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Isoforms Recommended:	Phospholipase C

Results for "

phospholipase C

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Phospholipase (42) 5-HT Receptor (1) Adenosine Receptor (1) Antibiotic (3) Apoptosis (3) Aurora Kinase (1) Bacterial (3) Biochemical Assay Reagents (6) Calcium Channel (5) Carbonic Anhydrase (1) Caspase (1) COX (1) Dopamine Receptor (2) Drug Derivative (2) Drug Metabolite (1) Endogenous Metabolite (4) Endothelin Receptor (1) Environmental Pollutants (1) Estrogen Receptor/ERR (1) Ferroptosis (1) Fluorescent Dye (1) Fungal (2) Isotope-Labeled Compounds (1) Lipoxygenase (1) mAChR (2) mGluR (2) Neurokinin Receptor (1) NO Synthase (1) P2Y Receptor (5) PARP (1) Phosphodiesterase (PDE) (2) PKA (1) PKC (3) Prostaglandin Receptor (1) Reference Standards (9) Reverse Transcriptase (1) TSH Receptor (1)
By Research Areas:	Cancer (18) Cardiovascular Disease (4) Endocrinology (3) Infection (10) Inflammation/Immunology (9) Metabolic Disease (14) Neurological Disease (14)

By Targets:

Phospholipase (42)

5-HT Receptor (1)

Adenosine Receptor (1)

Antibiotic (3)

Apoptosis (3)

Aurora Kinase (1)

Bacterial (3)

Biochemical Assay Reagents (6)

Calcium Channel (5)

Carbonic Anhydrase (1)

Caspase (1)

COX (1)

Dopamine Receptor (2)

Drug Derivative (2)

Drug Metabolite (1)

Endogenous Metabolite (4)

Endothelin Receptor (1)

Environmental Pollutants (1)

Estrogen Receptor/ERR (1)

Ferroptosis (1)

Fluorescent Dye (1)

Fungal (2)

Isotope-Labeled Compounds (1)

Lipoxygenase (1)

mAChR (2)

mGluR (2)

Neurokinin Receptor (1)

NO Synthase (1)

P2Y Receptor (5)

PARP (1)

Phosphodiesterase (PDE) (2)

PKA (1)

PKC (3)

Prostaglandin Receptor (1)

Reference Standards (9)

Reverse Transcriptase (1)

TSH Receptor (1)

By Research Areas:

Cancer (18)

Cardiovascular Disease (4)

Endocrinology (3)

Infection (10)

Inflammation/Immunology (9)

Metabolic Disease (14)

Neurological Disease (14)

Inhibitors & Agonists

Fluorescent Dyes

Biochemical Assay Reagents

Peptides

Inhibitory Antibodies

Natural
Products

Recombinant Proteins

Isotope-Labeled Compounds

Antibodies

Targets Recommended: Phospholipase PNPLA3

Cat. No.	Nombre del producto	Target	Áreas de investigación	Chemical Structure

HY-B0470

Neomycin sulfate 65+ Cited Publications	Environmental Pollutants Antibiotic Phospholipase Bacterial	Infection Metabolic Disease Cancer
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 .

HY-13419

U-73122 Maximum Cited Publications 98 Publications Verification	Phospholipase Lipoxygenase Ferroptosis	Inflammation/Immunology
U-73122 is a phospholipase C (PLC) and 5-LO (5-lipoxygenase) inhibitor with an IC₅₀of 1-2.1 µM for PLC.

HY-100168

BAPTA 35+ Cited Publications	Phospholipase	Others
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 .

HY-115768

Compound 48/80 5 Publications Verification Poly-p-methoxyphenethylmethylamine	Phospholipase	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 .

HY-70072

D609 5+ Cited Publications	Phospholipase	Infection Inflammation/Immunology Cancer
D609, an antitumoural xanthate, is a specific and competitive *phosphatidyl choline-specific phospholipase* C (PC-PLC) inhibitor with a K_i** of 6.4 μM. D609 is an antioxidative protector and has antiviral and anti-inflammatory activity .

HY-19619

m-3M3FBS 5+ Cited Publications	Phospholipase Apoptosis	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 .

HY-12598A

DHPG 4 Publications Verification (RS)-3,5-DHPG	mGluR	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) .

HY-130592

Compound 48/80 trihydrochloride 5 Publications Verification C48/80 trihydrochloride	Phospholipase	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 .

HY-N9480

Vinaxanthone 3 Publications Verification SM-345431	Phospholipase Bacterial	Infection Cancer
Vinaxanthone (SM-345431) is a potent and selective semaphorin3A, phospholipase C (PLC) and FabI inhibitor, with IC₅₀s of 0.1-0.2 μM and 0.9 mM for semaphorin3A and FabI. Vinaxanthone inhibits the substrate (t-o-NAC thioester) and the cofactor (NADPH) with K_is of 3.1 μM and 1.0 μM, respectively. Vinaxanthone can be used to handle infections caused by multidrug-resistant pathogens .

HY-100168A

BAPTA tetrasodium 35+ Cited Publications	Phospholipase	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 .

