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Merck
CN

610593

Meperidine solution

1 mg/mL in methanol, drug standard

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About This Item

Empirical Formula (Hill Notation):
C15H21NO2
CAS Number:
57-42-1
Molecular Weight:
247.33
UNSPSC Code:
41116107
PubChem Substance ID:
329759357
MDL number:
MFCD00057376

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InChI

1S/C15H21NO2/c1-3-18-14(17)15(9-11-16(2)12-10-15)13-7-5-4-6-8-13/h4-8H,3,9-12H2,1-2H3

SMILES string

CN1CCC(CC1)(C(OCC)=O)C2=CC=CC=C2

InChI key

XADCESSVHJOZHK-UHFFFAOYSA-N

grade

drug standard

drug control

kontrollierte Droge in Deutschland; regulated under CDSA - not available from Sigma-Aldrich Canada

availability

not available in Japan

concentration

1 mg/mL in methanol

application(s)

pharmaceutical (small molecule)

storage temp.

−20°C

Gene Information

human ... OPRD1(4985), OPRK1(4986), OPRM1(4988)
rat ... Oprm1(25601), Slc6a3(24898), Slc6a4(25553)

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Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

51.8 °F - closed cup

flash_point_c

11 °C - closed cup

Regulatory Information

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Chris Dockendorff et al.
Bioorganic & medicinal chemistry letters, 19(4), 1228-1232 (2009-01-27)
A series of 1-aminotetralin scaffolds was synthesized via metal-catalyzed ring-opening reactions of heterobicyclic alkenes. Small libraries of amides and amines were made using the amino group of each scaffold as a handle. Screening of these libraries against human opioid receptors
Mari Sithambaram Karthikeyan
European journal of medicinal chemistry, 44(2), 827-833 (2008-06-27)
A series of 2,4-dichloro-5-fluorophenyl containing thiazolotriazoles were synthesized starting from 3-(2,4-dichloro-5-fluorophenyl)-4H-1,2,4-triazole-3-thiol. The newly synthesized compounds were characterized by IR, 1H NMR, mass and elemental analysis. Some of the synthesized compounds were tested for their anti-inflammatory, analgesic and antimicrobial activities. Compounds
Alessio Coi et al.
European journal of medicinal chemistry, 43(11), 2479-2488 (2008-02-12)
Drugs delaying cardiac repolarization by blockade of hERG K(+) channel generally prolong the QT interval of the electrocardiogram, an effect regarded as a cardiac risk factor with the potential to cause 'torsade des pointes'-type arrhythmias in humans. The present study
Giulio Vistoli et al.
Bioorganic & medicinal chemistry, 18(1), 320-329 (2009-11-26)
Metabolic problems lead to numerous failures during clinical trials, and much effort is now devoted in developing in silico models predicting metabolic stability and metabolites. Such models are well known for cytochromes P450 and some transferases, whereas little has been
Motoi Tobita et al.
Bioorganic & medicinal chemistry letters, 15(11), 2886-2890 (2005-05-25)
HERG attracts attention as a risk factor for arrhythmia, which might trigger torsade de pointes. A highly accurate classifier of chemical compounds for inhibition of the HERG potassium channel is constructed using support vector machine. For two test sets, our
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