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Propicillin-M (di-HO-ring) MS3_2

Compound with spectra: 14 MS (LC)

Propicillin-M (di-HO-ring) MS3_2
SpectraBase Compound ID 89VArlu1dTL
InChI InChI=1S/C6H9NO2S/c1-6(2)4(5(8)9)7-3-10-6/h3-4,7H,1-2H3/p+1
InChIKey SXRBJFGRGFZRFM-UHFFFAOYSA-O
Mol Weight 160.21 g/mol
Molecular Formula C6H10NO2S
Exact Mass 160.043225 g/mol

View Spectrum of Propicillin-M (di-HO-ring) MS3_2

MS (LC) Spectrum
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS

View Spectrum of Propicillin-M (di-HO-ring) MS3_2

MS (LC) Spectrum
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS

View Spectrum of Propicillin-M (di-HO-ring) MS3_2

MS (LC) Spectrum
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS

View Spectrum of Propicillin-M (di-HO-ring) MS3_2

MS (LC) Spectrum
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS

View Spectrum of Propicillin-M (di-HO-ring) MS3_2

MS (LC) Spectrum
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS

View Spectrum of Propicillin-M (di-HO-ring) MS3_2

MS (LC) Spectrum
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS

View Spectrum of Propicillin-M (di-HO-ring) MS3_2

MS (LC) Spectrum
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS

View Spectrum of Propicillin-M (di-HO-ring) MS3_2

MS (LC) Spectrum
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS

View Spectrum of Propicillin-M (di-HO-ring) MS3_2

MS (LC) Spectrum
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS

View Spectrum of Propicillin-M (di-HO-ring) MS3_2

MS (LC) Spectrum
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS

View Spectrum of Propicillin-M (di-HO-ring) MS3_2

MS (LC) Spectrum
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS

View Spectrum of Propicillin-M (di-HO-ring) MS3_2

MS (LC) Spectrum
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS

View Spectrum of Propicillin-M (di-HO-ring) MS3_2

MS (LC) Spectrum
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS

View Spectrum of Propicillin-M (di-HO-ring) MS3_2

MS (LC) Spectrum
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS
  • Ampicillin MS3_1
  • Flucloxacillin-M (di-HO-ring) MS3_2
  • Ampicillin-M (350) MS3_1
  • Piperacilline MS3_2
  • Piperacilline-M (dealkyl-) MS3_2
  • Ampicillin-M (376) isomer 1 MS3_1
  • Ampicillin-M (376) isomer 2 MS3_1
  • Penicillin G artifact (367) MS3_1
  • Amoxicillin-M (penicilloic acid) MS3_2
  • Azidocillin artifact (381) MS3_1
  • Azidocillin artifact (408) MS3_1
  • Amoxicillin-M (penicilloic acid-glucuronide) MS3_2
  • Benzylpenicillin artifact (367) MS3_1
4-Thiazolidinecarboxylic acid, 5,5-dimethyl-
D-N-ACETYL-3-MERCAPTOVALINE
N-acetyl-3-mercaptovaline
L-Valine, N-[(ethylthio)thioxomethyl]-
N-Methoxycarbonyl-L-tert-leucine
Thiazole, 2-thio-4-methoxycarbonyl-
(R)-Methyl 2-oxothiazolidine-4-carboxylate
N-Formylthiazolidine-4-carboxylic acid
S-[2-(2-METHYL-1-CARBOXYPROPYL)CYSTEINE
N-Acetyl-D-allo-isoleucine
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