Phenols
Medchemexpress LLC P,p'-DDE; p,p'-dichlorodiphenyldichloroethylene | 72-55-9 | 99.9% | 250 MG
p,p'-DDE (4,4'-DDE) is the major and persistent metabolite of DDT. This orally active androgen receptor antagonist can affect the development and function of the male reproductive system by inhibiting androgen binding and transcriptional activity. High serum concentrations of p,p'-DDE may also be a risk factor for type 2 diabetes in women.
- Major and persistent metabolite of DDT
- Orally active androgen receptor antagonist
- Affects development and function of male reproductive system
- Inhibits androgen binding to the androgen receptor
- Inhibits androgen-induced transcriptional activity
- May be a risk factor for type 2 diabetes in women
Medchemexpress LLC N-trans-p-coumaroyloctopamine | 66648-45-1 | MFCD22417271 | 100 MG
N-trans-p-coumaroyloctopamine is a phenylpropanoid amide isolated from eggplant (Solanum melongena L.). This compound, with a molecular weight of 299.32 and chemical formula C17H17NO4, appears as a white to off-white solid. It is classified within phenylpropanoids, simple phenylpropanols, phenols, and polyphenols, originating from plants like Liliaceae and Ophiopogon japonicus (L. f.) Ker-Gawl.
- Isolated from eggplant (Solanum melongena L.)
- For research use only
- Molecular weight of 299.32
- Chemical formula C17H17NO4
- Appears as a white to off-white solid
- Purity of 99.70%
- Classified as a phenylpropanoid
- Soluble in DMSO at 83.33 mg/mL
- Store powder at -20°C for 3 years or 4°C for 2 years
- Store in solvent at -80°C for 6 months or -20°C for 1 month
Medchemexpress LLC STO-609 | 52029-86-4 | 98.20% | 314.29 | 5 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 ~0.02 g/ml.
- Inhibits activities of recombinant CaM-KKα and CaM-KKβ isoforms with Ki values of 80 and 15 ng/mL, respectively.
- Inhibits their autophosphorylation activities.
- Highly selective for CaM-KK without significant effect on downstream CaM kinases (CaM-KI and -IV).
- Inhibits constitutively active CaM-KKα as well as the wild-type enzyme.
- Suppresses Ca2+-induced activation of CaM-KIV in transfected HeLa cells in a dose-dependent manner.
- Reduces endogenous activity of CaM-KK in SH-SY5Y neuroblastoma cells at 1μg/mL (80% inhibitory rate).
Boston Bioproducts Inc BioAcryl-P Acrylamide/Bis-Acrylamide (40%, 37.5:1) - 500ml
BioAcryl-P Acrylamide/Bis-Acrylamide (40% 37 5/1) - 500ml (For Research Use and Further Manufacturing Only)