Conchigera Research Articles

Preliminary Phytochemical Screening and Determination of Anxiolytic, Analgesic, and Antibacterial Potentials of a Medicinal Plant – Alpinia conchigera Griff

Preliminary Phytochemical Screening and Determination of Anxiolytic, Analgesic, and Antibacterial Potentials of a Medicinal Plant – Alpinia conchigera Griff

Chemical Diversity of Essential Oils from Aerial Parts of Eight Species of Zingiberaceae Family from Vietnam

The objective of this work was to analyze the content and the chemical diversity of the essential oils from the aerial parts of eight species belonging to Zingiberaceae family collected in Binh Chau-Phuoc Buu Nature Reserve, Vietnam. The essential oils were isolated by hydrodistillation and their constituents were investigated by gas chromatography-mass spectrometry. The essential oils from the aerial parts of eight studied species, including Zingiber zerumbet, Zingiber pellitum, Curcuma pierreana, Globba macrocarpa, Globba globulifera, Alpinia conchigera, Stahlianthus campanulatus and Amomum sp. were obtained in a yield of 0.01%, 0.008%, 0.01%, 0.012%, 0.012%, 0.02%, 0.015 and 0.3%, respectively. There were a total of 75 compounds identified from the essential oils obtained from eight studied species. Four main clusters and three subclusters were formed by the cluster analysis. Cluster I consisted of A. conchigera with the presence of β-elemene (51.76%) and caryophyllene (28.1%). Cluster II contained five species, including Z. zerumbet, Z. pellitum, C. pierreana, G. globulifera and S. campanulatus with high concentration of β-pinene (11.81%, 5.32%, 4.43%, 25.42% and 1.57%), caryophyllene (13.61%, 23.45%, 19.78%, 34.26% and 18.72%), caryophyllene oxide (4.66%, 4.00%, 13.65%, 8.15% and 24.69%). Cluster III consisted of G. macrocarpa, and presented 4-isobutylquinoline (24.43%), β-copaene (21.69%), α-farnesene (20.73%), 2-tert-butylquinoline (6.05%), 3-Dihydroxydiphenylamine (5.47%), β-panasinsene (5.13%) as major compounds. Cluster IV contained Amomum sp. and had eucalyptol (25.22%), camphor (24.51%), camphene (14.57%), β-pinene (13.45%), Isoborneol (9.17%), α-Selinene (6.21%) as main constituents. The present study identified a total of 75 compounds of the essential oils from the aerial parts of eight species of the Zingiberaceae family collected in Binh-Chau_Phuoc-Buu Nature Reserve, Southern Vietnam. Four main clusters and three subclusters were formed by the cluster analysis. Cluster I consisted of A. conchigera with the presence of β-elemene (51.76%) and caryophyllene (28.1%). Cluster II contained five species, including Z. zerumbet, Z. pellitum, C. pierreana, G. globulifera and S. campanulatus with high concentration of β-pinene (11.81%, 5.32%, 4.43%, 25.42% and 1.57%), caryophyllene (13.61%, 23.45%, 19.78%, 34.26% and 18.72%), caryophyllene oxide (4.66%, 4.00%, 13.65%, 8.15% and 24.69%). Cluster III consisted of G. macrocarpa, and presented 4-isobutylquinoline (24.43%), β-copaene (21.69%), α-farnesene (20.73%), 2-tert-butylquinoline (6.05%), 3-dihydroxydiphenylamine (5.47%), β-Panasinsene (5.13%) as major compounds. Cluster IV contained Amomum sp. and had eucalyptol (25.22%), camphor (24.51%), camphene (14.57%), β-pinene (13.45%), isoborneol (9.17%), α-selinene (6.21%) as main constituents.

