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Cat No. | Product Name | Synonyms | Targets |
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T10674 | Potassium Channel Activator 1 | ZINC34634569 | Potassium Channel |
Potassium Channel Activator 1 can be used in studies about the treatment of disorders or conditions wherein the dopaminergic system is disrupted such as mood disorders ADHD, schizophrenia, and other psychotic states. | |||
T10101 | Calcium channel-modulator-1 | Others , Calcium Channel | |
Calcium channel-modulator-1 is a calcium channel-modulator (IC50:0.8 μM) with specialisation to block aortic constriction. | |||
T2604 | 1-EBIO | 1-EBIO | Calcium Channel |
1-EBIO (1-EBIO) is a calium channel agonist. | |||
T4669 | Fantofarone | SR 33557 | Calcium Channel , Parasite |
Fantofarone (SR 33557) is a highly potent antagonist of Calcium Channel. | |||
T10852 | CNS-5161 hydrochloride | CNS 5161A | NMDAR |
CNS-5161 hydrochloride (CNS 5161A) is a new antagonist of NMDA ion-channel. It interacts with the NMDA receptor/ion channel site to produce a noncompetitive blockade of the actions of glutamate. | |||
T10566 | BMS-191095 | Potassium Channel | |
BMS-191095 is mitochondrial ATP-sensitive potassium (mitoKATP) channel activator. | |||
T22537 | 9-Phenanthrol | TRP/TRPV Channel | |
9-Phenanthrol is inhibitor of the transient receptor potential melastatin 4 (TRPM) channel, a Ca2+ -activated non-selective cation channel. | |||
T10307 | AMPA receptor modulator-1 | iGluR | |
AMPA receptor modulator-1 can be activated by glutamate, thereby modulating ion channels. | |||
T22353 | Lanthanum(III) chloride heptahydrate | Calcium Channel | |
Lanthanum(III) chloride is an inorganic compound which used in biochemical research to block the activity of divalent cation channels, especially calcium channels. | |||
T7182 | Metaflumizone | BAS-320I | Sodium Channel , Parasite |
Metaflumizone (BAS-320I) is a sodium channel blocker insecticide. | |||
T1422 | Nilvadipine | FK235,FR34235,ARC029 | Calcium Channel |
Nilvadipine (FK235), a calcium channel blocker (CCB), is utilized for treatment of hypertension. | |||
T2342 | Raxatrigine | CNV1014802,CNV 1014802,GSK-1014802,CNV-1014802 | Sodium Channel |
Raxatrigine (CNV 1014802) has been investigated for the treatment of Bipolar Disorder and Bipolar Depression. | |||
T64561 | DPhPC | Others | |
DPhPC is a synthetic liposome used to synthesize liposomes commonly used in artificial membrane matrices.DPhPC bilayers do not allow ion leakage in the absence of pore/ion channels.DPhPC can be used to study channel prot... | |||
T0231 | Amlodipine Besylate | Amlodipine benzenesulfonate | Calcium Channel |
Amlodipine Besylate(Amlodipine benzenesulfonate) is a long-lasting calcium channel blocker. | |||
T12608 | QX-314 chloride | Sodium Channel | |
QX-314 chloride is a membrane-impermeable permanently charged blocker of sodium channel. | |||
T15053 | Darodipine | PY-108068,PY 108-068 | Calcium Channel |
Darodipine (PY-108068) is a dihydropyridine type Ca+2 antagonist. | |||
T15233 | Endovion | NS3728 | Chloride channel |
Endovion (NS3728) is a pharmacological anion channel and an Anoctamin-1 (ANO 1) channel inhibitor. Endovion is also the specific VRAC/VSOAC blocker. | |||
T16346 | NS1652 | Chloride channel | |
NS1652 is an anion conductance inhibitor. NS1652 blocks chloride channel has an IC50 of 1.6 μM in human and mouse red blood cells. | |||
