Chemical Compound

aspoxicillin

CAS Registry Number 63358-49-6
aspoxicillin chemical structure
Primary Record

aspoxicillin

In stock
1,961 g
Purity
99.7 %
CAS
63358-49-6

Compound Identifiers & Properties

CAS
63358-49-6
PubChem CID
71961
SMILES
CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)[C@@H](C3=CC=C(C=C3)O)NC(=O)[C@@H](CC(=O)NC)N)C(=O)O)C
Canonical SMILES
CNC(=O)C[C@@H](N)C(=O)N[C@@H](C(=O)N[C@@H]1C(=O)N2[C@@H]1SC(C)(C)[C@@H]2C(=O)O)c1ccc(O)cc1

Names & Synonyms

  • aspoxicillin
  • Aspoxicilina
  • Aspoxicilline
  • Doyle
  • Aspoxicillinum
  • Aspoxicillan
  • ASPC
  • Lecithovitellase
  • Aspoxicilina [Spanish]
  • Aspoxicilline [French]
  • Aspoxicillinum [Latin]
  • 63358-49-6
  • Doyle (TN)
  • Aspoxicillin [INN:JAN]
  • Aspoxicillin Trihydrate
  • Aspoxicillin (Standard)
  • Aspoxicillin (>80%)
  • AC1Q5QWB
  • RefChem:916399
  • Aspoxicillin (JAN/INN)
  • ASPOXICILLIN [MI]
  • CCRIS 2514
  • ASPOXICILLIN [INN]
  • DTXSID6046921
  • D0FD6E
  • UNII-0745KNO26J
  • AC1L2H5J
  • 0745KNO26J
  • SCHEMBL34176
  • TA 058
  • TA-058
  • ASPOXICILLIN [MART.]
  • DTXCID4026921
  • ASPOXICILLIN [WHO-DD]
  • orb1309971
  • CHEMBL1318150
  • C21H27N5O7S
  • CHEBI:31240
  • GTPL12293
  • J01CA19
  • BHELIUBJHYAEDK-OAIUPTLZSA-N
  • N-(N-Methylasparaginyl)amoxicillin
  • CID71961
  • ZINC3871610
  • N(sup 4)-Methyl-D-asparagininylamoxicillin
  • N4-Methyl-D-asparagininylamoxicillin
  • Tox21_112810
  • AR-1H7595
  • BBF-00569
  • C21-H27-N5-O7-S
  • CA0187
  • MSK000762
  • N(4)-methyl-D-asparaginylamoxicillin
  • NCGC00181352-01
  • AKOS040732482
  • DB13816
  • HY-135842R
  • DA-50752
  • J23.682I
  • LS-72203
  • MS-29166
  • CAS-63358-49-6
  • HY-135842
  • CS-0114376
  • NS00011613
  • C13269
  • D07469
  • G13896
  • (2S,5R,6R)-6-[[(2R)-2-[[(2R)-2-amino-4-(methylamino)-4-oxobutanoyl]amino]-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
  • A1204480
  • Q27114235
  • (2S,5R,6R)-6-((2R)-2-((2R)-2-Amino-3-(methylcarbamoyl)propionamido)-2-(p-hydroxyphenyl)acetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid
  • (2S,5R,6R)-6-[[(2R)-2-[[(2R)-2-amino-4-methylamino-4-oxobutanoyl]amino]-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
  • Glycinamide, N-methyl-D-asparaginyl-N-(2-carboxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)hept-6-yl)-D-2-(4-hydroxyphenyl)-, (2S-(2-alpha,5-alpha,6-beta))-
  • (2S,5R,6R)-6-(((2R)-2-(((2R)-2-amino-4-(methylamino)-4-oxo-butanoyl)amino)-2-(4-hydroxyphenyl)acetyl)amino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid
  • (2S,5R,6R)-6-(((2R)-2-(((2R)-2-amino-4-methylamino-4-oxobutanoyl)amino)-2-(4-hydroxyphenyl)acetyl)amino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid
  • (2S,5R,6R)-6-({(2R)-2-(4-hydroxyphenyl)-2-[(N-methyl-D-asparaginyl)amino]acetyl}amino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
  • (2S,5R,6R)-6-[(2R)-2-[(2R)-2-AMINO-3-(METHYLCARBAMOYL)PROPANAMIDO]-2-(4-HYDROXYPHENYL)ACETAMIDO]-3,3-DIMETHYL-7-OXO-4-THIA-1-AZABICYCLO[3.2.0]HEPTANE-2-CARBOXYLIC ACID
  • (2S,5R,6R)-6-[[(2R)-2-[[(2R)-2-amino-4-(methylamino)-4-oxo-butanoyl]amino]-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
  • (2S,5R,6R)-6alpha-[[(R)-[[(2R)-2-Amino-4-(methylamino)-1,4-dioxobutyl]amino](4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2beta-carboxylic acid
  • 6-[D-2-(D-2-amino-3-N-methylcarbamoylpropionamido)-2-p-hydroxyphenylacetamido]penicillanic acid
  • 634-698-9
  • 64045-99-4
  • 6alpha-[(R)-2-(4-Hydroxyphenyl)-2-[[(2R)-3-(methylcarbamoyl)-2-aminopropanoyl]amino]acetylamino]penicillanic acid
  • Glycinamide, N-methyl-D-asparaginyl-N-(2-carboxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-6-yl)-D-2-(4-hydroxyphenyl)-, [2S-(2a,5a,6ss)]-; ASPC; Aspoxicillin; Doyle; TA 058
  • N4-Methyl-D-Asn-4-hydroxy-D-phenyl Gly-N-[(2S,5beta)-2beta-carboxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-6alpha-yl]-NH2