S. Ahn

发表

Prediction of GPCR-Ligand Binding Using Machine Learning Algorithms

Sangmin Seo, Jinho Kim, Jaekwang Kim, 2018, Comput. Math. Methods Medicine.

Identification of chalcones as potent and selective PDE5A1 inhibitors.

Ky-Youb Nam, S. Ahn, N. Choi, 2012, Bioorganic & medicinal chemistry letters.

Structure-based virtual screening of novel tubulin inhibitors and their characterization as anti-mitotic agents.

Young Hoon Kim, Dae-Yeul Yu, Kyoung Tai No, 2010, Bioorganic & medicinal chemistry.

Asymmetric synthesis of enantiomerically pure (−)-(1′R,4′R)-dioxolane-thymine and its anti-HIV activity.

R. Schinazi, P. Roey, S. Ahn, 1991 .

Discrimination of Adzuki Bean (Vigna angularis) Geographical Origin by Targeted and Non-Targeted Metabolite Profiling with Gas Chromatography Time-of-Flight Mass Spectrometry

J. K. Kim, S. Ahn, K. Kim, 2020, Metabolites.

Enantiomers of higenamine inhibit LPS-induced iNOS in a macrophage cell line and improve the survival of mice with experimental endotoxemia.

Jae Heun Lee, S. Ahn, H. Seo, 2006, International immunopharmacology.

Targeting regulation of ATP synthase 5 alpha/beta dimerization alleviates senescence

S. Ahn, Youngjoo Byun, Yun Haeng Lee, 2022, Aging.

A novel highly potent and selective 11β-hydroxysteroid dehydrogenase type 1 inhibitor, UI-1499.

Ky-Youb Nam, S. Ahn, S. Byun, 2015, Life sciences.

Discovery of Novel 11β-HSD1 Inhibitors by Pharmacophore-Based Virtual Screening

S. Ahn, N. Kim, Chang-Kyun Han, 2012 .

Synthesis and biological activity of novel substituted pyridines and purines containing 2,4-thiazolidinedione.

S. Ahn, J. Shin, S. Kang, 2004, European journal of medicinal chemistry.

Identification and quantification of carotenoids in paprika fruits and cabbage, kale, and lettuce leaves

J. K. Kim, S. Ahn, K. Kim, 2014, Journal of the Korean Society for Applied Biological Chemistry.

A novel highly potent and selective 11&bgr;‐hydroxysteroid dehydrogenase type 1 inhibitor, INU‐101

S. Ahn, S. Hong, Dongoh Han, 2018, European journal of pharmacology.

Suppression of lytic replication of Kaposi’s sarcoma-associated herpesvirus by autophagy during initial infection in NIH 3T3 fibroblasts

S. Ahn, Michael Lee, Hara Kang, 2016, Archives of Virology.

Antitumor activity of 7-[2-(N-isopropylamino)ethyl]-(20S)-camptothecin, CKD602, as a potent DNA topoisomerase I inhibitor

S. Ahn, M. Kim, S. Jew, 1998, Archives of pharmacal research.

Differential inhibitory effects of two Raf-targeting drugs, sorafenib and PLX4720, on the growth of multidrug-resistant cells

S. Ahn, K. Eum, Michael Lee, 2012, Molecular and Cellular Biochemistry.

Development of locomotion in a subsocial spider

S. Ahn, K. Kim, 2015, Behavioural Processes.

Quinazolines as potent and highly selective PDE5 inhibitors as potential therapeutics for male erectile dysfunction.

S. Ahn, Young Hoon Kim, N. Choi, 2008, Bioorganic & medicinal chemistry letters.

Hantzsch Dihydropyridine: An Effective and Convenient Regioselective Reducing Agent for the 5-Benzylidene-2,4-thiazolidinedione Derivatives

S. Ahn, C. Hong, H. Lee, 2002 .

Manganese chloride-catalyzed cross-coupling and carbonylative cross-coupling of organostannanes with iodonium salts

J. Kim, W. Kim, S. Ahn, 1998 .

Discovery of potent, selective, and orally bioavailable PDE5 inhibitor: Methyl-4-(3-chloro-4-methoxybenzylamino)-8-(2-hydroxyethyl)-7-methoxyquinazolin-6-ylmethylcarbamate (CKD 533).

S. Ahn, Young Hoon Kim, N. Choi, 2010, Bioorganic & medicinal chemistry letters.

Studies towards the total synthesis of strychnine (I)

S. Ahn, Deukjoon Kim, Moohi Yoo Kim, 1987 .

Synthesis of novel diaryl ethers and their evaluation as antimitotic agents.

S. Ahn, J. Yang, N. Choi, 2007, Bioorganic & medicinal chemistry letters.

Identification of CKD-516: a potent tubulin polymerization inhibitor with marked antitumor activity against murine and human solid tumors.