T5183 | AUT1 | Potassium Channel | |
AUT1 (AUT-1) is a novel specific modulator of Kv3 channels (EC50: 4.7 and 4.9 uM for Kv3.1b and Kv3.2a). | |||
T16110 | ML418 | Potassium Channel | |
ML418 is a potent, selective and CNS penetrating Kir7.1 potassium channel blocker (IC50 = 310 nM), and also potently inhibits Kir6.2/SUR1. | |||
T0121 | Azelnidipine | CS 905,UR-12592 | Calcium Channel |
Azelnidipine (UR-12592) is a dihydropyridine used as calcium channel blocker. | |||
T0193 | Manidipine dihydrochloride | Manidipine 2HCl,CV-4093 | Calcium Channel |
Manidipine dihydrochloride (Manidipine 2HCl) is a potent calcium channel blocker for Ca2+ current(IC50=2.6 nM). | |||
TQ0014 | GNE-131 | Sodium Channel | |
GNE-131 is a potent and specific inhibitor of human sodium channel NaV1.7 (IC50: 3 nM). | |||
T1385 | Amlodipine | UK-48340 | Calcium Channel |
Amlodipine (UK-48340) is a synthetic dihydropyridine and a calcium channel blocker with antihypertensive and antianginal properties. | |||
T12032 | Mibefradil dihydrochloride | Ro 40-5967 (dihydrochloride) | Calcium Channel |
Mibefradil dihydrochloride (Ro 40-5967 (dihydrochloride)) is an blocker of calcium channel with moderate selectivity for T-type Ca2+ channels (T-type and L-type currents with IC50s of 2.7 μM and 18.6 μM, respectively). | |||
T10979 | DCPIB | Potassium Channel , Chloride channel | |
DCPIB, a known specific and potent inhibitor of volume-regulated anion channels (VRAC),DCPIB displayed superior selectivity toward TRESK with an IC50 of 0.14 μM, demonstrating at least 100-fold higher affinity over TREK1... | |||
T0693 | Niflumic acid | Nifluril,Forenol,Landruma | Others , Phospholipase , Chloride channel , COX , Monocarboxylate transporter , UGT |
Niflumic acid (Nifluril) is a Ca2+-activated Cl- channel blocker and an analgesic and anti-inflammatory agent used in the therapy of rheumatoid arthritis. | |||
T0946 | Mepivacaine hydrochloride | Mepivacaine HCl | Sodium Channel |
Mepivacaine hydrochloride (Mepivacaine HCl) is the hydrochloride salt form of mepivacaine, an amide derivative with local anesthetic properties. | |||
T68143 | Solpecainol | Sodium Channel | |
solpecainol is a sodium channel blocker used in the study of neurological and cardiovascular diseases. | |||
T3303 | ML277 | ML-277,CID-53347902 | Potassium Channel |
ML277 (CID-53347902) was identified as a potent activator of KCNQ1 channels (EC(50)=260 nM). | |||
T8617 | GMQ hydrochloride | NSC 403387 hydrochloride | Others |
GMQ hydrochloride (NSC-403387 hydrochloride) is a potent and selective acid-sensing ion channel (ASIC) modulator. It activates ASIC3 channels under neutral pH and blocks acid-induced maximal peak current. | |||
T4330 | CaCCinh-A01 | Chloride channel | |
CaCCinh-A01 is an inhibitor of the calcium-activated chloride channel (CaCC, 10 μM) and TMEM16A (IC50: 2.1 μM). | |||
TQ0033 | Zegocractin | CM-4620,N-(5-(6-Chloro-2,2-difluorobenzo[d][1,3]dioxol-5-yl)pyrazin-2-yl)-2-fluoro-6-methylbenzamide,CM4620 | Calcium Channel |
Zegocractin (CM-4620) is a calcium-release activated calcium-channel (CRAC channel) inhibitor. | |||
T7547 | Ralfinamide mesylate | FCE-26742A (mesylate) | Sodium Channel |
Ralfinamide mesylate (FCE-26742A (mesylate)) is an orally available Na+ channel blocker. | |||
T68038 | Celivarone | Potassium Channel | |
Celivarone is a potassium channel blocker used in the study of arrhythmias, atrial flutter and atrial fibrillation. | |||
