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Calcium Channel

A calcium channel is an ion channel which shows selective permeability to calcium ions. It is sometimes synonymous with voltage-gated calcium channel, although there are also ligand-gated calcium channels.
Signaling Pathways | Target | TargetMol
Cat. No. Product name CAS No. Purity Chemical Structure
T5457 SN 6 415697-08-4 98%
SN 6
SN 6 (SN6) is a selective Na+/Ca2+ exchanger (NCX) inhibitor (IC50s of NCX1: 2.9 μM , NCX2: 16 μM ,NCX3: 8.6 μM)
T7540 2,5-Di-tert-butylhydroquinone 88-58-4 98%
2,5-Di-tert-butylhydroquinone
2,5-Di-tert-butylhydroquinone (BHQ) is an effective and selective endoplasmic reticulum Ca2+-ATPase inhibitor.
T10884 CRAC intermediate 1 1249343-86-9 97.92%
CRAC intermediate 1
CRAC intermediate 1 (5-(S)-Fluorowillardiine) is a key intermediate in the chemical synthesis of a series of CRAC channel inhibitors.
TN2078 Pinocembrin chalcone 4197-97-1 97.82%
Pinocembrin chalcone
Pinocembrin chalcone is an inhibitor of tyrosinase with antimutagenic effects. Pinocembrin chalcone can be used in studies about the prevention of gastric ulcers...
T22788 FPL64176 120934-96-5 97.78%
FPL64176
FPL64176 is a L-type calcium channels activator.
T12385 PD0176078 248922-46-5 97.76%
PD0176078
PD0176078 () is a newly blocker of N-type Calcium channel.
T6856 Halofuginone 55837-20-2 97.67%
Halofuginone
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 ...
T34782 Tamolarizine 93035-32-6 97.46%
Tamolarizine
Tamolarizine (Tamolarizine free base) free base is a novel calcium antagonist.
T8867 RO2959 Hydrochloride 1219927-22-6 97.42%
RO2959 Hydrochloride
RO2959 Hydrochloride (RO2959 HCl) is a potent and selective inhibitor of CRAC channel(IC50: 402 nM). It is also a potent inhibitor of human IL-2.
T25263 Clopimozide 53179-12-7 97.18%
Clopimozide
Clopimozide (R-29764) acts as a calcium channel antagonist and inhibits [3H] nilandipine binding.Clopimozide is a novel and orally available long-acting antischi...
T37705 1,2,4-Trihydroxybenzene 533-73-3 97.16%
1,2,4-Trihydroxybenzene
1,2,4-Trihydroxybenzene (Benzene-1,2,4-triol) is a by-product of coffee bean roasting and is found in mouse, arabica coffee.1,2,4-Trihydroxybenzene is a benzotri...
T15553 Iganidipine 119687-33-1 96.85%
Iganidipine
Iganidipine(NKY 722) is a new water-soluble Ca2+ antagonist with antihypertensive activity for research and neurological related diseases.
TP1911L CALP3 acetate(261969-05-5 free base) TP1911L 96.49%
CALP3 acetate(261969-05-5 free base)
CALP3 acetate is a potent Ca2+ channel blocker that activates EF hand motifs of Ca2+-binding proteins. CALP3 acetate can functionally mimic increased [Ca2+]i by ...
T6848 GSK1016790A 942206-85-1 96.25%
GSK1016790A
GSK1016790A (GSK101) (GSK101) is a novel, potent activator of TRPV4 (transient receptor potential vanilloid 4) with EC50 of 34 nM in choroid plexus epithelial ce...
T24984 5J-4 827001-82-1 96.12%
5J-4
5J-4 is a potent a blocker of calcium release-activated calcium (CRAC) channel and store-operated calcium entry (SOCE). 5J-4 reduces the production of IL-17 and ...
T10814 Cinacalcet metabolite M4 104774-87-0 95.28%
Cinacalcet metabolite M4
Cinacalcet metabolite M4 (Rarechem AL BW 1078) is a metabolite of Cinacalcet. Cinacalcet is an allosteric agonist of Ca receptor.
TN5073 Strophanthidin 66-28-4 93%
Strophanthidin
Strophanthidin (Strophanthidine) can induce calcium overload in vivo.
