Material Feeders
Material Feeders
Selleck Chemical LLC ZD-4190
ZD-4190 is a submicromolar inhibitor of VEGF RTK activity in vitro with IC50 values of 29 4 nM and 708 63 nM for KDR and Flt-1 respectively
Cayman Chemical ANTIBODY ZD 4190 10mg
A racemic mixture of (S)-3-hydroxyphenylglycine and (R)-3-hydroxyphenylglycine
Cayman Chemical ANTIBODY ZD 4190 50mg
A racemic mixture of (S)-3-hydroxyphenylglycine and (R)-3-hydroxyphenylglycine
TARGETMOL CHEMICALS INC ZD 7155 HYDROCHLORIDE 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. ZD 7155 hydrochloride is an angiotensin II receptor type 1 (AT1 receptor) antagonist. purity: 99%
Cayman Chemical ZD 7155hydrochlorIde 25mg
An internal standard for the quantification of racecadotril by GC- or LC-MS
Cayman Chemical ANTIBODY ZD 4190 5mg
A co-inducer of heat shock proteins increases pancreatic Hsp60 and Hsp70 levels decreases MDA and protein carbonyl levels increases GPX activity and decreases Cu/Zn SOD activity in a rat model of CCK octapeptide-induced acute pancreatitis at 20 mg/kg increases spinal cord levels of Hsp70 and Hsp90 and motoneuron survival decreases disease severity and increases lifespan in an SOD1G93A transgenic mouse model of ALS at 10 mg/kg i.p.
Cayman Chemical ANTIBODY ZD 4190 1mg
A flavonoid with diverse biological activities inhibits NA activity in oseltamivir-sensitive and -resistant H1N1 influenza strains (IC50s 0.51 and 14.1 UM respectively) as well as PTP1B ACAT and DGAT (IC50s 0.31 24.6 and 8 UM respectively) cytotoxic to MCF-7 SW480 and HepG2 cells (IC50s 7.62 5.15 and 2.83 UM respectively) active against MRSA (MIC50 2 Ug/ml) binds to the benzodiazepine receptor (Ki 1.63 UM) and increases pentobarbital-induced sleep duration in mice at 50 mg/kg an effect that can be reversed by flumazenil
Cayman Chemical ZD 7155hydrochlorIde 10mg
A histamine H1 receptor antagonist (Ki 0 72 nM in a radioligand binding assay) selective for the histamine H1 receptor over mAChRs (Ki 38 nM in a radioligand binding assay) inhibits anti-IgE-induced histamine release from isolated human lung fragments (IC50 19 nM) but induces histamine release (RC50 1 03 UM) reduces SARS-CoV-2 replication in SARS-CoV-2-infected Vero E6 cells (EC50 1 76 UM) with a CC50 value of 19 73 UM
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