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(S)-(-)-3-(3-羟基苯基)-N-丙基哌啶盐酸盐

更新时间:2025-08-26 13:55:38

(S)-(-)-3-(3-羟基苯基)-N-丙基哌啶盐酸盐结构式
(S)-(-)-3-(3-羟基苯基)-N-丙基哌啶盐酸盐结构式
品牌特惠专场
常用名 (S)-(-)-3-(3-羟基苯基)-N-丙基哌啶盐酸盐 英文名 PRECLAMOL HYDROCHLORIDE
CAS号 88768-67-6 分子量 255.78
密度 N/A 沸点 342.2ºC at 760 mmHg
分子式 C14H22ClNO 熔点 N/A
MSDS 中文版 美版 闪点 158ºC

 用途


盐酸普瑞拉莫尔((-)-3-聚丙烯盐酸盐)是一种选择性多巴胺自身受体激动剂。盐酸普瑞拉莫尔具有研究精神分裂症的潜力[1][2]。

 (S)-(-)-3-(3-羟基苯基)-N-丙基哌啶盐酸盐名称

中文名 (S)-(-)-3-(3-羟基苯基)-N-丙基哌啶 盐酸盐
英文名 3-[(3S)-1-Propyl-3-piperidinyl]phenol hydrochloride (1:1)

 (S)-(-)-3-(3-羟基苯基)-N-丙基哌啶盐酸盐生物活性

描述 盐酸普瑞拉莫尔((-)-3-聚丙烯盐酸盐)是一种选择性多巴胺自身受体激动剂。盐酸普瑞拉莫尔具有研究精神分裂症的潜力[1][2]。
相关类别
参考文献

[1]. Seth-Olov Thorberg, et al. Large scale synthesis and absolute configuration of (-)-3-ppp, a selective dopamine autoreceptor agonist. Tetrahedron. 1985, 41(1): 129-139.

[2]. Tamminga CA, et al. Pharmacologic properties of (-)-3PPP (preclamol) in man. J Neural Transm Gen Sect. 1992;88(3):165-75.  

 (S)-(-)-3-(3-羟基苯基)-N-丙基哌啶盐酸盐物理化学性质

沸点 342.2ºC at 760 mmHg
分子式 C14H22ClNO
分子量 255.78
闪点 158ºC
精确质量 255.13900
PSA 23.47000
LogP 3.72150
InChIKey NRHUDETYKUBQJT-BTQNPOSSSA-N
SMILES CCCN1CCCC(c2cccc(O)c2)C1.Cl

 (S)-(-)-3-(3-羟基苯基)-N-丙基哌啶盐酸盐MSDS

 (S)-(-)-3-(3-羟基苯基)-N-丙基哌啶盐酸盐安全信息

个人防护装备 Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
危险品运输编码 NONH for all modes of transport
WGK德国 3
海关编码 2933399090

 (S)-(-)-3-(3-羟基苯基)-N-丙基哌啶盐酸盐海关

海关编码 2933399090
中文概述 2933399090. 其他结构含非稠合吡啶环的化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%
申报要素 品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期
Summary 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 (S)-(-)-3-(3-羟基苯基)-N-丙基哌啶盐酸盐文献3

更多文献
Central dopamine receptor agonist and antagonist actions of the enantiomers of 3-PPP.

Psychopharmacology 81 , 89-99, (1983)

The two enantiomers of the putative centrally acting dopamine (DA) autoreceptor agonist 3-(3-hydroxyphenyl)-N-n-propylpiperidine, 3-PPP (Hjorth et al. 1981), were pharmacologically evaluated. An exten...

Dopamine receptor agonistic and antagonistic effects of 3-PPP enantiomers.

Psychopharmacology 81 , 199-207, (1983)

The pharmacological profile of the enantiomers of the proposed selective dopamine (DA) autoreceptor agonist 3-PPP [3-(3-hydroxyphenyl)-N-n-propylpiperidine] has been studied. In vitro both enantiomers...

(+)-[3H]3-(3-hydroxyphenyl)-N-(1-propyl)-piperidine binding to sigma receptors in mouse brain in vivo.

Eur. J. Pharmacol. 161 , 263-266, (1989)

Binding of i.v. administered (+)-[3H]3-(3-hydroxyphenyl)-N-(1-propyl)piperidine ([3H]3-PPP) in the brain of intact mice is antagonized dose responsively by sigma receptor ligands. The correlation of p...

 (S)-(-)-3-(3-羟基苯基)-N-丙基哌啶盐酸盐靶点实验

查看更多实验

实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
实验名称:Inhibition of neurosphere proliferation of mouse neural precursor cells by MTT assay
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1266185
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
实验名称:Evaluated for dopa accumulation (biochemical activity) in rat limbic system
来源:ChEMBL
靶标:Rattus norvegicus
External Id:CHEMBL778855
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
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
实验名称:Evaluated for dopa accumulation (biochemical activity) in rat striatum
来源:ChEMBL
靶标:Rattus norvegicus
External Id:CHEMBL778857
实验名称:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
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