Merck
  • 252926
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252926

Millipore

N-Acetylneuraminic Acid, 2,3-Dehydro-2-deoxy-, Sodium Salt

Inhibitor of bacterial, viral, and mammalian neuraminidases. Ki = 4 µM for influenza virus neuraminidase. Believed to act by binding to the catalytic site of neuraminidase as a transition state analog.

All Photos(1)
Synonym(s):
N-Acetylneuraminic Acid, 2,3-Dehydro-2-deoxy-, Sodium Salt
Empirical Formula (Hill Notation):
C11H16NNaO8
Molecular Weight:
313.24

品質水準

100

アッセイ

≥95% (TLC)

形状

solid

manufacturer/tradename

Calbiochem®

保管条件

OK to freeze
desiccated (hygroscopic)

色

off-white to pale yellow

溶解性

water: 1 mM

輸送温度

ambient

保管温度

−20°C

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N-Acetylneuraminic Acid, 2,3-Dehydro-2-deoxy-, Sodium Salt

Adenosine 3′,5′-cyclic Monophosphate, 8-(4-Chlorophenylthio)-2′-O-Methyl-, Sodium Salt A potent, cell-permeable, and specific activator of the exchange protein activated by cyclic AMP (EPAC).

Millipore

116833

Adenosine 3′,5′-cyclic Monophosphate, 8-(4-Chlorophenylthio)-2′-O-Methyl-, Sodium Salt

N-Acetyl-α-D-15N glucosamine-1-phosphate disodium salt ≥98 atom % 15N, ≥95% (CP)

Sigma-Aldrich

905488

N-Acetyl-α-D-15N glucosamine-1-phosphate disodium salt

2′-Deoxycytidine-13C9,15N3 5′-monophosphate disodium salt ≥98 atom %, ≥95% (CP)

Sigma-Aldrich

648612

2'-デオキシシチジン-13C9,15N3 5'-一リン酸 ナトリウム塩

assay

≥95% (TLC)

assay

≥98% (HPLC)

assay

≥95% (CP)

assay

≥95% (CP)

form

solid

form

lyophilized

form

solid

form

solid

manufacturer/tradename

Calbiochem®

manufacturer/tradename

Calbiochem®

manufacturer/tradename

-

manufacturer/tradename

-

storage condition

OK to freeze

storage condition

OK to freeze, desiccated (hygroscopic)

storage condition

-

storage condition

-

color

off-white to pale yellow

color

-

color

-

color

-

solubility

water: 1 mM

solubility

water: 10 mg/mL

solubility

-

solubility

-

詳細

A ganglioside neuraminidase inhibitor that is believed to act by binding to the catalytic site of neuraminidase. Reported to inhibit influenza virus neuraminidase (Ki = 4 µM). Also inhibits bacterial, viral, and mammalian neuraminidases.
Inhibitor of bacterial, viral, and mammalian neuraminidases. Ki = 4 µM for influenza virus neuraminidase. Believed to act by binding to the catalytic site of neuraminidase as a transition state analog.

警告

Toxicity: Standard Handling (A)

再構成

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 1 month at -20°C.

その他情報

Kopitz, J., et al. 1997. Eur. J. Cell. Biol.73, 1.
Holzer, C.T., et al. 1993. Glycoconj. J.10, 40.
Chong, A.K., et al. 1991. Biochem. Int.24, 165.

法的情報

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

保管分類コード

11 - Combustible Solids

WGK

WGK 1

引火点(°F)

Not applicable

引火点(℃)

Not applicable

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