Determine the necessary mass, volume, or concentration for preparing a solution.
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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C133629-1g | 1g | In stock | $9.90 | |
C133629-5g | 5g | In stock | $28.90 | |
C133629-10g | 10g | In stock | $43.90 | |
C133629-50g | 50g | In stock | $127.90 |
Calcium channel antagonist
Synonyms | Artate | BPBio1_000172 | Cinnarizinum | Votegol | (E)-1-Benzhydryl-4-cinnamylpiperazine | cinnarizine | Folcodal | R 1575 | 516 MD | Aplexal | CINNARIZINE [MART.] | Sedatromin | Lopac0_000314 | Siptazin | UNII-3DI2E1X18L | DTXCID802821 | R-1575 | BSPBio_0 |
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Specifications & Purity | Moligand™, ≥98%(HPLC)(T) |
Biochemical and Physiological Mechanisms | Selective antagonist of T-type voltage-operated calcium ion channels. Antihistaminergic, antiserotoninergic and antidopaminergic effects in vitro . |
Shipped In | Normal |
Grade | Moligand™ |
Action Type | ANTAGONIST, BLOCKER, CHANNEL BLOCKER |
Mechanism of action | Histamine H1 receptor antagonist |
Note | Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Pubchem Sid | 488191943 |
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Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488191943 |
IUPAC Name | 1-benzhydryl-4-[(E)-3-phenylprop-2-enyl]piperazine |
INCHI | InChI=1S/C26H28N2/c1-4-11-23(12-5-1)13-10-18-27-19-21-28(22-20-27)26(24-14-6-2-7-15-24)25-16-8-3-9-17-25/h1-17,26H,18-22H2/b13-10+ |
InChi Key | DERZBLKQOCDDDZ-JLHYYAGUSA-N |
Canonical SMILES | C1CN(CCN1CC=CC2=CC=CC=C2)C(C3=CC=CC=C3)C4=CC=CC=C4 |
Isomeric SMILES | C1CN(CCN1C/C=C/C2=CC=CC=C2)C(C3=CC=CC=C3)C4=CC=CC=C4 |
WGK Germany | 2 |
RTECS | TL3430000 |
PubChem CID | 1547484 |
Molecular Weight | 368.51 |
PubChem CID | 1547484 |
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CAS Registry No. | 298-57-7 |
ChEMBL Ligand | CHEMBL43064 |
DrugBank Ligand | DB00568 |
BindingDB Ligand | 50017657 |
PEP | cinnarizine |
DrugCentral Ligand | 654 |
RCSB PDB Ligand | N90 |
PubChem SID | 488191943 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
---|---|---|---|
K2229358 | Certificate of Analysis | Sep 18, 2024 | C133629 |
K2229384 | Certificate of Analysis | Sep 18, 2024 | C133629 |
K2229385 | Certificate of Analysis | Sep 18, 2024 | C133629 |
K2229373 | Certificate of Analysis | Jul 12, 2024 | C133629 |
C23281059 | Certificate of Analysis | Nov 10, 2022 | C133629 |
C23281060 | Certificate of Analysis | Sep 13, 2022 | C133629 |
L1828013 | Certificate of Analysis | Sep 13, 2022 | C133629 |
L1828014 | Certificate of Analysis | Sep 13, 2022 | C133629 |
H2026253 | Certificate of Analysis | Jul 11, 2022 | C133629 |
Solubility | Solubility in water: Practically insoluble |
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Sensitivity | Heat Sensitive |
Melt Point(°C) | 119 °C |
1. Teive HA, Troiano AR, Germiniani FM, Werneck LC. (2004) Flunarizine and cinnarizine-induced parkinsonism: a historical and clinical analysis.. Parkinsonism Relat Disord, 10 (4): (243-5). [PMID:15120099] [10.1021/op500134e] |
2. Capellà D, Laporte JR, Castel JM, Tristán C, Cos A, Morales-Olivas FJ. (1988) Parkinsonism, tremor, and depression induced by cinnarizine and flunarizine.. BMJ, 297 (6650): (722-3). [PMID:3147743] [10.1021/op500134e] |
3. Kariya S, Isozaki S, Masubuchi Y, Suzuki T, Narimatsu S. (1995) Possible pharmacokinetic and pharmacodynamic factors affecting parkinsonism inducement by cinnarizine and flunarizine.. Biochem Pharmacol, 50 (10): (1645-50). [PMID:7503767] [10.1021/op500134e] |