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Iryanthera laevis

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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 UUID644021f1bef64780478171
Scientific name Iryanthera laevis
Authority Markgr.
First published in Notizbl. Bot. Gart. Berlin-Dahlem 9: 965 (1926)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Spanish cumala

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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil West-central
    • Northern South America
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000732332
Tropicos 21800015
KEW urn:lsid:ipni.org:names:130212-2
The Plant List kew-2866828
PFAF Iryanthera laevis
Open Tree Of Life 6028379
IPNI 130212-2
GBIF 3743937
USDA GRIN 450968

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)!
Title Authors Publication Released IDs
Dihydrochalcones from Iryanthera sagotiana Kazuko Kawanishi, Tomoko Takagaki, Yohei Hashimoto Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85234-7
Flavonolignoid from the fruit of Iryanthera laevis N. Liliana Garzon, E. Luis, S. Cuca, C. Juan, V. Martinez, Massayoshi Yoshida, Otto R. Gottlieb Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83600-6
Diarylpropanes from Iryanthera ulei Lucia M. Conserva, Massayoshi Yoshida, Otto R. Gottlieb Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85388-V
Iryantherins, lignoflavonoids of novel structural types from the myristicaceae Lucia M. Conserva, Massayoshi Yoshida, Otto R. Gottlieb, Juan C. Martinez V, Hugo E. Gottlieb Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85358-M
Flavonoids from Iryanthera laevis Raimundo Braz Filho, Marcelo S. Da Silva, Otto R. Gottlieb Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)83082-2