S. Ahn, Young Hoon Kim, N. Choi, 2010, Journal of medicinal chemistry.

Process Development and Scale-Up of PPAR α/γ Dual Agonist Lobeglitazone Sulfate (CKD-501)

S. Ahn, S. Kang, D. Ha, 2007 .

Novel α-Glucosidase Inhibitors, CKD-711 and CKD-711a Produced by Streptomyces sp. CK-4416

S. Ahn, S. Moon, C. Hong, 2002 .

Novel alpha-glucosidase inhibitors, CKD-711 and CKD-711a produced by Streptomyces sp. CK-4416. I. Taxonomy, fermentation and isolation.

S. Ahn, S. Moon, C. Hong, 2002, The Journal of antibiotics.

Synthesis and structure-activity relationship of 2-(5-substituted pyrrolidin-4-ylthio)-1β-carbapenems

S. Ahn, C. Hong, H. Lee, 1997 .

Studies on the Synthesis and Structure-Activity Relationships of 2-(2-Functionalized Pyrrolidin-4-ylthio)-1β-methylcarbapenems

S. Ahn, H. Lee, Chaewoon Lee, 1996 .

Molecular design, synthesis, and hypoglycemic and hypolipidemic activities of novel pyrimidine derivatives having thiazolidinedione.

S. Ahn, J. Shin, S. Kang, 2005, European journal of medicinal chemistry.

A Highly Stereoselective Synthesis of Anti‐HIV 2′,3′‐Dideoxy‐ and 2′,3′ ‐Didehydro‐2′,3′‐dideoxynucleosides.

Soon Kil Ahn, J. W. Beach, S. Ahn, 1992 .

A highly stereoselective synthesis of anti-HIV 2',3'-dideoxy- and 2',3'-didehydro-2',3'-dideoxynucleosides

S. Ahn, C. K. Chu, L. Jeong, 1992 .

A stereoselective asymmetric synthesis of antibiotic (-)-Fumagillol using claisen rearrangement and intramolecular ester enolate alkylation as key steps

S. Ahn, H. Kim, Deukjoon Kim, 2005, Archives of pharmacal research.

The efficacy and safety of clopidogrel resinate as a novel polymeric salt form of clopidogrel

S. Ahn, Min-Hyo Ki, Mee-Hwa Choi, 2008, Archives of pharmacal research.

Metabolite Profiling of Peppers of Various Colors Reveals Relationships Between Tocopherol, Carotenoid, and Phytosterol Content.

J. K. Kim, S. Ahn, K. Kim, 2017, Journal of food science.

Absorption, distribution, metabolism, and excretion of CKD-732, a novel antiangiogenic fumagillin derivative, in rats, mice, and dogs

S. Ahn, S. Myung, Sung Sook Lee, 2004, Archives of pharmacal research.

5-Demethoxyfumagillol, a potent angiogenesis inhibitor isolated from Aspergillus fumigatus.

S. Ahn, Jaeki Min, N. Choi, 2004, Chemical & pharmaceutical bulletin.

Quantification of Arbutin in Plant Extracts by Stable Isotope Dilution Gas Chromatography–Mass Spectrometry

J. K. Kim, S. Ahn, J. Na, 2018, Chromatographia.

A highly stereoselective glycosylation of 2-(phenylselenenyl)-2,3-dideoxyribose derivative with thymine: synthesis of 3'-deoxy-2',3'-didehydrothymidine and 3'-deoxythymidine

S. Ahn, C. K. Chu, L. Jeong, 1990 .

A Highly Stereoselective Glycosylation of 2-(Phenylselenenyl)-2,3-dideoxyribose Derivative with Thymine: Synthesis of 3′-Deoxy-2′,3′-didehydrothymidine and 3′-Deoxythymidine.

S. Ahn, C. K. Chu, L. Jeong, 1990 .

Synthesis of (±)-2′,3′-dideoxy-3′-fluoroapiosylpyrimidine nucleosides

S. Ahn, Deukjoon Kim, 1998 .

Synthesis and antihyperglycemic activity of erythrose, ribose and substituted pyrrolidine containing thiazolidinedione derivatives.

S. Ahn, J. Shin, T. Sim, 2003, Chemical & pharmaceutical bulletin.

Suppression of lytic replication of Kaposi’s sarcoma-associated herpesvirus by autophagy during initial infection in NIH 3T3 fibroblasts

S. Ahn, Michael Lee, Hara Kang, 2016, Archives of Virology.

Discovery of a novel pan‐RAF inhibitor with potent anti‐tumor activity in preclinical models of BRAFV600E mutant cancer

S. Ahn, S. Hong, 2017, Life sciences.

Differential sensitivity of melanoma cell lines with differing B-Raf mutational status to the new oncogenic B-Raf kinase inhibitor UI-152.

S. Ahn, Michael Lee, Jun‐Ho Ahn, 2012, Cancer letters.

Oncogenic BRAF inhibitor UAI-201 induces cell cycle arrest and autophagy in BRAF mutant glioma cells.