T13047 | Synta66 | Calcium Channel | |
Synta66 is a store-operated calcium entry channel Orai inhibitor, and used for the research of neurological disease. | |||
T0008 | Phenytoin sodium | 5,5-Diphenylhydantoin sodium salt,Diphantoine,Dilantin sodium,Diphenylhydantoin Sodium | Virus Protease , Sodium Channel |
Phenytoin sodium (Diphantoine) is an inactive stabilizer for voltage-gated sodium channel . | |||
T0386 | Ropivacaine hydrochloride | Ropivacaine monohydrochloride | Potassium Channel , Sodium Channel |
Ropivacaine hydrochloride (Ropivacaine monohydrochloride) is the hydrochloride salt of ropivacaine, a local anesthetic of the amide type with analgesic activity. | |||
T10884 | CRAC intermediate 1 | 5-(S)-Fluorowillardiine | Calcium Channel |
CRAC intermediate 1 (5-(S)-Fluorowillardiine) is a key intermediate in the chemical synthesis of a series of CRAC channel inhibitors. | |||
T2711 | Chembridge-5861528 | TCS 5861528 | TRP/TRPV Channel |
Chembridge-5861528 (TCS 5861528) is a TRPA1 channel blocker that antagonizes AITC- and 4-HNE-evoked calcium influx with IC50 values of 14.3 and 18.7 μM, respectively. | |||
T1406 | Amantadine hydrochloride | 1-adamantanamine HCl,1-Adamantanamine hydrochloride,Symmetrel,CI-719,Amantadine HCl,1-Adamantylamine hydrochloride | Dopamine Receptor , Influenza Virus |
Amantadine hydrochloride (CI-719) is an antiviral that is used in the prophylactic or symptomatic treatment of influenza A and Parkinson disease. | |||
TP1300 | GsMTx4 TFA (1209500-46-8 free base) | GsMTx4 TFA | Piezo Channel |
GsMTx4 TFA (1209500-46-8 free base) (GsMTx4 TFA) is a spider venom peptide that selectively inhibits cationic permeable mechanically-sensitive channels (MSCs) belonging to the Piezo and TRP channel families. | |||
T28020 | Mesendogen | TRP/TRPV Channel | |
Mesendogen is an inhibitor of TRPM6. Mesendogen alters magnesium homeostasis, promotes mesoderm and definitive endoderm differentiation. | |||
T4059 | Selamectin | UK-124114 | Chloride channel , P-gp , Parasite |
Selamectin (UK-124114) is a macrocyclic lactone derivative of ivermectin, an anthelmintic that potentiates glutamate- and GABA-gated chloride channel opening in nematodes. In an H. contortus larval development assay, sel... | |||
T10690 | Cav 2.2 blocker 1 | Calcium Channel | |
Cav 2.2 blocker 1 is an N-type calcium channel (Cav 2.2; IC50: 1 nM) blocker for the treatment of pain. | |||
T8401 | Efonidipine hydrochloride monoethanolate | NZ-105 hydrochloride monoethanolate | Calcium Channel |
Efonidipine hydrochloride monoethanolate (NZ-105 hydrochloride monoethanolate) is a Ca(2+)-channel Blocker, Enhances the Production of Dehydroepiandrosterone Sulfate in NCI-H295R Human Adrenocortical Carcinoma Cells | |||
T0386L | Ropivacaine | LEA-103 HCl | Potassium Channel , Sodium Channel |
Ropivacaine (LEA-103 HCl) is a local anaesthetic drug belonging to the amino amide group. | |||
T13059 | T16Ainh-A01 | Chloride channel | |
T16Ainh-A01 is a potent inhibitor of TMEM16A Chloride channel, inhibiting TMEM16A-mediated chloride currents (IC50 of 1 µM),and functions as a calcium-activated chloride channel (CaCC). | |||
T6645 | Ropivacaine hydrochloride monohydrate | Ropivacaine HCl,Ropivacaine HCl monohydrate,LEA 103,LEA-103 HCl | Potassium Channel , Sodium Channel |
Ropivacaine hydrochloride monohydrate (LEA-103 HCl) is an anaesthetic agent and blocks impulse conduction in nerve fibres through inhibiting sodium ion influx reversibly. | |||
