dBET1

dBET1 Struktur
1799711-21-9
CAS-Nr.
1799711-21-9
Englisch Name:
dBET1
Synonyma:
dBET1;CS-2706;DBET1;DBET-1 ;DBET 1;JQ1-Thalidomide conjugate;dBET1,inhibit,PROTACs,Epigenetic Reader Domain,Inhibitor,dBET 1,dBET-1;2-((S)-4-(4-Chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl)-N-(4-(2-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)oxy)acetamido)butyl)acetamide;6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetamide, 4-(4-chlorophenyl)-N-[4-[[2-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]oxy]acetyl]amino]butyl]-2,3,9-trimethyl-, (6S)-;N-(4-{2-[(9S)-7-(4-chlorophenyl)-4,5,13-trimethyl-3-thia-1,8,11,12-tetraazatricyclo[8.3.0.0,2,6]trideca-2 (6),4,7,10,12-pentaen-9-yl]acetamido}butyl)-2-{[2-( 2,6-dioxopiperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-i soindol-4-yl]oxy}acetamide
CBNumber:
CB23133361
Summenformel:
C38H37ClN8O7S
Molgewicht:
785.27
MOL-Datei:
1799711-21-9.mol

dBET1 Eigenschaften

Schmelzpunkt:
186 - 187°C
Dichte
1.55±0.1 g/cm3(Predicted)
storage temp. 
Hygroscopic, -20°C Freezer, Under inert atmosphere
Löslichkeit
DMSO (Slightly), Methanol (Slightly)
pka
10.68±0.40(Predicted)
Aggregatzustand
Solid
Farbe
Pale Yellow
Stabilität:
Hygroscopic

Sicherheit

HS Code  2933998090

dBET1 Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

dBET1 induces highly selective cereblon-dependent BET protein degradation in vitro and in vivo as well as delays leukemia progression in mice.

dBET1 Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


dBET1 Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 64)Lieferanten
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Shanghai finete Pharmaceutical Co., Ltd.
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Mandy@hangyubiotech.com China 11027 58
Jilin Chinese Academy of Sciences-yanshen Technology
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info@chemextension.com China 42057 58

  • dBET1
  • DBET1;DBET-1 ;DBET 1
  • CS-2706
  • 6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetamide, 4-(4-chlorophenyl)-N-[4-[[2-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]oxy]acetyl]amino]butyl]-2,3,9-trimethyl-, (6S)-
  • N-(4-{2-[(9S)-7-(4-chlorophenyl)-4,5,13-trimethyl-3-thia-1,8,11,12-tetraazatricyclo[8.3.0.0,2,6]trideca-2 (6),4,7,10,12-pentaen-9-yl]acetamido}butyl)-2-{[2-( 2,6-dioxopiperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-i soindol-4-yl]oxy}acetamide
  • 2-((S)-4-(4-Chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl)-N-(4-(2-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)oxy)acetamido)butyl)acetamide
  • dBET1,inhibit,PROTACs,Epigenetic Reader Domain,Inhibitor,dBET 1,dBET-1
  • JQ1-Thalidomide conjugate
  • 1799711-21-9
  • C38H37ClN8O7S
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