38396-39-3

Bupivacaine Chemical Structure
38396-39-3

Chemical Structure

Bupivacaine

  • CAS No.: 38396-39-3
  • Formula:C18H28N2O
  • Molecular Weight:288.43

IUPAC Name: 1-butyl-N-(2,6-dimethylphenyl)piperidine-2-carboxamide

InChIKey: LEBVLXFERQHONN-UHFFFAOYSA-N

SMILES: O=C(C1N(CCCC)CCCC1)NC2=C(C)C=CC=C2C

Biological Activity: Bupivacaine is a NMDA receptor inhibitor. Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels with the IC50 of 69.5 μM. Bupivacaine can be used for the research of chronic pain[1][2][3].

Cat. No. Product Name Purity Description Pricing
HY-B0405
Bupivacaine 99.95% Bupivacaine is a NMDA receptor inhibitor. Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels with the IC50 of 69.5 μM. Bupivacaine can be used for the research of chronic pain.
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HY-B0405R
Bupivacaine (Standard) ≥98% Bupivacaine (Standard) is the analytical standard of Bupivacaine. This product is intended for research and analytical applications. Bupivacaine is a NMDA receptor inhibitor. Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels with the IC50 of 69.5 μM. Bupivacaine can be used for the research of chronic pain.
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HY-B0405S
Bupivacaine-d9 99.04% Bupivacaine-d99 is a deuterium labeled Bupivacaine. Bupivacaine is a NMDA receptor inhibitor.Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels with the IC50 of 69.5 μM. Bupivacaine can be used for the research of chronic pain.
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