Dihydrocoumarin structure
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Common Name | Dihydrocoumarin | ||
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CAS Number | 119-84-6 | Molecular Weight | 148.159 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 272.0±15.0 °C at 760 mmHg | |
Molecular Formula | C9H8O2 | Melting Point | 24-25 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 108.4±17.8 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of DihydrocoumarinDihydrocoumarin is a compound found in Melilotus officinalis. Dihydrocoumarin is a yeast Sir2p inhibitor. Dihydrocoumarin also inhibits human SIRT1 and SIRT2 with IC50s of 208 μM and 295 μM, respectively[1]. |
Name | 3,4-dihydrocoumarin |
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Synonym | More Synonyms |
Description | Dihydrocoumarin is a compound found in Melilotus officinalis. Dihydrocoumarin is a yeast Sir2p inhibitor. Dihydrocoumarin also inhibits human SIRT1 and SIRT2 with IC50s of 208 μM and 295 μM, respectively[1]. |
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Related Catalog | |
Target |
hSIRT1:208 μM (IC50) hSIRT2:295 μM (IC50) |
In Vitro | Dihydrocoumarin induces a concentration-dependent inhibition of SIRT1 (IC50 of 208 μM) in an in vitro enzymatic assay. A decrease in SIRT1 deacetylase activity is observed even at micromolar doses (85±5.8 and 73±13.7% activity at 1.6 μM and 8 μM, respectively). The microtubule SIRT2 deacetylase is also inhibited with a similar dose dependency (IC50 of 295 μM)[1]. Dihydrocoumarin (1-5 mM) increases cytotoxicity in the TK6 cell line in a dose-dependent manner following a 24-h exposure. Dihydrocoumarin (1-5 mM) increases apoptosis in a dose-dependent manner in the TK6 cell line at the 6-h time point. A 5-mM dose of Dihydrocoumarin increases apoptosis at the 6-h time point in the TK6 cell line[1]. Dihydrocoumarin (1-5 mM) increases p53 lysine 373 and 382 acetylation in a dose-dependent manner in the TK6 cell line following a 24-h exposure period[1]. |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 272.0±15.0 °C at 760 mmHg |
Melting Point | 24-25 °C(lit.) |
Molecular Formula | C9H8O2 |
Molecular Weight | 148.159 |
Flash Point | 108.4±17.8 °C |
Exact Mass | 148.052429 |
PSA | 26.30000 |
LogP | 1.80 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.562 |
Water Solubility | insoluble |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | Xn:Harmful; |
Risk Phrases | R22;R36/37/38 |
Safety Phrases | S26-S36 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | MW5775000 |
HS Code | 29322980 |
HS Code | 2932209090 |
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Summary | 2932209090. other lactones. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Synthesis, carbonic anhydrase inhibition and cytotoxic activity of novel chromone-based sulfonamide derivatives.
Eur. J. Med. Chem. 96 , 425-35, (2015) Four series of sulfonamides incorporating chromone moieties were synthesized and assessed for their cytotoxic activity against MCF-7 and A-549 cell lines, considering the fact that some of these tumor... |
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DJ-1 interacts with and regulates paraoxonase-2, an enzyme critical for neuronal survival in response to oxidative stress.
PLoS ONE 9(9) , e106601, (2014) Loss-of-function mutations in DJ-1 (PARK7) gene account for about 1% of all familial Parkinson's disease (PD). While its physiological function(s) are not completely clear, DJ-1 protects neurons again... |
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The effect of temperature on the catalytic conversion of Kraft lignin using near-critical water.
Bioresour. Technol. 170 , 196-203, (2014) The catalytic conversion of suspended LignoBoost Kraft lignin was performed in near-critical water using ZrO2/K2CO3 as the catalytic system and phenol as the co-solvent and char suppressing agent. The... |
Dihydrocoumarin |
MFCD00006881 |
2-Chromanone |
EINECS 204-354-9 |
2H-1-Benzopyran-2-one, 3,4-dihydro- |
3,4-Dihydro-1-benzopyran-2-one,Benzodihydropyrone,Hydrocou |
3,4-dihydrochromen-2-one |
3,4-Dihydrocoumarin |
Hydrocoumarin |
chroman-2-one |