Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C34H50N4O9S.CH4O3S |
| Molecular Weight | 786.953 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CS(O)(=O)=O.CCN(CC)CCS(=O)(=O)[C@@H]1CCN2[C@H]1C(=O)O[C@H](C(C)C)[C@H](C)\C=C\C(=O)NC\C=C\C(C)=C\[C@@H](O)CC(=O)CC3=NC(=CO3)C2=O
InChI
InChIKey=ZUBXFMSQBHKVNC-ODOOVVHSSA-N
InChI=1S/C34H50N4O9S.CH4O3S/c1-7-37(8-2)16-17-48(44,45)28-13-15-38-31(28)34(43)47-32(22(3)4)24(6)11-12-29(41)35-14-9-10-23(5)18-25(39)19-26(40)20-30-36-27(21-46-30)33(38)42;1-5(2,3)4/h9-12,18,21-22,24-25,28,31-32,39H,7-8,13-17,19-20H2,1-6H3,(H,35,41);1H3,(H,2,3,4)/b10-9+,12-11+,23-18+;/t24-,25-,28-,31-,32-;/m1./s1
| Molecular Formula | C34H50N4O9S |
| Molecular Weight | 690.847 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
| Molecular Formula | CH4O3S |
| Molecular Weight | 96.106 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionCurator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/9511075
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/9511075
Dalfopristin is a pristinamycin-like component of anti-bacterial drug called Synercid which also containes quinupristin (quinupristin:dalfopristin ratio is 30:70 (w/w)). The drug was approved by FDA and used for the treatment of skin diseases caused by Staphylococcus aureus or Streptococcus pyogenes. Dalfopristin binds to the RNA of the 50S ribosomal subunit and thus inhibits the late phase of protein synthesis.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2363135 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Curative | SYNERCID Approved UseSynercid is indicated in adults for the treatment of the following infections when caused by susceptible strains of the designated microorganisms. Complicated skin and skin structure infections caused by Staphylococcus aureus (methicillin susceptible) or Streptococcus pyogenes. Launch Date1999 |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
7.96 μg/mL |
5.25 mg/kg bw 3 times / day steady-state, intravenous dose: 5.25 mg/kg bw route of administration: Intravenous experiment type: STEADY-STATE co-administered: QUINUPRISTIN |
DALFOPRISTIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
10.57 μg × h/mL |
5.25 mg/kg bw 3 times / day steady-state, intravenous dose: 5.25 mg/kg bw route of administration: Intravenous experiment type: STEADY-STATE co-administered: QUINUPRISTIN |
DALFOPRISTIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
1.04 h |
5.25 mg/kg bw 3 times / day steady-state, intravenous dose: 5.25 mg/kg bw route of administration: Intravenous experiment type: STEADY-STATE co-administered: QUINUPRISTIN |
DALFOPRISTIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
Doses
| Dose | Population | Adverse events |
|---|---|---|
5 mg/kg 3 times / day multiple, intravenous Recommended Dose: 5 mg/kg, 3 times / day Route: intravenous Route: multiple Dose: 5 mg/kg, 3 times / day Sources: |
unhealthy, 52.9 Health Status: unhealthy Age Group: 52.9 Sex: M+F Sources: |
Disc. AE: Arthralgia, Myalgia... AEs leading to discontinuation/dose reduction: Arthralgia (3%) Sources: Myalgia (2.6%) Nausea (1.1%) Myasthenia (0.7%) Flatulence (0.3%) Pain (0.3%) Pharyngitis (0.3%) Dysphagia (0.3%) Dizziness (0.3%) Chest pain (0.3%) Asthenia (0.3%) Rash (0.3%) Vomiting (0.3%) Anorexia (0.3%) |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Anorexia | 0.3% Disc. AE |
5 mg/kg 3 times / day multiple, intravenous Recommended Dose: 5 mg/kg, 3 times / day Route: intravenous Route: multiple Dose: 5 mg/kg, 3 times / day Sources: |
unhealthy, 52.9 Health Status: unhealthy Age Group: 52.9 Sex: M+F Sources: |
| Asthenia | 0.3% Disc. AE |
5 mg/kg 3 times / day multiple, intravenous Recommended Dose: 5 mg/kg, 3 times / day Route: intravenous Route: multiple Dose: 5 mg/kg, 3 times / day Sources: |
unhealthy, 52.9 Health Status: unhealthy Age Group: 52.9 Sex: M+F Sources: |
| Chest pain | 0.3% Disc. AE |
5 mg/kg 3 times / day multiple, intravenous Recommended Dose: 5 mg/kg, 3 times / day Route: intravenous Route: multiple Dose: 5 mg/kg, 3 times / day Sources: |
