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All Journal Jurnal Sains Materi Indonesia The Journal of Pure and Applied Chemistry Research Jurnal Kimia dan Kemasan Majalah Obat Tradisional KOVALEN: Jurnal Riset Kimia Acta Pharmaceutica Indonesia Chimica et Natura Acta Acta Pharmaciae Indonesia : Acta Pharm Indo Martabe : Jurnal Pengabdian Kepada Masyarakat PHARMACY: Jurnal Farmasi Indonesia (Pharmaceutical Journal of Indonesia) Acta Biochimica Indonesiana Jurnal Ilmiah Farmasi Farmasyifa BERNAS: Jurnal Pengabdian Kepada Masyarakat Jurnal Kimia dan Kemasan Indonesian Community Journal Pharmacy Reports Jurnal Sains dan Teknologi Farmasi Indonesia Kartika : Jurnal Ilmiah Farmasi Indonesian Journal of Chemical Science Jurnal Sains dan Kesehatan Journal of Chemistry Sciences and Education Indonesian Journal of Science and Education
Anjar Hermadi Saputro
Department Of Pharmacy, Faculty Of Science, Institut Teknologi Sumatera
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Molecular docking of several compounds in Bauhinia thonningii as alfa estrogen receptor inhibitors in breast cancer Zaqia, Lulu; Alhestha, Salsabila Zahra; Rahmadini, Celina Fadila; Kusumawati, Maiya; Dhiya, Syifa Nasywa; Andriani, Wellen Putri; Azzahra, Zeta Agustri; Auli, Winni Nur; Saputro, Anjar Hermadi
Pharmacy Reports Vol. 3 No. 3 (2023): Pharmacy Reports
Publisher : Indonesian Young Scientist Group and UPN Veteran Jakarta

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.51511/pr.70

Abstract

Compounds contained in Bauhinia thonningii have been proven in vitro to have anti-breast cancer effects. This research was carried out to validate in silico the compounds contained in Bauhinia thonningii. The molecular docking process begins with the ER target protein alpha (PDB id: 2BJ4) downloaded from the web http://www.rcsb.org/. After that, validation was carried out on natural ligands and target proteins using AutodockTools (Autodock 4.2 and Autogrid). Continued with optimization of the compounds to be tested, namely 6,8-Di-C-methyl kaempferol 3,7-dimethyl ether; 6-C-Methylquercetin-3,4'-dimethylether; Quercetin‑3‑O‑α‑L‑rhamnopyranoside and Tamoxifen as a positive control was downloaded at https://molview.org/ then geometrically optimized using Avogadro then docked with the target protein ER-α. Obtained bond energy results between natural ligands, 3 test compounds and 1 control compound 4-HYDROXYTAMOXIFEN; 6,8-Di-C-methyl kaempferol 3,7-dimethyl ether; 6-C-Methylquercetin-3,4'-dimethylether ;Quercetin-3–O-α-L-rhamnopyranoside and tamoxifen were -11.32,-6.07, -7.26,-8.88, -10.33 kcal/mol. If we look at the smallest bond energy, it is found that the compounds that have the greatest potential when sorted are the natural ligand, positive control, Quercetin‑3‑O‑α‑L‑rhamnopyranoside, 6-C-Methylquercetin-3,4'-dimethyl ether and 6,8-Di-C-methyl kaempferol 3,7-dimethyl ether.
Molecular docking analysis of guaiacin and chalcone from nutmeg (Myristica fragrans) as novel HSP90A inhibitors for skin cancer treatment Arrafi, Muhammad Zhafran; Cahyani, Ayu Sukma; Sitohang, Nada Nikita; Ulya, Salsa Nabila Ahlika; Anggraeni, Inggrid; Amalia, Miranti; Putri, Gladys Ellnora; Rajwa, Raihan M Dhiya; Auli, Winni Nur; Saputro, Anjar Hermadi
Pharmacy Reports Vol. 3 No. 3 (2023): Pharmacy Reports
Publisher : Indonesian Young Scientist Group and UPN Veteran Jakarta

