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Elvitegravir

Elvitegravir Struktur
697761-98-1
CAS-Nr.
697761-98-1
Englisch Name:
Elvitegravir
Synonyma:
EVG;D06677;CS-789;CS-456;JTK 303;GS 9137;Vitekta;For Mr Wei;Elvitegravi;Elvitegravir
CBNumber:
CB02464875
Summenformel:
C23H23ClFNO5
Molgewicht:
447.88
MOL-Datei:
697761-98-1.mol

Elvitegravir Eigenschaften

Schmelzpunkt:
93-96°C
Siedepunkt:
623.6±55.0 °C(Predicted)
Dichte
1.357±0.06 g/cm3(Predicted)
storage temp. 
Refrigerator
L?slichkeit
DMSO (Slightly), Methanol (Slightly)
pka
0.44±0.20(Predicted)
Aggregatzustand
Solid
Farbe
Off-White to Pale Yellow
Optische Rotation
[α]/D -26 to -34°, c =0.5 in methanol
InChIKey
JUZYLCPPVHEVSV-LJQANCHMSA-N
SMILES
N1([C@H](CO)C(C)C)C2=C(C=C(CC3=CC=CC(Cl)=C3F)C(OC)=C2)C(=O)C(C(O)=O)=C1
CAS Datenbank
697761-98-1
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
WGK Germany  WGK 3
Speicherklasse 11 - Combustible Solids
Hazard Classifications Aquatic Acute 1
Aquatic Chronic 2
Bildanzeige (GHS) Environment (GHS09)
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H412 Sch?dlich für Wasserorganismen, mit langfristiger Wirkung. Langfristig (chronisch) gew?ssergef?hrdend Kategorie 3 P273, P501
Sicherheit
P273 Freisetzung in die Umwelt vermeiden.
P501 Inhalt/Beh?lter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

Elvitegravir Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

In November 2013, the European Medicines Agency (EMA) approved elvitegravir (also known as GS 9137 and JTK 303) as a single agent to be used as part of an antiviral regimen that includes a ritonavir-boosted protease inhibitor for the treatment of HIV-1 in adults without mutations indicative of elvitegravir resistance. Elvitegravir is the second of three marketed HIV integrase strand transfer inhibitors (INSTIs) including raltegravir and dolutegravir (this volume of ARMC). Elvitegravir was discovered by modification of a literature naphthyridine HIV integrase inhibitor in which the naphthyridine core served as a bioisostere for the diketo acid moiety in an original series. Serendipitously, a 4-quinolone-3-carboxylic acid precursor en route to the desired bioisosteric glyoxylic acid demonstrated modest integrase inhibition (IC50=1600 nM). Further derivatization led to elvitegravir with enhanced inhibition of integrase strand transfer (IC50=7.2 nM) and significant antiviral activity (EC50=0.9 nM). Elvitegravir was prepared in seven synthetic steps from 2,4-difluoro-5-iodobenzoic acid. The corresponding acid chloride was coupled to ethyl 3-(dimethylamino) acrylate and further substituted with S-valinol. Base promoted cyclization afforded the quinolone which was protected as silyl ether. Negishi coupling installed the 2-fluoro-3-chlorobenzyl moiety. Subsequent hydrolysis and methoxylation afforded elvitegravir.

Chemische Eigenschaften

Off-White to Pale Yellow Solid

Verwenden

A novel inhibitor of human immunodeficiency virus type 1 integrase.

Definition

ChEBI: A quinolinemonocarboxylic acid that is 7-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid substited at position 1 by a 1-hydroxy-3-methylbutan-2-yl group and at position 6 by a 3-chloro-2-fluorobenzyl group (the S-enantiomer). It is us d in combination therapy for the treatment of HIV-1 infection.

