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Abstrak :
ABSTRAK
Gemuk lumas adalah semi cairan hingga padat yang merupakan campuran dari bahan dasar, pengental, dan aditif. Minyak jarak duri Ricinus communis L. memiliki peran potensial sebagai minyak dasar gemuk lumas, namun mudah teroksidasi. Penambahan aditif antioksidan dapat menunda reaksi oksidasi pada gemuk lumas food grade. Aditif antioksidan adalah BHT, TBHQ, dan HMWP. Li 12-hidroksistearat digunakan sebagai bahan pengental. Gemuk lumas food grade diformulasikan melalui proses saponifikasi-pelarutan-pendinginan-homogenisasi. Penelitian ini bertujuan untuk memperoleh gemuk lumas food grade yang memiliki performa pelumasan yang baik, stabil dan dapat dioperasikan pada suhu yang cukup tinggi dengan menggunakan minyak jarak duri Ricinus communis L. sebagai bahan dasar. Serta mempelajari pengaruh variasi konsentrasi bahan pengental 15 dan 17 , variasi konsentrasi 0, 0.5, 1, 1.5, dan 2 dan jenis aditif antioksidan terhadap karakteristik gemuk lumas. Karakteristik tersebut meliputi dropping point, konsistensi, klasifikasi NLGI, dan ketahanan korosi, serta ketahanan oksidasi pada minyak jarak duri. Hasil penelitian menunjukkan bahwa gemuk lumas food grade yang dihasilkan memiliki dropping point 189-194 oC, konsistensi kekerasan lunak hingga sedang, NLGI 1-3, ketahanan korosi 1a, serta semua antioksidan efektif meningkatkan ketahanan oksidasi pada minyak jarak duri.

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ABSTRACT
Grease is a semi fluid to solid mixture of a fluid lubricant, a thickener, and additives. Castor oil Ricinus communis L. has a potential roles as a grease lubricating base oil, but it has easily oxidized. The addition of antioxidant additives can delay oxidation reaction on food grade grease. Antioxidant additives are BHT, TBHQ, and HMWP. The thickening agent for the grease is Lithium 12 hydroxystearate soap. The food grade grease formulated through a saponification dilution cooling homogenization process. The aimed of this research is to obtain food grade grease which has a good lubrication performance, stable and can be operated at high temperature by using castor oil Ricinus communis L. as the based oil. And studying the effect of concentration variations of thickening agents 15 and 17 , concentration variations 0, 0.5, 1, 1.5, and 2 and types of antioxidant additives to the characteristics of grease. These characteristics included dropping point, consistency, NLGI classification, and corrosion resistance, and also oxidative resistance to castor oil. The results showed that the food grade grease had dropping point 189 194 oC, soft to moderate hardness consistency, NLGI 1 3, corrosion resistance 1a, and all the antioxidants effective to increased oxidative resistance of castor oil.

Abstrak :
Senyawa analog kurkumin merupakan kelas senyawa alami yang secara struktur ditandai dengan dua cincin aromatik yang dihubungkan oleh jembatan karbon, yang memiliki aktivitas biologis yang baik. Disisi lain, triazol merupakan senyawa heterosiklik  penting dalam kimia obat yang memiliki potensi terhadap anti bakteri dan antioksidan.Pada penelitian ini menggunakan berbagai variasi senyawa aldehida aromatik sebagai prekursor dalam mensintesis senyawa analog kurkumin. Senyawa analog kurkumin ini dapat disintesis dengan cara mereaksikan variasi aldehida aromatik seperti 4-hidroksi-3-metoksibenzaldehida (vanilin) dan 4-hidroksibenzaldehida dengan bantuan HCl.  Analog kurkumin yang terbentuk dapat dimodifikasi lebih lanjut membentuk bis-propargil dan bis-1,2,3-triazol. Produk yang terbentuk dimurnikan dengan kromatografi kolom, diindentifikasi menggunakan KLT dan dikarakterisasi menggunakan FTIR, LC-MS, dan NMR. Senyawa hasil sintesis dilakukan uji bioaktivitas sebagai antioksidan dengan menggunakan metode DPPH. Dengan memvariasikan aldehida memberikan hasil yang berbeda, yang akan dipengaruhi oleh ada atau tidak gugus pendorong elektron pada cincin benzena. Senyawa dihidroksi vanilin memiliki nilai persen inhibisi sebesar 95%, dihidroksi 4-hidroksibenzaldehida  95%, bis-propargil vanilin 53%, bis-propargil 4-hidroksibenzaldehida 45%, bis-1,2,3-triazol vanilin 25%, dan bis-1,2,3-triazol 4-hidroksibenzaldehida 20%. Diketahui bahwa senyawa dengan gugus metoksi memiliki nilai persen