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Chemical Structure Cat. No. Product Name CAS No.
MAT2A inhibitor Chemical Structure
BCP30524 MAT2A inhibitor 2201057-10-3
MAT2A inhibitor is a MATA2 inhibitor that are useful as therapeutic agents for treating malignancies.
Atrazine Chemical Structure
BCP12774 Atrazine 1912-24-9
Atrazine is an herbicide of the triazine class. Atrazine functions by binding to the plastoquinone-binding protein in photosystem II, which animals lack. Plant death results from starvation and oxidative damage caused by breakdown in the electron transport process.
TSPO1 Chemical Structure
BCP30513 TSPO1 1286708-86-8
TSPO1 is an electon transfer layer (ETL) or hole blocking layer (HBL) in OLED devices.
Salsoline Chemical Structure
BCP30496 Salsoline 89-31-6
(-)-Salsoline is a member of isoquinolines.
Tafamidis meglumine Chemical Structure
BCP30491 Tafamidis meglumine 951395-08-7
Tafamidis meglumine (Fx-1006A) is a potent and selective transthyretin (TTR) stabilizer, shows comparable potency and efficacy to the mutumant homotetramers V30M-TTR, V122I-TTR and wild type WT-TTR, with EC50s of 2.7-3.2 μM. Tafamidis meglumine inhibits amyloidogenesis.
Mycophenolate mofetil Chemical Structure
BCP12786 Mycophenolate mofetil 115007-34-6
Mycophenolate mofetil is an antimetabolite and potent immunosuppressive agent used as adjunctive therapy in prevention of allograft rejection and in the treatment of serious autoimmune diseases. Mycophenolate therapy can be associated with mild serum enzyme elevations and it has been linked to rare instances of clinically apparent liver injury.
McN-3716 Chemical Structure
BCP30486 McN-3716 69207-52-9
McN-3716 is a carnitine palmitoyltransferase I (CPT-1) inhibitor.
L-Cysteine methyl ester hydrochloride Chemical Structure
BCP30482 L-Cysteine methyl ester hydrochloride 18598-63-5
Mecysteine hydrochloride is an antitussive, and an expectorant agent, used to relieve breathing difficulties caused by mucus.
S-Gboxin Chemical Structure
BCP30480 S-Gboxin 2101317-21-7
S-Gboxin, a functional analogue of Gboxin, inhibits growth of mouse and human glioblastoma (GBM) with an IC50 of 470 nM. Antitumour activity.
SGC-GAK-1 Chemical Structure
BCP30478 SGC-GAK-1 2226517-76-4
SGC-GAK-1 is a potent and selective GAK kinase probe which targets the ATP-binding site.
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