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Internal ID UUID644014402d8ec777045453
Scientific name Cryptocarya kurzii
Authority Hook.f.
First published in Fl. Brit. India 5: 119 (1886)

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Synonyms Top

Scientific name Authority First published in
Cryptocarya wightiana var. griffithii Meisn. Prodr. 15(1): 70 1864
Cryptocarya argentea Gamble Bull. Misc. Inform. Kew 1910: 144 (1910)
Cryptocarya bicolor Merr. Philipp. J. Sci., C 4: 255 (1909)
Cryptocarya borneensis Kosterm. Reinwardtia 7: 302 (1968)
Cryptocarya kurzii var. argentea (Gamble) Airy Shaw Bull. Misc. Inform. Kew 1939: 535 (1939)
Cryptocarya kurzii var. subsericea Airy Shaw Bull. Misc. Inform. Kew 1939: 535 (1939)

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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
    • Indo-China
      • Myanmar
      • Thailand
    • Malesia
      • Borneo
      • Malaya
      • Philippines
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000627985
Tropicos 17800441
KEW urn:lsid:ipni.org:names:463954-1
The Plant List kew-2746031
Open Tree Of Life 6025994
NCBI Taxonomy 2580227
IUCN Red List 149618584
IPNI 463954-1
iNaturalist 427410
GBIF 4176116

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
Constituents of an Extract of Cryptocarya rubra Housed in a Repository with Cytotoxic and Glucose Transport Inhibitory Effects Ren Y, Yuan C, Qian Y, Chai HB, Chen X, Goetz M, Kinghorn AD J Nat Prod 17-Dec-2013
PMCID:PMC4047178
doi:10.1021/np400809w
PMID:24344605
Kurzilactone from Cryptocarya kurzii T.x. Fu, A. Sévenet, A. Hamid, Hadi, F. Remy, M. Païs Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85065-Y
Flavonone and chalcone derivatives from Cryptocarya kurzii. Fu X, Sévenet T, Remy F, Païs M, Hamid A, Hadi A, Zeng LM J Nat Prod 01-Jul-1993
doi:10.1021/NP50097A021
PMID:8377019

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 / Fatty Acyls / Fatty alcohols
(2S)-2-[(E,2S)-2-hydroxy-4-oxo-6-phenylhex-5-enyl]-2,3-dihydropyran-6-one 5468230 Click to see C1C=CC(=O)OC1CC(CC(=O)C=CC2=CC=CC=C2)O 286.32 unknown https://doi.org/10.1016/0031-9422(93)85065-Y
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(6aS,6bS,8aR,9S,12aR,14aR)-3,9-dihydroxy-4,6a,6b,8a,11,11,14a-heptamethyl-8,9,12,12a,13,14-hexahydro-7H-picene-2,10-dione 162883869 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(C(=O)C5O)(C)C)C)C)C)C)O 450.60 unknown https://doi.org/10.1021/NP50097A021
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
5,6-Dihydro-6-(2-hydroxy-4-oxo-6-phenyl-5-hexenyl)-2h-pyran-2-one 495689 Click to see C1C=CC(=O)OC1CC(CC(=O)C=CC2=CC=CC=C2)O 286.32 unknown https://doi.org/10.1016/0031-9422(93)85065-Y
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(1R,7S,17R,19S)-3,19-dihydroxy-7-phenyl-19-[(E)-2-phenylethenyl]-8,12,18-trioxatetracyclo[15.3.1.02,11.04,9]henicosa-2,4(9),10-triene-5,13-dione 162949389 Click to see C1CC2CC(CC(O2)(C=CC3=CC=CC=C3)O)C4=C(C5=C(C=C4OC(=O)C1)OC(CC5=O)C6=CC=CC=C6)O 526.60 unknown https://doi.org/10.1021/NP50097A021
(1S,5S,17R,19R)-9,19-dihydroxy-5-phenyl-19-[(E)-2-phenylethenyl]-4,12,18-trioxatetracyclo[15.3.1.02,11.03,8]henicosa-2(11),3(8),9-triene-7,13-dione 163099607 Click to see C1CC2CC(CC(O2)(C=CC3=CC=CC=C3)O)C4=C(C=C(C5=C4OC(CC5=O)C6=CC=CC=C6)O)OC(=O)C1 526.60 unknown https://doi.org/10.1021/NP50097A021
Kurziflavolactone A 53477539 Click to see C1CC2CC(CC(O2)(C=CC3=CC=CC=C3)O)C4=C(C=C(C5=C4OC(CC5=O)C6=CC=CC=C6)O)OC(=O)C1 526.60 unknown https://doi.org/10.1021/NP50097A021
kurziflavolactone B 53477540 Click to see C1CC2CC(CC(O2)(C=CC3=CC=CC=C3)O)C4=C(C=C(C5=C4OC(CC5=O)C6=CC=CC=C6)O)OC(=O)C1 526.60 unknown https://doi.org/10.1021/NP50097A021
Kurziflavolactone C 44260093 Click to see C1CC2CC(CC(O2)(C=CC3=CC=CC=C3)O)C4=C(C5=C(C=C4OC(=O)C1)OC(CC5=O)C6=CC=CC=C6)O 526.60 unknown https://doi.org/10.1021/NP50097A021
Kurziflavolactone D 44260094 Click to see C1CC2CC(CC(O2)(C=CC3=CC=CC=C3)O)C4=C(C5=C(C=C4OC(=O)C1)OC(CC5=O)C6=CC=CC=C6)O 526.60 unknown https://doi.org/10.1021/NP50097A021
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(1S,13R,15R)-3,5,15-trihydroxy-15-[(E)-2-phenylethenyl]-4-[(E)-3-phenylprop-2-enoyl]-8,14-dioxatricyclo[11.3.1.02,7]heptadeca-2(7),3,5-trien-9-one 162933642 Click to see C1CC2CC(CC(O2)(C=CC3=CC=CC=C3)O)C4=C(C=C(C(=C4O)C(=O)C=CC5=CC=CC=C5)O)OC(=O)C1 526.60 unknown https://doi.org/10.1021/NP50097A021

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