| Cat.No. | Name | Information |
|---|---|---|
| M14788 | MS-222 | Tricaine methanesulfonate (MS-222) is common used to immobilize fish for marking or transport and to suppress sensory systems during invasive procedures. |
| M14641 | Tribromoethyl alcohol | Tribromoethyl alcohol (2,2,2-Tribromoethanol) is used to animals, particularly rodents, before surgery. |
| M5358 | Tribromoethanol for ready use | 2,2,2-Tribromoethanol is an injectable anesthetic agent used in mice. |
| M25454 | Orthocaine | Orthocaine is a local anesthetic agent. |
| M25453 | Tolycaine | Tolycaine is an amide local anaesthetic. Tolycaine exhibits good anesthetic effects on mice. |
| M25452 | Etidocaine hydrochloride | Etidocaine hydrochloride is an amino acidamide that acts as a local anesthetic with fast onset and long-acting properties. |
| M21430 | Lidocaine N-ethyl bromide | Lidocaine N-ethyl bromide is a blocker of non-membrane-permeable,and Inhibits Acid-Induced Activation of Esophageal Nociceptive C Fiber Neurons. |
| M14275 | Ropivacaine hydrochloride | Ropivacaine hydrochloride is a potent sodium channel blocker and blocks impulse conduction via reversible inhibition of sodium ion influx in nerve fibrese. |
| M14272 | Propoxycaine hydrochloride | Propoxycaine hydrochloride inhibits voltage-gated sodium channels, and thereby inhibits the ionic flux required for the initiation and conduction of impulses. Propoxycaine hydrochloride application can lead to a loss of sensation. |
| M10492 | Ropivacaine | Ropivacaine is a member of the amino amide class of local anesthetics and acts as a potent sodium channel blocker. |
| M10074 | 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. |
| M9018 | Levobupivacaine | Levobupivacaine is a reversible neuronal sodium channel inhibitor. Levobupivacaine is a long-acting amide local anaesthetic. Levobupivacaine exerts anaesthetic and analgesic effects through reversible blockade of neuronal sodium channel. |
| M6049 | Vecuronium Bromide | Vecuronium is a non-depolarizing neuromuscular blocking agent, used for skeletal muscle relaxation during surgery. |
| M6006 | Tetracaine | Tetracaine is a topical local anesthetic for the eyes; works by interfering with entry of sodium ions into nerve cells. |
| M5899 | Procaine | Procaine is a benzoic acid derivative with local anesthetic and antiarrhythmic properties. Procaine binds to and inhibits voltage-gated sodium channels, thereby inhibiting the ionic flux required for the initiation and conduction of impulses. *The compound is unstable in solutions, freshly prepared is recommended |
| M5741 | Lidocaine | Lidocaine is a selective inverse peripheral histamine H1-receptor agonist with an IC50 of >32 μM. Lidocaine (Lignocaine) also inhibits sodium channels involving complex voltage and using dependence. |
| M5603 | Dyclonine HCl | Dyclonine HCl is an oral anaesthetic, reversibly binds to activated sodium channels on the neuronal membrane, thereby decreasing the neuronal membrane's permeability to sodium ions, leading to an increased threshold for excitation. |
| M5583 | Diperodon hydrochloride | Diperodon hydrochloride is a local anaesthetics, by the action of hydrolazes in blood serum is decomposed. |
| M5570 | Dibucaine | Dibucaine (Cinchocaine) is a sodium channel inhibitor. Dibucaine is a potent SChE inhibitor. Dibucaine is a local anesthetic of the amide type now generally used for surface anesthesia. |
| M5449 | Benzocaine hydrochloride | Benzocaine hydrochloride is a surface anesthetic that acts by preventing transmission of impulses along nerve fibers and at nerve endings. |
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