Material Feeders
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 ZD 7155hydrochlorIde 25mg
An internal standard for the quantification of racecadotril by GC- or LC-MS
Apexbio Technology LLC ZD 7288 25MG
ZD 7288 (CAS 133059-99-1) is a selective inhibitor of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels These channels mediate Na and K currents notably the hyperpolarization-activated current (I h) contributing to neuronal excitability and rhythmic activity ZD 7288 reduces I h in a concentration-dependent voltage- and time-sensitive manner as demonstrated in rat facial motoneurons (IC 50 0 2 M) and hippocampal CA1 pyramidal neurons Additionally it inhibits T-type calcium currents in rat CA1 pyramidal cells ZD 7288 is utilized in research investigating neuronal excitability mechanisms pain signaling and chronic visceral pain models
Apexbio Technology LLC ZD 7288 5MG
ZD 7288 (CAS 133059-99-1) is a selective inhibitor of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels These channels mediate Na and K currents notably the hyperpolarization-activated current (I h) contributing to neuronal excitability and rhythmic activity ZD 7288 reduces I h in a concentration-dependent voltage- and time-sensitive manner as demonstrated in rat facial motoneurons (IC 50 0 2 M) and hippocampal CA1 pyramidal neurons Additionally it inhibits T-type calcium currents in rat CA1 pyramidal cells ZD 7288 is utilized in research investigating neuronal excitability mechanisms pain signaling and chronic visceral pain models
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
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 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
Apexbio Technology LLC ZD 7288 10MG
ZD 7288 (CAS 133059-99-1) is a selective inhibitor of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels These channels mediate Na and K currents notably the hyperpolarization-activated current (I h) contributing to neuronal excitability and rhythmic activity ZD 7288 reduces I h in a concentration-dependent voltage- and time-sensitive manner as demonstrated in rat facial motoneurons (IC 50 0 2 M) and hippocampal CA1 pyramidal neurons Additionally it inhibits T-type calcium currents in rat CA1 pyramidal cells ZD 7288 is utilized in research investigating neuronal excitability mechanisms pain signaling and chronic visceral pain models
- 1
- 2