diallyl

Diallyl tetrasulfide is an organosulfur compound that has been found in A. sativum and has diverse biological activities, including antimicrobial, antioxidant, and anticancer properties.[1],[2],[3],[4] It is active against the bacteria S. aureus and methicillin-resistant S. aureus (MRSA; MICs = 0.5 and 2 mg/L, respectively), as well as the fungi C. albicans, C. krusei, C. glabrata, A. niger, A. flavus, and A. fumigatus (MICs = 0.5, 4, 2, 1, 2, and 4 mg/L, respectively).[1] It reduces cadmium-induced increases in hepatic levels of thiobarbituric acid reactive substances (TBARS) and increases cadmium-induced decreases in the hepatic activity of superoxide dismutase (SOD1), catalase, GST, and glucose-6-phosphate dehydrogenase (G6PDH) in rats when administered at a dose of 40 mg/kg.[2] Diallyl tetrasulfide is cytotoxic to MCF-7 breast cancer cells (IC50 = 92 μM) and reduces tumor growth in a BGC-823 mouse xenograft model when administered at doses of 20, 30, and 40 mg/kg for 32 days.[3],[4]

Diallyl disulfide has antitumor effect, the effect can be enhanced by miR-200b and miR-22.

Diallyl Trisulfide is an organic polysulfide compound found in garlic that acts as an H2S donor.

Diallyl phthalate (NSC 7667) is a widely used cross-linking agent for unsaturated polyesters and can cause fetal toxicity at certain concentrations.

Diallyl G is a delta-opioid receptor antagonist agent.

Fosamprenavir Calcium Salt (GW433908G) (GW433908G) is a phosphate ester prodrug of the antiretroviral protease inhibitor Amprenavir, with improved solubility. Fosamprenavir Calcium Salt has Anti-HIV infection.

Magnolol (5,5'-Diallyl-2,2'-biphenyldiol) is a dual agonist of RXRα( EC50=10.4 μM) and PPARγ(EC50=17.7 μM). It blocks TNF-α-induced NF-KB activation.

Propenyl-PEG3-Propenyl, a PEG-based linker for PROTACs, connects two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Methyl 2,3-O-diallyl-4,6-O-benzylidene-α-D-mannopyranoside is a reagent used in biochemical reactions.

(+)-N,N'-Diallyl-L-tartardiamide functions as a crosslinking agent in the preparation of hydrogels. It is suitable for use as a biomaterial or organic compound in life science research.

Diallyl phthalate (Standard) is the standard substance of Diallyl phthalate, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Diallyl phthalate (NSC 7667) is a widely used cross-linking agent for unsaturated polyesters and can cause fetal toxicity at certain concentrations.

Diallyl Trisulfide (Standard) is a reference standard for research and analysis in studies involving Diallyl Trisulfide. Diallyl Trisulfide is an organic polysulfide compound found in garlic that acts as an H2S donor.

Diallylmelamine is an anti-secretory agent for the stomach.

(3R,4R,5S)-Ethyl 4-(N-(tert-butyl)acetamido)-5-(diallylamino)-3-(pentan-3-yloxy)cyclohex-1-enecarboxylate hydrochloride is a useful organic compound for research related to life sciences and the catalog number is T66261.

Diallyldimethylammonium chloride (60% in water) is a quaternary ammonium compound classified as an alkyl ammonium salt. It is extensively utilized as a cationic monomer in the production of water-soluble polymers, particularly in manufacturing flocculants and coagulants for water treatment processes. Additionally, it serves as an antimicrobial agent, surfactant, or adhesive in various industrial applications. Its unique chemical properties make it a crucial component in several industrial processes, including papermaking, textiles, and personal care products.

2,3-Dimethyl-2,3-diphenylbutane is a byproduct of the decomposition of Dicumylperoxide (DCP) and serves as an initiator for Diallyl orthophthalate (DAOP), a reactive plasticizer used to enhance the processing of polyphenylene oxide (PPO) in manufacturing.

Magnolol (Standard) is a reference standard for research and analysis in studies involving Magnolol. Magnolol (5,5'-Diallyl-2,2'-biphenyldiol) is a dual agonist of RXRα( EC50=10.4 μM) and PPARγ(EC50=17.7 μM). It blocks TNF-α-induced NF-KB activation.