| Weight | 288.435 g/mol |
|---|---|
| Formula | C18H28N2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 5 |
Levobupivacaine (27262-47-1)
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- A comparison of the cardiovascular effects of levobupivacaine and rac-bupivacaine following intravenous administration to healthy volunteers (British Journal of Clinical Pharmacology, 2002)
- Levobupivacaine : A review of its pharmacology and use as a local anaesthetic (Drugs, 2000)
- Cardiovascular and central nervous system effects of intravenous levobupivacaine and bupivacaine in sheep. (Anesthesia & Analgesia, 1998)
- Levobupivacaineinduced seizures and cardiovascular collapse treated with Intralipid (Anaesthesia, 2007)
- Epidural pain relief in labour: potencies of levobupivacaine and racemic bupivacaine. (BJA: British Journal of Anaesthesia, 1998)
- Systemic toxicity and resuscitation in bupivacaine-, levobupivacaine-, or ropivacaine-infused rats. (Anesthesia & Analgesia, 2001)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCCN1CCCCC1C(=O)NC2=C(C=CC=C2C)C
-
InChIKeyLEBVLXFERQHONN-UHFFFAOYSA-N
- Pubchem - Levobupivacaine
- Wikipedia - levobupivacaine
Levobupivacaine (rINN) is a local anaesthetic drug belonging to the amino amide group. It is the S-enantiomer of bupivacaine. Levobupivacaine hydrochloride is commonly marketed by AbbVie under the trade name Chirocaine.
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