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· · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino LUF 6283 - Moligand™, ≥98% (HPLC) , Agonist of HCA 2 receptor, CAS No.92933-48-7, Agonist of HCA 2 receptor
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%(HPLC) Synonyms
acido 5-butil-2H-pirazolo-3-carbossilico | BDBM50220842 | AKOS000301963 | LUF6283;LUF-6283 | BBL030719 | ZJTXSGLJNBAMJS-UHFFFAOYSA-N | 3-butil-1H-pirazolo-5-carbossilico | VS-09994 | LUF 6283 | EN300-237993 | Acido 1H-pirazolo-3-carbossilico, 5-butil- | S
Storage
Conservare a 2-8°C
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Why this grade Moligand™, ≥98% (HPLC) Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Conservare a 2-8°C Ships Ghiaccio umido 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 Sinonimi
acido 5-butil-2H-pirazolo-3-carbossilico | BDBM50220842 | AKOS000301963 | LUF6283;LUF-6283 | BBL030719 | ZJTXSGLJNBAMJS-UHFFFAOYSA-N | 3-butil-1H-pirazolo-5-carbossilico | VS-09994 | LUF 6283 | EN300-237993 | Acido 1H-pirazolo-3-carbossilico, 5-butil- | S
Specifiche e purezza
Moligand™, ≥98% (HPLC)
Meccanismi biochimici e fisiologici
Agonista parziale del recettore 2 degli acidi idrossicarbossilici (HCA2) (Ki= 0,55μM). Si ritiene che riduca i livelli plasmatici di lipoproteine a bassissima densità (VLDL)-trigliceridi influenzando la produzione epatica di VLDL in topi C57BL/6 normolipi
Condizioni di conservazione di stoccaggio
Conservare a 2-8°C
Meccanismo d'azione
Agonist of HCA 2 receptor
Nomi e identificatori Pubchem Sid 528765310 Sorrisi canonici CCCCC1=CC(=NN1)C(=O)O IUPAC Name 5-butyl-1H-pyrazole-3-carboxylic acid InChIKey ZJTXSGLJNBAMJS-UHFFFAOYSA-N INCHI 1S/C8H12N2O2/c1-2-3-4-6-5-7(8(11)12)10-9-6/h5H,2-4H2,1H3,(H,9,10)(H,11,12) Isomeri SMILES CCCCC1=CC(=NN1)C(=O)O CAS alternativo 92933-48-7 Termini MeSH LUF6283 Peso molecolare 168.19 Reaxy-Rn 4649 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4649&ln=
Documentazione 📋 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 Classe Azoles Subclass Pyrazoles Intermediate Tree Nodes Not available Direct Parent Pyrazole carboxylic acids and derivatives Alternative Parents Heteroaromatic compounds Carboxylic acids Azacyclic compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents Pyrazole-3-carboxylic acid or derivatives - Pyrazole-5-carboxylic acid or derivatives - Heteroaromatic compound - Azacycle - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound Descrizione This compound belongs to the class of organic compounds known as pyrazole carboxylic acids and derivatives. These are heterocyclic compounds containing a pyrazole ring in which a hydrogen atom is replaced by a carboxylic acid 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.
Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Solubilità Solvent:DMSO, Max Conc. mg/mL: 16.82, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 16.82, Max Conc. mM: 100 Sensibilità Moisture sensitive Peso molecolare 168.190 g/mol XLogP3 1.800 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 4 Exact Mass 168.09 Da Monoisotopic Mass 168.09 Da Topological Polar Surface Area 66.000 Ų Heavy Atom Count 12 Formal Charge 0 Complexity 161.000 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
Calcolatori di soluzioni Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
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Reconstitution Calculator Recensioni 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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