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Spiranthera odoratissima

Spiranthera odoratissima - 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 UUID64404d8cafa44241625006
Scientific name Spiranthera odoratissima
Authority A.St.-Hil.
First published in Bull. Sci. Soc. Philom. Paris 1823: 130 (1823)

Description Top

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Synonyms Top

Scientific name Authority First published in
Terpnanthus jasminoides Nees & Mart. Nova Acta Phys.-Med. Acad. Caes. Leop.-Carol. Nat. Cur. 11: 178 (1823)
Spiranthera leopoldiana Bamps & A.Robyns Bull. Jard. Bot. Natl. Belg. 54: 483 (1984)

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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No germination or propagation data was added yet.

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
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001133219
Tropicos 28101612
KEW urn:lsid:ipni.org:names:775277-1
The Plant List tro-28101612
Open Tree Of Life 5747742
NCBI Taxonomy 2896588
IPNI 775277-1
iNaturalist 431769
GBIF 7269510

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
Antifungal Activity of Plantago lanceolata and Sida ovata Leaf Extracts against Dermatomycotic Fungi Jiru TM, Getahun M Evid Based Complement Alternat Med 05-Aug-2023
PMCID:PMC10423090
doi:10.1155/2023/9957892
PMID:37576453
Inhibition of Mixed Biofilms of Candida albicans and Staphylococcus aureus by β-Caryophyllene-Gold Nanoparticles Khan F, Tabassum N, Jeong GJ, Jung WK, Kim YM Antibiotics (Basel) 07-Apr-2023
PMCID:PMC10134979
doi:10.3390/antibiotics12040726
PMID:37107087
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831
Harvest time explains substantially more variance in yield, essential oil and quality performances of Salvia officinalis than irrigation and putrescine application Mohammadi-Cheraghabadi M, Modarres-Sanavy SA, Sefidkon F, Mokhtassi-Bidgoli A, Hazrati S Physiol Mol Biol Plants 04-Jan-2023
PMCID:PMC9886791
doi:10.1007/s12298-022-01272-7
PMID:36733840
Toxic Potential of Cerrado Plants on Different Organisms Rocha JD, Carneiro FM, Fernandes AS, Morais JM, Borges LL, Chen-Chen L, de Almeida LM, Bailão EF Int J Mol Sci 22-Mar-2022
PMCID:PMC8998518
doi:10.3390/ijms23073413
PMID:35408775
Integrative Alternative Tactics for Ixodid Control Showler AT, Saelao P Insects 18-Mar-2022
PMCID:PMC8948879
doi:10.3390/insects13030302
PMID:35323601
Effects of water‐deficit stress and putrescine on performances, photosynthetic gas exchange, and chlorophyll fluorescence parameters of Salvia officinalis in two cutting times Mohammadi‐Cheraghabadi M, Modarres‐Sanavy SA, Sefidkon F, Mokhtassi‐Bidgoli A, Hazrati S Food Sci Nutr 26-Feb-2022
PMCID:PMC9094464
doi:10.1002/fsn3.2741
PMID:35592300
Antibacterial Activity and Mode of Action of β-caryophyllene on Bacillus cereus MOO CL, YANG SK, OSMAN MA, YUSWAN MH, LOH JY, LIM WM, LIM SH, LAI KS Pol J Microbiol 12-Mar-2020
PMCID:PMC7256763
doi:10.33073/pjm-2020-007
PMID:32162852
The “Entourage Effect”: Terpenes Coupled with Cannabinoids for the Treatment of Mood Disorders and Anxiety Disorders Ferber SG, Namdar D, Hen-Shoval D, Eger G, Koltai H, Shoval G, Shbiro L, Weller A Curr Neuropharmacol 01-Feb-2020
PMCID:PMC7324885
doi:10.2174/1570159X17666190903103923
PMID:31481004
Essential Oil from Pinus Koraiensis Pinecones Inhibits Gastric Cancer Cells via the HIPPO/YAP Signaling Pathway Zhang Y, Xin C, Qiu J, Wang Z Molecules 25-Oct-2019
PMCID:PMC6864528
doi:10.3390/molecules24213851
PMID:31731517
Anxiolytic-Like Effects of Bergamot Essential Oil Are Insensitive to Flumazenil in Rats Rombolà L, Scuteri D, Adornetto A, Straface M, Sakurada T, Sakurada S, Mizoguchi H, Corasaniti MT, Bagetta G, Tonin P, Morrone LA Evid Based Complement Alternat Med 14-Aug-2019
PMCID:PMC6710760
doi:10.1155/2019/2156873
PMID:31485242
Flavonoids from Brazilian Cerrado: Biosynthesis, Chemical and Biological Profile Peixoto JD, Neves BJ, Vasconcelos FG, Napolitano HB, Barbalho MG, Silva SD, Rosseto LP Molecules 09-Aug-2019
PMCID:PMC6720525
doi:10.3390/molecules24162891
PMID:31395797
…Fell Upas Sits, the Hydra-Tree of Death , or the Phytotoxicity of Trees Lebedev VG, Krutovsky KV, Shestibratov KA Molecules 25-Apr-2019
PMCID:PMC6514861
doi:10.3390/molecules24081636
PMID:31027270
Use of β-caryophyllene to combat bacterial dental plaque formation in dogs Pieri FA, Souza MC, Vermelho LL, Vermelho ML, Perciano PG, Vargas FS, Borges AP, da Veiga-Junior VF, Moreira MA BMC Vet Res 01-Oct-2016
PMCID:PMC5045627
doi:10.1186/s12917-016-0842-1
PMID:27716286
A Systematic Review of the Anxiolytic-Like Effects of Essential Oils in Animal Models de Sousa DP, Soares Hocayen PD, Andrade LN, Andreatini R Molecules 14-Oct-2015
PMCID:PMC6332383
doi:10.3390/molecules201018620
PMID:26473822

