## Abstract Respiratory burst mediates crucial bactericidal mechanism in neutrophils. However, undesirable respiratory burst leads to pathological inflammation and tissue damage. This study investigates the effect and the underlying mechanism of 5‐hydroxy‐2‐(4‐hydroxy‐3‐methoxyphenyl)‐3,7‐dimethoxy
5,7-Dimethoxy-3-(4-methoxyphenyl)-4H-chromen-4-one
✍ Scribed by Li, Huan-Qiu ;Xiao, Zhu-Ping ;Han, Yue ;Fang, Rui-Qin ;Zhu, Hai-Liang
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 436 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
No coin nor oath required. For personal study only.
✦ Synopsis
In the genistein-related title molecule, C 18 H 16 O 5 , the dihedral angle between the two benzene rings is 59.25 (6) .
Related literature
For reference structural data, see: Allen et al. (1987). For background, see: Kim et al. (2004); Li et al. (2006). Experimental Crystal data C 18 H 16 O 5 M r = 312.31 Triclinic, P1 a = 8.5649 (10) A b = 10.3212 (13) A c = 10.5563 (13) A = 63.783 (2) = 71.937 (2) = 65.953 (2) V = 754.83 (16) A ˚3 Z = 2 Mo K radiation = 0.10 mm À1 T = 298 (2) K 0.20 Â 0.15 Â 0.15 mm Data collection Bruker SMART CCD diffractometer Absorption correction: multi-scan (SADABS; Bruker, 2001) T min = 0.980, T max = 0.985 4140 measured reflections 2855 independent reflections 2134 reflections with I > 2(I) R int = 0.016 Refinement R[F 2 > 2(F 2 )] = 0.053 wR(F 2 ) = 0.145 S = 1.03 2855 reflections
📜 SIMILAR VOLUMES
In the genistein-related title compound, C 19 H 16 O 6 , the dihedral angle between the two benzene-ring planes is 52.81 (9) .
Synthesis of 3-(4-Methoxyphenyl)-5,7-dimethoxy-(1H)-quinolin-2or 4-ones and Derivatives. -Various title compounds are prepared as nitrogen analogues of the pharmaceutically interesting genistein (XI). -
The title compound, C~16~H~11~ClO~2~, is a synthetic flavonoid. The fused-ring system is almost planar, with a mean deviation from the least-squares plane of 0.0204 (2) Å. The dihedral angle between the chromene group and the chlorophenyl ring is 50.9 (6)°, due to unfavourable steric interactions wi
The title compound, C 17 H 14 O 4 ÁCHCl 3 , was isolated from the rhizomes of Kaempferia parviflora. The benzopyran-4-one ring system and the phenyl substituent are approximately coplanar. The crystal structure is stabilized bystacking interactions between the benzopyran-4-one ring system of inversi