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4945-26-0 | 2-Styrylquinoline
CAS No: 4945-26-0 Catalog No: AG00E0FM MDL No:
Product Description
Catalog Number:
AG00E0FM
Chemical Name:
2-Styrylquinoline
CAS Number:
4945-26-0
IUPAC Name:
2-[(E)-2-phenylethenyl]quinoline
InChI:
InChI=1S/C17H13N/c1-2-6-14(7-3-1)10-12-16-13-11-15-8-4-5-9-17(15)18-16/h1-13H/b12-10+
InChI Key:
RLGKSXCGHMXELQ-ZRDIBKRKSA-N
Properties
Complexity:
277
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Exact Mass:
231.105g/mol
Formal Charge:
0
Heavy Atom Count:
18
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
231.298g/mol
Monoisotopic Mass:
231.105g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
12.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.5
Literature
| Title | Journal |
|---|---|
| (E)-5-styryl-1H-indole and (E)-6-styrylquinoline derivatives serve as probes for β-amyloid plaques. | Molecules (Basel, Switzerland) 20120410 |
| Simplified molecular input-line entry system and International Chemical Identifier in the QSAR analysis of styrylquinoline derivatives as HIV-1 integrase inhibitors. | Chemical biology & drug design 20110501 |
| Evaluation of the trypanocidal, cytotoxic and genotoxic activity of styrylquinoline analogs. | Journal of chemotherapy (Florence, Italy) 20100601 |
| Chemistry and structure-activity relationship of the styrylquinoline-type HIV integrase inhibitors. | Molecules (Basel, Switzerland) 20100427 |
| Solvent effects on the spectroscopic properties of styrylquinolinium dyes series. | Journal of fluorescence 20100101 |
| Synthesis and antiproliferative evaluations of certain 2-phenylvinylquinoline (2-styrylquinoline) and 2-furanylvinylquinoline derivatives. | Bioorganic & medicinal chemistry 20100101 |
| Exploring molecular shape analysis of styrylquinoline derivatives as HIV-1 integrase inhibitors. | European journal of medicinal chemistry 20080101 |
| Investigating the antiproliferative activity of quinoline-5,8-diones and styrylquinolinecarboxylic acids on tumor cell lines. | Bioorganic & medicinal chemistry letters 20071115 |
| Crystal and electronic structures of magnesium(II), copper(II), and mixed magnesium(II)-copper(II) complexes of the quinoline half of styrylquinoline-type HIV-1 integrase inhibitors. | The journal of physical chemistry. B 20070531 |
| Comparative molecular surface analysis (CoMSA) for virtual combinatorial library screening of styrylquinoline HIV-1 blocking agents. | Combinatorial chemistry & high throughput screening 20061201 |
| Microsphere-based protease assays and screening application for lethal factor and factor Xa. | Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501 |
| Experimental/theoretical electrostatic properties of a styrylquinoline-type HIV-1 integrase inhibitor and its progenitors. | The journal of physical chemistry. B 20060112 |
| Prediction of genotoxicity of chemical compounds by statistical learning methods. | Chemical research in toxicology 20050601 |
| Analogues of the styrylquinoline and styrylquinazoline HIV-1 integrase inhibitors: design and synthetic problems. | Acta poloniae pharmaceutica 20041201 |
| Nuclear import of HIV-1 integrase is inhibited in vitro by styrylquinoline derivatives. | Molecular pharmacology 20041001 |
| Exploring binding mode for styrylquinoline HIV-1 integrase inhibitors using comparative molecular field analysis and docking studies. | Acta pharmacologica Sinica 20040701 |
| Styrylquinolines, integrase inhibitors acting prior to integration: a new mechanism of action for anti-integrase agents. | Journal of virology 20040601 |
| Mechanism of HIV-1 integrase inhibition by styrylquinoline derivatives in vitro. | Molecular pharmacology 20040101 |
| Synthesis of styrylbenzofuran derivatives as styrylquinoline analogues for HIV-1 integrase inhibitor. | Farmaco (Societa chimica italiana : 1989) 20031201 |
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