HY-W039315

2,5-Anhydro-D-mannitol, 97%	Biochemical Assay Reagents	Metabolic Disease
2,5-Anhydro-D-mannitol, 97% is an antimetabolic fructose analogue. 2,5-Anhydro-D-mannitol, 97% depletes intracellular ATP, reduces oxygen consumption, regulates substrate oxidation, increases phosphomonoester levels, decreases inorganic phosphate levels, and promotes the release of intracellular calcium from intracellular calcium stores via phospholipase C-dependent activity in hepatocytes .

HY-150520

Neomycin	Antibiotic Phospholipase	Infection Cancer
Neomycin, an aminoglycoside antibiotic, exerts antibacterial activity through irreversible binding of the nuclear 30S ribosomal subunit, thereby blocking bacterial protein synthesis. Neomycin is a known phospholipase C (PLC) inhibitor. Neomycin potently inhibits both the nuclear translocation of angiogenin and angiogenin-induced cell proliferation and angiogenesis. Neomycin inhibits IP3-mediated Ca ²⁺ release, MgATP-dependent Ca ²⁺ uptake, and electrical excitation-evoked skeletal muscle Ca ²⁺ transients. Neomycin depletes gut microbiota in specific mouse models, causes hearing impairment, and kidney damage with prolonged exposure. Neomycin can be used for the research of cancer .

HY-108630

U-73343 5+ Cited Publications	Phospholipase	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 .

HY-111919

3-Nitrocoumarin 3 Publications Verification	Phospholipase Fungal	Infection
3-Nitrocoumarin is an inhibitor for phospholipase C that blocks the generation of inositol triphosphate (IP₃), thereby affecting the calcium signaling pathway .

HY-111208

CCT129957	Phospholipase	Cancer
CCT129957 is an indole derivative and a potent phospholipase C-γ (PLC-γ) inhibitor with an IC₅₀ of ~3 μM and a GC₅₀ of 15 μM. CCT129957 inhibits Ca ²⁺ release in squamous carcinoma cells at ~15 μM .

HY-100168B

BAPTA tetrapotassium 35+ Cited Publications	Phospholipase	Others
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 .

HY-100983

Protein kinase inhibitor H-7 dihydrochloride	PKC	Cancer
Protein kinase inhibitor H-7 dihydrochloride is a potent PKC (protein kinase C) inhibitor. At 100 μM, Protein kinase inhibitor H-7 dihydrochloride completely inhibits both TPA (skin tumour promoter, 12-O-tetradecanoylphorbol-13-acetate) and phospholipase C-induced ODC (ornithine decarboxylase) .

HY-116874

SKF 83822 1 Publications Verification	Dopamine Receptor	Neurological Disease
SKF 83822 is an atypical agonist of dopamine D1 receptor. SKF 83822 activates adenylyl cyclase (AC), but not phospholipase C (PLC). SKF 83822 is also proved to stimulate AC via cAMP production. SKF 83822 can be used for research of schizophrenia .

HY-14117

Enprofylline	Adenosine Receptor Phosphodiesterase (PDE)	Inflammation/Immunology
Enprofylline acts as a selective and competitive A2B receptor antagonist with the K_i of 7 μM. Enprofylline also acts as a phosphodiesterase inhibitor. Enprofylline can be used for the research of asthma, chronic obstructive pulmonary disease .

HY-150524

UDP-Galactose	Endogenous Metabolite P2Y Receptor	Metabolic Disease
UDP-Galactose is a monosaccharide and a key glycosyl donor molecule in cells that participates in nucleotide sugar metabolism. UDP-Galactose is the natural agonist of the P2Y₁₄ receptor coupled to G_i proteins in the immune system (IC₅₀= 0.67 μM, hP2Y₁₄). UDP-Galactose can be used to study cell signal transduction and substance metabolism .

HY-100045

p-Nitrophenyl phosphorylcholine 4-Nitrophenylphosphorylcholine; 4-Nitrophenylphosphorylcholine; O-(4-Nitrophenylphosphoryl)choline	Endogenous Metabolite	Metabolic Disease
p-Nitrophenyl phosphorylcholine (4-Nitrophenylphosphorylcholine) is a chromogenic substrate that is used to measure phospholipase C (PLC) activity. Hydrolysis of p-nitrophenylphosphorylcholine by PLC results in the liberation of p-nitrophenol, which can be measured at 405 nm at pH 7.2-7.5.

HY-N1773

5,7,3'-Tri-O-methyl (-)-epicatechin	Others	Cancer
5,7,3' -tri-O-Methyl (-)-epicatechin (Compound 13) is a phospholipase Cγ1 (PLCγ1) inhibitor. 5,7,3' -tri-o-methyl (-)-epicatechin has a methylene dioxy benzene ring and can express inhibitory activity against PLCγ1. 5,7,3' -tri-O-Methyl (-)-epicatechin can be used in the study of chemotherapy and chemopexic agents for cancer .

HY-W100403

Choline tosylate Choline p-toluenesulfonate	Phospholipase	Others
Choline tosylate (Choline p-toluenesulfonate) is an intermediate and also a substrate of choline acetyltransferase (CHAT). Choline tosylate inhibits phospholipase A2 and phospholipase C .

