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Results for "

Erythrocytes

" in MedChemExpress (MCE) Product Catalog:

82

Inhibitors & Agonists

2

Biochemical Assay Reagents

15

Peptides

1

Inhibitory Antibodies

7

Natural
Products

6

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-129064
    Superoxide dismutase, Porcine erythrocytes

    SOD

    		 SOD Inflammation/Immunology Cancer
    Superoxide dismutase, Porcine erythrocytes (SOD) is the only antioxidant enzyme that scavenges the superoxide anion by converting this free radical to oxygen and hydrogen peroxide, thus preventing peroxynitrite production and further damage. Superoxide dismutase, Porcine erythrocytes is extensively researched and used in anti-inflammatory, antitumor, radiation protection, and antisenility applications .
    Superoxide dismutase, Porcine erythrocytes
  • HY-P1775
    Carbonic anhydrase, Bovine erythrocytes

    EC 4.2.1.1

    		 Carbonic Anhydrase Neurological Disease Metabolic Disease Cancer
    Carbonic anhydrase, Bovine erythrocytes (EC 4.2.1.1) is ubiquitous zinc-containing metalloenzyme present in prokaryotes and eukaryotes. Carbonic anhydrase can catalyze reversible conversion of carbon dioxide to bicarbonate and protons. Carbonic anhydrase can be used for the research of cancer, glaucoma, obesity and epilepsy .
    Carbonic anhydrase, Bovine erythrocytes
  • HY-Y0525
    AAPH

    2,2'-Azodiisobutyramidine dihydrochloride

    		 Others Inflammation/Immunology
    AAPH (2,2'-Azodiisobutyramidine dihydrochloride) has an effect of radical generation. AAPH induces oxidative stress and erythrocyte hemolysis .
    AAPH
  • HY-139573
    Etavopivat

    FT-4202

    		 Pyruvate Kinase Cardiovascular Disease
    Etavopivat is a potent, selective, and orally active erythrocyte pyruvate kinase (PKR) activator. Etavopivat has potent antisickling effects that can be used in studies of sickle cell disease and other haemoglobinopathies .
    Etavopivat
  • HY-111355B
    Cholesteryl sulfate sodium

    		Endogenous Metabolite Metabolic Disease
    Cholesteryl sulfate sodium is an important regulatory molecule. Cholesterol sulfate sodium is a component of cell membranes where it has a stabilizing role and protects erythrocytes from osmotic lysis and regulating sperm capacitation .
    Cholesteryl sulfate sodium
  • HY-D0844
    Glutathione oxidized
    4 Publications Verification

    L-Glutathione oxidized; GSSG; Oxiglutatione

    		 Endogenous Metabolite Reactive Oxygen Species Metabolic Disease
    Glutathione oxidized (L-Glutathione oxidized) is produced by the oxidation of glutathione. Detoxification of reactive oxygen species is accompanied by production of glutathione oxidized. Glutathione oxidized can be used for the research of sickle cells and erythrocytes .
    Glutathione oxidized
  • HY-B1829
    Dexamethasone phosphate

    Dexamethasone 21-phosphate

    		 Glucocorticoid Receptor Others
    Dexamethasone phosphate (Dexamethasone 21-phosphate) disodium is a biologically inactive compound which undergoes dephosphorylation by intra-erythrocyte enzymes. The active metabolite, Dexamethasone, is then released into the circulation by simple passive diffusion through cell membranes. Dexamethasone phosphate disodium-encapsulated erythrocyte has the potential for steroid-dependent ulcerative colitis research .
    Dexamethasone phosphate
  • HY-P2807C
    Lactate Dehydrogenase 2 (LDH-2), Human Erythrocytes

    LDH-2 (3H1M), LD2

    		 Others Others
    Lactate Dehydrogenase 2 (LDH-2), Human Erythrocytes (LDH-2 (3H1M), LD2) is a biological material or organic compound that can be used in life science research .
    Lactate Dehydrogenase 2 (LDH-2), Human Erythrocytes
  • HY-N3087
    Phaseollin

