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224,000+ productos de investigación · Triple ISO certified · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 5-Hydroxyindole - Moligand™, ≥98% , Allosteric modulator of 5-HT 3A, CAS No.1953-54-4, Allosteric modulator of 5-HT 3A
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
5-hydroxy indole | AC-5464 | DTXSID00173187 | EN300-79057 | Hydroxy-5 indole [French] | SCHEMBL50566 | H-6044 | AKOS005206937 | 1h-indole-5-ol | 1H-indol-5-ol. | 3fuh | UNII-320UN7XZYN | (R)-(+)-7-Methoxy2-aminotetralin | 5-21-03-00018 (Beilstein Handboo
Storage
Store at 2-8°C,Protected from light,Argon charged
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Why this grade Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Protected from light,Argon charged Ships Wet ice 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 Reactants for the preparation of antitumor agents (oximidazolyl / oxpyrimidinyl) benzenesulfonate and tubulin inhibitors
Reactants for preparation of o-aminobenzoic acid
It is used to prepare indole compounds as reactants of dopamine D2 receptor antagonists
Reactants for preparation of human β - adrenoceptor ligands containing naphthalimide or carbazole
Reactants for preparation of natural radiation protective agent melanin
Reactants for the preparation of 5-vinyl-3-pyridinonitrile, a PKC θ inhibitor
Specifications Sinónimos
5-hydroxy indole | AC-5464 | DTXSID00173187 | EN300-79057 | Hydroxy-5 indole [French] | SCHEMBL50566 | H-6044 | AKOS005206937 | 1h-indole-5-ol | 1H-indol-5-ol. | 3fuh | UNII-320UN7XZYN | (R)-(+)-7-Methoxy2-aminotetralin | 5-21-03-00018 (Beilstein Handboo
Especificaciones y pureza
Moligand™, ≥98%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Protected from light, Argon charged
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
ALLOSTERIC MODULATOR
Mecanismo de acción
Allosteric modulator of 5-HT 3A
Nombres e identificadores Pubchem Sid 504752730 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504752730 Sonrisas canónicas C1=CC2=C(C=CN2)C=C1O IUPAC Name 1H-indol-5-ol InChIKey LMIQERWZRIFWNZ-UHFFFAOYSA-N INCHI 1S/C8H7NO/c10-7-1-2-8-6(5-7)3-4-9-8/h1-5,9-10H Isómeros SMILES C1=CC2=C(C=CN2)C=C1O WGK Alemania 3 RTECS NM2430000 Peso molecular 133.15 Beilstein 112349 Reaxy-Rn 112349 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=112349&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 Clase Indoles and derivatives Subclass Hydroxyindoles Intermediate Tree Nodes Not available Direct Parent Hydroxyindoles Alternative Parents Indoles 1-hydroxy-2-unsubstituted benzenoids Pyrroles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Hydroxyindole - Indole - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as hydroxyindoles. These are organic compounds containing an indole moiety that carries a hydroxyl 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Sensibilidad Air sensitive ,Light sensitive Punto de fusión (°C) 107-110°C Peso molecular 133.150 g/mol XLogP3 2.000 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 0 Exact Mass 133.053 Da Monoisotopic Mass 133.053 Da Topological Polar Surface Area 36.000 Ų Heavy Atom Count 10 Formal Charge 0 Complexity 126.000 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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Reconstitution Calculator Reseñas Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →
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