Chemical diversity of essential oils of rhizomes of six species of Zingiberaceae family

In this study, the essential oils from the rhizomes of six species belonging to the Zingiberaceae family, including Zingiber zerumbet, Curcuma pierreana, Globba macrocarpa, Alpinia conchigera, Stahlianthus campanulatus and Amomum sp., collected in Binh Chau-Phuoc Buu Nature Reserve were isolated using hydrodistillation, and their constituents were identified via Gas Chromatography-Mass Spectrometry. A total of 91 constituents have been identified from essential oils. These compounds were classified into 4 clusters by Agglomerative Hierarchical Clustering (AHC) and Principal Component Analysis (PCA) analysis. The principal constituents of the essential oils isolated from four species, C. pierreana, S. campanulatus, A. conchigera, and Z. zerumbet contained camphene (18.82%), α-copaene (11.75%), p-xylene (21.86%), and α-santalene (17.91%), which were significantly different from those in previous reports. Furthermore, this study revealed the chemical constituents of essential oils of G. macrocarpa and Amomum sp. for the first time. Accordingly, artemisia triene (22.21%), β-pinene (13.57%), 4,6,8-trimethylazulene (11.1%), 2-tert-butylquinoline (9.86%), β-patchoulene (7.06%), α-elemene (6.93%), and β-ocimene (6.0%) were the major compounds in essential oils of G. macrocarpa rhizomes whereas the oil of Amomum sp. was found to be rich in 2-carene (21.82%), fenchyl acetate (14.26%), 3-carene (8.28%), bornyl acetate (7.7%), and D-limonene (7.13%).

Chemicals Constituents Isolated from Cultivate Alpinia conchigera Griff. and Antimicrobial Activity.

Alpinia conchigera Griff. is a plant species from the family Zingiberaceae. Coloquially known as wild ginger, Alpinia conchigera Griff. is used as food condiment and for traditional treatment of skin diseases. Isolation studies to identify bioactive compounds of rhizomes of Alpinia conchigera yielded seven compounds; 1′S-1′-acetoxychavicol acetate (1), trans-p-coumaryl diacetate (2), p-hydroxycinnamyl acetate (3), 1′S-1′-hydroxychavicol acetate (4) p-hydroxybenzaldehyde (5), stigmasterol (6) and β-sitosterol (7). Compounds 1, 2 and 5 were evaluated for antimicrobial activity against methicillin-resistant Staphylococcus aureus (MRSA). Among the compounds tested, Compound 1 showed good antimicrobial activity against the strain of MRSA with minimum inhibition concentration (MIC) value of 0.5 mg/mL. Meanwhile, Compounds 2 and 5 exhibited moderate activity with MIC value between 1.0 and 2.0 mg/mL. These findings indicate antimicrobial potential of 1′S-1′-acetoxychavicol acetate (1), compound derived from rhizome of Alpinia conchigera Griff. against MRSA, which warrant further investigation.

Hoạt tính kháng oxy hóa và kháng nấm của một số cao chiết thực vật thuộc họ gừng (Zingiberaceae) và họ củ nâu (Dioscoreaceae)

The antioxidant and antifungal activity of ethanol extracts of Curcuma longa, Curcuma yunnanensis, Hedychium coronarium, Alpinia conchigera, Dioscorea bulbifera, Dioscorea membranacea, Dioscorea hispida and Dioscorea pentaphylla were tested. The highest total polyphenol (44,87±0,14 mg GAE/g extract) and flavonoid (110,75±6,38 mg QE/g extract) content were observed in Curcuma longa extract. The correlation was observed between biological activities and the amount of polyphenol, flavonoid compounds. All extracts exhibited antioxidant activity in FRAP (ferric reducing-antioxidant power), ABTS (2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) and RP (reducing power) assay. Poisoned food technique was used to determine the inhibition of mycelial growth, minimum inhibitory concentration, and minimum fungicidal concentration of the extracts on the test pathogens. The C. longa produced complete mycelial growth inhibition in Corynespora cassiicola pathogens at a concentration of 5,000 µg/mL after three days of incubation. The minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) of the C. longa on the test fungi were in the range of 2,500-5,000 ����L/mL and >5000 ����L/mL, respectively. These findings confirm the fungicidal properties of plants extract and their potential use in the management of economically important C. cassiicola and as possible alternatives to synthetic fungicides. C. longa used in this study could be potential sources of new antifungal and antioxidant.

A literature-based phyto-pharmacological review on A. conchigera Griff

This paper aims to sketch an up-to-date phyto-pharmacological reports on Alpinia conchigera Griff. For this, published scientific reports found in the databases: PubMed, Science Direct and Google Scholar were considered. The findings suggest that A. conchigera contains various important secondary metabolites, including alkaloids, steroids, flavonoids, saponins, triterpenes, and phenols. Rhizomes contain essential oils. A. conchigera possesses various important biological activities such as antioxidant, anti-inflammatory and membrane stabilizing, anti-microbial, anthelmintic, larvicidal, anti-diarrheal and anti-motility, anti-cancer, anti-nociceptive, sedative, pesticidal, melanin synthesis inhibitory, anti-pyretic, and anti-atherothrombosis effects. The anti-cancer effects of A. conchigera and its derivatives have been found by causing cytotoxicity, cell cycle arrest, apoptosis, autophagy and anti-proliferative effects in the test systems. Of note, A. conchigera may be one of the best sources of phytotherapeutic lead compounds.