    		Others Others
    Phaseollin is an isoflavonoid phytoalexin that can be isolated from Phaseolus vulgaris . Phaseollin is toxic to bean hypocotyl and endocarp cells, and causes a complete lysis of sheep erythrocytes .
    Phaseollin
  • HY-P2807B
    Lactate Dehydrogenase 1 (LDH-1), Human Erythrocytes

    LDH-1, LD1 isoenzyme, 4H isoenzyme, Lactic Dehydrogenase

    		 Others Others
    Lactate Dehydrogenase 1 (LDH-1), Human Erythrocytes (LDH-1, LD1 isoenzyme, 4H isoenzyme, Lactic Dehydrogenase) is a biological material or organic compound that can be used in life science research .
    Lactate Dehydrogenase 1 (LDH-1), Human Erythrocytes
  • HY-P2807D
    Lactate Dehydrogenase 3 (LDH-3), Human Erythrocytes

    LDH-3, LD3, LD-3, 2H2M

    		 Others Others
    Lactate Dehydrogenase 3 (LDH-3), Human Erythrocytes (LDH-3, LD3, LD-3, 2H2M) is a biological material or organic compound that can be used in life science research .
    Lactate Dehydrogenase 3 (LDH-3), Human Erythrocytes
  • HY-P1629
    Temporin A

    		Bacterial Fungal Antibiotic Infection
    Temporin A is a short alpha-helical antimicrobial peptide isolated from the skin of the frog Rana temporaria. Temporin A is effective against a broad spectrum of Gram-positive bacteria. Temporin A interacts directly with the cell membrane of the microorganism and it is non-toxic to erythrocytes at concentrations that are antimicrobial. Temporin A also has antifungal activities (against yeast-like Candida albicans) .
    Temporin A
  • HY-123962
    G6PD activator AG1
    3 Publications Verification

    		 Others Metabolic Disease
    G6PD activator AG1 is a potent and selective glucose-6-phosphate dehydrogenase (G6PD) activator with an EC50 of 3 µΜ . G6PD activator AG1 reduces hemolysis of human erythrocytes .
    G6PD activator AG1
  • HY-147327
    N-Formylsarcolysine

    		Others Cancer
    N-Formylsarcolysine has antitumor activity, and inhibits leukemia by increasing the Hb and erythrocyte levels and decreasing the number of leukocytes. N-Formylsarcolysine also involves in glioblastoma and other diseases research .
    N-Formylsarcolysine
  • HY-117569
    KF24345 free base

    		TNF Receptor Inflammation/Immunology
    KF24345 free base is an orally active adenosine uptake inhibitor. KF24345 free base inhibits adenosine uptake by human, mouse, rabbit and hamster erythrocytes with IC50 values ??of 59.5, 130.1, 104.2 and 30.9 nM, respectively. KF24345 free base has anti-inflammatory activity and can inhibit LPS-induced TNF-α production and leukopenia in mice .
    KF24345 free base
  • HY-P99720
    Luspatercept

    ACE-536; luspatercept–aamt

    		 TGF-beta/Smad Metabolic Disease Cancer
    Luspatercept (ACE-536) is a recombinant modified ActRIIB fusion protein that binds with transforming growth factor β superfamily ligands. Luspatercept increases the erythrocyte numbers and promotes maturation of erythroid precursors. Luspatercept binds with GDF11 and inhibits Smad2/3 signaling. Luspatercept can be used for the research of anemia .
    Luspatercept
  • HY-135849B
    Catalase, Human Erythrocyte

    		Reactive Oxygen Species Cancer
    Catalase, Human Erythrocyte is an important antioxidant enzyme. Catalase, Human Erythrocyte plays an important role in removing ROS and maintaining the balance of redox state. Catalase, Human Erythrocyte is closely related to the occurrence and development of tumors. Catalase, Human Erythrocyte has the potential to be used in tumor prevention research .
    Catalase, Human Erythrocyte
  • HY-W008344
    2-Chloroadenosine

