Clerodendrum calamitosum - Unknown
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Internal ID UUID6440315c70d39606588703
Scientific name Clerodendrum calamitosum
Authority L.
First published in Mant. Pl. 1: 90 (1767)

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Synonyms Top

Scientific name Authority First published in
Volkameria alternifolia Burm.f. Fl. Indica : 137 (1768)

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Language Common/alternative name
Indonesian bugang
jv bugang
Vietnamese ngọc nữ cúc phương
Chinese 化石樹
Chinese 白蝶大青

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Varieties (abbr. var.) 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
  • Asia-tropical
    • Indian Subcontinent
      • India
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Nicobar Nicobar
    • Malesia
      • Borneo
      • Christmas Island
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000880089
Tropicos 100424896
KEW urn:lsid:ipni.org:names:861967-1
The Plant List kew-42445
Open Tree Of Life 6086132
NCBI Taxonomy 2571307
IPNI 861967-1
iNaturalist 480110
GBIF 3894771
EOL 5387829

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)!
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Title Authors Publication Released IDs
Shallow- and Deep-Water Ophiura Species Produce a Panel of Chlorin Compounds with Potent Photodynamic Anticancer Activities Klimenko A, Huber R, Marcourt L, Tabakaev D, Koval A, Dautov SS, Dautova TN, Wolfender JL, Thew R, Khotimchenko Y, Queiroz EF, Katanaev VL Antioxidants (Basel) 05-Feb-2023
PMCID:PMC9952619
doi:10.3390/antiox12020386
PMID:36829945
Novel Approaches for the Recovery of Natural Pigments with Potential Health Effects Carrillo C, Nieto G, Martínez-Zamora L, Ros G, Kamiloglu S, Munekata PE, Pateiro M, Lorenzo JM, Fernández-López J, Viuda-Martos M, Pérez-Álvarez JÁ, Barba FJ J Agric Food Chem 18-Jan-2022
PMCID:PMC9204822
doi:10.1021/acs.jafc.1c07208
PMID:35040324
Lysophosphatidylcholines and Chlorophyll-Derived Molecules from the Diatom Cylindrotheca closterium with Anti-Inflammatory Activity Lauritano C, Helland K, Riccio G, Andersen JH, Ianora A, Hansen EH Mar Drugs 17-Mar-2020
PMCID:PMC7143213
doi:10.3390/md18030166
PMID:32192075
First identification of marine diatoms with anti-tuberculosis activity Lauritano C, Martín J, de la Cruz M, Reyes F, Romano G, Ianora A Sci Rep 02-Feb-2018
PMCID:PMC5797112
doi:10.1038/s41598-018-20611-x
PMID:29396507
Anti-Tumor Action, Clinical Biochemistry Profile and Phytochemical Constituents of a Pharmacologically Active Fraction of S. crispus in NMU-Induced Rat Mammary Tumour Model Yaacob NS, Yankuzo HM, Devaraj S, Wong JK, Lai CS PLoS One 22-May-2015
PMCID:PMC4441459
doi:10.1371/journal.pone.0126426
PMID:26000968
Cytotoxic pheophorbide-related compounds from Clerodendrum calamitosum and C. cyrtophyllum. Cheng HH, Wang HK, Ito J, Bastow KF, Tachibana Y, Nakanishi Y, Xu Z, Luo TY, Lee KH J Nat Prod 01-Jul-2001
doi:10.1021/NP000595B
PMID:11473423

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 / Triterpenoids
norquadrangularic acid A 10790237 Click to see CC(CCC(=O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)O)O)C)C 462.60 unknown https://doi.org/10.1021/NP000595B
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(2R)-2-[(1S)-1-[(4S,8S,9S,10R,13S,14S)-4-hydroxy-10,13-dimethyl-1-oxo-4,7,8,9,11,12,14,15-octahydrocyclopenta[a]phenanthren-17-yl]ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 46939347 Click to see CC1=C(C(=O)OC(C1)C(C)C2=CCC3C2(CCC4C3CC=C5C4(C(=O)C=CC5O)C)C)CO 452.60 unknown https://doi.org/10.1021/NP000595B
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(1S,2S,10R,14S,15R,16S,17R,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-7-yl]oxy]oxane-3,4,5-triol 160496 Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C 559.80 unknown https://doi.org/10.1021/NP000595B
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
[5-[3-[5-[3-[(5-Hydroxy-3-methylpent-2-enoyl)amino]propyl]-3,6-dioxopiperazin-2-yl]propylamino]-3-methyl-5-oxopent-3-enyl] acetate 163005577 Click to see CC(=CC(=O)NCCCC1C(=O)NC(C(=O)N1)CCCNC(=O)C=C(C)CCOC(=O)C)CCO 494.60 unknown https://doi.org/10.1021/NP000595B
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,3S,4S,5'S,8S,9R,10R,12R)-5'-(furan-3-yl)-3-hydroxy-12-(hydroxymethyl)-10-methylspiro[2-oxatricyclo[6.3.1.04,12]dodecane-9,3'-oxolane]-2'-one 54598293 Click to see CC1CC2C3(C(CCCC3C14CC(OC4=O)C5=COC=C5)C(O2)O)CO 362.40 unknown https://doi.org/10.1021/NP000595B
> Organoheterocyclic compounds / Tetrapyrroles and derivatives / Chlorins
3-(16-ethenyl-11-ethyl-3-methoxycarbonyl-12,17,21,26-tetramethyl-4-oxo-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaen-22-yl)propanoic acid 5901209 Click to see CCC1=C(C2=CC3=C(C(=C(N3)C=C4C(C(C(=N4)C5=C6C(=C(C(=N6)C=C1N2)C)C(=O)C5C(=O)OC)CCC(=O)O)C)C)C=C)C 592.70 unknown https://doi.org/10.1021/NP000595B
3-[(3R,21S,22S)-16-ethenyl-11-ethyl-3-methoxycarbonyl-12,17,21,26-tetramethyl-4-oxo-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaen-22-yl]propanoic acid 5323510 Click to see CCC1=C(C2=CC3=C(C(=C(N3)C=C4C(C(C(=N4)C5=C6C(=C(C(=N6)C=C1N2)C)C(=O)C5C(=O)OC)CCC(=O)O)C)C)C=C)C 592.70 unknown https://doi.org/10.1021/NP000595B

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