Nitrophenols
Selleck Chemical LLC STO-609
STO-609 is a specific inhibitor of the Ca2 /Calmodulin-dependent protein kinase kinase(CaM-KK) that inhibits the activities of recombinant CaM-KK and CaM-KK isoforms with Ki values of 80 and 15 ng/ml respectively and also inhibits their autophosphorylation activities STO-609 inhibits AMPKK activity and inhibits autophagy
Selleck Chemical LLC FHD-609-E1859-5MG
FHD-609 acts as a selective inhibitor and degrader of BRD9 protein (bromodomain-containing protein 9) FHD-609 targets ncBAF and can be used in research of various cancers involving mutations in a BAF complex subunit
eMolecules 2-Methyl-6-nitrophenol | 13073-29-5 | MFCD00031116 | 1g
Combi-Blocks | 2-Methyl-6-nitrophenol | 1g | 205380804 | AN-2925 | 98.000 | 13073-29-5 | MFCD00031116 | 153.137 | C7H7NO3
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Selleck Chemical LLC STO-609
STO-609 is a specific inhibitor of the Ca2 /Calmodulin-dependent protein kinase kinase(CaM-KK) that inhibits the activities of recombinant CaM-KK and CaM-KK isoforms with Ki values of 80 and 15 ng/ml respectively and also inhibits their autophosphorylation activities STO-609 inhibits AMPKK activity and inhibits autophagy
Medchemexpress LLC 3,5-Dinitrosalicylic acid | 609-99-4 | 100.0% | 228.12 | 25 G
3,5-Dinitrosalicylic acid is a derivative of salicylic acid. It is utilized in α-amylase assays, carbohydrase assays, and for the colorimetric determination of reducing substances. This product functions as a commonly used reducing sugar detection reagent, undergoing an oxidation-reduction reaction with reducing sugars to generate derivatives, which results in a color change for quantitative detection of reducing sugar content.
- Derivative of salicylic acid.
- Utilized in α-amylase assays.
- Utilized in carbohydrase assays.
- Used for the colorimetric determination of reducing substances.
- Functions as a commonly used reducing sugar detection reagent.
- Undergoes an oxidation-reduction reaction with reducing sugars to generate derivatives.
- Results in a color change for quantitative detection of reducing sugar content.
Apexbio Technology LLC STO-609 acetate 1173022-21-3 10mg
STO-609 acetate (CAS 1173022-21-3) is a selective inhibitor of Ca2 /calmodulin-dependent protein kinase kinase (CaM-KK) demonstrating Ki values of 80 ng/ml for CaM-KK and 15 ng/ml for CaM-KK This compound exhibits marked specificity for CaM-KK isoforms with minimal activity against downstream CaM kinases such as CaM-KI and CaM-KIV and an IC50 of approximately 10 g/ml for CaM-KII In cell-based studies STO-609 suppresses Ca2 -induced activation of CaM-KIV and reduces endogenous CaM-KK activity In vivo STO-609 administration enhances osteoblast formation and inhibits osteoclast differentiation in mouse models highlighting its utility in studies of calcium signaling and bone metabolism
Chem-Impex International, Inc. 3,5-Dinitrosalicylic acid | 609-99-4 | MFCD00007104 | 25G
3,5-Dinitrosalicylic acid, 609-99-4, MFCD00007104, 25G
Medchemexpress LLC Sto-609 | 52029-86-4 | 98.20% | 314.29 | 50 MG
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).
Medchemexpress LLC STO-609 | 52029-86-4 | 98.2% | 314.29 | 25 MG
STO-609 | 52029-86-4 | 98.2% | 314.29 | 25 MG
Medchemexpress LLC STO-609 | 52029-86-4 | 98.2% | 314.29 | 100 MG
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
Medchemexpress LLC 2R -2- 3 5-Dinitro 100g
(2R)-2-[(3 5-Dinitrobenzoyl)amino]-2-phenyl-acetic acid is a Glycine (HY-Y0966) derivative[1]
TARGETMOL CHEMICALS INC A 21960 5MG
Also available in 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. A 21960 (Ethyl 2-chloroacetoacetate) inhibits synapse formation between resolvase and two directly repeated res sites blocks site-specific recombination reactions and can be used to study bacterial infections. purity: 99%