| 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. |
| M2881 | Nicardipine hydrochloride | Nicardipine is a dihydropyridine calcium-channel blocking agent used for the treatment of vascular disorders. |
| M2820 | Lomerizine dihydrochloride | Lomerizine dihydrochloride is a relatively new L- and T-type calcium channel blocker used in the treatment of migraine. |
| M2520 | Cinepazide maleate | Cinepazide maleate is a maleate salt form of cinepazide which is a vasodilator. |
| M2496 | Catharanthine | Catharanthine inhibits nicotinic receptor mediated diaphragm contractions with IC50 of 59.6 μM |
| M2425 | Azelnidipine | Azelnidipine is a novel dihydropyridine derivative, a L-type calcium channel blocker, and an antihypertensive. |
| M2248 | Cilnidipine | Cilnidipine is a dual L- and N-type calcium channel blocker that displays antihypertensive, sympatholytic and neuroprotective activity. |
| M1927 | KB-R7943 mesylate | KB-R7943 mesylate is a potent, selective inhibitor of the reverse mode of the Na+/Ca2+ exchanger (IC50 = 0.7 mM). |
| 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. |
| 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. |
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