Shivaji V. More - Concepedia

Author

Shivaji V. More

Institute of Chemistry, Academia Sinica

Also Known As

S. V. More, Shivaji V. More, Shravani More

Publications

859

Citations

H-Index

Concepts

All Affiliations

Institute of Chemistry, Academia Sinica National Taiwan Normal University National Sun Yat-sen University Institute of Biological Chemistry, Academia Sinica National Chemical Laboratory

About

Shivaji V. More is an author at Institute of Chemistry, Academia Sinica specializing in medicine, cell biology, and cancer research.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	257
2	Cell Biology	6	6	244
3	Engineering	4	4	524
4	Chemical Engineering	3	3	464
5	Health Sciences	1	1	30

Shivaji V. More

Publications

829

Citations

H-Index

Page 1

	Year	Citations
Cerium (iv) ammonium nitrate (CAN) as a catalyst in tap water: A simple, proficient and green approach for the synthesis of quinoxalines Shivaji V. More, M. N. V. Sastry, Ching‐Fa Yao Green Chemistry EngineeringImportant Quinoxaline DerivativesGreen ChemistryOrganic ChemistryChemistry	2005	243
Molecular iodine: a powerful catalyst for the easy and efficient synthesis of quinoxalines Shivaji V. More, M. N. V. Sastry, Chieh-Chieh Wang, Tetrahedron Letters Chemical EngineeringEngineeringMolecular IodineOrganic ChemistryCatalysis	2005	196
A novel sialyltransferase inhibitor AL10 suppresses invasion and metastasis of lung cancer cells by inhibiting integrin‐mediated signaling Chih-Po Chiang, Chie‐Hong Wang, Hui‐Chiu Chang, Journal of Cellular Physiology Total SialylationChemoprevention StrategyIntegrin‐mediated SignalingMedicinePharmacology	2010	97
Isomalyngamide A, A-1 and their analogs suppress cancer cell migration in vitro Tzu Ting Chang, Shivaji V. More, I-Hsuan Lu, European Journal of Medicinal Chemistry Tumor BiologyOncogenic AgentMedicineAnti-cancer AgentTumor Suppressor	2011	63
NBS as an efficient catalyst for the synthesis of 1,5-benzodiazepine derivatives under mild conditions Chun-Wei Kuo, Shivaji V. More, Ching‐Fa Yao Tetrahedron Letters Combinatorial ChemistryEngineeringMild ConditionsOrganic ChemistryCatalysis	2006	60
The novel indole compound SK228 induces apoptosis and FAK/Paxillin disruption in tumor cell lines and inhibits growth of tumor graft in the nude mouse Sin‐Ming Huang, Pei‐Chun Hsu, Mei‐Yu Chen, International Journal of Cancer Antitumor GrowthApoptosisCell DeathCell ProliferationCancer Biology	2011	30
Pictet‐spengler cyclization in room temperature ionic liquid: A convenient access to tetrahydro β‐carbolines M. Muthukrishnan, Shivaji V. More, Dinesh R. Garud, Journal of Heterocyclic Chemistry Chemical EngineeringEngineeringConvenient AccessIndustrial CatalysisPictet‐spengler Cyclization	2006	25
Synthesis and Evaluation of the Cytotoxicities of Tetraindoles: Observation that the 5-Hydroxy Tetraindole (SK228) Induces G<sub>2</sub>Arrest and Apoptosis in Human Breast Cancer Cells Wen‐Shan Li, Chie‐Hong Wang, Shengkai Ko, Journal of Medicinal Chemistry Medicinal Chemistry5-Hydroxy TetraindoleMedicineApoptosisCancer Cell Biology	2012	24
Synthesis and antibacterial activity of new Schiff bases, 4-thiazolidinones and 2-azetidinones Shivaji V. More, D. V. Dongarkhadekar, RP Chavan, Zenodo (CERN European Organization for Nuclear Research)	2002	23
Polyfluorinated bipyridine cisplatins manipulate cytotoxicity through the induction of S-G2/M arrest and partial intercalation mechanism Tzu Ting Chang, Shivaji V. More, Norman Lu, Bioorganic & Medicinal Chemistry Medicinal ChemistryS-g2/m ArrestPartial Intercalation MechanismMedicineAnti-cancer Agent	2011	19

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