Mutagenesis Research Chemicals
Items 91 to 100 of 172 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
CAY10594 | 1130067-34-3 | sc-223874 sc-223874A | 1 mg 5 mg | $80.00 $261.00 | 8 | |
CAY10594 is a specialized chemical that acts as a potent mutagenesis research tool, exhibiting unique reactivity patterns that facilitate the formation of DNA adducts. Its structure allows for selective interactions with nucleophilic sites, promoting the generation of reactive species that can disrupt normal base pairing. The compound's behavior is influenced by various environmental conditions, which can modulate its reaction kinetics and pathways, making it a critical subject in the study of mutagenic mechanisms. | ||||||
4-Chloro-N-methylaniline | 932-96-7 | sc-232582 | 10 g | $86.00 | ||
4-Chloro-N-methylaniline is a distinctive chemical utilized in mutagenesis research, characterized by its ability to form covalent bonds with biomolecules. Its electrophilic nature enables it to engage with nucleophilic sites on DNA, leading to potential alterations in genetic material. The compound's reactivity is influenced by pH and solvent polarity, which can affect its stability and interaction dynamics, making it a valuable subject for exploring mutagenic processes and mechanisms. | ||||||
(S)-N-Nitroso Anabasine | 1133-64-8 | sc-397413A sc-397413B sc-397413C sc-397413 sc-397413D sc-397413E | 1 mg 2 mg 5 mg 10 mg 25 mg 100 mg | $194.00 $235.00 $265.00 $296.00 $714.00 $2040.00 | ||
(S)-N-Nitroso Anabasine is a notable compound in mutagenesis research, recognized for its capacity to induce genetic mutations through specific interactions with cellular components. Its nitroso group enhances electrophilicity, facilitating reactions with nucleophilic sites in nucleic acids. The compound's unique stereochemistry may influence its binding affinity and reaction kinetics, providing insights into mutagenic pathways and the mechanisms of DNA damage. Its behavior in various biological environments offers a rich area for exploration in genetic studies. | ||||||
3,5-Diamino-2,4,6-triiodobenzoic Acid | 5505-16-8 | sc-209714 | 100 mg | $300.00 | ||
3,5-Diamino-2,4,6-triiodobenzoic Acid is a significant compound in mutagenesis research, characterized by its ability to interact with DNA through its multiple amino and iodine substituents. These functional groups can form hydrogen bonds and participate in electrophilic attacks, potentially leading to alterations in genetic material. Its unique structural features may influence the stability of DNA adducts, providing insights into mutagenic mechanisms and the dynamics of genetic alterations. | ||||||
1,2-Bis(2,4,6-tribromophenoxy)ethane | 37853-59-1 | sc-397466 sc-397466A sc-397466B sc-397466C | 1 g 5 g 10 g 50 g | $275.00 $575.00 $665.00 $2655.00 | ||
1,2-Bis(2,4,6-tribromophenoxy)ethane is a notable compound in mutagenesis research, distinguished by its extensive bromination and ether linkages. The presence of multiple tribromophenoxy groups enhances its reactivity, allowing for significant interactions with nucleophilic sites on DNA. This compound can induce oxidative stress and generate reactive intermediates, which may lead to strand breaks and mutations. Its unique structure facilitates the study of mutagenic pathways and the mechanisms of genetic instability. | ||||||
Aristolochic Acid B | 475-80-9 | sc-358881 | 5 mg | $460.00 | ||
Aristolochic Acid B is a potent compound in mutagenesis research, characterized by its ability to intercalate into DNA, disrupting normal base pairing. This interaction can lead to the formation of adducts, resulting in mispairing during replication. Its unique structure promotes the generation of reactive oxygen species, contributing to oxidative damage. The compound's distinct pathways of mutagenesis provide valuable insights into the mechanisms underlying genetic alterations and carcinogenesis. | ||||||
2′-Deoxyadenosine | 958-09-8 | sc-275525 sc-275525A sc-275525B sc-275525C | 5 g 10 g 25 g 100 g | $39.00 $70.00 $164.00 $607.00 | ||
2'-Deoxyadenosine is a pivotal compound in mutagenesis research, known for its role in DNA synthesis and repair mechanisms. Its unique structure allows for incorporation into DNA strands, potentially leading to mispairing during replication. This misincorporation can trigger mutations, providing insights into genetic stability. The compound's interactions with polymerases and its influence on nucleotide pool dynamics are critical for studying mutagenic pathways and their implications in genomic integrity. | ||||||
FTI-277 trifluoroacetate salt | 170006-73-2 (free base) | sc-215058 sc-215058A | 1 mg 5 mg | $160.00 $581.00 | 1 | |
FTI-277 trifluoroacetate salt is a notable compound in mutagenesis research, recognized for its ability to inhibit specific protein interactions that are crucial for cellular signaling pathways. This inhibition can lead to altered gene expression and subsequent genomic instability. Its unique trifluoroacetate moiety enhances solubility and reactivity, facilitating studies on mutagenic mechanisms. The compound's distinct kinetic profile allows for precise exploration of its effects on cellular processes, making it a valuable tool in understanding mutagenesis. | ||||||
(−)-Cotinine | 486-56-6 | sc-205267 sc-205267A sc-205267B | 50 mg 250 mg 1 g | $70.00 $115.00 $265.00 | 3 | |
(-)-Cotinine is a significant compound in mutagenesis research, recognized for its ability to interact with cellular signaling pathways and influence gene expression. Its structural features enable it to form stable complexes with various biomolecules, potentially altering transcriptional activity. The compound's kinetics in cellular environments can lead to oxidative stress, which may induce DNA damage and subsequent mutagenesis. Understanding these interactions is crucial for elucidating mechanisms of genetic variability. | ||||||
Stearoyl chloride | 112-76-5 | sc-215905 | 100 ml | $77.00 | ||
Stearoyl chloride, an acid chloride, plays a pivotal role in mutagenesis research due to its reactivity with nucleophiles, particularly amines and alcohols. This compound can facilitate acylation reactions, leading to the formation of amides and esters, which may impact cellular processes. Its unique ability to modify lipid membranes can alter membrane fluidity and permeability, potentially influencing cellular signaling and gene expression pathways. The kinetics of its reactions can provide insights into mutagenic mechanisms at the molecular level. | ||||||