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenols / Methoxyphenols
5-Methoxy-2-[3-(6-methoxy-1,3-benzodioxol-5-yl)propyl]phenol 162890657 Click to see COC1=CC(=C(C=C1)CCCC2=CC3=C(C=C2OC)OCO3)O 316.30 unknown https://doi.org/10.1016/0031-9422(80)83082-2
6-[3-(2-Hydroxy-4-methoxy-5-methylphenyl)propyl]-1,3-benzodioxol-5-ol 14213548 Click to see CC1=CC(=C(C=C1OC)O)CCCC2=CC3=C(C=C2O)OCO3 316.30 unknown https://doi.org/10.1016/0031-9422(80)83082-2
6-[3-(4-Hydroxy-2-methoxy-5-methylphenyl)propyl]-1,3-benzodioxol-5-ol 15730627 Click to see CC1=CC(=C(C=C1O)OC)CCCC2=CC3=C(C=C2O)OCO3 316.30 unknown https://doi.org/10.1016/0031-9422(80)83082-2
> Organoheterocyclic compounds / Benzodioxoles
4-[3-(6-Hydroxy-1,3-benzodioxol-5-yl)propyl]-2,6-dimethylbenzene-1,3-diol 14213547 Click to see CC1=CC(=C(C(=C1O)C)O)CCCC2=CC3=C(C=C2O)OCO3 316.30 unknown https://doi.org/10.1016/0031-9422(80)83082-2
4-[3-(6-Methoxy-1,3-benzodioxol-5-yl)propyl]benzene-1,3-diol 15730625 Click to see COC1=CC2=C(C=C1CCCC3=C(C=C(C=C3)O)O)OCO2 302.32 unknown https://doi.org/10.1016/0031-9422(80)83082-2
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
1-[2,4-dihydroxy-3-[(1R)-1-(4-hydroxyphenyl)prop-2-enyl]-6-methoxyphenyl]-3-(4-methoxyphenyl)propan-1-one 162920927 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C(=C2O)C(C=C)C3=CC=C(C=C3)O)O)OC 434.50 unknown https://doi.org/10.1016/S0031-9422(00)83600-6
1-[2,4-Dihydroxy-3-[1-(4-hydroxyphenyl)prop-2-enyl]-6-methoxyphenyl]-3-(4-methoxyphenyl)propan-1-one 13915682 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C(=C2O)C(C=C)C3=CC=C(C=C3)O)O)OC 434.50 unknown https://doi.org/10.1016/0031-9422(90)85358-M
https://doi.org/10.1016/S0031-9422(00)83600-6
1-[3-[(1S,2S,3S)-1,4-bis(4-hydroxyphenyl)-2,3-dimethylbutyl]-2,4-dihydroxy-6-methoxyphenyl]-3-(4-methoxyphenyl)propan-1-one 162996894 Click to see CC(CC1=CC=C(C=C1)O)C(C)C(C2=CC=C(C=C2)O)C3=C(C(=C(C=C3O)OC)C(=O)CCC4=CC=C(C=C4)OC)O 570.70 unknown https://doi.org/10.1016/0031-9422(90)85234-7
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
1-[(2R,3S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(E)-3-(4-hydroxyphenyl)prop-2-enyl]-3,4-dihydro-2H-chromen-8-yl]-3-(4-methoxyphenyl)propan-1-one 163185618 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C3=C2OC(C(C3)CC=CC4=CC=C(C=C4)O)C5=CC=C(C=C5)O)O)O 552.60 unknown https://doi.org/10.1016/0031-9422(90)85388-V
1-[5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(E)-3-(4-hydroxyphenyl)prop-2-enyl]-3,4-dihydro-2H-chromen-8-yl]-3-(4-methoxyphenyl)propan-1-one 15160719 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C3=C2OC(C(C3)CC=CC4=CC=C(C=C4)O)C5=CC=C(C=C5)O)O)O 552.60 unknown https://doi.org/10.1016/0031-9422(90)85358-M
1-[5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[3-(4-hydroxyphenyl)prop-2-enyl]-3,4-dihydro-2H-chromen-8-yl]-3-(4-methoxyphenyl)propan-1-one 162964777 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C3=C2OC(C(C3)CC=CC4=CC=C(C=C4)O)C5=CC=C(C=C5)O)O)O 552.60 unknown https://doi.org/10.1016/0031-9422(90)85388-V
2-(6-hydroxy-1,3-benzodioxol-5-yl)-5,8-dimethyl-3,4-dihydro-2H-chromen-7-ol 74977218 Click to see CC1=CC(=C(C2=C1CCC(O2)C3=CC4=C(C=C3O)OCO4)C)O 314.30 unknown https://doi.org/10.1016/0031-9422(80)83082-2
2-(6-hydroxy-1,3-benzodioxol-5-yl)-6,8-dimethyl-3,4-dihydro-2H-chromen-7-ol 74977217 Click to see CC1=CC2=C(C(=C1O)C)OC(CC2)C3=CC4=C(C=C3O)OCO4 314.30 unknown https://doi.org/10.1016/0031-9422(80)83082-2
7,2'-Dihydroxy-5,8-dimethyl-4',5'-methylenedioxyflavan 44257182 Click to see CC1=CC(=C(C2=C1CCC(O2)C3=CC4=C(C=C3O)OCO4)C)O 314.30 unknown https://doi.org/10.1016/0031-9422(80)83082-2
7,2'-Dihydroxy-6,8-dimethyl-4',5'-methylenedioxyflavan 44257181 Click to see CC1=CC2=C(C(=C1O)C)OC(CC2)C3=CC4=C(C=C3O)OCO4 314.30 unknown https://doi.org/10.1016/0031-9422(80)83082-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
