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Micromeria biflora

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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 UUID643fe35ea70e2710332998
Scientific name Micromeria biflora
Authority Benth.
First published in Labiat. Gen. Spec. : 378 (1834)

Description Top

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Synonyms Top

Scientific name Authority First published in
Satureja biflora Briq. Nat. Pflanzenfam. 4(3a): 299 (1896)
Thymus biflorus Buch.-Ham. ex D.Don Prodr. Fl. Nepal. : 112 (1825)
Micromeria biflora var. indica Elly Walther & K.H.Walther Mitt. Thüring. Bot. Ges. 1(4): 6 (1957)
Clinopodium biflorum Kuntze Revis. Gen. Pl. 2: 515 (1891)

Common names Top

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Language Common/alternative name
Arabic بيوسة
Arabic شمسية
Chinese 姜味草
Chinese 小姜草
Chinese 小香草
Chinese 柏枝草
Chinese 桂子香
Chinese 灵芝草
Chinese 胡椒草

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
  • Asia-temperate
    • China
      • China South-central
    • Western Asia
      • Afghanistan
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • India
      • Pakistan
      • West Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000243157
Tropicos 17600162
KEW urn:lsid:ipni.org:names:451719-1
The Plant List kew-127122
Open Tree Of Life 5801200
Observations.org 119828
NCBI Taxonomy 1898872
IPNI 451719-1
iNaturalist 1181310
GBIF 7307212
EOL 2893962
Elurikkus 586183

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
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Ethnobotanical study of medicinal plants used by the people of Mosop, Nandi County in Kenya Maiyo ZC, Njeru SN, Toroitich FJ, Indieka SA, Obonyo MA Front Pharmacol 19-Jan-2024
PMCID:PMC10834697
doi:10.3389/fphar.2023.1328903
PMID:38313073
HPLC- and NMR-Based Chemical Profiling, Wound-Healing Potential, Anti-Inflammatory and Antibacterial Activities of Satureja pilosa (Lamiaceae), a Neglected Medicinal–Aromatic Herb Panagiotidou C, Burgers LD, Tsadila C, Almpani C, Krigas N, Mossialos D, Rallis MC, Fürst R, Karioti A Plants (Basel) 08-Dec-2023
PMCID:PMC10747026
doi:10.3390/plants12244114
PMID:38140440
Vegetation diversity pattern during spring season in relation to topographic and edaphic variables in sub-tropical zone Ali H, Muhammad Z, Majeed M, Aziz R, Khan A, Mangrio WM, Abdo HG, Almohamad H, Al Dughairi AA Bot Stud 16-Sep-2023
PMCID:PMC10505133
doi:10.1186/s40529-023-00398-5
PMID:37716923
One Pot Synthesis, Biological Efficacy of AuNPs and Au-Amoxicillin Conjugates Functionalized with Crude Flavonoids Extract of Micromeria biflora Jalil K, Ahmad S, Islam N, Ullah R, Jalil Q, Sulaiman S, Sajjad A, Ullah R, Alqahtani AS, Bari A, Hussain H, Ali EA Molecules 09-Apr-2023
PMCID:PMC10140876
doi:10.3390/molecules28083320
PMID:37110554
In Vivo and In Vitro Biological Evaluation and Molecular Docking Studies of Compounds Isolated from Micromeria biflora (Buch. Ham. ex D.Don) Benth Aljohani AS, Alhumaydhi FA, Rauf A, Hamad EM, Rashid U Molecules 24-May-2022
PMCID:PMC9181852
doi:10.3390/molecules27113377
PMID:35684311
Ethnobotanical inventory and medicinal perspectives of herbal flora of Shiwalik mountainous range of District Bhimber, Azad Jammu and Kashmir, Pakistan Ishtiaq M, Khanum H, Hussain I, Parveen A, Maqbool M, Thind S, Hussain T, Azeem M, Shabir F, Elansary HO PLoS One 29-Mar-2022
PMCID:PMC8963552
doi:10.1371/journal.pone.0265028
PMID:35349579
Traditions for Future Cross-National Food Security—Food and Foraging Practices among Different Native Communities in the Western Himalayas Haq SM, Hassan M, Jan HA, Al-Ghamdi AA, Ahmad K, Abbasi AM Biology (Basel) 16-Mar-2022
PMCID:PMC8944997
doi:10.3390/biology11030455
PMID:35336828
Environmental variables drive plant species composition and distribution in the moist temperate forests of Northwestern Himalaya, Pakistan Rahman IU, Hart RE, Ijaz F, Afzal A, Iqbal Z, Calixto ES, Abd_Allah EF, Alqarawi AA, Hashem A, Al-Arjani AB, Kausar R, Haq SM PLoS One 24-Feb-2022
PMCID:PMC8870539
doi:10.1371/journal.pone.0260687
PMID:35202409
Classification and Characterization of the Manoor Valley’s (Lesser Himalaya) Vegetation from the Subtropical-Temperate Ecotonal Forests to the Alpine Pastures along Ecological Variables Rahman IU, Afzal A, Iqbal Z, Alzain MN, Al-Arjani AB, Alqarawi AA, Abd_Allah EF, Ali N, Sakhi S, Khan MA, Khan U, Ijaz F, Mumtaz S, Calixto ES Plants (Basel) 28-Dec-2021
PMCID:PMC8747448
doi:10.3390/plants11010087
PMID:35009089
Species Distribution Pattern and Their Contribution in Plant Community Assembly in Response to Ecological Gradients of the Ecotonal Zone in the Himalayan Region Rahman IU, Afzal A, Iqbal Z, Hashem A, Al-Arjani AB, Alqarawi AA, Abd_Allah EF, Abdalla M, Calixto ES, Sakhi S, Ali N, Bussmann RW Plants (Basel) 04-Nov-2021
PMCID:PMC8623140
doi:10.3390/plants10112372
PMID:34834735
Plants predict the mineral mines – A methodological approach to use indicator plant species for the discovery of mining sites Ahmad Z, Mulk Khan S, Page S, Alamri S, Hashem M J Adv Res 18-Oct-2021
PMCID:PMC9263987
doi:10.1016/j.jare.2021.10.005
PMID:35777902
A Brief Overview of Potential Treatments for Viral Diseases Using Natural Plant Compounds: The Case of SARS-Cov Abiri R, Abdul-Hamid H, Sytar O, Abiri R, Bezerra de Almeida E Jr, Sharma SK, Bulgakov VP, Arroo RR, Malik S Molecules 24-Jun-2021
PMCID:PMC8270261
doi:10.3390/molecules26133868
PMID:34202844
The Botanical, Chemical and Ethnobotanical Diversity of Southern African Lamiaceae Rattray RD, Van Wyk BE Molecules 18-Jun-2021
PMCID:PMC8233991
doi:10.3390/molecules26123712
PMID:34207006
An ethnopharmacological survey and comparative analysis of plants from the Sudhnoti District, Azad Jammu and Kashmir, Pakistan Khan MF, Mashwani ZU, Mehmood A, Qureshi R, Sarwar R, Ahmad KS, Quave CL J Ethnobiol Ethnomed 20-Mar-2021
PMCID:PMC7980561
doi:10.1186/s13002-021-00435-2
PMID:33743778

