C. Liang

发表

Kinase Cells Transformed by the Oncogenic TPR-MET Tyrosine A Novel Small Molecule Met Inhibitor Induces Apoptosis in Updated

J. Christensen, R. Salgia, Yuri B. Pride, 2003 .

Rational design of 4,5-disubstituted-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-ones as a novel class of inhibitors of epidermal growth factor receptor (EGF-R) and Her2(p185(erbB)) tyrosine kinases.

C. Liang, Hui Chen, Li Sun, 2002, Bioorganic & medicinal chemistry letters.

Structure-based design and discovery of novel inhibitors of protein tyrosine phosphatases.

G. Mcmahon, C. Liang, B. Jallal, 2003, Bioorganic & medicinal chemistry.

Double bond deformation: cumulenes, cumulenones, and Group IV ethylene analogs

C. Liang, L. C. Allen, 1991 .

Density functional study of model species for nucleic acids and lipids

C. Liang, J. Hill, Jörg-Rüdiger Hill, 1997 .

Finite Td symmetry models for diamond: from adamantane to super-adamantane (C35H36)

H. Schaefer, N. L. Allinger, P. Schleyer, 1992 .

Properties of Small Group IIIA Hydrides Including the Cyclic and Pentacoordinate Structures of Trialane (Al3H9) and Trigallane (Ga3H9): Can Dialane Be Isolated?

H. Schaefer, C. Liang, B. Duke, 1991 .

AB INITIO STUDIES OF LIPID MODEL SPECIES. II: CONFORMATIONAL ANALYSIS OF INOSITOLS

A. Hagler, T. Stouch, C. Liang, 1994 .

.sigma.-Bridged-.pi. bonding in small-ring compounds

C. Liang, L. C. Allen, 1991 .

SU6668 is a potent antiangiogenic and antitumor agent that induces regression of established tumors.

Cherrington, R A Blake, S. Hubbard, 2000, Cancer research.

Group IV double bonds : shape deformation and substituent effects

C. Liang, L. C. Allen, 1990 .

The tetramer of borane and its heavier valence-isoelectronic analogs: M4H12 with M = B, Al, and Ga

H. Schaefer, C. Liang, M. Shen, 1993 .

Infrared spectra of the unknown dialane (Al2H6) and recently observed digallane (Ga2H6) molecules

H. Schaefer, C. Liang, R. Davy, 1989 .

Vibrational Spectra of Butatriene (C4H4) and Pentatetraene (C5H4): Is Pentatetraene Bent?

H. S. Kim, H. Schaefer, C. Liang, 1991 .

Electronic structures of linear C4, C6, C8, and C10 carbon clusters and a symmetry breaking phenomenon

Congxin Liang, H. Schaefer, C. Liang, 1990 .

Carbon clusters: The structure of C10 studied with configuration interaction methods

H. Schaefer, C. Liang, 1990 .

Ab initio studies of electron transfer: pathway analysis of effective transfer integrals

M. Newton, C. Liang, 1992 .

Ab initio studies of lipid model species. 1. Dimethyl phosphate and methyl propyl phosphate anions

Terry R. Stouch, Arnold T. Hagler, Congxin Liang, 1993 .

Force field studies of cholesterol and cholesteryl acetate crystals and cholesterol–cholesterol intermolecular interactions

Terry R. Stouch, Arnold T. Hagler, Jörg-Rüdiger Hill, 1995, J. Comput. Chem..

Classical and nonclassical forms of the vinyl cation: A coupled cluster study

H. Schaefer, T. Hamilton, C. Liang, 1990 .

Potent and selective inhibitors of the Met [hepatocyte growth factor/scatter factor (HGF/SF) receptor] tyrosine kinase block HGF/SF-induced tumor cell growth and invasion.

A. Howlett, G. Mcmahon, C. Liang, 2003, Molecular cancer therapeutics.

PND-1186 FAK inhibitor selectively promotes tumor cell apoptosis in three-dimensional environments

G. Mcmahon, S. Lim, D. Schlaepfer, 2010, Cancer biology & therapy.

A novel small molecule met inhibitor induces apoptosis in cells transformed by the oncogenic TPR-MET tyrosine kinase.

J. Christensen, R. Salgia, P. Ma, 2003, Cancer research.

Inhibition Of Vascular Endothelial Growth Factor ( Vegf) And Stem- Cell Factor ( Scf) Receptor Kinases As Therapeutic Targets For The Treatment Of Human Diseases

G. Mcmahon, C. Liang, Li Sun, 2000 .

The Met kinase inhibitor SU11274 exhibits a selective inhibition pattern toward different receptor mutated variants

L. Schmidt, A. Howlett, D. Candinas, 2004, Oncogene.

Growth of Small Cell Lung Cancer Cells Indolinone Tyrosine Kinase Inhibitors Block Kit Activation and Updated

S. Honsawek, G. Mcmahon, C. Liang, 2001 .

Induces Regression of Established Tumors SU 6668 Is a Potent Antiangiogenic and Antitumor Agent That Updated

S. Hubbard, A. Ullrich, N. Shenoy, 2000 .

SU 6668 Is a Potent Antiangiogenic and Antitumor Agent That Induces Regression of Established Tumors 1

S. Hubbard, A. Ullrich, N. Shenoy, 2000 .

Ab initio studies of electron transfer. 2. Pathway analysis for homologous organic spacers

Congxin Liang, M. Newton, C. Liang, 1993 .

Sulfur Does Not Form Double Bonds in Phosphorothioate Anions.

C. Liang, L. C. Allen, 1988 .

Sulfur does not form double bonds in phosphorothioate anions

C. Liang, L. C. Allen, 1987 .

Design, synthesis, and evaluations of substituted 3-[(3- or 4-carboxyethylpyrrol-2-yl)methylidenyl]indolin-2-ones as inhibitors of VEGF, FGF, and PDGF receptor tyrosine kinases.

G. Mcmahon, L. Sun, C. Tang, 1999, Journal of medicinal chemistry.

Development of SU5416, a selective small molecule inhibitor of VEGF receptor tyrosine kinase activity, as an anti-angiogenesis agent.

L. Ellis, C. Liang, J. Cherrington, 2000, Anti-cancer drug design.

盐酸恩沙替尼胶囊的药理与临床评价

C. Liang, Yongbin Ma, Yang Wang, 2020, Zhongguo fei ai za zhi = Chinese journal of lung cancer.