|  Gen info - Canthium is a genus of flowering plants in the family Rubiaceae. They are shrubs and small trees, with deciduous leaves and usually thorny stems.
 - Etymology: The genus  Canthium
       was named by Jean-Baptiste Lamarck in 1785 in Encyclopédie Méthodique. The name is a latinisation of "kantankara". a Malayalam name from Kerala for Canthium coromandelicum. Kantan means "shining" and kara means "spiny shrub". (11)
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     The Canthium taxonomy has been problematic; its final circumscription remains in doubt until phylogenetic studies achieve greater resolution for the clade containing Canthium coromandelicum and its closest relatives. (11)
 Botany• Kuliak-daga is a shrub or a small tree growing up to 2 to 5 meters. Branches are somewhat hairy and armed with sharp, slender axillary spines 5 to 10 millimeters in length. Leaves are ovate to elliptic-ovate, 1 to 2.5 centimeters long, short-petioled, and pointed at both ends. Flowers are greenish-yellow or nearly white, about 6 millimeters long, borne singly in the axils of the leaves. Fruit is red, fleshy, ovoid, about 7 millimeters long.
  • Shrubs, 2-3 m tall; branches flattened to subterete, often rather slender, strigillose to strigose or pilosulous, sometimes with lateral short shoots to 0.5 cm; thorns slender to stout, 3-30 mm, straight, or sometimes absent. Leaves paired along developed stems or sometimes clustered on lateral short shoots; petiole 2-3 mm, strigillose to pilosulous; blade drying papery, ovate to lanceolate or elliptic, 2-6 × 1-3.5 cm, adaxially glabrous or strigillose to hispidulous along principal veins or throughout, abaxially puberulent to strigillose or hispidulous, base rounded or obtuse, apex obtuse, acute, or weakly acuminate; secondary veins 2 or 3 pairs, in abaxial axils with pilosulous and/or foveolate domatia; stipules deciduous after distalmost several nodes, triangular to ovate, 2-3 mm, densely strigillose to strigose, acute. Inflorescences fasciculate, 0.5-1 cm, few flowered, strigillose to glabrescent; peduncles 1-3 mm, each with a pair of triangular bracteoles ca. 1 mm and fused in pairs. Calyx puberulent to glabrous; ovary portion obconic, ca. 0.8 mm; limb 0.5-0.8 mm, truncate to undulate. Corolla white, funnelform, outside glabrous; tube suburceolate, ca. 2 mm; lobes 5, triangular-oblong, ca. 3 mm, acuminate. Ovary 2-locular; stigma ca. 0.5 mm. Drupes yellow, ovoid to subglobose, obovoid, or somewhat dicoccous, laterally somewhat flattened, 15-25 × 10-20 mm, smooth, glabrous, with calyx limb persistent; pyrenes 2, weakly tuberculate. (Flora of China)
  Distribution - Native to the Philippines.
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          Found in dry thickets 
          at low altitudes in Pangasinan, Zambales, Bulacan, Rizal, Camarines, and Sorsogon Provinces in Luzon.
 - Also native to Bangladesh, Borneo, Cambodia, China South-Central, China Southeast, Hainan, Jawa, Lesser Sunda Is., Malaya, Philippines, Sumatera, Vietnam. (6)
 Constituents• Phytochemical study showed 
          the roots to predominantly consist of triterpenes, alkaloids, anthraquinones, 
          steroids, organic acid, phenols and carbohydrates.
 
