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KH7

KH7
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Purity:98.43%
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KH7

Catalog No. T15658Cas No. 330676-02-3
KH7 is a soluble inhibitor of adenylyl cyclase (sAC)-specific. It has IC50s of 3-10 μM toward both recombinant purified human sACt protein and heterologously expressed sACt in cellular assays. KH7 is also a cAMP inhibitor.
With extensive experience in compound synthesis, we can provide rapid custom synthesis services for this product according to your research needs.
Pack SizePriceAvailabilityQuantity
1 mg$37In Stock
2 mg$50In Stock
5 mg$82In Stock
10 mg$132In Stock
25 mg$265In Stock
50 mgInquiryIn Stock
1 mL x 10 mM (in DMSO)$91In Stock
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Product Introduction

Bioactivity
Description
KH7 is a soluble inhibitor of adenylyl cyclase (sAC)-specific. It has IC50s of 3-10 μM toward both recombinant purified human sACt protein and heterologously expressed sACt in cellular assays. KH7 is also a cAMP inhibitor.
Targets&IC50
sAC:3-10 μM
In vitro
KH7 prevents the generation of CaSF. KH7 (10 μM) blocks this capacitation-induced cAMP increase. At higher concentrations (50 μM), 5- to 10-fold above its IC50 but still selective for sAC relative to tmACs, KH7 resulted in a significant decrease in the basal cAMP accumulation in sperm regardless of the incubation medium. The myocytes exert a negative inotropic effect (NIE) of approximately 20%, in the presence of KH7. This suggesting that sAC is involved in the normal generation of basal cardiac contractility [1,2].
Chemical Properties
Molecular Weight419.3
FormulaC17H15BrN4O2S
Cas No.330676-02-3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: < 0.1 mg/mL (insoluble)
DMSO: 100 mg/mL (238.49 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.3849 mL11.9246 mL23.8493 mL119.2464 mL
5 mM0.4770 mL2.3849 mL4.7699 mL23.8493 mL
10 mM0.2385 mL1.1925 mL2.3849 mL11.9246 mL
20 mM0.1192 mL0.5962 mL1.1925 mL5.9623 mL
50 mM0.0477 mL0.2385 mL0.4770 mL2.3849 mL
100 mM0.0238 mL0.1192 mL0.2385 mL1.1925 mL

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