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Merck
CN

P103

(S)-(-)-3-(3-羟基苯基)-N-丙基哌啶 盐酸盐

≥98% (HPLC), solid

别名:

S-(-)-3-PPP, 丙克拉莫

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经验公式(希尔记法):
C14H21NO · HCl
化学文摘社编号:
分子量:
255.78
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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InChI

1S/C14H21NO.ClH/c1-2-8-15-9-4-6-13(11-15)12-5-3-7-14(16)10-12;/h3,5,7,10,13,16H,2,4,6,8-9,11H2,1H3;1H/t13-;/m1./s1

SMILES string

Cl.CCCN1CCC[C@H](C1)c2cccc(O)c2

InChI key

NRHUDETYKUBQJT-BTQNPOSSSA-N

assay

≥98% (HPLC)

form

solid

color

white

solubility

H2O: 150 mg/mL (Solutions should be freshly prepared.), ethanol: slightly soluble (Solutions should be freshly prepared.)

Gene Information

Biochem/physiol Actions

Dopamine autoreceptor agonist; postsynaptic dopamine receptor antagonist.

Legal Information

Sold with the permission of Astra Pharmaceutical Co.

存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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J Arnt et al.
Psychopharmacology, 81(3), 199-207 (1983-01-01)
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 showed weak DA agonistic activity, and (--)-3-PPP some DA antagonistic effect on DA-stimulated adenylate cyclase activity. Both
S Hjorth et al.
Psychopharmacology, 81(2), 89-99 (1983-01-01)
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 extensive series of biochemical and behavioural experiments unexpectedly revealed that both (+)- and (-)-3-PPP showed clear, but differential
B K Koe et al.
European journal of pharmacology, 161(2-3), 263-266 (1989-02-28)
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 potencies for inhibition of binding in vivo and in vitro indicates that sigma receptors in mouse brain

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