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Documentos

1134062

USP

Cimetidine

United States Pharmacopeia (USP) Reference Standard

Sinónimos:

SKF-92334

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About This Item

Fórmula empírica (notación de Hill):
C10H16N6S
Número de CAS:
51481-61-9
Peso molecular:
252.34
Número MDL:
MFCD00133296
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
329749396
NACRES:
NA.24

grado

pharmaceutical primary standard

familia API

cimetidine

fabricante / nombre comercial

USP

aplicaciones

pharmaceutical (small molecule)

formato

neat

temp. de almacenamiento

2-8°C

cadena SMILES

CN\C(NC#N)=N\CCSCc1nc[nH]c1C

InChI

1S/C10H16N6S/c1-8-9(16-7-15-8)5-17-4-3-13-10(12-2)14-6-11/h7H,3-5H2,1-2H3,(H,15,16)(H2,12,13,14)

Clave InChI

AQIXAKUUQRKLND-UHFFFAOYSA-N

Información sobre el gen

human ... HRH2(3274)

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Descripción general

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Aplicación

Cimetidine USP reference standard, intended for use in specified quality tests and assays as specified in the USP compendia.

Nota de análisis

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.  ​

Otras notas

Sales restrictions may apply.

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Descripción
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BP475

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PHR2242

Cimetidine Impurity D, Pharmaceutical Secondary Standard; Certified Reference Material

PHR2220

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PHR2250

Cimetidine Impurity B, pharmaceutical secondary standard, certified reference material

PHR2251

Cimetidine Impurity C, Pharmaceutical Secondary Standard; Certified Reference Material

PHR2252

Cimetidine Impurity J, certified reference material, pharmaceutical secondary standard

PHR2259

Cimetidine Impurity G, Pharmaceutical Secondary Standard; Certified Reference Material

PHR2260

Cimetidine Impurity I, Pharmaceutical Secondary Standard; Certified Reference Material

PHR2255

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PHR2243

Cimetidine Impurity E, Pharmaceutical Secondary Standard; Certified Reference Material

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Catherine H Olson et al.
Journal of biomedical informatics, 51, 60-71 (2014-04-17)
Create an automated algorithm for predicting elderly patients' medication-related risks for readmission and validate it by comparing results with a manual analysis of the same patient population. Outcome and Assessment Information Set (OASIS) and medication data were reused from a
Zhuo Wang et al.
Cancer chemotherapy and pharmacology, 74(2), 239-247 (2014-06-01)
We investigated E-selectin expression in mice and rabbits with vinorelbine-induced phlebitis and the effect of cimetidine. To find the relationship between E-selectin expression and vinorelbine-induced phlebitis. Mouse and rabbit model of vinorelbine-induced phlebitis was established by intravenous infusion of vinorelbine.
Jia-Xing Yue et al.
CNS neuroscience & therapeutics, 20(10), 883-892 (2014-07-06)
The upregulation of Nav1.8 in primary afferents plays a critical role in the development and persistence of neuropathic pain. The mechanisms underlying the upregulation are not fully understood. The present study aims to investigate the regulatory effect of histamine on
Kan Zhong et al.
Antimicrobial agents and chemotherapy, 58(7), 4153-4161 (2014-05-14)
Morinidazole is a novel 5-nitroimidazole antimicrobial drug that undergoes extensive metabolism in humans via N(+)-glucuronidation (N(+)-glucuronide of S-morinidazole [M8-1] and N(+)-glucuronide of R-morinidazole [M8-2]) and sulfation (sulfate conjugate of morinidazole [M7]). Our objectives were to assess the effects of renal
Ryan J Schutte et al.
Journal of neurophysiology, 112(4), 903-912 (2014-05-09)
Hundreds of mutations in the SCN1A sodium channel gene confer a wide spectrum of epileptic disorders, requiring efficient model systems to study cellular mechanisms and identify potential therapeutic targets. We recently demonstrated that Drosophila knock-in flies carrying the K1270T SCN1A
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