Jiangnan Peng

发表

Reducing oyster-associated bacteria levels using supercritical fluid CO2 as an agent of warm pasteurization.

M. Hamann, J. Bowling, D. A. Meujo, 2008, International journal of food microbiology.

Euphocactoside, a New Megastigmane Glycoside from Euphorbia cactus Growing in Saudi Arabia

S. Perveen, O. Taglialatela‐Scafati, A. Al-Taweel, 2022, Plants.

Batzelladine alkaloids from the caribbean sponge Monanchora unguifera and the significant activities against HIV-1 and AIDS opportunistic infectious pathogens

R. Schinazi, M. Hamann, C. Cuevas, 2007 .

Lamellarins and Related Pyrrole-Derived Alkaloids from Marine Organisms

M. Hamann, Jin-Feng Hu, Jiangnan Peng, 2008 .

Potent taccalonolides, AF and AJ, inform significant structure-activity relationships and tubulin as the binding site of these microtubule stabilizers.

Lihong Hu, A. L. Risinger, S. Mooberry, 2011, Journal of the American Chemical Society.

Metabonomics study of urine from Sprague-Dawley rats exposed to Huang-yao-zi using (1)H NMR spectroscopy.

Honglin Huang, Rong-qing Huang, Bing-kun Xiao, 2010, Journal of pharmaceutical and biomedical analysis.

Taccalonolides: A Novel Class of Microtubule-Stabilizing Anticancer Agents

Hongtao Yu, A. Winstead, Jiangnan Peng, 2021, Cancers.

Chemically diverse microtubule stabilizing agents initiate distinct mitotic defects and dysregulated expression of key mitotic kinases.

Tyler A. Johnson, P. Crews, S. Mooberry, 2013, Biochemical pharmacology.

Identification of Compounds with Efficacy against Malaria Parasites from Common North American Plants.

D. Powell, T. Anderson, R. Cichewicz, 2016, Journal of natural products.

Glycogen synthase kinase-3 (GSK-3) inhibitory activity and structure-activity relationship (SAR) studies of the manzamine alkaloids. Potential for Alzheimer's disease.

Ana Martínez, S. Wahyuono, M. Hamann, 2007, Journal of natural products.

Microbial metabolism studies of cyanthiwigin B and synergetic antibiotic effects.

M. Hamann, F. Fronczek, Jiangnan Peng, 2006, Journal of natural products.

New cytotoxic trichothecene macrolide epimers from endophytic Myrothecium roridum IFB-E012

Ju Xie, D. Wan, Jiangnan Peng, 2016, The Journal of Antibiotics.

Manzamine B and E and ircinal A related alkaloids from an Indonesian Acanthostrongylophora sponge and their activity against infectious, tropical parasitic, and Alzheimer's diseases.

B. Tekwani, S. Wahyuono, Shabana I. Khan, 2006, Journal of natural products.

New manzamine alkaloids from an Indo-Pacific sponge. Pharmacokinetics, oral availability, and the significant activity of several manzamines against HIV-I, AIDS opportunistic infections, and inflammatory diseases.

S. Wahyuono, M. Hamann, W. Charman, 2004, Journal of medicinal chemistry.

The bat flower: a source of microtubule-destabilizing and -stabilizing compounds with synergistic antiproliferative actions.

A. L. Risinger, S. Mooberry, D. Frantz, 2013, Journal of natural products.

Contents of Cannabinoids in Hemp Varieties Grown in Maryland

Jiangnan Peng, Hua Deng, D. Puthoff, 2021, ACS omega.

Identification and biological activities of new taccalonolide microtubule stabilizers.

G. Helms, A. L. Risinger, S. Mooberry, 2011, Journal of medicinal chemistry.

Lamellarins and related pyrrole-derived alkaloids from marine organisms.

Mark T Hamann, M. Hamann, Jin-Feng Hu, 2008, Chemical reviews.

Microwave-Assisted Synthesis of Organometallic Rhenium (I) Pentylcarbonato Complexes: New Synthon for Carboxylato, Sulfonato and Chlorido Complexes.

P. Zavalij, S. Mandal, J. Krause, 2021, Journal of organometallic chemistry.

Marine natural products as prototype agrochemical agents.

M. Hamann, K. E. El Sayed, J. Huesing, 2003, Journal of agricultural and food chemistry.

Structural activity relationship studies of zebra mussel antifouling and antimicrobial agents from verongid sponges.

