What is the Difference Between Combinatorial and Parallel Synthesis?
🆚 Go to Comparative Table 🆚Combinatorial and parallel synthesis are both important synthetic techniques used in drug discovery and development, but they have distinct differences:
- Method: Combinatorial synthesis involves preparing a large number of compounds in a single process using a split synthesis method. Parallel synthesis, on the other hand, uses an individual compound for reactions and employs a one-bead-one-compound method.
- Compound Production: Combinatorial synthesis allows for the rapid generation of large numbers of compounds, often ranging from tens to thousands or even millions of compounds. Parallel synthesis focuses on synthesizing individual peptides in separate reaction vessels, defining the sequence of a peptide based on the vessel used.
- Applications: Combinatorial synthesis can be used to create diverse chemical libraries and accelerate the discovery of new compounds. Parallel synthesis is primarily used for developing chemical libraries and searching for potential drug candidates in the pharmaceutical industry.
- Compound Identification: Parallel synthesis simplifies the process of identifying and preparing individual compounds for use, making it easier to work with large compound libraries.
In summary, combinatorial synthesis is a powerful method for rapidly generating large numbers of compounds, while parallel synthesis focuses on individual compound synthesis and development of chemical libraries. Both techniques have proven valuable in drug discovery and development, particularly in the pharmaceutical industry.
Comparative Table: Combinatorial vs Parallel Synthesis
Here is a table comparing the differences between combinatorial and parallel synthesis:
Feature | Combinatorial Synthesis | Parallel Synthesis |
---|---|---|
Definition | A chemical synthesis method that enables preparing a large number of compounds in a single process. | An important technique used in accelerating the discovery of new compounds, where individual compounds are prepared independently. |
Method | Combinatorial synthesis uses a split synthesis method. | Parallel synthesis uses a one-bead-one-compound method. |
Compound Preparation | Synthesizes compound libraries as mixtures, sets of individual compounds, or chemical structures. | Each compound is prepared independently, typically by linking a reactant to the surface of polymer beads. |
Process | The initial reactant is linked to the surface of polymer beads, which are then divided into several groups. A different building block is added to each group, the different groups are combined, and the reassembled mix is again split to form new groups. This process is repeated multiple times. | The reactant is first linked to the surface of polymer beads, which are then placed into small wells on a 96-well glass plate. Programmable robotic instruments add different sequences of building blocks to the different wells, thereby making multiple different products. |
Application | Combinatorial and parallel synthesis are important synthetic techniques mainly useful in drug discovery and drug development. | Both techniques are used in drug discovery and drug development. |
The key difference between combinatorial and parallel synthesis is that combinatorial synthesis uses a split synthesis method and prepares compound libraries, while parallel synthesis uses a one-bead-one-compound method and prepares individual compounds independently.
- Linear vs Convergent Synthesis
- Analysis vs Synthesis
- Synthesis vs Retrosynthesis
- Synthesis vs Biosynthesis
- Synthesis vs Decomposition
- Synthon vs Synthetic Equivalent
- Combinational vs Sequential Logic
- Synthesis Reaction vs Substitution Reaction
- Permutations vs Combinations
- Purine vs Pyrimidine Synthesis
- Combination vs Decomposition Reaction
- Partial vs Absolute Asymmetric Synthesis
- DNA vs RNA Synthesis
- Combinational Logic Circuit vs Sequential Logic Circuit
- Syn vs Anti Addition
- Hydrolysis vs Dehydration Synthesis
- Complementation vs Recombination
- Homocyclic vs Heterocyclic Compounds
- Synapsis vs Crossing Over