Piperidines
Medchemexpress LLC 1,2-pyrrolidinedicarboxylic acid, 5-oxo-, 1-(1,1-dimethylethyl) 2-(phenylmethyl) ester, (2R)- | 400626-71-3 | MFCD14635665 | 10g
Avibactam impurity 1 is an impurity of Avibactam (HY-14879)
eMolecules 1373765-19-5 | Medchem Express | IPSU | 5mg | 446263520 | HY-13796 | MFCD25976654 | 405.502 | C23H27N5O2
Ambeed | 6-Fluorobenzo[c][12]oxaborol-1(3H)-ol | 100mg | 600844860 | A647056 | 174671-89-7 | MFCD10699481 | 151.930 | C7H6BFO2
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Medchemexpress LLC Levobupivacaine hydrochloride | 27262-48-2 | >99.8% | 5 MG
Levobupivacaine hydrochloride is a long-acting amide local agent that can suppress or relieve pain. It exerts analgesic effects through reversible blockade of neuronal sodium channels. It can inhibit impulse transmission and conduction in cardiovascular and other tissues, possessing certain cardiac and CNS toxicity. It is metabolized by hepatic cytochrome P450 (CYP450) enzymes in vivo and can also induce ferroptosis by miR-489-3p/SLC7A11 signaling in gastric cancer.
- Long-acting amide local agent
- Suppresses or relieves pain
- Exerts analgesic effects through reversible blockade of neuronal sodium channels
- Inhibits impulse transmission and conduction in cardiovascular and other tissues
- Metabolized by hepatic cytochrome P450 (CYP450) enzymes in vivo
- Induces ferroptosis by miR-489-3p/SLC7A11 signaling in gastric cancer
Medchemexpress LLC HY-14879B 200mg , Avibactam (sodium hydrate) CAS: Purity:98%
Medchemexpress, HY-14879B 200mg Avibactam (sodium hydrate) CAS: Formula:C7H12N3NaO7S IC50: 8 nM (TEM-1), 5 nM (CTX-M-15) Purity:98% Avibactam sodium hydrate is a covalent, reversible β-lactamase inhibitor, inhibits β-lactamase TEM-1 and CTX-M-15 with IC 50 of 8 nM and 5 nM, respectively. Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Med Vet International Zoetis Carbocaine-V 2% Sterile Aqueous Solution, 50mL
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
CARBOCAINE-V Sterile Aqueous Solution (2% mepivacaine hydrochloride, USP) is recommended for infiltration, nerve block, intra-articular and epidural anesthesia for horses. It has also been found useful for topical anesthesia of the laryngeal mucosa prior to ventriculectomy.
Accela Chembio Inc 1 | 1'-(azodicarbonyl)dipiperidine (addp) | 5g | 10465-81-3 | MFCD00010111 | 98% | Shelf Life: 1260 Days | +4
1 | 1'-(azodicarbonyl)dipiperidine (addp) | 5g | 10465-81-3 | MFCD00010111 | 98% | Shelf Life: 1260 Days | +4
![eMolecules 27262-47-1 | LEVOBUPIVACAINE | AstaTech | MFCD00936851 | 288.435 | C18H28N2O | 95.000 | CCCCN1CCCC[C@H]1C(=O)Nc1c(C)cccc1C | 0.25g | 796988911](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502456373.PNG-250.jpg)
eMolecules 27262-47-1 | LEVOBUPIVACAINE | AstaTech | MFCD00936851 | 288.435 | C18H28N2O | 95.000 | CCCCN1CCCC[C@H]1C(=O)Nc1c(C)cccc1C | 0.25g | 796988911
LEVOBUPIVACAINE | AstaTech | 27262-47-1 | MFCD00936851 | 288.435 | C18H28N2O | 95.000 | CCCCN1CCCC[C@H]1C(=O)Nc1c(C)cccc1C | 0.25g | 796988911
AdipoGen Ropivacaine
Chemical. CAS 84057-95-4. Formula C17H26N2O. MW 274.4. Synthetic. Ropivacaine is a long-acting amide local anaesthetic agent. Ropivacaine is a potent and reversible blocker of sodium channels in nerve fibers. It is a pure S-enantiomer and less lipophilic than racemic sodium channel blockers, such as bupivacaine and is less likely to penetrate large myelinated motor fibres, resulting in a relatively reduced motor blockade. Thus, ropivacaine has a greater degree of motor sensory differentiation, which could be useful when motor blockade is undesirable. The reduced lipophilicity is also associated with decreased potential for central nervous system toxicity and cardiotoxicity.
Medchemexpress LLC Mepivacaine hydrochloride | 1722-62-9 | 99.68% | 1 G
Mepivacaine hydrochloride is a local anesthetic that inhibits nerve impulse initiation and conduction by binding to voltage-gated sodium ion channels in neuronal cell membranes. This action blocks sodium influx and membrane depolarization, leading to a reversible loss of sensation. It is characterized by a rapid onset and moderate duration of action compared to other local anesthetics.
- Exhibits a more rapid onset than some other local anesthetics.
- Provides a moderate duration of action.
- Shows preferential use-dependent block of Na(v)1.8 channels.
- For research use only.
Aobchem Methanone cyclopropyl(3 4-difluorophenyl)- | ≥95% | CAS 898790-32-4 | C10H8F2O | 500mg
Methanone cyclopropyl(3 4-difluorophenyl)- | ≥95% | CAS 898790-32-4 | C10H8F2O | 500mg
Aobchem Pyridin-3-yl(p-tolyl)methanone | ≥95% | CAS 34950-04-4 | C13H11NO | 250mg
Pyridin-3-yl(p-tolyl)methanone | ≥95% | CAS 34950-04-4 | C13H11NO | 250mg