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| Product | Description | |
|---|---|---|
| Levobupivacaine hydrochloride | Levobupivacaine hydrochloride ((S)-(-)-Bupivacaine monohydrochloride) is a long-acting amide local agent that can suppress or relieve pain. Levobupivacaine hydrochloride exerts agent that can suppress or relieve pain. and analgesic effects through reversible blockade of neuronal sodium channel. Levobupivacaine hydrochloride can inhibit impulse transmission and conduction in cardiovascular and other tissues, possessing certain cardiac and CNS toxicity. Levobupivacaine hydrochloride is metabolized by hepatic cytochrome P450 (CYP450) enzymes in vivo. Levobupivacaine hydrochloride can also induce ferroptosis by miR-489-3p/SLC7A11 signaling in gastric cancer [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: (S)-(-)-Bupivacaine monohydrochloride. CAS No. 27262-48-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-B0653A. |  |
| Levobupivacaine free base | Levobupivacaine is a local anaesthetic drug belonging to the amino amide group. It is the S-enantiomer of bupivacaine. Levobupivacaine hydrochloride is commonly marketed by Abbott under the trade name Chirocaine. It acts via reversibly binding voltage-gated sodium channels to modulate ionic flux and block the initiation and transmission of nerve impulses. Uses: Local anaesthetic drug. Synonyms: (S)-1-butyl-N-(2,6-dimethylphenyl)piperidine-2-carboxamide; Levobupivacaine free base; (S)-1-Butyl-2',6'-pipecoloxylidide; L(-)-Bupivacaine. Grades: 98%. CAS No. 27262-47-1. Molecular formula: C18H28N2O. Mole weight: 288.44. |  |
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