Yong Woo Lee, S. Ahn, Michael Lee, 2014, Life sciences.

Prediction Models of P-Glycoprotein Substrates Using Simple 2D and 3D Descriptors by a Recursive Partitioning Approach

Jong Young Joung, Kyoung Tai No, Soon Kil Ahn, 2012 .

The role of autophagy in cytotoxicity induced by new oncogenic B-Raf inhibitor UI-152 in v-Ha-ras transformed fibroblasts.

S. Ahn, Michael Lee, Jun‐Ho Ahn, 2012, Biochemical and biophysical research communications.

Design, synthesis, and antiangiogenic effects of a series of potent novel fumagillin analogues.

S. Ahn, J. Shin, S. Kang, 2007, Chemical & pharmaceutical bulletin.

Total synthesis and antiangiogenic activity of cyclopentane analogues of fumagillol.

S. Ahn, N. Choi, H. Kim, 2005, Bioorganic & medicinal chemistry letters.

Development of parenteral formulation for a novel angiogenesis inhibitor, CKD-732 through complexation with hydroxypropyl-beta-cyclodextrin.

S. Ahn, Su‐Kyung Lee, Su-Kyung Lee, 2004, International journal of pharmaceutics.

An asymmetric total synthesis of (−)-fumagillol

S. Ahn, H. Kim, Deukjoon Kim, 1997 .

Identification of Polo-Like Kinase 1 Inhibitors Using Structure-Based Molecular Design

K. No, Ky-Youb Nam, S. Ahn, 2014 .

Effects of Heavy Metals on Plant Growths and Pigment Contents in Arabidopsis thaliana

S. Ahn, Sukchan Lee, Hara Kang, 2012 .

Development of Three-Dimensional Descriptors Represented by Tensors: Free Energy of Hydration Density Tensor

Kyoung Tai No, Su Hwan Son, Cheol Kyu Han, 1999, J. Chem. Inf. Comput. Sci..

Targeting Mitochondrial Oxidative Stress as a Strategy to Treat Aging and Age-Related Diseases

S. Ahn, Yun Haeng Lee, Myeong Uk Kuk, 2023, Antioxidants.

Metabolic profiling reveals an increase in stress-related metabolites in Arabidopsis thaliana exposed to honeybees

Jaegyoon Ahn, S. Ahn, K. Kim, 2021, Journal of Applied Biological Chemistry.

Methyl Aryloxy Gallates as Regulators of Vascular Smooth Muscle Cell Proliferation

S. Ahn, Y. Yun, J. Hong, 2009 .

Chemical profiling of insect-resistant rice shows that geographical variations produce greater differences in chemical composition than genetic modifications

S. Ahn, S. Park, Jaehyuk Choi, 2023, Plant Biotechnology Reports.

Discovery of a potent tubulin polymerization inhibitor: synthesis and evaluation of water-soluble prodrugs of benzophenone analog.

S. Ahn, Young Hoon Kim, N. Choi, 2010, Bioorganic & medicinal chemistry letters.

Practical synthesis of (S)‐7‐(2‐isopropylamino)ethylcamptothecin hydrochloride, potent topoisomerase I inhibitor

S. Ahn, N. Choi, Byeong-Seon Jeong, 2000 .

An Efficient Method for the Large-Scale Synthesis of Atorvastatin Calcium

S. Ahn, S. Kang, H. Lee, 2008 .

Discovery of novel HCV polymerase inhibitors using pharmacophore-based virtual screening.

S. Ahn, Jaewon Yang, N. Kim, 2011, Bioorganic & medicinal chemistry letters.

Inhibition of GLI Transcriptional Activity and Prostate Cancer Cell Growth and Proliferation by DAX1

S. Ahn, K. Kim, S. Hong, 2023, Current issues in molecular biology.

Metabolic profiling reveals glucose and fructose accumulation in gcr1 knock-out mutant of Arabidopsis

Jaegyoon Ahn, S. Ahn, K. Kim, 2019, Applied Biological Chemistry.

Discovery of 11β-hydroxysteroid dehydrogenase type 1 inhibitor.

Ky-Youb Nam, S. Ahn, K. Kim, 2015, Bioorganic & medicinal chemistry letters.

Quinazolines as potent and highly selective PDE5 inhibitors as potential therapeutics for male erectile dysfunction.

S. Ahn, Young Hoon Kim, N. Choi, 2008, Bioorganic & medicinal chemistry letters.

Discovery of a Highly Specific and Potent Pan-RAF Inhibitor

Ky-Youb Nam, S. Ahn, N. Choi, 2016 .

Asymmetric synthesis of 1,3-dioxolane-pyrimidine nucleosides and their anti-HIV activity.

R. Schinazi, S. Ahn, C. K. Chu, 1992, Journal of medicinal chemistry.