Bactericidal Efficacy of Selected Medicinal Plant Crude Extracts and their Fractions against Common Fish Pathogens

The emergence of new diseases and the increased use of antibiotics have led to the development of resistant bacterial strains. Thus, there is greater attention to seek new antibacterial agents from the natural sources for combating fish diseases in the aquaculture industry. The present study evaluated the bactericidal efficacy of crude methanolic and aqueous extracts from Polygonum chinense, Syzygium polyanthum, Premna foetida, Pimenta dioica, Brucea javanica, Vitex negundo, Alpinia conchigera and Clinacanthus nutans against Vibrio harveyi, Vibrio alginolyticus, Vibrio parahaemolyticus and Aeromonas hydrophila using disc diffusion method. The results showed that methanolic extracts of P. dioica, P. foetida and P. chinense, and aqueous extracts of P. dioica and S. polyanthum showed moderate to strong activity (10.8 to 17.2 mm) against all the tested bacteria. These five potential crude extracts were fractionated using liquid-liquid extraction method to obtain the methanol, dichloromethane and ethyl acetate fractions. Among the fractions, ethyl acetate fraction showed the highest activity against all tested bacteria, with minimum inhibition concentration (MIC) values between 0.625 and 10.000 mg/mL. In addition, the five potential crude extracts had low to moderate toxicity with LC50 >100 μg/mL using brine shrimp cytotoxicity assays. The results of this study indicated that methanolic extracts of P. chinense and P. foetida that showed high bactericidal activity and low toxicity could be good potentials for use in fish culture.

Cardamonin Induces Cell Cycle Arrest, Apoptosis and Alters Apoptosis Associated Gene Expression in WEHI-3 Mouse Leukemia Cells.

Cardamonin, the chalcone class, is one of the natural components from the spicy herbaceous plant (Alpinia conchigera Griff) and has anticancer activities in many human cancer cell lines. There is, however, no information to show that cardamonin induces cell apoptosis and alters apoptosis associated gene expressions in mouse leukemia cells. Thus, we investigated the effects of cardamonin on the apoptotic cell death and associated gene expression in mouse leukemia WEHI-3 cells in vitro. Results indicated that cardamonin decreased total viable cell number via induced cell morphological changes and apoptotic cell death in WEHI-3 cells that were assay by contrast-phase microscopy and flow cytometry examinations, respectively. The flow cytometry assay indicated that cardamonin increased reactive oxygen species (ROS) and Ca production, decreased the levels of mitochondrial membrane potential ( and increased caspase-3, -8 and -9 activities in WEHI-3 cells. Western blotting was performed to analyze expression of relevant pro- and anti-apoptotic proteins and results showed that cardamonin decreased anti-apoptotic protein of Bcl-2 but increased pro-apoptotic protein of Bax in WEHI-3 cells. Furthermore, cardamonin increased cytochrome c, AIF and Endo G release, increased GRP78, caspase-12 that were associated with ER stress and increased Fas, Fas-Ligand and FADD expression. Furthermore, cardamonin increased the gene expressions of DAP (death-associated protein), TMBIM4 transmembrane (BAX inhibitor motif containing 4), ATG5 (autophagy related 5) but decreased the gene expression of DDIT3 (DNA-damage inducible transcript 3), DDIT4 (DNA-damage-inducible transcript 4), BAG6 (BCL2-associated athanogene 6), BCL2L13 [BCL2-like 13 (apoptosis facilitator)] and BRAT1 (BRCA1-associated ATM activator 1) that are associated with apoptosis pathways. Based on those findings, we may suggest cardamonin induced apoptotic cell death through Fas and Fas-Ligand-, caspase- and mitochondria-dependently pathways and also affects the apoptotic gene expression in WEHI-3 cells in vitro.

Preliminary Phytochemical and Pharmacological Screenings of Plumbago indica L. and Alpinia conchigera Griff.

