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KH7

Cat. No. M7874
KH7 Structure
Size Price Availability Quantity
5mg USD 240  USD240 In stock
10mg USD 384  USD384 In stock
50mg USD 1306  USD1306 In stock
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Quality Control & Documentation
Biological Activity

KH7 is a specific inhibitor of soluble adenylate cyclase (sAC) with IC50 values of 3-10 μM against recombinant sACt proteins (human and others) in cells. KH7 is also an inhibitor of cAMP.

Chemical Information
Molecular Weight 419.3
Formula C17H15BrN4O2S
CAS Number 330676-02-3
Form Solid
Solubility (25°C) DMSO: ≥20 mg/mL
Storage -20°C
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Hemanoel Passarelli-Araujo, et al. Phylogenetic analysis and population structure of Pseudomonas alloputida

[2] Sarder Arifuzzaman, et al. Research update and opportunity of non-hormonal male contraception: Histone demethylase KDM5B-based targeting

[3] Emil Jakobsen, et al. The inhibitors of soluble adenylate cyclase 2-OHE, KH7, and bithionol compromise mitochondrial ATP production by distinct mechanisms

[4] Jarel K Gandhi, et al. Differential Intraocular Pressure Measurements by Tonometry and Direct Cannulation After Treatment with Soluble Adenylyl Cyclase Inhibitors

[5] Domenico De Rasmo, et al. Intramitochondrial adenylyl cyclase controls the turnover of nuclear-encoded subunits and activity of mammalian complex I of the respiratory chain

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Keywords: KH7 supplier, Adenylate Cyclase, inhibitors, activators


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