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"This article provides a comprehensive review of the contamination by Butylin compounds (BTa) and its possible implications on the marine and coastal environments of the Philippines...."

"Telah dilakukan penelitian tentang sintesis senyawa koordinasi inti ganda krom(III)-polipiridil dengan ligan gugus jembatan 4,4'-bipiridin dan pyrazin (L'). Ligan polipiridil yang digunakan adalah 1,10-phenantrolin dan 2,2'-bipiridin (L). Sintesis dilakukan berdasarkan penentuan stoikiometri antara krom(III)-ligan polipiridil-ligan gugus jembatan secara spektrofotometri. Berdasarkan penentuan stoikiometri, diperoleh perbandingan mol krom(III):L=1:3, yang berarti bahwa rumus molekul senyawa koordinasi krom(III)-L adalah [CrL3]3+. Senyawa koordinasi ini berstruktur rang oktahedral yang mengandung enam ikatan koordinasi antara atom-atom N pada ligan L dengan ion krom(III). Senyawa koordinasi [CrL2L'2]3+ disintesis melalui subtitusi 4,4'-bipiridin dan pyrazin pada [CrL3]3+. Formula tersebut mempunyai perbandingan mol krom(III):L:L'=1:2;2 yang diperoleh melalui penentuan stoikiometri. Berdasarkan perbandingan stoikiometri ini selanjutnya disintesis senyawa koordinasi [Cr(phen)2(bpy')2]3+ , [Cr(phen)2(pyz)2] 3+, [Cr(bpy)2(bpy')2]3+ , [Cr(bpy)2(pyz)2] 3+ Senyawa koordinasi [CrL2L'2]3+ terbentuk melalui tahapan pembentukan senyawa [CrL2(H2O)L'] 3+ dengan perbandingan mol krom(III):L:L'=1:2:1 yang cukup stabil. Hal ini mengindikasikan bahwa ligan gugus jembatan terikat pada ion krom(III) melalui satu sisi koordinasi, sedangkan sisi koordinasi yang lain masih bebas. Sisi koordinasi yang masih bebas ini mampu mengikat ion krom(III) lainnya sehingga terbentuklah senyawa koordinasi inti ganda. Senyawa koordinasi inti ganda krom(III) - ligan polipiridil - ligan gugus jembatan disintesis berdasarkan perbandingan mol krom (III):L:L'=2:4:1 ([L2(H2O)CrL'Cr(H2O)L2]6+). Senyawa koordinasi yang disintesis adalah [(phen)2 (H2O) Cr(bpy')Cr(H2O)(phen)2]6+, [(phen)2(H2O)Cr(pyz)Cr(H2O)(phen)2]6+, [(bpy)2(H2O)Cr(bpy')Cr(H2O)(bpy) 2]6+, dan [(bpy)2(H2O)Cr(pyz)Cr(H2O)(bpy) 2]6+. Karakterisasi senyawa koordinasi hasil sintesis ([CrL3]3+, [CrL2L'2]3+ dan [L2(H2O)CrL'2Cr(H2O)L2]6+ di daerah ultraungu dekat-tampak menunjukkan adanya transisi elektronik dari 4A2g à 4T2g1 4A2g à a4T1g dan 4A29 à b4T19. Hal ini mengindikasikan adanya transisi d-d. Dari spektrum IR yang diperoleh dapat disimpulkan adanya substitusi ligan gugus jembatan pada senyawa koordinasi [CrL3]3+ mengakibatkan pergeseran puncak serapan. Adanya puncak baru di daerah 400-450 cm-' mengindikasikan adanya vibrasi M-N yang berarti senyawa koordinasi telah terbentuk. Pola difraksi sinar-X pada senyawa koordinasi hasil sintesis menunjukkan sudut 20 dan intensitas maksimum yang berbeda satu sama lain. Hal ini menunjukkan adanya perbedaan bidang-bidang hal dalam kristal senyawa-senyawa koordinasi tersebut.

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Synthesis and characterization of polynuclear coordination compounds of chrom(III)-polypiridyls with bridging ligands of 4,4'-bipiridine and pyrazine;Synthesis and characterization of polynuclear coordination compounds of chrom(III)-polypiridyls with bridging ligands of 4,4'-bipiridine and pyrazine.

Polynuclear coordination compounds of chrom(lll)-polypiridyls with bridging ligands of 4,4'-bipyridine and pyrazine (l') have been synthesized using 1,10- phenanthroline and 2,2'-bipyridine (L). The compounds were prepared based on the stoichiometry between chrom(lll)-polypiridyls-bridging ligands determined by spectra photometry.

