Explore: Conformation Molecular
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Books Results
Source: The Open Library
The Open Library Search Results
Search results from The Open Library
1Drug stereochemistry
By Irving W. Wainer

“Drug stereochemistry” Metadata:
- Title: Drug stereochemistry
- Author: Irving W. Wainer
- Language: English
- Number of Pages: Median: 424
- Publisher: M. Dekker - CRC Press
- Publish Date: 1993
- Publish Location: New York
“Drug stereochemistry” Subjects and Themes:
- Subjects: ➤ Chiral drugs - Methods - Stereoismers - Stereochemistry - Conformation Molecular - Pharmaceutical Chemistry - Stereoisomers - Molecular Conformation - Stereoisomerism
Edition Identifiers:
- The Open Library ID: OL1741530M
- Online Computer Library Center (OCLC) ID: 27187740
- Library of Congress Control Number (LCCN): 92048364
- All ISBNs: 9780824788193 - 0824788192
Access and General Info:
- First Year Published: 1993
- Is Full Text Available: No
- Is The Book Public: No
- Access Status: Unclassified
Online Access
Downloads Are Not Available:
The book is not public therefore the download links will not allow the download of the entire book, however, borrowing the book online is available.
Online Borrowing:
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2Drug Stereochemistry
By Irving Wainer

“Drug Stereochemistry” Metadata:
- Title: Drug Stereochemistry
- Author: Irving Wainer
- Language: English
- Number of Pages: Median: 432
- Publisher: CRC
- Publish Date: 1993
“Drug Stereochemistry” Subjects and Themes:
- Subjects: ➤ Chiral drugs - Methods - Stereoismers - Stereochemistry - Conformation Molecular - Pharmaceutical Chemistry - Pharmaceutical chemistry
Edition Identifiers:
- The Open Library ID: OL8160545M
- All ISBNs: 0824788192 - 9780824788193
First Setence:
"The first half of the nineteenth century was the great age of geometrical optics."
Access and General Info:
- First Year Published: 1993
- Is Full Text Available: No
- Is The Book Public: No
- Access Status: No_ebook
Online Access
Downloads Are Not Available:
The book is not public therefore the download links will not allow the download of the entire book, however, borrowing the book online is available.
Online Borrowing:
Online Marketplaces
Find Drug Stereochemistry at online marketplaces:
- Amazon: Audiable, Kindle and printed editions.
- Ebay: New & used books.
Wiki
Source: Wikipedia
Wikipedia Results
Search Results from Wikipedia
Rotamer
differ by rotation about single bonds can also be referred to as conformations. Conformations, which represent local minima on the potential energy surface
Central dogma of molecular biology
The central dogma of molecular biology deals with the flow of genetic information within a biological system. It is often stated as "DNA makes RNA, and
Eclipsed conformation
In chemistry an eclipsed conformation is a conformation in which two substituents X and Y on adjacent atoms A, B are in closest proximity, implying that
Cyclohexane conformation
Cyclohexane conformations are any of several three-dimensional shapes adopted by cyclohexane. Because many compounds feature structurally similar six-membered
Docking (molecular)
Molecular docking is one of the most frequently used methods in structure-based drug design, due to its ability to predict the binding-conformation of
Molecular geometry
Molecular geometry is the three-dimensional arrangement of the atoms that constitute a molecule. It includes the general shape of the molecule as well
Molecular machine
motion within molecular components for further applications. This led to the design of "proto-molecular machines" featuring conformational changes such
Protein structure
exhibits intrinsic structure resembling the Cdk2/cyclin A-bound conformation". Journal of Molecular Biology. 353 (5): 1118–1128. doi:10.1016/j.jmb.2005.08.074
Structural formula
condensed formulas, skeletal formulas, Newman projections, Cyclohexane conformations, Haworth projections, and Fischer projections. Several systematic chemical
Molecular dynamics
implemented molecular dynamics simulations to identify compounds that complement a receptor while causing minimal disruption to the conformation and flexibility