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Nitrophenols

Organic compounds derived from phenols that contain a nitro functional group (-NO2).
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61 – 65 of 65 results
61

eMolecules​ 23282-55-5 | Sulfachloropyridazine sodium | Combi-Blocks306.700 | C10H8ClN4NaO2S | 98.000 | [Na+].Nc1ccc(cc1)S(=O)(=O)[N-]c1ccc(Cl)nn1 | 5g | 205403345

Sulfachloropyridazine sodium | Combi-Blocks | 23282-55-5306.700 | C10H8ClN4NaO2S | 98.000 | [Na+].Nc1ccc(cc1)S(=O)(=O)[N-]c1ccc(Cl)nn1 | 5g | 205403345

ENCOMPASS_PREFERRED
62

Chemscene CHEMSCENE
SDP

5000578420 1-METHYL-3 5-DINITRO-1 2-D 50G

ENCOMPASS_PREFERRED
63

Medchemexpress LLC MEDCHEMEXPRESS LLC
SDP

5000771898 4 4 -DINITRO-1 1 -B 1G

ENCOMPASS_PREFERRED
64

Medchemexpress LLC STO-609 | 52029-86-4 | 98.2% | 314.29 | 100 MG
SDP

STO-609 is a selective and cell-permeable inhibitor of the Ca2+/calmodulin-dependent protein kinase kinase (CaM-KK), with Ki values of 80 and 15 ng/mL for recombinant CaM-KKα and CaM-KKβ, respectively. It inhibits AMP-activated protein kinase kinase (AMPKK) activity in HeLa cell lysates with an IC50 ~0.02 g/ml.

  • Selective inhibitor of CaM-KK
  • Cell-permeable
  • Inhibits AMPKK activity

ENCOMPASS_PREFERRED
65

Medchemexpress LLC Sto-609 | 52029-86-4 | 98.20% | 314.29 | 50 MG
SDP

STO-609 is a selective and cell-permeable inhibitor of the Ca2+/calmodulin-dependent protein kinase kinase (CaM-KK). It inhibits AMP-activated protein kinase kinase (AMPKK) activity in HeLa cell lysates with an IC50 of approximately 0.02 g/ml. It is highly selective for CaM-KK without significant effect on downstream CaM kinases.

  • Inhibits recombinant CaM-KKα and CaM-KKβ isoforms and their autophosphorylation activities.
  • Has an IC50 value against CaM-KII of 10 μg/mL.
  • Inhibits constitutively active CaM-KKα and wild-type enzyme.
  • Suppresses Ca2+-induced activation of CaM-KIV in a dose-dependent manner in transfected HeLa cells.
  • Reduces endogenous activity of CaM-KK in SH-SY5Y neuroblastoma cells at 1μg/mL (80% inhibitory rate).

ENCOMPASS_PREFERRED