application(s)
pharmaceutical (small molecule)
format
neat
General description
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.
Packaging
Unit quantity: 50 mg. Subject to change. The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.
Other Notes
Sales restrictions may apply.
法规信息
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Doxycycline desensitization for a suspected case of ehrlichiosis.
Joanna L Stollings et al.
The journal of allergy and clinical immunology. In practice, 2(1), 103-104 (2014-02-26)
Artem K Efremov et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(3), E334-E343 (2014-01-10)
Characterizing the collective functions of cytoskeletal motors is critical to understanding mechanisms that regulate the internal organization of eukaryotic cells as well as the roles various transport defects play in human diseases. Though in vitro assays using synthetic motor complexes
Fever and a solitary papule on the foot.
Stephanie D Gan et al.
JAMA dermatology, 150(2), 203-204 (2013-12-27)
Sridhar Arumugam et al.
Experimental parasitology, 138, 30-39 (2014-02-01)
Wolbachia of filarial nematodes are essential, obligate endobacteria. When depleted by doxycycline worm embryogenesis, larval development and worm survival are inhibited. The molecular basis governing the endosymbiosis between Wolbachia and their filarial host is still being deciphered. In rodent filarial
Jamil A Haque et al.
Blood, 123(4), 582-589 (2013-12-04)
Warfarin and other 4-hydroxycoumarins inhibit vitamin K epoxide reductase (VKOR) by depleting reduced vitamin K that is required for posttranslational modification of vitamin K-dependent clotting factors. In vitro prediction of the in vivo potency of vitamin K antagonists is complicated
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