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Results for "

A1 and pi4k Inhibitors

" in MedChemExpress (MCE) Product Catalog:

2096

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3

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9

Fluorescent Dye

72

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1301

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24

Inhibitory Antibodies

105

Natural
Products

446

Recombinant Proteins

43

Isotope-Labeled Compounds

158

Antibodies

12

Click Chemistry

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-106012

    PI4K PI3K Cancer
    PI4K-IN-1 (compound 44) is a potent PI4KIII inhibitor, with pIC50 values of 9.0 and 6.6 for PI4KIIIα and PI4KIIIβ, respectively. PI4K-IN-1 also inhibits PI3Kα/β/γ/δ, with pIC50 values of 4.0/<3.7/5.0/<4.1, respectively [1].
    <em>PI4</em>K-IN-<em>1</em>
  • HY-N2344
    Procyanidin A1
    1 Publications Verification

    Proanthocyanidin A1

    PKC Inflammation/Immunology
    Procyanidin A1 (Proanthocyanidin A1) is a procyanidin dimer, which inhibits degranulation downstream of protein kinase C activation or Ca 2+ influx from an internal store in RBL-213 cells. Procyanidin A1 has antiallergic effects [1].
    Procyanidin <em>A1</em>
  • HY-150598

    PI4K PI3K Infection
    CHMFL-PI4K-127 (compound 15g) is an orally active, potent and high selective PfPI4K (Plasmodium falciparum PI4K kinase) inhibitor, with an IC50 of 0.9 nM. CHMFL-PI4K-127 exhibits potent activity against 3D7 Plasmodium falciparum, with an EC50 of 25.1 nM. CHMFL-PI4K-127 shows antimalaria efficacy [1].
    CHMFL-<em>PI4</em>K-127
  • HY-135077

    Others Others
    Prostaglandin A1 ethyl ester is a prodrug form of Prostaglandin A1. Prostaglandin A1 inhibits the activation of platelets [1].
    Prostaglandin <em>A1</em> ethyl ester
  • HY-N7452

    JAK Bacterial Orthopoxvirus Metabolic Disease
    Coumermycin A1 is a JAK2 signal activator. Coumermycin A1 inhibits DNA Gyrase which thereby inhibits cell division in bacteria. Coumermycin A1 shows anti-orthopoxvirus activity.
    Coumermycin <em>A1</em>
  • HY-136652

    YL-704 A1

    Antibiotic Infection
    Platenomycin A1 (compound 1) is a macrolide antibiotic [1].
    Platenomycin <em>A1</em>
  • HY-125560

    Endogenous Metabolite Antibiotic Infection
    Leucomycin A1 is a main component of the leucomycin complex produced by Streptomyces kitasatoensis, Leucomycin A1 is an antibiotic [1].
    Leucomycin <em>A1</em>
  • HY-123121

    Antibiotic Apoptosis Bacterial NF-κB Infection Inflammation/Immunology Cancer
    Nargenicin A1 is an antibiotic agent against various Gram-positive bacteria. Nargenicin A1 shows anti-inflammatory activity. Nargenicin A1 protects HINAE cells against Tacrolimus (HY-13756)-induced DNA damage and apoptosis. Nargenicin A1 can also be used for the research of acute myeloid leukemia [1].
    Nargenicin <em>A1</em>
  • HY-N7443

    Others Others
    Gibberellin A1 is a kind of plant hormones. Gibberellin A1 is a growth-promoting acids isolated from immature seed of Phaseolus multiflorus [1].
    Gibberellin <em>A1</em>
  • HY-16147

    Oxi4503; CA1P; Combretastatin A1 diphosphate

    Others Cancer
    Combretastatin A1 phosphate (Oxi4503; CA1P; Combretastatin A1 diphosphate) is a potent vascular disruptive agent. Combretastatin A1 phosphate exerts anti-angiogenic effects on tumors. Combretastatin A1 phosphate has the potential for the research of pancreatic neuroendocrine tumors [1] .
    Combretastatin <em>A1</em> phosphate
  • HY-P2569

    Apoptosis Cancer
    Malformin A1, a cyclic pentapeptide isolated from Aspergillus niger, possess a range of bioactive properties including antibacterial activity. Malformin A1 shows potent cytotoxic activities on human colorectal cancer cells. Malformin A1 induces apoptosis by activating PARP, caspase 3, -7, and -9 [1].
    Malformin <em>A1</em>
  • HY-105237

    Antibiotic DNA/RNA Synthesis Cancer
    Esperamicin A1, as an extremely potent antitumor antibiotic, is isolated from cultures of Actinomadura verrucosospora. Esperamicin A1 can be used for the research of antitumor [1]. Eesperamicin A1 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    Eesperamicin <em>A1</em>
  • HY-N7480A

