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Oxacillin

HCID 6196
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Grundinformationen

CAS
1173-88-2
Standard-SMILES
Cc1onc(-c2ccccc2)c1C(=O)N[C@@H]1C(=O)N2[C@@H]1SC(C)(C)[C@@H]2C(=O)O
InChIKey
UWYHMGVUTGAWSP-JKIFEVAISA-N
Summenformel
C19H19N3O5S
Durchschnittliche Molmasse
401,4 g/mol
Monoisotopische Masse
401,10454189

Überblick

Oxacillin is a penicillin antibiotic carrying a 5-methyl-3-phenylisoxazole-4-carboxamide group at position 6beta. It has a role as an antibacterial agent and an antibacterial drug. It is a conjugate acid of an oxacillin(1-).

Namen und Bezeichner

Bevorzugter Name
Oxacillin
IUPAC
(2S,5R,6R)-3,3-dimethyl-6-[(5-methyl-3-phenyl-1,2-oxazole-4-carbonyl)amino]-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
Lokaler Name
Oxacillin
Englischer Name
OXACILLIN
Summenformel
C19H19N3O5S
Molmasse
401.44

Namen und Synonyme

oxacillin66-79-5OxazocillinOxazocillineOxacilinaOxacillineOxacillinum5-Methyl-3-phenyl-4-isoxazolyl-penicillin(2S,5R,6R)-3,3-dimethyl-6-(5-methyl-3-phenyl-1,2-oxazole-4-amido)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid(2S,5R,6R)-3,3-dimethyl-6-[(5-methyl-3-phenyl-1,2-oxazole-4-carbonyl)amino]-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acidResistopenOxabel
Weitere Namen anzeigen
OxazinaBactocilPenstaphoOXACILLIN USP/EP/BPAnnamycin Impurity 100UWYHMGVUTGAWSP-JKIFEVAISA-NOxacillinQ: What is Oxacillin Q: What is the CAS Number of Oxacillin[2S-(2,5,6)]-3,3-dimethyl-6-(methyl-3-phenylisoxaz-4-ole-carboxamide-7-oxy-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid(2S,5R,6R)-3,3-Dimethyl-6-[(5-methyl-3-phenylisoxazol-4-yl)carbonylamino]-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
CHEBI:7809UH95VD7V76Staphcillin V(5-methyl-3-phenyl-4-isoxazolyl)penicillin6beta-(5-methyl-3-phenylisoxazol-4-yl)penicillanic acidDTXSID8023397(2S,5R,6R)-3,3-dimethyl-6-{[(5-methyl-3-phenylisoxazol-4-yl)carbonyl]amino}-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-6-(((5-methyl-3-phenyl-4-isoxazolyl)carbonyl)amino)-7-oxo-, (2S-(2alpha,5alpha,6beta))-

Eigenschaften

Berechnete Struktureigenschaften

XLogP
2,4
Polarare Oberfläche (TPSA)
138 Ų
H-Brücken-Donoren
2
H-Brücken-Akzeptoren
7
Frei drehbare Bindungen
4
Schwere Atome
28
Formalladung
0
Komplexität
680

Experimentelle und physikochemische Eigenschaften

Drugs · 3 Einträge

Pharmaceuticals -> Antibiotics (Penicillins)

Pharmaceuticals -> Antibiotics

Pharmaceuticals -> Listed in ZINC15

LogP2.4
Solubility8.62e-02 g/L
Human Drugs · 2 Einträge

Breast Feeding; Lactation; Milk, Human; Anti-Infective Agents; Antibacterial Agents; Penicillins

Access group antibiotics

Animal DrugsPharmaceuticals -> Animal Drugs -> Approved in Taiwan
Physical DescriptionSolid
Dissociation Constants2.72
Collision Cross Section · 3 Einträge

195.4 Ų [M+Na]+ [CCS Type: TW; Method: calibrated with Waters Major Mix]

193.63 Ų [M+K]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]

187.73 Ų [M+H]+

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

GHS-Klassifizierung

GHS Classification · 4 Einträge

Danger

H315 (40%): Causes skin irritation [Warning Skin corrosion/irritation]

P233, P260, P261, P264, P264+P265, P271, P272, P280, P284, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P333+P317, P337+P317, P342+P316, P362+P364, P403, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 5 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Gefahrenhinweise

Other Safety Information · 2 Einträge

IMAP assessments - 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-6-[[(5-methyl-3-phenyl-4-isoxazolyl)carbonyl]amino]-7-oxo-, monosodium salt, [2S-(2.alpha.,5.alpha.,6.beta.)]-: Environment tier I assessment

IMAP assessments - 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-6-[[(5-methyl-3-phenyl-4-isoxazolyl)carbonyl]amino]-7-oxo-, [2S-(2.alpha.,5.alpha.,6.beta.)]-: Environment tier I assessment

Hazard Classes and CategoriesSkin Irrit. 2 (40%)

Toxikologische Informationen

Hepatotoxicity · 1 Eintrag

Oxacillin has been linked to two forms of hepatotoxicity, first an acute andtransient elevation in serum aminotransferase levels occurring with highdoses of intravenous therapy; and second, a more prolonged, usuallycholestatic, idiosyncratic liver injury that is similar to thehepatotoxicity of other second-generation penicillins such as dicloxacillin,flucloxacillin, and nafcillin.

