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Internal ID UUID643fd681b320f601222262
Scientific name Andira surinamensis
Authority (Bondt) Splitg. ex Pulle
First published in Enum. Vasc. Pl. Surinam: 229 (1906)

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Synonyms Top

Scientific name Authority First published in
Geoffroea surinamensis Bondt Cort. Geoffr. Surinam.: 9 (1788)
Andira retusa var. oblonga Benth. J. Proc. Linn. Soc., Bot.4(Suppl.): 121 (1860)
Andira surinamensis var. surinamensis (Bondt) Pulle
Andira oblonga Benth. J. Proc. Linn. Soc., Bot.4(Suppl.): 121 (1860)
Andira retusa (Poir.) DC. Prodr. [A. P. de Candolle] 2: 475. 1825 [mid Nov 1825]
Vouacapoua surinamensis Kuntze Revis. Gen. Pl.1: 212 (1891)
Geoffroea pubescens Rich. Actes Soc. Hist. Nat. Paris1: 121 (1792)
Andira retusa var. surinamensis (Bondt) DC. Prodr.2: 476 (1825)
Andira retusa var. paraguariensis Chodat & Hassl. Bull. Herb. Boissier, sér. 2, 4: 894 (1904)
Andira surinamensis var. ovatifoliolata Mattos Loefgrenia58: 3 (1973)

Common names Top

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Language Common/alternative name
Arabic أنديرة سورينامية
Chinese 苏里南甘蓝豆
Chinese 苏里南甘蓝豆木

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Trinidad-Tobago
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000169589
Tropicos 13015710
INPN 733690
KEW urn:lsid:ipni.org:names:12607-2
The Plant List ild-15887
Open Tree Of Life 134778
NCBI Taxonomy 588922
IUCN Red List 144275633
IPNI 12607-2
iNaturalist 415559
GBIF 2952202
EPPO ANDSU
EOL 638839
USDA GRIN 435635
CMAUP NPO10936

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
Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants Kirker GT, Hassan B, Mankowski ME, Eller FJ Insects 18-Jan-2024
PMCID:PMC10816604
doi:10.3390/insects15010069
PMID:38249075
Unveiling the potential anti‐cancer activity of calycosin against multivarious cancers with molecular insights: A promising frontier in cancer research Sohel M, Zahra Shova FT, shuvo S, Mahjabin T, Mojnu Mia M, Halder D, Islam H, Roman Mogal M, Biswas P, Saha HR, Sarkar BC, Mamun AA Cancer Med 17-Jan-2024
PMCID:PMC10905684
doi:10.1002/cam4.6924
PMID:38230908
Present practices and emerging opportunities in bioengineering for slope stabilization in Malaysia: An overview Dorairaj D, Osman N PeerJ 12-Jan-2021
PMCID:PMC7810040
doi:10.7717/peerj.10477
PMID:33520435
Dataset on wood density of trees in ecotone forests in Northern Brazilian Amazonia Farias HL, Silva WR, Perdiz RD, Citó AC, Carvalho LC, Barbosa RI Data Brief 07-Mar-2020
PMCID:PMC7090334
doi:10.1016/j.dib.2020.105378
PMID:32215302
Prunetin Relaxed Isolated Rat Aortic Rings by Blocking Calcium Channels Kim B, Jo C, Choi HY, Lee K Molecules 17-Sep-2018
PMCID:PMC6225200
doi:10.3390/molecules23092372
PMID:30227625
Production and Anti-Melanoma Activity of Methoxyisoflavones from the Biotransformation of Genistein by Two Recombinant Escherichia coli Strains Chiang CM, Chang YJ, Wu JY, Chang TS Molecules 04-Jan-2017
PMCID:PMC6155705
doi:10.3390/molecules22010087
PMID:28054996
NMR spectral assignments of a new [C--O--C] isoflavone dimer from Andira surinamensis. de Almeida JG, Silveira ER, Pessoa OD Magn Reson Chem 01-Jan-2008
doi:10.1002/MRC.2138
PMID:18098226