HY-114457

Phosphatidylinositol 4,5-bisphosphate L-alpha-Phosphatidylinositol-4,5-bisphosphate; (PtdIns)-(4,5)-P2	Phospholipase	Inflammation/Immunology
Phosphatidylinositol 4,5-bisphosphate (L-alpha-Phosphatidylinositol-4,5-bisphosphate) is a plasma membrane lipid that is enriched in the cytoplasmic leaflet of the plasma membrane. Phosphatidylinositol 4,5-bisphosphate serves as a substrate for phospholipase C and class I PI3K, generating diacylglycerol, inositol (1,4,5)-trisphosphate, and phosphatidylinositol (3,4,5)-trisphosphate. Phosphatidylinositol 4,5-bisphosphate contributes to lamellipodial protrusion, directional cell migration, focal adhesion lipid generation, and trafficking of the GABA_A receptor. Phosphatidylinositol 4,5-bisphosphate can be used in research related to acute lung injury and pulmonary edema .

HY-107544

8-pCPT-2'-O-Me-cAMP-AM	PKA	Metabolic Disease
8-pCPT-2'-O-Me-cAMP-AM is a cyclic AMP analogue, selectively activates Epac-Rap signaling pathway. 8-pCPT-2'-O-Me-cAMP-AM protects renal function by activating Epac from ischemia injury. 8-pCPT-2'-O-Me-cAMP-AM also stimulates insulin secretion by interaction with PKA pathway .

HY-P2705

Mastoparan X	Endogenous Metabolite	Others
Mastoparan X is a GTP-binding regulatory protein (G protein)-activating peptide, and a tetradecapeptide from wasp venom. Mastoparan X acts function by the direct activation of G protein that couple to phospholipase C to cause secretion from various kinds of cells .

HY-70083

SPK-601 LMV-601	Phospholipase Reverse Transcriptase	Infection
SPK-601 (LMV-601) is an inhibitor of the *phosphatidylcholine-specific phospholipase* C (PC-PLC)**. SPK-601 also can be used as an antimicrobial agent .

HY-153213A

Org 274178-0	TSH Receptor	Endocrinology
Org 274178-0 is a selective thyroid-stimulating hormone receptor (TSHR) antagonist with a pIC₅₀ value for TSHR is 5.03. Org 274178-0 inhibits the activation of cAMP signaling pathway and phospholipase C (PLC) signaling pathway mediated by thyroid-stimulating hormone (TSH) and TSH receptor-stimulating immunoglobulins (TSIs). Org 274178-0 is promising for research of Graves’ disease and Graves’ ophthalmopathy .

HY-B0470R

Neomycin sulfate (Standard)	Reference Standards Bacterial Antibiotic Phospholipase	Infection Cancer
Neomycin (sulfate) (Standard) is the analytical standard of Neomycin (sulfate). This product is intended for research and analytical applications. 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 nuclear translocation of angiogenin and angiogenin-induced cell proliferation and angiogenesis .

HY-P2817

Phospholipase C PLCs	Phospholipase	Infection Metabolic Disease
Phospholipase C (PLCs) is a class of phospholipases. Phospholipase C participates in cellular signaling and regulation by virtue of its ability to hydrolyze membrane phospholipids into di-acyl-glycerol (DAG) and inositol triphosphate (IP3), which further causes the activation of other signaling pathways involved in various processes, including immune response .

HY-P10053

sPLA2-IIA Inhibitor	Phospholipase	Metabolic Disease
sPLA2-IIA Inhibitor is a cyclic pentapeptide analog of FLSYK (cyclic 2-Nal-Leu-Ser-2-Nal-Arg (c2)), that binds to hGIIA (human IIA phospholipase A2) and inhibits its hydrolytic ability. sPLA2 is a member of the esterase superfamily that catalyzes the hydrolysis of the ester bond at the sn-2 position of glycerophospholipids, releasing free fatty acids such as arachidonic acid and lysophospholipids .

HY-117168

1,2-Dilinoleoyl-sn-glycerol	Endogenous Metabolite	Metabolic Disease
1,2-Dilinoleoyl-sn-glycerol is a diacylglycerol (DAG) with linoleic acid (HY-N0729) (18:2) side chains attached at both the sn-1 and sn-2 positions . 1,2-Dilinoleoyl-sn-glycerol can be prepared from L-dilinoleoylphosphatidylcholine via hydrolysis with phospholipase C .

HY-137311

(S)-Albuterol hydrochloride	Calcium Channel Phospholipase mAChR	Neurological Disease
(S)-Albuterol hydrochloride is a muscarinic receptor and phospholipase C activator. (S)-Albuterol hydrochloride increases intracellular free calcium in airway smooth muscle .

HY-148388

N-Stearoylsphingomyelin N-Stearoyl-D-sphingomyelin	Phospholipase	Cancer
N-Stearoylsphingomyelin (N-Stearoyl-D-sphingomyelin) is a sphingolipid, which can inhibit Phospholipase Cδ1 (PLCδ1) .

HY-N1450

Aristolochic acid C	Phospholipase	Cancer
Aristolochic acid C is a derivative of Aristolochic acid. Aristolochic acid is a phospholipase A₂ (PLA2) inhibitor, which disrupts cortical microtubule arrays and root growth in Arabidopsis .

