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Micromelum hirsutum

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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 UUID643ffe61c00b0599064298
Scientific name Micromelum hirsutum
Authority Oliv.
First published in J. Proc. Linn. Soc., Bot. 5(Suppl. 2): 40 (1861)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 月橘
Chinese 粗毛小芸木

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-tropical
    • Indian Subcontinent
      • Bangladesh
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Vietnam
    • Malesia
      • Malaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000452911
Tropicos 50172242
KEW urn:lsid:ipni.org:names:774389-1
Open Tree Of Life 755732
NCBI Taxonomy 159058
IUCN Red List 200400945
IPNI 774389-1
GBIF 3837612

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
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
Discovery of Bioactive Compounds by the UIC-ICBG Drug Discovery Program in the 18 Years Since 1998 Zhang HJ, Li WF, Fong HH, Soejarto DD Molecules 31-Oct-2016
PMCID:PMC6273581
doi:10.3390/molecules21111448
PMID:27809237
Larvae of the parasitoid wasp Ampulex compressa sanitize their host, the American cockroach, with a blend of antimicrobials Herzner G, Schlecht A, Dollhofer V, Parzefall C, Harrar K, Kreuzer A, Pilsl L, Ruther J Proc Natl Acad Sci U S A 07-Jan-2013
PMCID:PMC3557021
doi:10.1073/pnas.1213384110
PMID:23297195
Study on chemical constituents of Picrasma quassioides ZHU Chenchen China Journal of Chinese Materia Medica 01-Jun-2011
doi:10.4268/CJCMM20110714
Anti-Tuberculosis Constituents from the Stem Bark of Micromelum hirsutum Ma C, Case RJ, Wang Y, Zhang HJ, Tan GT, Van Hung N, Cuong NM, Franzblau SG, Soejarto DD, Fong HH, Pauli GF Planta Med 01-Mar-2005
PMCID:PMC2940840
doi:10.1055/s-2005-837826
PMID:15770548

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 / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
5Alpha-Epoxyalantolactone 474521 Click to see CC1CCCC2(C13C(O3)C4C(C2)OC(=O)C4=C)C 248.32 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940840/
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
2-hydroxy-6-methoxy-9H-carbazole-3-carbaldehyde 5278451 Click to see COC1=CC2=C(C=C1)NC3=C2C=C(C(=C3)O)C=O 241.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940840/
3-Methyl-9H-carbazole 20746 Click to see CC1=CC2=C(C=C1)NC3=CC=CC=C32 181.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940840/
6-hydroxy-5-(3-methylbut-2-enyl)-9H-carbazole-3-carbaldehyde 5278450 Click to see CC(=CCC1=C(C=CC2=C1C3=C(N2)C=CC(=C3)C=O)O)C 279.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940840/
6-methoxy-9H-carbazole-3-carbaldehyde 5278452 Click to see COC1=CC2=C(C=C1)NC3=C2C=C(C=C3)C=O 225.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940840/
9H-Carbazole-3-carbaldehyde 504067 Click to see C1=CC=C2C(=C1)C3=C(N2)C=CC(=C3)C=O 195.22 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940840/
9H-Carbazole-3-carboxaldehyde, 2,7-dimethoxy- 5317755 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=C(C(=C3)C=O)OC 255.27 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940840/
Methyl 3-carbazolecarboxylate 504069 Click to see COC(=O)C1=CC2=C(C=C1)NC3=CC=CC=C32 225.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940840/
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
9Z-octadecadien-4R-olide 11323473 Click to see CCCCCCCCC=CCCCCC1CCC(=O)O1 280.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940840/
Dihydro-5-(5-tetradecenyl)-2-(3h)-furanone 6320932 Click to see CCCCCCCCC=CCCCCC1CCC(=O)O1 280.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940840/
> Phenylpropanoids and polyketides / Coumarins and derivatives
Micromelin 73230 Click to see CC12C(O1)C(OC2=O)C3=C(C=C4C(=C3)C=CC(=O)O4)OC 288.25 unknown https://doi.org/10.4268/CJCMM20110714
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Magnolioside 3084335 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.4268/CJCMM20110714
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Santin 5281695 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 344.30 unknown https://doi.org/10.4268/CJCMM20110714

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