Compound ID | 2756

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Suncillin

Class: Beta-lactam

Spectrum of activity: Gram-positive  &  Gram-negative
Details of activity: Broad-spectrum activity with notable effect towards Pseudomonas aeruginosa
Description: Semisynthetic antibiotic; derived from penicillin (ureidopenicillin); shows similar but inferior activity profile to carbenicillin
Institute where first reported: Bristol-Myers Squibb Pharmaceutical
Year first mentioned: 1968
Development status: Experimental
Chemical structure(s):
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Molecular weight: 429.47
Iso. SMILES: CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)[C@@H](C3=CC=CC=C3)NS(=O)(=O)O)C(=O)O)C
InChI Key: OIECDSKSPRTZHG-NJBDSQKTSA-N
Can. SMILES: CC1(C)[C@H](C(=O)O)N2C(=O)[C@H]([C@H]2S1)NC(=O)[C@@H](C3=CC=CC=C3)NS(=O)(=O)O
InChI: InChI=1S/C16H19N3O7S2/c1-16(2)11(15(22)23)19-13(21)10(14(19)27-16)17-12(20)9(18-28(24,25)26)8-6-4-3-5-7-8/h3-7,9-11,14,18H,1-2H3,(H,17,20)(H,22,23)(H,24,25,26)/t9-,10-,11+,14-/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/3034014
Citations:
  • https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=web&cd=&cad=rja&uact=8&ved=2ahUKEwihmemL_JiEAxXVT0EAHbn_AYQ4FBAWegQIAhAB&url=https%3A%2F%2Frmmg.org%2Fexportar-pdf%2F4016%2Fen_e33209.pdf&usg=AOvVaw1m1uml2kDyA40DB4mzYu9-&opi=89978449
  • https://www.jstage.jst.go.jp/article/antibiotics1968/31/10/31_10_1013/_pdf

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