5' o dmt n4 ac dc

5'-O-DMT-N4-Ac-dC (N4-Acetyl-2'-deoxy-5'-O-DMT-cytidine, compound 7) is a deoxynucleoside used in synthesizing dodecyl phosphoramidite, a crucial precursor for dod-DNA production. Dod-DNA is amphiphilic DNA with dodecyl phosphotriester linkages, featuring an internal hydrophobic region[1][2].

2-(4-methyl-1,3-thiazol-5-yl)ethyl decanoate is a long-chain fatty acid ester containing thiazole that is used in organic synthesis and biochemical experiments.

Heptanoic acid sodium is the sodium salt of Heptanoate.The C(5) ketogenicity of Heptanoate is much lower than the C(4) ketogenicity of octanoate, and it can inhibit the osteoporosis and gluconeogenesis of Heptanoate.

2-Deoxy-D-ribonic-1,4-lactone ((4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-one) is an oxolane-containing compound used in organic synthesis and biochemical experiments.

Nocardamine is a ferrioxamine siderophore that has been found inStreptomycesand has diverse biological activities.1,2,3,4It chelates iron in a chrome azurol S assay (IC50= 9.9 μM).1Nocardamine inhibitsM. smegmatisandM. bovisbiofilm formation (MIC = 10 μM for both), an effect that can be reversed by iron.2It is cytotoxic to T47D, SK-MEL-5, SK-MEL-28, and RPMI-7951 cancer cells (IC50s = 6, 18, 12, and 14 μM, respectively).3Nocardamine also induces morphological changes in BM-N4 insect cells.4 1.Lopez, J.A.V., Nogawa, T., Futamura, Y., et al.Nocardamin glucuronide, a new member of the ferrioxamine siderophores isolated from the ascamycin-producing strain Streptomyces sp. 80H647J. Antibiot. (Tokyo)72(12)991-995(2019) 2.Ishida, S., Arai, M., Niikawa, H., et al.Inhibitory effect of cyclic trihydroxamate siderophore, desferrioxamine E, on the biofilm formation of Mycobacterium speciesBiol. Pharm. Bull.34(6)917-920(2011) 3.Kalinovskaya, N.I., Romaneko, L.A., Irisawa, T., et al.Marine isolate Citricoccus sp. KMM 3890 as a source of a cyclic siderophore nocardamine with antitumor activityMicrobiol. Res.166(8)654-661(2011) 4.Matsubara, K., Sakuda, S., Tanaka, M., et al.Morphological changes in insect BM-N4 cells induced by nocardamineBiosci. Biotechnol. Biochem.62(10)2049-2051(1998)

AzoMethine-H Monosodium salt hydrate (Sodium 5-hydroxy-4-((2-hydroxybenzylidene)amino)-7-sulfonaphthalene-2-sulfonate hydrate) is a reagent used for the colorimetric determination of boron in soil, plants, composts, manure, water and nutrient solutions.

18:1 PI(4,5)P2 (1,2-Dioleoyl-sn-glycero-3-phospho-(1′-myo-inositol-4′,5′-bisphosphate) (ammonium)) is utilized as a biomaterial or organic compound in life sciences research.

18:0-20:4 PI(3,4,5)P3 is a reagent used in biochemical reactions.

1,2-Dioctanoyl-sn-glycero-3-phospho-(1'-myo-inositol-3',4',5'-trisphosphate) ammonium is a membrane-associated signaling molecule that plays a crucial role in cell physiology. It is involved in regulating cell growth, metabolism, proliferation, and survival, and participates in various signal transduction pathways, significantly influencing intracellular signal transmission.

Bis(Benz-15-crown-5) [Bis[(Benzo-15-crowN-5)-4-methyl]pimelate] is a biochemical analysis reagent suitable for use in chemical synthesis.

Diethylene glycol monopentyl ether is a reagent used in biochemical reactions.

2-Amino-5-bromo-4-methylpyridine is a biochemical reagent that can be used as a biomaterial for life science related research and as a sulfonylation reagent for organic synthesis and drug discovery.

5-Bromo-4-chloro-3-indolyl-α-D-mannopyranoside, 93%, is a cationic surfactant commonly used in micelle experiments.

5-Bromo-4-chloro-3-indolyl octanoate has potential applications in glycobiology research.

5-Bromo-4-chloro-1H-indol-3-yl β-D-xylopyranoside has potential applications in glycobiology research.

5-Bromo-4-chloro-3-indolyl-α-D-glucopyranoside, 98% is a reagent used in biochemical reactions.

5-Bromo-4-chloro-1H-indol-3-yl-β-D-mannopyranoside has potential applications in glycobiology research.

Sodium 5-bromo-4-chloro-1H-indol-3-yl phosphate is often employed in biochemistry and molecular biology as a substrate for phosphatase assays. This compound is converted by phosphatase into a yellow product, which can be easily quantified using spectrophotometric or fluorometric methods. Additionally, it serves as a valuable reagent in enzyme-catalyzed reactions and as a tool for studying signal transduction pathways.

5-Bromo-4-chloro-3-indolyl β-D-fucopyranoside is a substrate for β-galactosidase.

5-Bromo-4-chloro-3-indolyl sulfate potassium is a reagent used in biochemical reactions.

5-Bromo-4-chloro-1H-indol-3-yl nonanoate is a fluorescent substrate used for enzyme detection. It reacts with various enzymes to produce fluorescent products and has demonstrated activity with β-galactosidase, α-chymotrypsin, and β-glucuronidase.

5-Bromo-4-chloro-3-indolyl-α-L-fucopyranoside can serve as a chromogenic substrate for α-L-Fucosidase.

5-Bromo-4-chloro-3-indolyl β-L-fucopyranoside has potential applications in glycobiology research.

5-Bromo-4-chloro-3-indoxyl palmitate is a reagent used in biochemical reactions.