inhibisi DPPH yang lebih tinggi. ......Curcumin analogs are a class of chemical compounds structurally characterized by two aromatic rings connected by a carbon bridge, which have good biological activity. On the other hand, triazoles are important heterocyclic compounds in medicinal chemistry that have antibacterial and antioxidant potential. In this study, a variety of aromatic aldehyde compounds were used as precursors in synthesizing curcumin analogues. This curcumin analog compound can be synthesized by reacting various aromatic aldehydes such as vanillin and 4-hydroxybenzaldehyde with the help of HCl. The curcumin analogs formed can be further modified to form bis-propargyl and bis-1,2,3-triazol. The product formed was purified by column chromatography, identified using TLC and characterized using FTIR, LC-MS, and NMR. The synthesized compound was tested for bioactivity as an antioxidant using the DPPH method. Varying the aldehydes gives different results, which will be affected by the presence or absence of electron-donating groups on the benzene ring. The compound dihydroxy vanillin had a percentage inhibition value of 95%, dihydroxy 4-hydroxybenzaldehyde 95%, bis-propargyl vanillin 53%, bis-propargyl 4-hydroxybenzaldehyde 45%, bis-1,2,3-triazole vanillin 25%, and bis- 1,2,3-triazole 4-hydroxybenzaldehyde 20%. It can be concluded that compounds with methoxy groups have a higher percentage value of DPPH inhibition.

Abstrak :
Kurkumin merupakan senyawa bahan alam yang memiliki berbagai aktivitas biologis seperti antiinflamasi dan antioksidan. Akan tetapi aplikasi klinis kurkumin masih belum optimal karena profil farmakokinetiknya yang buruk seperti bioavaibilitas yang rendah, metabolisme yang cepat, dan buruknya stabilitas kimia (Rajasekaran, 2011). Oleh karena itu, untuk meningkatkan aktivitas farmakologi kurkumin, maka perlu dilakukan modifikasi struktur kimia kurkumin. Pada penelitian ini dilakukan modifikasi struktur kurkumin menjadi beberapa senyawa analog kurkumin monokarbonil asimetrik (AKMA) (5a-f) dan AKMA yang tersubstitusi basa Mannich morfolin (7a-f) yang diharapkan mampu meningkatkan aktivitas antiinflamasi dan antioksidan. Sintesis dilakukan dalam 3 tahap. Tahap pertama dan kedua dilakukan dengan melibatkan reaksi kondensasi Claisen-Schmidt, sedangkan tahap ketiga dengan reaksi Mannich. Kemurnian setiap senyawa hasil sintesis tahap 2 dan 3 diuji menggunakan Kromatografi Lapis Tipis dan penetapan jarak lebur. Struktur setiap senyawa hasil sintesis tahap 2 dan 3 dianalisis menggunakan spektrofotometer FTIR, spektrometri 1H-NMR dan 13CNMR, dan HR-MS. Setiap senyawa hasil sintesis ini terbukti memiliki aktivitas antiinflamasi dan antioksidan, namun dengan aktivitas yang masih di bawah standard dan senyawa pembanding. Senyawa 7c (IC50=25,26 μM) dan 7d (IC50=26,27 μM) terbukti memiliki aktivitas yang hampir sama dengan standard Na-diklofenak (IC50=20,35 μM) dan senyawa pembanding siklovalon (IC50= 22,38 μM). Selain itu, senyawa 5d (IC50= 68,91 μM) terbukti memiliki aktivitas antioksidan yang hampir sama dengan siklovalon (IC50= 72,04 μM). Substitusi basa Mannich morfolin pada senyawa AKMA terbukti dapat meningkatkan aktivitas antiinflamasi, akan tetapi dapat menurunkan aktivitas antioksidan

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Curcumin is a natural active product that has various pharmacological activities such as anti-inflammatory and antioxidant. However, the clinical application of curcumin is still not optimal because of the poor pharmacokinetic profiles such as low bioavailability, rapid metabolism, and poor chemical stability (Rajasekaran, 2011). Therefore, to increase the curcumin pharmacological activity, it is necessary to modify the chemical structure of curcumin. In this study, structure modification of cyclovalone into asymmetric monocarbonyl analogs of curcumin (AMACs) (5a-f) and asymmetric monocarbonyl analogs of curcumin substituted Mannich base of morpholine (7a-f) are expected to enhance its anti-inflammatory and antioxidant activity. Synthesis was conducted in 3 stages. The first and second stages were done by the Claisen-Schmidt condensation reaction to obtain compound 5a-f, while the third stage was by the Mannich reaction to obtain compound 7a-f. The purity of the synthesized compounds were