The mole ratio of chrom(lll):polypiridyls ligands was 1:3 which means that the formula of the chrom(lll)-polypiridyls coordination compounds were [Crl3]3+. The,compounds have octahedral structure with six coordination bond which was fanned,through the,N atoms of the L ligands.

The coordination compounds [CrL2L'2]3+ were synthesized by substitution of bridging ligands 4,4'-bipyridine and pyrazin on [CrL3]3+. This formula was determined by the stoichiometry of chrom(III):L:L'=1 :2:2. Based on these results coordination compounds of [Cr(phen)z(bpy'h)3+. [Cr(phen)z(pyz)2]3+, [Cr(bpy)2(bpy'h]3+, [Cr(bpyh(pyz)2]3+ were synthesised. The coordination compounds [CrL2L'2]3+ were formed through the formation step of stable compound [Crl2{H20)L']3+ using mole ratio of chrom(III):L:L'=1:2:1. This results showed that the bridging ligands coordinated chrom(lll) ion only on one side, while the other side was able to coordinate with another chrom(lll) ion to form the polynuclear coordination compounds.

The polynuclear compounds chrom(lll}-polypiridyl ligands-bridging ligands were synthesised with mole ratio chrom(III}:L:L';::2:4:1 {[L2(H20)CrL'Cr(H20)LiJ'"". The compounds were [(phen)2(H20)Cr(pyz}Cr(H20}(phen)2]8+, [ (b py)2(H20)C r(pyz)Cr(H20)(bpy)2]&+. [(phen)2(H20)Cr(bpy')Cr(H20)(phen)iJ&+, [(bpy)2{H20)Cr{bpy')Cr(H20)(bpy)2]6+, Characterization of synthesized coordination compounds [Cr4]3+ , [CrL2L'2]3+, and [L2(H20)CrL'Cr(H20)L2]&+ using UV-VIS spectrum showed the electronic transition 4A2g -7 ~29 , 4A2g -7 a+r1g , 4A2g -7 b"T19 . This result indicates the d-d transition.

From the IR-Spectra, it can be concluded that the substitution of the bridging ligands on to [Cr4]J+ causes peak shift. The formation of a new peak at 400-450 cm·1 were related to M-N vibration which means the coordination compounds were fanned. X-ray diffraction studies of the synthesized coordination compounds show different 29 angles and the maximum intensities. This result indicates the difference in the hkl planes on the crystals."

"Kandidiasis merupakan suatu penyakit kulit yang diakibatkan oleh Candida krusei yang telah resisten terhadap antijamur Flukonazol. Resistensi disebabkan gen penanda: ERG11, FKS1, ABC1 dan ABC2 yang meningkatkan aktivitas membran transporter. Maka diperlukan pencarian kandidat antijamur yang dapat menggantikan Flukonazol, dimulai dengan memanfaatkan senyawa fenolik yang terdapat pada tanaman herbal. Penelitian ini dilakukan untuk mencari kandidat antijamur Candida krusei dari golongan senyawa fenolik melalui perspektif studi In Silico dengan protein target Enzim lanosterol 14 α-demetilase dengan kode PDB 5V5Z. Aplikasi LiganScout digunakan untuk Virtual Screening, ditemukan beberapa senyawa fenolik, diambil tiga senyawa yaitu Eugenol, Kuersetin, dan Asam Galat. Dilanjutkan dengan penambatan molekular menggunakan Aplikasi Molegro 2011. Hasil penambatan molekular senyawa ligan natif, Flukonazol, dan ketiga senyawa fenolik terhadap Enzim lanosterol 14α-demetilase wild type menunjukkan rerank score berturut-turut: -154.433; -98.3027; -97.4626; -66.4573 dan -65.2084, sedangkan rerank score mutan: -31.0348; -99.4858; -92.1078; -63.9848; dan -62.6408. Ketiga senyawa fenolik menunjukkan potensi antijamur karena rerank score lebih baik dari ligan natif, meski tidak lebih baik dari rerank score Flukonazole. Dilakukan uji aktivitas Antijamur ketiga senyawa fenolik dan Flukonazol, didapatkan nilai uji hambat berturut-turut 3,33; 1,25; 0,63 dan 0 mm. Hal ini menunjukkan ketiga senyawa fenolik berpotensi sebagai Antijamur menggantikan Flukonazol di masa depan.

