Browse publications by year: 2014

  1. Al-Astani Tengku Din TA, Shamsuddin SH, Idris FM, Ariffin Wan Mansor WN, Abdul Jalal MI, Jaafar H
    Asian Pac J Cancer Prev, 2014;15(9):3939-44.
    PMID: 24935577
    BACKGROUND: To elucidate the role of rapamycin and PF4 on apoptosis regulation via Bax (pro-apoptosis), Bcl-2 (anti-apoptosis) and survivin activation on the growth in the 1-methyl-1-nitrosourea -induced invasive breast carcinoma model.

    MATERIALS AND METHODS: Thirty five female Sprague Dawley rats at age 21-day old were divided into 4 groups; Group 1 (control, n=10), Group 2 (PF4, n=5), Group 3 (rapamycin, n=10) and Group 4 (rapamycin+PF4, n=10). MNU was administered intraperitionally, dosed at 70 mg/kg body weight. The rats were treated when the tumors reached the size of 14.5 ± 0.5 mm and subsequently sacrificed after 5 days. Rapamycin and PF4 were administered as focal intralesional injections at the dose of 20 μg/lesion. The tumor tissue was then subjected to histopathological examinations for morphological appraisal and immunohistochemical assessment of the pro-apoptotic marker, Bax and anti-apoptotic markers, Bcl-2 and survivin.

    RESULTS: The histopathological pattern of the untreated control cohort showed that the severity of the malignancy augments with mammary tumor growth. Tumors developing in untreated groups were more aggressive whilst those in treated groups demonstrated a transformation to a less aggressive subtype. Combined treatment resulted in a significant reduction of tumor size without phenotypic changes. Bax, the pro-apoptotic marker, was significantly expressed at higher levels in the rapamycin-treated and rapamycin+PF4-treated groups compared to controls (p<0.05). Consequently, survivin was also significantly downregulated in the rapamycin-treated and rapamycin+PF4-treated group and this was significantly different when compared to controls (p).

    CONCLUSIONS: In our rat model, it could be clearly shown that rapamycin specifically affects Bax and survivin signaling pathways in activation of apoptosis. We conclude that rapamycin plays a critical role in the induction of apoptosis in MNU-induced mammary carcinoma.

    MeSH terms: Animals; Cell Transformation, Neoplastic; Female; Mammary Glands, Animal/pathology; Mammary Neoplasms, Experimental/chemically induced; Mammary Neoplasms, Experimental/drug therapy*; Methylnitrosourea; Microtubule-Associated Proteins/biosynthesis*; Platelet Factor 4/pharmacology*; Signal Transduction/drug effects; Transcriptional Activation; Down-Regulation; Up-Regulation; Rats, Sprague-Dawley; Apoptosis/drug effects*; Proto-Oncogene Proteins c-bcl-2/biosynthesis; Sirolimus/pharmacology*; bcl-2-Associated X Protein/biosynthesis*; Rats
  2. Azlin AH, Looi LM, Cheah PL
    Asian Pac J Cancer Prev, 2014;15(9):3959-63.
    PMID: 24935581
    The tumour suppressor genes, p53 and pRb, are known to play important roles in neoplastic transformation. While molecular routes to the uncontrolled growth of hepatocytes, leading to primary liver cancer have generated considerable interest, the roles of p53 and pRb mutations in hepatocellular carcinoma (HCC) and hepatoblastoma (HB) remain to be clarified. We examined the immunohistochemical expression of p53 and pRb gene products in 26 HCC and 9 HB, sampled into tissue microarray blocks. 10 (38%) of 26 HCC showed > 10% tumour nuclear staining for p53 protein, 3 of these also being HbsAg positive. Conversely, none of 9 HB expressed nuclear p53 immunopositivity. Some 24 (92%) HCC and 8 (89%) HB showed loss of pRb nuclear expression. Two of the 26 HCC and one of the 9 HB showed >10% tumour nuclear staining for pRb protein. Our results suggest that p53 does not have an important role in the development of HB but may contribute in HCC. There is also loss of pRb expression in the majority of HCC and HB, supporting loss of pRb gene function in the hepatocarcinogenesis pathway. However, a comparison of the staining profiles of p53 and pRb proteins in HCC and HB did not reveal a consistent pattern to differentiate between the two types of tumours immunohistochemically. Hence the use of p53 and pRB protein expression has no contribution in the situation where there is a diagnostic difficulty in deciding between HCC and HB.