tested using Thin Layer Chromatography and determination of the melting range. The synthesized compounds were characterized by FTIR, 1H-NMR, 13C-NMR, and HRMS. All the synthesized compounds showed lower activity than symmetrical MAC, cyclovalone. Compound 7c and 7d exhibited a potent anti‐inflammatory activity (IC50=25,26 μM and 26,27 μM, respectively), which almost comparable to cyclovalone (IC50=22,38 μM) and the standard diclofenac sodium (IC50=20,35 μM). All the synthesized compounds showed lower antioxidant activity than the symmetrical MAC, cyclovalone and quercetin. However, compound 5d showed antioxidant activity, which is comparable to cyclovalone (IC50=72,04μM). The substitution of morpholine Mannich base in AMACs has been shown to enhance anti-inflammatory activity, but may decrease antioxidant activity.

Abstrak :
Research through a metabolomics approach is carried out withoutisolating a single active compound responsible for an activity. Empirically the root, stem, and leaf preparations of Rhinachantus nasutus (L.) Kurz have long been used in traditional medicine such as the treatment of diabetes, eczema, pulmonary tuberculosis, herpes, hepatitis, and hypertension. This dissertation aims to evaluate compounds that have antioxidant and antidiabetic activity through inhibition of alpha-glucosidase activity of plant R. Nasutus metabolomics and molecular tethering based liquid chromatography very high performance mass spectrometry/mass spectrometry (KCKST SM/SM). The stages of research carried out include: (1) Extraction of leaves, flowers, and bark using 70% ethanol with ultrasonic wave-assisted extraction method. (2) Fractionation of selected extracts using centrifugation partition chromatography (PPP). (3) Testing of antidiabetic activity through the mechanism of alpha-glucosidase inhibition of selected extracts and their PPP fractions in vitro. (4) Testing of antioxidant activity by 1,1-diphenyl-2-picrylhydrazil (DPPH) method; ferric reducing antioxidant power (FRAP); cupric ion reducing antioxidant capacity (CUPRAC) in vitro against extracts and PPP fractions whose alpha-glucosidase inhibitory activity is very active and/or active. (5) Determination of metabolite profiles using KCKST SM/SM Q-Orbitrap on PPP fractions whose alpha-glucosidase inhibitory activity is very active and/or active. (6) Chemometric analysis with multivariate data analysis using SIMCA software against metabolite area area data and bioactivity data. (7) Verification of compounds that contribute significantly as inhibitors of alpha-glucosidase activity resulting from metabolomics by molecular tethering. This study obtained 10 active compounds in the inhibition of alpha-glucosidase in the KPS fraction of R. nasutus, namely compounds (5) bis(2-ethylhexyl) amines, (6) choline, (7) leu gly, (8) N-methyltanolamine phosphate, (11) N-methyldioctylamine, (14) dodesiltrimethethlammonium, (15) austalida J, (17) DL-β-leucine, (22) cemilicoisoflavone B, and (26) licoflavone B. In addition, 6 compounds (compounds 5, 8, 11, 14, 15, and 22) contributed significantly as alpha-glucosidase inhibitors as well as very strong antioxidants with the FRAP method and 3 compounds (compounds 5, 11, and 15) with the CRAPC method. ......In the metabolomics approach, research is done without isolating any active compounds that cause activity. Empirically, preparations of the roots, stems, and leaves of Rhinachantus nasutus (L.) Kurz have long been used in traditional medicine for such purposes as the treatment of diabetes, eczema, pulmonary tuberculosis, herpes, hepatitis, and hypertension. This dissertation aims to evaluate compounds with antioxidant and anti-diabetic activity by inhibiting the alpha-glucosidase activity of the plant R. nasutus using a metabolomics approach and molecular docking based on ultra-high performance liquid chromatography mass spectrometry/mass spectrometry (UHPL MS/MS). The stages of the research included: (1) extraction of leaves, flowers, and stem bark using 70% ethanol using an ultrasound-assisted extraction (UAE) method. (2) Fractionation of selected extracts using centrifugation partition chromatography (CPC). (3) In vitro testing of antidiabetic activity through the mechanism of alpha-glucosidase inhibition of selected extracts and their CPC