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Candidiasis is a dermatological condition caused by the fungus Candida krusei, which exhibits resistance to the antifungal medication Fluconazole. The presence of marker genes, namely ERG11, FKS1, ABC1, and ABC2, leads to resistance via enhancing the function of membrane transporters. It is imperative to seek other antifungal options to replace Fluconazole. This can be achieved by harnessing the potential of phenolic chemicals derived from herbal plants. The purpose of this study was to identify potential antifungal agents for Candida krusei from the phenolic chemical category using In Silico experiments, focusing on the lanosterol 14 α-demethylase enzyme with the PDB code 5V5Z. The LiganScout software was employed for Virtual Screening, resulting in the identification of many phenolic compounds. Three specific compounds were selected, namely Eugenol, Kuersetin, and Gallic Acid. Subsequently, molecular docking was performed utilizing the Molegro 2011 Application. The molecular docking results of the natif ligan compound, Fluconazole, and the three phenolic compounds against the wild type lanosterol 14α-demethylase enzyme yielded rerank scores of -154.433, -98.3027, -97.4626, -66.4573, and -65.2084 respectively. The mutant rerank scores were -31.0348, -99.4858, -92.1078, -63.9848, and -62.6408. The three phenolic compounds exhibited antifungal efficacy as their rerank score surpassed that of the natural ligan, while it did not surpass the rerank score of Fluconazole. The antifungal activity of the three phenolic compounds and Fluconazole was individually examined using an inhibition test. The corresponding inhibition test values were 3.33 mm, 1.25 mm, 0.63 mm, and 0 mm, respectively. These findings demonstrate that the three phenolic compounds possess the capacity to function as antifungal agents, potentially replacing Fluconazole in the future."

"Ekstraksi senyawa bioaktif menggunakan Deep Eutectic Solvent (DES) semakin masif digunakan karena memiliki toksisitas rendah, biodegradable, mudah disintesis, dapat diatur polaritas serta selektivitasnya sesuai kebutuhan, dan aman bagi lingkungan jika dibandingkan dengan pelarut organik. Sintesis DES dari pencampuran Hidrogen Bond Acceptor (HBA) dan Hidrogen Bond Donor (HBD) akan memberikan jenis yang beragam sehingga sulit untuk menentukan campuran DES yang akan memberikan hasil ekstraksi terbaik. Penelitian ini menggunakan mangostin sebagai representatif dari ribuan senyawa bioaktif dan difokuskan untuk mencari korelasi antara polaritas DES dengan hasil ekstraksi menggunakan Nile Red sebagai parameter kepolaran. Hipotesis dari korelasi tersebut akan diuji pada senyawa bioaktif lainnya yaitu (kuersetin, rutin, polifenol, fenolik), ekstraksi cair-cair (asam palmitat), dan ekstraksi cair-gas (CO2) Penelitian ini menggunakan data sekunder untuk mendapatkan data yang ekstensif terkait hasil ekstraksi senyawa bioaktif alfa-mangostin, kuersetin, rutin, polifenol, fenolik, asam palmitat, dan CO2 menggunakan DES dan data polar parameter Nile Red (Enr). Selanjutnya, akan dilakukan uji polaritas DES jika data polaritas yang tidak tersedia pada literatur. Hasil akhir menunjukkan adanya korelasi kuadratik yang ditunjukkan oleh kurva regresi maupun secara kuantitatif yang ditunjukkan dari nilai regresi kuadratik antara hasil esktraksi dengan polaritas DES.

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Extraction of bioactive compounds using Deep Eutectic Solvent (DES) has emerged as a highly promising category of green solvents due to the low toxicity, biodegradable, easy to synthesize, and considered safe for the environment compared to organic solvents. The synthesis of DES from mixing Hydrogen Bond Acceptor (HBA) and Hydrogen Bond Donor (HBD) has provided various types, making it difficult to determine the DES mixture that will give the best extraction yield. This study used mangosteen as a representative of thousands of bioactive compounds and focused on finding the correlation between the polarity of DES and the extraction using Nile Red as a polarity parameter. The hypothesis of the correlation will be tested on other bioactive compounds (quercetin, rutin, polyphenols, phenolics), liquid-liquid extraction (palmitic acid), and liquid-gas extraction (CO2). This study uses secondary data to obtain extensive data regarding the extraction results of the bioactive compounds alpha-mangosteen, quercetin, rutin, polyphenols, phenolics, palmitic acid, and CO2 using DES and data on polar parameters Nile red (Enr). Furthermore, the polarity value of DES (Enr) will be carried out through experimental research if the polarity data are not available in the literature. The final result qualitatively shows that there is a quadratic correlation based on the curve as well as quantitatively which is indicated by the value of the quadratic correlation between the extraction yield and the polarity of DES (Enr)

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