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.51511/pr.73

Abstract

Skin cancer represents one of the most prevalent malignancies globally, with Indonesia reporting the third highest incidence among cancer types. Despite advances in treatment, there remains a critical need for novel therapeutic agents. Heat Shock Protein 90 Alpha (HSP90A) has emerged as a promising target for cancer therapy due to its critical role in stabilizing oncogenic proteins. This study aimed to evaluate the potential of guaiacin and chalcone from nutmeg (Myristica fragrans) as HSP90A inhibitors for skin cancer treatment through computational analysis. Molecular docking was performed using AutoDock Tools with the HSP90A crystal structure (PDB ID: 2VCJ). The compounds were assessed for binding affinity, molecular interactions, and drug-likeness properties according to Lipinski's Rule of Five. Redocking validation yielded an RMSD of 1.24 Å, confirming protocol reliability. Guaiacin demonstrated promising binding affinity (-7.40 kcal/mol) with key hydrogen bonds to Asp93 and Lys58, while chalcone showed moderate affinity (-5.99 kcal/mol) with a single hydrogen bond to Thr184. Both compounds exhibited favorable drug-like properties with high predicted gastrointestinal absorption. Guaiacin emerges as a promising natural HSP90A inhibitor candidate with binding energy exceeding the stability threshold (-7.00 kcal/mol) and interactions with critical residues in the ATP-binding pocket, providing a foundation for further development of nutmeg-derived compounds as potential anticancer agents.
Molecular docking of capsaicin and its derivatives as acetylcholinesterase (AChE) inhibitors in Alzheimer disease Syah, Vicky Ardian; Geralda, Rifka; Sakti, Nickyta Salsabila Ira; Febriyanti, Kharisma; Bokshow, Rency Violita Vanden; Wulandari, Valentri; Hasanah, Siti Fadhilatul; Fadillah, Muhammad Zakki; Auli, Winni Nur; Saputro, Anjar Hermadi
Pharmacy Reports Vol. 4 No. 1 (2024): Pharmacy Reports
Publisher : Indonesian Young Scientist Group and UPN Veteran Jakarta

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.51511/pr.74

Abstract

Alzheimer's disease (AD) is a progressive neurodegenerative disorder predominantly affecting older adults, characterized by pathological processes that include excessive acetylcholinesterase (AChE) activity leading to depleted acetylcholine levels. Although synthetic AChE inhibitors such as donepezil are used therapeutically, their clinical application is often limited by adverse effects and high costs. Capsaicin, a bioactive compound derived from chili peppers, has exhibited neuroprotective properties—including cognitive enhancement and amyloid-β reduction—suggesting its potential as a natural alternative for AD treatment. This study investigated capsaicin and six structural derivatives as potential AChE inhibitors through in silico molecular docking simulations against the human AChE crystal structure (PDB: 4EY7), using donepezil as a reference ligand. The docking protocol was validated with a root-mean-square deviation (RMSD) value of 0.71 Å, confirming reproducibility and reliability. The calculated binding affinities of the evaluated compounds ranged from –6.13 to –11.60 kcal/mol. Among them, 2-Hydroxy-3-(octyloxy)phenyl-5-(acrylamido)methylbenzophenone (Compound 2) exhibited the strongest binding affinity (–11.60 kcal/mol), slightly exceeding that of donepezil (–11.45 kcal/mol). Compound 2 formed four hydrogen bonds within the active site and shared key interactions with residues Phe338 and Trp286, consistent with the binding mode of donepezil. These results suggest that Compound 2 may serve as a potent natural AChE inhibitor and warrant further investigation as a candidate for Alzheimer’s disease therapy.
Molecular docking analysis of flavonoid compounds from gandaria (Bouea macrophlla Griff) as potential alpha-glucosidase inhibitors Azzahrah, Qurrota A’yun; Novelina, Laras; Rosviena, Nyi Ayu Fayza; Saabirah, Ghania Parsa; Adilla, Annisa Rahma; Saeli, Pinka Mustika; Uswatunhasanah, Putri; Auli, Winni Nur; Saputro, Anjar Hermadi
Pharmacy Reports Vol. 4 No. 1 (2024): Pharmacy Reports
Publisher : Indonesian Young Scientist Group and UPN Veteran Jakarta

