Vatalanib Dihydrochloride, VEGFR inhibitor
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Catalog numberSIH-484-10MG
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Price:
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Size10 mg
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Stock availabilitIn StockIn Stock
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CAS number212141-51-0
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DescriptionVEGFR inhibitor
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Molecular weight419,7 g/mol
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Primary research fieldsCell Signaling, Cancer, Apoptosis, Cardiovascular System, Cancer Growth Inhibitors, Growth Factor Receptor Inhibitors
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Other nameN-(4-Chlorophenyl)-4-(4-pyridinylmethyl)-1-phthalazinamine dihydrochloride
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Product categorySmall Molecules
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Product typeInhibitor
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Chemical formulaC20H17Cl3N4
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OriginSynthetic
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Purity pourcentage≥96%
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Soluble inSoluble in DMSO (30 mg/ml), ethanol (10 mg/ml) with warming; very poorly soluble in water; maximum solubility in plain water is estimated to be about 10-20 µM; buffers, serum, or other additives may increase or decrease the aqueous solubility.Also soluble in methanol, and water ( ≥10 mg/ml )
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Physical appearanceSolid
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Storage recommendations-20ºC
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Shipping recommendationsShipped Ambient
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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.
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PubChem number22386467
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Scientific contextVatalanib Dihydrochloride is an inhibitor of Flk, c-Kit and PDGFR-β. It has been shown to inhibit VEGFR-dependent tumor angiogenesis and EGFR- and RET-dependent tumor cell proliferation and survival.
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Bibliography1. Herbst R.S., Heymach J.V., O’Reilly M. S., Onn A., & Ryan A.J. (2007) Expert Opin. Invest. Drugs. 16(2): 239–249.
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Release date1-Oct-2014
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PubMed numberRefer to PubMed
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Tested applicationsTo be tested
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Tested reactivityTo be tested
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Representative figure legendChemical structure of Vatalanib Dihydrochloride (SIH-484), a VEGFRK inhibitor. CAS #: 212141-51-0. Molecular Formula: C20H17Cl3N4. Molecular Weight: 419.7 g/mol. Chemical structure of Vatalanib Dihydrochloride, a VEGFRK inhibitor (SIH-484). CAS # 212141-51-0. Molecular Formula: C20H17Cl3N4.
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Warning informationNon-hazardous
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Country of productionCanada
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Total weight kg0.25
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Net weight g0.01
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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.
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Gene target
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Gene symbolFLT4, KDR
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Short nameVatalanib Dihydrochloride, VEGFR inhibitor
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Alternative nameVatalanib Dihydrochloride, VEGFR suppressor
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Gene info
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Identity
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Gene
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Long gene namefms related receptor tyrosine kinase 4
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Synonyms gene name
- fms-related tyrosine kinase 4
- fms related tyrosine kinase 4
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Synonyms
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Synonyms name
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GenBank acession
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Locus
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Discovery year1991-10-25
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Entrez gene record
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Pubmed identfication
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Classification
- I-set domain containing
- Receptor tyrosine kinases
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VEGA ID
Gene info
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Identity
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Gene
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Long gene namekinase insert domain receptor
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Synonyms gene name
- kinase insert domain receptor (a type III receptor tyrosine kinase)
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Synonyms
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Synonyms name
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GenBank acession
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Locus
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Discovery year1991-07-10
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Entrez gene record
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Pubmed identfication
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Classification
- Receptor tyrosine kinases
- CD molecules
- I-set domain containing
- V-set domain containing
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VEGA ID
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Locus Specific Databases