fractions. (4) Testing the antioxidant activity with the 1,1-diphenyl-2-picrylhydrazyl (DPPH) method, ferric reducing antioxidant power (FRAP), and cupric ion reducing antioxidant capacity (CUPRAC) in vitro against extracts and CPC fractions with highly active, active, or slightly active alpha-glucosidase inhibitory activity. (5) Determination of metabolite profiles using KCKST SM/SM Q-Orbitrap on CPC fractions with highly active or slightly active alpha-glucosidase inhibitory activity. (6) Chemometric analysis in the form of multivariate data analysis using SIMCA software on metabolite area data and bioactivity data. (7) Verification of compounds that contribute significantly as inhibitors of alpha-glucosidase activity in metabolomics by molecular docking.This study obtained 10 active compounds in alpha-glucosidase inhibition in the R. nasutus CPC fraction, namely compounds (5) bis(2-ethylhexyl) amine, (6) choline, (7) leugly, (8) N-methylethanolamine phosphate, (11) N-methyldioctylamine, (14) dodecyltrimethylammonium, (15) austalide J, (17) DL-β-Leucine, (22) semilicoisoflavone B, and (26) licoflavone B. In addition, it was also found that six compounds (compounds 5, 8, 11, 14, 15, and 22) significantly contributed as alpha-glucosidase inhibitors as well as very strong antioxidants with the FRAP method and three compounds (compounds 5, 11, and 15) with the CUPRAC method.

Abstrak :
Lemak dan minyak mudah mengalami kerusakan akibat proses oksidasi. Untuk memperlambat proses oksidasi tersebut, diperlukan antioksidan. Namun, penggunaan antioksidan sintetik sekarang mi ditinjau kembali karena ada yang bersifat merugikan. Oleh karena itu pengembangan antioksidan yang berasal dari alam, yang reiatif lebih aman tengah digalakkan saat ini.

Abstrak :
Kurkumin sebagai senyawa alami yang memiliki aktivitas biologis yang beragam salah satunya antioksidan dan banyak digunakan sebagai senyawa obat. Akan tetapi, aplikasi kurkumin sebagai senyawa obat belum dapat optimal karena memiliki masalah pada stabilitas dan profil farmakokinetik yang buruk. Untuk memperbaiki masalah tersebut dapat dilakukan dengan memodifikasi struktur kurkumin menjadi analog kurkumin monokarbonil non-simetri yang bermotif 1,2,3-triazol. Pada penelitiaan ini, senyawa analog kurkumin monokarbonil disintesis dengan beberapa prinsip reaksi seperti propargilasi, kondensasi Claisen- Schmidt, dan sikloadisi azida-alkuna dengan variasi azido aromatik untuk membentuk cincin triazol. Senyawa hasil sintesis akan dimurnikan dengan kromatografi kolom dan diidentifikasi dengan KLT serta dikarakterisasi dengan uji titik leleh, HRMS, FTIR, dan NMR. Hasil sintesis senyawa produk akhir memiliki rendemen berturut-turut untuk senyawa triazol 4-NO2 monokarbonil kurkumin 4- OCH3, triazol 4-Cl monokarbonil kurkumin 4-OCH3, triazol 4-COCH3 monokarbonil kurkumin 4-OCH3 adalah 70%; 83%; 86%, serta uji aktivitas antioksidan seluruh senyawa produk akhir terhadap radikal DPPH berturut-turut menunjukkan nilai inhibisi sebesar 68,17%; 73,35%; 71,94%. ......Curcumin is a natural compound that has various biological activities, one of which is antioxidant and is widely used as a medicinal compound. However, the application of curcumin as a medicinal compound has not been optimal because it has problems with stability and a poor pharmacokinetic profile. To fix this problem, it can be done by modifying the structure of curcumin into a non-symmetrical monocarbonyl analog curcumin with a 1,2,3-triazole pattern. In this research, a monocarbonyl curcumin analog compound was synthesized using several reaction principles such as propargylation, Claisen-Schmidt condensation, and azide-alkyne cycloaddition with various aromatic azidos to form a triazole ring. The synthesized compound will be purified by column chromatography and identified by TLC. It will also be characterized by melting point, HRMS, FTIR, and NMR tests. The results of the synthesis of the final product compounds showed successive yields for triazole 4-NO2 monocarbonyl curcumin 4-OCH3, triazole 4-Cl monocarbonyl curcumin 4-OCH3, and triazole 4-COCH3 monocarbonyl curcumin 4-OCH3 of 70%, 83%, and 86%, respectively. The antioxidant activity test of all compounds of the final product against DPPH radicals showed inhibition value of 68.17%, 73.35%, 71.94%, respectively.