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.51511/pr.75

Abstract

Diabetes mellitus represents a significant metabolic disorder with elevated global prevalence, necessitating development of effective antidiabetic therapies. This study investigates flavonoid compounds from gandaria (Bouea macrophylla Griff) as potential α-glucosidase inhibitors through molecular docking analysis. Eight flavonoid compounds were evaluated against human α-glucosidase enzyme (PDB ID: 2QMJ) using AutoDock Tools version 1.5.6. The methodology achieved validation with an RMSD value of 1.98 Å, confirming computational reliability. Lipinski's Rule of Five assessment identified four compounds meeting drug-likeness criteria for analysis. Quercetin demonstrated the strongest binding affinity among tested compounds with a binding energy of -4.72 kcal/mol, compared to the native ligand N-acetylglucosamine at -5.12 kcal/mol. Interaction analysis revealed quercetin formed significant hydrogen bonds with key active site residues including Lys389, Asn393, and Asn417, indicating potential competitive inhibition mechanisms. All flavonoid compounds exhibited consistent binding patterns with Lys389 serving as a critical interaction site. These computational findings establish quercetin as the most promising flavonoid candidate for α-glucosidase inhibition, supporting its potential as a natural antidiabetic agent.
Molecular docking of hybrid coumarin thiazole derivative as anti-breast cancer on VEGFR-2 protein Liswatini, Putri; Rahma, Sophia; Mariska, Putri; Anggraeni, Fibria; Agustin, Desti; Sari, Desi Puspita; Afrian, Mahisa Shzara; Auli, Winni Nur; Saputro, Anjar Hermadi
Pharmacy Reports Vol. 4 No. 2 (2024): Pharmacy Reports
Publisher : Indonesian Young Scientist Group and UPN Veteran Jakarta

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.51511/pr.76

Abstract

VEGFR-2 is a tyrosine kinase receptor located on cell membranes, originally identified in endothelial cells but also expressed in tumor cells and various cancer types, including breast cancer. In breast cancer, VEGFR-2 expression is upregulated during early stages of primary tumors and invasive metastases, with elevated levels associated with lymph node metastasis and reduced survival outcomes. This computational study evaluated the potential of coumarin-thiazole derivative compounds against VEGFR-2 as anticancer agents using molecular docking analysis. Three coumarin-thiazole hybrid compounds (42a, 54a, and 54b) were assessed for their binding affinity to VEGFR-2, with sorafenib serving as the reference drug. The docking analysis utilized the three-dimensional structure of VEGFR-2 (PDB ID: 2OH4) downloaded from the RCSB Protein Data Bank. Ligand structures were prepared using molecular modeling software and converted to appropriate formats for analysis. Molecular docking was performed using AutoDockTools v.1.5.7, and protein-ligand interactions were visualized using BIOVIA Discovery Studio 2024 software.Method validation using the native GIG ligand yielded a binding energy of -10.88 kcal/mol. The binding energy values for the three test compounds were -9.81 kcal/mol for compound 42a, -12.71 kcal/mol for compound 54a, and -12.77 kcal/mol for compound 54b. Compound 54b demonstrated the strongest binding affinity to VEGFR-2, surpassing the native ligand GIG, the reference drug sorafenib, and the other test compounds. These results indicate that compound 54b represents the most promising candidate for anti-breast cancer therapy through VEGFR-2 targeting, warranting further experimental validation.
Molecular docking of several compounds in katuk (Sauropus androgynus (L.)) leaves as anti-breast cancer in AKT1 protein Sutjiningsih, Ni Nyoman Ota; Ulisya, Azzaima Ayu; Utami, Amalda; Natalia, Christine; Mumtaz, Fakhira Chairunnisa; Yulanda, Nola Rohmi Eka; Sari, Victoria Rekina; Auli, Winni Nur; Saputro, Anjar Hermadi
Pharmacy Reports Vol. 4 No. 3 (2024): Pharmacy Reports
Publisher : Indonesian Young Scientist Group and UPN Veteran Jakarta

