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Dasymaschalon dasymaschalum

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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 UUID64400558ccbfb535191009
Scientific name Dasymaschalon dasymaschalum
Authority (Blume) I.M.Turner
First published in Gard. Bull. Singapore 58: 276 (2007)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pelticalyx argentea Griff. Not. Pl. Asiat. 4: 706 (1854)
Uvaria alphonsii Müll.Berol. Ann. Bot. Syst. 4: 67 (1857)
Unona cleistogama Burck ex Boerl. Icon. Bogor. 1: 127 (1899)
Unona dasymaschala Blume Fl. Javae 23-24: 55 (1830)
Unona coelophloea Scheff. Flora 52: 300 (1869)
Unona alphonsii Wall. Numer. List [Wallich] n. 6426. 1832
Dasymaschalon blumei Finet & Gagnep. Mém. Soc. Bot. France 4: 143 (1906)
Dasymaschalon blumei var. suratense Bân Bot. Zhurn. (Moscow & Leningrad) 60: 229 (1975)
Dasymaschalon cleistogamum Merr. Philipp. J. Sci., C 10: 237 (1915)
Dasymaschalon coelophloeum Merr. Philipp. J. Sci., C 10: 237 (1915)
Desmos dasymaschalus Saff. Bull. Torrey Bot. Club 39: 507 (1912)
Uvaria dasymaschala (Blume) Walp. Repert. Bot. Syst. 1: 77 (1842)

Common names Top

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Language Common/alternative name
Thai บุหรง

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
    • Indo-China
      • Andaman Islands
      • Nicobar Nicobar
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000506972
Tropicos 100320634
KEW urn:lsid:ipni.org:names:77085883-1
The Plant List kew-2604143
Open Tree Of Life 541913
NCBI Taxonomy 1202393
IUCN Red List 136138979
IPNI 77085883-1
iNaturalist 430926
GBIF 6027815
CMAUP NPO19311

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
Implementation of a MS/MS database for isoquinoline alkaloids and other annonaceous metabolites Agnès SA, Okpekon T, Kouadio YA, Jagora A, Bréard D, Costa EV, da Silva FM, Koolen HH, Le Ray-Richomme AM, Richomme P, Champy P, Beniddir MA, Le Pogam P Sci Data 06-Jun-2022
PMCID:PMC9170680
doi:10.1038/s41597-022-01345-y
PMID:35668110
DNA Barcoding Medicinal Plant Species from Indonesia Cahyaningsih R, Compton LJ, Rahayu S, Magos Brehm J, Maxted N Plants (Basel) 21-May-2022
PMCID:PMC9147630
doi:10.3390/plants11101375
PMID:35631799
Natural Bioactive Cinnamoyltyramine Alkylamides and Co-Metabolites Evidente A, Masi M Biomolecules 25-Nov-2021
PMCID:PMC8698393
doi:10.3390/biom11121765
PMID:34944409
Floral evolution by simplification in Monanthotaxis (Annonaceae) and hypotheses for pollination system shifts Hoekstra PH, Wieringa JJ, Smets E, Chatrou LW Sci Rep 13-Aug-2018
PMCID:PMC6089970
doi:10.1038/s41598-018-30607-2
PMID:30104579
Organ Homologies and Perianth Evolution in the Dasymaschalon Alliance (Annonaceae): Inner Petal Loss and Its Functional Consequences Guo X, Thomas DC, Saunders RM Front Plant Sci 20-Feb-2018
PMCID:PMC5826315
doi:10.3389/fpls.2018.00174
PMID:29515600
Southeast Asian Medicinal Plants as a Potential Source of Antituberculosis Agent Sanusi SB, Abu Bakar MF, Mohamed M, Sabran SF, Mainasara MM Evid Based Complement Alternat Med 03-Jul-2017
PMCID:PMC5610802
doi:10.1155/2017/7185649
PMID:29081822
Cytotoxic alkaloids from stems, leaves and twigs of Dasymaschalon blumei. Chanakul W, Tuchinda P, Anantachoke N, Pohmakotr M, Piyachaturawat P, Jariyawat S, Suksen K, Jaipetch T, Nuntasaen N, Reutrakul V Fitoterapia 01-Oct-2011
doi:10.1016/J.FITOTE.2011.05.012
PMID:21641972
Trypanocidal constituents of Dracocephalum komarovi Nahoko Uchiyama, Fumiyuki Kiuchi, Michiho Ito, Gisho Honda, Yoshio Takeda, Olimjon K. Khodzhimatov, Ozodbek A. Ashurmetov Elsevier BV 24-Mar-2006
doi:10.1016/J.TET.2006.02.067
A 7-hydroxyaporphine alkaloid from desmos dasymachalus K.C. Chan, H.T. Toh Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81197-8

