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LDC000067

Cat. No. M5328
LDC000067 Structure
Synonym:

LDC067

Size Price Availability Quantity
5mg USD 55  USD55 In stock
10mg USD 95  USD95 In stock
25mg USD 210  USD210 In stock
50mg USD 380  USD380 In stock
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Quality Control & Documentation
Biological Activity

LDC000067 reduces Ser2-P, induces p53 activation and leads to apoptosis in mESCs. In addition, LDC067 also dose-dependently inhibits P-TEFb-dependent de novo RNA synthesis of cellular genes.

Chemical Information
Molecular Weight 370.43
Formula C18H18N4O3S
CAS Number 1073485-20-7
Solubility (25°C) 64 mg/mL in DMSO
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
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] Albert TK, et al. Br J Pharmacol. Characterization of molecular and cellular functions of the cyclin-dependent kinase CDK9 using a novel specific inhibitor.

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  Catalog
Abmole Inhibitor Catalog




Keywords: LDC000067, LDC067 supplier, CDK, inhibitors, activators


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