Sultamicillin
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Description

Sultamicillin is a penicillanic acid ester. It is functionally related to an ampicillin and a sulbactam.

From NIH 3D

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Source creator
Hamza Gad
Source license
CC-BY
Archived copies are shared under the license shown.
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Tags

#nih-3d
#small molecules
#sultamicillin
#76497-13-7
#sultamicilina
#sultamicillinum
#vd 1827
#cp-49,952
#chebi:51770
#65dt0ml581
#76497-13-7 (free)
#4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid, 6-[[(2r)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-,[[[(2s,5r)-3,3-dimethyl-4,4-dioxido-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-yl]carbonyl]oxy]methylester, (2s,5r,6r)-
#vd-1827
#cp-49952
#(((2s,5r,6r)-6-((r)-2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carbonyl)oxy)methyl (2s,5r)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide
#({6beta-[(2r)-2-amino-2-phenylacetamido]-2,2-dimethylpenam-3alpha-carbonyl}oxy)methyl 2,2-dimethylpenam-3alpha-carboxylate 1,1-dioxide
#[(2,2-dimethyl-1,1-dioxidopenam-3alpha-carbonyl)oxy]methyl 6beta-[(2r)-2-amino-2-phenylacetamido]-2,2-dimethylpenam-3alpha-carboxylate
#[(2s,5r)-3,3-dimethyl-4,4,7-trioxo-4lambda6-thia-1-azabicyclo[3.2.0]heptane-2-carbonyl]oxymethyl (2s,5r,6r)-6-[[(2r)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
#hydroxymethyl (2s,5r,6r)-6-((r)-(2-amino-2-phenylacetamido))-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylate, (2s,5r)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylate (ester) s,s-dioxide
#sultamicilina [spanish]
#sultamicillinum [latin]
#cp 49952
#unii-65dt0ml581
#sultamicillin [usan:inn:ban]
#hydroxymethyl (2s,5r,6r)-6-[(r)-(2-amino-2-phenylacetamido)]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate, (2s,5r)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (ester) s,s-dioxide
#sultamicillin [mi]
#sultamicillin [inn]
#sultamicillin (usan/inn)
#sultamicillin [usan]
#schembl34392
#sultamicillin [mart.]
#sultamicillin [who-dd]
#chembl506110
#gtpl12290
#dtxsid501010077
#hy-n7115
#sultamicillin [ep monograph]
#sultamicillin for peak identification
#s5411
#akos015963376
#ccg-270182
#db12127
#(2s,5r)-3,3-dimethyl-4,4,7-trioxo-4-thia-1-azabicyclo(3.2.0)heptan-2-carbonyloxymethyl (2s,5r,6r)-6-((r)-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptan-2-carboxylat
#4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 6-((aminophenylacetyl)amino)-3,3-dimethyl-7-oxo-, (((3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)hept-2-yl)carbonyl)oxy)methyl ester, s,s-dioxide, (2s-(2alpha(2r*,5s*),5alpha,6beta(s*)))-
#as-14087
#cs-0082687
#d05972
#en300-19766280
#6'-(2-amino-2-phenylacetamido)penicillanoyloxymethyl penicillanate 1,1-dioxide
#[(2s,5r,6r)-6-[(2r)-2-amino-2-phenylacetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carbonyloxy]methyl (2s,5r)-3,3-dimethyl-4,4,7-trioxo-4lambda6-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
#1,1-dioxopenicillanoyloxymethyl 6-(d-.alpha.-amino-.alpha.-phenylacetamido)penicillanate
#sultamicilline
#sultamicilli
#((2s,5r)-3,3-dimethyl-4,4,7-trioxo-4lambda6-thia-1-azabicyclo(3.2.0)heptane-2-carbonyl)oxymethyl (2s,5r,6r)-6-(((2r)-2-amino-2-phenylacetyl)amino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylate
#((6beta-((2r)-2-amino-2-phenylacetamido)-2,2-dimethylpenam-3alpha-carbonyl)oxy)methyl 2,2-dimethylpenam-3alpha-carboxylate 1,1-dioxide
#refchem:890030
#j01cr04
#dtxcid501436497
#sultamycillin
#c25h30n4o9s2
#3mf
#blend
#fbx
#glb
#jpg
#mtl
#obj
#ply
#png
#stl
#wrl
#x3d

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Sultamicillin

From NIH 3D
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Category

learning

License

CC-BY

Published

8/29/2026

Availability

free on NIH 3D