SR-6 Inhibitors
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Items 11 to 20 of 23 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
BGC 20-761 | 17375-63-2 | sc-361120 sc-361120A | 10 mg 50 mg | $155.00 $620.00 | ||
BGC 20-761, an SR-6 acid halide, exhibits exceptional reactivity due to its strong electrophilic nature, facilitating rapid nucleophilic attacks. The compound's unique steric and electronic properties create a favorable environment for the formation of stable acyl complexes. Its distinctive interaction with solvents enhances solubility and reactivity, while its ability to engage in multiple reaction pathways allows for diverse synthetic strategies, making it a versatile reagent in organic chemistry. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $64.00 $246.00 | 136 | |
MEK inhibitor, can alter ERK pathway activity, possibly regulating SR-6. | ||||||
Ro 04-6790 dihydrochloride | 202466-68-0 | sc-396661 | 10 mg | $150.00 | ||
Ro 04-6790 dihydrochloride, an SR-6 acid halide, exhibits distinctive reactivity due to its highly polarized carbonyl moiety, which facilitates rapid nucleophilic addition. The compound's unique electronic configuration enhances its interaction with various nucleophiles, leading to diverse acylation products. Additionally, its ability to stabilize reactive intermediates through resonance effects allows for efficient transformation pathways, making it a versatile agent in synthetic chemistry. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
p38 MAPK inhibitor, may impact pathways that modulate SR-6 function. | ||||||
NPS ALX Compound 4a dihydrochloride | 299433-10-6 | sc-204134 sc-204134A | 10 mg 50 mg | $169.00 $712.00 | ||
NPS ALX Compound 4a dihydrochloride, classified as an SR-6 acid halide, showcases remarkable reactivity stemming from its electrophilic carbonyl group, which promotes swift nucleophilic attack. The compound's structural features enable it to engage in selective acylation reactions, yielding a variety of derivatives. Its unique steric and electronic properties also facilitate the formation of stable transition states, enhancing reaction kinetics and expanding its utility in complex synthetic routes. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
JNK inhibitor, could affect signaling processes that SR-6 is part of. | ||||||
Dimebolin dihydrochloride | 97657-92-6 | sc-294348 sc-294348A sc-294348B | 1 mg 5 mg 50 mg | $37.00 $96.00 $384.00 | ||
Dimebolin dihydrochloride, an SR-6 acid halide, exhibits distinctive reactivity due to its highly polarized carbonyl moiety, which enhances its susceptibility to nucleophilic addition. The compound's unique steric hindrance and electronic distribution allow for selective interactions with various nucleophiles, leading to diverse acylation products. Additionally, its ability to stabilize intermediates contributes to efficient reaction pathways, making it a versatile candidate in synthetic chemistry. | ||||||
SB-258585 dihydrochloride | sc-301789 | 10 mg | $185.00 | |||
SB-258585 dihydrochloride, classified as an SR-6 acid halide, showcases remarkable reactivity stemming from its unique electronic configuration and spatial arrangement. The compound's carbonyl group engages in strong dipole-dipole interactions, facilitating rapid acyl transfer reactions. Its distinctive steric profile promotes selective reactivity with specific nucleophiles, resulting in tailored synthetic pathways. Furthermore, the compound's stability under varying conditions enhances its utility in complex reaction schemes. | ||||||
BAY 11-7082 | 19542-67-7 | sc-200615B sc-200615 sc-200615A | 5 mg 10 mg 50 mg | $62.00 $85.00 $356.00 | 155 | |
NF-κB pathway inhibitor, potentially influencing SR-6 mediated signaling. | ||||||
Asenapine maleate | 65576-45-6 | sc-361110 sc-361110A | 10 mg 50 mg | $145.00 $615.00 | ||
Asenapine maleate, an SR-6 acid halide, exhibits intriguing reactivity due to its unique stereochemistry and electronic characteristics. The presence of the maleate moiety introduces a conjugated system that enhances electrophilicity, allowing for efficient nucleophilic attack. Its ability to form stable intermediates during reactions is influenced by intramolecular hydrogen bonding, which can modulate reaction kinetics. Additionally, the compound's solubility profile aids in facilitating diverse synthetic transformations. | ||||||