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.51511/pr.77

Abstract

Breast cancer represents a leading cause of cancer-related mortality among women worldwide. Katuk leaves (Sauropus androgynus L.) demonstrate potential as anticancer agents through their ability to inhibit metastatic processes. The AKT1 protein plays a critical role in preventing apoptosis in breast cancer cells, making it an important therapeutic target. This study employed molecular docking analysis to evaluate the binding affinity of bioactive compounds from katuk leaves to the AKT1 protein. The docking methodology involved protein preparation using structures obtained from the Protein Data Bank (PDB ID 3O96), followed by ligand preparation and validation using AutoDockTools version 1.5.6. Chemical interaction analysis was performed using BIOVIA Discovery Studio 2021 software. The binding energy analysis encompassed one native ligand, one reference drug (afuresertib), and five katuk-derived compounds: kaempferol, catechin, coumarin, squalene, and phytol. The respective binding energies were determined as -12.59, -8.70, -5.92, -6.44, -5.05, -8.11, and -6.70 kcal/mol. Among the tested compounds, squalene exhibited the strongest binding affinity (-8.11 kcal/mol), demonstrating superior interaction with the AKT1 protein compared to other katuk-derived bioactive compounds. The in silico screening results indicate that bioactive constituents in katuk leaves possess favorable binding characteristics for breast cancer protein targets, with squalene showing particular promise as a natural AKT1 inhibitor.
Molecular docking of piperine, limonene, and eugenol in black pepper (Piper nigrum L.) as anti-stroke Azzahra, Fauzia; Nadapdap, Ezra Gabriella Oktaviany; Cahyani, Nabila; Salsabila, Fathul Aini; Afada, M. Mufti; Auli, Winni Nur; Saputro, Anjar Hermadi
Pharmacy Reports Vol. 4 No. 3 (2024): Pharmacy Reports
Publisher : Indonesian Young Scientist Group and UPN Veteran Jakarta

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.51511/pr.79

Abstract

Stroke remains a leading cause of death and disability worldwide, necessitating the development of effective therapeutic agents. This study explores the potential of bioactive compounds from Piper nigrum L. (black pepper) as anti-stroke candidates targeting the cGMP-specific phosphodiesterase 5A (PDE5A) receptor (PDB ID: 3BJC). The evaluation employed molecular docking and drug-likeness assessment methodologies. Piperine, limonene, and eugenol were assessed using Lipinski's Rule of Five (RO5) to predict oral bioavailability. All compounds met the RO5 criteria, indicating favorable drug-likeness characteristics. Molecular docking was validated through re-docking of the native ligand WAN, yielding an RMSD ≤ 2 Å, confirming the accuracy of the docking protocol. Following validation, molecular docking analysis revealed that piperine demonstrated the lowest binding energy (-7.71 kcal/mol), followed by limonene (-5.28 kcal/mol) and eugenol (-4.86 kcal/mol). Visualization results revealed that piperine shared key interaction motifs and amino acid residues with the native ligand, including hydrogen bonding and hydrophobic interactions, indicating strong receptor affinity and molecular stability. Additionally, the ligand-receptor interaction distance of piperine (2.21 Å) closely resembled the native ligand (2.15 Å), further supporting its structural and functional similarity. These findings highlighted piperine as the most promising anti-stroke candidate among the tested compounds. Further in vitro and in vivo studies are recommended to validate its pharmacological efficacy and safety.
Perbandingan Metode Ekstraksi Maserasi, Sokletasi, Dan Sonikasi Terhadap Nilai Rendemen Ekstrak Rimpang Kunyit (Curcuma Longa L.) Annisa Rahma Aryanti; Made Helen Susanti; Anjar Hermadi Saputro; Herayati; Indah Puspita Sari; Syahjoko Saputra, Iwan
Journal of Chemistry Sciences and Education Vol 2 No 01 (2025): Journal of Chemistry Sciences and Education
Publisher : PT. Pubsains Nur Cendekia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.69606/jcse.v2i01.237