The present study was conducted to evaluate the phytochemical constituents, anti-inflammatory, antipyretic, thrombolytic and CNS modulatory activities of the methanol, chloroform and n-hexane extracts of Plumbago indica L. and Alpinia conchigera Griff. The plants are used in the treatment of inflammations and fever in traditional systems of medicine in Bangladesh. Qualitative tests revealed that the crude extracts of the plants contain reducing sugars, steroids, alkaloids and flavonoids. The anti-inflammatory activity was evaluated by means of protein denaturation and membrane stabilization assay. The methanol extract of P. indica and A. conchigera demonstrated inhibition of protein denaturation by 34.55 and 29.55% while their n-hexane soluble extract exhibited 46.87 and 37.21% inhibition of lysis of erythrocyte membrane, respectively which were considerable as compared to the standard drug acetyl salicylic acid. The methanol extract of P. indica and A. conchigera prominently reduced Brewer’s yeast-induced pyrexia which were close to the standard drug, paracetamol. A considerable thrombolytic activity was exhibited by the chloroform soluble extract of A. conchigera (48.27%) compared to the reference drug, streptokinase (72.13%) in red blood cell clot lysis test. The chloroform soluble materials of P. indica extract demonstrated noticeable reduction of CNS depression activity (63.52 % inhibition of locomotion), compared to reference drug diazepam (80.69 %) in open field experiment. The study justifies the medicinal applications of P. indica and A. conchigera in traditional systems and reveals the bioactivity of the plants which could be suitable for isolation and identification of the bioactive compounds.Dhaka Univ. J. Pharm. Sci. 17(1): 73-79, 2018 (June)

In vitro inhibitory mechanisms and molecular docking of 1′-S-1′-acetoxychavicol acetate on human cytochrome P450 enzymes

BackgroundThe compound, 1′-S-1′-acetoxychavicol acetate (ACA), isolated from the rhizomes of a Malaysian ethno-medicinal plant, Alpinia conchigera Griff. (Zingiberaceae), was previously shown to have potential in vivo antitumour activities. In the development of a new drug entity, potential interactions of the compound with the cytochrome P450 superfamily metabolizing enzymes need to be ascertain. PurposeThe concomitant use of therapeutic drugs may cause potential drug-drug interactions by decreasing or increasing plasma levels of the administered drugs, leading to a suboptimal clinical efficacy or a higher risk of toxicity. Thus, evaluating the inhibitory potential of a new chemical entity, and to clarify the mechanism of inhibition and kinetics in the various CYP enzymes is an important step to predict drug-drug interactions. Study designThis study was designed to assess the potential inhibitory effects of Alpinia conchigera Griff. rhizomes extract and its active constituent, ACA, on nine c-DNA expressed human cytochrome P450s (CYPs) enzymes using fluorescent CYP inhibition assay. Methods/ResultsThe half maximal inhibitory concentration (IC50) of Alpinia conchigera Griff. rhizomes extract and ACA was determined for CYP1A2, CYP2A6, CYP2B6, CYP2C8, CYP2C19, CYP2D6, CYP2E1, CYP3A4 and CYP3A5. A. conchigera extract only moderately inhibits on CYP3A4 (IC50 = 6.76 ± 1.88µg/ml) whereas ACA moderately inhibits the activities of CYP1A2 (IC50 = 4.50 ± 0.10µM), CYP2D6 (IC50 = 7.50 ± 0.17µM) and CYP3A4 (IC50 = 9.50 ± 0.57µM) while other isoenzymes are weakly inhibited. In addition, mechanism-based inhibition studies reveal that CYP1A2 and CYP3A4 exhibited non-mechanism based inhibition whereas CYP2D6 showed mechanism-based inhibition. Lineweaver-Burk plots depict that ACA competitively inhibited both CYP1A2 and CYP3A4, with a Ki values of 2.36 ± 0.03 µM and 5.55 ± 0.06µM, respectively, and mixed inhibition towards CYP2D6 with a Ki value of 4.50 ± 0.08µM. Further, molecular docking studies show that ACA is bound to a few key amino acid residues in the active sites of CYP1A2 and CYP3A4, while one amino residue of CYP2D6 through predominantly Pi-Pi interactions. ConclusionOverall, ACA may demonstrate drug-drug interactions when co-administered with other therapeutic drugs that are metabolized by CYP1A2, CYP2D6 or CYP3A4 enzymes. Further in vivo studies, however, are needed to evaluate the clinical significance of these interactions.