HY-12598AR

DHPG (Standard) (RS)-3,5-DHPG (Standard)	mGluR Reference Standards	Neurological Disease
DHPG (Standard) is the analytical standard of DHPG. This product is intended for research and analytical applications. 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) .

HY-175982

AURKA-IN-3	Aurora Kinase	Cancer
AURKA-IN-3 (Compound AL8) is an irreversible covalent Aurora kinase A (AURKA) inhibitor with an IC₅₀ value of 23.0 nM. AURKA-IN-3 inhibits the activation of cAMP signaling pathway and phospholipase C (PLC) signaling pathway mediated by AURKA, and reduces the autophosphorylation level of AURKA. AURKA-IN-3 is promising for research of malignant tumors associated with high AURKA expression (e.g., leukemia, lymphoma) .

HY-127008

N-Butylfluorescein	Fluorescent Dye	Others
N-Butylfluorescein is an alkyl-substituted fluorescein, can be used for synthesis of fluorogenic substrates for assaying phosphatidylinositol-specific phospholipase C .

HY-108654

PSB 0474	P2Y Receptor Apoptosis Drug Derivative Phospholipase NO Synthase	Neurological Disease Inflammation/Immunology Endocrinology
PSB 0474 (3-phenacyl-UDP) is a UDP (HY-113359) analog and selective P2Y₆ receptor agonist, with an EC₅₀ value of 70 nM for the hP2Y₆ receptor. PSB 0474 activates Phospholipase C-coupled receptors to increase intracellular inositol phosphate levels. PSB 0474 enhances NO release by upregulating inducible iNOS and induces Apoptosis. PSB 0474 increases micturition frequency in urine of anesthetized rats, without altering bladder contraction amplitude/duration or causing urothelial damage. PSB 0474 can be used in studies related to chronic brain inflammation .

HY-123202

MRS2603	P2Y Receptor	Cancer
MRS2603 is a pyridoxal derivative. MRS2603 antagonized both P2Y1 and P2Y13 receptors .

HY-N14292

Hispidospermidin	Phospholipase	Infection
Hispidospermidin is a phospholipase C inhibitor found in Chaetosphaeronema hispidulum .

HY-137311A

(S)-Albuterol	Calcium Channel Phospholipase mAChR	Neurological Disease
(S)-Albuterol is a muscarinic receptor and phospholipase C activator. (S)-Albuterol increases intracellular free calcium in airway smooth muscle .

HY-N14103

Cinatrin C1	Phospholipase	Others
Cinatrin C1 is a phospholipase A2 (PLA2) inhibitor that can be extracted from Circinotrichum falcatisporum RF-641 .

HY-N1450R

Aristolochic acid C (Standard)	Reference Standards Phospholipase	Cancer
Aristolochic acid C (Standard) is the analytical standard of Aristolochic acid C. This product is intended for research and analytical applications. Aristolochic acid C is a derivative of Aristolochic acid. Aristolochic acid is a phospholipase A2 (PLA2) inhibitor, which disrupts cortical microtubule arrays and root growth in Arabidopsis .

HY-N14104

Cinatrin C2	Phospholipase	Others
Cinatrin C2 is a phospholipase A2 (PLA2) inhibitor with an IC₅₀ of 800 μM and can be extracted from Circinotrichum falcatisporum RF-641 .

HY-N14105

Cinatrin C3	Phospholipase	Others
Cinatrin C3 is a phospholipase A2 (PLA2) inhibitor with an IC₅₀ of 70 μM and can be extracted from Circinotrichum falcatisporum RF-641 .

HY-P10658

ARF1 (2-17)	Phospholipase	Others
ARF1 (2-17) inhibits both ARF-independent (PLC-β) and ARF-dependent (PLD) pathways. ARF1 (2-17) inhibits GTP-γ-S-stimulated PLD activity, phospholipase C-β (PLC-β), and exocytosis .

HY-103411

SKF83822 hydrobromide	Dopamine Receptor	Neurological Disease
SKF83822 hydrobromide is a potent dopamine D1 receptor agonist. SKF83822 hydrobromide activates G_s/_olf/adenylyl cyclase (AC)-coupled D1 receptors, but not phospholipase C (PLC)-coupled D1-like receptors .

HY-176008

Lauric acid leelamide	Drug Derivative	Inflammation/Immunology
Lauric acid leelamide is the lauric acid (C-12) amide analog of Leelamine (HY-W005629). Leelamine exhibits inhibitory activity against pyruvate dehydrogenase kinase (PDHK) with an IC₅₀ value of 9.5 µM. Leelamine derivatives possess anti-inflammatory effects and can inhibit phospholipase A2 activity from various sources .

HY-100983R

Protein kinase inhibitor H-7 dihydrochloride (Standard)	Reference Standards PKC	Cancer
Protein kinase inhibitor H-7 (dihydrochloride) (Standard) is the analytical standard of Protein kinase inhibitor H-7 (dihydrochloride). This product is intended for research and analytical applications. Protein kinase inhibitor H-7 dihydrochloride is a potent PKC (protein kinase C) inhibitor. At 100 μM, Protein kinase inhibitor H-7 dihydrochloride completely inhibits both TPA (skin tumour promoter, 12-O-tetradecanoylphorbol-13-acetate) and phospholipase C-induced ODC (ornithine decarboxylase) .

