Piperidines
TARGETMOL CHEMICALS INC AVIBACTAM SODIUM 50MG
Also available in 2 mg 5 mg 10 mg 25 mg 100 mg 200 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Avibactam sodium (NXL-104) is a reversible (beta)-lactamase inhibitor (IC50 8/80/38 nM for TEM-1/P99/KPC-2 (beta)-lactamases). purity: 99%
Selleck Chemical LLC Avibactam sodium S3732-1g
Avibactam (AVE-1330A NXL104) is a covalent reversible non- -lactam -lactamase inhibitor with IC50 values of 8 80 and 38 nM for TEM-1 P99 and KPC-2 -lactamases respectively
Selleck Chemical LLC Avibactam sodium S3732-100mg
Avibactam (AVE-1330A NXL104) is a covalent reversible non- -lactam -lactamase inhibitor with IC50 values of 8 80 and 38 nM for TEM-1 P99 and KPC-2 -lactamases respectively
Selleck Chemical LLC Avibactam sodium S3732-10mM/1mL
Avibactam (AVE-1330A NXL104) is a covalent reversible non- -lactam -lactamase inhibitor with IC50 values of 8 80 and 38 nM for TEM-1 P99 and KPC-2 -lactamases respectively
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.
Medchemexpress LLC HY-14879A 200mg , Avibactam (sodium) NXL-104 CAS:1192491-61-4 Purity:98%
Medchemexpress, HY-14879A 200mg Avibactam (sodium) NXL-104 CAS:1192491-61-4 Formula:C7H10N3NaO6S IC50: 8 nM (TEM-1), 5 nM (CTX-M-15) Purity:98% Avibactam sodium 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.
![eMolecules Medchem Express / Avibactam (sodium hydrate) / 5mg / 446264703 / HY-14879B / / 2938989-90-1 / [null] / 305.240 / C7H12N3NaO7S](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502443142.PNG-250.jpg)
eMolecules Medchem Express / Avibactam (sodium hydrate) / 5mg / 446264703 / HY-14879B / / 2938989-90-1 / [null] / 305.240 / C7H12N3NaO7S
Medchem Express / Avibactam (sodium hydrate) / 5mg / 446264703 / HY-14879B / / 2938989-90-1 / [null] / 305.240 / C7H12N3NaO7S
Selleck Chemical LLC Ropivacaine HCl S4058-50mg
Ropivacaine HCl (LEA-103) is an anaesthetic agent and blocks impulse conduction in nerve fibres through inhibiting sodium ion influx reversibly
Selleck Chemical LLC Levobupivacaine HCl S4061-50mg
Levobupivacaine HCl ((S)-(-)-Bupivacaine) the pure S(-)-enantiomer of bupivacaine is a reversible neuronal sodium channel inhibitor used as a long-acting local anesthetic
Selleck Chemical LLC Levobupivacaine S5181-25mg
Levobupivacaine (Chirocaine (S)-(-)-Bupivacaine L-(-)-Bupivacaine) the S (-)-enantiomer of bupivacaine is a long-acting amide local anaesthetic used in analgesia and anaesthesia Levobupivacaine exhibits effects on motor and sensory nerves by inhibiting the opening of voltage-gated sodium channels
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.
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.
AdipoGen Ropivacaine HCl H2O
Chemical. CAS 132112-35-7. Formula C17H26N2O . HCl . H2O. MW 274.4 . 36.5 . 18.0. 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.
AdipoGen Ropivacaine HCl H2O
Chemical. CAS 132112-35-7. Formula C17H26N2O . HCl . H2O. MW 274.4 . 36.5 . 18.0. 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.
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