  • Study of essential oils from C. horridum yielded 27 peaks and identified 26 compounds.  The main components were 1,2-benzenedicarboxylic acid bis(2-methylpropyl) ester (36.08%), bis(2-ethylhexyl) phthalate (13.82%), n-hexadecanoic acid (8.32%), (Z,Z,Z)-9,12,15octadecatrien-1-ol (9.61%) among others.  (1) • Study of CH stems yielded ten compounds: (+)-syringaresinol (1), scoparone (2), scopoletin (3), 3'-methoxy-4'-hydroxy-trans-cinnamaldehyde (4), sinapic aldehyde (5), syringic acid (6), mannitol (7), vanillic acid 4-O-beta-D-glucopyranoside (8), beta-daucosterol (9) and beta-sitosterol (10). (see study below)    (3)
 • Study of stem extract isolated 20 compounds:
        syringaresinol (1), quercetin(2), scoparone(3), scopoletin(4), fraxidin(5), sinapic aldehyde(6), 3-methoxy-4-hydroxy-trans-cinnamaldehyde (7), coniferyl alcohol (8), p-hydroxybenzoic acid (9), vanillic acid (10), syringic acid (11), syringaldehyde (12), di-isobutyl phthalate (13), vanillic acid 4-O-β-D-glucopyranoside(14), 3-(1-C-β-D-glucopyranosyl)-2,6-dihydroxy-5-methoxybenzoic acid (15), mannitol (16), β-daucosterol (17), β-sitosterol (18), nonadecanoic acid (19), dibutyl phthalate (20). (see study below)  (8)
 • Bioassay-guided study of stem extract of C. horridum yielded ten compounds: (+)-syringaresinol (1), scoparone (2), scopoletin (3), 3'-methoxy-4'-hydroxy-trans-cinnamaldehyde (4), sinapic aldehyde (5), syringic acid (6), mannitol (7), vanillic acid 4-O-beta-D-glucopyranoside (8), beta-daucosterol (9), and beta-sitosterol (10). (see study below) (10)
 • Optimized ultrasound-assisted extraction of CH leaves using polyols yielded major antioxidant bioactive compounds, including: 4-(Butoxymethyl) phenol, 3-O-Caffeoyl-4-O-methylquinic acid, Quercetin 3-(2G-glucosylrutinoside), 2,4-Dihydroxybenzoic acid and other bioactive compounds. (see study below) (12)
 Properties- Studies have suggested antimicrobial, antioxidant, cytotoxicity properties.
 Parts used Leaves and bark.
  Uses Edibility
 · In Java, confections are made from the acid fruit. Leaves are pounded in water to prepare a sweet cincau jelly.
 Folkloric
 • In the Philippines, boiled  leaves and bark used to hasten menstruation.
 • In Malaya, plant is used for wounds and fevers.
 • In Indo-China, bark and young twigs used for dysentery.
 • Decoction also used after childbirth.
 • In Indonesia,  used to soothe inflamed eyes. In  Malaysia,  used to heal wounds and promote recovery from childbirth.  (7)
 • In 
Vietnam bark and young stems used to treat dysentery. (7)
 • In China, folk healers of the Lahu people apply mashed leaves on snake bites. Plaster from mashed leaves used for 
          foot pains.
 • In China, used for cough, diabetes and hypertension. (11)
 • Boiled fruits used to treat foot wounds.
 Studies• Anti-Bacterial: Study 
          isolated compounds found for the first time, Carulignan, lupeol, b-sitosterol, 
          among many others. The chloroform fraction showed anti-bacterial activities.
 • Phytochemicals / Antibacterial: Study 
          of the chemical composition of the roots of C horridum yielded triterpene, alkaloid, anthraquinone, steroid, organic acid, phenol, carbohydrates among others. The chloroform fraction was shown to have antibacterial properties.  (2)
 • Constituents / Antimicrobial: Study of CH stems yielded ten compounds. Syringic acid (compound 6) had the highest activity against Bacillus subtilis; syringaresinol (Compound 1) showed good activity against E coli, B subtilis and S aureus.  None of the compounds showed inhibitory activity against Aspergillus niger. (see constituents above) (3)
 • Phenolics / Antioxidant: Study 
          of leaves showed the polyphenol content of 0.4879%. Results show the leaves had strong antioxidant activity, with an IC50 value of 0.35mg/mL.   (5)
 • Antibacterial / Stems:          Bioassay-guided isolated studies of stem extract isolated 20 compounds. Compound 1 showed high inhibitory activity against Escherichia coli, Bacillus subtilis and Staphylococcus aureus. Compounds 3 and 7 had medium activity against these bacteria.  No compounds showed activity against Aspergillus niger. (8)
 • Antimicrobial / Stem:  Bioassay-guided study of C. horridum stem extract yielded ten compounds. Compound 6 showed highest activity against Bacillus subtilis, while compound 1 should good activity against E. coli, B. subtilis and S. aureus. No compound showed activity against Aspergillus niger. (see constituents above) (10)
 • Ultrasound-Assisted Extraction of Compounds Using Polyols  / Leaves: Study evaluated phenolic compounds in C. horridum leaves using UHPLC-ESI-QTOF-MS/MS. Polyols-based ultrasound-assisted extraction resulted in higher amount of bioactive substances and improved in vitro antioxidant properties compared to use of single polyols. The aqueous-polyols extract from CH leaves exhibited low toxicity.  The extract also showed cellular antioxidant properties on NIH/3T3 fibroblasts and reduced melanogenesis in B16F10 melanoma. Study identified potential application of leaves in cosmetic and pharmaceutical applications. (see constituents above) (12)
 
 Availability
 Wild-crafted.
 
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