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Calmodulin Related Products (53)
Related Products (53)
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Probimane
0 ImagesSynonyms: AT-2153Probimane (AT-2153) is a potent anticancer agent. Probimane is effective against mouse tumors S37, S180, Lewis lung carcinoma, L1210 and human pulmonary adenocarcinoma heterotransplanted into nude mice. -
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CALP1
0 ImagesCALP1 is a calmodulin (CaM) agonist (Kd of 88 µM) with binding to the CaM EF-hand/Ca2+-binding site. CALP1 blocks calcium influx and apoptosis (IC50 of 44.78 µM) through inhibition of calcium channel opening. CALP1 blocks glutamate receptor channels and blocks a store-operated nonselective cation channel. CALP1 activates CaM-dependent phosphodiesterase activity. -
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Albanin A
0 ImagesCat. No.: HY-N10772CAS No.: 73343-42-7Albanin A, a flavonoid, suppresses glutamate release by decreasing Ca2+/calmodulin/adenylate Cyclase 1 (AC1) activation in synaptosomes and exerts neuroprotective effect in vivo. Albanin A has anti-inflflammatory activity. -
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A-7 hydrochloride
0 ImagesSynonyms: Ophobolin AA-7 hydrochloride (Ophobolin A) is a calmodulin antagonist and can be used for the research of cancer. -
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Metofenazate
0 ImagesMetofenazate is a selective calmodulin inhibitor. -
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Calmodulin antagonist-1
0 ImagesCalmodulin antagonist-1 (A-5) is a calmodulin (CaM) antagonist. Calmodulin antagonist-1 inhibits calmodulin-activated Ca2+-phosphodiesterase (PDE) (IC50=66 μM). Calmodulin antagonist-1 also inhibits trypsin-treated Ca2+-PDE (IC50=560 μM) in a competitive fashion with respect to cyclic GMP. -
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L-6355
0 ImagesCat. No.: HY-124176CAS No.: 85642-08-6L-6355 is an Amiodarone (HY-14187) related compound, which inhibits Ca2+/calmodulin activated cyclic nucleotide phosphodiesterase with an IC50 value of 0.65 μM. L-6355 is promising for research of antiarrhythmic and antianginal agent. -
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- Neurogranin (48-76), mouse
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E6 Berbamine
0 ImagesCat. No.: HY-120997CAS No.: 114784-59-7Synonyms: Berbamine p-nitrobenzoateE6 Berbamine (Berbamine p-nitrobenzoate) is a potent calmodulin (CaM) antagonist. E6 Berbamine inhibits the activities of calmodulin-dependent myosin light chain kinase (MLCK) and phosphodiesterase (PDE). E6 Berbamine exhibits anti-leukemic activity. E6 Berbamine can be used in research related to cardiovascular abnormalities and chronic myeloid leukemia. -
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Zaldaride
0 ImagesCat. No.: HY-105118CAS No.: 109826-26-8Synonyms: CGS-9343B free base; KW 5617 free baseZaldaride (CGS-9343B free base) is a potent, orally active and selective inhibitor of calmodulin. Zaldaride inhibits CaM (calmodulin)-stimulated cAMP phosphodiesterase activity, with an IC50 of 3.3 nM. Zaldaride prevents estrogen-induced transcription activation by ER, reversibly blocks voltage-activated Na+, Ca2+ and K+ currents in PC12 cells and inhibits nAChR. -
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Bovine calmodulin
0 ImagesCat. No.: HY-NP0230Bovine calmodulin can be used for the in vitro phosphorylation assay of recombinant retinoic acid-induced gene I protein. Bovine calmodulin has also been used in studies of the hydrolysis and deamidation of the endopeptide Glu-C protein. -
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KS 501
0 ImagesCat. No.: HY-117232CAS No.: 120634-86-8KS 501 is a potent and selective calmodulin inhibitor. KS 501 inhibits the activation of calmodulin kinase I and II, but has less effect against cyclic adenosine 3’,5’-monophosphate (cyclic AMP)-sensitive kinase. KS 501 inhibits the enzyme through interfering with calmodulin activation rather than through a direct effect on the enzyme. KS 501 can be used for the study of leukemia. -
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CALP2
0 ImagesCat. No.: HY-P1076CAS No.: 261969-04-4CALP2 is a calmodulin (CaM) antagonist ( (Kd of 7.9 µM)) with high affinity for binding to the CaM EF-hand/Ca2+-binding site. CALP2 inhibits CaM-dependent phosphodiesterase activity and increases intracellular Ca2+ concentrations. CALP2 potently inhibits of adhesion and degranulation. CALP2 is also a strong activator of alveolar macrophages. -
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RU 45144
0 ImagesCat. No.: HY-118242CAS No.: 119286-92-9RU 45144 is an anti-estrogen compound that has the activity of antagonizing the binding of estrogen receptors to calmodulin. RU 45144 can inhibit the binding of estrogen receptors to calmodulin, and its effect is similar to that of tamoxifen. Its anti-estrogen effect may be related to specific side chains in the molecular structure, and the steroid skeleton may be involved in its anti-proliferative activity. -
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- (S)-O-Methylencecalinol
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Encecalinol
0 ImagesCat. No.: HY-N12405CAS No.: 88728-56-7Encecalinol, extracted from aerial parts of Ageratina grandifolia, is a potent inhibitor of calmodulin inhibitor. -
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Cloxacepride
0 ImagesCat. No.: HY-106645CAS No.: 65569-29-1Cloxacepride is an orally active and potent antiallergic agent. Cloxacepride is a CaM (calmodulin) antagonist. Cloxacepride has anti-PCA (passive cutaneous anaphylaxis) activity. -
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- RyR1(3614-3643)
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Calmodulin-Dependent Protein Kinase II (281-309)
0 ImagesCat. No.: HY-P1874CAS No.: 116826-37-0Calmodulin-Dependent Protein Kinase II (281-309) is a peptide of calcium/calmodulin-dependent protein kinase II (CaM-kinase II). -
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CV-159
0 ImagesCat. No.: HY-19025CAS No.: 86384-98-7CV-159 is a unique dihydropyridine Ca2+ antagonist with an anti-calmodulin (CaM) action, and has antiinflammatory activities. -
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