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Tandutinib

Tandutinib Struktur
387867-13-2
CAS-Nr.
387867-13-2
Englisch Name:
Tandutinib
Synonyma:
CS-309;MLN 518;CT 53518;CID 3231;NSC726292;Tandutinib;Unii-E1io3icj9a;CT53518; MLN518;Tandutinib(TINIBS);MLN518, Tandutinib
CBNumber:
CB31011758
Summenformel:
C31H42N6O4
Molgewicht:
562.7
MOL-Datei:
387867-13-2.mol

Tandutinib Eigenschaften

Schmelzpunkt:
177-178°C
Siedepunkt:
769.5±60.0 °C(Predicted)
Dichte
1.213±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Store in freezer, under -20°C
L?slichkeit
Chloroform (Slightly), Methanol (Slightly)
Aggregatzustand
Solid
pka
13.39±0.70(Predicted)
Farbe
White to Off-White
Wasserl?slichkeit
H2O: 2mg/mL, clear
InChIKey
UXXQOJXBIDBUAC-UHFFFAOYSA-N
SMILES
N1(C(NC2=CC=C(OC(C)C)C=C2)=O)CCN(C2=C3C(=NC=N2)C=C(OCCCN2CCCCC2)C(OC)=C3)CC1
CAS Datenbank
387867-13-2(CAS DataBase Reference)

Sicherheit

WGK Germany  WGK 3
Speicherklasse 11 - Combustible Solids

Tandutinib Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

Tandutinib is a potent antagonist of platelet-derived growth factor receptor β (PDGFRβ), FLT3, and c-Kit (IC50 = 200, 220, and 170 nM, respectively). It less potently inhibits macrophage colony-stimulating factor 1 receptor (IC50 = 3.4 μM) and does not significantly inhibit other tyrosine or serine/threonine kinases. Tandutinib blocks the growth of cells expressing an internal tandem duplication within the juxtamembrane domain of the FLT3 receptor, found in some acute myelogenous leukemia cells. It also impairs the growth of colon cancer cells through its actions on the c-Kit receptor. Tandutinib reverses multidrug resistance in vitro by impairing the efflux activity of the multidrug resistance protein 7.

Chemische Eigenschaften

White Solid

Verwenden

An oral, small-molecule inhibitor of FLT3 for the treatment of AML (acute myelogenous leukemia) and other cancer indications. The drug exhibited limited activity as a single agent in phase I and II clinical trials in patients with AML and myelody

Definition

ChEBI: An N-arylpiperazine that is piperazine in which the hydrogen attached to the nitrogen at position 1 is replaced by a 6-methoxy-7-[3-(piperidin-1-yl)propoxy]quinazolin-4-yl group, while the hydrogen attached to the nitrogen at position 4 s replaced by a (p-isopropoxyphenyl)aminocarbonyl group. Tandutinib is an inhibitor of tyrosine kinases FLT3, PDGFR and KIT.

Tandutinib Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Tandutinib Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 198)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Sinoway Industrial co., ltd.
+86-0592-5800732 +86-13806035118
xie@china-sinoway.com China 1369 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806
sales@capot.com China 29640 60
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795
ivan@atkchemical.com China 33024 60
Xiamen AmoyChem Co., Ltd
+86-86-5926051114 +8615060885618
sales@amoychem.com China 6366 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427
sales@conier.com China 49979 58
career henan chemical co
+86-0371-86658258 +8613203830695
factory@coreychem.com China 29792 58
SIMAGCHEM CORP
+86-5922680277 +86-13806087780
sale@simagchem.com China 17346 58
TargetMol Chemicals Inc.
+1-781-999-5354; +17819995354
marketing@targetmol.com United States 32467 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 28509 58

387867-13-2()Verwandte Suche:


  • Tandutinib
  • 1-Piperazinecarboxamide, 4-(6-methoxy-7-(3-(1-piperidinyl)propoxy)-4-quinazolinyl)-N-(4-(1-methylethoxy)phenyl)-
  • 4-(6-Methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin-4-yl)piperazine-1-carboxylic acid (4-isopropoxyphenyl)amide
  • Unii-E1io3icj9a
  • Tandutinib(CT 53518)
  • Tandutinib (MLN518)
  • CT53518; MLN518
  • Tandutinib(TINIBS)
  • (4-(6-Methoxy-7-(3-piperidylpropoxy)quinazolin-4-yl)piperazinyl)-N-(4-(methylethoxy)phenyl)carboxamide
  • 4-[6-Methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin-4-yl]-N-(4-propan-2-yloxyphenyl)piperazine-1-carboxamide
  • 4-[6-Methoxy-7-[3-(1-piperidinyl)propoxy]-4-quinazolinyl]-N-[4-(1-methylethoxy)phenyl]-1-piperazinecarboxamide
  • CT 53518
  • MLN 518
  • Tandutinib for research
  • N-(4-isopropoxyphenyl)-4-(6-methoxy-7-(3-(piperidin-1-yl)propoxy)quinazolin-4-yl)piperazine-1-carboxamide
  • NSC726292
  • (4-(6-Methoxy-7-(3-piperidylpropoxy)quinazolin-4-yl)piperazinyl)-N-(4-(methylethoxy)phenyl)carboxamide Tandutinib(MLN518)
  • 4-[6-Methoxy-7-[3-(1-piperidinyl)propoxy]-4-quinazolinyl]-N-[4-(1-Methylethoxy)phenyl]-
  • N-(4-Isopropoxyphenyl)-4-(6-methoxy-7-(3-(piperidin-1-yl)propoxy)quinazolin-4-yl)piperazine-1-
  • MLN518; CT53518; MLN 518; CT 53518; MLN-518; CT-53518;
  • Tandutinib (CT53518, MLN518)
  • CS-309
  • Tandutinib(MLN518, CT53518)
  • Tandutinib USP/EP/BP
  • Tandutinib (MLN518, CT53518, NSC-726292)
  • 4-[6-Methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin-4-yl]-N-(...
  • MLN518, Tandutinib
  • Tandutinib CT53518 MLN518 CT-53518 MLN-518
  • CID 3231
  • Tandutinib, 10 mM in DMSO
  • Abmole M1828-200mg Tandutinib 387867-13-2
  • 387867-13-2
  • C31H42N6O4
  • C27H31Br2ClN4O2
  • Inhibitors
  • ZUBRIN
  • API
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Tyrosine Kinase Inhibitors
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