T3651 | YM-58483 | YM 58483,BTP2 | Calcium Channel |
YM-58483 (BTP2) is a specific and effective inhibitor of CRAC channels and subsequent Ca2+ signals. |
Cat No. | Product Name | Synonyms | Targets |
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T8040 | Cholesterol myristate | Cholesteryl myristate,Cholesteryl tetradecanoate | Others , Potassium Channel , GABA Receptor , Endogenous Metabolite , AChR |
Cholesterol myristate (Cholesteryl myristate) is a natural steroid present in traditional Chinese medicine. Cholesterol myristate binds to several ion channels such as GABAA receptor, the nicotinic acetylcholine receptor... | |||
T1381 | Milbemycin oxime | Others , Antibiotic , Parasite | |
Milbemycin oxime is a broad spectrum antiparasitic, used as a veterinary drug. | |||
T2996 | Tetrandrine | NSC-77037,d-Tetrandrine,Hanfangchin A,Fanchinine,Sinomenine A | Potassium Channel , Calcium Channel |
Tetrandrine (Sinomenine A) is a natural, bis-benzylisoquinoline alkaloid isolated from the root of the plant. Tetrandrine non-selectively inhibits calcium channel activity and induces G1 blockade of the G1 phase of the c... | |||
T2807 | Caffeic Acid | Lipoxygenase , Endogenous Metabolite , TRP/TRPV Channel | |
Caffeic Acid is an orally bioavailable, hydroxycinnamic acid derivative and polyphenol, with potential anti-oxidant, anti-inflammatory, and antineoplastic activities. | |||
T2782 | Catharanthine | (+)-3, 4-Didehydrocoronaridine,(+)-3,4-Didehydrocoronaridine | Calcium Channel , AChR |
Catharanthine ((+)-3,4-Didehydrocoronaridine) suppresses nicotinic receptor-mediated diaphragm contractions (IC50=59.6 μM). | |||
TN1081 | Hirsuteine | Dopamine Receptor | |
Hirsuteine is a natural product. It non-competitively antagonizes nicotine-mediated dopamine release by blocking ion permeation through nicotinic receptor channel complexes. | |||
T3S0156 | Atractyloside potassium salt | Atractyloside Dipotassium Salt | Others |
1. Atractyloside potassium salt (Atractyloside Dipotassium Salt) inhibits oxidative phosphorylation by blocking the transfer of adenosine nucleotides through the mitochondrial membrane. | |||
T16535 | Picrotoxinin | Chloride channel , GABA Receptor | |
Picrotoxinin is a blocker of chloride channel and a noncompetitive antagonist of GABAA with an IC50 of 1.15 μM for α1β2γ2L GABAA. Picrotoxinin shows convulsant properties. | |||
T2720 | Ginsenoside Rc | Panaxoside Rc | Others , TNF , GABA Receptor , Interleukin |
Ginsenoside Rc (Panaxoside Rc) is one of the ginsenosides from Panax ginseng, inhibits the expression of TNF-α and IL-1β. | |||
T3013 | Catharanthine tartrate | Catharanthine hemitartrate | Others , Calcium Channel |
Catharanthine tartrate (Catharanthine hemitartrate) is an alkaloid from periwinkle that inhibits voltage-gated L-type calcium channels and has antitumor and hypotensive activities. | |||
T1130 | Gramicidin | Gramicidinum,Gramicidine,Gramicidina | MRP , Antibacterial , Antibiotic |
A group of peptide antibiotics from BACILLUS brevis. Gramicidin (Gramicidine) C or S is a cyclic, ten-amino acid polypeptide and gramicidins A, B, D are linear. Gramicidin is one of the two principal components of TYROTH... | |||
T4S1876 | 3-Deoxyaconitine | Sodium Channel | |
3- Deoxyaconitine is a derivative of Aconitine (A189875), which activates tetrodotoxin-sensitive Na+ channels, inducing presynaptic depolarization, thus blocking the nerve action potential which, in turn, blocks the rele... | |||
