ChemicalBook--->CAS DataBase List--->690206-97-4

690206-97-4

690206-97-4 Structure

690206-97-4 Structure
IdentificationBack Directory
[Name]

ZM 306416
[CAS]

690206-97-4
[Synonyms]

CS-616
CB676475
CB-676475
CB 676475
ZM 306416, >=99%
ZM306416/ZM-306416
ZM 306416 USP/EP/BP
ZM-306416(CB 676475)
ZM 306416 HYDROCHLORIDE
ZM 213689 DisodiuM Salt (MeropeneM iMpurity)
N-(4-chloro-2-fluorophenyl)-6,7-dimethoxyquinazolin-4-amine
N-(4-Chloro-2-fluorophenyl)-6,7-dimethoxy-4-quinazolinamine
N-(3-chloro-4-fluorophenyl)-6,7-dimethoxyquinazolin-4-amine
4-QuinazolinaMine,N-(4-chloro-2-fluorophenyl)-6,7-diMethoxy-
ZM-306416;ZM 306416;CB 676475;ZM-306416;ZM306416;CB-676475;CB676475
N-(4-fluorophenyl)-7-methoxy-6-(3-morpholinopropoxy)quinazolin-4-amine
4-[(4'-CHLORO-2'-FLUORO)PHENYLAMINO]-6,7-DIMETHOXYQUINAZOLINE HYDROCHLORIDE
ZM 213689 DisodiuM Salt (MeropeneM iMpurity) (Mixture of double bond isoMers)
[Molecular Formula]

C16H14Cl2FN3O2
[MDL Number]

MFCD08703133
[MOL File]

690206-97-4.mol
[Molecular Weight]

370.206
Chemical PropertiesBack Directory
[Melting point ]

>161°C (dec.)
[Boiling point ]

434.1±45.0 °C(Predicted)
[density ]

1.389±0.06 g/cm3(Predicted)
[storage temp. ]

Desiccate at RT
[solubility ]

Methanol (Slightly), Water (Sparingly)
[form ]

Off-white solid.
[pka]

5.49±0.30(Predicted)
[color ]

Light Orange to Brown
[Stability:]

Hygroscopic
Hazard InformationBack Directory
[Uses]

ZM 306416 an inhibitor of tyrosine kinase RTK signaling pathway involved in anti-cancer agents. Anti-tumor, anti-metastatic agent.
[Uses]

ZM-306416 is a VEGFR inhibitor, inhibiting Src, VEGFR1 and Abl with IC50 of 0.33 μM, 0.33 μM and 1.3 μM, respectively.
[Definition]

ChEBI: N-(4-chloro-2-fluorophenyl)-6,7-dimethoxy-4-quinazolinamine is a member of quinazolines.
[Biological Activity]

VEGF receptor tyrosine kinase inhibitor. Inhibits KDR (IC50=100nM) and Flt (IC50=2μM) tyrosine kinases.
[target]

VEGFR1
[IC 50]

KDR: 100 nM (IC50); Flt-1: 2 μM (IC50)
[References]

1. antczak, c., et al., a high-content biosensor-based screen identifies cell-permeable activators and inhibitors of egfr function: implications in drug discovery. j biomol screen, 2012. 17(7): p. 885-99.2. choi kj, baik ih, ye sk et al. molecular targeted therapy for hepatocellular carcinoma: present status and future directions. biol pharm bull. 2015;38(7):986-91. 3. choi, k.j., et al., molecular targeted therapy for hepatocellular carcinoma: present status and future directions. biol pharm bull, 2015. 38(7): p. 986-91.4. susarla, r., j.c. watkinson, and m.c. eggo, regulation of human thyroid follicular cell function by inhibition of vascular endothelial growth factor receptor signalling. mol cell endocrinol, 2012. 351(2): p. 199-207.
Spectrum DetailBack Directory
[Spectrum Detail]

ZM 306416(690206-97-4)1HNMR
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