    MeSH terms: Adult; Aged; Cell Transformation, Neoplastic/genetics; Child, Preschool; Female; Hepatitis B Surface Antigens/analysis; Carcinoma, Hepatocellular/genetics*; Carcinoma, Hepatocellular/pathology; Humans; Immunohistochemistry; Infant; Liver Neoplasms/genetics*; Liver Neoplasms/pathology; Male; Middle Aged; Retrospective Studies; Tissue Preservation; Tumor Suppressor Protein p53/analysis; Tumor Suppressor Protein p53/genetics*; Retinoblastoma Protein/analysis; Retinoblastoma Protein/genetics*; Hepatoblastoma/genetics*; Hepatoblastoma/pathology; Tissue Array Analysis; Young Adult
  3. Huang CJ, Nguyen PN, Choo KB, Sugii S, Wee K, Cheong SK, et al.
    Int J Med Sci, 2014;11(8):824-33.
    PMID: 24936146 DOI: 10.7150/ijms.8358
    A miRNA precursor generally gives rise to one major miRNA species derived from the 5' arm, and are called miRNA-5p. However, more recent studies have shown co-expression of miRNA-5p and -3p, albeit in different concentrations, in cancer cells targeting different sets of transcripts. Co-expression and regulation of the -5p and -3p miRNA species in stem cells, particularly in the reprogramming process, have not been studied.
    MeSH terms: Cell Differentiation; Humans; Gene Expression Regulation, Developmental; MicroRNAs/biosynthesis*; MicroRNAs/genetics; Embryonic Stem Cells/metabolism*; Induced Pluripotent Stem Cells/metabolism*; Mesenchymal Stromal Cells/metabolism*; Cellular Reprogramming/genetics
  4. Hussain AI, Rathore HA, Sattar MZ, Chatha SA, Sarker SD, Gilani AH
    J Ethnopharmacol, 2014 Aug 8;155(1):54-66.
    PMID: 24936768 DOI: 10.1016/j.jep.2014.06.011
    Citrullus colocynthis (L.) Schrad is a valuable cucurbit plant, widely distributed in the desert areas of the world. Citrullus colocynthis fruits are usually recognized for its wide range of medicinal uses as well as pharmaceutical and nutraceutical potential. This review aims to appraise the published information on the ethnobotanical knowledge, phytochemistry, ethnopharmacology, nutraceutical potential and safety studies of Citrullus colocynthis (bitter apple) fruit, with critical analysis on the gaps and potential for future studies.
    MeSH terms: Animals; Fruit; Humans; Medicine, Traditional/methods*; Plant Extracts/adverse effects; Plant Extracts/pharmacology*; Ethnopharmacology; Citrullus colocynthis/chemistry*
  5. Hong W, Li J, Laughton CA, Yap LF, Paterson IC, Wang H
    J Mol Graph Model, 2014 Jun;51:193-202.
    PMID: 24937176 DOI: 10.1016/j.jmgm.2014.05.010
    Protein arginine methyltransferases (PRMTs) catalyse the methylation of arginine residues of target proteins. PRMTs utilise S-adenosyl methionine (SAM) as the methyl group donor, leading to S-adenosyl homocysteine (SAH) and monomethylarginine (mMA). A combination of homology modelling, molecular docking, Active Site Pressurisation, molecular dynamic simulations and MM-PBSA free energy calculations is used to investigate the binding poses of three PRMT1 inhibitors (ligands 1-3), which target both SAM and substrate arginine binding sites by containing a guanidine group joined by short linkers with the SAM derivative. It was assumed initially that the adenine moieties of the inhibitors would bind in sub-site 1 (PHE44, GLU137, VAL136 and GLU108), the guanidine side chain would occupy sub-site 2 (GLU 161, TYR160, TYR156 and TRP302), with the amino acid side chain occupying sub-site 3 (GLU152, ARG62, GLY86 and ASP84; pose 1). However, the SAH homocysteine moiety does not fully occupy sub-site 3, suggesting another binding pose may exist (pose 2), whereby the adenine moiety binds in sub-site 1, the guanidine side chain occupies sub-site 3, and the amino acid side chain occupies sub-site 2. Our results indicate that ligand 1 (pose 1 or 2), ligand 2 (pose 2) and ligand 3 (pose 1) are the predominant binding poses and we demonstrate for the first time that sub-site 3 contains a large space that could be exploited in the future to develop novel inhibitors with higher binding affinities.
