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T1787 |
Levobupivacaine
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Sodium Channel
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Levobupivacaine is an amino-amide local anaesthetic drug belonging to the family of n-alkylsubstituted pipecoloxylidide. It is the S-enantiomer of bupivacaine. Levobupivacaine hydrochloride is commonly marketed by AstraZ... |
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T19658 |
Enflurane
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NSC115944,Ethrane,NSC-115944,Efrane,NSC 115944 |
Others
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Enflurane (Efrane), a volatile anaesthetic, is a potent inhibitor of high conductance Ca2+-activated K+ channels of Chara australis. Enflurane is an internal standard in monitoring halogenated volatile anaesthetics by he... |
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T0386L |
Ropivacaine
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LEA-103 HCl |
Potassium Channel
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Sodium Channel
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Ropivacaine (LEA-103 HCl) is a local anaesthetic drug belonging to the amino amide group. |
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T0386 |
Ropivacaine hydrochloride
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Ropivacaine monohydrochloride |
Potassium Channel
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Sodium Channel
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Ropivacaine hydrochloride (Ropivacaine monohydrochloride) is the hydrochloride salt of ropivacaine, a local anesthetic of the amide type with analgesic activity. |
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T6566 |
Levobupivacaine hydrochloride
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Levobupivacaine HCl,(S)-(-)-Bupivacaine HCl,(S)-(-)-Bupivacaine monohydrochloride |
Sodium Channel
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Levobupivacaine hydrochloride ((S)-(-)-Bupivacaine monohydrochloride) is a reversible neuronal sodium channel inhibitor, which is the pure S(-)-enantiomer of bupivacaine. It was utilized as a long-acting local anesthetic... |
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T27572 |
Ibuprofen diethylaminoethyl ester
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Brufen diethylaminoethyl ester,BF-DEAE,BF DEAE |
Others
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Ibuprofen diethylaminoethyl ester (BF DEAE) has anti-inflammatory activity, acts as a local anaesthetic and can be used in the study of neurological disorders. |
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T0726 |
Benzydamine hydrochloride
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Benzydamine HCl,AF864 |
COX
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PGE Synthase
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Antibacterial
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Benzydamine hydrochloride (AF864), a locally-acting nonsteroidal anti-inflammatory drug, has local anaesthetic and analgesic properties. |
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T21787L |
Azepexole hydrochloride
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4H-Oxazolo[4,5-d]azepin-2-amine, 6-ethyl-5,6,7,8-tetrahydro-, hydrochloride (1:1) |
Adrenergic Receptor
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Azepexole hydrochloride (4H-Oxazolo[4,5-d]azepin-2-amine, 6-ethyl-5,6,7,8-tetrahydro-, hydrochloride (1:1)) is a potent α2-Adrenoceptor agonist with anaesthetic effects. |
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T1198 |
Tetracaine hydrochloride
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Amethocaine hydrochloride,Amethocalne HCl,Tetracaine HCl |
Calcium Channel
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Sodium Channel
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Tetracaine hydrochloride (Amethocalne HCl) (Pontocaine), a potent local anaesthetic, is a channel function allosteric inhibitor. It is primarily used as an antipruritic and topically in ophthalmology, and it has been use... |
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T6645 |
Ropivacaine hydrochloride monohydrate
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Ropivacaine HCl,Ropivacaine HCl monohydrate,LEA 103,LEA-103 HCl |
Potassium Channel
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Sodium Channel
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Ropivacaine hydrochloride monohydrate (LEA-103 HCl) is an anaesthetic agent and blocks impulse conduction in nerve fibres through inhibiting sodium ion influx reversibly. |
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T0901 |
Chlorobutanol
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Chlortran,Chloretone,YM-57158,Chlorbutol,Chloreton |
Antibacterial
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Antibiotic
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Antifungal
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Chlorobutanol (Chlortran) is a chemical preservative, sedative hypnotic and weak local anaesthetic. It has Antibacterial and Antifungal properties. Chlorobutanol is typically used at a concentration of 0.5% where it lend... |
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T31843 |
Fomocaine HCl
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P-652 HCl,Fomocaine,P652 hydrochloride,P-652 hydrochloride,Panacaine hydrochloride,P 652 hydrochloride |
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Fomocaine is an type of anaesthetic agent blocking voltage-gated Na(+) currents in neurons. |
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T68941 |
Dioxadrol
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Dioxadrol is a dissociative anaesthetic drug which has been found to be an NMDA antagonist and produces similar effects to PCP in animals. |
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T60423 |
Etoxadrol
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Etoxadrol (CL-1848C) is a potent and high affinity N-methyl-D-aspartic acid (NMDA) antagonist that can be used for anaesthetic research [1]. |
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T80043 |
µ-Conotoxin-CnIIIC
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Sodium Channel
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μ-Conotoxin-CnIIIC, a 22-residue conopeptide derived from Conus consors, acts as a potent and persistent NaV1.4 channel blocker, exhibiting analgesic, anaesthetic, and myorelaxant properties [1] [2]. |
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T61475 |
Ropivacaine mesylate
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Ropivacaine mesylate, a long-acting amide local anaesthetic, is used for spinal block and effectively mitigates neuropathic pain. It achieves analgesia by reversibly inhibiting sodium ion influx in nerve fibers, thus blo... |
