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AD80

SKU: orb1222721

Description

AD80 is a multikinase inhibitor. It potently targets human RET, BRAF, S6K, and SRC.

Images & Validation

Key Properties

CAS Number1384071-99-1
MW473.44
Purity>98% (HPLC)
FormulaC22H19F4N7O
SMILESCC(C)N1C2=C(C(=N1)C3=CC=C(C=C3)NC(=O)NC4=C(C=CC(=C4)C(F)(F)F)F)C(=NC=N2)N
TargetCXCR
SolubilityDMSO : ≥ 150 mg/mL; 316.84 mM

Bioactivity

In Vivo
Oral administration of either AD80 or AD81 results in a notable 70-90% of animals developing to adulthood in Drosophila ptc>dRetMEN2Bmodel, a considerable improvement over the efficacy observed with AD57. AD80 also promotes enhanced tumour growth inhibition and reduces body-weight modulation relative to vandetanib in a mouse xenograft model. AD80 rescues 50% of mice transplanted with PTEN-deficient leukemia cells.
In Vitro
AD80 is a polypharmacological agent with an optimal balance of activity against Ret, Raf, Src, Tor and S6K that show high efficacy with very low toxicity. AD80 and AD81 inhibits RET, RAF, SRC and S6K, with greatly reduced mTOR activity relative to AD57 and AD58.AD80 is optimal for Ras-Erk pathway inhibition. AD80 inhibits proliferation of MZ-CRC-1 and TT thyroid cancer cells in culture, probably through the induction of apoptosis. Immunoblot analysis demonstrates potent downregulation of phosphorylated Ret and several downstream biomarkers within these cells. AD80 coordinately inhibits S6K1 together with the TAM family tyrosine kinase AXL. AD80 avoides S6K1 phosphorylation and mTOR co-association, resulting in durable suppression of S6K1-induced signaling and protein synthesis.

Storage & Handling

StorageStorage temperature: -20°C. Stability: ≥ 2 years
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

AD80 | AD-80 | AD 80

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    1384071-99-1

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    C22H19F4N7O

    1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 500 mg, 1 ml x 10 mM (in DMSO)
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AD80 (orb1222721)

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Available Sizes

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5 mg
$ 150.00
10 mg
$ 220.00
25 mg
$ 410.00
50 mg
$ 650.00
100 mg
$ 940.00
500 mg
$ 1,920.00