Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C15H16N6O.2C2H6O4S |
| Molecular Weight | 548.59 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OCCS(O)(=O)=O.OCCS(O)(=O)=O.NC(=N)C1=CC=CC(NC(=O)NC2=CC(=CC=C2)C(N)=N)=C1
InChI
InChIKey=PWUMRNFCZFZXAE-UHFFFAOYSA-N
InChI=1S/C15H16N6O.2C2H6O4S/c16-13(17)9-3-1-5-11(7-9)20-15(22)21-12-6-2-4-10(8-12)14(18)19;2*3-1-2-7(4,5)6/h1-8H,(H3,16,17)(H3,18,19)(H2,20,21,22);2*3H,1-2H2,(H,4,5,6)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| New drug developments for opportunistic infections in immunosuppressed patients: Pneumocystis carinii. | 1995-11-24 |
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| Treatment of experimental pneumocystosis: review of 7 years of experience and development of a new system for classifying antimicrobial drugs. | 1992-09 |
|
| Cationic antitrypanosomal and other antimicrobial agents in the therapy of experimental Pneumocystis carinii pneumonia. | 1988-06 |
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FCC0RF48XI
Created by
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528032
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3671-72-5
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DTXSID80190175
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222-937-6
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12883609
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m556
Created by
admin on Mon Mar 31 21:54:02 GMT 2025 , Edited by admin on Mon Mar 31 21:54:02 GMT 2025
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PRIMARY | Merck Index |
ACTIVE MOIETY
SUBSTANCE RECORD