Cat.No. | Name | Information |
---|---|---|
M3621 | Ionomycin | Ionomycin is a calcium ionophor and an antibiotic produced by Streptomyces conglobatus. |
M3807 | Ionomycin (Calcium salt) | Ionomycin is a calcium ionophor and an antibiotic produced by Streptomyces conglobatus. |
M7409 | Thapsigargin | Thapsigargin is an endoplasmic reticulum (ER) stress inducer, it is also an inhibitor of microsomal Ca2+-ATPase. |
M5073 | (R)-(+)-BAY K 8644 | (R)-(+)-BAY K 8644 is a calcium channel inhibitor, inhibits Ba2+ currents (IBa) with IC50 of 975 nM. |
M3424 | Nifedipine | Nifedipine (BAY-a-1040) is a potent vasodilator agent with calcium antagonistic action. |
M14204 | Verapamil | Verapamil ((±)-Verapamil) is a calcium channel blocker and a potent and orally active first-generation P-glycoprotein (P-gp) inhibitor. |
M52801 | Imperatoxin A | Imperatoxin A is an activator of Ca2+-release channels/ryanodine receptors (RyRs) enhances the influx of Ca2+ from the sarcoplasmatic reticulum into the cell. |
M52800 | Calcicludine | Calcicludine is a protein toxin from the venom of the green mamba Dendroaspis angusticeps that inhibits high-voltage-activated calcium channel, especially L-type calcium channel with the IC50 of 88 nM. |
M52799 | Huwentoxin I | Huwentoxin I (HWTX-I) is a peptide toxin that inhibits voltage-gated sodium channels and N-type calcium channels. |
M52797 | Calciseptin | Calciseptine, a natural neurotoxin isolated from the black mamba Dendroaspis p. |
M52796 | Verticilide | Verticilide is a ryanodine-binding inhibitor and inhibits ryanodine binding to ryanodine receptors in the cockroach at an IC50 value of 4.2 μM (whereas inhibition against mouse ryanodine receptors was weak (IC50=53.9 μM)). |
M52795 | Myomodulin | Myomodulin is a neuropeptide present in molluscs, insects, and gastropods. |
M52794 | Agelenin | Agelenin is a polypeptide composed of 35 amino acids. |
M52793 | ProTx-I | ProTx-I, a venom toxin of the tarantula Thrixopelma pruriens, is a potent, selective CaV3.1 channel blocker with IC50 values of 0.2 μM and 31.8 μM for hCaV3.1 and hCaV3.2 respectively. |
M49729 | N-Salicyloyltryptamine | N-Salicyloyltryptamine acts on voltage-dependent Na+, Ca2+, and K+ ion channels inhibitor. |
M49487 | AP30663 | AP30663 is a negatively variable modulator of KCa2 channels and can be used in studies related to atrial fibrillation. |
M42170 | Caloxin 3A1 | Caloxin 3A1 is a biological active peptide. |
M42169 | BBT | BBT is an enhancer of impaired glucose-stimulated insulin secretion (GSIS). |
M42168 | Prenylamine | Prenylamine is a calcium channel blocker of the amphetamine chemical class. |
M42167 | Budiodarone | Budiodarone (ATI-2042) is an analogue of Amiodarone with a half-life of 7 h. |
M42166 | TROX-1 | TROX-1 is an N-type calcium channel (CaV2.2) inhibitor with an IC50 value of 0.11 μM. |
M42165 | Cav 3.2 inhibitor 4 | Cav 3.2 inhibitor 4 is a potent, peripherally restricted, selective T-type calcium channel (Cav3.2) inhibitor, with an IC50 of 0.6 μM. |
M42164 | ω-Tbo-IT1 | ω-Tbo-IT1 is a peptide toxin that can be isolated from the venom of Tibellus oblongus.ω-Tbo-IT1 is an inhibitor of insect calcium channel. |
M41122 | PptT-IN-4 | PptT-IN-4 is a PptT inhibitor (IC50: 0.71 μM). |
M31048 | Ziconotide TFA | Ziconotide TFA (SNX-111 TFA), a peptide, is a potent and selective block of N-type calcium channels antagonist. Ziconotide TFA reduces synaptic transmission, and can be used for chronic pain research. |
M30967 | TTA-A2 | TTA-A2 is a potent, selective and orally active t-type voltage gated calcium channel antagonist with reduced pregnane X receptor (PXR) activation. TTA-A2 is equally potent against the Cav3.1 (a1G) and Cav3.2 (a1H) channels with IC50 values of 89 nM and 92 nM, respectively, at -80 and -100 mV holding potentials. TTA-A2 can be used for the research of a variety of human neurological diseases, including sleep disorders and epilepsy. |
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