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. |
M56455 | Nexopamil | Nexopamil is a calcium antagonist of Ca2+ channel, 5HT2, 5HT1A, 5HT1C and dopamine D2 receptors. |
M56454 | Azumolene sodium | Azumolene sodium (EU4093) is an analog of Dantrolene that inhibits malignant hyperthermia (MH) syndrome and intracellular Ca2+ homeostasis failure caused by Halothane/Succinylcholine. |
M56453 | 2-Chloro-ATP sodium | 2-Chloro-ATP sodium (2-Chloro ATP) is an adenine nucleotide and an analog of ATP. |
M56452 | ML218 hydrochloride | ML218 hydrochloride is a potent, selective and orally active T-type Ca2+ channels (Cav3.1, Cav3.2, Cav3.3) inhibitor with IC50s of 310 nM and 270 nM for Cav3.2 and Cav3.3, respectively. |
M56451 | YS 035 hydrochloride | YS 035 hydrochloride is a Ca2+ antagonist on cellular uptake and mitochondrial efflux of calcium ions. |
M56450 | Ca2+ channel agonist 1 | Ca2+ channel agonist 1 is an agonist of N-type Ca2+ channel and an inhibitor of Cdk2, with EC50s of 14.23 μM and 3.34 μM, respectively, and is used as a potential treatment for motor nerve terminal dysfunction. |
M56449 | D-myo-Inositol 1,4,5-trisphosphate tripotassium | D-myo-Inositol 1,4,5-trisphosphate tripotassium, a second messenger, elicits Ca2+ mobilization. |
M55649 | Monatepil maleate | Monatepil maleate (AJ-2615) is a potent and orally active Ca2+-channel antagonist and a noncompetitive ACAT inhibitor. Monatepil maleate (AJ-2615) is also an α1-adrenoceptor antagonist. |
M53706 | ω-Agatoxin TK | ω-Agatoxin TK, a peptidyl toxin of the venom of Agelenopsis aperta, is a potent and selective P/Q type Ca2+ channel blocker. |
M53705 | SNX-482 | SNX-482, a peptidyl toxin of the spider Hysterocrates gigas, is a potent, high affinity, selective and voltage-dependent R-type CaV2.3 channel blocker with an IC50 of 30 nM. |
M52811 | ω-Conotoxin MVIIC | ω-Conotoxin MVIIC is a N- and P/Q-type Ca2+ channel blocker, significantly suppresses the 11-keto-βboswellic acid-mediated inhibition of glutamate release. |
M52810 | ω-Conotoxin GVIA | ω-Conotoxin GVIA is an inhibitor of the N-type Ca2+ channel. |
M52809 | ω-Conotoxin CnVIIA | ω-Conotoxin CnVIIA, a 27 amino acid neuropeptide toxin, is a N-type calcium current blocker. |
M52808 | ω-Conotoxin SO3 | ω-Conotoxin SO3 is a blocker of N-type voltage-sensitive calcium channel. |
M52807 | ω-Conotoxin CVIA | ω-Conotoxin CVIA, a 27 amino acid neuropeptide toxin, is an voltage sensitive calcium channels blocker. |
M52806 | ω-Conotoxin CVID | ω-Conotoxin CVID (Leconotide, AM336, CNSB004) blocks neuronal voltage sensitive calcium channel. |
M52805 | ω-Hexatoxin-Hv1a | ω-Hexatoxin-Hv1a is a neurotoxin that can be isolated from the venom spider (Hadronyche versuta).ω-Hexatoxin-Hv1a blocks voltage-gated calcium channels. |
M52804 | ω-Grammotoxin SIA | ω-Grammotoxin SIA (GrTx) is P/Q and N-type voltage-gated Calcium channels inhibitor. |
M52803 | Ser-Ala-alloresact | Ser-Ala-alloresact is a sperm activating peptide (SAP). |
M52802 | Huwentoxin XVI | Huwentoxin XVI, an analgesic, is a highly reversible and selective mammalian N-type calcium channel (IC50 of ~60 nM) antagonist from Chinese tarantula Ornithoctonus huwena. |
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