Hamaudol structure
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Common Name | Hamaudol | ||
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CAS Number | 735-46-6 | Molecular Weight | 276.28500 | |
Density | N/A | Boiling Point | 464.7±45.0 °C at 760 mmHg | |
Molecular Formula | C15H16O5 | Melting Point | 197.0-197.5 °C | |
MSDS | N/A | Flash Point | N/A |
Use of HamaudolHamaudol is a chromone isolated from Saposhnikovia divaricata. Hamaudol shows significant inhibitory activity on cyclooxygenase (COX)-1 and COX-2 activities with IC50 values of 0.30, 0.57 mM, respectively, and has potent analgesia and anti-inflammary effects[1][2]. |
Name | (3S)-3,5-dihydroxy-2,2,8-trimethyl-3,4-dihydropyrano[3,2-g]chromen-6-one |
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Synonym | More Synonyms |
Description | Hamaudol is a chromone isolated from Saposhnikovia divaricata. Hamaudol shows significant inhibitory activity on cyclooxygenase (COX)-1 and COX-2 activities with IC50 values of 0.30, 0.57 mM, respectively, and has potent analgesia and anti-inflammary effects[1][2]. |
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Related Catalog | |
Target |
COX-1:0.3 mM (IC50) COX-2:0.57 mM (IC50) |
In Vivo | Hamaudol (Compound 7) increases the potency to exhibit a potent analgesia at doses of 1, 5 and 10 mg/kg in mice, although it do not show clear dose dependency[1]. |
References |
Boiling Point | 464.7±45.0 °C at 760 mmHg |
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Melting Point | 197.0-197.5 °C |
Molecular Formula | C15H16O5 |
Molecular Weight | 276.28500 |
Exact Mass | 276.10000 |
PSA | 79.90000 |
LogP | 1.88140 |
Storage condition | 2-8°C |
Hamaudol |