Elvitegravir Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Elvitegravir Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 262)Lieferanten
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Hangzhou Benoy Chemical Co., Ltd
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+15184799099
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CONIER CHEM AND PHARMA LIMITED
+8618523575427
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SHANGHAI T&W PHARMACEUTICAL CO., LTD.
+86-021-61551413 +8618813727289
contact@trustwe.com China 5745 58

697761-98-1()Verwandte Suche:


  • Elvitegravir,EVG,GS-9137,JTK-303
  • (S)-6-(3-CHLORO-2-FLUOROBENZYL)-1-(1-HYDROXY-3-METHYLBUTAN-2-YL)-7-METHOXY-4-OXO
  • 6-[(3-chloro-2-fluorophenyl)Methyl]-1-[(2S)-1-hydroxy-2,3-diMethylbutan-2-yl]-7-Methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
  • GS 9137
  • JTK 303
  • 6-[(3-Chloro-2-fluorophenyl)Methyl]-1,4-dihydro-1-[(1S)-1-(hydroxyMethyl)-2-Methylpropyl]-7-Methoxy-4-oxo-3-quinolinecarboxylic Acid
  • D06677
  • Elvitegravir (GS-9137)
  • Vitekta
  • 6-(3-Chloro-2-fluorobenzyl)-1-[1(S)-(hydroxymethyl)-2-methylpropyl]-7-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid Elvitegravir (GS-9137, JTK-303)
  • (S)-6-(3-CHLORO-2-FLUOROBENZYL)-1-(1-HYDROXY-3-METHYLBUTAN-2-YL)-4-OXO-1,4-DIHYDROQUINOLINE-3-CARBOXYLIC ACID
  • (S)-6-(3-Chloro-2-fluorobenzyl)-1-(1-hydroxy-3-methylBUTAN-2-YL)-7-methoxy-4-oxo-1,4-dihydroqu
  • 1-ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid
  • (S)-6-(3-CHLORO-2-FLUOROBENZYL)-1-(1-HYDROXY-2,3-DIMETHYLBUTAN-2-YL)-7-METHOXY-4-OXO-1,4-DIHYDROQUINOLINE-3-CARBOXYLIC ACID
  • Elvitegravir(GS-9137,JTK-303)
  • Elvitegravir
  • 6-(3-Chloro-2-fluorobenzyl)-1-[1(S)-(hydroxymethyl)-2-methylpropyl]-7-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
  • (S)-6-(3-CHLORO-2-FLUOROBENZYL)-1-(1-HYDROXY-3-METHYLBUTAN-2-YL)-7-METHOXY-4-OXO-1,4-DIHYDROQUINOLINE-3-CARBOXYLIC ACID
  • CS-789
  • CS-456
  • GS9137;GS-9137;GS 9137
  • brand name: Stribild
  • GS-9137; GS9137; GS 9137; JTK 303; JTK-303; JTK303; EVG; ELVITEGRAVIR; BRAND NAME: STRIBILD
  • 3-Quinolinecarboxylic acid, 6-[(3-chloro-2-fluorophenyl)methyl]-1,4-dihydro-1-[(1S)-1-(hydroxymethyl)-2-methylpropyl]-7-methoxy-4-oxo-
  • Elvitegravi
  • ELVITEGRAVIR CAS 697761-98-1
  • (S)-6-(3-CHLORO-2-FLUOROBENZYL)-1-(1-HYDROXY-3-METHYLBUTAN-2-YL)-7-METHOXY-4-OXO-1,4-DIHYDROQUINOLINE-3-CARBOXYLIC ACID USP/EP/BP
  • 6-[(3-chloro-2-fluorophenyl)methyl]-1-[(2S)-1-hydroxy-3-methylbutan-2-yl]-7-methoxy-4-oxoquinoline-3-carboxylic acid
  • ElvitegravirQ: What is Elvitegravir Q: What is the CAS Number of Elvitegravir Q: What is the storage condition of Elvitegravir Q: What are the applications of Elvitegravir
  • Elvitegravir (JTK-303)
  • For Mr Wei
  • Elvitegravir, quinolone HIV integrase inhibitor
  • Elvitegravir, 10 mM in DMSO
  • EVG
  • 697761-98-1
  • 595037-20-2
  • C23H23ClFNO5
  • API
  • Inhibitor
  • Aromatics
  • Heterocycles
  • Inhibitors
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • 697761-98-1
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