    Cholinesterase (ChE) Neurological Disease
    Quinolactacin A1 is a potent acetylcholinesterase (AChE) inhibitor from solid state fermentation of Penicillium citrinum 90648. Quinolactacin A1 can be used for the research of Alzheimer disease [1].
    Quinolactacin <em>A1</em>
  • HY-N6704

    ERK Apoptosis Cancer
    Enniatin A1 isolated from Fusarium mycotoxins is a cyclic hexadepsipeptide consisting of alternating D-α-hydroxyisovaleric acids and N-methyl-L-amino acids. Enniatin A1 possesses anticarcinogenic properties by induction of apoptosis and disruption of ERK signalling pathway. Enniatin A1 inhibits ACAT with an IC50 of 49 μM in rat liver microsomes [1].
    Enniatin <em>A1</em>
  • HY-125738

    Phosphodiesterase (PDE) Neurological Disease Inflammation/Immunology
    Obscurolide A1 is a Phosphodiesterase (PDE) inhibitor (IC50=8 mM) that can be obtained from Streptomyces viridochromogenes culture. Obscurolide A1 has the potential to study neurological and inflammatory diseases [1].
    Obscurolide <em>A1</em>
  • HY-113053

    Endogenous Metabolite Apoptosis Neurological Disease Inflammation/Immunology Endocrinology Cancer
    Prostaglandin A1 is a dehydration derivate of Prostaglandin E1. Prostaglandin A1 exhibits inhibitory activities against tumor growth, inflammation, virus replication, platelet aggregation and excitotoxin-induced neurons apoptosis [1].
    Prostaglandin <em>A1</em>
  • HY-N4133

    Others Others
    Ciwujianoside A1 is isolated from the Eleutherococcus senticosus leaf [1].
    Ciwujianoside <em>A1</em>
  • HY-N2264

    Wulignan A1 is isolated from the stems of Schisandra henryi. Wulignan A1 exhibits anti-influenza virus H1N1 and H1N1-TR (a Tamiflu agent resistant virus strain) activities [1].
    Wulignan <em>A1</em>
  • HY-N6079

    Others Others
    Timosaponin A1 is a coprostane type steroidal saponin isolated from Rhizoma Anemarrhenae.
    Timosaponin <em>A1</em>
  • HY-100558
    Bafilomycin A1
    Maximum Cited Publications
    369 Publications Verification

    BafA1

    Proton Pump Autophagy Antibiotic Bacterial Apoptosis Infection Cancer
    Bafilomycin A1 (BafA1) is a specific and reversible inhibitor of vacuolar H +-ATPase (V-ATPase) with IC50 values of 4-400 nmol/mg. Bafilomycin A1, a macrolide antibiotic, is also used as an autophagy inhibitor at the late stage. Bafilomycin A1 blocks autophagosome-lysosome fusion and inhibits acidification and protein degradation in lysosomes of cultured cells. Bafilomycin A1 induces apoptosis [1] .
    Bafilomycin <em>A1</em>
  • HY-N8252

    Antibiotic Infection
    Xanthoquinodin A1 is an anticoccidial antibiotic having a new xanthone-anthraquinone conjugate system [1].
    Xanthoquinodin <em>A1</em>
  • HY-N6950
    Hederacolchiside A1
    1 Publications Verification

    PI3K Akt mTOR Parasite Apoptosis Infection Cancer
    Hederacolchiside A1, isolated from Pulsatilla chinensis, suppresses proliferation of tumor cells by inducing apoptosis through modulating PI3K/Akt/mTOR signaling pathway [1]. Hederacolchiside A1 has antischistosomal activity, affecting parasite viability both in vivo and in vitro .
    Hederacolchiside <em>A1</em>
  • HY-112435

    PI4K Parasite Infection
    UCT943 is a next-generation Plasmodium falciparum PI4K inhibitor. UCT943 inhibits the P. vivax PI4K (PvPI4K) enzyme with an IC50 of 23 nM [1].
    UCT943
  • HY-118834

    Lyngbyatoxin A

    PKC Cancer
    Teleocidin A1 (Lyngbyatoxin A), a highly toxic skin irritant, is a potent activator of protein kinase C (PKC). Teleocidin A1 shows antiproliferative activity against HeLa cancer cells (IC50=9.2 nM) [1] .
    Teleocidin <em>A1</em>
  • HY-106199
    Adenosine A1 receptor activator T62
    1 Publications Verification

    Adenosine Receptor Neurological Disease Inflammation/Immunology
    Adenosine A1 receptor activator T62 is an allosteric enhancer of adenosine A1 receptor. Adenosine A1 receptor activator T62 produces antinociception in animal models of acute pain and also reduces hypersensitivity in models of inflammatory and nerve-injury pain [1] .
    Adenosine <em>A1</em> receptor activator T62
  • HY-136824