Cat. No.	Nombre del producto	Type

HY-100168

BAPTA 35+ Cited Publications	Biochemical Assay Reagents
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 .

HY-W039315

2,5-Anhydro-D-mannitol, 97%	Biochemical Assay Reagents
2,5-Anhydro-D-mannitol, 97% is an antimetabolic fructose analogue. 2,5-Anhydro-D-mannitol, 97% depletes intracellular ATP, reduces oxygen consumption, regulates substrate oxidation, increases phosphomonoester levels, decreases inorganic phosphate levels, and promotes the release of intracellular calcium from intracellular calcium stores via phospholipase C-dependent activity in hepatocytes .

HY-100168B

BAPTA tetrapotassium 35+ Cited Publications	Biochemical Assay Reagents
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 .

HY-W100403

Choline tosylate Choline p-toluenesulfonate	Biochemical Assay Reagents
Choline tosylate (Choline p-toluenesulfonate) is an intermediate and also a substrate of choline acetyltransferase (CHAT). Choline tosylate inhibits phospholipase A2 and phospholipase C .

HY-100168R

BAPTA (Standard)

Biochemical Assay Reagents

BAPTA (Standard) is the analytical standard of BAPTA. This product is intended for research and analytical applications. BBAPTA is a selective and cell-impermeant chelator for calcium. BAPTA, as calcium indicator, has high selectivity against magnesium and calcium. BAPTA is widely used as an intracellular buffer for investigating the effects of Ca ²⁺ release from intracellular stores or influx via Ca ²⁺-permeable channels in the plasma membrane. BAPTA can also inhibit phospholipase C activity independently of their role as Ca ²⁺ chelators .

HY-100168BR

BAPTA tetrapotassium (Standard)

Biochemical Assay Reagents

BAPTA tetrapotassium (Standard) is the analytical standard of BAPTA tetrapotassium (HY-100168B). This product is intended for research and analytical applications. BAPTA tetrapotassium is a selective and cell-impermeant chelator for calcium. BAPTA tetrapotassium, as calcium indicator, has high selectivity against magnesium and calcium. BAPTA tetrapotassium is widely used as an intracellular buffer for investigating the effects of Ca ²⁺ release from intracellular stores or influx via Ca ²⁺-permeable channels in the plasma membrane. BAPTA tetrapotassium can also inhibit phospholipase C activity independently of their role as Ca ²⁺ chelators .

Cat. No.	Nombre del producto	Target	Research Area

HY-P2705

Mastoparan X	Endogenous Metabolite	Others
Mastoparan X is a GTP-binding regulatory protein (G protein)-activating peptide, and a tetradecapeptide from wasp venom. Mastoparan X acts function by the direct activation of G protein that couple to phospholipase C to cause secretion from various kinds of cells .

HY-P10053

sPLA2-IIA Inhibitor	Phospholipase	Metabolic Disease
sPLA2-IIA Inhibitor is a cyclic pentapeptide analog of FLSYK (cyclic 2-Nal-Leu-Ser-2-Nal-Arg (c2)), that binds to hGIIA (human IIA phospholipase A2) and inhibits its hydrolytic ability. sPLA2 is a member of the esterase superfamily that catalyzes the hydrolysis of the ester bond at the sn-2 position of glycerophospholipids, releasing free fatty acids such as arachidonic acid and lysophospholipids .

HY-P1834

MARCKS Peptide(151-175), Phosphorylated	Peptides	Inflammation/Immunology
MARCKS Peptide(151-175), Phosphorylated is a phosphorylated peptide corresponding to the basic effector domain of myristoylated alanine-rich protein kinase C substrate protein (MARCKS). Phosphorylation of MARCKS Peptide (151-175) reverses its inhibition of phospholipase C (PLC)-catalyzed hydrolysis of phosphatidylinositol 4,5-bisphosphate (PIP2) .

HY-P10658

ARF1 (2-17)	Phospholipase	Others
ARF1 (2-17) inhibits both ARF-independent (PLC-β) and ARF-dependent (PLD) pathways. ARF1 (2-17) inhibits GTP-γ-S-stimulated PLD activity, phospholipase C-β (PLC-β), and exocytosis .

HY-P2139

Ranakinin	Neurokinin Receptor Phospholipase	Others
Ranakinin is a NK1R agonist. Ranakinin inhibits the binding of selective NK1 radioligands to NK1 receptors. Ranakinin activates phospholipase C (Phospholipase C), thereby enhancing polyphosphoinositide hydrolysis. Ranakinin stimulates inositol phosphate production and reduces membrane polyphosphoinositide levels. Ranakinin stimulates corticosterone and aldosterone secretion .