    		Nucleoside Antimetabolite/Analog Others
    2-Chloroadenosine, a stable adenosine analogue, protects against long term development of ischaemic cell loss in the rat hippocampus. 2-Chloroadenosine is an apparent competitive inhibitor of uridine influx (apparent Ki=33 μM) and high-affinity nitrobenzylthioinosine binding (apparent Ki=0.18 mM). 2-Chloroadenosine is a transported permeant for the nucleoside transporter in human erythrocytes .
    2-Chloroadenosine
  • HY-E70197A
    Calpain-1, Human Erythrocyte

    		Calcium Channel Neurological Disease
    Calpain-1, Human Erythrocyte is an intracellular Ca 2+-regulated cysteine protease. Calpain-1, Human Erythrocyte exhibits neuroprotective effect .
    Calpain-1, Human Erythrocyte
  • HY-129560
    DNDS disodium

    		Others Metabolic Disease
    DNDS disodium is a potent erythrocyte sedimentation inhibitor .
    DNDS disodium
  • HY-123294
    Fentrazamide

    YRC 2388; BAY-YRC 2388; NBA 061

    		 Others Neurological Disease Metabolic Disease
    Fentrazamide (YRC 2388) is a herbicide. Fentrazamide has specific toxic effects on the nervous system and erythrocytes in rats, affecting the energy supply of cells mainly by interfering with the glycolysis process. Fentrazamide can be used as a useful tool to study the mechanisms of neurodegenerative diseases and erythrocyte dysfunction .
    Fentrazamide
  • HY-12784
    Cycloguanil

    		Parasite Drug Metabolite Infection
    Cycloguanil, the active metabolite of Proguanil, acts on malaria schizonts in erythrocytes and hepatocytes .
    Cycloguanil
  • HY-12784A
    Cycloguanil hydrochloride

    		Parasite Drug Metabolite Infection
    Cycloguanil hydrochloride, the active metabolite of Proguanil, acts on malaria schizonts in erythrocytes and hepatocytes .
    Cycloguanil hydrochloride
  • HY-163753
    Carbonic anhydrase inhibitor 25

    		Carbonic Anhydrase Others
    Carbonic anhydrase inhibitor 25 (compound 6a) is a potent carbonic anhydrase inhibitor. Carbonic anhydrase inhibitor 25 shows inhibition for hCA I and hCA II receptor .
    Carbonic anhydrase inhibitor 25
  • HY-14830
    SAR 97276

    Albitiazolium bromide

    		 Parasite Infection
    SAR 97276 (Albitiazolium bromide) is an antimalarial agent. SAR 97276 interfers with the phospholipid metabolism of malarial parasites, especially the biosynthesis of phosphatidylcholine (PC). SAR 97276 enters erythrocytes through the new permeability pathways (NPP) of infected erythrocytes, and is transported into the malarial parasite by a poly-specific cation carrier .
    SAR 97276
  • HY-B0204B
    (-)-Pimobendan

    (-)-UD-CG115

    		 Others Cardiovascular Disease
    (-)-Pimobedan is an isomer of pimobedan. It has the property of stereoselective partitioning or distribution into erythrocytes. The clearance of (-)-pimobedan from erythrocytes is significantly lower than that of (+)-pimobedan, which is entirely due to its stereoselective distribution into erythrocytes. This stereoselective property of (-)-pimobedan may explain the phenomenon previously reported that it produces a 1.5-fold greater contractile force than the (+)-isomer in detergent-treated myocardial specimens of guinea pigs and dogs. These properties suggest that (-)-pimobedan may have unique advantages in terms of in vivo distribution and pharmacological action, which may have important implications for its clinical use.
    (-)-Pimobendan
  • HY-P5652
    Bombolitin II

    		Bacterial Infection
    Bombolitin II is an antimicrobial peptide derived from bumblebee venom. Bombolitin II can lysate erythrocyte and liposome .
    Bombolitin II
  • HY-P5653
    Bombolitin III

    		Bacterial Infection
    Bombolitin III is an antimicrobial peptide derived from bumblebee venom. Bombolitin III can lysate erythrocyte and liposome .
    Bombolitin III
  • HY-P5654
    Bombolitin IV

