成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

返回ChemicalBook首頁(yè)>CAS數(shù)據(jù)庫(kù)列表>1033836-12-2

1033836-12-2

中文名稱 6-(3-氟苯基)-N-[1-(2,2,2-三氟乙基)-4-哌啶基]-3-吡啶羧酰胺
英文名稱 3-PYRIDINECARBOXAMIDE, 6-(3-FLUOROPHENYL)-N-[1-(2,2,2-TRIFLUOROETHYL)-4-PIPERIDINYL]-
CAS 1033836-12-2
分子式 C19H19F4N3O
分子量 381.37
MOL 文件 1033836-12-2.mol
更新日期 2025/01/22 01:55:23
1033836-12-2 結(jié)構(gòu)式 1033836-12-2 結(jié)構(gòu)式

基本信息

中文別名
6-(3-氟苯基)-N-[1-(2,2,2-三氟乙基)-4-哌啶基]-3-吡啶羧酰胺
6-(3-氟苯基)-N-[1-(2,2,2-三氟乙基)-4-哌啶基]-3-吡啶甲酰胺
6-(3-氟苯基)-N-[1-(2,2,2-三氟乙基)-4-哌啶基]-3-吡啶羧酰胺, >98%
英文別名
CS-1438
MDK36122
HPGDS inhibitor 1
HPGDS inhibitor 1, >=98%
Prostaglandin D Synthase (hematopoietic-type) Inhibitor I
6-(3-fluorophenyl)-N-(1-(2,2,2-trifluoroethyl)piperidin-4-yl)nicotinaMide
6-(3-Fluorophenyl)-N-[1-(2,2,2-trifluoroethyl)-4-piperidinyl]-3-pyridinecarboxamide
3-PYRIDINECARBOXAMIDE, 6-(3-FLUOROPHENYL)-N-[1-(2,2,2-TRIFLUOROETHYL)-4-PIPERIDINYL]-
所屬類別
生物化工:激動(dòng)劑抑制劑

物理化學(xué)性質(zhì)

沸點(diǎn)487.2±45.0 °C(Predicted)
密度1.33±0.1 g/cm3(Predicted)
儲(chǔ)存條件Sealed in dry,2-8°C
溶解度溶于二甲基亞砜
酸度系數(shù)(pKa)9.55±0.20(Predicted)
形態(tài)結(jié)晶固體
顏色White to off-white
6-(3-氟苯基)-N-[1-(2,2,2-三氟乙基)-4-哌啶基]-3-吡啶羧酰胺價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2024/11/11XW1033836122026-(3-氟苯基)-N-[1-(2,2,2-三氟乙基)-4-哌啶基]-3-吡啶羧酰胺1033836-12-25MG153元
2024/11/08HY-104396-(3-氟苯基)-N-[1-(2,2,2-三氟乙基)-4-哌啶基]-3-吡啶羧酰胺
HPGDS inhibitor 1
1033836-12-25mg1860元
2024/11/08HY-104396-(3-氟苯基)-N-[1-(2,2,2-三氟乙基)-4-哌啶基]-3-吡啶羧酰胺
HPGDS inhibitor 1
1033836-12-210mM * 1mLin DMSO2046元

常見問題列表

生物活性
HPGDS inhibitor 1 是一種有效的,選擇性的和具有口服活性的 HPGDS 抑制劑,在酶和細(xì)胞分析中的 IC50 值分別為 0.6 nM 和 32 nM。HPGDS inhibitor 1 不抑制人 L-PGDS,mPGES,COX-1,COX-2 或 5-LOX。
靶點(diǎn)

IC50: 0.6 nM (HPGDS in enzyme assays) and 32 nM (HPGDS in cellular assays)

體外研究

HPGDS inhibitor 1 has equal potency against purified HPGDS from human, rat, dog, and sheep (IC 50 , 0.5-2.3 nM).

體內(nèi)研究

HPGDS inhibitor 1 (compound 8; 1 mg/kg) has excellent PK characteristics with 76% bioavailability, and the T 1/2 is 4.1 hours in rats.
Rats dosed orally with 1 mg/kg and 10 mg/kg HPGDS inhibitor 1 (compound 8) are sacrificed at various times. Oral administration of HPGDS inhibitor 1 blocks PGD2 production in the rat spleen; inhibition of PGD2 is inversely correlated with the plasma concentration of HPGDS inhibitor 1 in a time- and dose-dependent manner.
HPGDS inhibitor 1 (compound 8; 1 mg/mL) illustrates efficacy in an in vivo sheep model of asthma.

"1033836-12-2" 相關(guān)產(chǎn)品信息
101-54-2 613-93-4