the hemostatic abnormalities induced by Bothrops jararaca snake venom Assafim M, Ferreira MS, Frattani FS, Guimarães JA, Monteiro RQ, Zingali RB Br J Pharmacol 05-Jun-2006
PMCID:PMC1617072
doi:10.1038/sj.bjp.0706786
PMID:16751793
Chamaedrydiol, an ursane triterpene from Marsypianthes chamaedrys Fábio de Sousa Menezes, Ângelo Saboia Borsatto, Nuno Alvares Pereira, Francisco José de Abreu Matos, Maria Auxiliadora Coelho Kaplan Elsevier BV 23-Apr-2003
doi:10.1016/S0031-9422(97)01137-0
Molluscicidal constituents of Marsypianthes chamaedrys Fábio de Sousa Menezes, Célia Santos da Silva, Nuno Alvares Pereira, Francisco José de Abreu Matos, Ângelo Saboia Borsatto, Maria Auxiliadora Coelho Kaplan Wiley 25-Aug-2002
doi:10.1002/(SICI)1099-1573(199908/09)13:5<433::AID-PTR457>3.0.CO;2-4

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 / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.2001.9699601
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.2001.9699601
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.2001.9699601
> 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/10.1080/10412905.2001.9699601
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.2001.9699601
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.2001.9699601
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.2001.9699601
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9R,10R,11aR,11bR,13aR,13bS)-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]chrysene-9,10-diol 162878713 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
(1S,3S,4aS,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-1,3-diol 15380486 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(CC(C5(C)C)O)O)C)C)C2C1)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
(2R,3R,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-2,3-diol 15380485 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
(2S,3S,4aR,6aS,6aR,6bR,8aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicene-2,3-diol 163190208 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
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]chrysene-9,10-diol 72745631 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicene-2,3-diol 23132192 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-2,3-diol 57575193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
https://doi.org/10.1002/(SICI)1099-1573(199908/09)13:5<433::AID-PTR457>3.0.CO;2-4
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
https://doi.org/10.1002/(SICI)1099-1573(199908/09)13:5<433::AID-PTR457>3.0.CO;2-4
Epigermanidiol 69569298 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
Germanicol 122857 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
https://doi.org/10.1002/(SICI)1099-1573(199908/09)13:5<433::AID-PTR457>3.0.CO;2-4
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
Lup-20(29)-ene-2alpha,3beta-diol 15127233 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1002/(SICI)1099-1573(199908/09)13:5<433::AID-PTR457>3.0.CO;2-4
https://doi.org/10.1016/S0031-9422(97)01137-0
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
Olean-18-en-3-ol 609334 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
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/10.1002/(SICI)1099-1573(199908/09)13:5<433::AID-PTR457>3.0.CO;2-4
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1002/(SICI)1099-1573(199908/09)13:5<433::AID-PTR457>3.0.CO;2-4
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1002/(SICI)1099-1573(199908/09)13:5<433::AID-PTR457>3.0.CO;2-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(1S,2S,4S,5R,10R,11S,14S,15R,18S)-15-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-5,15-dihydroxy-10,14-dimethyl-3-oxapentacyclo[9.7.0.02,4.05,10.014,18]octadec-7-en-9-one 101942518 Click to see CC1=C(C(=O)OC(C1)C(C)C2(CCC3C2(CCC4C3C5C(O5)C6(C4(C(=O)C=CC6)C)O)C)O)C 470.60 unknown https://doi.org/10.1016/S0031-9422(97)01137-0
> 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/10.1002/(SICI)1099-1573(199908/09)13:5<433::AID-PTR457>3.0.CO;2-4
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1002/(SICI)1099-1573(199908/09)13:5<433::AID-PTR457>3.0.CO;2-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1002/(SICI)1099-1573(199908/09)13:5<433::AID-PTR457>3.0.CO;2-4

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