    		Bacterial Infection
    Bombolitin IV is an antimicrobial peptide derived from bumblebee venom. Bombolitin IV can lysate erythrocyte and liposome .
    Bombolitin IV
  • HY-12784AS1
    Cycloguanil-d6 hydrochloride

    		Isotope-Labeled Compounds Parasite Drug Metabolite Infection
    Cycloguanil-d6 hydrochloride is the deuterium labeled Cycloguanil hydrochloride. Cycloguanil hydrochloride, the active metabolite of Proguanil, acts on malaria schizonts in erythrocytes and hepatocytes .
    Cycloguanil-d6 hydrochloride
  • HY-110389
    Pitofenone hydrochloride

    		Cholinesterase (ChE) Neurological Disease
    Pitofenone hydrochloride, a spasmolytic compound, inhibits the acetylcholinesterase (AChE) activity from bovine erythrocytes and from electric eel with Kis of 36 and 45 μM, respectively.
    Pitofenone hydrochloride
  • HY-12784AS
    Cycloguanil-d4 hydrochloride

    		Parasite Drug Metabolite Infection
    Cycloguanil-d4 (hydrochloride) is the deuterium labeled Cycloguanil hydrochloride. Cycloguanil hydrochloride, the active metabolite of Proguanil, acts on malaria schizonts in erythrocytes and hepatocytes[1].
    Cycloguanil-d4 hydrochloride
  • HY-B0312S1
    Dipyridamole-d16

    		Phosphodiesterase (PDE) Cardiovascular Disease
    Dipyridamole-d16 is the deuterium labeled Dipyridamole. Dipyridamole (Persantine) is a phosphodiesterase inhibitor that blocks uptake and metabolism of adenosine by erythrocytes and vascular endothelial cells.
    Dipyridamole-d16
  • HY-W011293
    DTA

    2,4-Disulfamyl-5-trifluoromethylaniline

    		 Phosphodiesterase (PDE) Others
    DTA (2,4-Disulfamyl-5-trifluoromethylaniline) is a cyclic AMP phosphodiesterase inhibitor that binds to erythrocyte carbonic anhydrase .
    DTA
  • HY-126021
    Mobam

    		Cholinesterase (ChE) Neurological Disease
    Mobam is a insecticide against Anoplura Pediculidae. Mobam inhibits cholinesterase (ChE) levels in rats plasma, erythrocytes, and brain, suppresses the avoidance behavior in rats .
    Mobam
  • HY-B0312S
    Dipyridamole-d20

    		Phosphodiesterase (PDE) Cardiovascular Disease
    Dipyridamole-d20 is the deuterium labeled Dipyridamole. Dipyridamole is a phosphodiesterase inhibitor that blocks uptake and metabolism of adenosine by erythrocytes and vascular endothelial cells[1][2][3].
    Dipyridamole-d20
  • HY-W016188
    1-Naphthyl acetate

    		Cholinesterase (ChE) Others
    1-Naphthyl acetate is an attractive chromogenic substrate for the detection of erythrocyte acetylcholinesterase (AChE) activity. 1-Naphthyl acetate has the potential to detect organophosphorus pesticide (OP) poisoning .
    1-Naphthyl acetate
  • HY-W371164
    C1s-IN-1

    		Complement System Inflammation/Immunology
    C1s-IN-1 (compound A1) is a selective and competitive inhibitor of C1s. C1s-IN-1 binds directly to C1s with a Kd of 9.8 μM .
    C1s-IN-1
  • HY-115731
    Tocol

    Desmethyltocopherol; DL-Tocol; rac-Tocol

    		 Endogenous Metabolite Metabolic Disease
    (±)-Tocol is a synthetic vitamin E derivative.nlike (±)-α-tocopherol, (±)-tocol does not suppress retinol-induced erythrocyte hemolysis or increase microviscosity of rat liver phosphatidylcholine (PC) liposomes.
    Tocol
  • HY-100322
    H100