T1215 Nicardipine hydrochloride 54527-84-3 100%
Nicardipine hydrochloride
Nicardipine hydrochloride (YC-93 Hydrochloride) is the hydrochloride salt form of nicardipine, a synthetic derivative of nitrophenyl-pyridine and potent calcium ...
T1641 Strontium ranelate 135459-87-9 100%
Strontium ranelate
Strontium ranelate (S12911), a strontium (II) salt of the ranelic acid, is a medication for osteoporosis. Studies indicate it can also slow the course of osteoar...
T0207 Ranolazine dihydrochloride 95635-56-6 100%
Ranolazine dihydrochloride
Ranolazine dihydrochloride (Ranolazine 2HCl) , an antianginal agent, can treat arrhythmia via a novel mechanism of action (inhibition of the late phase of the in...
SN 6
T5457
SN 6 (SN6) is a selective Na+/Ca2+ exchanger (NCX) inhibitor (IC50s of NCX1: 2.9 μM , NCX2: 16 μM ,NCX3: 8.6 μM)
2,5-Di-tert-butylhydroquinone
T7540
2,5-Di-tert-butylhydroquinone (BHQ) is an effective and selective endoplasmic reticulum Ca2+-ATPase inhibitor.
CRAC intermediate 1
T10884
CRAC intermediate 1 (5-(S)-Fluorowillardiine) is a key intermediate in the chemical synthesis of a series of CRAC channel inhibitors.
Pinocembrin chalcone
TN2078
Pinocembrin chalcone is an inhibitor of tyrosinase with antimutagenic effects. Pinocembrin chalcone can be used in studies about the prevention of gastric ulcers...
FPL64176
T22788
FPL64176 is a L-type calcium channels activator.
PD0176078
T12385
PD0176078 () is a newly blocker of N-type Calcium channel.
Halofuginone
T6856
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 ...
Tamolarizine
T34782
Tamolarizine (Tamolarizine free base) free base is a novel calcium antagonist.
RO2959 Hydrochloride
T8867
RO2959 Hydrochloride (RO2959 HCl) is a potent and selective inhibitor of CRAC channel(IC50: 402 nM). It is also a potent inhibitor of human IL-2.
Clopimozide
T25263
Clopimozide (R-29764) acts as a calcium channel antagonist and inhibits [3H] nilandipine binding.Clopimozide is a novel and orally available long-acting antischi...
1,2,4-Trihydroxybenzene
T37705
1,2,4-Trihydroxybenzene (Benzene-1,2,4-triol) is a by-product of coffee bean roasting and is found in mouse, arabica coffee.1,2,4-Trihydroxybenzene is a benzotri...
Iganidipine
T15553
Iganidipine(NKY 722) is a new water-soluble Ca2+ antagonist with antihypertensive activity for research and neurological related diseases.
CALP3 acetate(261969-05-5 free base)
TP1911L
CALP3 acetate is a potent Ca2+ channel blocker that activates EF hand motifs of Ca2+-binding proteins. CALP3 acetate can functionally mimic increased [Ca2+]i by ...
GSK1016790A
T6848
GSK1016790A (GSK101) (GSK101) is a novel, potent activator of TRPV4 (transient receptor potential vanilloid 4) with EC50 of 34 nM in choroid plexus epithelial ce...
5J-4
T24984
5J-4 is a potent a blocker of calcium release-activated calcium (CRAC) channel and store-operated calcium entry (SOCE). 5J-4 reduces the production of IL-17 and ...
Cinacalcet metabolite M4
T10814
Cinacalcet metabolite M4 (Rarechem AL BW 1078) is a metabolite of Cinacalcet. Cinacalcet is an allosteric agonist of Ca receptor.
Strophanthidin
TN5073
Strophanthidin (Strophanthidine) can induce calcium overload in vivo.
Nicardipine hydrochloride
T1215
Nicardipine hydrochloride (YC-93 Hydrochloride) is the hydrochloride salt form of nicardipine, a synthetic derivative of nitrophenyl-pyridine and potent calcium ...
Strontium ranelate
T1641
Strontium ranelate (S12911), a strontium (II) salt of the ranelic acid, is a medication for osteoporosis. Studies indicate it can also slow the course of osteoar...
Ranolazine dihydrochloride
T0207
Ranolazine dihydrochloride (Ranolazine 2HCl) , an antianginal agent, can treat arrhythmia via a novel mechanism of action (inhibition of the late phase of the in...
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TargetMol