Cat. No.	Nombre del producto	Target	Research Area	Image

HY-P991964

Rendomab B4 Rendomab-B49	Endothelin Receptor	Cancer
Rendomab B4 (Rendomab-B49) is a monoclonal antibody targeting ETB. Rendomab B4 preferentially binds to ETB in the active conformational state and exhibits selectivity for ETB on melanoma cells. Rendomab B4 inhibits the G protein-dependent phospholipase C (PLC) pathway, blocks ET-3-induced Gαi/o-mediated inhibition of adenylate cyclase, and does not affect the activation of the ERK1/2 pathway. Rendomab B4 is applicable to melanoma-related research .

Cat. No.	Nombre del producto	Category	Target	Chemical Structure

HY-B0470

Neomycin sulfate 65+ Cited Publications	Structural Classification Classification of Application Fields Antibacterial Disease Research Other Antibiotics Infection Microorganisms Antibiotics Animal Husbandry Mammalian Cell Culture Anticancer Disease Research Fields Source Classification	Environmental Pollutants Antibiotic Phospholipase Bacterial
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 .

HY-N9480

Vinaxanthone 3 Publications Verification SM-345431	Microorganisms Xanthones Classification of Application Fields Phenols Disease Research Fields Cancer Source Classification	Phospholipase Bacterial
Vinaxanthone (SM-345431) is a potent and selective semaphorin3A, phospholipase C (PLC) and FabI inhibitor, with IC₅₀s of 0.1-0.2 μM and 0.9 mM for semaphorin3A and FabI. Vinaxanthone inhibits the substrate (t-o-NAC thioester) and the cofactor (NADPH) with K_is of 3.1 μM and 1.0 μM, respectively. Vinaxanthone can be used to handle infections caused by multidrug-resistant pathogens .

HY-150524

UDP-Galactose	Structural Classification Productos naturales Human Gut Microbiota Metabolites Classification of Application Fields Metabolic Disease Endogenous metabolite Disease Research Fields Source Classification	Endogenous Metabolite P2Y Receptor
UDP-Galactose is a monosaccharide and a key glycosyl donor molecule in cells that participates in nucleotide sugar metabolism. UDP-Galactose is the natural agonist of the P2Y₁₄ receptor coupled to G_i proteins in the immune system (IC₅₀= 0.67 μM, hP2Y₁₄). UDP-Galactose can be used to study cell signal transduction and substance metabolism .

HY-N1773

5,7,3'-Tri-O-methyl (-)-epicatechin	Machilus thunbergii Sieb. et Zucc. Flavonoids Flavanols Plants Lauraceae Source Classification	Others
5,7,3' -tri-O-Methyl (-)-epicatechin (Compound 13) is a phospholipase Cγ1 (PLCγ1) inhibitor. 5,7,3' -tri-o-methyl (-)-epicatechin has a methylene dioxy benzene ring and can express inhibitory activity against PLCγ1. 5,7,3' -tri-O-Methyl (-)-epicatechin can be used in the study of chemotherapy and chemopexic agents for cancer .

HY-114457

Phosphatidylinositol 4,5-bisphosphate L-alpha-Phosphatidylinositol-4,5-bisphosphate; (PtdIns)-(4,5)-P2	Structural Classification Human Gut Microbiota Metabolites Classification of Application Fields Other Diseases Endogenous metabolite Disease Research Fields Lipid Source Classification	Phospholipase
Phosphatidylinositol 4,5-bisphosphate (L-alpha-Phosphatidylinositol-4,5-bisphosphate) is a plasma membrane lipid that is enriched in the cytoplasmic leaflet of the plasma membrane. Phosphatidylinositol 4,5-bisphosphate serves as a substrate for phospholipase C and class I PI3K, generating diacylglycerol, inositol (1,4,5)-trisphosphate, and phosphatidylinositol (3,4,5)-trisphosphate. Phosphatidylinositol 4,5-bisphosphate contributes to lamellipodial protrusion, directional cell migration, focal adhesion lipid generation, and trafficking of the GABA_A receptor. Phosphatidylinositol 4,5-bisphosphate can be used in research related to acute lung injury and pulmonary edema .

HY-B0470R

Neomycin sulfate (Standard)	Structural Classification Microorganisms Antibiotics Animal Husbandry Mammalian Cell Culture Antibacterial Disease Research Anticancer Other Antibiotics Source Classification	Reference Standards Bacterial Antibiotic Phospholipase
Neomycin (sulfate) (Standard) is the analytical standard of Neomycin (sulfate). This product is intended for research and analytical applications. 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 nuclear translocation of angiogenin and angiogenin-induced cell proliferation and angiogenesis .

HY-N1450

Aristolochic acid C	Monophenols other families Classification of Application Fields Phenols Plants Disease Research Fields Source Classification Cancer	Phospholipase
Aristolochic acid C is a derivative of Aristolochic acid. Aristolochic acid is a phospholipase A₂ (PLA2) inhibitor, which disrupts cortical microtubule arrays and root growth in Arabidopsis .

HY-N14292

Hispidospermidin	Productos naturales Microorganisms Source Classification	Phospholipase
Hispidospermidin is a phospholipase C inhibitor found in Chaetosphaeronema hispidulum .

HY-N14103

Cinatrin C1	Productos naturales Microorganisms Source Classification	Phospholipase
Cinatrin C1 is a phospholipase A2 (PLA2) inhibitor that can be extracted from Circinotrichum falcatisporum RF-641 .