Abstrak :
Minyak biji kelor memiliki potensi antioksidan yang baik, namun secara topikal dapat menyebabkan iritasi dan rasa tidak nyaman pada kulit. Minyak biji kelor dirancang menggunakan sistem penghantaran Solid Lipid Nanoparticle (SLN). Penelitian ini bertujuan untuk memformulasikan dan menguji aktivitas antioksidan minyak biji kelor dalam bentuk topikal dengan sistem penghantaran SLN pada sediaan lotion. Minyak biji kelor dilakukan karakterisasi, lalu dijadikan zat aktif pada pembuatan SLN. Formula SLN dikarakterisasi dan dipilih satu formula untuk diinkorporasikan ke dalam sediaan lotion. Lotion dievaluasi serta diuji aktivitas antioksidan metode DPPH dengan spektrofotometer UV-Vis. Formula SLN minyak biji kelor dengan konsentrasi gliseril monostearat 2,5% menunjukkan karakterisasi dengan ukuran globul (Dv90) 141 nm, indeks polidispersitas 0,174, zeta potensial -35,4 mV dan efisiensi penjerapan sebesar 22,6887%. Formula lotion yang mengandung SLN sebanyak 10% memiliki ukuran globul 322 nm, indeks polidispersitas 0,350, dan zeta potensial sebesar -35,9 mV. Hasil uji aktivitas antioksidan pada minyak biji kelor menunjukkan nilai IC50 sebesar 147,027 µg/mL dan nilai IC50 sediaan lotion pada minggu ke-0 dan ke-12 menunjukkan penurunan aktivitas yaitu dari 11.993,868 µg/mL menjadi 37.661,615µg/mL. Hal ini dapat disimpulkan bahwa sediaan lotion yang mengandung 10% SLN minyak biji kelor tidak memiliki aktivitas antioksidan. ......Moringa seed oil has good antioxidant potential, but topically it can cause irritation and discomfort in the skin. Moringa seed oil is designed using a Solid Lipid Nanoparticle (SLN) delivery system that can form a film layer on the skin and can increase stability. This study aims to formulate and test antioxidant activity of Moringa seed oil in topical form with the SLN delivery system. Moringa seed oil was characterized, then used as an active substance in the preparation of SLN. The SLN formula was characterized and one formula was selected to be incorporated into the lotion preparation. Lotion preparations were evaluated and tested for antioxidant activity by the DPPH method with a UV-Vis spectrophotometer. The SLN formula of Moringa seed oil with a glyceryl monostearate concentration of 2.5% showed characterization with a globul size (Dv90) of 141 nm, a polydispersity index of 0.174, a potential zeta of -35.4 mV and entrapment efficiency of 22.6887%. The lotion formula containing 10% SLN had a globul size of 322 nm, a polydispersity index of 0.350, and a potential zeta of -35.9 mV. Lotion preparations showed good physical stability for 12 weeks at various temperatures, but were unstable at testing for viscosity, globul size, and potential zeta. The antioxidant activity of Moringa seed oil showed an IC50 value of 147.027 μg/mL and the IC50 value of Moringa seed oil SLN lotion preparations at the 0th and 12th weeks showed a decreased activity, namely from 11.993.868 μg/mL to 37.661.615μg/mL. It can be concluded that lotion preparations containing 10% SLN of Moringa seed oil does not have antioxidant activity.

