We have 36 products in: Biochemicals >> Research Area >> Diabetes >> Signaling >> Ca2+ signaling

Ca2+ signaling

Code

Name

Details

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A23187 (Calcimycin) 

Ca2+ ionophore

Purity: > 98%

 
 
 
 
  

ω-Agatoxin IVA 

Ca2+ channel blocker (P and Q type)

Purity: > 95%

 
Specific publication references
 
 
 
  

Amiodarone hydrochloride 

Broad-spectrum ion channel blocker. Antiarrhythmic agent.

Purity: > 98%

 
 
 
 
  

2-APB 

Ca2+ release modulator

Purity: > 98%

 
 
 
 
  

BAPTA-AM 

Selective Ca2+ chelator. Analogue of BAPTA.

Purity: > 98%

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BAPTA sodium salt 

Selective Ca2+ chelator

Purity: > 98%

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CGP 37157 

Na+-Ca2+ exchange inhibitor

Purity: > 99%

 
Specific publication references
 
 
 
  

ω-Conotoxin GVIA 

Ca2+ channel blocker (N type)

Purity: > 96%

 
Specific publication references
 
 
 
  

ω-Conotoxin MVIIC 

Ca2+ channel blocker (P and Q-type)

Purity: > 95%

 
Specific publication references
 
 
 
  

Cyclopiazonic acid from Penicillium grisefulvum 

Ca2+-ATPase inhibitor

Purity: > 99%

 
Specific publication references
 
 
 
  

D890 

Intracellular Ca2+ channel blocker

Purity: > 99%

 
 
 
 
  

Diltiazem 

L-type Ca2+ channel antagonist

Purity: > 99%

 
 
 
 
  

Fura-2 AM (Fura-2 acetoxymethyl ester) 

Selective Ca2+ chelator; fluorescent indicator

Purity: > 95%

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Gabapentin 

α2δ ligand

Purity: > 99%

 
 
 
 
  

Ionomycin (free acid) 

Ca2+ ionophore

Purity: > 99%

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Specific publication references
 
 
 
  

Ionomycin Ca2+ Salt 

Ca2+ ionophore

Purity: > 99%

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Specific publication references
 
 
 
  

Isradipine 

L-type Ca2+ channel blocker

Purity: > 98%

 
 
 
 
  

K252a 

Highly potent inhibitor of protein and CAM kinases

Purity: > 99%

 
 
 
 
  

KB-R7943 

NCX inhibitor. TRPC blocker.

Purity: > 99%

 
 
 
 
  

KN-62 

CaM kinase II inhibitor. P2X7 antagonist.

Purity: > 98%

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KN-93 (water soluble) 

Potent, specific CaMK II inhibitor

Purity: > 99%

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Monastrol 

Potent and cell permeable mitosis inhibitor. Kinesin Eg5 inhibitor.

Purity: > 99%

 
 
 
 
  

Nicardipine hydrochloride 

L-type Ca2+ channel antagonist

Purity: > 99%

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Nifedipine 

L-type Ca2+ channel blocker

Purity: > 99%

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Specific publication references
 
 
 
  

Nimodipine 

L-type Ca2+ channel blocker

Purity: > 98%

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Specific publication references
 
 
 
  

Nitrendipine 

L-type Ca2+ channel blocker

Purity: > 98%

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Ruthenium red 

Calcium signalling inhibitor

 
Specific publication references
 
 
 
  

Ryanodine 

Ca2+ release modulator

Purity: > 98%

 
Specific publication references
 
 
 
  

SKF 96365 

Blocker of TRP cation channels. Inhibits capacitative Ca2+ entry.

Purity: > 99%

 
Specific publication references
 
 
 
  

SNX 482 

R-Type Ca2+ (Cav2.3) channel blocker

Purity: > 96%

 
Specific publication references
 
 
 
  

tBuBHQ (BHQ) 

Sarco-endoplasmic reticulum Ca2+-ATPase (SERCA) inhibitor

Purity: > 99%

 
 
 
 
  

Thapsigargin 

Ca2+-ATPase inhibitor

Purity: > 98%

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Specific publication references
 
 
 
  

Trifluoperazine dihydrochloride 

Cell permeable calmodulin antagonist

Purity: > 99%

 
 
 
 
  

Verapamil hydrochloride 

L-type Ca2+ channel blocker

Purity: > 99%

 
Specific publication references
 
 
 
  

Xestospongin C 

Potent, selective, reversible IP3 receptor antagonist

Purity: > 90%

 
 
 
 
  

Zonisamide 

Non-selective Na+ / Ca2+channel blocker

Purity: > 99%