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· · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino Sophoridine - ≥98%(GC)(T) , CAS No.6882-68-4
Synonyms
(41S,7aR,13aR,13bR)-Dodecahydro-1H-dipyrido[2,1-f:3',2',1'-ij][1,6]naphthyridin-10(41H)-one | 6.beta.-Matrine | s3895 | C15H24N2O | Matridin-15-one, (6.beta.)- | Z54065866 | Matridin-15-one, (5-beta)- | Q-100773 | 5-Epidihydrosophocarpine | Q27292355 | d-
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Why this grade ≥98%(GC)(T) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinonimi
(41S,7aR,13aR,13bR)-Dodecahydro-1H-dipyrido[2,1-f:3',2',1'-ij][1,6]naphthyridin-10(41H)-one | 6.beta.-Matrine | s3895 | C15H24N2O | Matridin-15-one, (6.beta.)- | Z54065866 | Matridin-15-one, (5-beta)- | Q-100773 | 5-Epidihydrosophocarpine | Q27292355 | d-
Specifiche e purezza
≥98%(GC)(T)
Condizioni di conservazione di stoccaggio
Store at 2-8°C
Spedito in
Wet ice
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Nomi e identificatori Pubchem Sid 504757578 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504757578 Sorrisi canonici C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 IUPAC Name (1R,2R,9R,17S)-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one InChIKey ZSBXGIUJOOQZMP-BHPKHCPMSA-N INCHI 1S/C15H24N2O/c18-14-7-1-6-13-12-5-3-9-16-8-2-4-11(15(12)16)10-17(13)14/h11-13,15H,1-10H2/t11-,12-,13-,15+/m1/s1 Isomeri SMILES C1C[C@@H]2[C@H]3CCCN4[C@H]3[C@H](CCC4)CN2C(=O)C1 RTECS WG1250000 Numero UN 1544 Gruppo di imballaggio III Peso molecolare 248.37 Reaxy-Rn 102206 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=102206&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 Alkaloids and derivatives Classe Lupin alkaloids Subclass Matrine alkaloids Intermediate Tree Nodes Not available Direct Parent Matrine alkaloids Alternative Parents Quinolizidinones Naphthyridines Piperidinones Delta lactams Tertiary carboxylic acid amides Trialkylamines Amino acids and derivatives Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic heteropolycyclic compounds Substituents Matrine - Quinolizidinone - Diazanaphthalene - Naphthyridine - Quinolizidine - Delta-lactam - Piperidinone - Piperidine - Tertiary carboxylic acid amide - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Carboxamide group - Lactam - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Amine - Carbonyl group - Organopnictogen compound - Organic oxide - Aliphatic heteropolycyclic compound Descrizione This compound belongs to the class of organic compounds known as matrine alkaloids. These are lupin alkaloids with a structure based on the matrine skeleton, a four-ring skeleton that based on a saturated dipyrido[2,1-f:3',2',1'-ij][1,6]naphthyridin-10-one skeleton. 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 Sensibilità Heat Sensitive Rotazione specifica [α] -70° (C=1,EtOH) Punto di fusione (°C) 109 °C Peso molecolare 248.360 g/mol XLogP3 1.600 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 0 Exact Mass 248.189 Da Monoisotopic Mass 248.189 Da Topological Polar Surface Area 23.600 Ų Heavy Atom Count 18 Formal Charge 0 Complexity 356.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 4 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
Citations of This Product Riferimenti 1. Kunmei Xie, Jingquan Dong, Xiguang Liu, Xiao Liu, Shasha Zhang, Yan Cao, Long Chen, Wanyi Xu, Panpan Zhao, Zibo Dong. (2025) Sophoridine alleviates sepsis-associated encephalopathy by inhibiting MARK4 and NLRP3 signaling. FREE RADICAL BIOLOGY AND MEDICINE, [PMID:41167535 ] [10.1016/j.freeradbiomed.2025.10.293 ] 2. Shasha Zhang, Huilin Sun, Xinran Li, Kunmei Xie, Yusa Li, Hongyu Huang, Huizhen Chen, Jingquan Dong. (2026) Sophoridine alleviates spleen injury in sepsis by inhibiting ASK1-mediated inflammation, oxidative stress, and apoptosis. EUROPEAN JOURNAL OF PHARMACOLOGY, [PMID:41621573 ] [10.1016/j.ejphar.2026.178593 ]
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