Antimicrobial compounds from Alpinia conchigera

Ethnopharmacological relevanceThe rhizome of Alpinia conchigerahas been used as a condiment in the northern states of Peninsular Malaysia and occasionally in folk medicine in the east coast to treat fungal infections. In some states of Peninsular Malaysia, the rhizomes are consumed as a post-partum medicine and the young shoots are prepared into a vegetable dish. This study aimed to investigate the chemical constituents of the pseudostems and rhizomes of Malaysian Alpinia conchigera and to evaluate the antimicrobial activity of the dichloromethane (DCM) extracts of the pseudostems, rhizomes and the isolated compounds against three selected fungi and five strains of Staphylococcus aureus. Materials and methodsThe dried and ground pseudostems (0.8kg) and rhizomes (1.0kg) were successively extracted in Soxhlet extractor using n-hexane, dichloromethane (DCM) and methanol. The n-hexane and DCM extracts of the pseudostem and rhizome were subjected to isolation and purification using column chromatography on silica gel using a stepwise gradient system (n-hexane to methanol). Briefly, a serial two fold dilutions of the test materials dissolved in DMSO were prepared prior to addition of 100μl overnight microbial suspension (108 cfu/ml) followed by incubation at 37°C (bacteria) or 26°C (dermatophytes and candida) for 24h. The highest concentration of DMSO remaining after dilution (5%, v/v) caused no inhibition to bacterial/candida/dermatophytes’ growth. Antibiotic cycloheximide was used as reference for anticandidal and antidermatophyte comparison while oxacilin was used as reference for antibacterial testing. DMSO served as negative control. Turbidity was taken as indication of growth, thus the lowest concentration which remains clear after macroscopic evaluation was taken as the minimum inhibitory concentration (MIC). ResultsThe isolation of n-hexane and DCM extracts of the rhizomes and pseudostems of Alpinia conchigera via column chromatography yielded two triterpenes isolated as a mixture of stigmasterol and β-sitosterol: caryophyllene oxide, chavicol acetate 1, p-hydroxy cinnamaldehyde 2, 1′S-1′-acetoxychavicol acetate 3, trans-p-coumaryl diacetate 4, 1′S-1′-acetoxyeugenol acetate 5, 1′-hydroxychavicol acetate 6, p-hydroxycinnamyl acetate 7 and 4-hydroxybenzaldehyde.The DCM extract of the rhizome of Alpinia conchigera indicated potent antifungal activity against Candida albicans, Microsporum canis and Trycophyton rubrum with MIC values of 625μg/ml, 156μg/ml and 156μg/ml, respectively. It also showed significant inhibitory activity with MIC values between 17.88 and 35.75μg/ml against the mutant Staphylococci isolates MSSA, MRSA and Sa7.Amongst the isolated compounds, the lowest inhibition observed were of 1′S-1′-acetoxyeugenol against the dermatophytes (MIC 313μg/ml) followed by trans-p-coumaryl diacetate against both dermatophytes and candida (MIC 625μg/ml). The compound p-hydroxycinnamyl acetate strongly inhibited Staphylococcusaureus strain VISA (MIC 39μg/ml) followed by trans-p-coumaryl diacetate and 1′-hydroxychavicol acetate with MIC value of 156μg/ml. ConclusionIn conclusion, the observed antibacterial, anticandidal and antidermatophyte activity of the extracts and compounds obtained from the rhizome confirm the traditional use of Alpinia cochigera rhizome in the treatment of skin infection.

In-vitro anti-atherothrombosis activity of four Bangladeshi plants

Thrombous formation inside the blood vessels obstructs blood flow through the circulatory system leading hypertension, stroke to the heart, anoxia and so on. The complete deprivation of oxygen and infarction is a mode of cell death. Crude biologicals and their components possessing anti-thrombotic activity have been reported before. This study was aimed to investigate thrombolytic activity of ethanol extracts of four traditionally used medicinal plants. For this an in-vitro thrombolytic study was carried out along with streptokinase, and ethanol was taken as reference standard and negative control, respectively. The ethanol extracts (5 μg/μl) of Alpinia conchigera, Lannea grandis, Aglaonema hookerianum and Tridax procumbens 24.50%, 13.31%, 11.18%, and 8.70% clot lysis, respectively. Among the extracts studied Alpinia conchigera showed significant percent of clot lysis (24.50%) with reference to streptokinase (81.08%). Preliminary chemical group identification revealed the presence of alkaloids, glycosides, steroids, terpenoids, tannins and reducing sugars important secondary metabolites. Key words: Crude extracts, streptokinase, thrombolytic, traditional medicine

