Others Products Targets
- Oxidative Phosphorylation (6)
- NHE (3)
- Monocarboxylate Transporter (3)
- Matrix Metalloprotease (16)
- LXR-like Receptor (6)
- Voltage-gated Sodium (NaV) Channel (30)
- Voltage-gated Potassium (KV) Channel (38)
- Voltage-gated Calcium Channel (CaV) (38)
- Cell Adhesion Molecule (21)
- TRPV (30)
- Lipoxygenase (8)
- Bradykinin Receptor (12)
- Others (16)
- Cyclooxygenase (24)
- Apelin Receptor (5)
- TRPP (3)
- TRPML (3)
- TRPC (4)
- TRPA1 (7)
- Glycine Receptor (6)
- Epithelial Sodium Channel (3)
- STIM-Orai Channel (4)
- Ryanodine Receptor (6)
- Angiotensin-Converting Enzyme (8)
- 5-HT3 Receptor (39)
- IP3 Receptor (2)
- TRPM (8)
- Acid-Sensing Ion Channel (3)
- Calcium-Activated Potassium (KCa) Channel (19)
- VIP Receptor (7)
- Inward Rectifier Potassium (Kir) Channel (21)
- Stearoyl-CoA 9-Desaturase (1)
- Vasopressin Receptor (6)
- NADPH Oxidase (2)
- Monoamine Oxidase (10)
- Heme Oxygenase (2)
- NO donors and precursors (9)
- nNOS (5)
- iNOS (11)
- eNOS (1)
- Sodium and Potassium ATPase (3)
- KCC2 (1)
- H+-ATPase (3)
- Urotensin-II Receptor (8)
- H+,K+-ATPase (4)
- Ionophore (6)
- Chloride Channel (17)
- ETB Receptor (6)
- ETA Receptor (5)
- Angiotensin AT2 Receptor (3)
- Angiotensin AT1 Receptor (9)
- M5 Receptor (2)
- M4 Receptor (3)
- M3 Receptor (4)
- Purinergic (P2Y) Receptor (31)
- M2 Receptor (5)
- M1 Receptor (8)
- NCX (5)
- Ca2+-ATPase (7)
- Purinergic (P2X) Receptor (32)
- NKCC (2)
- Adrenergic α2 Receptor (33)
- Adrenergic α1 Receptor (22)
- HCN Channel (4)
- Adrenergic β3 Receptor (12)
- Adrenergic β2 Receptor (6)
- Adrenergic β1 Receptor (7)
- Protease-Activated Receptor (23)
- Prostanoid Receptor (24)
- Platelet-Activating Factor (PAF) Receptor (5)
- Phosphodiesterase (34)
Products for Others - Page 41
- Cat.No. Product Name Information/Activity
-
BCC6952
Thapsigargin
Thapsigargin is an inhibitor of microsomal Ca2+-ATPase. Thapsigargin is a well characterized Endoplasmic Reticulum (ER) stress inducing agent.
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BCC7008
Ochratoxin A
303-47-9
-
BCC7235
Paxilline
Paxilline is an indole alkaloid mycotoxin from Penicillium paxilli, acts as a potent BK channels inhibitor by an almost exclusively closed-channel block mechanism. Paxilline also inhibits the sarco/endoplasmic reticulum Ca2+ ATPase (SERCA) with IC50s between 5 μM and 50 μM for differing isoforms. Paxilline possesses significant anticonvulsant activity.
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BCC1058
Lansoprazole
Lansoprazole(AG 1749) is a proton pump inhibitor which prevents the stomach from producing acid.
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BCC1254
Omeprazole
Omeprazole (H 16868), a proton pump inhibitor (PPI), is available for treatment of acid-related gastrointestinal disorders. Omeprazole shows competitive inhibition of CYP2C19 activity with a Ki of 2 to 6 μM. Omeprazole also inhibits growth of Gram-positive and Gram-negative bacteria.
-
BCC2084
PF-03716556
PF 03716556 is a potent, and selective H+, K+-ATPase antagonist, with a pIC50 value of 6.009.
-
BCC7154
SCH 28080
SCH28080 inhibits gastric H+/K+-ATPase by K+-competitive binding, with an IC50 value of 20 nM in rabbit microsomal membranes. Antisecretory and cytoprotective activities.
-
BCC3914
Bafilomycin A1
Bafilomycin A1, a macrolide antibiotic isolated from the Streptomyces species, is a specific inhibitor of vacuolar-type H+ ATPase (V-ATPase). Bafilomycin A1 inhibits autophagy and induces apoptosis.
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BCC3919
Concanamycin A
Concanamycin A (Antibiotic X 4357B) is a macrolide antibiotic and a specific vacuolar type H+-ATPase (V-ATPase) inhibitor.
-
BCC5424
VU 0240551
VU 0240551 is a small molecule inhibitor of the neuronal K-Cl cotransporter, KCC2 (IC50 = 560 nM for K+ uptake assay in KCC2-overexpressing cells).