    MeSH terms: Enzyme Inhibitors/chemistry*; Humans; Hydrogen Bonding; Ligands; Methylation; Protein-Arginine N-Methyltransferases/antagonists & inhibitors*; Protein-Arginine N-Methyltransferases/chemistry; Protein Binding; Repressor Proteins/antagonists & inhibitors*; Repressor Proteins/chemistry; Thermodynamics; Protein Structure, Secondary; Catalytic Domain; Structural Homology, Protein; Molecular Dynamics Simulation*; Molecular Docking Simulation
  6. Li J, Lindström LS, Foo JN, Rafiq S, Schmidt MK, Pharoah PD, et al.
    Nat Commun, 2014 Jun 17;5:4051.
    PMID: 24937182 DOI: 10.1038/ncomms5051
    Large population-based registry studies have shown that breast cancer prognosis is inherited. Here we analyse single-nucleotide polymorphisms (SNPs) of genes implicated in human immunology and inflammation as candidates for prognostic markers of breast cancer survival involving 1,804 oestrogen receptor (ER)-negative patients treated with chemotherapy (279 events) from 14 European studies in a prior large-scale genotyping experiment, which is part of the Collaborative Oncological Gene-environment Study (COGS) initiative. We carry out replication using Asian COGS samples (n=522, 53 events) and the Prospective Study of Outcomes in Sporadic versus Hereditary breast cancer (POSH) study (n=315, 108 events). Rs4458204_A near CCL20 (2q36.3) is found to be associated with breast cancer-specific death at a genome-wide significant level (n=2,641, 440 events, combined allelic hazard ratio (HR)=1.81 (1.49-2.19); P for trend=1.90 × 10(-9)). Such survival-associated variants can represent ideal targets for tailored therapeutics, and may also enhance our current prognostic prediction capabilities.
    MeSH terms: Breast Neoplasms/diagnosis*; Breast Neoplasms/drug therapy*; Breast Neoplasms/genetics*; Chromosomes, Human, Pair 2/genetics*; Drug Therapy/methods*; Female; Genetic Markers/genetics*; Humans; Prognosis; Linkage Disequilibrium; Proportional Hazards Models; Polymorphism, Single Nucleotide/genetics; European Continental Ancestry Group/genetics; Kaplan-Meier Estimate
  7. Qaeed MA, Ibrahim K, Saron KM, Ahmed MA, Allam NK
    ACS Appl Mater Interfaces, 2014 Jul 9;6(13):9925-31.
    PMID: 24937197 DOI: 10.1021/am502217b
    Indium gallium nitride nanocubes were syntheized via a low-temperature chemical route. Energy-dispersive X-ray spectroscopy and X-ray diffraction analyses confirmed the successful fabrication of (In,Ga)N with various indium mole fractions. The bandgap of the material was tunded as a function of the indium content. The fabricated nanocubes showed a deep level photoluminescence emission at 734 nm as well as in the visible region at 435-520 nm. The Hall effect measurements showed the hole concentration to constantly increase from 6.2 × 10(16) to 2.3 × 10(18) cm(-3), while the hole mobility to decrease from 0.92 to 0.1 cm(2) /(V s) as the doping ratio increases from 0.005 to 0.025 cm(-3). The solar cell device made of nanocubes film containing 0.4 indium on flexible substrates showed a short-circuit current density of 12.47 mA/cm(2) and an open-circuit voltage (Voc) of 0.48 V with 54% fill factor. The relationship between Voc and indium content in the fabricated films was also investigated.
  8. Moy FM, Hoe VC, Hairi NN, Buckley B, Wark PA, Koh D, et al.
    BMC Public Health, 2014;14:611.
    PMID: 24938383 DOI: 10.1186/1471-2458-14-611
    The study on Clustering of Lifestyle risk factors and Understanding its association with Stress on health and wellbeing among school Teachers in Malaysia (CLUSTer) is a prospective cohort study which aims to extensively study teachers in Malaysia with respect to clustering of lifestyle risk factors and stress, and subsequently, to follow-up the population for important health outcomes.
