2-bromoethanol-d4 is the deuterated derivative of 2-bromoethanol. 2-bromoethanol is a cytotoxic alkylating agent.

Ethane-d4-1,2-diamine dihydrochloride is the deuterated form of 1,2-diaminoethane dihydrochloride.1,2-diaminoethane dihydrochloride is a laboratory reagent with protein cross-linking effect, mainly used in molecular modification or cell inhibition experiments in biochemical research.

Collagenase,Type II is a microbially derived matrix metalloproteinase (MMP) and zinc-dependent peptidase that degrades collagens 1, 3, 5, 7, 8, 10, as well as fibronectin, gelatin, and aggrecan. It can be commonly used in research of human cell isolation, wound healing, and wound debridement.

Morpholine-d8 Hydrochloride is the deuterated derivative of morpholin hydrochloride. Morpholine hydrochloride is an antiviral drug that works by inhibiting influenza virus, herpes virus, etc. Its synthesis involves morpholine derivatives as intermediates.

N-Boc-piperazine-d8 is the deuterated derivative of 1-t-Butoxycarbonylpiperazine.1-t-Butoxycarbonylpiperazine is a piperazine organic intermediate, which is often used to synthesize drug molecules with antiviral, antibacterial and other biological activities.

Tanzisertib (CC-930) is a potent JNK1/2/3 inhibitor with IC50s of 61/7/6 nM, respectively.

cGAMP (Cyclic GMP-AMPP) functions as an endogenous second messenger in metazoans and triggers interferon production in response to cytosolic DNA. cGAMP activates stimulator of interferon genes (STING), which activates a signaling cascade leading to the production of type I interferons and other immune mediators.

Minocycline is an orally active, potent and BBB-penetrated semi-synthetic tetracycline antibiotic. Minocycline is a hypoxia-inducible factor (HIF)-1α inhibitor. Minocycline shows anti-cancer, anti-inflammatory, and glutamate antagonist effects. Minocycline reduces glutamate neurotransmission and shows neuroprotective properties and antidepressant effects. Minocycline inhibits bacterial protein synthesis through binding with the 30S subunit of the bacterial ribosome, resulting in a […]

Alvespimycin (17-DMAG) is a potent inhibitor of Hsp90, binding to Hsp90 with an EC50 of 62 ± 29 nM.

RO-9187 is a potent inhibitor of HCV virus replication with an IC50 of 171 nM. RO-9187 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.