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Product introduction
In Vivo Humulone (10 or 20 mg/kg; IP; single dose) shortens sleep onset and increases the duration of sleep induced by pentobarbital and decreases the spontaneous locomotion in open field at 20 mg/kg. Humulone (10 μmol; applied topically to the dorsal shaved area) pre-treatment significantly inhibited TPA (10 nmol)-induced COX-2 expression in Female ICR mice (6-7 weeks of age) skin. Humulone (1, 10 μmol; applied topical; pre-treatment 30 min) suppresses TPA-induced NF-κB DNA binding. Humulone attenuates TPA-stimulated nuclear translocation of p65 and p50 subunit proteins of NF-κB. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Male BALB/cAnNRj mice (9-11 weeks of age)Dosage: 10 or 20 mg/kg Administration: IP; pre-treatment before sodium pentobarbital (35 mg/kg; i.p.) and ethanol (3.5 g/kg) Result: Significantly decreased the latency and prolonged the duration of sleep induced by pentobarbital at 20 mg/kg dose. These effects were not observed at a lower dose of 10 mg/kg. Showed no effect on the onset of sleep induced by ethanol, but significantly increased sleep duration dose-dependently. Form:Oil
Chinese name
律草酮
English name
Humulone
Chinese alias
葎草酮 | (R)-3,5,6-三羟基-4,6-双(3-甲基丁-2-烯-1-基)-2-(3-甲基丁酰基)环己-2,4-二烯酮
English alias
SCHEMBL144835 | Humulone | NCGC00016682-02 | SCHEMBL13629033 | ((r)-3,5,6-trihydroxy-4,6-bis(3-methyl-2-butenyl)-2-(3-methyl-1oxobutyl)-2,4-cyclohexadien-1-one) | 3,5,6-Trihydroxy-2-(3-methylbutanoyl)-4,6-bis(3-methyl-2-butenyl)-2,4-cyclohexadien-1-one #
CAS number
26472-41-3
molecular formula
C21H30O5
molecular weight
362.46 g/mol
Exact mass
-
PSA
94.800 Ų
Logp
4.200
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Research chemical 5mg; ≥98%

Research chemical 5mg; ≥98%; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: 5mg; ≥98%.

item number:H648732-5mg
Product model:5mg
level: 5mg; ≥98%
Lead Time:30days
sold 968 Items
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5mg

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