97162 Results for: "CAPITAL+SAFETY&pageNo=9"
DEA NONOate ≥98% (by NMR), white to off-white solid
Supplier: Enzo Life Sciences
DEA NONOate is used as a nitric oxide donor.
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5,5-Dimethyl-1-pyrroline-N-oxide ≥98% (by ELSD)
Supplier: Enzo Life Sciences
Spin trapping reagent
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MnTMPyP pentachloride ≥95% (by TLC), black powder
Supplier: Enzo Life Sciences
SOD mimetic. Peroxynitrite scavenger.
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PPH hydrochloride ≥99%
Supplier: Enzo Life Sciences
Effective, non-cell permeable and non-toxic analog of CPH for the detection of superoxide radicals.
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DIPPMPO ≥98% (by TLC, 1H-NMR, 13C-NMR)
Supplier: Enzo Life Sciences
Most efficient spin trap for the in vitro and in vivo detection of O-, N-, S-, and C-centered free radicals.
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1-Methyl-3,4-bis(3-indolyl)maleimide ≥98%
Supplier: Enzo Life Sciences
Negative control for the protein kinase C (PKC)-inhibitory activity.
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Captopril ≥98%
Supplier: Enzo Life Sciences
Inhibitor of ACE and leukotriene hydrolase
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Y-27632 dihydrochloride ≥98% (by HPCE)
Supplier: Enzo Life Sciences
ROCK inhibitor
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Pioglitazone ≥97% (by HPLC)
Supplier: Enzo Life Sciences
PPARgamma activator.
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D-myo-Inositol-1,3,4,5,6-pentakisphosphate pentapotassium salt ≥98% (by HPLC)
Supplier: Enzo Life Sciences
D-myo-Inositol-1,3,4,5,6-pentakisphosphate pentapotassium salt ≥98% (by HPLC)
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(S)-(+)-Camptothecin ≥98%
Supplier: Enzo Life Sciences
Potent antitumor agent
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Compound E ≥98% (by HPLC)
Supplier: Enzo Life Sciences
gamma-Secretase inhibitor
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AS-604850 ≥98% (by HPLC and UV method)
Supplier: Enzo Life Sciences
Potent, cell permeable and ATP-competitive inhibitor of phosphoinositide 3-kinase γ (PI(3)Kγ). Exhibits selectivity over other PI(3)K isoforms.
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CK-666 ≥95%
Supplier: Enzo Life Sciences
Cell permeable inhibitor human (IC50=4µM), fission yeast (IC50=5µM), S. cerevisiae (IC50=12µM) and bovine (IC50=17µM) Arp2/3 complex between Arp2 and Arp3. Inhibits Listeria motility (IC50=7µM).
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SB 225002 ≥98% (by HPLC)
Supplier: Enzo Life Sciences
Chemokine receptor ligand
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TCS JNK 5a ≥95% (by HPLC)
Supplier: Enzo Life Sciences
Thienylnaphthamide compound. Potent inhibitor of JNK2 (pIC50=6.5) and JNK3 (pIC50=6.7) targeting the ATP-binding site. Has no activity against JNK1.
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Sulindac Sulphide ≥99% (by TLC)
Supplier: Enzo Life Sciences
Active metabolite of sulindac. Inhibits cyclooxygenase. More selective for PGHS-1 (ID50=0.5 µM) over PGHS-2 (ID50=14 µM). Induces apoptosis by a cyclooxygenase-independent mechanism. Inhibits colorectal cancer growth and γ-secretase. NF-κB inhibitor. Inhibits Ras signaling.
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ICI-118,551 ≥98% (by HPLC)
Supplier: Enzo Life Sciences
Adrenergic receptor ligand.
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N-(6-Aminohexyl)-5-chloro-1-naphthalenesulphonamide hydrochloride ≥98% (by TLC)
Supplier: Enzo Life Sciences
Binds to calmodulin, inhibiting Ca²⁺-calmodulin-regulated enzyme activity. It inhibits the Ca²⁺/calmodulin-induced activation of myosin light chain kinase in a concentration dependent manner (IC50=25 µM). Cell permeable.
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Mifepristone ≥99%
Supplier: Enzo Life Sciences
Progesterone receptor ligand.
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Supplier: GRANT INSTRUMENTS
Supplier: BOCHEM
Supplier: VWR Collection
Supplier: OMEGA BIO-TEK
Supplier: DWK Life Sciences
Supplier: Thermo Fisher Scientific
Supplier: VWR Collection
Supplier: Oxford Nanopore Technologies
Supplier: Industrial Physics
Supplier: AAT BIOQUEST
Supplier: Integra
Supplier: Palbam
Supplier: VWR Collection
Supplier: Integra
Supplier: VWR Collection
Supplier: FACELLITATE
Supplier: NANOENTEK
Supplier: Greiner Bio-One