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569-77-7

中文名稱 紅陪酚
英文名稱 PURPUROGALLIN
CAS 569-77-7
分子式 C11H8O5
分子量 220.18
MOL 文件 569-77-7.mol
569-77-7 結(jié)構(gòu)式 569-77-7 結(jié)構(gòu)式

基本信息

中文別名
紅倍酚
紅陪酚
1,2,3,9-四羥基苯并[7]環(huán)庚烯-8-酮
1,2,3,9-四羥基-8-苯并[7]環(huán)庚烯酮
5H-苯并環(huán)庚烯-5-酮,2,3,4,6-四羥基-
2,3,4,6-四羥基-5H-苯并[A]環(huán)庚烯-5-酮
2,3,4,6-四羥基-5H-苯并[7]環(huán)庚烯-5-酮
英文別名
C09964
MLS0007
NSC 35676
NSC 646653
AIDS138915
CHEBI:8647
AIDS-138915
AKOS 209-004
KBio1_001351
KBio2_000828

物理化學(xué)性質(zhì)

熔點(diǎn)275 °C (dec.)(lit.)
沸點(diǎn)321.11°C (rough estimate)
密度1.3824 (rough estimate)
折射率1.5140 (estimate)
儲(chǔ)存條件−20°C
溶解度可溶于DMSO(少許)、甲醇(少許)
酸度系數(shù)(pKa)6.75±0.20(Predicted)
形態(tài)固體
顏色深棕色
Merck7946
穩(wěn)定性空氣敏感
LogP2.050 (est)

安全數(shù)據(jù)

危險(xiǎn)性符號(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險(xiǎn)性描述H319-H315-H335
危險(xiǎn)品標(biāo)志Xi
危險(xiǎn)類別碼36/37/38
安全說明26-36
WGK Germany3
RTECS號DE8380000

常見問題列表

生物活性
Purpurogallin 是從櫟屬植物中提取的天然酚,具有強(qiáng)的黃嘌呤氧化酶 (Xanthine Oxidase) 抑制活性,其 IC50 為 0.2 μM。Purpurogallin 具有抗氧化和抗炎作用。
靶點(diǎn)

IC50: 0.2 μM (xanthine oxidase)

體外研究

Purpurogallin (50 or 100 μM; 7 or 25 hours; BV2 murine microglial cells) treatment attenuates the production of pro-inflammatory cytokines, including interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α) by suppressing their mRNA and protein expression in LPS-stimulated BV2 microglial cells.
Purpurogallin (100 μM; 75-120 minutes; BV2 murine microglial cells) exhibits anti-inflammatory properties by suppressing the phosphatidylinositol 3-kinase/Akt and mitogen-activated protein kinase signaling pathways in LPS-stimulated BV2 microglial cells.

RT-PCR

Cell Line: BV2 murine microglial cells
Concentration: 50 or 100 μM
Incubation Time: 7 or 25 hours
Result: Attenuated the production of pro-inflammatory cytokines, including interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α) by suppressing their mRNA and protein expression.

Western Blot Analysis

Cell Line: BV2 murine microglial cells
Concentration: 100 μM
Incubation Time: 75 minutes, 90 minutes, 120 minutes
Result: Suppressed the phosphatidylinositol 3-kinase/Akt and mitogen-activated protein kinase signaling pathways.
體內(nèi)研究

Purpurogallin (100-400?μg/kg; intraperitoneal injection; for 48 or 72 hours; male Sprague-Dawley rats) exerts its neuroinflammation effect through the dual effect of inhibiting IL-6 and TNF-α mRNA expression and reducing HMGB1 protein and mRNA expression.

Animal Model: Fifty-four male Sprague-Dawley rats (250-350?g) with subarachnoid hemorrhage (SAH)
Dosage: 100?μg/kg, 200?μg/kg, 400?μg/kg
Administration: Intraperitoneal injection; for 48 or 72 hours
Result: Dose-dependently reduced HMGB1 protein expression. High dose reduced TNF-α and HMGB1 mRNA levels.
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