aza 1

AZA1 (Rac1/Cdc42-IN-1) is a potent dual inhibitor of Rac1 and Cdc42. AZA1 induced apoptosis of prostate cancer cells and inhibited cell proliferation, migration and invasion.

N-1H-imidazo[4,5d ]pyridazin-7-yl benzamideN4-Benzoyl-2-aza-3'-deazaadenine is a Heterocyclic Compound - Purine; Intermediates and Building Blocks - Nucleoside bases.

AZA197 (AZA-197) is a selective Cdc42 inhibitor. It acts by inhibiting primary colon cancer growth and prolonging survival in a preclinical mouse xenograft model by downregulation of PAK1 activity.

Spermine (Neuridine) is an endogenous polyamine in the human body. As a direct free radical scavenger, it exhibits antiviral activity and protects DNA from free radical damage; it is also a key regulator of cell proliferation, differentiation, and apoptosis. Spermine inhibits certain bacteria, particularly strains of Staphylococcus aureus. Spermine induces striatal neurotoxicity in a dose-dependent manner. Spermine reversibly inhibits DNA synthesis, mixed lymphocyte reactions, and the induction of cytolytic lymphocyte reactions in primary cultures of mouse splenocytes.

3-Trifluoromethyl-5-aza-1H-indazole, with CAS No. 230305-81-4, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 3-Trifluoromethyl-5-aza-1H-indazole provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

2-Aza-ε-adenosine (2-Aza-1,N6-ethenoadenosine) serves as a versatile dye with broad applications in various fields. As essential components in biological experimentation, dyes enable scientists to examine and track cell structures, monitor biomolecules, assess cellular functions, differentiate among cell types, explore tissue pathology, and scrutinize microorganisms. Their utility extends beyond biological research into clinical diagnostics, influencing a wide spectrum of industries including traditional textile dyeing, innovative textile processing, food coloring, and dye-sensitized solar cells.

AAZ-A 154 hydrobromide is a selective, competitive, non-hallucinogenic 5-HT2AR antagonist. It promotes neuronal growth in rodents and yields enduring beneficial behavioral effects.

AAZ-A 154 mesylate mesylate is a selective, competitive, and non-hallucinogenic antagonist of 5-HT2AR. It enhances neuronal growth in rodents and produces enduring beneficial behavioral effects.

AAZ-A 154 benzoate is a selective, competitive, and non-hallucinogenic 5-HT2AR antagonist. This compound facilitates neuronal growth in rodents and produces lasting beneficial behavioral effects.

AAZ-A 154 hydrochloride is a selective, competitive, non-hallucinogenic antagonist of 5-HT2AR. It promotes neuronal growth in rodents and results in enduring beneficial behavioral effects.

AAZ-A 154, as a selective, competitive, and non-psychoactive 5-HT2AR antagonist, promotes neuronal growth in rodents.

Hexacyclen is an analogue of 18-crown-6, exhibiting antagonistic and blocking effects on the extracellular calcium-sensing receptor with an EC50 of 20 μM. Possessing multiple secondary amine groups, Hexacyclen serves as an excellent electron donor and functions as a block copolymer.

Diaza-15-crown-5, a crown ether compound, can extend the lifespan of the M intermediate in BR membranes. By altering the surface charge of the BR membrane, Diaza-15-crown-5 affects the interactions between BR molecules and enhances the overall stability of the membrane, allowing the M state to be sustained longer.

Hexacyclen, also known as Cycloolefin, is an organic compound with a unique macrocyclic structure composed of six nitrogen-containing rings. It serves as a chelating agent in chemistry and biochemistry due to its ability to bind metal ions and functions as an inhibitor for certain diseases like cancer. In biochemistry, Hexacyclen is utilized to selectively bind metal ions within proteins or enzymes, aiding in the study of their structure and function. Due to its large size and complex structure, Hexacyclen is not widely used in everyday products or applications.

Hexacyclen (Cycloalkene) is an organic compound characterized by a distinctive macrocyclic structure composed of six nitrogen-containing rings. Known for its metal ion-binding capability, Hexacyclen is frequently employed as a chelating agent in chemistry and biochemistry for selectively binding metal ions in proteins or enzymes to study their structure and function. Additionally, Hexacyclen can serve as a cancer inhibitor.

Ixabepilone (Azaepothilone B) is an orally bioavailable microtubule inhibitor. It binds to tubulin and promotes tubulin polymerization and microtubule stabilization, thereby arresting cells in the G2-M phase of the cell cycle and inducing tumor cell apoptosis.

(5Alpha)-23-methyl-4-aza-21-norchol-1-ene-3,20-dione is a bioactive chemical.

GS-441524tris-isobutyryl ester is a prodrug form of the antiviral nucleoside analog and remdesivir metabolite GS-441524 .1It reduces the cytopathic effect of respiratory syncytial virus (RSV) in infected HEp-2 cells with an EC50value of 0.26 μM. 1.Mackman, R.L., Hui, H.C., Perron, M., et al.Prodrugs of a 1'-CN-4-aza-7,9-dideazaadenosine C-nucleoside leading to the discovery of remdesivir (GS-5734) as a potent inhibitor of respiratory syncytial virus with efficacy in the african green monkey model of RSVJ. Med. Chem.64(8)5001-5017(2021)

GM 1489 is a broad-spectrum inhibitor of matrix metalloproteinases (MMPs) with Ki values of 0.002, 0.1, 0.5, 0.2, and 20 μM for MMP-1, MMP-8, MMP-2, MMP-9, and MMP-3, respectively. It reduces 5-aza-2'-deoxycytidine-induced increases in MMP-1, MMP-2, MMP-3, MMP-7, MMP-9, and MMP-14 expression as well as cell invasion in AsPC-1, BxPC-3, Hs766T, MiaPaCa2, and PANC-1 cancer cells. Topical administration of GM 1489 (100 μg) inhibits increases in ear thickness and epidermal hyperplasia induced by phorbol 12-myristate 13-acetate and phorbol dibutyrate (PdiBu) in mice.

2-Amino-8-aza-7-deaza-7-iodoguanosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis , etc [1] .

5-Azacitidine, a purine nucleoside analog, exhibits wide-ranging antitumor efficacy against indolent lymphoid malignancies by inhibiting DNA synthesis and inducing apoptosis, among other mechanisms [1].

5-Azacytidine 5′-triphosphate (5-aza-CMP), a cytidine analog, selectively inhibits the incorporation of [^3H]CTP into RNA during the DNA-dependent RNA polymerase reaction without affecting the incorporation of [^3H]UTP [1].

5-Aza-4'-thio-2'-deoxycytidine (5-Aza-T-dCyd), a sulfur-containing deoxy-cytidine analog, serves as an orally active inhibitor of DNA methyltransferase I (DNMT1). It exhibits potential antitumor effects and DNA hypomethylating properties [1].

1-(b-D-Xylofuranosyl)-6-azauracil is a Nucleoside Derivative - Xylo-nucleoside; 6-Aza-uridine.