Abstract

This study aims to determine the comparison of maceration, soxhletation, and sonication extraction methods on the yield value of turmeric rhizome (Curcuma longa L.). Extraction was carried out using methanol and n-hexane solvents. The extraction process produces turmeric extract with different colors, textures, and aromas depending on the method used. The maceration, soxhletation, and sonication methods have different impacts on the yield of the extract, but the basic principle is the same in filtering active substances from the sample. The yield value obtained from the maceration method is 0.4996% soxhletation 0.0013% and sonication 0.0071%. The maceration method is proven to provide the highest extract yield compared to the soxhletation and sonication methods, which is 0.4996%.
PEMBERDAYAAN USAHA EKONOMI KREATIF MELALUI PENDEKATAN PELATIHAN DAN PENDAMPINGAN USAHA PEMBUATAN PRODUK JAMU KEKINIAN SEBAGAI UPAYA PENCAPAIAN SDGS DI KELURAHAN YOSOREJO, KOTA METRO Yulianti Suprahman, Nisa; Hidayaturahmah, Rizky; Hermadi Saputro, Anjar; Irna Windari, Nurul; Sarmoko, Sarmoko
Martabe : Jurnal Pengabdian Kepada Masyarakat Vol 7, No 11 (2024): MARTABE : JURNAL PENGABDIAN MASYARAKAT
Publisher : Universitas Muhammadiyah Tapanuli Selatan

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.31604/jpm.v7i11.4924-4929

Abstract

Sebagian besar masyarakat di Kelurahan Yosorejo, Kecamatan Metro Timur memiliki pekarangan rumah atau kebun yang sebagian ditanami tanaman obat keluarga (TOGA) seperti kunyit, temulawak, temugiring, jahe kencur, sirih, kecombrang, sambiloto, binahong dan lain-lain. Kendala utama yang dihadapi adalah belum optimalnya pemanfaatan tanaman obat keluarga (TOGA), rendahnya pengetahuan dan teknologi untuk membuat jamu kekinian yang berkualitas, jumlah diproduksi masih terbatas, jenis dan variasi produk juga masih sedikit dan market share masih rendah. Selain produk jamu, tanaman TOGA belum dilakukan pengembangan teknologi menjadi produk herbal yang bernilai ekonomi tinggi seperti sabun.  Faktor tersebut yang membuat industri jamu tradisional tidak bisa berkembang. Maksud Pengabdian Kepada Masyarakat (PKM) adalah mengembangkan usaha jamu kekinian pada Ibu-ibu PKK kelurahan Yosorejo agar dapat membantu meningkatkan pendapatan masyarakat. Tujuannya Mengembangkan dan memperbaiki usaha jamu tradisional menjadi jamu kekinian yang modern yang bisa mengangkat salah satu produk warisan leluhur turun temurun. Dengan cara memproses tahap-tahapan pembuatan produk secara benar, mengedukasi Ibu-Ibu PKK untuk giat mengembangkan usaha yang menguntungkan dan memiliki peluang yang sangat terbuka. Kegiatan dilakukan dengan metode pelatihan secara langsung serta pembagian produk jamu kekinian dan sabun organik ke masyarakat. Hasil dari kegiatan ini adalah masyarakat dapat memahami dan mampu membuat jamu dan sabun organik berbahan dasar tanaman TOGA.
Molecular Docking Senyawa Fiscalin b, Isoleutherin, Eleutherol, Kaempferol, dan Luteolin pada Tumbuhan Physalis angulata Linn. sebagai Anti Kanker Lidah pada Protein MMP-9 Riani, Nadia Nanda; Saputro, Anjar Hermadi; Auli, Winni Nur; Azizah, Nadya Nur; Simorangkir, Nanda Lenny Yuniaty br; Hutabarat, Stefanny Herlin Natalya; Natalia, Dela
Indonesian Journal of Chemical Science Vol. 14 No. 3 (2025): Indonesian Journal of Chemical Science
Publisher : Prodi Kimia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.15294/ijcs.v14i3.25817