S. Duke, M. Hamann, J. Bowling, 2004, Journal of Natural Products.

Reductive amidation of nitroarenes: a practical approach for the amidation of natural products

M. Hamann, A. Wahba, Jiangnan Peng, 2009 .

Structure and absolute configuration of karlotoxin-2, an ichthyotoxin from the marine dinoflagellate Karlodinium veneficum.

C. Anklin, M. Hamann, A. Place, 2010, Journal of the American Chemical Society.

The marine bromotyrosine derivatives.

M. Hamann, Jiangnan Peng, Jing Li, 2005, The Alkaloids. Chemistry and biology.

Crystallographic and NMR studies of antiinfective tricyclic guanidine alkaloids from the sponge Monanchora unguifera.

M. Hamann, F. Fronczek, M. Kelly, 2004, Bioorganic & medicinal chemistry.

Cyclic heptapeptides from the Jamaican sponge Stylissa caribica.

M. Hamann, M. Kelly, Jiangnan Peng, 2006, Journal of natural products.

Cyanthiwigin AC and AD, two novel diterpene skeletons from the Jamaican sponge Myrmekioderma styx.

M. Hamann, M. Avery, Jiangnan Peng, 2003, Organic letters.

The new bioactive diterpenes cyanthiwigins E–AA from the Jamaican sponge Myrmekioderma styx

M. Hamann, M. Kelly, Kelly R. Walsh, 2002 .

Chemical transformation and biological studies of marine sesquiterpene (S)-(+)-curcuphenol and its analogs.

M. Hamann, M. Yousaf, W. Gul, 2007, Biochimica et biophysica acta.

Polyketide-peroxides from a Species of Jamaican Plakortis (Porifera: Demospongiae)

R. J. Doerksen, Z. Bie, A. Xie, 2010 .

Reductive Amidation of Nitroarenes: A Practical Approach for the Amidation of Natural Products.

M. Hamann, A. Wahba, Jiangnan Peng, 2009 .

A Simple and Noninvasive DOSY NMR Method for Droplet Size Measurement of Intact Oil-In-Water Emulsion Drug Products.

Kang Chen, D. Keire, D. Kozak, 2019, Journal of pharmaceutical sciences.

An Iridoid Glucoside and the Related Aglycones from Cornus florida

M. Hamann, L. West, Jiangnan Peng, 2014, Journal of natural products.

Corrigendum to “Lamellarins and Related Pyrrole-Derived Alkaloids from Marine Organisms”: [Chemical Review 108 (2008) 264−287]

M. Hamann, Jin-Feng Hu, Jiangnan Peng, 2010 .

Evaluation of the Antifungal, Antioxidant, and Anti-Diabetic Potential of the Essential Oil of Curcuma longa Leaves from the North-Western Himalayas by In Vitro and In Silico Analysis

Prof Vikas Kumar, S. Perveen, C. Patel, 2022, Molecules.

Texas Native Plants Yield Compounds with Cytotoxic Activities against Prostate Cancer Cells.

Andrew J. Robles, D. Powell, R. Cichewicz, 2016, Journal of natural products.

Novel sesquiterpenes and a lactone from the Jamaican sponge Myrmekioderma styx

M. Hamann, S. Franzblau, Fangqiu Zhang, 2002 .

Novel Sesquiterpenes and a Lactone from the Jamaican Sponge Myrmekioderma styx.

M. Hamann, S. Franzblau, Fangqiu Zhang, 2003 .

Structure and Antimicrobial Activity of Rare Lactone Lipids from the Sooty Mold (Scorias spongiosa).

R. Schumacher, M. Hamann, Y. Zou, 2022, Journal of natural products.

Amyrisins A-C, O-prenylated flavonoids from Amyris madrensis.

S. Mooberry, Jiangnan Peng, Rachel M. Hartley, 2012, Journal of natural products.

Structure-activity relationship and mechanism of action studies of manzamine analogues for the control of neuroinflammation and cerebral infections.

R. J. Doerksen, B. Tekwani, S. Prasanna, 2010, Journal of medicinal chemistry.

Kahalalides V-Y isolated from a Hawaiian collection of the sacoglossan mollusk Elysia rufescens.

M. Hamann, M. Na, R. Matsumoto, 2008, Journal of natural products.

Manadomanzamines A and B: a novel alkaloid ring system with potent activity against mycobacteria and HIV-1.