    MeSH terms: Adult; Alcohol Drinking; Anxiety/etiology; Chronic Disease; Depression/etiology; Depressive Disorder; Female; Health Status*; Humans; Life Style*; Malaysia/epidemiology; Male; Middle Aged; Obesity/etiology; Personal Satisfaction*; Prospective Studies; Quality of Life*; Surveys and Questionnaires; Risk Factors; Schools; Smoking/epidemiology; Socioeconomic Factors; Stress, Psychological/etiology*; Stress, Psychological/epidemiology; Cluster Analysis; Workplace/psychology; School Teachers
  9. Bukhari SN, Lauro G, Jantan I, Bifulco G, Amjad MW
    Bioorg Med Chem, 2014 Aug 1;22(15):4151-61.
    PMID: 24938495 DOI: 10.1016/j.bmc.2014.05.052
    Arachidonic acid and its metabolites have generated high level of interest among researchers due to their vital role in inflammation. The inhibition of enzymes involved in arachidonic acid metabolism has been considered as synergistic anti-inflammatory effect. A series of novel α,β-unsaturated carbonyl based compounds were synthesized and evaluated for their inhibitory activity on secretory phospholipase A₂ (sPLA₂), cyclooxygenases (COX), soybean lipoxygenase (LOX) in addition to proinflammatory cytokines comprising IL-6 and TNF-α. Six α,β-unsaturated carbonyl based compounds (2, 3, 4, 12, 13 and 14) exhibited strong inhibition of sPLA₂ activity, with IC₅₀ values in the range of 2.19-8.76 μM. Nine compounds 1-4 and 10-14 displayed inhibition of COX-1 with IC₅₀ values ranging from 0.37 to 1.77 μM (lower than that of reference compound), whereas compounds 2, 10, 13 and 14 strongly inhibited the COX-2. The compounds 10-14 exhibited strong inhibitory activity against LOX enzyme. All compounds were evaluated for the inhibitory activities against LPS-induced TNF-α and IL-6 release in the macrophages. On the basis of screening results, five active compounds 3, 4, 12, 13 and 14 were found strong inhibitors of TNF-α and IL-6 release in a dose-dependent manner. Molecular docking experiments were performed to clarify the molecular aspects of the observed COX and LOX inhibitory activities of the investigated compounds. Present findings increases the possibility that these α,β-unsaturated carbonyl based compounds might serve as beneficial starting point for the design and development of improved anti-inflammatory agents.
    MeSH terms: Animals; Binding Sites; Cell Line; Curcumin/pharmacology; Curcumin/chemistry; Lipoxygenase/metabolism; Lipoxygenase/chemistry*; Macrophages/cytology; Macrophages/drug effects; Macrophages/metabolism; Prostaglandin-Endoperoxide Synthases/metabolism; Prostaglandin-Endoperoxide Synthases/chemistry*; Protein Binding; Soybeans/enzymology; Structure-Activity Relationship; Tumor Necrosis Factor-alpha/antagonists & inhibitors*; Tumor Necrosis Factor-alpha/metabolism; Interleukin-6/antagonists & inhibitors*; Interleukin-6/metabolism; Lipoxygenase Inhibitors/chemical synthesis; Lipoxygenase Inhibitors/pharmacology; Lipoxygenase Inhibitors/chemistry*; Cyclooxygenase Inhibitors/chemical synthesis; Cyclooxygenase Inhibitors/pharmacology; Cyclooxygenase Inhibitors/chemistry*; Protein Structure, Tertiary; Mice; Phospholipases A2, Secretory/antagonists & inhibitors*; Phospholipases A2, Secretory/metabolism; Molecular Docking Simulation; Phospholipase A2 Inhibitors/chemical synthesis; Phospholipase A2 Inhibitors/pharmacology; Phospholipase A2 Inhibitors/chemistry*
  10. Patil PG, Nimbalkar-Patil SP, Karandikar AB
    J Contemp Dent Pract, 2014 Jan 1;15(1):112-5.
    PMID: 24939276
    This case report demonstrates sequential periodontic, orthodontic and prosthodontic treatment modalities to save and restore deep horizontally fractured maxillary central incisor. The location of fracture was deep in the mucosa which reveals less than 2 mm of tooth structure to receive the crown. The procedures like surgical crown lengthening, endodontic post placement, orthodontic forced eruption, core build-up and metal-ceramic crown restoration were sequentially performed to conserve the fractured tooth. Forced eruption is preferred to surgical removal of supporting alveolar bone, since forced eruption preserves the biologic width, maintains esthetics, and at the same time exposes sound tooth structure for the placement of restorative margins.
