Category: Reagents

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  • Brand: Boster
  • Brand: MedChemExpress 
  • Brand: Technoclone
Reference: HY-107260

Lucidenic acid D (Lucidenic acid D2) is a highly oxidized lanostane-type triterpenoid.

Reference: HY-147584

BTK-IN-14 is a potent inhibitor of BTK. BTK plays an important role in signaling mediated by B cell antigen receptor (BCR) and Fcγreceptor (FcγR) in B cells and myeloid cells, respectively. BTK-IN-14 has the potential for the research of related diseases, especially autoimmune diseases, inflammatory diseases or cancer (extracted from patent WO2022057894A1, compound 1).

Reference: HY-151701

DiSulfo-Cy5 alkyne is a fluorescent dye can be used as a click chemistry reagent.

Reference: HY-B0863S2

Glyphosate-d2-1 is the deuterium labeled Glyphosate[1]. Glyphosate is an herbicidal derivative of the amino acid glycine. Glyphosate targets and blocks a plant metabolic pathway not found in animals, the shikimate pathway, required for the synthesis of aromatic amino acids in plants[2].

Reference: HY-N11663

Dugesin C is a diterpenoid isolated from the plant Salvia dugesii with a spiro carbocyclic ring system derived from the normal neocrotane skeleton.

Reference: HY-115729

PROTAC CDK9 ligand-1 is a CDK9 ligand that can be used in the synthesis of PROTACs.

Reference: HY-W014787S

Decanedioic acid-d4 is the deuterium labeled Decanedioic acid[1]. Decanedioic acid, a normal urinary acid, is found to be associated with carnitine-acylcarnitine translocase deficiency and medium chain acyl-CoA dehydrogenase deficiency[2].

Reference: HY-135636

Ponatinib Acid, an analogue of Ponatinib, is usually used as a labeled chemical or fluorescent probe.

Reference: HY-154660

N4-Benzoyl-2’-deoxy-5-iodocytidine 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.

Reference: HY-N6712

Thiolutin (Acetopyrrothin) is a disulfide-containing antibiotic and anti-angiogenic compound produced by Streptomyces. Thiolutin inhibits the JAMM metalloproteases Csn5, Associated-molecule-with-the-SH3-Domain-of-STAM (AMSH) and Brcc36. Thiolutin is a potent and selective inhibitor of endothelial cell adhesion accompanied by rapid induction of Heat-shock protein beta-1 (Hsp27) phosphorylation.

Reference: HY-19329

HA130 is a selective autotaxin (ATX) inhibitor with an IC50 of 28 nM.

Reference: HY-133321

N3-PEG24-Hydrazide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.