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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items THDOC - Moligand™, ≥95%(HPLC) , CAS No.567-02-2
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%(HPLC) Synonyms
3beta,21-Dihydroxy-5alpha-pregnan-20-one | Allotetrahydrocortexone | deoxycorticosterone-21-aminopropane | HY-123489 | A8Z | BRD-K36764776-001-01-4 | 21-Hydroxyallopregnanolone | EINECS 209-300-8 | (3?,5?)-3,21-Dihydroxypregnan-20-one | Aradinum | NSC 113
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™, ≥95%(HPLC) Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads 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.
Specifications Sinónimos
3beta, 21-Dihydroxy-5alpha-pregnan-20-one | Allotetrahydrocortexone | deoxycorticosterone-21-aminopropane | HY-123489 | A8Z | BRD-K36764776-001-01-4 | 21-Hydroxyallopregnanolone | EINECS 209-300-8 | (3?, 5?)-3, 21-Dihydroxypregnan-20-one | Aradinum | NSC 113
Especificaciones y pureza
Moligand™, ≥95%(HPLC)
Mecanismos bioquímicos y fisiológicos
Positive modulator of GABAAreceptors. Potentiates neuronal response to low concentrations of GABA at α4β1δ GABAAreceptorsin vitro. Endogenous neurosteroid.
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Sonrisas canónicas CC12CCC(CC1CCC3C2CCC4(C3CCC4C(=O)CO)C)O IUPAC Name 2-hydroxy-1-[(3R,5S,8R,9S,10S,13S,14S,17S)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone InChIKey CYKYBWRSLLXBOW-GDYGHMJCSA-N INCHI 1S/C21H34O3/c1-20-9-7-14(23)11-13(20)3-4-15-16-5-6-18(19(24)12-22)21(16,2)10-8-17(15)20/h13-18,22-23H,3-12H2,1-2H3/t13-,14+,15-,16-,17-,18+,20-,21-/m0/s1 Isómeros SMILES C[C@]12CC[C@H](C[C@@H]1CC[C@@H]3[C@@H]2CC[C@]4([C@H]3CC[C@@H]4C(=O)CO)C)O WGK Alemania 3 Peso molecular 334.49 Reaxy-Rn 3391514 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3391514&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 Lipids and lipid-like molecules Clase Steroids and steroid derivatives Subclass Hydroxysteroids Intermediate Tree Nodes Not available Direct Parent 21-hydroxysteroids Alternative Parents Gluco/mineralocorticoids, progestogins and derivatives 20-oxosteroids 3-alpha-hydroxysteroids Alpha-hydroxy ketones Secondary alcohols Cyclic alcohols and derivatives Primary alcohols Organic oxides Hydrocarbon derivatives Molecular Framework Aliphatic homopolycyclic compounds Substituents Progestogin-skeleton - 21-hydroxysteroid - Pregnane-skeleton - 20-oxosteroid - 3-hydroxysteroid - 3-alpha-hydroxysteroid - Oxosteroid - Alpha-hydroxy ketone - Cyclic alcohol - Secondary alcohol - Ketone - Organic oxygen compound - Organooxygen compound - Primary alcohol - Hydrocarbon derivative - Carbonyl group - Organic oxide - Alcohol - Aliphatic homopolycyclic compound Descripción This compound belongs to the class of organic compounds known as 21-hydroxysteroids. These are steroids carrying a hydroxyl group at the 21-position of the steroid backbone. External Descriptors Glycine conjugates 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 Solubilidad Solvent:DMSO, Max Conc. mg/mL: 33.45, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 33.45, Max Conc. mM: 100 Peso molecular 334.500 g/mol XLogP3 4.200 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 2 Exact Mass 334.251 Da Monoisotopic Mass 334.251 Da Topological Polar Surface Area 57.500 Ų Heavy Atom Count 24 Formal Charge 0 Complexity 517.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 8 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
Calculadoras de soluciones Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
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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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