unhealthy, 52.9 Health Status: unhealthy Age Group: 52.9 Sex: M+F Sources: |
| Dizziness | 0.3% Disc. AE |
5 mg/kg 3 times / day multiple, intravenous Recommended Dose: 5 mg/kg, 3 times / day Route: intravenous Route: multiple Dose: 5 mg/kg, 3 times / day Sources: |
unhealthy, 52.9 Health Status: unhealthy Age Group: 52.9 Sex: M+F Sources: |
| Dysphagia | 0.3% Disc. AE |
5 mg/kg 3 times / day multiple, intravenous Recommended Dose: 5 mg/kg, 3 times / day Route: intravenous Route: multiple Dose: 5 mg/kg, 3 times / day Sources: |
unhealthy, 52.9 Health Status: unhealthy Age Group: 52.9 Sex: M+F Sources: |
| Flatulence | 0.3% Disc. AE |
5 mg/kg 3 times / day multiple, intravenous Recommended Dose: 5 mg/kg, 3 times / day Route: intravenous Route: multiple Dose: 5 mg/kg, 3 times / day Sources: |
unhealthy, 52.9 Health Status: unhealthy Age Group: 52.9 Sex: M+F Sources: |
| Pain | 0.3% Disc. AE |
5 mg/kg 3 times / day multiple, intravenous Recommended Dose: 5 mg/kg, 3 times / day Route: intravenous Route: multiple Dose: 5 mg/kg, 3 times / day Sources: |
unhealthy, 52.9 Health Status: unhealthy Age Group: 52.9 Sex: M+F Sources: |
| Pharyngitis | 0.3% Disc. AE |
5 mg/kg 3 times / day multiple, intravenous Recommended Dose: 5 mg/kg, 3 times / day Route: intravenous Route: multiple Dose: 5 mg/kg, 3 times / day Sources: |
unhealthy, 52.9 Health Status: unhealthy Age Group: 52.9 Sex: M+F Sources: |
| Rash | 0.3% Disc. AE |
5 mg/kg 3 times / day multiple, intravenous Recommended Dose: 5 mg/kg, 3 times / day Route: intravenous Route: multiple Dose: 5 mg/kg, 3 times / day Sources: |
unhealthy, 52.9 Health Status: unhealthy Age Group: 52.9 Sex: M+F Sources: |
| Vomiting | 0.3% Disc. AE |
5 mg/kg 3 times / day multiple, intravenous Recommended Dose: 5 mg/kg, 3 times / day Route: intravenous Route: multiple Dose: 5 mg/kg, 3 times / day Sources: |
unhealthy, 52.9 Health Status: unhealthy Age Group: 52.9 Sex: M+F Sources: |
| Myasthenia | 0.7% Disc. AE |
5 mg/kg 3 times / day multiple, intravenous Recommended Dose: 5 mg/kg, 3 times / day Route: intravenous Route: multiple Dose: 5 mg/kg, 3 times / day Sources: |
unhealthy, 52.9 Health Status: unhealthy Age Group: 52.9 Sex: M+F Sources: |
| Nausea | 1.1% Disc. AE |
5 mg/kg 3 times / day multiple, intravenous Recommended Dose: 5 mg/kg, 3 times / day Route: intravenous Route: multiple Dose: 5 mg/kg, 3 times / day Sources: |
unhealthy, 52.9 Health Status: unhealthy Age Group: 52.9 Sex: M+F Sources: |
| Myalgia | 2.6% Disc. AE |
5 mg/kg 3 times / day multiple, intravenous Recommended Dose: 5 mg/kg, 3 times / day Route: intravenous Route: multiple Dose: 5 mg/kg, 3 times / day Sources: |
unhealthy, 52.9 Health Status: unhealthy Age Group: 52.9 Sex: M+F Sources: |
| Arthralgia | 3% Disc. AE |
5 mg/kg 3 times / day multiple, intravenous Recommended Dose: 5 mg/kg, 3 times / day Route: intravenous Route: multiple Dose: 5 mg/kg, 3 times / day Sources: |
unhealthy, 52.9 Health Status: unhealthy Age Group: 52.9 Sex: M+F Sources: |
Sample Use Guides
The recommended dosage for the treatment of complicated skin and skin structure infections is 7.5 mg/kg q12h.
Route of Administration:
Intravenous
The combination of quinupristin and dalfopristin (Synercid) exhibits in vitro minimum inhibitory concentrations (MIC's) of ≤1.0 ug/mL against most (≥90%) isolates of the following microorganisms: Corynebacterium jeikeium, Staphylococcus aureus (methicillin-resistant isolates), Staphylococcus epidermidis (including methicillin-resistant isolates, Streptococcus agalactiae.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:26:11 GMT 2025
by
admin
on
Mon Mar 31 22:26:11 GMT 2025
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| Record UNII |
R5U9EZY06G
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| Record Status |
Validated (UNII)
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| Record Version |
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DBSALT002330
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PARENT -> SALT/SOLVATE |
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ACTIVE MOIETY |