Details
Stereochemistry | ACHIRAL |
Molecular Formula | C21H34N2O |
Molecular Weight | 330.5075 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCN1CCC(CC1)(C(=O)N(C)CC)C2=CC=CC=C2
InChI
InChIKey=TYWUGCGYWNSRPS-UHFFFAOYSA-N
InChI=1S/C21H34N2O/c1-4-6-7-11-16-23-17-14-21(15-18-23,20(24)22(3)5-2)19-12-9-8-10-13-19/h8-10,12-13H,4-7,11,14-18H2,1-3H3
Sameridine was developed as a compound with both local anesthetic and opioid properties (partial micro-opioid receptor agonist). This drug participated in clinical trials when administered intrathecally to provide anesthesia for surgery and extended postoperative analgesia. However, further development of this drug was discontinued.
Originator
Approval Year
PubMed
Title | Date | PubMed |
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Determination of sameridine in blood plasma by nitrogen-selective gas chromatography. | 2001 Aug 25 |
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Novel local anaesthetics and novel indications for local anaesthetics. | 2001 Dec |
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The effects on hypercarbic ventilatory response of sameridine compared to morphine and placebo. | 2001 Feb |
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Hypercarbic and hypoxic ventilatory responses after intrathecal administration of bupivacaine and sameridine. | 2003 Feb |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/12538214
Twenty-four healthy volunteers received either 25 mg of sameridine or 15 mg of bupivacaine intrathecally. Ventilation was measured by pneumotachography and in-line capnography
Route of Administration:
Other
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C241
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NCI_THESAURUS |
C1506
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DTXSID30162367
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C72174
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CHEMBL2104504
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SAMERIDINE
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NQP2Y50Y6B
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143257-97-0
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SUB10436MIG
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100000080549
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7050
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C113809
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65996
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ACTIVE MOIETY
SALT/SOLVATE (PARENT)