Abstrak :
Penyakit ikan mengkhawatirkan para pembudidaya karena dapat menurunkan kualitas ikan dan ikan meningkatkan kematian ikan. Penyakit pada ikan bisa disebabkan oleh infeksi bakteri dan stres oksidatif yang disebabkan oleh kontaminan di lingkungan. Senyawa dari tumbuhan seperti polifenol yang memiliki aktivitas antioksidan sekaligus antibakteri Patogen ikan sangat diminati sebagai pilihan alternatif untuk mengobati kedua penyakit tersebut. Berdasarkan penelitian sebelumnya, ekstrak metanol daun Kjellbergiodendron celebicum (Coord.) Merr. terbukti mengandung senyawa polifenol. Penelitian ini bertujuan untuk menguji aktivitas antioksidan dan antibakteri ekstrak etanol daun 70% Kjellbergiodendron celebicum (Coord.) Merr. yang diekstraksi menggunakan 2 metode berbeda yaitu maserasi dan UAE untuk membandingkan hasil tes, sekaligus mengerjakan penentuan kandungan fenolik total. Uji aktivitas antioksidan dilakukan dengan menggunakan metode tersebut DPPH dan FRAP, serta dilakukan uji antibakteri terhadap 3 bakteri patogen pada ikan, yaitu Aeromonas hydrophila, Edwardsiella ictaluri, dan Flavobacterium columnare menggunakan metode difusi cakram kertas dan mikrodilusi. Penentuan kandungan fenolik total dilakukan dengan menggunakan metode Folin-Ciocalteu dan kadar fenol yang diekspresikan dalam EAG (Setara Asam Galat). Uji aktivitas antioksidan metode DPPH menunjukkan IC50 ekstrak dari metode maserasi 11,48 μg / mL dan 9,82 μg / mL dari UAE. Metode Nilai FRAP FeEAC ekstrak hasil maserasi 1,581,6 μmol / g dan ekstrak dari UAE sebesar 1.661,3 μmol / gr. Dalam metode difusi cakram kertas, diameter area hambat Ekstrak dari metode maserasi adalah 14 mm pada Aeromonas hydrophila, 9,7 mm pada Edwardsiella ictaluri, dan 13,3 mm di Flavobacterium columnare, sedangkan pada Metode UAE 17,3 mm di Aeromonas hydrophila, di Edwardsiella ictaluri dari 10,7 mm dan 13,8 mm di kolom Flavobacterium. Dalam metode mikrodilusi, ekstrak menunjukkan penghambatan pertumbuhan bakteri pada ketiga bakteri tersebut patogen dengan MIC sebesar 781,25 µg / mL untuk diekstrak dari metode maserasi dan 390,6 μg / mL untuk ekstrak dari UAE. Dalam menentukan kandungan fenolik total dari ekstrak yang dimaserasi mengandung ekstrak 224,84 mgEAG / gr sedangkan ekstrak UEA mengandung 319,36 Ekstrak mgEAG / gr. Dari hasil penelitian dapat disimpulkan bahwa ekstrak etanol daun 70% Kjellbergiodendron celebicum (Coord.) Merr. memiliki aktivitas antioksidan dan antibakteri, dan ekstrak dari metode UAE memberikan aktivitas yang lebih baik dibandingkan dengan metode maserasi. ......Fish disease worries farmers because it can reduce fish quality and fish increases fish mortality. Diseases in fish can be caused by bacterial infections and oxidative stress caused by contaminants in the environment. Compounds from plants such as polyphenols which have antioxidant and antibacterial activity. Fish pathogens are in great demand as an alternative option for treating both diseases. Based on previous research, the methanol extract of the leaves of Kjellbergiodendron celebicum (Coord.) Merr. proven to contain polyphenol compounds. This study aims to test the antioxidant and antibacterial activity of the ethanol extract of leaves 70% Kjellbergiodendron celebicum (Coord.) Merr. which was extracted using 2 methods different namely maceration and UAE to compare test results, as well as to determine the total phenolic content. Antioxidant activity tests were carried out using the DPPH and FRAP methods, and antibacterial tests were carried out against 3 pathogenic bacteria in fish, namely Aeromonas hydrophila, Edwardsiella ictaluri, and Flavobacterium columnare using paper disc diffusion and microdilution methods. Determination of the total phenolic content was carried out using the Folin-Ciocalteu method and the phenol content expressed in EAG (Gallic Acid Equivalent). The DPPH antioxidant activity test showed that the IC50 extract from the maceration method was 11.48 μg / mL and 9.82 μg / mL from the UAE. Methods The value of the FRAP FeEAC extract from maceration results was 1.581.6 μmol / g and the extract from the UAE was 1.661.3 μmol / g. In the paper disc diffusion method, the diameter of the inhibitory area of ​​the extract from the maceration method was 14 mm in Aeromonas hydrophila, 9.7 mm in Edwardsiella ictaluri, and 13.3 mm in Flavobacterium columnare, whereas in the UAE method it was 17.3 mm in Aeromonas hydrophila, in Edwardsiella ictaluri from 10.7 mm and 13.8 mm in the Flavobacterium column. In the microdilution method, the extract showed inhibition of bacterial growth in the three pathogenic bacteria with an MIC of 781.25 µg / mL for extracting from the maceration method and 390.6 µg / mL for the extract from the UAE. In determining the total phenolic content of the macerated extract contained 224.84 mgEAG / gr extract while UEA extract contained 319.36 mgEAG / gr extract. From the research results, it can be concluded that the ethanol extract of the leaves of 70% Kjellbergiodendron celebicum (Coord.) Merr. has antioxidant and antibacterial activity, and the extract from the UAE method provides better activity compared to the maceration method.

