![2-[2-[(6-Methoxy-3-methyl-1H-pyrazolo[3,4-b]quinolin-4-yl)amino]ethoxy]ethanol](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F395063-ras-rac-transformation-blocker-sch-51344.webp&w=3840&q=75)
CAS 171927-40-5
:2-[2-[(6-Methoxy-3-methyl-1H-pyrazolo[3,4-b]quinolin-4-yl)amino]ethoxy]ethanol
Description:
2-[2-[(6-Methoxy-3-methyl-1H-pyrazolo[3,4-b]quinolin-4-yl)amino]ethoxy]ethanol, with CAS number 171927-40-5, is a chemical compound characterized by its complex structure, which includes a pyrazoloquinoline core. This compound features an amino group linked to an ethoxyethanol moiety, contributing to its potential solubility and reactivity. The presence of a methoxy group enhances its lipophilicity, which may influence its biological activity and interaction with cellular targets. The pyrazoloquinoline framework is known for its pharmacological properties, often associated with activities such as anti-inflammatory or anticancer effects. The compound's molecular structure suggests it may participate in hydrogen bonding and other intermolecular interactions, which are critical for its function in biological systems. Overall, this substance is of interest in medicinal chemistry and drug development, particularly for its potential therapeutic applications. However, specific biological activities and safety profiles would require further investigation through empirical studies.
Formula:C16H20N4O3
InChI: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)
InChI key:InChIKey=YWEGXZZAORIRQR-UHFFFAOYSA-N
SMILES:N(CCOCCO)C=1C=2C(NC=3C1C(C)=NN3)=CC=C(OC)C2
Synonyms:- 2-[2-[(6-Methoxy-3-methyl-1H-pyrazolo[3,4-b]quinolin-4-yl)amino]ethoxy]ethanol
- Ethanol, 2-[2-[(6-methoxy-3-methyl-1H-pyrazolo[3,4-b]quinolin-4-yl)amino]ethoxy]-
- Sch-51344
- Ras/Rac Transformation Blocker, SCH 51344
- 2-[2-[(6-methoxy-3-methyl-2H-pyrazolo[3,4-b]quinolin-4-yl)amino]ethoxy]ethanol
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Found 4 products.
SCH 51344
CAS:<p>SCH 51344 inhibits Ras induced malignant transformation. SCH 51344 prevents anchorage-independent growth of oncogene transformed fibroblasts [1].</p>Formula:C16H20N4O3Color and Shape:SolidMolecular weight:316.36
