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G-1 is a nonsteroidal, high-affinity, and selective GPR30 agonist (Ki: 11 nM).

Aflatoxin G1 9,10-epoxide is a biochemical.

PKG drug G1 targets PKG Iα C42. PKG drug G1 can couple to vasodilation and blood pressure lowering by a C42 PKG Iα-independent mechanism.

Aflatoxin G1 is a mycotoxin produced by Aspergillus flavus and Aspergillus parasiticus, which is hepatotoxic, teratogenic, immunosuppressive, and carcinogenic, and is mainly found in contaminated cereals. Aflatoxin G1 inhibits RNA polymerase activity, affects RNA and protein synthesis, and causes damage to the liver and kidney.

Cucumarioside G1 is a triterpene glycoside of holothurian from Cucumaria fraudatrix.

Hemsloside G1 is a useful organic compound for research related to life sciences. The catalog number is T126090 and the CAS number is 129385-80-4.

G1-OC2-K3-E10, an ionizable lipid, facilitates mRNA delivery through lipid nanoparticles (LNPs) [1].

Prostaglandin G1 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.

Monamycin G1 is an ester-peptide antibiotic [esterpeptid]. It shows activity against Gram-positive bacteria.

Luminacin G1 exhibits a potent inhibitory effect on capillary formation, with an IC50 of less than 0.1 μg/mL.

Human Immunoglobulin G1 (IgG1) is a monoclonal antibody of human origin.

Mouse Immunoglobulin G1 is a type of serum immunoglobulin from mice, suitable for use as an immunolabeling and coating protein in various immunoassays, including ELISA.

A2[3]G1 & A2[6]G1 glycan (G1) is a type of poly N-glycoprotein that serves as a multifunctional fluorescent linker. The resulting conjugate simulates the antennae elements of N-glycans, providing high sensitivity and specificity.

FA2[3]G1 & FA2[6]G1 glycan (G1F), procainamide labelled, is a poly-N-glycoprotein serving as a versatile fluorescent linkage (Linker). The resulting conjugate, mimicking the antenna elements of N-glycans, exhibits high sensitivity and specificity.

A2[3]G1 N-glycan is a Lewis X (LeX) polysaccharide with two asymmetric antennae and serves as a precursor to A2G1F1(a1-3) and asymmetric biantennary N-glycan. SLeX, a ligand for the cell adhesion molecule E-selectin, is specifically expressed at sites of inflammatory lesions. Conjugates of SLeX polysaccharides are designed to deliver drugs to these inflammation sites.

A2[3]G1 & A2[6]G1 glycan (G1), 2-AA labelled, is a type of poly N-glycoprotein and serves as a versatile fluorescent linker. The resulting conjugates, which mimic structural elements of N-glycan antennae, exhibit high sensitivity and specificity.

FA2[3]G1 & FA2[6]G1 glycan (G1F), APTS labelled, is a type of N-glycoprotein with multiple glycans and serves as a multifunctional fluorescent linker. The resulting conjugate, characterized by high sensitivity and specificity, mimics the antenna structures of N-glycans.

A2[3]G1 & A2[6]G1 glycan (G1), 2-AB labelled is an N-glycan featuring two asymmetric antennary Lewis X (LeX) structures with a 2-AB (2-aminobenzamide) label. SLeX serves as a ligand for the cell adhesion molecule E-selectin, which is specifically expressed at sites of inflammatory lesions. Designing conjugates with SLeX polysaccharides enables targeted drug delivery to inflamed areas.

FA2[3]G1 & FA2[6]G1 glycan (G1F), 2-AA labelled is a type of polymeric N-glycoprotein that acts as a multifunctional fluorescent linker. The resulting conjugates, simulating N-glycan antenna elements, exhibit high sensitivity and specificity.

FA2[3]G1 & FA2[6]G1 glycan (G1F) is a type of poly-N-glycoprotein that serves as a multifunctional fluorescent linker. The resulting conjugate, by mimicking the arm components of N-glycans, exhibits high sensitivity and specificity.

FA2[3]G1 & FA2[6]G1 glycan (G1F), 2-AB labelled is a multifunctional fluorescent linker comprising a polymeric N-glycoprotein. The resulting conjugate simulates the antenna components of N-glycans, offering high sensitivity and specificity.

KRas G12C inhibitor 1 is a compound that selectively inhibits the KRas G12C protein.

G6PD activator AG1 is a glucose-6-phosphate dehydrogenase (G6PD) agonist that promotes glucose-6-phosphate dehydrogenase (G6PD) oligomerization to a catalytically competent form. G6PD activator AG1 reduces oxidative stress in cells and zebrafish, reduces chloroquine or diamide-induced oxidative stress in human erythrocytes, and can be used to study glucose-6-phosphate dehydrogenase deficiency.

Dipyrithione appears to have novel cytotoxicity and potent broad-spectrum antitumor activity