    MeSH terms: Bicycling/injuries; Crowns; Esthetics, Dental; Gingiva/anatomy & histology; Humans; Incisor/injuries*; Male; Maxilla; Patient Care Planning; Patient Care Team*; Post and Core Technique; Tooth Fractures/therapy*; Crown Lengthening/methods; Metal Ceramic Alloys/chemistry; Dental Prosthesis Design; Root Canal Preparation/methods; Tooth, Nonvital/therapy; Orthodontic Extrusion/instrumentation; Young Adult
  11. Mutalik VS, Nichat P, Carnelio S, Solomon M, Radhakrishnan R
    J Contemp Dent Pract, 2014 Jan 1;15(1):119-21.
    PMID: 24939279
    Calcifying epithelial odontogenic tumor (CEOT) is a rare, benign, locally aggressive odontogenic epithelial tumor that affects the jaws. Although there are numerous reports on the variants of CEOT, occurrence of clear cells with complete absence of calcification has been a rarity. Histochemical analysis of tumor cells revealed glycogen granules with PAS staining, with absence of CD 1a staining in clear cells, while the amyloid-like deposit associated with clear cells showed green birefringence with Congo red. We report an unusual variant of CEOT occurring in a 27 years old male patient.
    MeSH terms: Adult; Amyloid/analysis; Congo Red; Cytoplasm/pathology; Coloring Agents; Epithelial Cells/pathology; Humans; Male; Mandibular Neoplasms/pathology*; Odontogenic Tumors/pathology*; Skin Neoplasms/pathology; Antigens, CD1/analysis
  12. Xu Y, Zhang H, Lit LC, Grothey A, Athanasiadou M, Kiritsi M, et al.
    Sci Signal, 2014 Jun 17;7(330):ra58.
    PMID: 24939894 DOI: 10.1126/scisignal.2005170
    Lemur tyrosine kinase 3 (LMTK3) is associated with cell proliferation and endocrine resistance in breast cancer. We found that, in cultured breast cancer cell lines, LMTK3 promotes the development of a metastatic phenotype by inducing the expression of genes encoding integrin subunits. Invasive behavior in various breast cancer cell lines positively correlated with the abundance of LMTK3. Overexpression of LMTK3 in a breast cancer cell line with low endogenous LMTK3 abundance promoted actin cytoskeleton remodeling, focal adhesion formation, and adhesion to collagen and fibronectin in culture. Using SILAC (stable isotope labeling by amino acids in cell culture) proteomic analysis, we found that LMTK3 increased the abundance of integrin subunits α5 and β1, encoded by ITGA5 and ITGB1. This effect depended on the CDC42 Rho family guanosine triphosphatase, which was in turn activated by the interaction between LMTK3 and growth factor receptor-bound protein 2 (GRB2), an adaptor protein that mediates receptor tyrosine kinase-induced activation of RAS and downstream signaling. Knockdown of GRB2 suppressed LMTK3-induced CDC42 activation, blocked ITGA5 and ITGB1 expression promoted by the transcription factor serum response factor (SRF), and reduced invasive activity. Furthermore, abundance of LMTK3 positively correlated with that of the integrin β1 subunit in breast cancer patient's tumors. Our findings suggest a role for LMTK3 in promoting integrin activity during breast cancer progression and metastasis.
    MeSH terms: Breast Neoplasms/enzymology; Breast Neoplasms/metabolism; Breast Neoplasms/pathology*; Female; Humans; Membrane Proteins/metabolism*; Neoplasm Invasiveness; Protein-Serine-Threonine Kinases/metabolism*; Antigens, CD29/physiology*; GRB2 Adaptor Protein/physiology*
  13. Abdul Nasir NA, Agarwal R, Vasudevan S, Tripathy M, Alyautdin R, Ismail NM
    Mol Vis, 2014;20:822-35.
    PMID: 24940038
    Oxidative and nitrosative stress underlies cataractogenesis, and therefore, various antioxidants have been investigated for anticataract properties. Several vitamin E analogs have also been studied for anticataract effects due to their antioxidant properties; however, the anticataract properties of tocotrienols have not been investigated. In this study, we investigated the effects of topically applied tocotrienol on the onset and progression of cataract and lenticular oxidative and nitrosative stress in galactosemic rats.
