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Protease/Metabolic Enzyme
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Research Areas
- Metabolic Disease
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Nature products
Antibodies
Peptides
Catalysts
Impurities
Intermediate
- Amino acid
- Ammonia Series
- Azaindazole
- Pyridazine Series
- Nucleoside Series
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- Saccharide
- Azaindole
- Indole Series
- Piperidine Series
- Indazole Series
- Heterocyclic Series
- Benzene Series
- Pyridine Series
Raw Materials
Phospholipase
Chemical Structure | Cat. No. | Product Name | CAS No. |
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BCP48475 | Varespladibmethyl New | 172733-08-3 | |
Varespladib methyl is a selective inhibitor of group II secretory phospholipase A2 (PLA2).
|
BCP45093 | SB-435495 New | 304694-39-1 | |
SB-435495 is a potent, orally active inhibitor of Lp-PLA2 with IC50 of 0.06 nM.
|
BCP37987 | ML298 New | 1426916-02-0 | |
ML-298 is a potent inhibitor of phospholipase D2 (PLD2) displaying selectivity for PLD2 over PLD1 with IC50 values of 355 and 20000 nM, respectively.
|
BCP37902 | ML349 New | 890819-86-0 | |
ML 349 is a lysophospholipase 2 inhibitor with IC50 value of 144 nM.
|
BCP37841 | ML-299 New | 1426916-00-8 | |
ML-299 is a dual PLD1/2 inhibitor (PLD1 IC50 = 6 nM, PLD2 IC50 = 20 nM).
|
BCP37836 | YM 26734 New | 144337-18-8 | |
YM-26734 is an inhibitor of rabbit platelet sPLA2.
|
BCP33391 | Aacocf3 New | 149301-79-1 | |
AACOCF3 is a fatty acid derivative that is arachidonic acid in which the OH part of the carboxy group has been replaced by a trifluoromethyl group
|
BCP32595 | CAY10650 New | 1233706-88-1 | |
CAY10650 is a potent cPLA2a inhibitor, demonstrating strong anti-inflammatory effects.
|
BCP30845 | N-(p-amylcinnamoyl) Anthranilic Acid New | 110683-10-8 | |
N-(p-amylcinnamoyl) Anthranilic Acid (ACA) is a broad spectrum Phospholipase A2 (PLA2) inhibitor and TRP channel blocker. N-(p-amylcinnamoyl) Anthranilic Acid (ACA) is also an effective reversible inhibitor of calcium-activated chloride channels, has potential to treat arrhythmia.
|
BCP30751 | CAY10594 New | 1130067-34-3 | |
CAY10594 is a potent PLD2 inhibitor, both in vitro (IC50 = 140 nM) and in cells (IC50 = 110 nM). It is also effective as a PLD1 inhibitor at higher concentrations (IC50 = 5.1 μM in vitro, 1.0 μM in cells). CAY10594 strongly inhibits the invasive migration of breast cancer cells in transwell assays, suggesting that PLD might be a useful target in blocking tumor cell invasion.
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