[³H](-)CGP 12177 - Moligand™ , Agonist of β 1-adrenoceptor;Antagonist of β 1-adrenoceptor, CAS No.H614072, Agonist of β 1-adrenoceptor;Antagonist of β 1-adrenoceptor

CAS: H614072 Cat. No.: H614072 PubChem CID: 6603756
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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.
Synonyms
Z7YP8B158Q|UNII-Z7YP8B158Q|CGP-12177, (S)-|CHEMBL36060|(-)-CGP 12177|[3H](-)CGP 12177|(S)-(-)-CGP-12177|CGP-12177A|2H-Benzimidazol-2-one, 4-((2S)-3-((1,1-dimethylethyl)amino)-2-hydroxypropoxy)-1,3-dihydro-|95840-76-9|Tocris-1134|Lopac-C-125|GTPL531|SCHEMB
Storage
Room temperature
★
Size
Deutschland (EU)
USA*
Price
Qty
5mg
H614072-5mg
Auf Bestellung · 8–12 Wochen
694,10€
25mg
H614072-25mg
Auf Bestellung · 8–12 Wochen
1.488,09€
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships 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.

Specifications

Synonyme
Z7YP8B158Q | UNII-Z7YP8B158Q | CGP-12177, (S)- | CHEMBL36060 | (-)-CGP 12177 | [3H](-)CGP 12177 | (S)-(-)-CGP-12177 | CGP-12177A | 2H-Benzimidazol-2-one, 4-((2S)-3-((1,1-dimethylethyl)amino)-2-hydroxypropoxy)-1,3-dihydro- | 95840-76-9 | Tocris-1134 | Lopac-C-125 | GTPL531 | SCHEMB
Spezifikationen & Reinheit
Moligand™
Storage
Room temperature
Note
Moligand™
Aktionsart
AGONIST, ANTAGONIST
Mechanismus der Wirkung
Agonist of β 1-adrenoceptor;Antagonist of β 1-adrenoceptor
Namen und Kennungen
Kanonisches Lächeln
O[C@H](COc1cccc2c1[nH]c(=O)[nH]2)CNC(C)(C)C
IUPAC Name
4-[(2S)-3-(tert-butylamino)-2-hydroxypropoxy]-1,3-dihydrobenzimidazol-2-one
InChIKey
UMQUQWCJKFOUGV-VIFPVBQESA-N
INCHI
1S/C14H21N3O3/c1-14(2,3)15-7-9(18)8-20-11-6-4-5-10-12(11)17-13(19)16-10/h4-6,9,15,18H,7-8H2,1-3H3,(H2,16,17,19)/t9-/m0/s1
Isomere SMILES
CC(C)(C)NC[C@@H](COC1=CC=CC2=C1NC(=O)N2)O
PubChem CID
6603756

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
SuperclassOrganoheterocyclic compounds
KlasseBenzimidazoles
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzimidazoles
Alternative Parents Phenol ethers  Alkyl aryl ethers  Imidazoles  Heteroaromatic compounds  Ureas  Secondary alcohols  1,2-aminoalcohols  Dialkylamines  Azacyclic compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Benzimidazole - Phenol ether - Alkyl aryl ether - Benzenoid - Azole - Imidazole - Heteroaromatic compound - Urea - Secondary alcohol - 1,2-aminoalcohol - Secondary amine - Ether - Secondary aliphatic amine - Azacycle - Organic oxide - Organooxygen compound - Organonitrogen compound - Alcohol - Organic oxygen compound - Amine - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteropolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as benzimidazoles. These are organic compounds containing a benzene ring fused to an imidazole ring (five member ring containing a nitrogen atom, 4 carbon atoms, and two double bonds).
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
ADRB2 Tclin Beta-2 adrenergic receptor (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ADRB1 Tclin Beta-1 adrenergic receptor (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Zugehörige Ziele (nicht menschlich)
lef Anthrax lethal factor (7585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Lösungsrechner
Bewertungen

Kundenbewertungen

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