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    Camaric acid
    Camaric acid
    Information
    CAS No. 146450-83-1 Price
    Catalog No.CFN99606Purity>=98%
    Molecular Weight568.8 Type of CompoundTriterpenoids
    FormulaC35H52O6Physical DescriptionPowder
    Download Manual    COA    MSDSSimilar structuralComparison (Web)
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    According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
    Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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    Our products had been exported to the following research institutions and universities, And still growing.
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    Related Libraries
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  • Biological Activity
    Description: Camaric acid shows antibacterial activity against Staphylococcus aureus and methicillin resistant S. aureus with IC50 values 8.74 and 8.09 uM, respectively, it also shows moderate antileishmanial activity and highly potent antitrypanosomal activity. Camaric acid possesses nematicidal activity. Camaric acid shows significant topical anti-inflammatory activity with IC50 value of 0.67 mg/ear in the assay of TPA mouse ear oedema model.
    Targets: Antifection
    In vitro:
    Chem Biodivers. 2014 May;11(5):709-18.
    Leishmanicidal Triterpenes from Lantana camara.[Pubmed: 24827681]

    METHODS AND RESULTS:
    Two new natural triterpenes, lantaninilic acid and lantoic acid, along with the known triterpenes lantadene A, and oleanolic, ursolic, betulinic, lantanolic, and Camaric acid, were obtained from the aerial parts of Lantana camara through bioassay-guided isolation, monitoring the in vitro antileishmanial activity against promastigotes of Leishmania major. Oleanolic acid (3), ursolic acid (4), lantadene A (5), and lantanilic acid (7) showed significant leishmanicidal activities with IC50 values of 53.0, 12.4, 20.4, and 21.3 μM, respectively. The IC50 value of ursolic acid (4; 12.4 μM) was found to be comparable with that of the standard drugs, pentamidine (IC50 15.0 μM) and amphotericin B (IC50 0.31 μM).
    CONCLUSIONS:
    The in vitro activities of L. camara and its constituents against promastigotes of Leishmania major are reported here for the first time.
    Pharmaceutical Biology, 2008 , 37 (1) :63-66
    Antibacterial Triterpenoids Isolated from Lantana camara.[Reference: WebLink]
    The known triterpenoids lantic acid, Camaric acid, camarinic acid and lantanilic acid were isolated from Lantana camara (L.) cultivated in Egypt.
    METHODS AND RESULTS:
    The antibacterial activity of lantic acid was carried out using bioautography assays for Gram-positive and Gram-negative bacteria. Lantic acid was found to possess strong antibacterial activity against Escherichia coli and Bacillus cereus, in which 0.08 and 0.1 μg were the minimum inhibition doses, respectively, compared to 0.05 and 0.005 μg for chloramphenicol, respectively.
    CONCLUSIONS:
    The results indicate that lantic acid has broad spectrum antibacterial activity and may hold potential as a non-selective antimicrobial agent.
    Fitoterapia. 2004 Jun;75(3-4):327-31.
    Oleanene constituents of Lantana cujabensis.[Pubmed: 15158990]

    METHODS AND RESULTS:
    A new compound, 3beta,25-epoxy-3alpha-hydroxy-22beta-isobutanoyloxyolean-12-ene-28-oic acid (1), and two known triterpenoids lantanilic acid (2) and Camaric acid (3) were isolated from the stem and leaves of Lantana cujabensis. Their structures were elucidated by spectroscopic methods.
    CONCLUSIONS:
    The ethanol extracts did not show significant in vitro antiplasmodial activity against chloroquine-sensitive or resistant strains of Plasmodium falciparum.
    Nat Prod Res. 2005 Sep;19(6):609-13.
    Nematicidal natural products from the aerial parts of Lantana camara Linn.[Pubmed: 16010828]

    METHODS AND RESULTS:
    Lantanilic acid, Camaric acid and oleanolic acid possessing nematicidal activity were isolated from the methanolic extract of the aerial parts of Lantana camara Linn. through bio-assay guided fractionation.
    CONCLUSIONS:
    These compounds exhibited 98%, 95% and 70% mortality respectively against root-knot nematode Meloidogyne incognita at 0.5% concentration. Conventional nematicide furadan showed 100% mortality at this concentration.
    Spatula Dd, 2011,4(1):213-8.
    Antibacterial and cytotoxic triterpenoids from Lantana viburnoides ssp viburnoides var kisi[Reference: WebLink]

    METHODS AND RESULTS:
    The stem and root bark ethanol extracts exhibited strong antibacterial activity against    (195.3 μg/ml) and      (390.6 μg/ml). Camaric acid (1), isolated from the dichloromethane fraction of root bark extract, exhibited antimicrobial activity against   (MIC = 19.5 μg/ml)     (MIC = 19.5 μg/ml)   (MIC = 9.76 μg/ml),    (MIC = 4.88 μg/ml), and  (MIC = 19.5 μg/ml), and was toxic to the shrimps (LC50 = 4.1 μg/ml). Betulinic acid (2) also from the same fraction exhibited poor anti-bacterial activity against all bacteria tested but showed high cytotoxic activity against brine shrimp larvae (LC50 = 2.4 μg/ml).
    CONCLUSIONS:
    Detection of antibacterial activity and isolation of an antibacterial compound, Camaric acid, from extracts of     ssp.     var.  supports the traditional use of extracts of the plant for treatment of gastrointestinal problems. Betulinic acid and Camaric acid are already established to have anticancer activity.
    Camaric acid Description
    Source: The herbs of Lantana camara
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

    After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.7581 mL 8.7904 mL 17.5809 mL 35.1617 mL 43.9522 mL
    5 mM 0.3516 mL 1.7581 mL 3.5162 mL 7.0323 mL 8.7904 mL
    10 mM 0.1758 mL 0.879 mL 1.7581 mL 3.5162 mL 4.3952 mL
    50 mM 0.0352 mL 0.1758 mL 0.3516 mL 0.7032 mL 0.879 mL
    100 mM 0.0176 mL 0.0879 mL 0.1758 mL 0.3516 mL 0.4395 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    Protocol
    Animal Research:
    Kean. OngBoo.,2004.
    Anti-inflammatory activity of camaric acid from Lantana camara[Reference: WebLink]

    METHODS AND RESULTS:
    The chemical studies on the leaves of Lantana camara Linn (Verbanaceae) have successfully afforded linoleic acid, β-sitosterol and phytol together with four pentacyclic triterpenoid acids; oleanonic acid, lantadene B, Camaric acid and oleanolic acid.
    CONCLUSIONS:
    Camaric acid showed significant topical anti-inflammatory activity with IC50 value of 0.67 mg/ear in the assay of TPA mouse ear oedema model.