2-Hydroxysaclofen - Moligand™, ≥95% , Antagonist of GABA B1;Antagonist of GABA B receptor, CAS No.117354-64-0, Antagonist of GABA B1;Antagonist of GABA B receptor

CAS: 117354-64-0 Cat. No.: H286964 Peso molecular: 265.71 Número EC: 634-206-2
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. ≥95%
Synonyms
2-OH-Saclofen | 3-amino-2-(4-chlorophenyl)-2-hydroxypropane-1-sulfonic acid | 2-Hydroxy-saclofen | (RS)-3-Amino-2-(4-chlorophenyl)-2-hydroxypropyl-sulfonic acid | 3-Amino-2-(4-chlorophenyl)-2-hydroxypropanesulfonic acid
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1mg
H286964-1mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
105,90US$
5mg
H286964-5mg
1
377,90US$
10mg
H286964-10mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
599,90US$
25mg
H286964-25mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
1.199,90US$
50mg
H286964-50mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
1.919,90US$
100mg
H286964-100mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
3.079,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, ≥95% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal 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.

Descripción general

2-Hydroxysaclofen is a potent γ-amino-butyric-acid-B (GABAB) receptor antagonist. 2-Hydroxysaclofen can abolish nicotine-induced hypolocomotor effects and increases the antinociceptive effects. 2-Hydroxysaclofen can stimulate luteinizing hormone (LH) secretion in female rats.

Specifications

Sinónimos
2-OH-Saclofen | 3-amino-2-(4-chlorophenyl)-2-hydroxypropane-1-sulfonic acid | 2-Hydroxy-saclofen | (RS)-3-Amino-2-(4-chlorophenyl)-2-hydroxypropyl-sulfonic acid | 3-Amino-2-(4-chlorophenyl)-2-hydroxypropanesulfonic acid
Especificaciones y pureza
Moligand™, ≥95%
Mecanismos bioquímicos y fisiológicos
Selective antagonist at GABABreceptors.
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Grado
Moligand™
Tipo de acción
ANTAGONIST
Mecanismo de acción
Antagonist of GABA B1;Antagonist of GABA B receptor
Pureza
≥95%
Nombres e identificadores
Sonrisas canónicasC1=CC(=CC=C1C(CN)(CS(=O)(=O)O)O)Cl
IUPAC Name3-amino-2-(4-chlorophenyl)-2-hydroxypropane-1-sulfonic acid
InChIKeyWBSMZVIMANOCNX-UHFFFAOYSA-N
INCHI1S/C9H12ClNO4S/c10-8-3-1-7(2-4-8)9(12,5-11)6-16(13,14)15/h1-4,12H,5-6,11H2,(H,13,14,15)
Isómeros SMILES C1=CC(=CC=C1C(CN)(CS(=O)(=O)O)O)Cl
Peso molecular 265.71
Reaxy-Rn 3593140
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3593140&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

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassHalobenzenes
Intermediate Tree Nodes Not available
Direct ParentChlorobenzenes
Alternative Parents Aralkylamines  Aryl chlorides  Tertiary alcohols  Sulfonyls  Organosulfonic acids  Alkanesulfonic acids  1,2-aminoalcohols  Organopnictogen compounds  Organochlorides  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Aromatic alcohols  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Chlorobenzene - Aralkylamine - Aryl chloride - Aryl halide - Organic sulfonic acid or derivatives - Alkanesulfonic acid - Organosulfonic acid or derivatives - Tertiary alcohol - Sulfonyl - Organosulfonic acid - 1,2-aminoalcohol - Organic nitrogen compound - Aromatic alcohol - Hydrocarbon derivative - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Primary aliphatic amine - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Alcohol - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as chlorobenzenes. These are compounds containing one or more chlorine atoms attached to a benzene moiety.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
KCTD8 Tbio BTB/POZ domain-containing protein KCTD8 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GABBR2 Tclin Gamma-aminobutyric acid type B receptor subunit 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GABBR1 Tclin Gamma-aminobutyric acid type B receptor subunit 1 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCTD12 Tchem BTB/POZ domain-containing protein KCTD12 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCTD16 Tbio BTB/POZ domain-containing protein KCTD16 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BLM Tchem Bloom syndrome protein (4248 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MPHOSPH8 Tbio M-phase phosphoprotein 8 (656 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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.

5 results found

Lot NumberCertificate TypeFechaArticulo
F2503364Certificate of AnalysisNov 04, 2024 H286964
F2503366Certificate of AnalysisNov 04, 2024 H286964
F2503367Certificate of AnalysisNov 04, 2024 H286964
F2503368Certificate of AnalysisNov 04, 2024 H286964
F2503369Certificate of AnalysisNov 04, 2024 H286964
Propiedades químicas y físicas
SolubilidadSolvent:water, Max Conc. mg/mL: None, Max Conc. mM: 5; Solvent:1eq. NaOH, Max Conc. mg/mL: None, Max Conc. mM: 100
Peso molecular265.710 g/mol
XLogP3-2.800
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass265.018 Da
Monoisotopic Mass265.018 Da
Topological Polar Surface Area109.000 Ų
Heavy Atom Count16
Formal Charge0
Complexity321.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluciones
Reseñas

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