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56985-40-1

中文名稱(chēng) 9,11-二脫氧基-9Α,11Α-亞甲基環(huán)氧前列腺素 F2Α溶液
英文名稱(chēng) U-46619
CAS 56985-40-1
分子式 C21H34O4
分子量 350.49
MOL 文件 56985-40-1.mol
56985-40-1 結(jié)構(gòu)式 56985-40-1 結(jié)構(gòu)式

基本信息

中文別名
9,11-二脫氧基-9Α,11Α-亞甲基環(huán)氧前列腺素
9,11-二脫氧基-11Α,9Α-亞甲基環(huán)氧前列腺素 F2Α
9,11-二脫氧基-9Α,11Α-亞甲基環(huán)氧前列腺素 F2Α溶液
9,11-DIDEOXY-11Α,9Α-EPOXYMETHANOPROSTAGLANDIN F2Α
英文別名
U-46619
9,11-Methanoxy-PGH2
9,11-Methanoepoxy PGH2
11α,9α-Epoxymethanoprostaglandin H2
U-46619 - CAS 56985-40-1 - Calbiochem
9,11-DIDEOXY-11ALPHA,9ALPHA-EPOXYMETHANO
4-alpha,5-beta(z),6-alpha(1e,3s*)))-r-(1-alph
9,11-dideoxy-11α,9α-epoxymethanoprostaglandin f2α
9,11-dideoxy-11A,9A-epoxymethano-*prostaglandin F
9,11-DIDEOXY-9ALPHA,11ALPHA-METHANOEPOXY PGF2ALPHA
所屬類(lèi)別
生物化工:激動(dòng)劑抑制劑

物理化學(xué)性質(zhì)

沸點(diǎn)519.7±30.0 °C(Predicted)
密度1.092±0.06 g/cm3(Predicted)
閃點(diǎn)-10 °C
儲(chǔ)存條件-20°C
溶解度≥100 mg/mL in DMSO, ≥100 mg/mL in Ethanol, ≥100 mg/mL in DMF, ≥2 mg/mL in PBS pH 7.2
酸度系數(shù)(pKa)4.76±0.10(Predicted)
形態(tài)solution
顏色Colorless to light yellow
BRN4267334

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07
警示詞危險(xiǎn)
危險(xiǎn)性描述H225-H319-H336
防范說(shuō)明P210-P305+P351+P338
危險(xiǎn)品標(biāo)志F,Xi
危險(xiǎn)類(lèi)別碼11-36-66-67
安全說(shuō)明16-26
危險(xiǎn)品運(yùn)輸編號(hào)UN 1231 3/PG 2
危險(xiǎn)品運(yùn)輸編號(hào)UN 1231 3/PG 2
WGK Germany2
WGK Germany2
RTECS號(hào)MJ9681090
毒性LD50 intravenous in mouse: 66ug/kg

常見(jiàn)問(wèn)題列表

用途

U-46619是一種PGH2類(lèi)似物,可以用作血栓烷A2(TP)受體激動(dòng)劑,影響人類(lèi)血管平滑肌的促有絲分裂生長(zhǎng)。U 46619是穩(wěn)定的血栓烷A2模擬物,是H2內(nèi)過(guò)氧化物前列腺素的類(lèi)似物,用作血管收縮劑和血栓烷受體激動(dòng)劑。

生物活性
U-46619 (9,11-Methanoepoxy PGH2) 是一種穩(wěn)定的血栓素 A2 (TXA2) 的類(lèi)似物,也是一種有效的 TXA2 激動(dòng)劑。
靶點(diǎn)

TXA2

體外研究

U-46619 (1 nM-10 μM) causes platelets shape change and aggregation in a concentration-dependent manner, and with EC 50 s of 0.58 μM and 0.013 μM for aggregation and shape change, respectively.
U-46619 (10 nM-10 μM) increases internal Ca 2+ concentration ([Ca 2+ ]i) and activates phosphoinositide (PI) hydrolysis in a concentration-dependent manner with a similar concentration-dependency.
U-46619 (3 nM-10 μM) also activates GTPase concentration-dependently in the membranes derived from platelets.
U-46619 improves the differentiation efficiency of human induced pluripotent stem cells into endothelial cells by activating both p38MAPK and ERK1/2 signaling pathways.

體內(nèi)研究

U-46619 (5 μg/kg; i.v.) increases blood pressure in male spontaneously hypertensive rats (SHR).

Animal Model: 12-15 weeks-old male and female SHR
Dosage: 5 μg/kg
Administration: Intravenous injection
Result: Induceed a significant increase of MABP after 1 min in male SHR.
9,11-二脫氧基-9Α,11Α-亞甲基環(huán)氧前列腺素 F2Α溶液價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱(chēng)CAS號(hào)包裝價(jià)格
2024/11/08HY-1085669,11-二脫氧基-9Α,11Α-亞甲基環(huán)氧前列腺素 F2Α溶液
U-46619
56985-40-11mg(28.5mM * 100μL in Methyl acetate)3300元
2024/08/19HY-1085669,11-二脫氧基-9Α,11Α-亞甲基環(huán)氧前列腺素 F2Α溶液
U-46619
56985-40-15mg(28.5mM * 500μL in Methyl acetate)9900元
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