Mibefradil dihydrochloride - Moligand™, ≥98% , Voltage-gated T-type calcium channel blocker, CAS No.116666-63-8, Voltage-gated T-type calcium channel blocker

CAS: 116666-63-8 Cat. No.: M275143 Peso molecular: 568.56 Número EC: 848-218-2 PubChem CID: 60662
Disponible para pedir
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
HY-15553A | Mibefradil hydrochloride | FD5011 | RO 40-5967/001 | MIBEFRADIL DIHYDROCHLORIDE [MI] | MIBEFRADIL HYDROCHLORIDE [WHO-DD] | UNII-842TUP3PQ8 | [(1S,2S)-2-[2-[3-(1H-benzimidazol-2-yl)propyl-methyl-amino]ethyl]-6-fluoro-1-isopropyl-tetralin-2-yl]
Storage
Store at -20°C,Argon charged,Desiccated
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1mg
M275143-1mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
99,90US$
5mg
M275143-5mg
7
249,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C,Argon charged,Desiccated Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Mibefradil dihydrochloride (Ro 40-5967 dihydrochloride) is a calcium channel blocker with moderate selectivity for T-type Ca2+ channels (IC50s of 2.7 μM and 18.6 μM for T-type and L-type currents, respectively)

Specifications

Sinónimos
HY-15553A | Mibefradil hydrochloride | FD5011 | RO 40-5967/001 | MIBEFRADIL DIHYDROCHLORIDE [MI] | MIBEFRADIL HYDROCHLORIDE [WHO-DD] | UNII-842TUP3PQ8 | [(1S, 2S)-2-[2-[3-(1H-benzimidazol-2-yl)propyl-methyl-amino]ethyl]-6-fluoro-1-isopropyl-tetralin-2-yl]
Especificaciones y pureza
Moligand™, ≥98%
Mecanismos bioquímicos y fisiológicos
Ca 2+ channel blocker. Shows moderate selectivity for T-type channels (IC 50 values are 2.7 and 18.6 μM for T-type and L-type respectively). Shows antihypertensive effects in vivo. Orally active.
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Argon charged, Desiccated
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Grado
Moligand™
Tipo de acción
BLOCKER
Mecanismo de acción
Voltage-gated T-type calcium channel blocker
Nota
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.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504753713
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504753713
Sonrisas canónicasCC(C)C1C2=C(CCC1(CCN(C)CCCC3=NC4=CC=CC=C4N3)OC(=O)COC)C=C(C=C2)F.Cl.Cl
IUPAC Name[(1S,2S)-2-[2-[3-(1H-benzimidazol-2-yl)propyl-methylamino]ethyl]-6-fluoro-1-propan-2-yl-3,4-dihydro-1H-naphthalen-2-yl] 2-methoxyacetate;dihydrochloride
InChIKeyMTJLQTFHJIHXIX-GDUXWEAWSA-N
INCHI1S/C29H38FN3O3.2ClH/c1-20(2)28-23-12-11-22(30)18-21(23)13-14-29(28,36-27(34)19-35-4)15-17-33(3)16-7-10-26-31-24-8-5-6-9-25(24)32-26;;/h5-6,8-9,11-12,18,20,28H,7,10,13-17,19H2,1-4H3,(H,31,32);2*1H/t28-,29-;;/m0../s1
Isómeros SMILES CC(C)[C@H]1C2=C(CC[C@@]1(CCN(C)CCCC3=NC4=CC=CC=C4N3)OC(=O)COC)C=C(C=C2)F.Cl.Cl
PubChem CID 60662
Peso molecular 568.56

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseTetralins
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentTetralins
Alternative Parents Benzimidazoles  Aralkylamines  Aryl fluorides  Heteroaromatic compounds  Imidazoles  Trialkylamines  Amino acids and derivatives  Carboxylic acid esters  Dialkyl ethers  Azacyclic compounds  Monocarboxylic acids and derivatives  Hydrochlorides  Hydrocarbon derivatives  Carbonyl compounds  Organofluorides  Organopnictogen compounds  Organic oxides  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Tetralin - Benzimidazole - Aralkylamine - Aryl fluoride - Aryl halide - Azole - Heteroaromatic compound - Imidazole - Tertiary aliphatic amine - Amino acid or derivatives - Tertiary amine - Carboxylic acid ester - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Dialkyl ether - Ether - Amine - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Hydrochloride - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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Objetivos asociados (no humanos)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Kcnk9 Potassium channel subfamily K member 9 (8 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Npsr1 Neuropeptide S receptor (260 Activities)
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rep Replicase polyprotein 1ab (378 Activities)
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Rorc Nuclear receptor ROR-gamma (89407 Activities)
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ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
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FTL Ferritin light chain (43324 Activities)
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nfo Endonuclease 4 (425 Activities)
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Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

6 results found

Lot NumberCertificate TypeFechaArticulo
A2613150Certificate of AnalysisJan 17, 2026 M275143
D2508052Certificate of AnalysisApr 11, 2025 M275143
F23271036Certificate of AnalysisFeb 11, 2025 M275143
F2327695Certificate of AnalysisFeb 11, 2025 M275143
F2327680Certificate of AnalysisJan 13, 2025 M275143
F2327689Certificate of AnalysisJan 13, 2025 M275143
Propiedades químicas y físicas
SolubilidadSoluble in\xa0water to\xa050 mM
SensibilidadMoisture sensitive
Peso molecular568.500 g/mol
XLogP3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count6
Rotatable Bond Count12
Exact Mass567.243 Da
Monoisotopic Mass567.243 Da
Topological Polar Surface Area67.500 Ų
Heavy Atom Count38
Formal Charge0
Complexity709.000
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
Calculadoras de soluciones
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