TN1035 | Irisolidone | IL Receptor , NF-κB , Chloride channel | |
Irisolidone is a potent volume-regulated anion channel (VRAC) current inhibitor, it exhibits high efficacy for VRAC blockade with IC50s of 5-13 μM. | |||
T0690 | Quinine | 奎宁 | Potassium Channel , Platelet aggregation , Parasite |
Quinine is a natural cinchona alkaloid that has been used for centuries in the prevention and therapy of malaria. Quinine is also used for idiopathic muscle cramps. Quinine therapy has been associated with rare instances... | |||
TWS1563 | Incensole | Others | |
1. Incensole has a protective or stimulating effect on β-cells of the rat pancreas, it also can increase the insulin secretion, which evidenced by a significant increase both in body weight and in liver glycogen. | |||
T1131 | Ivermectin | MK-933 | Mitophagy , GluCls , P2X Receptor , SARS-CoV , HIV Protease , Antibiotic , Parasite , Autophagy , HSV |
Ivermectin (MK-933) is a glutamate-gated chloride channel (GluCls) activator, with antiparasitic activity. | |||
T6856 | Halofuginone | Tempostatin,empostatin,RU-19110 | Calcium Channel , DNA/RNA Synthesis , Sodium Channel , Parasite , TGF-beta/Smad |
Halofuginone (RU-19110), the competitive inhibitor of prolyl-tRNA synthetase(Ki=18.3 nM), could also down-regulate Smad3 and blocked TGF-β signaling at 10 ng/ml in the mammal. | |||
T1125 | Shikonin | NSC 252844,Isoarnebin 4,(+)-Shikonin,Alkanna Red,C.I. 75535,Anchusa acid | TNF , NF-κB , Chloride channel , HIV Protease , PKM |
Shikonin (Anchusa acid) is an TMEM16A chloride channel inhibitor (IC50: 6.5 μM). Shikonin is also a selective PKM2 inhibitor and can also suppress activation of the NF-κB pathway and inhibit TNF-α. Shikonin decreases exo... | |||
T7177 | Capsazepine | Apoptosis , TRP/TRPV Channel | |
Capsazepine is an antagonist of TRPV1 receptor ( IC50 : 562 nM). Capsazepine blocks the painful sensation of heat caused by capsaicin (the active ingredient of chilli pepper) which activates the TRPV1 ion channel. It is ... | |||
T2994 | (E)-Cardamonin | Alpinetin chalcone,Cardamomin,Cardamonin,(E)-Cardamoni | Apoptosis , TRP/TRPV Channel |
(E)-Cardamonin (Alpinetin chalcone) is a chalconoid that has been isolated from several plants including Alpinia katsumadai and Alpinia conchigera. It is a novel antagonist of hTRPA1 cation channel with an IC50 of 454 nM... | |||
T1407 | (-)-Menthol | L-Menthol,Levomenthol,Menthomenthol,Menthacamphor | Opioid Receptor , Endogenous Metabolite , TRP/TRPV Channel |
(-)-Menthol (Levomenthol) is a levo isomer of menthol, an organic compound made synthetically or obtained from peppermint or mint oils with flavoring and local anesthetic properties. When added to pharmaceuticals and foo... | |||
T4808 | Agmatine sulfate | Agmatine sulfate salt | Endogenous Metabolite , NO Synthase , Imidazoline Receptor |
Agmatine sulfate (Agmatine sulfate salt) is a bioactive metabolite of the arginine amino acid. It exerts modulatory action at multiple molecular targets, such as neurotransmitter systems, ion channels and nitric oxide sy... | |||
T23735 | Jamaicin | An-Co-A4,AnCoA-4,An Co A4,AnCoA4 | Calcium Channel |
Jamaicin (AnCoA4), an isoflavone derived from the chickweed plant, is an inhibitor of the STIM1-Orai1 channel that blocks calcium influx, reduces its interaction with STIM1, and inhibits T-cell activation. | |||