HY-N1450R

Aristolochic acid C (Standard)	Structural Classification Monophenols other families Phenols Plants Source Classification	Reference Standards Phospholipase
Aristolochic acid C (Standard) is the analytical standard of Aristolochic acid C. This product is intended for research and analytical applications. Aristolochic acid C is a derivative of Aristolochic acid. Aristolochic acid is a phospholipase A2 (PLA2) inhibitor, which disrupts cortical microtubule arrays and root growth in Arabidopsis .

HY-N14104

Cinatrin C2	Microorganisms Antibiotics Other Antibiotics Source Classification	Phospholipase
Cinatrin C2 is a phospholipase A2 (PLA2) inhibitor with an IC₅₀ of 800 μM and can be extracted from Circinotrichum falcatisporum RF-641 .

HY-N14105

Cinatrin C3	Productos naturales Microorganisms Source Classification	Phospholipase
Cinatrin C3 is a phospholipase A2 (PLA2) inhibitor with an IC₅₀ of 70 μM and can be extracted from Circinotrichum falcatisporum RF-641 .

HY-N16865

Myristinin B/C	Structural Classification Horsfieldia amygdalina (Wall. ex Hook. f. & Thomson) Warb. Coumarins Myristicaceae Phenylpropanoids Plants Source Classification	COX Prostaglandin Receptor Fungal
Myristinin B/C is a mixture of Myristinin B and Myristinin C. Myristinin B/C is a flavan compound found in Horsfieldia amygdaline and Myristica cinnamomea. Myristinin B/C can selectively inhibit COX-2 activity with an IC₅₀ of 2.1 μg/mL. Myristinin B/C can reduce the production of prostaglandin E2 (PGE2) and inhibit phospholipase A2 (PLA2), thereby blocking the release of inflammatory mediators. Myristinin B/C can inhibit Candida albicans with an IC₅₀ of 6 μg/mL. Myristinin B/C can be used for the research of inflammation and infection, such as rheumatoid arthritis .

Species:	Human (2)
Tag:	His (2) Tag Free (1) GST (1)
Source:	E. coli Cell-free (1) Sf9 insect cells (1) E. coli (2)

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HY-P701964

	Phospholipase C Protein, Bacillus cereus BC_0670; Phosphatidylcholine cholinephosphohydrolase; phospholipase C	Others	E. coli
	Phospholipase C Protein, Bacillus cereus is the recombinant Phospholipase C protein, expressed by E. coli, with tag free.

HY-P701965

	Phospholipase C Protein, Bacillus cereus (His) BC_0670; Phosphatidylcholine cholinephosphohydrolase; phospholipase C	Others	E. coli
	Phospholipase C Protein, Bacillus cereus (His) is the recombinant Phospholipase C protein, expressed by E. coli, with N-6*His labeled tag.

HY-P703036

	PLCD4 Protein, Human (sf9, GST) 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-4; hPLCD4; Phosphoinositide phospholipase C-delta-4; phospholipase C-delta-4 (PLC-delta-4)	Human	Sf9 insect cells
	PLCD4 Protein, Human (sf9, GST) is the recombinant human-derived PLCD4, expressed by Sf9 insect cells , with GST labeled tag. ,

HY-P702447

	SMPD2 Protein, Human (Cell-Free, His) Sphingomyelin phosphodiesterase 2; Lyso-platelet-activating factor-phospholipase C; Lyso-PAF-PLC; Neutral sphingomyelinase; N-SMase; nSMase; nSMase1	Human	E. coli Cell-free
	In vitro experiments have demonstrated that the sphingomyelin phosphodiesterase 2 (SMPD2) protein plays a key role in catalyzing the hydrolysis of sphingomyelin, leading to the formation of ceramide and phosphocholine. Furthermore, SMPD2 exhibits its enzymatic activity by hydrolyzing 1-O-alkyl-2-lyso-sn-glycero-3-phosphocholine (hemolytic platelet-activating factor) in vivo. SMPD2 Protein, Human (Cell-Free, His) is the recombinant human-derived SMPD2 protein, expressed by E. coli Cell-free , with N-10*His labeled tag.

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HY-N1393S

2-Methoxybenzoic acid-13C6

2-Methoxybenzoic acid (NSC 3778; O-Methylsalicylic acid; Salicylic acid methyl ether)- ¹³C₆ is the ¹³C-labeled 2-Methoxybenzoic acid (HY-N1393). 2-Methoxybenzoic acid is a natural compound with potential salicylate-like effect. 2-Methoxybenzoic acid inhibits carbonic anhydrase activity, elevates intraplatelet cyclic guanosine monophosphate level, and suppresses cytosolic phospholipase A₂ phosphorylation. 2-Methoxybenzoic acid suppresses platelet reactivity, including decreased spreading, retraction, and aggregation in platelets. 2-Methoxybenzoic acid ameliorates arterial thrombosis in a dose-dependent manner without affecting normal hemostasis in mice. 2-Methoxybenzoic acid can be used for the research of arterial thrombosis .

