265 Results for "

phospholipase-d

" in MedChemExpress (MCE) Product Catalog:
Products (265)

265 Results for "phospholipase-d" in MCE Product Catalog:

110
110 Publications Verification
製品番号: HY-13419
CAS 番号: 112648-68-7
純度:  98.41%
U-73122 is a phospholipase C (PLC) and 5-LO (5-lipoxygenase) inhibitor with an IC50of 1-2.1 µM for PLC.
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76
76 Cited Publications
製品番号: HY-B0470
CAS 番号: 1405-10-3
Neomycin sulfate, an aminoglycoside antibiotic, exerts antibacterial activity through irreversible binding of the nuclear 30S ribosomal subunit, thereby blocking bacterial protein synthesis. Neomycin sulfate is a known phospholipase C (PLC) inhibitor. Neomycin sulfate potently inhibits both the nuclear translocation of angiogenin and angiogenin-induced cell proliferation and angiogenesis. Neomycin sulfate inhibits IP3-mediated Ca 2+ release, MgATP-dependent Ca 2+ uptake, and electrical excitation-evoked skeletal muscle Ca 2+ transients. Neomycin sulfate depletes gut microbiota in specific mouse models, causes hearing impairment, and kidney damage with prolonged exposure. Neomycin sulfate can be used for the research of cancer .
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37
37 Cited Publications
製品番号: HY-100168
CAS 番号: 85233-19-8
純度:  98.10%
BAPTA is a selective and cell-impermeant chelator for calcium. BAPTA has high selectivity against magnesium and calcium. BAPTA can also inhibit phospholipase C activity independently of their role as Ca 2+ chelators .
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37
37 Cited Publications
製品番号: HY-100168A
CAS 番号: 126824-24-6
純度:  99.70%
Target:  

Phospholipase

研究分野:  

Others

BAPTA tetrasodium is a selective and cell-impermeant chelator for calcium. BAPTA tetrasodium has high selectivity against magnesium and calcium. BAPTA can also inhibit phospholipase C activity independently of their role as Ca 2+ chelators .
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37
37 Cited Publications
製品番号: HY-100168B
CAS 番号: 73630-08-7
純度:  99.45%
BAPTA tetrapotassium is a selective and cell-impermeant chelator for calcium. BAPTA has high selectivity against magnesium and calcium. BAPTA tetrapotassium can also inhibit phospholipase C activity independently of their role as Ca 2+ chelators .
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10
10 Cited Publications
製品番号: HY-19619
CAS 番号: 200933-14-8
Target:  

Phospholipase Apoptosis

研究分野:  

Cancer

m-3M3FBS is a potent phospholipase C (PLC) activator. m-3M3FBS stimulates superoxide generation in human neutrophils, upregulates intracellular calcium concentration, and stimulates inositol phosphate generation in various cell lines. m-3M3FBS induces monocytic leukemia cell apoptosis .
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9
9 Cited Publications
製品番号: HY-13402
CAS 番号: 172732-68-2
純度:  99.23%
別名: LY315920
Target:  

Phospholipase

研究分野:  

Inflammation/Immunology

Varespladib (LY315920) is a potent and selective group IIA, secretory phospholipase A2 (sPLA2) inhibitor with an IC50 of 9 nM. Varespladib exhibits the significant inhibitory effect on sPLA2 activity in serum from various species including rat, rabbit, guinea pig and human with IC50s of 8.1 nM, 5.0 nM, 3.2 nM and 6.2 nM, respectively .
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9
9 Cited Publications
製品番号: HY-13402A
CAS 番号: 172733-42-5
純度:  ≥98.0%
別名: LY315920 sodium
Target:  

Phospholipase

研究分野:  

Inflammation/Immunology

Varespladib sodium (LY315920 sodium) is a potent and selective group IIA, secretory phospholipase A2 (sPLA2) inhibitor with an IC50 of 9 nM. Varespladib sodium exhibits the significant inhibitory effect on sPLA2 activity in serum from various species including rat, rabbit, guinea pig and human with IC50s of 8.1 nM, 5.0 nM, 3.2 nM and 6.2 nM, respectively .
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8
8 Cited Publications
製品番号: HY-10801
CAS 番号: 1233706-88-1
純度:  ≥98.0%
Target:  

Phospholipase

研究分野:  

Inflammation/Immunology

CAY10650 is a highly potent cytosolic phospholipase A2α (cPLA2α) inhibitor with an IC50 value of 12 nM. CAY10650 suppresses lipid droplets formation and PGE2 secretion .
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8
8 Cited Publications
製品番号: HY-70072
CAS 番号: 83373-60-8
Target:  

Phospholipase

D609, an antitumoural xanthate, is a specific and competitive phosphatidyl choline-specific phospholipase C (PC-PLC) inhibitor with a Ki of 6.4 μM. D609 is an antioxidative protector and has antiviral and anti-inflammatory activity .
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8
8 Cited Publications
製品番号: HY-108630
CAS 番号: 142878-12-4
純度:  99.31%
Target:  

