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Isradipine - >98.0%(HPLC), high purity , CAS No.75695-93-1, Gating inhibitor of Ca v1.2;Gating inhibitor of Ca v1.3;Gating inhibitor of Ca v1.4

Specifications & Purity:  >98.0%(HPLC)
Item Number
I157715
Grouped product items
SKUSizeAvailabilityPrice Qty
I157715-5mg
5mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$26.90
I157715-25mg
25mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$110.90
I157715-100mg
100mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$367.90
I157715-250mg
250mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$828.90

L-type Ca 2+ channel blocker

Basic Description

Synonymsisradipine|75695-93-1|DynaCirc|Isradipin|Prescal|Lomir|Isrodipine|Dynacirc CR|Esradin|Clivoten|PN 200-110|Dynacrine|Isradipinum [Latin]|Isradipino [Spanish]|PN-200-110|Isradipino|Isradipinum|Rebriden|(+-)-Isradipine|DynaCire|DynaCire CR|PN 200|(+/-)-Israd
Specifications & Purity>98.0%(HPLC)
Storage TempStore at -20°C
Shipped InDry ice
Action TypeGATING INHIBITOR
Mechanism of actionGating inhibitor of Ca v1.2;Gating inhibitor of Ca v1.3;Gating inhibitor of Ca v1.4

Associated Targets

CACNA1C Tclin Voltage-dependent L-type calcium channel subunit alpha-1C 4 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CACNA1D Tclin Voltage-dependent L-type calcium channel subunit alpha-1D 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CACNA1F Tchem Voltage-dependent L-type calcium channel subunit alpha-1F 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 3-O-methyl 5-O-propan-2-yl 4-(2,1,3-benzoxadiazol-4-yl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
INCHI InChI=1S/C19H21N3O5/c1-9(2)26-19(24)15-11(4)20-10(3)14(18(23)25-5)16(15)12-7-6-8-13-17(12)22-27-21-13/h6-9,16,20H,1-5H3
InChi Key HMJIYCCIJYRONP-UHFFFAOYSA-N
Canonical SMILES CC1=C(C(C(=C(N1)C)C(=O)OC(C)C)C2=CC=CC3=NON=C32)C(=O)OC
Isomeric SMILES CC1=C(C(C(=C(N1)C)C(=O)OC(C)C)C2=CC=CC3=NON=C32)C(=O)OC
WGK Germany 3
PubChem CID 3784
Molecular Weight 371.39

Certificates

Certificate of Analysis(COA)

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1 results found

Lot NumberCertificate TypeDateItem
F1927090Certificate of AnalysisApr 13, 2023 I157715

Chemical and Physical Properties

SensitivityHeat sensitive
Melt Point(°C)169 °C

Safety and Hazards(GHS)

Pictogram(s) GHS06,GHS08,GHS09,GHS07
Signal Danger
Hazard Statements H319,H301,H400,H410,H372
Precautionary Statements P305+P351+P338,P273,P280,P321,P405,P501,P264,P260,P270,P391,P330,P264+P265,P301+P316,P337+P317,P319
WGK Germany 3
Merck Index 5240

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References

1. Jurkovicová-Tarabová B et al..  (2012)  Repertoire of high voltage-activated Ca2+ channels in the lateral superior olive: functional analysis in wild-type, Ca(v)1.3(-/-), and Ca(v)1.2DHP(-/-) mice..  J Neurophysiol,  108  (2): (365-79).  [PMID:22539826]
2. Díaz-García CM et al..  (2021)  The distinct roles of calcium in rapid control of neuronal glycolysis and the tricarboxylic acid cycle..  Elife,  10    [PMID:33555254]
3. Meyer DJ et al..  (2022)  The Na+/K+ pump dominates control of glycolysis in hippocampal dentate granule cells..  Elife,  11    [PMID:36222651]

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