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 / Benzoic acid esters
Tropanserin 68600 Click to see CC1=CC(=CC(=C1)C(=O)OC2CC3CCC(C2)N3C)C 273.37 unknown https://doi.org/10.1590/S0103-50532005000800007
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Pinene 15837102 Click to see CC1=C2CC(C2(C)C)CC1 136.23 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> 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/10.1016/S0305-1978(03)00039-5
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> 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/10.1016/S0305-1978(03)00039-5
Germacrene B 5281519 Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C 204.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Auraptene 1550607 Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C 298.40 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,7S,10R,13R,14R,16S,19R,20S)-19-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 98050000 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=CC(=O)OC7O)C)C)C 502.50 unknown https://doi.org/10.1590/S0103-50532010000500016
(2R,7S,10R,13R,14R,16S,19S,20S)-19-(furan-3-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 162918693 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271672/
Evodia fruit 235284 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown https://doi.org/10.1590/S0103-50532010000500016
Limonexin 76419898 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=CC(=O)OC7O)C)C)C 502.50 unknown https://doi.org/10.1590/S0103-50532010000500016
Limonin 179651 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown https://doi.org/10.1590/S0103-50532010000500016
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271672/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
19-(2-hydroxy-5-oxo-2H-furan-4-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 13996851 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=CC(OC7=O)O)C)C)C 502.50 unknown https://doi.org/10.1590/S0103-50532010000500016
Isolimonexic acid 5321282 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=CC(OC7=O)O)C)C)C 502.50 unknown https://doi.org/10.1590/S0103-50532010000500016
methyl (Z)-3-[(1R,2R,4S,7S,8S,10R,12R)-10-acetyloxy-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,13,18-trioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-12-yl]prop-2-enoate 163185981 Click to see CC(=O)OC1CC2(C(OC(=O)C3C2(O3)C4(C1C5(C(CC4=O)C(OC5=O)(C)C)C=CC(=O)OC)C)C6=COC=C6)C 556.60 unknown https://doi.org/10.1590/S0103-50532005000800007
methyl (Z)-3-[(1R,2R,4S,7S,8S,10R,12R)-7-(furan-3-yl)-10-hydroxy-1,8,15,15-tetramethyl-5,13,18-trioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-12-yl]prop-2-enoate 163195246 Click to see CC1(C2CC(=O)C3(C(C2(C(=O)O1)C=CC(=O)OC)C(CC4(C35C(O5)C(=O)OC4C6=COC=C6)C)O)C)C 514.50 unknown https://doi.org/10.1590/S0103-50532005000800007
Methyl 3-[10-acetyloxy-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,13,18-trioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-12-yl]prop-2-enoate 162820375 Click to see CC(=O)OC1CC2(C(OC(=O)C3C2(O3)C4(C1C5(C(CC4=O)C(OC5=O)(C)C)C=CC(=O)OC)C)C6=COC=C6)C 556.60 unknown https://doi.org/10.1590/S0103-50532005000800007
Methyl 3-[7-(furan-3-yl)-10-hydroxy-1,8,15,15-tetramethyl-5,13,18-trioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-12-yl]prop-2-enoate 163067086 Click to see CC1(C2CC(=O)C3(C(C2(C(=O)O1)C=CC(=O)OC)C(CC4(C35C(O5)C(=O)OC4C6=COC=C6)C)O)C)C 514.50 unknown https://doi.org/10.1590/S0103-50532005000800007
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
1-Hydroxyrutaecarpine 10447696 Click to see C1CN2C(=NC3=C(C2=O)C=CC=C3O)C4=C1C5=CC=CC=C5N4 303.30 unknown https://doi.org/10.1590/S0103-50532005000800007
https://doi.org/10.1590/S0100-40422009000800010
d-Evodiamine 442088 Click to see CN1C2C3=C(CCN2C(=O)C4=CC=CC=C41)C5=CC=CC=C5N3 303.40 unknown https://doi.org/10.1590/S0103-50532005000800007
Evodiamine 151289 Click to see CN1C2C3=C(CCN2C(=O)C4=CC=CC=C41)C5=CC=CC=C5N3 303.40 unknown https://doi.org/10.1590/S0103-50532005000800007
Rutaecarpine 65752 Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C4=C1C5=CC=CC=C5N4 287.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271672/
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271672/
https://doi.org/10.1590/S0103-50532010000500016
gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271672/
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
https://doi.org/10.1590/S0103-50532010000500016
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
1-Methyl-2-phenyl-4(1H)-quinolinone 776143 Click to see CN1C2=CC=CC=C2C(=O)C=C1C3=CC=CC=C3 235.28 unknown https://doi.org/10.1590/S0103-50532010000500016
> Phenylpropanoids and polyketides / Coumarins and derivatives
Osthol 10228 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC)C 244.28 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Braylin 618370 Click to see CC1(C=CC2=C3C(=CC(=C2O1)OC)C=CC(=O)O3)C 258.27 unknown https://doi.org/10.1016/S0305-1978(03)00039-5

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