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AL 8697

SKU: orb1940830

Description

AL 8697 is a selective p38α MAPK inhibitor (IC50 = 6 nM) with 14-fold selectivity over p38β (IC50 = 82 nM) and 300-fold selectivity over a panel of 91 kinases. AL 8697 has anti-inflammatory activity.(In Vivo):In male Wistar rats, AL 8697 (1, 3, 10, 30 mg/kg; p.o.) decreases the oedema in right and left paws in a dose-dependent manner thereby causing a larger improvement in the contralateral un-injected paw.

Images & Validation

Key Properties

CAS Number1057394-06-5
MW402.421
Purity>98% (HPLC)
FormulaC21H21F3N4O
SMILESCc1c(F)cc(cc1-c1c(F)cn2c(nnc2c1F)C(C)(C)C)C(=O)NC1CC1
Targetp38 MAPK
SolubilityIn Vitro: DMSO : 100 mg/mL (248.50 mM)

Bioactivity

In Vivo
AL 8697 (1-30 mg/kg; p.o. ; once daily for 10 days) dose-dependently decreases the oedema in right and left paws. Animal model: Male Wistar rats. Dosage: 1, 3, 10, 30 mg/kg. Administration: Oral gavage; once daily for 10 days. Result: Dose-dependently decreased the oedema in right and left paws, causing a larger improvement in the contralateral un-injected paw.

Storage & Handling

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

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AL 8697 (orb1940830)

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Step 1: Enter information below

(Recommended: An additional animal making an allowance for loss during the experiment)

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Available Sizes

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5 mg
$ 350.00
10 mg
$ 490.00
25 mg
$ 810.00
50 mg
$ 1,140.00
100 mg
$ 1,550.00
500 mg
$ 3,080.00