盐酸地匹福林结构式
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常用名 | 盐酸地匹福林 | 英文名 | Dipivefrin HCl |
|---|---|---|---|---|
| CAS号 | 64019-93-8 | 分子量 | 387.89800 | |
| 密度 | N/A | 沸点 | 473.7ºC at 760 mmHg | |
| 分子式 | C19H30ClNO5 | 熔点 | 158-159° | |
| MSDS | N/A | 闪点 | 240.3ºC |
盐酸地匹福林用途Dipivefrin hydrochloride (Dipivefrine hydrochloride) 是一种抗青光眼前体药物,通过角膜中的酯酶水解为其活性化合物肾上腺素。 |
| 中文名 | 盐酸地匹福林 |
|---|---|
| 英文名 | dipivefrin hydrochloride |
| 中文别名 | 4-(1-羟基-2-(甲基氨基)乙基)-1,2-苯二醇二特戊酸酯盐酸盐 |
| 英文别名 | 更多 |
| 描述 | Dipivefrin hydrochloride (Dipivefrine hydrochloride) 是一种抗青光眼前体药物,通过角膜中的酯酶水解为其活性化合物肾上腺素。 |
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| 相关类别 | |
| 体内研究 | 盐酸二吡氟林(0.3-10μg/kg;i.p.;)诱导记忆增强涉及中枢β-而不是α肾上腺素能机制[3]。动物模型:雄性60日龄CFW小鼠(23-28g)[3]剂量:0.3μg/kg、1.0μg/kg、3.0μg/kg、10μg/kg;腹腔注射;训练后结果:抑制回避和Y迷宫辨别任务的保留率均显著提高,且呈剂量依赖性。 |
| 参考文献 |
| 沸点 | 473.7ºC at 760 mmHg |
|---|---|
| 熔点 | 158-159° |
| 分子式 | C19H30ClNO5 |
| 分子量 | 387.89800 |
| 闪点 | 240.3ºC |
| 精确质量 | 387.18100 |
| PSA | 84.86000 |
| LogP | 4.03530 |
| InChIKey | VKFAUCPBMAGVRG-UHFFFAOYSA-N |
| SMILES | CNCC(O)c1ccc(OC(=O)C(C)(C)C)c(OC(=O)C(C)(C)C)c1.Cl |
| 储存条件 | -20°C, 充氩 |
| 水溶解性 | Freely soluble in water, very soluble in methanol, freely soluble in ethanol (96 per cent) and in methylene chloride. |
| 危险品运输编码 | UN 2811 6.1 / PGIII |
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Bikini dermatitis due to mercaptobenzothiazole.
Contact Dermatitis 54(6) , 345-6, (2006)
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[Radiation protective effect of beta-ketoanalogs of hydroxyphenyl ethanolamines].
Radiats. Biol. Radioecol. 37(6) , 914-7, (1997) Experiments are carried out on 3400 mice, irradiated in dose 8 Gy (LD97/30). beta-Ketoanalogs of adrenaline (adrenalone, 50-150 mumol/kg), m,p-dipivaloyladrenaline (20 mumol/kg) and phenylephrine (but... |
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Effects of dipivefrin and pilocarpine on pupil diameter, automated perimetry and LogMAR acuity.
Graefes Arch. Clin. Exp. Ophthalmol. 237(2) , 117-24, (1999) A study was carried out to ascertain, in ophthalmologically normal subjects, the short-term effects of dipivefrin hydrochloride 0.1% on visual performance and make comparisons with pilocarpine.Twelve ... |
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来源:The Scripps Research Institute Molecular Screening Center
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External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
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靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
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靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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实验名称:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
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External Id:TargetID_659_CEMA
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
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靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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靶标:RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
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靶标:N/A
External Id:SPEC167MG
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| Dipivefrin HCL |
| EINECS 264-609-5 |
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