R. Hill, R. Schinazi, S. Wahyuono, 2003, Journal of the American Chemical Society.

Resource Utilization of Lake Sediment to Prepare “Sponge” Light Aggregate: Pore Structure and Water Retention Mechanism Study

B. Liang, Chi Zhou, Kunpeng Li, 2022, Processes.

Melampodium leucanthum, a source of cytotoxic sesquiterpenes with antimitotic activities.

Andrew J. Robles, S. Mooberry, Susan L Mooberry, 2015, Journal of natural products.

Bromopyrrole Alkaloids from the Jamaican Sponge Didiscus Oxeata

M. Hamann, A. Kazi, M. Kelly, 2005 .

Taccalonolide Microtubule Stabilizers Generated Using Semisynthesis Define the Effects of Mono Acyloxy Moieties at C-7 or C-15 and Disubstitutions at C-7 and C-25.

R. Cichewicz, L. Du, S. Mooberry, 2018, Journal of natural products.

Evelynin, a cytotoxic benzoquinone-type Retro-dihydrochalcone from Tacca chantrieri.

G. Helms, S. Mooberry, D. Frantz, 2010, Journal of natural products.

NMR-Based Metabolomics for Geographical Discrimination of Adhatoda vasica Leaves

R. Verpoorte, M. Jahangir, I. Khan, 2023, Plants.

Antiproliferative effects of curcuphenol, a sesquiterpene phenol.

M. Hamann, Yajun Cheng, R. Duan, 2010, Fitoterapia.

Effects of Green Tea (-)-Epigallocatechin-3-Gallate (EGCG) on Cardiac Function - A Review of the Therapeutic Mechanism and Potentials.

Jiangnan Peng, Yuejin Li, Md. Rezaul Karim, 2022, Mini reviews in medicinal chemistry.

Chemical Structure and Composition of Major Glycans Covalently Linked to Therapeutic Monoclonal Antibodies by Middle-Down Nuclear Magnetic Resonance.

Kang Chen, D. Keire, Sharadrao M. Patil, 2018, Analytical chemistry.

Polycyclic aromatic hydrocarbons as a potential source of carcinogenicity of mate

S. Dawsey, F. Kamangar, Jiangnan Peng, 2018, Journal of environmental science and health. Part C, Environmental carcinogenesis & ecotoxicology reviews.

Structure-activity relationships of retro-dihydrochalcones isolated from Tacca sp.

G. Kellogg, S. Mooberry, Chenxiao Da, 2013, Journal of natural products.

Phenolic constituents from Rheum nobile and their antioxidant activity

Juan Wang, J. Chen, Zu-ping Zeng, 2017, Natural product research.

Synthetic Reactions with Rare Taccalonolides Reveal the Value of C-22,23 Epoxidation for Microtubule Stabilizing Potency

S. Mooberry, Jiangnan Peng, Jing Li, 2014, Journal of medicinal chemistry.

Structure-activity relationship studies of manzamine A: amidation of positions 6 and 8 of the beta-carboline moiety.

B. Tekwani, M. Hamann, A. Wahba, 2009, Bioorganic & medicinal chemistry.

Phytochemical Analysis of Anvillea garcinii Leaves: Identification of Garcinamines F–H and Their Antiproliferative Activities

S. Tabassum, S. Perveen, M. Abdel-Kader, 2021, Plants.

Epoxidation at C22-C23 significantly increases the potency of microtubule stabilizing taccalonolides

Jiangnan Peng, Jing Li, A. Risinger, 2012 .

Polygamain, a New Microtubule Depolymerizing Agent That Occupies a Unique Pharmacophore in the Colchicine Site

S. Dakshanamurthy, J. Peng, S. Mooberry, 2012, Molecular Pharmacology.

Taccalonolide binding to tubulin imparts microtubule stability and potent in vivo activity.

D. Schriemer, A. L. Risinger, S. Mooberry, 2013, Cancer research.

A cost-effective o-toulidine-based Schiff base as an efficient sorbent for metal ion uptake from aqueous and soil samples: Synthesis, antimicrobial, and acute toxicity analyses

S. Perveen, M. M. Akhtar, A. Al-Taweel, 2023, Frontiers in Environmental Science.

Polygamain, a New Microtubule Depolymerizing Agent That Occupies a Unique Pharmacophore in the Colchicine Site

S. Dakshanamurthy, S. Mooberry, Milton L. Brown, 2012, Molecular Pharmacology.

Chemically diverse microtubule stabilizing agents initiate distinct mitotic defects and dysregulated expression of key mitotic kinases.

Tyler A. Johnson, P. Crews, S. Mooberry, 2013, Biochemical pharmacology.