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
> Alkaloids and derivatives / Aporphines
7,16,18-Trimethoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),9,11,14(19),15,17-octaen-13-one 162868000 Click to see COC1=CC2=C(C(=C1)OC)C3=C4C(=C(C5=C3C(=NC=C5)C2=O)OC)OCO4 365.30 unknown https://doi.org/10.1016/J.FITOTE.2011.05.012
Dicentrinone 177744 Click to see COC1=C(C=C2C(=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O)OC 335.30 unknown https://doi.org/10.1016/S0031-9422(00)81197-8
https://doi.org/10.1016/J.TET.2006.02.067
https://doi.org/10.1016/J.FITOTE.2011.05.012
Oxodiscoguattine 16126692 Click to see COC1=CC2=C(C(=C1)OC)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O 335.30 unknown https://doi.org/10.1016/J.FITOTE.2011.05.012
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
16,17-Dimethoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaen-13-ol 75090874 Click to see CN1CCC2=CC3=C(C4=C2C1C(C5=CC(=C(C=C54)OC)OC)O)OCO3 355.40 unknown https://doi.org/10.1016/S0031-9422(00)81197-8
https://doi.org/10.1016/J.TET.2006.02.067
> Alkaloids and derivatives / Aristolactams
6,14,15-Trimethoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1,3,5,7,9(16),12,14-heptaen-11-one 10859838 Click to see COC1=CC=CC2=C3C4=C(C=C21)NC(=O)C4=CC(=C3OC)OC 309.30 unknown https://doi.org/10.1016/J.FITOTE.2011.05.012
Goniopedaline 183523 Click to see COC1=C(C(=C2C3=C1C4=CC=CC=C4C=C3NC2=O)OC)O 295.29 unknown https://doi.org/10.1016/J.FITOTE.2011.05.012
Griffithinam 5317823 Click to see COC1=CC=CC2=C3C4=C(C=C21)NC(=O)C4=CC(=C3O)OC 295.29 unknown https://doi.org/10.1016/J.FITOTE.2011.05.012
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
3,14-Dihydroxy-13,15-dimethoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1,3,5,7,9(16),12,14-heptaen-11-one 163076198 Click to see COC1=C(C(=C2C3=C(C=C4C=CC=C(C4=C31)O)NC2=O)OC)O 311.29 unknown https://doi.org/10.1016/J.FITOTE.2011.05.012
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,8S,10S)-4-methoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-3-ol 21632855 Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)CO3)O)OC 330.50 unknown via CMAUP database
(3S,4aS,10aR)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-3,6-diol 92966440 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CC(CC3(C)C)O)C)O 302.50 unknown via CMAUP database
(4aR)-1,1-Dimethyl-5,6-dimethoxy-7-isopropyl-1,3,4,10aalpha-tetrahydrophenanthrene-4abeta(2H)-carboxylic acid methyl ester 10761833 Click to see CC(C)C1=C(C(=C2C(=C1)C=CC3C2(CCCC3(C)C)C(=O)OC)OC)OC 372.50 unknown via CMAUP database
11-Hydroxysugiol 10403490 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)O 316.40 unknown via CMAUP database
6alpha-Hydroxydemethylcryptojaponol 76326386 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C(C3C2(CCCC3(C)C)C)O)O)O 332.40 unknown via CMAUP database
Arucatriol 102239782 Click to see CC(C)C1=C(C(=C2C(=C1)C(=CC3=C2C(=O)CCC3(C)C)O)O)O 314.40 unknown via CMAUP database
Carnosic acid 65126 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O 332.40 unknown via CMAUP database
Salvicanol 101607178 Click to see CC(C)C1=C(C(=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O)OC 332.50 unknown via CMAUP database
Sugiol 94162 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Clovanediol 15599878 Click to see CC1(CC(C23C1CCC(C2)(C(CC3)O)C)O)C 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
16-Hydroxycarnosol 12966869 Click to see CC(CO)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O 346.40 unknown via CMAUP database
7-Ethoxyrosmanol 23243693 Click to see CCOC1C2C3C(CCCC3(C4=C(C(=C(C=C14)C(C)C)O)O)C(=O)O2)(C)C 374.50 unknown via CMAUP database
7-O-Methylrosmanol 23243692 Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)OC)O)O 360.40 unknown via CMAUP database
Carnosol 442009 Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O 330.40 unknown via CMAUP database
Galdosol 13966127 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C3C4C2(CCCC4(C)C)C(=O)O3)O)O 344.40 unknown via CMAUP database
Isorosmanol 13820511 Click to see CC(C)C1=C(C(=C2C(=C1)C3C(C4C2(CCCC4(C)C)C(=O)O3)O)O)O 346.40 unknown via CMAUP database
Rosmanol 13966122 Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O 346.40 unknown via CMAUP database
Rosmaquinone 23243691 Click to see CC(C)C1=CC2=C(C(=O)C1=O)C34CCCC(C3C(C2O)OC4=O)(C)C 344.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database

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