Phospholipase

研究分野:  

Others

U-73343, works as a protonophore, is an inactive analog of U-73122 and can be used as a negative control. U-73343 dose-dependently inhibits acid secretion irrespective of the stimulant. U-73122 is a phospholipase C (PLC) and 5-LO (5-lipoxygenase) inhibitor with an IC50 of 1-2.1 μM for PLC .
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8
8 Cited Publications
製品番号: HY-118628
CAS 番号: 110683-10-8
純度:  99.63%
別名: N-(p-Amylcinnamoyl) anthranilic acid; ACA
研究分野:  

Cardiovascular Disease

(E/Z)-BML264 (N-(p-amylcinnamoyl) Anthranilic Acid) is a broad spectrum Phospholipase A2 (PLA2) inhibitor and TRP channel blocker . (E/Z)-BML264 is a SLC13A3 inhibitor. (E/Z)-BML264 (N-(p-amylcinnamoyl) Anthranilic Acid) is also an effective reversible inhibitor of calcium-activated chloride channels, has potential to treat arrhythmia .
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7
7 Cited Publications
製品番号: HY-115768
CAS 番号: 94724-12-6
純度:  99.98%
別名: Poly-p-methoxyphenethylmethylamine
Target:  

Phospholipase

研究分野:  

Neurological Disease Cancer

Compound 48/80 (Poly-p-methoxyphenethylmethylamine) is widely used in animal and tissue models as a "selective" mast cell activator. Compound 48/80 acts at the mast cell membrane to stimulate trimeric G-proteins and induces degranulation via phospholipase C and D pathways .
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7
7 Cited Publications
製品番号: HY-130592
CAS 番号: 848035-21-2
純度:  99.95%
別名: C48/80 trihydrochloride
Target:  

Phospholipase

研究分野:  

Neurological Disease

Compound 48/80 trihydrochloride (C48/80 trihydrochloride) is a mixture of condensation products of N-methyl-p-methoxyphenethylamine with formaldehyde. Compound 48/80 trihydrochloride is also a histamine releaser and a mast cell degranulator. Compound 48/80 inhibits phosphatidylinositol-specific phospholipase C activity from human platelets .
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6
6 Cited Publications
製品番号: HY-108611
CAS 番号: 149301-79-1
純度:  ≥99.0%
別名: Arachidonyl trifluoromethyl ketone
Target:  

Phospholipase

研究分野:  

Cardiovascular Disease

AACOCF3 (Arachidonyl trifluoromethyl ketone) is a cell-permeant trifluoromethyl ketone analog of arachidonic acid. AACOCF3 is a potent and selective slow binding inhibitor of the 85-kDa cytosolic phospholipase A2 (cPLA2). AACOCF3 blocks production of arachidonate and 12-hydroxyeicosatetraenoic acid by calcium ionophore-challenged platelets. AACOCF3 inhibits glucose-induced insulin secretion from isolated rat islets. AACOCF3 has the potential for the research of cardiovascular disease .
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5
5 Cited Publications
製品番号: HY-12807
CAS 番号: 939055-18-2
純度:  98.00%
別名: 5-Fluoro-2-indolyl deschlorohalopemide
FIPI is a phospholipase D (PLD) inhibitor with an IC50 for PLD1 and PLD2 of about 25 nM. FIPI regulates cytoskeletal recombination, cell diffusion and chemotaxis. FIPI can be used in cancer research. In addition, FIPI can enhance the secretion and aggregation of platelet dense particles, inhibit thrombosis, reduce ischemic stroke infarct volume and improve nerve function .
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4
4 Cited Publications
製品番号: HY-12598A
CAS 番号: 146255-66-5
純度:  99.65%
別名: (RS)-3,5-DHPG
Target:  

mGluR

研究分野:  

Neurological Disease

DHPG is the agonist for mGluR 1/5 (EC50 for mGluR 1 is 60 nM) that activates the phospholipase C (PLC) pathway, and leads ultimately to the activation of protein kinase C (PKC) .
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4
4 Cited Publications
製品番号: HY-111376
CAS 番号: 341973-06-6
純度:  99.60%
Pyrrophenone is a potent and specific cytosolic phospholipase A2α (cPLA2α) inhibitor with an IC50 value of 4.2 nM .
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4
4 Cited Publications
製品番号: HY-111919
CAS 番号: 28448-04-6
純度:  100.0%
Target:  

Phospholipase Fungal

研究分野:  

Infection

3-Nitrocoumarin is an inhibitor for phospholipase C that blocks the generation of inositol triphosphate (IP3), thereby affecting the calcium signaling pathway .
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3
3 Cited Publications
製品番号: HY-131181
CAS 番号: 2393840-15-6
純度:  99.73%
Target:  

Phospholipase

研究分野:  

Neurological Disease

LEI-401 is a first-in-class, selective, and CNS-active NAPE-PLD (N-acylphosphatidylethanolamine phospholipase D) inhibitor, with an IC50 of 27 nM. LEI-401 modulates emotional behavior in mice .
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