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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag auf Lager Lerisetron - 10mM in DMSO , CAS No.143257-98-1
GRADE & PURITY 10mM in DMSO
Synonyms
PWWDCRQZITYKDV-UHFFFAOYSA-N | Lerisetron [INN] | Q6528811 | 1-benzyl-2-piperazin-1-ylbenzimidazole. | BCP33052 | s2644 | UNII-Q36R82SXRG | Z2049693817 | 1-benzyl-2-(piperazin-1-yl)-1H-1,3-benzodiazole | EX-A7543 | L-175 | 1-Benzyl-2-(1-piperazinyl)benzimi
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Übersicht Information
Lerisetron (F 0930, F 0930RS) is a5-HT3 receptorantagonist with IC50 of 0.81μM.
Targets
5-HT3 receptor (Cell-free assay) 0.81 μM
Specifications Synonyme
PWWDCRQZITYKDV-UHFFFAOYSA-N | Lerisetron [INN] | Q6528811 | 1-benzyl-2-piperazin-1-ylbenzimidazole. | BCP33052 | s2644 | UNII-Q36R82SXRG | Z2049693817 | 1-benzyl-2-(piperazin-1-yl)-1H-1,3-benzodiazole | EX-A7543 | L-175 | 1-Benzyl-2-(1-piperazinyl)benzimi
Spezifikationen & Reinheit
10mM in DMSO
Biochemische und physiologische Mechanismen
Lerisetron (F 0930, F 0930RS) is a 5-HT3 receptor antagonist with IC50 of 0.81μM.
Verschickt in
Dry ice packs + Cold packs
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Produkteigenschaften ALogP 3.26 hba_count 1 HBD-Zahl 1 Rotationsfähige Bindung 3
Namen und Kennungen Pubchem Sid 528772131 Kanonisches Lächeln C1CN(CCN1)C2=NC3=CC=CC=C3N2CC4=CC=CC=C4 IUPAC Name 1-benzyl-2-piperazin-1-ylbenzimidazole InChIKey PWWDCRQZITYKDV-UHFFFAOYSA-N INCHI 1S/C18H20N4/c1-2-6-15(7-3-1)14-22-17-9-5-4-8-16(17)20-18(22)21-12-10-19-11-13-21/h1-9,19H,10-14H2 Isomere SMILES C1CN(CCN1)C2=NC3=CC=CC=C3N2CC4=CC=CC=C4 Molekulargewicht 292.38 Reaxy-Rn 7651816 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7651816&ln=
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 Kingdom Organic compounds Superclass Organoheterocyclic compounds Klasse Diazinanes Subclass Piperazines Intermediate Tree Nodes Not available Direct Parent N-arylpiperazines Alternative Parents Benzimidazoles Dialkylarylamines N-substituted imidazoles Benzene and substituted derivatives Aminoimidazoles Heteroaromatic compounds Dialkylamines Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents N-arylpiperazine - Benzimidazole - Dialkylarylamine - Aminoimidazole - Monocyclic benzene moiety - N-substituted imidazole - Benzenoid - Imidazole - Azole - Heteroaromatic compound - Secondary amine - Secondary aliphatic amine - Azacycle - Organopnictogen compound - Organonitrogen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Aromatic heteropolycyclic compound Beschreibung This compound belongs to the class of organic compounds known as n-arylpiperazines. These are organic compounds containing a piperazine ring where the nitrogen ring atom carries an aryl group. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften DMSO (mg/ml) Maximale Löslichkeit 58 DMSO (mM) Maximale Löslichkeit 198.371981667693 Wasser (mg/ml) Maximale Löslichkeit ＜1 Molekulargewicht 292.400 g/mol XLogP3 2.800 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 3 Exact Mass 292.169 Da Monoisotopic Mass 292.169 Da Topological Polar Surface Area 33.100 Ų Heavy Atom Count 22 Formal Charge 0 Complexity 349.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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