Abstrak :
Senyawa basa Schiff memiliki aktivitas biologis seperti antioksidan, antibakteri, antikanker, dan antitumor. Pada penelitian ini dilakukan sintesis senyawa basa Schiff turunan asam lemak yang mengandung gugus aromatik melalui tiga tahapan reaksi. Prekursor awal yang digunakan untuk mensintesis senyawa basa Schiff ini adalah asam lemak yang terkandung dalam palm fatty acid distillate (PFAD) menghasilkan senyawa intermediet ester. Senyawa basa Schiff disintesis dengan mereaksikan intermediet hidrazida dengan tiga aldehida aromatik yang berbeda, yaitu benzaldehida, 2- hidroksibenzaldehida, dan sinamaldehida. Senyawa basa Schiff yang terbentuk diidentifikasi menggunakan KLT dan titik leleh serta dikarakterisasi menggunakan FTIR, Spektrofotometer UV-Vis, dan LC-MS. Kemudian produk akhir senyawa basa Schiff turunan asam lemak berbasis aldehida aromatik yang terbentuk diuji aktivitas antioksidannya dengan menggunakan metode DPPH. Hasil penelitian ini diperoleh senyawa basa Schiff turunan asam lemak berbasis benzaldehida dengan persen rendemen sebesar 76,65%, senyawa basa Schiff turunan asam lemak berbasis 2- hidroksibenzaldehida dengan persen rendemen sebesar 49,51%, dan senyawa basa Schiff turunan asam lemak berbasis sinamaldehida dengan persen rendemen sebesar 59,17%. Kemampuan antioksidan tertinggi diperoleh oleh senyawa basa Schiff turunan asam lemak berbasis 2-hidroksibenzaldehida dengan nilai IC50 sebesar 108,59 ppm dan kemampuan antioksidan terendah diperoleh oleh senyawa basa Schiff turunan asam lemak berbasis benzaldehida dengan nilai IC50 sebesar 345,27 ppm. ......Schiff base compounds have a biological activity, such as antioxidant, antibacterial, anticancer, and antitumor. In this study, synthesized of Schiff base compounds derived from fatty acid via three steps reaction. The initial precursor used to synthesize Schiff base compounds was the fatty acid from palm fatty acid distillate (PFAD) to formed intermediate ester compound. Schiff base compounds were synthesized by reacting the intermediate hydrazide with three different aromatic aldehydes: benzaldehyde, 2-hydroxybenzaldehyde, and cinnamaldehyde. The product formed Schiff base compounds will be identified using TLC, melting point, and characterized using instrument FTIR, UV-Vis Spectrophotometry, and LC-MS. Then, the final product Schiff base compounds based on aromatic aldehydes were tested for antioxidant activity using DPPH method. The fatty acid – Schiff base derived from benzaldehyde compound gave a yield percentage of 76.65%, the fatty acid-Schiff base derived from 2-hydroxybenzaldehyde compound gave a yield percentage of 49.51%, and the fatty acid-Schiff base derived from cinnamaldehyde compound gave a yield percentage of 59,.7%. The highest antioxidant activity was obtained by fatty acid-Schiff base derived from 2-hydroxybenzaldehyda with an IC50 value of 108.59 ppm and the lowest antioxidant activity was obtained by fatty acid-Schiff base derived from benzaldehyde with an IC50 value of 345.37 ppm.