ZM 306416, VEGFR kinase inhibitor
-
Catalog numberSIH-487-25MG
-
PricePlease ask
-
Size25 mg
-
-
Stock availabilitIn StockIn Stock
-
CAS number690206-97-4
-
DescriptionVEGFR kinase inhibitor
-
Molecular weight333,7 g/mol
-
Primary research fieldsCell Signaling, Cancer, Apoptosis, Cardiovascular System, Cancer Growth Inhibitors, Tyrosine Kinase Inhibitors
-
Other nameZM-306416
-
Product categorySmall Molecules
-
Product typeInhibitor
-
Chemical formulaC16H13ClFN3O2
-
OriginSynthetic
-
Purity pourcentage≥98% (TLC)
-
Soluble inSoluble in DMSO (3 mg/ml) or ethanol (1 mg/ml)
-
Physical appearanceOff-white solid
-
Storage recommendations-20ºC
-
Shipping recommendationsShipped Ambient
-
Safety informationClassification: Not a hazardous substance or mixture. Safety Phrases: S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
-
PubChem number5329006
-
Scientific contextZM 306416 is a potent and selective VEGF receptor tyrosine kinase inhibitor. Specifically, it inhibits Flk-1 (KDR) and Flt.
-
Bibliography1. Hennequin L.F., et al. (1999) J. Med. Chem. 42(26): 5369–5389. 2. Kawai, T., et al. (2006) Neurosci. 141(3): 1209–1216.
-
Release date1-Oct-2014
-
PubMed numberRefer to PubMed
-
Tested applicationsTo be tested
-
Tested reactivityTo be tested
-
Representative figure legendChemical structure of ZM 306416 (SIH-487), a VEGFR kinase inhibitor. CAS #: 690206-97-4. Molecular Formula: C16H13ClFN3O2. Molecular Weight: 333.7 g/mol. Chemical structure of ZM 306416, a VEGFR kinase inhibitor (SIH-487). CAS # 690206-97-4. Molecular Formula: C16H13ClFN3O2.
-
Warning informationNon-hazardous
-
Country of productionCanada
-
Total weight kg0.25
-
Net weight g0.025
-
Additional descriptionTissue, pathway, proteinase, peptidase, protease ,acrosin, lipoprotein, activator, caspase, trypsin, papain, esterase inhibitors are proteins or receptor ligands or receptor antagonists that bind to an enzyme receptor and decreases its activity. Since blocking an enzyme's activity can kill a pathogen or correct a metabolic imbalance, many drugs are enzyme inhibitors. Not all receptor antagonist that bind to enzymes are inhibitors; enzyme activator ligands or agonists bind to enzymes and increase their enzymatic activity, while enzyme substrates bind and are converted to products in the normal catalytic cycle of the enzyme.
-
Gene target
-
Gene symbolFLT4, KDR
-
Short nameZM 306416, VEGFR kinase inhibitor
-
Alternative nameZM 306416, VEGFR phosphorylation catalyst suppressor
-
Gene info
-
Identity
-
Gene
-
Long gene namefms related receptor tyrosine kinase 4
-
Synonyms gene name
- fms-related tyrosine kinase 4
- fms related tyrosine kinase 4
-
Synonyms
-
Synonyms name
-
GenBank acession
-
Locus
-
Discovery year1991-10-25
-
Entrez gene record
-
Pubmed identfication
-
Classification
- I-set domain containing
- Receptor tyrosine kinases
-
VEGA ID
Gene info
-
Identity
-
Gene
-
Long gene namekinase insert domain receptor
-
Synonyms gene name
- kinase insert domain receptor (a type III receptor tyrosine kinase)
-
Synonyms
-
Synonyms name
-
GenBank acession
-
Locus
-
Discovery year1991-07-10
-
Entrez gene record
-
Pubmed identfication
-
Classification
- Receptor tyrosine kinases
- CD molecules
- I-set domain containing
- V-set domain containing
-
VEGA ID
-
Locus Specific Databases