1-[(2R,3R)-7-hydroxy-2-(4-hydroxyphenyl)-3-[(E)-3-(4-hydroxyphenyl)prop-2-enyl]-5-methoxy-3,4-dihydro-2H-chromen-8-yl]-3-(4-methoxyphenyl)propan-1-one 163194406 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C3C(=C(C=C2O)OC)CC(C(O3)C4=CC=C(C=C4)O)CC=CC5=CC=C(C=C5)O 566.60 unknown https://doi.org/10.1016/0031-9422(90)85388-V
1-[7-hydroxy-2-(4-hydroxyphenyl)-3-[(E)-3-(4-hydroxyphenyl)prop-2-enyl]-5-methoxy-3,4-dihydro-2H-chromen-8-yl]-3-(4-methoxyphenyl)propan-1-one 15160721 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C3C(=C(C=C2O)OC)CC(C(O3)C4=CC=C(C=C4)O)CC=CC5=CC=C(C=C5)O 566.60 unknown https://doi.org/10.1016/0031-9422(90)85358-M
1-[7-hydroxy-2-(4-hydroxyphenyl)-3-[3-(4-hydroxyphenyl)prop-2-enyl]-5-methoxy-3,4-dihydro-2H-chromen-8-yl]-3-(4-methoxyphenyl)propan-1-one 163094403 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C3C(=C(C=C2O)OC)CC(C(O3)C4=CC=C(C=C4)O)CC=CC5=CC=C(C=C5)O 566.60 unknown https://doi.org/10.1016/0031-9422(90)85388-V
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-2-(6-hydroxy-1,3-benzodioxol-5-yl)-7-methoxy-6,8-dimethyl-3,4-dihydro-2H-chromen-5-ol 162848988 Click to see CC1=C(C2=C(C(=C1OC)C)OC(CC2)C3=CC4=C(C=C3O)OCO4)O 344.40 unknown https://doi.org/10.1016/0031-9422(80)83082-2
(2S)-2-(6-hydroxy-1,3-benzodioxol-5-yl)-7-methoxy-6,8-dimethyl-3,4-dihydro-2H-chromen-5-ol 162848987 Click to see CC1=C(C2=C(C(=C1OC)C)OC(CC2)C3=CC4=C(C=C3O)OCO4)O 344.40 unknown https://doi.org/10.1016/0031-9422(80)83082-2
5,2'-Dihydroxy-7-methoxy-6,8-dimethyl-4',5'-methylenedioxyflavan 44257195 Click to see CC1=C(C2=C(C(=C1OC)C)OC(CC2)C3=CC4=C(C=C3O)OCO4)O 344.40 unknown https://doi.org/10.1016/0031-9422(80)83082-2
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids
[3-Acetyloxy-5-methoxy-4-[3-(4-methoxyphenyl)propanoyl]phenyl] acetate 162820247 Click to see CC(=O)OC1=CC(=C(C(=C1)OC(=O)C)C(=O)CCC2=CC=C(C=C2)OC)OC 386.40 unknown https://doi.org/10.1016/0031-9422(80)83082-2
[3,5-Dimethoxy-2-[3-(4-methoxyphenyl)propanoyl]phenyl] acetate 162873543 Click to see CC(=O)OC1=CC(=CC(=C1C(=O)CCC2=CC=C(C=C2)OC)OC)OC 358.40 unknown https://doi.org/10.1016/0031-9422(80)83082-2
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',4'-Dihydroxy-3,4,6'-trimethoxydihydrochalcone 15730629 Click to see COC1=C(C=C(C=C1)CCC(=O)C2=C(C=C(C=C2OC)O)O)OC 332.30 unknown https://doi.org/10.1016/0031-9422(90)85234-7
2',4'-Dihydroxy-4,6'-dimethoxydihydrochalcone 637162 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2OC)O)O 302.32 unknown https://doi.org/10.1016/S0031-9422(00)83600-6
3-(4-Methoxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one 3086055 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2O)O)O 288.29 unknown https://doi.org/10.1016/S0031-9422(00)83600-6
3-(4-methoxyphenyl)-1-[(9S)-1,6,7-trihydroxy-9-[(2R,3R)-4-(4-hydroxyphenyl)-3-methylbutan-2-yl]-3-methoxy-9H-xanthen-2-yl]propan-1-one 162975895 Click to see CC(CC1=CC=C(C=C1)O)C(C)C2C3=CC(=C(C=C3OC4=CC(=C(C(=C24)O)C(=O)CCC5=CC=C(C=C5)OC)OC)O)O 584.70 unknown https://doi.org/10.1016/0031-9422(90)85388-V
3-(4-methoxyphenyl)-1-[(9S)-1,6,7-trihydroxy-9-[(2S,3R)-4-(4-hydroxyphenyl)-3-methylbutan-2-yl]-3-methoxy-9H-xanthen-2-yl]propan-1-one 162975894 Click to see CC(CC1=CC=C(C=C1)O)C(C)C2C3=CC(=C(C=C3OC4=CC(=C(C(=C24)O)C(=O)CCC5=CC=C(C=C5)OC)OC)O)O 584.70 unknown https://doi.org/10.1016/0031-9422(90)85234-7
3-(4-methoxyphenyl)-1-[1,6,7-trihydroxy-9-[4-(4-hydroxyphenyl)-3-methylbutan-2-yl]-3-methoxy-9H-xanthen-2-yl]propan-1-one 15160717 Click to see CC(CC1=CC=C(C=C1)O)C(C)C2C3=CC(=C(C=C3OC4=CC(=C(C(=C24)O)C(=O)CCC5=CC=C(C=C5)OC)OC)O)O 584.70 unknown https://doi.org/10.1016/0031-9422(90)85358-M
https://doi.org/10.1016/0031-9422(90)85388-V
Flavokawin A 270057 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2OC)OC)O 316.30 unknown https://doi.org/10.1016/0031-9422(80)83082-2

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