Host:	Mouse (4) Rabbit (8)
Reactivity:	Human (10) Rat (6) Mouse (4) Monkey (2)
Application:	IHC-P (9) ICC/IF (7) IP (3) WB (12) FC (5) ELISA (5)
Isotype:	IgG (8) IgG1 (4)
Conjugation:	Non-conjugated (12)
Clonality:	Monoclonal (5) Monoclonal Antibody (2) Recombinant (4)
Modification:	Unmodified (7)

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HY-P86178

	Phospholipase C gamma 1 Antibody (YA5870) PLCG1; PLC1; 1-phosphatidylinositol 4; 5-bisphosphate phosphodiesterase gamma-1; PLC-148; Phosphoinositide phospholipase C-gamma-1; phospholipase C-II; PLC-II; phospholipase C-gamma-1; PLC-gamma-1	WB, IHC-P, ICC/IF, IP, ELISA	Human, Mouse, Rat
	Phospholipase C gamma 1 Antibody (YA5870) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Phospholipase C gamma 1.

HY-P810555

	Phospholipase C beta 3/PLCB3 Antibody (YA9824) PLCB3; 1-phosphatidylinositol 4; 5-bisphosphate phosphodiesterase beta-3; Phosphoinositide phospholipase C-beta-3; phospholipase C-beta-3; PLC-beta-3	WB, IHC-P	Human
	Phospholipase C beta 3/PLCB3 Antibody (YA9824) is a Rabbit-derived and non-conjugated IgG Recombinant, Monoclonal antibody, targeting to Phospholipase C beta 3/PLCB3.

HY-P82949

	Phospholipase C beta 3 Antibody (YA2694) PLCB3; 1-phosphatidylinositol 4; 5-bisphosphate phosphodiesterase beta-3; Phosphoinositide phospholipase C-beta-3; phospholipase C-beta-3; PLC-beta-3	WB, IHC-P	Human
	Phospholipase C beta 3 Antibody (YA2694) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Phospholipase C beta 3.

HY-P81881

	Phospholipase C beta 1 Antibody (YA1626) Plcb; AI132408; mKIAA0581; 3110043I21Rik	WB	Rat
	Phospholipase C beta 1 Antibody (YA1626) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Phospholipase C beta 1.

HY-P84153

	Phospholipase C gamma 1 Antibody (YA3850) PLC1; NCKAP3; PLC-II; PLC148; PLCgamma1	WB, IHC-P, ICC/IF, FC, ELISA	Human, Rat, Monkey
	Phospholipase C gamma 1 Antibody (YA3850) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to Phospholipase C gamma 1.

HY-P84154

	Phospholipase C gamma 1 Antibody (YA3851) PLC1; NCKAP3; PLC-II; PLC148; PLCgamma1	WB, IHC-P, ICC/IF, FC, ELISA	Human, Mouse
	Phospholipase C gamma 1 Antibody (YA3851) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to Phospholipase C gamma 1.

HY-P81881A

	Phospholipase C beta 1 Antibody (YA1626)(PBS only) Plcb; AI132408; mKIAA0581; 3110043I21Rik	WB	Rat
	Phospholipase C beta 1 Antibody (YA1626) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Phospholipase C beta 1.

HY-P84153A

	Phospholipase C gamma 1 Antibody (YA3850)(PBS only) PLC1; NCKAP3; PLC-II; PLC148; PLCgamma1	WB, IHC-P, ICC/IF, FC, ELISA	Human, Rat, Monkey
	Phospholipase C gamma 1 Antibody (YA3850) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to Phospholipase C gamma 1.

HY-P84154A

	Phospholipase C gamma 1 Antibody (YA3851)(PBS only) PLC1; NCKAP3; PLC-II; PLC148; PLCgamma1	WB, IHC-P, ICC/IF, FC, ELISA	Human, Mouse
	Phospholipase C gamma 1 Antibody (YA3851) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to Phospholipase C gamma 1.

HY-P83555

	ERp57 Antibody (YA3300) ERp57; ERp60; ERp61; Glucose Regulated Protein 58 Kd; HsT17083; p58; PDIA3; phospholipase C alpha; PI PLC	WB, IHC-P, IP	Human
	ERp57 Antibody (YA3300) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to ERp57.

HY-P80427

	Phospholipase C gamma 1 Antibody (YA179) PLC gamma 1 antibody; PLC II antibody; PLC-148 antibody; PLCgamma1 antibody; PLCG1; NCKAP3	WB, ICC/IF, IP	Human
	Phospholipase C gamma 1 Antibody (YA179) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Phospholipase C gamma 1.

HY-P810538

	Phospholipase C beta 1 Antibody 1 phosphatidylinositol 4,5 bisphosphate phosphodiesterase beta 1; 1-phosphatidyl-D-myo-inositol-4,5-bisphosphate; 1-phosphatidylinositol 4; 1-phosphatidylinositol-4; 5-bisphosphate phosphodiesterase beta-1; EIEE12; Inositoltrisphosphohydrolase; Monophosphatidylinositol phosphodiesterase; Phosphb; Phosphoinositidase C	WB, IHC-P, ICC/IF, FC	Human, Mouse, Rat
	Phospholipase C beta 1 Antibody is a Rabbit-derived and non-conjugated IgG Polyclonal antibody, targeting to Phospholipase C beta 1.

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phospholipase C

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