    		Chloride Channel Cardiovascular Disease
    H100 is a Cl - transport inhibitor, with partial effects against both the NaK2Cl cotransporter and the Band 3 anion exchanger, but no effect against KCl cotransporter, in human erythrocytes.
    H100
  • HY-B1726
    Phenacaine

    Holocaine

    		 Phosphodiesterase (PDE) Metabolic Disease
    Phenacaine (Holocaine) is a local anesthetic. Phenacaine inhibits the specific calmodulin-dependent stimulation of erythrocyte Ca 2+-ATPase and cyclic nucleotide phosphodiesterases from brain and heart .
    Phenacaine
  • HY-120690
    RO5464466

    		Influenza Virus Infection
    RO5464466 is an hemagglutinin (HA) inhibitor of influenza H1N1 viruses. RO5464466 inhibits HA-mediated hemolysis of chicken erythrocytes with the IC50 of 0.29 μM .
    RO5464466
  • HY-106745
    Elziverine

    Ro 22-4839

    		 Calmodulin Cardiovascular Disease
    Elziverine (Ro 22-4839) is a brain circulation improvement agent with vasospasm antispasmodic effects. Elziverine is a calmodulin antagonist. Elziverine inhibits erythrocyte cell membrane rupture, platelet aggregation and lipid peroxidation .
    Elziverine
  • HY-P4836
    LL-37 FK-13

    		Parasite Infection
    LL-37 FK-13 is an antimicrobial agent, that inhibits Trichomonas vaginalis. LL-37 FK-13 exhibits slight hemolytic effects on human erythrocytes and low cytotoxicity to human fibroblasts .
    LL-37 FK-13
  • HY-139899
    S6821

    		Others Others
    S6821 is a TAS2R8 antagonist with IC50 value of 0.035 μM. S6821 is not found to be mutagenic or disruptive in vitro, nor is it found to induce micronucleus in bone marrow polychromatic erythrocytes in vivo .
    S6821
  • HY-139573A
    (Rac)-Etavopivat

    (Rac)-FT-4202

    		 Pyruvate Kinase Cardiovascular Disease
    (Rac)-Etavopivat ((Rac)-FT-4202) is an isomer of Etavopivat (HY-139573). Etavopivat is an orally active erythrocyte pyruvate kinase-R (PKR) activator that can be used in studies of sickle cell disease and other haemoglobinopathies .
    (Rac)-Etavopivat
  • HY-151575
    PfGSK3/PfPK6-IN-2

    		GSK-3 Infection
    PfGSK3/PfPK6-IN-2 is a potent dual PfGSK3/PfPK6 (Plasmodium falciparum GSK3/PK6) inhibitor (IC50: 172 nM and 11 nM respectively). PfGSK3/PfPK6-IN-2 can be used in the research of Malaria .
    PfGSK3/PfPK6-IN-2
  • HY-121556
    Rufigallol

    		Reactive Oxygen Species Parasite Infection
    Rufigallol is one of the earliest systems reported to form columnar mesophases. Rufigallol is also an oxidant agent. Rufigallol acts in a pro-oxidant fashion to produce oxygen radicals inside parasitized erythrocytes. Rufigallol has vitamin K activity and antimalarial activity .
    Rufigallol
  • HY-160610A
    Carbamoyl phosphate dilithium salt

    		Others Others
    Carbamoyl phosphate dilithium salt is an antisickling agent and plays a significant role in the urea cycle. Carbamoyl phosphate dilithium salt carbamylates the amino-terminal valine residues of hemoglobin S in erythrocytes, which interferes with the sickling phenomenon. Carbamoyl phosphate dilithium salt exhibits toxicity due to the lithium cation .
    Carbamoyl phosphate dilithium salt
  • HY-145996
    STC314

    		Bacterial Infection
    STC314 is a small polyanion that interact electrostatically with histones. STC314 blocks disruption of lipid-bilayers by histones that inhibits the cytotoxic, platelet-activating and erythrocyte-damaging effects of histones. STC314 has anti-infective effects and can be uesd for sepsis research .
    STC314

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