Vochysia divergens - Unknown
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Internal ID UUID64404fd268710680367728
Scientific name Vochysia divergens
Authority Pohl
First published in Pl. Bras. Icon. Descr. 2: 19 (1828)

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No known synonyms.

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Language Common/alternative name
Arabic فوتشي منتشرة
Portuguese cambará

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil West-central
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001146140
Tropicos 34100067
KEW urn:lsid:ipni.org:names:871064-1
The Plant List tro-34100067
Open Tree Of Life 6123580
IPNI 871064-1
iNaturalist 603439
GBIF 4030794
EOL 5497771

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
Antifungal activity from 14-helical beta-peptides. Karlsson AJ, Pomerantz WC, Weisblum B, Gellman SH, Palecek SP J Am Chem Soc 04-Oct-2006
doi:10.1021/JA064630Y
PMID:17002340
Divergioic Acid, a Triterpene from Vochysia divergens Sonia C. Hess, Franco Delle Monache FapUNIFESP (SciELO) 25-Apr-2005
doi:10.1590/S0103-50531999000200005
Anti-allodynic action of the tormentic acid, a triterpene isolated from plant, against neuropathic and inflammatory persistent pain in mice. Bortalanza LB, Ferreira J, Hess SC, Delle Monache F, Yunes RA, Calixto JB Eur J Pharmacol 25-Oct-2002
doi:10.1016/S0014-2999(02)02428-7
PMID:12398905
Antibacterial activity and phytochemical analysis of Vochysia divergens (Vochysiaceae). Hess SC, Brum RL, Honda NK, Cruz AB, Moretto E, Cruz RB, Messana I, Ferrari F, Cechinel Filho V, Yunes RA J Ethnopharmacol 07-Jul-1995
doi:10.1016/0378-8741(95)01260-K
PMID:7500642

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 / Prenol lipids / Triterpenoids
24-Hydroxytormentic acid 14055737 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)O 504.70 unknown https://doi.org/10.1590/S0103-50531999000200005
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1021/JA064630Y
https://doi.org/10.1590/S0103-50531999000200005
https://doi.org/10.1016/0378-8741(95)01260-K
Sericic acid 124214 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1O)C)C(=O)O)C 504.70 unknown https://doi.org/10.1021/JA064630Y
https://doi.org/10.1016/0378-8741(95)01260-K
https://doi.org/10.1590/S0103-50531999000200005
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/S0014-2999(02)02428-7
> 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/10.1016/0378-8741(95)01260-K
https://doi.org/10.1021/JA064630Y
https://doi.org/10.1590/S0103-50531999000200005
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/10.1016/0378-8741(95)01260-K
https://doi.org/10.1590/S0103-50531999000200005

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