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Haploclathra paniculata

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64405b75ef8ca379486216
Scientific name Haploclathra paniculata
Authority Benth.
First published in J. Proc. Linn. Soc., Bot. 5: 64 (1860)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Caraipa paniculata Mart. Nov. Gen. Sp. Pl. 1: 104 (1826)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Haploclathra paniculata var. verticillata (Ducke) Lleras Mem. New York Bot. Gard. 22(4): 134 (1972)
Haploclathra paniculata var. paniculata Unknown

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
    • Western South America
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001295699
Tropicos 7800266
KEW urn:lsid:ipni.org:names:828939-1
The Plant List tro-7800266
Open Tree Of Life 576891
NCBI Taxonomy 280743
IPNI 828939-1
GBIF 7330014
EOL 5711016

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
A 1,3,7,8-tetraoxygenated xanthone from haploclathra paniculata Tanus J. Nagem, José C.Da Silveira Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84543-4
Clathraxanthone, a 1,2,7-trioxygenated xanthone from Haploclathra paniculata Tanus J. Nagem, Marilda C. Da Silva, José C. Da Silveira Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83665-L
Haploxanthone from Haploclathra species Tanus J. Nagem, Jost C. Da Silveira Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97949-4

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 / Biphenyls and derivatives
Aucuparin 442508 Click to see COC1=CC(=CC(=C1O)OC)C2=CC=CC=C2 230.26 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Hexanoic Acid 8892 Click to see 116.16 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
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/10.1016/S0031-9422(00)84543-4
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1-Hydroxy-3,5-dimethoxy-xanthen-9-one 5479773 Click to see COC1=CC=CC2=C1OC3=CC(=CC(=C3C2=O)O)OC 272.25 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
1-Hydroxy-7-methoxyxanthone 12214329 Click to see COC1=CC2=C(C=C1)OC3=CC=CC(=C3C2=O)O 242.23 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
1,3,5-Trimethoxyxanthone 11953368 Click to see 286.28 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
1,3,7-Trihydroxyxanthone 5281635 Click to see 244.20 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
1,5-Dihydroxy-3-methoxyxanthone 5281651 Click to see 258.23 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
1,6-Dihydroxy-2,8-dimethoxy-9H-xanthen-9-one 5465786 Click to see 288.25 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
1,7-Dihydroxy-3,8-dimethoxyxanthone 5281634 Click to see 288.25 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
2,6-Dihydroxy-1,8-dimethoxyxanthen-9-one 129684944 Click to see 288.25 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
2,6,8-Trihydroxy-1-methoxyxanthone 5322072 Click to see 274.22 unknown https://doi.org/10.1016/S0031-9422(00)97949-4
2,7-Dihydroxy-1-methoxyxanthen-9-one 11623029 Click to see COC1=C(C=CC2=C1C(=O)C3=C(O2)C=CC(=C3)O)O 258.23 unknown https://doi.org/10.1016/0031-9422(92)83665-L
2,8-Dihydroxy-1-methoxyxanthone 5464640 Click to see 258.23 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
5-Hydroxy-1,3-dimethoxyxanthone 378687 Click to see 272.25 unknown https://doi.org/10.1016/S0031-9422(00)84543-4
8-Hydroxy-1,2-dimethoxyxanthen-9-one 85948687 Click to see 272.25 unknown https://doi.org/10.1016/S0031-9422(00)84543-4

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Collections Top

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