    Bacterial Antibiotic Infection Cancer
    Napyradiomycin A1 is one enantioselective compound of napyradiomycins. napyradiomycins are an intriguing family of halogenated natural products with activity against several tumor cell lines as well as some bacterial strains [1].
    Napyradiomycin <em>A1</em>
  • HY-N6854

    Others Metabolic Disease Cancer
    Mogroside I A1 is a triterpenoid glycoside and a nonsugar sweetener. Mogrosides are sweeter than sucrose. Mogrosides exhibit antioxidant, antidiabetic and anticancer activities [1].
    Mogroside I <em>A1</em>
  • HY-N0258
    Epimedin A1
    1 Publications Verification

    Hexandraside F

    Others Cancer
    Epimedin A1 is a flavonoid extracted from Herba Epimedii which is one of commonly used Chinese medicines.
    Epimedin <em>A1</em>
  • HY-N2046

    Jujuboside A1

    Others Others
    Jujuboside D (Jujuboside A1) is a dammarane-type saponin that can be isolated from the seeds of Ziziphus jujube [1].
    Jujuboside D
  • HY-N11009

    EBV Infection
    11-Oxomogroside II A1 (compound 7) is an oxidized cucurbitin. It can be isolated from the ethanol extract of Rohanberry fruit. 11-Oxomogroside II A1 inhibits the activation of Epstein-Barr virus (EBV) early antigen (EBV-EA) induced by 12-O-tetradecanoylphorbol-13-acetate (TPA). 11-Oxomogroside II A1 also weakly inhibits the activation of (±)-(E)-methyl-2-[(E)-hydroxyimino]-5-nitro-6-methoxy-3-hexemide (NOR 1), a nitric oxide (NO) donor [1].
    11-Oxomogroside II <em>A1</em>
  • HY-121993

    Microtubule/Tubulin Cancer
    Combretastatin A-1 is a microtubule polymerization inhibitor that binds to the colchicine-binding site of tubulin. Combretastatin A-1 inhibits the Wnt/β-catenin pathway through tubulin depolymerization mediated AKT deactivation. Combretastatin A-1 exhibits anti-tumor and anti-vascular effects [1] .
    Combretastatin <em>A-1</em>
  • HY-114599

    Endogenous Metabolite Others
    8-iso Prostaglandin A1 is an active substrate for Arabidopsis thaliana OPR3 (AtOPR3), with a KM of 22 μM [1].
    8-iso Prostaglandin <em>A1</em>
  • HY-134135

    PGA1 methyl ester

    Others Others
    Prostaglandin A1 methyl ester (PGA1 methyl ester) is a cyclopentenone analog [1].
    Prostaglandin <em>A1</em> methyl ester
  • HY-N5045

    Others Inflammation/Immunology
    Jionoside A1 isolated from Radix Rehmanniae Praeparata displays dose dependent immune-enhancement activity and possesses moderate protective activities on H2O2-treated SH-SY5Y cells [1].
    Jionoside <em>A1</em>
  • HY-N0541
    Pseudoginsenoside F11
    1 Publications Verification

    Ginsenoside A1

    Endogenous Metabolite Others
    Pseudoginsenoside F11 (Ginsenoside A1), a component of Panax quinquefolium (American ginseng), has been demonstrated to antagonize the learning and memory deficits induced by scopolamine, morphine and methamphetamine in mice.
    Pseudoginsenoside F11
  • HY-118101

    Apoptosis NF-κB Inflammation/Immunology
    15-Deoxy-Δ12,14-prostaglandin A1 is a deoxyanalog of prostaglandins that inhibits NF-κB signaling and induces apoptosis. 15-Deoxy-Δ12,14-prostaglandin A1 inhibits TNF-α-induced upregulation of inflammatory endothelial cell adhesion molecule (CAM) and avoids monocyte arrest [1].
    15-Deoxy-Δ12,14-prostaglandin <em>A1</em>
  • HY-100540C

    GCA-1

    Others Infection
    Golgicide A-1 (GCA-1) is a less active cis-diastereomer of Golgicide A (GCA). Golgicide A-1 weakly inhibits mosquito reproduction [1].
    Golgicide <em>A-1</em>
  • HY-156685

    PI4K Parasite Infection
    EDI048 (compound 1.16) is an orally active Cryptosporidium PI4K inhibitor for the research of cryptosporidiosis [1].
    EDI048
  • HY-N125722

