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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag auf Lager SCH 51344 - ≥99%(HPLC) , CAS No.171927-40-5
Synonyms
BCP17385 | EX-A4182 | WGA92740 | Ras/Rac Transformation Blocker, SCH 51344 | HMS3674M09 | NCGC00384193-04 | 2-[2-[(6-Methoxy-3-methyl-1H-pyrazolo[3,4-b]quinolin-4-yl)amino]ethoxy]ethanol | DTXSID10433926 | 2-(2-((6-methoxy-3-methyl-1H-pyrazolo[3,4-b]quino
Shipped In
Ice chest + Ice pads
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Why this grade ≥99%(HPLC) 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 Synonyme
BCP17385 | EX-A4182 | WGA92740 | Ras/Rac Transformation Blocker, SCH 51344 | HMS3674M09 | NCGC00384193-04 | 2-[2-[(6-Methoxy-3-methyl-1H-pyrazolo[3,4-b]quinolin-4-yl)amino]ethoxy]ethanol | DTXSID10433926 | 2-(2-((6-methoxy-3-methyl-1H-pyrazolo[3,4-b]quino
Spezifikationen & Reinheit
≥99%(HPLC)
Biochemische und physiologische Mechanismen
Potent MTH1 inhibitor (Kd= 49 nM). Inhibits Ras-induced malignant transformation and increasesα-actin promoter-driven CAT activity in Ras-transformed cells. Has no effect on Ras-induced ERK and JNK activation. Inhibits Ras-induced membrane ruffling in REF
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Namen und Kennungen Kanonisches Lächeln CC1=C2C(=C3C=C(C=CC3=NC2=NN1)OC)NCCOCCO IUPAC Name 2-[2-[(6-methoxy-3-methyl-2H-pyrazolo[3,4-b]quinolin-4-yl)amino]ethoxy]ethanol InChIKey YWEGXZZAORIRQR-UHFFFAOYSA-N INCHI 1S/C16H20N4O3/c1-10-14-15(17-5-7-23-8-6-21)12-9-11(22-2)3-4-13(12)18-16(14)20-19-10/h3-4,9,21H,5-8H2,1-2H3,(H2,17,18,19,20) Isomere SMILES CC1=C2C(=C3C=C(C=CC3=NC2=NN1)OC)NCCOCCO PubChem CID 9995890 Molekulargewicht 316.35
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 Klasse Quinolines and derivatives Subclass Aminoquinolines and derivatives Intermediate Tree Nodes Not available Direct Parent 4-aminoquinolines Alternative Parents Pyrazolopyridines Anisoles Secondary alkylarylamines Aminopyridines and derivatives Alkyl aryl ethers Pyrazoles Heteroaromatic compounds Dialkyl ethers Azacyclic compounds Primary alcohols Organopnictogen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents 4-aminoquinoline - Pyrazolopyridine - Anisole - Alkyl aryl ether - Aminopyridine - Secondary aliphatic/aromatic amine - Pyridine - Benzenoid - Azole - Pyrazole - Heteroaromatic compound - Ether - Dialkyl ether - Azacycle - Secondary amine - Hydrocarbon derivative - Organic nitrogen compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Alcohol - Organopnictogen compound - Organic oxygen compound - Amine - Aromatic heteropolycyclic compound Beschreibung This compound belongs to the class of organic compounds known as 4-aminoquinolines. These are organic compounds containing an amino group attached to the 4-position of a quinoline ring system. External Descriptors aromatic ether - secondary amino compound - primary alcohol - aromatic amine - pyrazoloquinoline 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.
3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Löslichkeit Solvent:DMSO, Max Conc. mg/mL: 31.64, Max Conc. mM: 100 Molekulargewicht 316.350 g/mol XLogP3 1.700 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 7 Exact Mass 316.154 Da Monoisotopic Mass 316.154 Da Topological Polar Surface Area 92.300 Ų Heavy Atom Count 23 Formal Charge 0 Complexity 373.000 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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