Drug Induced Liver Injury · 5 Einträge

Chemie und Industrie

Pharmakologische Informationen

ATC Code · 4 Einträge

J - Antiinfectives for systemic use

QJ - Antiinfectives for systemic use

QJ - Antiinfectives for systemic use

J01CF02

Protein Binding94.2 +/- 2.1% (binds to serum protein, mainly albumin)
Pharmacodynamics · 1 Eintrag

Oxacillin is a penicillin beta-lactam antibiotic used in the treatment of bacterial infections caused by susceptible, usually gram-positive, organisms. The name "penicillin" can either refer to several variants of penicillin available, or to the group of antibiotics derived from the penicillins. Oxacillin has in vitro activity against gram-positive and gram-negative aerobic and anaerobic bacteria. The bactericidal activity of Oxacillin results from the inhibition of cell wall synthesis and is mediated through Oxacillin binding to penicillin binding proteins (PBPs). Oxacillin is stable against hydrolysis by a variety of beta-lactamases, including penicillinases, and cephalosporinases and extended spectrum beta-lactamases.

Mechanism of Action · 1 Eintrag

By binding to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall, Oxacillin inhibits the third and last stage of bacterial cell wall synthesis. Cell lysis is then mediated by bacterial cell wall autolytic enzymes such as autolysins; it is possible that Oxacillin interferes with an autolysin inhibitor.

Biological Half-Life20 to 30 minutes
FDA Pharmacological Classification · 6 Einträge

UH95VD7V76

OXACILLIN

Established Pharmacologic Class [EPC] - Penicillin-class Antibacterial

Chemical Structure [CS] - Penicillins

Oxacillin is a Penicillin-class Antibacterial.

OXACILLIN

MeSH Pharmacological ClassificationSubstances that inhibit the growth or reproduction of BACTERIA.

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Auf dieser SeiteGrundinformationenÜberblickNamen und BezeichnerEigenschaftenSicherheit und RegulatorischesChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung

Datenbank-Bezeichner

CAS
1173-88-2、66-79-5
PubChem CID
6196
DTXSID
DTXSID8023397
ChEMBL
CHEMBL819
ChEBI
CHEBI:7809
UNII
UH95VD7V76
EC Number
200-635-5、214-636-3
Nikkaji
J4.514D

Physikochemische Eigenschaften

Schmelzpunkt
188 °C · 188 °C
Siedepunkt
686.8 · 686.8±55.0 °C(Predicted)
Dichte
1.49 · 1.49±0.1 g/cm3(Predicted)
pka
2.72 · pKa 2.72 (Uncertain)
CAS Datenbank
66 · 66-79-5
EPA chemische Informationen
4 · 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-6-[[(5-methyl-3-phenyl-4-isoxazolyl)carbonyl]amino]-7-oxo-, (2S,5R,6R)- (66-79-5)

Drug-Induced Liver Injury Severity and Toxicity (DILIst)

oxacillin

DILI Positive

Intravenous

DOI:10.1016/j.drudis.2019.09.022

Effects During Pregnancy and Lactation◉ Summary of Use during Lactation

Sicherheitsdaten

Alarmwort
Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code H302
Absorption, Distribution and Excretion
Oxacillin Sodium is rapidly excreted as unchanged drug in the urine by glomerular filtration and active tubular secretion.
Cellular LocationsCytoplasm

Verwendung und Herstellung

Use ClassificationPharmaceuticals -> Animal Drugs -> Approved in Taiwan
Anwendungen · 1 Eintrag

BeschreibungChemically this is 3-methyl-5-phenyl-4-isoxazolyl penicillin. It was synthesized in 1961 and has been extensively used in North America. It is available as an oral solution of 120 mg/5 ml. It usually comes in an injectable formulation of 1 and 2 g. A 10-g injectable formulation is also marketed.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

ChlorHydroxylaminThionyldichlorid6-AminopenicillansureEthylacetoacetatBenzaldehydNatriumhydrogencarbonat

Anbieter23 Anbieter

北京华美互利生物化工010-56205725 · [email protected]
上海瀚香生物科技有限公司177-54423994 17754423994 · [email protected]
BOC Sciences1-631-485-4226; 16314854226 · [email protected]
玺标(上海)科技有限公司18512111473 18512111473 · [email protected]
陕西缔都医药化工有限公司+86-29-87569262 +86-15003564040 · [email protected]
陕西缔都医药化工有限公司029-81024372 17792795018 · [email protected]
上海谱科生物技术有限公司021-64705760 18027310741 · [email protected]
天津阿尔塔科技有限公司022-6537-8550 15522853686 · [email protected]
HANGZHOU LEAP CHEM CO., LTD.+86-571-87711850 +86-15355479329 · [email protected]
上海阿拉丁生化科技股份有限公司6206333 13167063860 · [email protected]
上海一飞生物科技有限公司021-65675885 18964387627 · [email protected]
上海源叶生物科技有限公司18916372613 · [email protected]
上海陶术生物科技股份有限公司13564774135 · [email protected]
成都标样生物科技有限公司028-81700200 13308200041 · [email protected]
湖北扬信医药科技有限公司15374522761 · [email protected]
Shaanxi Dideu New Materials Co. Ltd18192503167 · [email protected]
阿勒山(广州)生物科技有限公司18636736628 · [email protected]
湖北康鑫源顺医药化工有限公司027-51831887 15337167856 · [email protected]
湖北摩科化学有限公司18627753421; 18627756402 · [email protected]
TargetMol中国(陶术生物)4008200310 15002144251 · [email protected]
广州安纳医药科技有限公司020-86211473 13925088720 · [email protected]
南京世洲生物科技有限公司17301488900 · [email protected]
上海阿摩尔生物科技有限公司13370042665 18916960931 · [email protected]

Ergänzende Hinweise

DefinitionChEBI: A penicillin antibiotic carrying a 5-methyl-3-phenylisoxazole-4-carboxamide group at position 6.