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Cryptocarya amygdalina

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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 UUID64401433452b1405217032
Scientific name Cryptocarya amygdalina
Authority Nees
First published in Pl. Asiat. Rar. 2: 69 (1831)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cryptocarya ferrea var. scortechinii (Gamble) Ng Gard. Bull. Singapore 57: 66 (2005)
Cryptocarya floribunda Nees Pl. Asiat. Rar. 2: 69 (1831)
Cryptocarya scortechinii Gamble Bull. Misc. Inform. Kew 1910: 143 (1910)
Laurus floribunda Wall. Numer. List: n.° 2593 (1830)

Common names Top

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Language Common/alternative name
Chinese 杏仁厚壳桂

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • Nepal
    • Indo-China
      • Andaman Islands
      • Myanmar
      • Thailand
    • Malesia
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000627764
Tropicos 17800690
KEW urn:lsid:ipni.org:names:463791-1
The Plant List kew-2745829
Open Tree Of Life 6025881
NCBI Taxonomy 2580221
IPNI 463791-1
iNaturalist 560046
GBIF 4178658
EOL 2886413

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
The ethoxycarbonyl group as both activating and protective group in N-acyl-Pictet–Spengler reactions using methoxystyrenes. A short approach to racemic 1-benzyltetrahydroisoquinoline alkaloids Keller M, Sauvageot-Witzku K, Geisslinger F, Urban N, Schaefer M, Bartel K, Bracher F Beilstein J Org Chem 05-Nov-2021
PMCID:PMC8576818
doi:10.3762/bjoc.17.183
PMID:34804241
The Constituents and Synthesis of Cryptamygin‐A from the Stem Bark of <i>Cryptocarya Amygadalina</i> Yu‐Yi Charf, Chia‐Hung Wu, Shwu‐Jen Wu, Tian‐Shung Wu Wiley 01-May-2015
doi:10.1002/JCCS.200200041
Alkaloids and olefinic acids from Cryptocarya amygdalina N. Borthakur, P.K. Mahanta, R.C. Rastogi Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84175-8

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown https://doi.org/10.1002/JCCS.200200041
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1002/JCCS.200200041
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3,4-Dimethoxybenzoic acid 7121 Click to see COC1=C(C=C(C=C1)C(=O)O)OC 182.17 unknown https://doi.org/10.1002/JCCS.200200041
> Benzenoids / Benzene and substituted derivatives / Styrenes
[(E)-3-(2-hydroxyphenyl)prop-2-enyl] acetate 66886152 Click to see CC(=O)OCC=CC1=CC=CC=C1O 192.21 unknown https://doi.org/10.1002/JCCS.200200041
3-(2-Hydroxyphenyl)prop-2-enyl acetate 77162741 Click to see CC(=O)OCC=CC1=CC=CC=C1O 192.21 unknown https://doi.org/10.1002/JCCS.200200041
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(2S,4E,8E,10E,12E)-2-[(1S,2R,3R,4R,6S,7R)-1-tetracyclo[4.3.0.02,4.03,7]non-8-enyl]pentadeca-4,8,10,12-tetraenoic acid 163031963 Click to see CCC=CC=CC=CCCC=CCC(C(=O)O)C12C=CC3C1CC4C3C24 350.50 unknown https://doi.org/10.1016/S0031-9422(00)84175-8
(2S,6E,8E,10E)-2-[(1S,2R,3R,4R,6S,7R)-1-tetracyclo[4.3.0.02,4.03,7]non-8-enyl]trideca-6,8,10-trienoic acid 163076055 Click to see CCC=CC=CC=CCCCC(C(=O)O)C12C=CC3C1CC4C3C24 324.50 unknown https://doi.org/10.1016/S0031-9422(00)84175-8
2-(1-Tetracyclo[4.3.0.02,4.03,7]non-8-enyl)pentadeca-4,8,10,12-tetraenoic acid 163031962 Click to see CCC=CC=CC=CCCC=CCC(C(=O)O)C12C=CC3C1CC4C3C24 350.50 unknown https://doi.org/10.1016/S0031-9422(00)84175-8
2-(1-Tetracyclo[4.3.0.02,4.03,7]non-8-enyl)trideca-6,8,10-trienoic acid 163076054 Click to see CCC=CC=CC=CCCCC(C(=O)O)C12C=CC3C1CC4C3C24 324.50 unknown https://doi.org/10.1016/S0031-9422(00)84175-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
1,1,7,7a-Tetramethyl-1a,4,5,6,7,7b-hexahydrocyclopropa[a]naphthalen-2-one 522300 Click to see CC1CCCC2=CC(=O)C3C(C12C)C3(C)C 218.33 unknown https://doi.org/10.1002/JCCS.200200041
Aristolone 165536 Click to see CC1CCCC2=CC(=O)C3C(C12C)C3(C)C 218.33 unknown https://doi.org/10.1002/JCCS.200200041
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/JCCS.200200041
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/JCCS.200200041
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/JCCS.200200041
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-[2-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]propanoic acid 162849989 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC=CC=C3CCC(=O)O)O)O)O)O)(CO)O 460.40 unknown https://doi.org/10.1002/JCCS.200200041
3-[2-[6-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]propanoic acid 162849988 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC=CC=C3CCC(=O)O)O)O)O)O)(CO)O 460.40 unknown https://doi.org/10.1002/JCCS.200200041
Dihydrocoumaroyl Hexoside 73981563 Click to see C1=CC=C(C(=C1)CCC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 328.31 unknown https://doi.org/10.1002/JCCS.200200041
Dihydromelilotoside 5316728 Click to see C1=CC=C(C(=C1)CCC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 328.31 unknown https://doi.org/10.1002/JCCS.200200041
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1R)-1-[(4-hydroxy-3-methoxyphenyl)methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-ol 101306759 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)O)OC)O)OC 329.40 unknown https://doi.org/10.1016/S0031-9422(00)84175-8
(S)-Laudanine 821396 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)OC)OC 343.40 unknown https://doi.org/10.1016/S0031-9422(00)84175-8
7-Isoquinolinol, 1,2,3,4-tetrahydro-1-((4-hydroxy-3-methoxyphenyl)methyl)-6-methoxy-2-methyl-, (+-)- 14357386 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)O)OC)O)OC 329.40 unknown https://doi.org/10.1016/S0031-9422(00)84175-8
Laudanine 92732 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)OC)OC 343.40 unknown https://doi.org/10.1016/S0031-9422(00)84175-8
> Phenylpropanoids and polyketides / Cinnamaldehydes
2-Hydroxycinnamaldehyde 5318169 Click to see C1=CC=C(C(=C1)C=CC=O)O 148.16 unknown https://doi.org/10.1002/JCCS.200200041
3-Phenyl-propenal 307 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown https://doi.org/10.1002/JCCS.200200041
Cinnamaldehyde 637511 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown https://doi.org/10.1002/JCCS.200200041
o-Hydroxy-trans-cinnamaldehyde 98373 Click to see C1=CC=C(C(=C1)C=CC=O)O 148.16 unknown https://doi.org/10.1002/JCCS.200200041
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1002/JCCS.200200041
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1002/JCCS.200200041
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1002/JCCS.200200041
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1002/JCCS.200200041
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Cinnamyl alcohol 5315892 Click to see C1=CC=C(C=C1)C=CCO 134.17 unknown https://doi.org/10.1002/JCCS.200200041
Phenylallyl alcohol 308 Click to see C1=CC=C(C=C1)C=CCO 134.17 unknown https://doi.org/10.1002/JCCS.200200041
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown https://doi.org/10.1002/JCCS.200200041

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