97209 Results for: "R\u0119czne+pompki+pró\u017Cniowe&pageNo=9"
NS-2028 ≥98% (by TLC)
Supplier: ENZO LIFE SCIENCES
A potent and selective, cell-permeable inhibitor of nitric oxide (NO)-sensitive soluble guanylyl cyclase (sGC). Inhibition is irreversible. Inhibits also the basal, the YC-1 and the coenhanced sGC activity. Complete inhibition of NO-induced relaxation in vascular and nonvascular smooth muscle at 1μM.
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Chlorpromazine hydrochloride ≥98% (by HPLC)
Supplier: ENZO LIFE SCIENCES
Antipsychotic working on a variety of receptors in the CNS
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NPC-15437 dihydrochloride ≥98% (by HPLC)
Supplier: ENZO LIFE SCIENCES
PKC inhibitor
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Tyrphostin AG 527 ≥98% (by HPLC)
Supplier: ENZO LIFE SCIENCES
Tyrphostin AG 527 ≥98% (by HPLC)
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4-(Dimethylamino)-N-[7-(hydroxyamino)-7-oxoheptyl]benzamide ≥98% (by HPLC)
Supplier: ENZO LIFE SCIENCES
Potent inhibitor of histone deacetylases (HDACs) (IC50≤1µM).
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Curcumin (from Curcuma longa) ≥98% (by HPLC), high purity
Supplier: ENZO LIFE SCIENCES
Curcumin (from Curcuma longa) ≥98% (by HPLC), high purity
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Catharanthine tartrate (from Catharanthus roseus) ≥90% (dry basis)
Supplier: ENZO LIFE SCIENCES
Starting material for the synthesis of the antitumor drugs vinblastine and vincristine. It is less active as an inhibitor of tubulin self-assembly into microtubules than the latter two compounds.
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D-myo-Inositol-1,4,5-trisphosphate, hexapotassium salt ≥98% (by TLC)
Supplier: ENZO LIFE SCIENCES
Product of phosphatidylinositol phospholipid hydrolysis.
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Salubrinal ≥98% (by HPLC)
Supplier: ENZO LIFE SCIENCES
Salubrinal ≥98% (by HPLC)
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Rockout ≥98% (by HPLC)
Supplier: ENZO LIFE SCIENCES
A cell permeable, selective, and ATP-competitive inhibitor of Rho kinase (ROCK) activity (IC50=25µM). Does not inhibit the activation of Rho nor does it affect the in vitro activities of MLCK, PKCα, and SAPK2a/p38α. Shown to be less potent than Y-27632.
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1-Azakenpaullone ≥95% (by NMR)
Supplier: ENZO LIFE SCIENCES
GSK-3beta inhibitor
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SU 9516 ≥95% (by HPLC)
Supplier: ENZO LIFE SCIENCES
Cell permeable, potent, selective and ATP-competitive inhibitor of CDK2/cyclin A (IC50=22nM), CDK1/cyclin B (IC50=40nM) and CDK4/cyclin D1 (IC50=200nM). Has no effect on the activity of PKC, p38, PDGFRβ and EGFR (IC50>10µM). Displays anti-proliferative and pro-apoptotic properties in tumor cells. Inhibits proliferation of growth factor-stimulated colon carcinoma cells by binding to CDK2 and thus preventing the phosphorylation of pRb and its dissociation from E2F.
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CDK1/2 Inhibitor III ≥95% (by HPLC)
Supplier: ENZO LIFE SCIENCES
Cell permeable triazolo-diamine compound that displays anti-proliferative properties in various human cancer cells (IC50=20nM, 35nM and 92nM in HCT-116, HeLa, and A375 cells). Acts as a highly potent, ATP-competitive inhibitor of CDK1/cyclin B and CDK2/cyclin A (IC50=600pM and 500pM) with selectivity over VEGF-R2 and GSK-3β (IC50=32nM and 140nM).
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6,7-Dihydro-5H-cyclopenta[b]pyridin-7-amine hydrochloride 97+%
Supplier: Apollo Scientific
6,7-Dihydro-5H-cyclopenta[b]pyridin-7-amine hydrochloride 97+%
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(+)-1-Deoxynojirimycin 99% min
Supplier: Apollo Scientific
(+)-1-Deoxynojirimycin 99% min
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1-Bromo-4-butoxybenzene 97%
Supplier: Apollo Scientific
1-Bromo-4-butoxybenzene 97%
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Benzylammonium chloride 99%
Supplier: Apollo Scientific
Benzylammonium chloride 99%
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Ethyl-2-chloronicotinate 98%
Supplier: Apollo Scientific
Ethyl-2-chloronicotinate 98%
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NG-Hydroxy-L-arginine monoacetate ≥98%
Supplier: ENZO LIFE SCIENCES
Intermediate in NO biosynthesis
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N-ω-Hydroxy-L-norarginine acetate salt ≥97% (by TLC)
Supplier: ENZO LIFE SCIENCES
Potent and reversible arginase inhibitor. Specifically interacts with the manganese-cluster of the arginase active site. Does not act as a substrate or as an inhibitor of NOS.
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BIX 01294 trihydrochloride, hydrate ≥95% (by HPLC)
Supplier: ENZO LIFE SCIENCES
Selective and cell permeable inhibitor of G9a histone methyltransferase.
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TGX-221 ≥98% (by NMR)
Supplier: ENZO LIFE SCIENCES
PI3 kinase p110beta inhibitor
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PI103 ≥97% (by HPLC)
Supplier: ENZO LIFE SCIENCES
Potent, cell permeable and ATP-competitive inhibitor of DNA-PK, phosphoinositide 3-kinase (PI(3)K), the rapamycin-sensitive (mTORC1) and rapamycin-insensitive (mTORC2) complexes of the protein kinase mTOR. Exhibits little activity towards a panel of more than 40 other kinases even at concentrations as high as 10µM. Effectively blocks cell proliferation in glioma cell lines both in vitro and in vivo.
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UPF1035 ≥95% (by HPLC)
Supplier: ENZO LIFE SCIENCES
PARP-2 specific inhibitor with 60-fold selectivity for PARP-2 (IC50=0.15 ± 0.04μM) over PARP-1 (IC50=9.0 ± 0.7μM). Can be used for further characterization of PARP-2 in pathophysiological conditions.
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4-(3-Pyridin-2-yl-1H-pyrazol-4-yl)quinoline ≥97% (by 1H-NMR)
Supplier: ENZO LIFE SCIENCES
Cell permeable, potent, selective and ATP-competitive inhibitor of TGF-β RI kinase (IC50=51nM). Displays ~15-fold greater selectivity over p38α MAPK (IC50=740nM). Inhibits TGF-β-dependent cellular growth (IC50=89nM in NIH 3T3 mouse fibroblasts) and transcription activation (IC50=47nM in mink lung cells). Suppresses invasion of MDA-MB-231 breast cancer cells in a matrigel invasion assay.
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Resibufogenin (from Bufonis venom) ≥98% (by HPLC)
Supplier: ENZO LIFE SCIENCES
Specific Na⁺/K⁺-ATPase inhibitor.
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: GRANT INSTRUMENTS
: BOCHEM
: VWR Collection
: DWK Life Sciences
: Thermo Fisher Scientific
: VWR Collection
: Oxford Nanopore Technologies
: Industrial Physics
: AAT BIOQUEST
: Integra
: Palbam
: VWR Collection
: Integra
: VWR Collection
: FACELLITATE
: NANOENTEK
: Greiner Bio-One