    MeSH terms: Administration, Topical; Animals; Anterior Eye Segment/drug effects; Anterior Eye Segment/pathology; Catalase/metabolism; Cataract/complications*; Cataract/drug therapy*; Cataract/metabolism; Emulsions; Eye Proteins/metabolism; Galactosemias/complications*; Galactosemias/metabolism; Glutathione/metabolism; Lens, Crystalline/drug effects; Lens, Crystalline/enzymology; Lens, Crystalline/metabolism*; Lens, Crystalline/pathology*; Liposomes/chemistry; Malondialdehyde/metabolism; Oxidation-Reduction/drug effects; Particle Size; Stress, Physiological/drug effects; Superoxide Dismutase/metabolism; Tyrosine/analogs & derivatives; Tyrosine/metabolism; Viscosity; Rats, Sprague-Dawley; Disease Progression; Tocotrienols/administration & dosage*; Tocotrienols/pharmacology; Tocotrienols/therapeutic use*; Rats; Nitric Oxide Synthase Type II/metabolism; Static Electricity
  14. Joseph B, Sithambaresan M, Kurup MR, Ng SW
    Acta Crystallogr Sect E Struct Rep Online, 2014 Jun 1;70(Pt 6):m211-2.
    PMID: 24940200 DOI: 10.1107/S1600536814010150
    The molecule of the title complex, [Ni2(C21H15N3O5)2(H2O)4]·4C3H7NO, is located on an inversion centre. This results in a dimeric Ni(II) complex, with the two Ni(II) atoms bridged by phenolate O atoms. The tridentate ligand is chelated to each Ni(II) atom via one N and two O atoms of the imino-late form of the hydrazide moiety, which has the same conformation as the free ligand. The coordination geometry around each Ni(II) ion is slightly distorted octa-hedral. A supra-molecular three-dimensional architecture is created by dominant inter-molecular O-H⋯N, O-H⋯O and C-H⋯O hydrogen-bonding inter-actions. These are augmented by two C-H⋯π inter-actions and a π-π inter-action with a centroid-centroid distance of 3.681 (2) Å.
  15. Dhanabalan N, Thanigaimani K, Arshad S, Razak IA, Santhanaraj KJ
    Acta Crystallogr Sect E Struct Rep Online, 2014 Jun 1;70(Pt 6):o657-8.
    PMID: 24940241 DOI: 10.1107/S160053681401023X
    The asymmetric unit of the title hydrated salt, C13H11N2 (+)·C7H6NO2 (-)·2H2O, consists of two independent 9-amino-acridinium cations, two 4-amino-benzoate anions and four water mol-ecules. Both 9-amino-acridinium cations are essentially planar, with maximum deviations of 0.034 (1) and 0.025 (2) Å, and are protonated at the pyridine N atoms. The 4-amino-benzoate anions are approximately planar, with dihedral angles of 9.16 (19) and 5.4 (2)° between the benzene ring and the carboxyl-ate group. In the crystal, the two independent anions are connected by N-H⋯O hydrogen bonds, forming a layer parallel to (100). The layers are connected through the cations by N-H⋯N and N-H⋯O hydrogen bonds. The water mol-ecules, which form O-H⋯O hydrogen-bonded chains along the b-axis direction, connect the anions and the cations by O-H⋯O, N-H⋯O and C-H⋯O hydrogen bonds. The crystal structure also features π-π inter-actions [centroid-centroid distances = 3.6343 (9)-3.8366 (10) Å] and a C-H⋯π inter-action.
  16. Abosadiya HM, Hasbullah SA, Yamin BM, Fadzil AH
    PMID: 24940255 DOI: 10.1107/S1600536814009295
    The two independent mol-ecules in the asymmetric unit of the title compound, C11H12Cl2N2OS, exhibit different conformations, with the benzene ring and the N2CS thio-urea group forming dihedral angles of 87.40 (18) and 69.42 (15)°. An intra-molecular N-H⋯O hydrogen bond is present in each mol-ecule. Two further N-H⋯O hydrogen bonds link the independent mol-ecules into a dimer. In the crystal, the dimers are linked by N-H⋯S and C-H⋯S hydrogen bonds, forming chains parallel to the c axis.
