- Sultamicillin
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-
2026-09-01
- CAS:76497-13-7
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 100kg
- Sultamicillin
-
- $33.00
-
2026-08-04
- CAS:76497-13-7
- Purity: 99.34%
- Supply Ability: 10g
- Sultamicillin
-
- $33.00
-
2026-08-04
- CAS:76497-13-7
- Purity: 99.34%
- Supply Ability: 10g
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| | Sultamicillin Basic information |
| Product Name: | Sultamicillin | | Synonyms: | 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[(aminophenylacetyl)amino]-3,3-dimethyl-7-oxo-, [[(3,3-dimethyl-4,4-dioxido-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-yl)carbonyl]oxy]methyl ester, [2S-[2a(2R*,5S*),5a,6b(S*)]]-;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-[2a(2R*,5S*),5a,6b(S*)]]-;4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-aminophenylacetyl]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]methyl ester, (2S,5R,6R)- (9CI);CP 49952;Unacid PD;VD 1827;SULTAMICILLIN BASE;SULTAMICILLIN | | CAS: | 76497-13-7 | | MF: | C25H30N4O9S2 | | MW: | 594.66 | | EINECS: | 1312995-182-4 | | Product Categories: | | | Mol File: | 76497-13-7.mol |  |
| | Sultamicillin Chemical Properties |
| Melting point | 190° | | Boiling point | 907.7±65.0 °C(Predicted) | | density | 1.55±0.1 g/cm3(Predicted) | | storage temp. | 2-8°C | | solubility | Practically insoluble in water, very slightly soluble in methanol, practically insoluble in ethanol (96 per cent). | | form | Solid | | pka | 12.15±0.60(Predicted) | | color | White to off-white | | InChIKey | OPYGFNJSCUDTBT-PMLPCWDUSA-N | | SMILES | N12[C@@]([H])([C@H](NC([C@H](N)C3=CC=CC=C3)=O)C1=O)SC(C)(C)[C@@H]2C(OCOC([C@H]1C(C)(C)S(=O)(=O)[C@@]2([H])N1C(=O)C2)=O)=O |
| | Sultamicillin Usage And Synthesis |
| Chemical Properties | White or almost white, slightly hygroscopic, crystalline powder. | | Uses | Antibacterial. | | Definition | ChEBI: Sultamicillin is a penicillanic acid ester. It is functionally related to an ampicillin and a sulbactam. | | in vivo | Upon oral absorption, Sultamicillin is hydrolyzed to Sulbactam (HY-B0334) and Ampicillin (HY-B0522)[2].
Sultamicillin (oral gavage, every 12 h) combined with immunosuppression agent (eg: Mycophenolate mofetil (HY-B0199) and Methylprednisolone (HY-B0260)) markedly improves survival of experimental polymicrobial sepsis in mice, and enhances bacterial clearance[3].
| | IC 50 | β-lactam |
| | Sultamicillin Preparation Products And Raw materials |
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