Abstract

Kanker lidah adalah jenis kanker rongga mulut yang agresif dengan angka kejadian dan kematian tinggi, terutama karena diagnosis terlambat dan terbatasnya pilihan terapi efektif. Protein Matrix Metalloproteinase-9 (MMP-9) berperan penting dalam invasi dan metastasis sel kanker lidah dengan kemampuan mendegradasi matriks ekstraseluler, sehingga memfasilitasi penyebaran kanker. Tanaman herbal ciplukan (Physalis angulata Linn.) mengandung senyawa aktif seperti Lutheolin, Isoleutherin, yang berpotensi sebagai agen antikanker. Penelitian ini mengevaluasi afinitas senyawa Isoleutherin, Luteolin, Fiscalin b, Eleutherol, Kaempferol terhadap protein MMP-9 menggunakan metode molecular docking. Hasil menunjukkan Isoeleutherin memiliki energi ikatan bebas terendah (-8,49 kkal/mol), lebih rendah dibandingkan senyawa lain seperti Fiscalin b (-7,74 kkal/mol), Eleutherol (-7,73 kkal/mol), Kaempferol (-7,47 kkal/mol), dan Luteolin (-8,07 kkal/mol). Isoeleutherin memiliki potensi sebagai antikanker lidah walaupun kemampuannya tidak lebih baik dari ligan alaminya.
Co-Authors Achmad Gus Fahmi Adilla, Annisa Rahma Afada, M. Mufti Afrian, Mahisa Shzara Aghalfi, Revin Rindra Aghalfi Agustin, Desti Ahmad Bayu Satriawan Ahmad, Winda Tiara Ainiya, Aliva Ainun, Hadhistia Nur Al-Husni, Ihza Adzkiya Mubarak Alhestha, Salsabila Zahra Aluna Monalaika Izzati Amalia, Miranti Andriani, Wellen Putri Anggini, Joya Talitha Anggraeni, Fibria Anggraeni, Inggrid Anjani, Arfina Puteri Annisa Nofriani Annisa Rahma Aryanti Arrafi, Muhammad Zhafran Aulia, Nanda Aulia, Yasinta Sahma Ayuwulanda, Aditya Azizah, Nadya Nur Azti, Zahara Azzahra, Zeta Agustri Azzahrah, Qurrota A’yun Balqis, Selvi Billa, Firly Shalsha Bokshow, Rency Violita Vanden Cahyani, Ayu Sukma Cahyani, Nabila Chandra, Nabella Oktaviana Choiriah, Ika Putri Chrisnanda, Anang Agung Christine Natalia Citra Andini Cristiannanda, Daniel Dhiya, Syifa Nasywa Dwinna Rahmi Elisa Grace Clarensia Erniningsih, Ni Ketut Esa Amelia Ratri Yuniasri Fadillah, Muhammad Zakki Farah Zahira Shofa Fauziyya, Riri Fazilla, Rizki Fakhri Febrian, Tobi Febriyanti, Kharisma Fida, Marsa Jannatul Fransisca, Ni Putu Vina Geralda, Rifka Gusman, Adisti Faradilla Hafid, Gina Mutia Hasanah, Siti Fadhilatul Hati, Dinda Mutiara Herayati, Herayati Hidayati, Putri Aulia Nurul Hidayaturahmah, Rizky Hutabarat, Stefanny Herlin Natalya I Dewa Gde Mayun