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Cediranib

Cediranib Struktur
288383-20-0
CAS-Nr.
288383-20-0
Englisch Name:
Cediranib
Synonyma:
Cediranib dihydrochloride;CS-377;AZD2171;Recentin;Cediranib;Cadiranib;NSC-732208;Cediranib R;Cediranib, >=99%;Cediranib (AZD217)
CBNumber:
CB3947063
Summenformel:
C25H27FN4O3
Molgewicht:
450.51
MOL-Datei:
288383-20-0.mol

Cediranib Eigenschaften

Schmelzpunkt:
135-138°C
Siedepunkt:
626.6±55.0 °C(Predicted)
Dichte
1.285
storage temp. 
Sealed in dry,Store in freezer, under -20°C
L?slichkeit
Acetone (Slightly), DMSO (Slightly), Methanol (Slightly)
Aggregatzustand
Solid
pka
16.14±0.30(Predicted)
Farbe
White to Off-White
InChI
InChI=1S/C25H27FN4O3/c1-16-12-17-19(29-16)6-7-21(24(17)26)33-25-18-13-22(31-2)23(14-20(18)27-15-28-25)32-11-5-10-30-8-3-4-9-30/h6-7,12-15,29H,3-5,8-11H2,1-2H3
InChIKey
XXJWYDDUDKYVKI-UHFFFAOYSA-N
SMILES
N1=C2C(C=C(OC)C(OCCCN3CCCC3)=C2)=C(OC2C=CC3=C(C=2F)C=C(C)N3)N=C1
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
WGK Germany  WGK 3
HS Code  2933599590
Speicherklasse 11 - Combustible Solids
Bildanzeige (GHS) Exclamation Mark (GHS07)
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitssch?dlich bei Verschlucken. Akute Toxizit?t oral Kategorie 4 Warnung P264, P270, P301+P312, P330, P501
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung P264, P280, P302+P352, P321,P332+P313, P362
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung P264, P280, P305+P351+P338,P337+P313P
H335 Kann die Atemwege reizen. Spezifische Zielorgan-Toxizit?t (einmalige Exposition) Kategorie 3 (Atemwegsreizung) Warnung
Sicherheit
P261 Einatmen von Staub vermeiden.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach M?glichkeit entfernen. Weiter spülen.

Cediranib Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

Receptors for VEGF have central roles in vasculogenesis and angiogenesis and thus serve as targets for cancer therapy. Cediranib is a potent inhibitor of VEGF receptor tyrosine kinases, including VEGFR1, 2, and 3 (IC50s = 5, 1, and 3 nM, respectively). It also potently inhibits a variety of other receptor and non-receptor tyrosine kinases, including several in the platelet-derived growth factor, fibroblast growth factor, and endothelial growth factor receptor families. Cediranib blocks tubule formation by human umbilical vein endothelial cells in vitro and prevents angiogenesis as well as xenograft tumor growth in vivo. Because of these effects, cediranib has potential use in a range of cancers.

Verwenden

Cediranib (AZD2171) inhibited VEGF-stimulated proliferation and KDR phosphorylation with IC50 of 0.4 and 0.5 nM, respectively.

Cediranib Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Cediranib Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 272)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hebei Chuanghai Biotechnology Co., Ltd
+8615350571055
Sibel@chuanghaibio.com China 8738 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21587 55
Nanjing ChemLin Chemical Industry Co., Ltd.
025-83697070
product@chemlin.com.cn CHINA 3009 60
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795
ivan@atkchemical.com China 33024 60
career henan chemical co
+86-0371-86658258 +8613203830695
sales@coreychem.com China 29815 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427
sales@conier.com China 49979 58
TargetMol Chemicals Inc.
+1-781-999-5354; +17819995354
marketing@targetmol.com United States 32466 58
ANHUI WITOP BIOTECH CO., LTD
+8615255079626
eric@witopchemical.com China 23541 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250
1026@dideu.com China 20581 58
AFINE CHEMICALS LIMITED
+86-0571-85134551
sales@afinechem.com China 15075 58

288383-20-0()Verwandte Suche:


  • Cediranib
  • 4-(4-Fluoro-2-methylindol-5-yloxy)-6-methoxy-7-[3-(pyrrolidin-1-yl)propoxy]quinazoline
  • Cadiranib (AZD2171)
  • Cediranib(AZD2171)
  • AZD2171
  • Recentin
  • Cadiranib
  • Cediranib R
  • 4-((4-fluoro-2-Methyl-1H-indol-5-yl)oxy)-6-Methoxy-7-(3-(pyrrolidin-1-yl)propoxy)quinazoline
  • Cediranib (AZD217)
  • NSC-732208
  • 4-(4-Fluoro-2-methylindol-5-yloxy)-6-methoxy-7-[3-(pyrrolidin-1-yl)propoxy]quinazoline Cediranib (AZD2171)
  • Cediranib 4-(4-Fluoro-2-methylindol-5-yloxy)-6-methoxy-7-[3-(pyrrolidin-1-yl)propoxy]quinazoline
  • Cediranib, >=99%
  • RECENTIN;AZD2171;AZD 2171;AZD-2171
  • CS-377
  • Quinazoline, 4-[(4-fluoro-2-methyl-1H-indol-5-yl)oxy]-6-methoxy-7-[3-(1-pyrrolidinyl)propoxy]-
  • Cediranib (free base)
  • Cediranib USP/EP/BP
  • Cediranib (NSC-732208
  • 288383-20-0 Cediranib
  • AZD2171, Cediranib
  • AZD2171|||NSC-732208
  • Carprofen Impurity 8(Carprofen EP Impurity H )
  • Cediranib, 10 mM in DMSO
  • Cediranib dihydrochloride
  • 288383-20-0
  • C25H27FN4O3
  • Inhibitors
  • Antineoplastic
  • APIs
  • 288383-20-0
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