T4S0969 | Obtusifolin | Antioxidant , NF-κB | |
1. Obtusifolin has antioxidant properties and improves chemically induced diabetes and its complications by modulation of oxidative stress. 2. Obtusifolin suppresses phthalate esters-mediated bone resorption, thus may be... | |||
T3243 | Betaine | Abromine,glycine betaine,oxyneurine,trimethylglycine,lycine | Others , Endogenous Metabolite |
Betaine (trimethylglycine) is a methyl derivative of glycine first isolated from sugar beets. It has been shown to have potential benefits for fighting heart disease, improving body composition, and helping promote muscl... | |||
T5065 | GUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SOD | Monosodium-GMP,cGMP sodium salt,Cyclic GMP | PKA |
GUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SOD (cGMP sodium salt) , also known as cGMP, is a cellular regulatory agent and has been described as a second messenger. Its levels increase in response to a variety of hormones, inc... | |||
T82764 | Cd1a | β-TRTX-cd1a,β-Theraphotoxin-cd1a | |
Cd1a, a β-toxin from the African spider Ceratogyrus darlingi, modulates calcium ion channels and inhibits human calcium ion channels (Ca v 2.2)(IC 50 2.6 μM) as well as mouse sodium ion channels (Na v 1.7). This compound... | |||
T75722 | Chlorotoxin TFA | ||
Chlorotoxin TFA is a peptide isolated from the venom of the scorpion Leiurus quinquestriatus , acts as a chloride channel blocker [1] . Anti-cancer activity [2] . | |||
T36439 | Gramicidin A | Antibacterial , HIF , Parasite | |
Gramicidin A is a peptide antibiotic isolated from B. brevis.Gramicidin A is a highly hydrophobic channel-forming ion carrier that forms monovalent cation-permeable channels in artificial membranes.Gramicidin A induces t... | |||
T38484 | Englerin A | (-)-Englerin A | TRP/TRPV Channel |
Englerin A, a TRPC4 and TRPC5 channel agonist, is a compound from the East African plant Phyllanthus engleri with analgesic, anti-inflammatory, and anticancer activities that induces necrosis in human renal cancer cells. | |||
T75333 | Quinine hemisulfate hydrate | ||
Quinine hemisulfate hydrate, an alkaloid derived from the bark of the cinchona tree, acts as an anti-malaria agent. Quinine hemisulfate hydrate is a potassium channel inhibitor that inhibits WT mouse Slo3 (K Ca 5.1) chan... |
Cat No. | Product Name | ||
---|---|---|---|
L2300 | Ion Channel Inhibitor Library | 946 compounds | |
A unique collection of 946 compounds targeting ion channels for research in ion channels-related diseases and ion channel drug discovery; | |||
L7300 | Potassium Channel Blocker Library | 160 compounds | |
A unique collection of 160 potassium channel blockers and agonists for high throughput and high content screening; | |||
L7400 | Sodium Channel Blocker Library | 128 compounds | |
A unique collection of 128 sodium channel blockers and agonists for high throughput and high content screening; | |||
L7200 | Calcium Channel Compound Library | 143 compounds | |
A unique collection of 143 calcium channel blockers and agonists for high throughput and high content screening; | |||
L2800 | Serotonin Receptor-Targeted Compound Library | 275 compounds | |
A unique collection of 275 compounds targeting serotonin receptors for high throughput screening and high content screening; | |||
L9420 | Exosome Compound Library | 80 compounds | |
80 exosome-related compounds that can be used for high-throughput and high-content screening. |