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BBT594

Cat. No. M10934
BBT594 Structure
Synonym:

NVP-BBT594

Size Price Availability Quantity
5mg USD 220  USD220 In stock
10mg USD 355  USD355 In stock
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Quality Control & Documentation
Biological Activity

BBT594 IS A POTENT RECEPTOR TYROSINE KINASE RET INHIBITOR COMMONLY USED IN CANCER RESEARCH.

Chemical Information
Molecular Weight 569.58
Formula C28H30F3N7O3
CAS Number 882405-89-2
Form Solid
Solubility (25°C) DMSO ≥ 20 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] Qi Zhang, et al. Oncotarget. Inhibition of mTORC1/C2 signaling improves anti-leukemia efficacy of JAK/STAT blockade in CRLF2 rearranged and/or JAK driven Philadelphia chromosome-like acute B-cell lymphoblastic leukemia

[2] Xiaotian Kong, et al. Sci Rep. How Does the L884P Mutation Confer Resistance to Type-II Inhibitors of JAK2 Kinase: A Comprehensive Molecular Modeling Study

[3] Elena Andreucci, et al. Oncotarget. Targeting the receptor tyrosine kinase RET in combination with aromatase inhibitors in ER positive breast cancer xenografts

[4] Andrea Morandi, et al. Cancer Res. GDNF-RET signaling in ER-positive breast cancers is a key determinant of response and resistance to aromatase inhibitors

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  Catalog
Abmole Inhibitor Catalog




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