  17. Abosadiya HM, Hasbullah SA, Yamin BM, Fadzil AH
    PMID: 24940263 DOI: 10.1107/S1600536814011209
    The title compound, C10H10BrClN2OS, adopts a trans-cis conformation with respect to the position of the 3-chloro-propanoyl and 4-bromo-phenyl groups, respectively, against the thiono C=S bond across their C-N bonds. The benzene ring makes a dihedral angle of 9.55 (16)° with the N2CS thio-urea moiety. Intra-molecular N-H⋯O and C-H⋯S hydrogen bonds occur. In the crystal, mol-ecules are linked into chains along the c-axis direction by N-H⋯S, C-H⋯S and C-H⋯O hydrogen bonds.
  18. Rahman ML, Srinivasa HT, Mohd Yusoff M, Kwong HC, Quah CK
    Acta Crystallogr Sect E Struct Rep Online, 2014 Jun 1;70(Pt 6):o696-7.
    PMID: 24940271 DOI: 10.1107/S1600536814010642
    The asymmetric unit of the title compound, C17H18O3, comprises three independent mol-ecules with similar geometries. In each mol-ecule, the carbonyl group is twisted away from the napthalene ring system, making dihedral angles of 1.0 (2), 1.05 (19)° and 1.5 (2)°. The butene group in all three mol-ecules are disordered over two sets of sites, with a refined occupancy ratio of 0.664 (6):0.336 (6). In the crystal, mol-ecules are oriented with respect to their carbonyl groups, forming head-to-head dimers via O-H⋯O hydrogen bonds. Adjacent dimers are further inter-connected by C-H⋯O hydrogen bonds into chains along the a-axis direction. The crystal structure is further stabilized by weak C-H⋯π inter-actions.
  19. Ngah N, Mohamed NA, Yamin BM, Mohd Zaki H
    PMID: 24940277 DOI: 10.1107/S1600536814011404
    In the title compound, C10H11FN3O3S, the 2-fluoro-benzoyl and proponic acid groups maintain a trans-cis conformation with respect to the thiono C=S bond across their C-N bonds. The propionic acid group adopts an anti conformation about the C-C bond, with an N-C-C-C torsion angle of 173.8 (2)°. The amino groups are involved in the formation of intra-molecular N-H⋯O and N-H⋯F hydrogen bonds. In the crystal, pairs of O-H⋯O hydrogen bonds link mol-ecules into inversion dimers.
  20. Radhakrishnan A, Tudawe D, Chakravarthi S, Chiew GS, Haleagrahara N
    Exp Ther Med, 2014 May;7(5):1408-1414.
    PMID: 24940448
    Tocotrienols exhibit a significant anti-inflammatory and antioxidant effect in numerous human diseases. However, the anti-inflammatory and antioxidant effects of tocotrienols in arthritic conditions are not well documented. Therefore, the effect of γ-tocotrienol supplementation against oxidative stress and joint pathology in collagen-induced arthritis in rats was investigated in the present study. Adult female Dark Agouti rats were randomly divided into groups: Control, γ-tocotrienol alone, arthritis alone and arthritis with γ-tocotrienol. Arthritis was induced using 4 mg/kg body weight collagen in complete Freund's adjuvant. The rats were treated orally with 5 mg/kg body weight of γ-tocotrienol between day 21 and day 45. After 45 days, serum C-reactive protein (CRP), tumor necrosis factor (TNF)-α, superoxide dismutase (SOD) and total glutathione (GSH) assays were conducted. γ-tocotrienol significantly reduced the arthritis-induced changes in body weight, CRP, TNF-α, SOD and the total GSH levels. There was a significant reduction in the arthritis-induced histopathological changes in the γ-tocotrienol treatment group. The data indicated that administration of γ-tocotrienol resulted in a significant antioxidant and anti-inflammatory effect on collagen-induced arthritis; therefore, γ-tocotrienol may have therapeutic potential as a long-term anti-arthritic agent in rheumatoid arthritis therapy.
    MeSH terms: Adult; Animals; Anti-Inflammatory Agents; Antioxidants; Arthritis, Experimental; Arthritis, Rheumatoid; C-Reactive Protein; Chromans; Female; Freund's Adjuvant; Glutathione; Humans; Superoxide Dismutase; Tumor Necrosis Factor-alpha; Vitamin E; Oxidative Stress; Tocotrienols; Rats; Dasyproctidae
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