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Tyrphostin 9

Cat. No. M3096
Tyrphostin 9  Structure
Synonym:

SF 6847, RG-50872

Size Price Availability
25mg USD 50  USD50 Out of stock
50mg USD 80  USD80 Out of stock
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Quality Control & Documentation
Biological Activity

Tyrphostin 9 is firstly designed as an EGFR inhibitor with IC50 of 460 μM, but is also found to be more potent to PDGFR with IC50 of 0.5 μM.

Chemical Information
Molecular Weight 282.38
Formula C18H22N2O
CAS Number 10537-47-0
Solubility (25°C) DMSO 40 mg/mL
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] Amanda Chow, et al. Dasatinib inhibits peripapillary scleral myofibroblast differentiation

[2] Salanee Kandandapani, et al. Exploring the interaction between tyrphostin 9 and human serum albumin using biophysical and computational methods

[3] Lyndsey F Meyer, et al. Development and validation of an LC-MS/MS method for tyrphostin A9

[4] Zo Lama, et al. Kinase inhibitors tyrphostin 9 and rottlerin block early steps of rabies virus cycle

[5] Alberto Camacho, et al. Tyrphostin AG17 inhibits adipocyte differentiation in vivo and in vitro

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Keywords: Tyrphostin 9 , SF 6847, RG-50872 supplier, VEGFR/PDGFR, inhibitors, activators


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