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 / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol 14529 Click to see CC1=CC=C(C=C1)C(C)(C)O 150.22 unknown https://doi.org/10.1080/10412905.1997.9700709
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1997.9700709
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl acetate 9017 Click to see CC(CCC=C(C)C)CCOC(=O)C 198.30 unknown https://doi.org/10.1080/10412905.1997.9700709
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1997.9700709
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-CITRONELLOL, (+/-)- 8842 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1080/10412905.1997.9700709
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1997.9700709
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.1997.9700709
Citronellal 7794 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1080/10412905.1997.9700709
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1997.9700709
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.1997.9700709
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1997.9700709
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.1997.9700709
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1080/10412905.1997.9700709
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-Isoborneol 6973640 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1997.9700709
(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one 6973628 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1080/10412905.1997.9700709
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene 6451618 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1997.9700709
(1S,2R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol 88298 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1080/10412905.1997.9700709
(1S,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol 10975683 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1080/10412905.1997.9700709
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1080/10412905.1997.9700709
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1997.9700709
3-Thujanone 11027 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1997.9700709
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1997.9700709
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1997.9700709
beta-Thujone 91456 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1997.9700709
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1997.9700709
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1997.9700709
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1080/10412905.1997.9700709
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1080/10412905.1997.9700709
cis-Verbenol 164888 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1080/10412905.1997.9700709
Thujone 261491 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1997.9700709
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1997.9700709
trans-Verbenol 89664 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1080/10412905.1997.9700709
Verbenone 29025 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1080/10412905.1997.9700709
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1997.9700709
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1997.9700709
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1997.9700709
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1080/10412905.1997.9700709
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.1997.9700709
Carvone, (+/-)- 7439 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.1997.9700709
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1997.9700709
Piperitenone 381152 Click to see CC1=CC(=O)C(=C(C)C)CC1 150.22 unknown https://doi.org/10.1080/10412905.1997.9700709
Piperitone 6987 Click to see CC1=CC(=O)C(CC1)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1997.9700709
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1080/10412905.1997.9700709
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700709
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1997.9700709
1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane 5317024 Click to see CC(=C1CCC(C(C1)(C)C(=C)C)(C)C=C)C 218.38 unknown https://doi.org/10.1080/10412905.1997.9700709
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane 6432312 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700709
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1997.9700709
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1997.9700709
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700709
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700709
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1997.9700709
Cedrelanol 160799 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1997.9700709
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700709
trans-Nerolidol 5284507 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1080/10412905.1997.9700709
> 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/10.1080/10412905.1997.9700709
(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/10.1080/10412905.1997.9700709
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexyl)propan-2-ol 547972 Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O 222.37 unknown https://doi.org/10.1080/10412905.1997.9700709
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700709
Elemol 92138 Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O 222.37 unknown https://doi.org/10.1080/10412905.1997.9700709
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Decanal 8175 Click to see CCCCCCCCCC=O 156.26 unknown https://doi.org/10.1080/10412905.1997.9700709
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown https://doi.org/10.1080/10412905.1997.9700709
Octanal 454 Click to see CCCCCCCC=O 128.21 unknown https://doi.org/10.1080/10412905.1997.9700709
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one 9862 Click to see CC(=CCCC(=O)C)C 126.20 unknown https://doi.org/10.1080/10412905.1997.9700709

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Collections Top

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