Comparative study of essential oil composition of leaves and rhizomes of Alpinia conchigera Griff. at different post- harvest drying periods

Essential oils from the leaves and rhizomes of Alpinia conchigera Griff. dried for different times (0 (fresh), 1, 2, 3 and 7 days of drying, respectively) were isolated using hydrodistillation. The chemical composition of oils was analyzed by using GC and GC-MS. The identified components constituted 95.06, 94.51, 94.64 and 91.60% of the leaf oil and 47.71, 64.19, 49.96, 94.47 and 91.56% of the rhizome oil of fresh, 1, 2, 3 and 7 days drying samples, respectively. Thirty four components were identified, among which 31 had not been detected previously. The major constituents in fresh, one, two and three days dried leaves were cyclohexene, 1-methyl-4-(5-methyl-1-methylene-4-hexenyl), while for leaves dried for seven days were 1, 6, 10-dodecatriene, 7 and 11-dimethyl-3-methylene. β-pinene was the major component for fresh and two days dried rhizomes, while 1-methyl-4-(5-methyl-1-methylene-4-hexenyl) was the major constituent for one, three and seven days dried rhizomes. The post-harvest drying period had a positive effect on the oil yield of both leaf and rhizome. The highest oil yield was obtained from leaves dried for 7 days (0.300 v/w) and rhizomes dried for 3 days (0.162 v/w). This study suggests that the yield and content ofessential oils from the leaves and rhizomes of A. conchigera could be increased by drying leaves and rhizomes for 3 and 7 days, respectively. Key words: Alpinia conchigera Griff., essential oil, GC-MS, post-harvest drying, Zingiberaceae.

Essential oils analysis of the rhizomes of Alpinia conchigera Griff. and leaves of Alpinia malaccensis (Burm. f.) Roscoe from Bangladesh

The essential oils obtained by hydrodistillation of the rhizomes of Alpinia conchigera Griff. and leaves of Alpinia malaccensis (Burm. f.) Roscoe were analysed by gas chromatography mass spectrometry (GC-MS). 74 compounds were identified in A. conchigera rhizome oil among them, 40 had not been detected previously. The major chemical class was terpenoids, with eucalyptol (25.85%), chavicol (25.08%), b-pinene (6.71%) and caryophyllene (3.38%), as the major components. A. malaccensis leaves yielded 47 identified constituents: the majority were terpenoids, but the oil was clearly dominated by a-phellandrene (31.80%), eucalyptol (13.76%), O-cymene (11.45%), b-pinene (11.34%) and limonene (6.44%). The compositions of both oils varied qualitatively and quantitatively. Key words: Alpinia conchigera, Alpinia malaccensis, GC-MS analysis, essential oil composition, eucalyptol, a-phellandrene.

Antinociceptive and anti-inflammatory effects of the ethanolic extract of alpinia conchigera Griff. leaves in various animal models

The ethanolic extract of Alpinia conchigera Griff. leaves (EACL) was evaluated for its antinociceptive and anti-inflammatory activities in several in vivo experimental models. Antinociceptive activity was determined using the acetic acid-induced abdominal writhing test, the hot plate test and the formalin test. Anti-inflammatory activity was determined using the carrageenan-induced paw edema test. The extract (30, 100 and 300 mg/kg i.p.) was found to possess significant, dose-dependent inhibitory activity in all test models. In addition, the antinociceptive effect of the extract in the acetic acid-induced writhing and hot plate tests was reversed by naloxone, suggesting that this activity is mediated through activation of the opioid system. These findings suggest that EACL presents notable analgesic and anti-inflammatory activities, which support its folkloric use for painful and inflammatory conditions.

A 17-Diarylheptanoid from Alpinia conchigera

The rhizomes of Alpinia conchigera were found to contain a new 1,7-diarylheptanoid, which was identified as 1,7-diphenyl-3,5-heptanedione, together with four other diarylheptanoids, two flavonoids and four phenylpropanoids.