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Chemical Structure Cat. No. Product Name CAS No.
Phlorizin Chemical Structure
BCP29914 Phlorizin 60-81-1
Phlorizin is a non-selective SGLT inhibitor with Kis of 300 and 39 nM for hSGLT1 and hSGLT2, respectively. Phlorizin is also a Na+/K+-ATPase inhibitor.
Luseogliflozin Chemical Structure
BCP20937 Luseogliflozin 898537-18-3
Luseogliflozin, also known as TS-71 and TS-071, is a potent and competitive inhibitor of sodium-dependent glucose cotransporter 2 (SGLT2 inhibitor).
Ipragliflozin L-proline Chemical Structure
BCP28794 Ipragliflozin L-proline 951382-34-6
Ipragliflozin is a Sodium/glucose cotransporter 2 (SGLT2) inhibitor (gliflozin).
Ipragliflozin Chemical Structure
BCP07718 Ipragliflozin 761423-87-4
Ipragliflozin (ASP1941) is a highly potent and selective SGLT2 inhibitor with IC50 of 2.8 nM; little and NO potency for SGLT1/3/4/5/6.
PF-04971729 Chemical Structure
BCP02525 PF-04971729 1210344-57-2
PF-04971729, a potent and selective inhibitor.PF-04971729(Ertugliflozin) is a potent and selective inhibitor of the sodium-dependent glucose cotransporter 2(SGLT2).
PF-04971729 Chemical Structure
BCP18768 PF-04971729 1210344-83-4
PF-04971729(Ertugliflozin) is a potent and selective inhibitor of the sodium-dependent glucose cotransporter 2(SGLT2).
Tofogliflozin hydrate (1:1) Chemical Structure
BCP14576 Tofogliflozin hydrate (1:1) 1201913-82-7
Tofogliflozin(CSG-452) hydrate is a potent and highly specific sodium/glucose cotransporter 2(SGLT2) inhibitor with Ki values of 2.9, 14.9, and 6.4 nM for human, rat, and mouse SGLT2.
Phloretin Chemical Structure
BCP28296 Phloretin 60-82-2
Phloretin(NSC 407292; RJC 02792) is a dihydrochalcone, a type of natural phenols. Phloretin inhibits the active transport of glucose into cells by SGLT1 and SGLT2.
Dapagliflozin propylene glycolate hydrate Chemical Structure
BCP24058 Dapagliflozin propylene glycolate hydrate 960404-48-2
Dapagliflozin propylene glycolate hydrate is the S-enantiomer of Dapagliflozin 1,2-propanediol, hydrate. Dapagliflozin inhibits sodium/glucose cotransporter 2 (SGLT2), which results in excretion of glucose into the urine.
Canagliflozin hemihydrate Chemical Structure
BCP09300 Canagliflozin hemihydrate 928672-86-0
Canagliflozin hemihydrate is a highly potent and selective SGLT2 inhibitor for hSGLT2 with IC50 of 2.2 nM, exhibits 413-fold selectivity over hSGLT1.
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