    Aabomycin A1

    ATP Synthase Antibiotic Infection
    Venturicidin A (Aabomycin A1), from actinomycetes, is a membrane-active natural product inhibitor of ATP synthase. Venturicidin A potentiates the aminoglycoside antibiotic gentamicin against multidrug-resistant clinical isolates of Staphylococcus, Enterococcus, and Pseudomonas aeruginosa. Venturicidin A shows noticeable toxicity toward human embryonic-kidney (HEK)cells with an IC50 of 31 μg/mL.
    Venturicidin A
  • HY-116758

    di-Me-PGA1

    DNA/RNA Synthesis HIV HSV Infection Cancer
    16,16-Dimethyl prostaglandin A1 (di-Me-PGA1) is a prostaglandin analog that can inhibit DNA synthesis in Lewis lung carcinoma and B 16 amelanotic melanoma cells. 16,16-Dimethyl prostaglandin A1 also inhibits viral replication in both HSV and HIV-1 infection systems [1] .
    16,16-Dimethyl prostaglandin <em>A1</em>
  • HY-16146

    OXi-4503 tetrasodium

    Microtubule/Tubulin Cancer
    Combretastatin A-1 phosphate (OXi-4503) tetrasodium, a proagent of Combretastatin A-1, is a microtubule polymerization inhibitor that binds to the colchicine-binding site of tubulin. Combretastatin A-1 phosphate tetrasodium inhibits the Wnt/β-catenin pathway through tubulin depolymerization mediated AKT deactivation. Combretastatin A-1 phosphate tetrasodium exhibits anti-tumor and anti-vascular effects [1] .
    Combretastatin <em>A-1</em> phosphate tetrasodium
  • HY-106005
    MMV390048
    2 Publications Verification

    Parasite PI4K Infection
    MMV390048 is a representative of a new chemical class of Plasmodium PI4K inhibitor (Kd app=0.3 µM). MMV390048 binds to the ATP binding site of Plasmodium PI4K and does not bind to other P. falciparum and human kinases apart from human PIP4K2C, thus alleviating potential kinase-mediated safety concerns. MMV390048 is an antimalarial agent [1].
    MMV390048
  • HY-16668

    Tyrphostin 1; AG9

    Interleukin Related Inflammation/Immunology
    Tyrphostin A1(AG9) inhibits CD40L-stimulated IL-12 production in macrophage cultures and antigen-induced generation of Th1 cells.
    Tyrphostin <em>A1</em>
  • HY-12912

    PI4K Parasite Infection
    KDU691, an imidazopyrazine with potent anti-parasitic activity against blood stage schizonts, gametocytes and liver stages, is a Plasmodium PI4K inhibitor. KDU691 selectively inhibits dihydroartemisinin-pretreated Plasmodium falciparum ring-stage parasites [1].
    KDU691
  • HY-12016
    KU-55933
    30+ Cited Publications

    ATM/ATR Autophagy Cancer
    KU-55933 is a potent ATM inhibitor with an IC50 and Ki of 12.9 and 2.2 nM, respectively, and is highly selective for ATM as compared to DNA-PK, PI3K/PI4K, ATR and mTOR.
    KU-55933
  • HY-12046
    PIK-93
    4 Publications Verification

    PI4K PI3K Virus Protease Cancer
    PIK-93 is the first potent, synthetic PI4K (PI4KIIIβ) inhibitor with IC50 of 19 nM, and also inhibits PI3Kγ and PI3Kα with IC50 of 16 nM and 39 nM, respectively.
    PIK-93
  • HY-103583

    PI4K Parasite Infection
    KDU731, an orally active C. parvum PI4K inhibitor with an IC50 value of 25 nM, blocks Cryptosporidium infection in vitro and in vivo [1] . KDU731 is a promising agent candidate for the treatment of diarrhea caused by Cryptosporidium and meets a broad range of safety .
    KDU731
  • HY-145706

    Adenosine Receptor Neurological Disease
    A2A/A1 AR antagonist-1 (compound 1a) is dual potent A2A/A1 AR antagonist with Kis of 5.58 and 24.2 nM, respectively. A2A/A1 AR antagonist-1 has the potential for the research of ischemic stroke [1].
    A2A/<em>A1</em> AR antagonist-<em>1</em>
  • HY-147543

    Adenosine Receptor Neurological Disease
    A1AR antagonist 4 (compound 22) is a potent and selective A1AR (A1 adenosine receptor) antagonist, with a pIC50 of 5.51 and a pKi of 6.29 [1].
    <em>A1</em>AR antagonist <em>4</em>
  • HY-147544

    Adenosine Receptor Neurological Disease
    A1AR antagonist 5 (compound 20) is a potent and selective A1AR (A1 adenosine receptor) antagonist, with a pIC50 of 5.83 and a pKi of 6.11 [1].
    <em>A1</em>AR antagonist 5

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