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Chemical Structure Cat. No. Product Name CAS No.
S0859 Chemical Structure
BCP06882 S0859 1019331-10-2
S0859, an N-cyanosulphonamide compound, reversibly inhibited NBC-mediated pH(i) recovery (K (i)=1.7 microM, full inhibition at approximately 30 microM). Na(+)-coupled HCO(3)(-) transporters (NBCs) mediate the transport of bicarbonate ions across cell membranes and are thus ubiquitous regulators of intracellular pH.
JNJ1661010 Chemical Structure
BCP06935 JNJ1661010 681136-29-8
JNJ-1661010 is a potent and selective FAAH inhibitor with IC50 of 10 nM (rat) and 12 nM (human), exhibits >100-fold selectivity for FAAH-1 when compared to FAAH-2.
Gemcitabine hydrochloride Chemical Structure
BCP04160 Gemcitabine hydrochloride 122111-03-9
Gemcitabine HCl is a DNA synthesis inhibitor with IC50 of 50 nM, 40 nM, 18 nM and 12 nM in PANC1, MIAPaCa2, BxPC3 and Capan2 cells, respectively.
Doxercalciferol Chemical Structure
BCP01411 Doxercalciferol 54573-75-0
Doxercalciferol is a synthetic analog of vitamin D.
Sapropterin Chemical Structure
BCP03735 Sapropterin 62989-33-7
Sapropterin is a Phenylalanine Hydroxylase Activator. The mechanism of action of sapropterin is as a Phenylalanine Hydroxylase Activator, and Breast Cancer Resistance Protein Inhibitor, and P-Glycoprotein Inhibitor.
Argatroban Chemical Structure
BCP06831 Argatroban 74863-84-6
Argatroban is a direct, selective thrombin inhibitor.
Roflumilast Chemical Structure
BCP03736 Roflumilast 162401-32-3
Roflumilast is a selective inhibitor of PDE4 with IC50 of 0.2-4.3 nM.
Cilostazol Chemical Structure
BCP03724 Cilostazol 73963-72-1
Cilostazol(OPC 13013; OPC 21) is a potent inhibitor of PDE3A, the isoform of PDE 3 in the cardiovascular system (IC50=0.2 uM).
UK 383367 Chemical Structure
BCP02332 UK 383367 348622-88-8
UK-383367 (UK 383367) is a Potent and selective inhibitor of BMP-1 (procollagen C-proteinase; PCP) (IC50 = 44 nM).
Vardenafil hydrochloride trihydrate Chemical Structure
BCP02961 Vardenafil hydrochloride trihydrate 224785-90-4
Vardenafil Hydrochloride Trihydrate (Vivanza) is a new type PDE inhibitor with IC50 of 0.7 and 180 nM for PDE5 and PDE1, respectively.
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