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
(-)-Isoboldine 6971182 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown via CMAUP database
Isoboldine 133323 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown via CMAUP database
> Alkaloids and derivatives / Pavine alkaloids
(-)-Argemonine 442168 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)OC)OC)OC)OC 355.40 unknown via CMAUP database
(+)-Caryachine 12305286 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O 325.40 unknown via CMAUP database
(1R,12R)-16-Methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol 3082467 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4 325.40 unknown via CMAUP database
(1R,12S)-15,16-dimethoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-1-ol 10948236 Click to see CN1C2CC3=CC4=C(C=C3C1(CC5=CC(=C(C=C25)OC)OC)O)OCO4 355.40 unknown via CMAUP database
(1R,12S)-23-methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-1-ol 11110561 Click to see CN1C2CC3=CC4=C(C=C3C1(CC5=CC6=C(C=C25)OCO6)O)OCO4 339.30 unknown via CMAUP database
(1R,9R)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol 11869664 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O 327.40 unknown via CMAUP database
(1S,12S,20R)-15-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 102304441 Click to see C[N+]1(C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O)[O-] 341.40 unknown via CMAUP database
(1S,12S,20R)-16-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol 102304443 Click to see C[N+]1(C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4)[O-] 341.40 unknown via CMAUP database
(1S,12S)-15-methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 11823545 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O 325.40 unknown via CMAUP database
(1S,12S)-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaene 11012304 Click to see C1C2C3=CC4=C(C=C3CC(N2)C5=CC6=C(C=C51)OCO6)OCO4 309.30 unknown via CMAUP database
(1S,9S)-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2(7),3,5,10,12,14-hexaene-3,12-diol 92856799 Click to see CN1C2CC3=C(C1CC4=CC(=C(C=C24)O)OC)C(=C(C=C3)OC)O 327.40 unknown via CMAUP database
(1S,9S)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol 12300156 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O 327.40 unknown via CMAUP database
Caryachine 44575219 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4 325.40 unknown via CMAUP database
Crychine 193382 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC6=C(C=C25)OCO6)OCO4 323.30 unknown via CMAUP database
Escholtzine 12304178 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC6=C(C=C25)OCO6)OCO4 323.30 unknown via CMAUP database
> Alkaloids and derivatives / Proaporphines
(+)-8,9-Dihydrostepharine 13819281 Click to see COC1=C(C2=C3C(CC24CCC(=O)C=C4)NCCC3=C1)OC 299.40 unknown via CMAUP database
(1'S,2S,4R)-10-methoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1',11-diol 10870351 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(C=C4)O)O)OC 301.40 unknown via CMAUP database
Isoamuronine 12306127 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(=O)C=C4)OC)OC 313.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 336.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
alpha-Tocopherolquinone 2734086 Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Cryptocaryone 10379026 Click to see C1C2C(C=CC(=O)C2=C(C=CC3=CC=CC=C3)O)OC1=O 282.29 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives
6-Methyl-[1,3]dioxolo[4,5-g]isoquinolin-6-ium 2753983 Click to see C[N+]1=CC2=CC3=C(C=C2C=C1)OCO3 188.20 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-(6,7-Dimethoxyisoquinoline-1-ylmethyl)phenol 21814573 Click to see COC1=C(C=C2C(=C1)C=CN=C2CC3=CC=C(C=C3)O)OC 295.30 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
Doryanin 12998814 Click to see CN1C=CC2=CC3=C(C=C2C1=O)OCO3 203.19 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
7-O-Methylcryptochinone A 46939685 Click to see COC1CC2=C(C3C1OC(=O)C3)C(=O)CC(O2)C4=CC=CC=C4 314.30 unknown via CMAUP database
Cryptocaryanone A 10356404 Click to see C1C2C(C=CC3=C2C(=O)CC(O3)C4=CC=CC=C4)OC1=O 282.29 unknown via CMAUP database
Cryptochinone A 46939683 Click to see C1C2C(C(CC3=C2C(=O)CC(O3)C4=CC=CC=C4)O)OC1=O 300.30 unknown via CMAUP database
Cryptochinone B 46939684 Click to see C1C2C(C(CC3=C2C(=O)CC(O3)C4=CC=CC=C4)O)OC1=O 300.30 unknown via CMAUP database
Cryptochinone D 46939686 Click to see COC1CC2=C(C3C1OC(=O)C3)C(=O)CC(O2)C4=CC=CC=C4 314.30 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(1'S,2R,4R)-10,11-dimethoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,6'-cyclohex-2-ene]-1'-ol 10914050 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC=CC4O)OC)OC 315.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Hexacosyl (E)-ferulate 5318033 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 558.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone 688857 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Epitaxifolin 712318 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4H-1-Benzopyran-4-one, 5-hydroxy-3,7-dimethoxy-2-phenyl- 5748697 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=CC=C3)O 298.29 unknown via CMAUP database
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
Mosloflavone 471722 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O)OC 298.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Hydroxy-3,7,8-trimethoxyflavone 21632881 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(=C(O2)C3=CC=CC=C3)OC)OC 328.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin 5280448 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown https://doi.org/10.1002/MRC.2138
Pratensein 5281803 Click to see COC1=C(C=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown https://doi.org/10.1002/MRC.2138
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
7-[3-(1,3-Benzodioxol-5-yl)-4-oxochromen-7-yl]oxy-3-(4-methoxyphenyl)chromen-4-one 163042234 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4=CC5=C(C=C4)C(=O)C(=CO5)C6=CC7=C(C=C6)OCO7 532.50 unknown https://doi.org/10.1002/MRC.2138
Biochanin A 5280373 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O 284.26 unknown https://doi.org/10.1002/MRC.2138
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Prunetin 5281804 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1002/MRC.2138
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Larrein 9993268 Click to see COC1=C(C=CC(=C1O)C(=O)C=CC2=CC=CC=C2)O 270.28 unknown via CMAUP database

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