Permana Ihsanti Dwi Rahayu Indah Puspita Sari Indah Puspita Sari, Indah Puspita Indah Wulandari Ine Pebriyanti intan kusuma wardani Irna Windari, Nurul Iwan Syahjoko Saputra Iwan Syahjoko Saputra Iwan Syahjoko Saputra Iwan Syahjoko Saputra Kamilaini, Diva Arisanti Karima, Miska Aulia Kumara, Gusti Made Bagus Kusumawati, Maiya Liswatini, Putri Made Helen Susanti Maharani, Ayu Puspita Maharani, Gita Putri Mariska, Putri Mariska, Soraya Mega Fatimah Rosana Melki, Yana Putri Amelia Mellina, Echa Dian Mentari, Corona Mubarika Sekarsari Yusuf Muflihah, Hanny Muhammad Aditya Nugraha Mumtaz, Fakhira Chairunnisa Mutiara Putri, Mutiara Nadapdap, Ezra Gabriella Oktaviany Napitu, Ade Shinta Maria Br Natalia, Dela Natasya, Zaskiya Naurah Rosyidah Hasna Nisa Yulianti Suprahman Nisa Yulianti Suprahman Nopiandi, Yogi Novelina, Laras Nur Adliani Nur Adliani Pangestu, Maryo Adjie Panggabean, Diva Selviana Pasaribu, Romualdo Pebriyanti, Ine Pinanga, Yangie Dwi Marga Pravita, Nabila Cahya Prawicha, Ertika Agtha Primasty, Ratna Dewi Putri Amelia Rooswita Putri, Adelia Ofira Putri, Amalia Sonita Putri, Esterike Alfatien Putri, Gladys Ellnora Raden Mohamad Herdian Bhakti Rahma, Annisa Nur Rahma, Sophia Rahmadini, Celina Fadila Rajwa, Raihan M Dhiya Rasida, Rima Regita, Putu Ayu Reny Haryani Riani, Nadia Nanda Rifka Noor Azizah Rina Andriyani Riri Fauziyya Riri Fauziyya Rislia, Rana Atikah Rosviena, Nyi Ayu Fayza Saabirah, Ghania Parsa Sabrina Rakhel Zahirah Saeli, Pinka Mustika Sakti, Nickyta Salsabila Ira Salsabila, Fathul Aini Saputri, Mutiara Anggun Sari, Desi Puspita Sari, Victoria Rekina Sarini, Sarini Sarmoko Sarmoko Sarmoko Sarmoko Sativa, Nasywa Oryza Setiawati, Luh Gede Elen Simanullang, Gayatri Simorangkir, Nanda Lenny Yuniaty br Sitohang, Nada Nikita Sophi Damayanti Sudarsono Sudarsono Sudewi Mukaromah Khoirunnisa Sudewi Mukaromah Khoirunnisa Sudirman Sudirman Sutjiningsih, Ni Nyoman Ota Syaadatun Nadiah Syah, Vicky Ardian Syahjoko Saputra, Iwan Syakilla, Nadia Nur Tantri Liris Nareswari Tikarahayu Putri Ulfa, Lutfiyana Ulisya, Azzaima Ayu Ulya, Salsa Nabila Ahlika Ummi, Ummi Uswatun Hasanah Uswatunhasanah, Putri Utami, Amalda Utami, Firanti Putri Utami, Widia Vega, Amelia Vernanda, Pramyudha Winni Nur Auli Wulandari, Valentri Yogi Nopiandi Permana Yogi Nopiandi Permana Yoki Yulizar Yulanda, Nola Rohmi Eka Yunita, Nadia Rahma Zaqia, Lulu Zusela, Titah