Phospholipase
Phospholipases are enzymes that catalyze the hydrolysis of phospholipids into fatty acids and other lipid mediators. It plays a variety of roles in tumorgenesis , inflammation and brain disorders etc.
Products Related to Phospholipase(136)
- GC14521ONO-RS-082CAS: 99754-06-0Purity: >98%
reversible inhibitor of Ca2+-independent phospholipase A2
- GC15888VU 0155069CAS: 1130067-06-9Purity: >98.00%
VU 0155069 is a selective phospholipase D1 (PLD1) inhibitor (IC 50 =46nM).
- GC16115AACOCF3CAS: 149301-79-1Purity: >98.00%
AACOCF3 (arachidonyl trifluoromethyl ketone) is a potent inhibitor of cytosolic phospholipase A2 (cPLA2) with an IC 50 value of approximately 10μM. By irreversibly alkylating the enzyme's active site, AACOCF3 blocks the release of arachidonic acid and the subsequent production of pro-inflammatory eicosanoids. AACOCF3 is widely used in the study of inflammatory pathways, neuroinflammation, and lipid signaling mechanisms.
- GC16687(R)-EdelfosineCAS: 77286-66-9Purity: >99.00%
(R)-Edelfosine is a synthetic lipid agent belonging to a class of compounds with antitumor and antiparasitic activities. (R)-Edelfosine can induce apoptosis-like cell death in tumor cells by targeting FOF1-ATP synthase on mitochondria and lipid rafts.
- GC17203Varespladib (LY315920)CAS: 172732-68-2Purity: >98.00%
Varespladib (LY315920) is a potent and selective inhibitor of group IIA, nonpancreatic secretory PLA2 (sPLA2) with an IC 50 value of 9nM.
- GC18559Lysophosphatidylethanolamines (egg)CAS: 97281-40-8Purity: >98%
Lysophosphatidylethanolamine (LPE) is a naturally-occurring lysophospholipid that can be generated via deacylation of phosphatidylethanolamine by phospholipase A2 (PLA2).
- GC30464Ecopladib (PLA 725)CAS: 381683-92-7Purity: >98%
Ecopladib (PLA 725) is a sub-micromolar inhibitor of cytosolic phospholipase A2α (cPLA2α), with IC50s of 0.15 μM and 0.11 μM in the GLU micelle and rat whole blood assays, respectively.
- GC305612-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfideCAS: 137089-36-2Purity: >98%
2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide is a compound that inhibits stress-induced ulcer and low toxicity, and can maintain the content of phospholipase A2 and prostaglandin E2 in ulcerated rats induced by water immersed restrained stress.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC14521 | ONO-RS-082 | 99754-06-0 | >98% | |
reversible inhibitor of Ca2+-independent phospholipase A2 | ||||
| GC15877 | CP 316819 | 186392-43-8 | >98% | |
Selective glycogen phosphorylase inhibitor | ||||
| GC15888 | VU 0155069 | 1130067-06-9 | >98.00% | |
VU 0155069 is a selective phospholipase D1 (PLD1) inhibitor (IC 50 =46nM). | ||||
| GC16115 | AACOCF3 | 149301-79-1 | >98.00% | |
AACOCF3 (arachidonyl trifluoromethyl ketone) is a potent inhibitor of cytosolic phospholipase A2 (cPLA2) with an IC 50 value of approximately 10μM. By irreversibly alkylating the enzyme's active site, AACOCF3 blocks the release of arachidonic acid and the subsequent production of pro-inflammatory eicosanoids. AACOCF3 is widely used in the study of inflammatory pathways, neuroinflammation, and lipid signaling mechanisms. | ||||
| GC16286 | m-3M3FBS | 200933-14-8 | >98.00% | |
PLC activator | ||||
| GC16364 | LY 311727 | 164083-84-5 | >98.00% | |
secreted phospholipase A2 (sPLA2) inhibitor | ||||
| GC16687 | (R)-Edelfosine | 77286-66-9 | >99.00% | |
(R)-Edelfosine is a synthetic lipid agent belonging to a class of compounds with antitumor and antiparasitic activities. (R)-Edelfosine can induce apoptosis-like cell death in tumor cells by targeting FOF1-ATP synthase on mitochondria and lipid rafts. | ||||
| GC16714 | PACOCF3 | 141022-99-3 | >98.00% | |
CPLA2 and iPLA2 inhibitor | ||||
| GC16770 | Arachidonic Acid Leelamide | - | >98% | |
phospholipase A2 inhibitor | ||||
| GC17203 | Varespladib (LY315920) | 172732-68-2 | >98.00% | |
Varespladib (LY315920) is a potent and selective inhibitor of group IIA, nonpancreatic secretory PLA2 (sPLA2) with an IC 50 value of 9nM. | ||||
| GC17420 | OBAA | 221632-26-4 | >98% | |
OBAA is a potent phospholipase A2 (PLA2) inhibitor, with an IC50 of 70 nM. | ||||
| GC17684 | VU 0364739 hydrochloride | 1244640-48-9 | >98% | |
phospholipase D2 (PLD2) inhibitor | ||||
| GC17851 | D609 | 83373-60-8 | >98.00% | |
A competitive inhibitor of PC-specific PLC | ||||
| GC17889 | ML 349 | 890819-86-0 | >99.00% | |
ML 349 is the active-site competitive acyl protein thioesterase 2 (APT2) inhibitor, with K i = 0.120μM. | ||||
| GC17960 | U 73343 | 142878-12-4 | >99.00% | |
U 73343 is an inactive analogue of U 73122. | ||||
| GC18039 | ML 348 | 899713-86-1 | >99.50% | |
ML 348 is a selective and reversible lysophospholipase 1 (LYPLA1) inhibitor with an IC 50 of approximately 210nM, exhibiting 14-fold selectivity for LYPLA1 over LYPLA2. | ||||
| GC18141 | EA4 | 389614-94-2 | >98.50% | |
rPLA2 inhibitor | ||||
| GC18305 | CAY10650 | 1233706-88-1 | >98.00% | |
CAY10650 is a highly potent cytosolic phospholipase A2α (cPLA2α) inhibitor with an IC 50 value of 12nM. | ||||
| GC18559 | Lysophosphatidylethanolamines (egg) | 97281-40-8 | >98% | |
Lysophosphatidylethanolamine (LPE) is a naturally-occurring lysophospholipid that can be generated via deacylation of phosphatidylethanolamine by phospholipase A2 (PLA2). | ||||
| GC18691 | CAY10594 | 1130067-34-3 | >98% | |
CAY10594 is an orally active phospholipase D2 (PLD2) inhibitor (IC 50 =140nM). | ||||
| GC19745 | hnps-PLA Inhibitor | 185298-58-2 | >98% | |
| GC30180 | ST271 | 106392-48-7 | >98.50% | |
ST271 is a potent inhibitor of protein tyrosine kinase (PTK), inhibits phospholipase D activation stimulated by fMet-Leu-Phe and PAF, with IC50s of 6.7 and 9 μM, respectively. | ||||
| GC30464 | Ecopladib (PLA 725) | 381683-92-7 | >98% | |
Ecopladib (PLA 725) is a sub-micromolar inhibitor of cytosolic phospholipase A2α (cPLA2α), with IC50s of 0.15 μM and 0.11 μM in the GLU micelle and rat whole blood assays, respectively. | ||||
| GC30561 | 2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide | 137089-36-2 | >98% | |
2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide is a compound that inhibits stress-induced ulcer and low toxicity, and can maintain the content of phospholipase A2 and prostaglandin E2 in ulcerated rats induced by water immersed restrained stress. | ||||
