Cefonicid: Difference between revisions

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Cefonicid
Clinical data
AHFS/Drugs.com	Micromedex Detailed Consumer Information
MedlinePlus	a601206
ATC code	J01DC06 (WHO) ;
Identifiers
	IUPAC name (6R,7R)-7-[(2R)-2-hydroxy-2-phenylacetyl)amino]-8-oxo-; 3-{[1-(sulfomethyl)tetrazol-5-yl]sulfanylmethyl}-; 5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid;
CAS Number	61270-58-4;
PubChem CID	43594;
ChemSpider	39734 ;
UNII	6532B86WFG;
KEGG	D07644 ;
ChEBI	CHEBI:3491 ;
ChEMBL	ChEMBL1601 ;
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	C18H18N6O8S3
Molar mass	542.569 g/mol
3D model (JSmol)	Interactive image;
	SMILES O=C2N1/C(=C(\CS[C@@H]1[C@@H]2NC(=O)[C@H](O)c3ccccc3)CSc4nnnn4CS(=O)(=O)O)C(=O)O;
	InChI InChI=1S/C18H18N6O8S3/c25-13(9-4-2-1-3-5-9)14(26)19-11-15(27)24-12(17(28)29)10(6-33-16(11)24)7-34-18-20-21-22-23(18)8-35(30,31)32/h1-5,11,13,16,25H,6-8H2,(H,19,26)(H,28,29)(H,30,31,32)/t11-,13-,16-/m1/s1 ; Key:DYAIAHUQIPBDIP-AXAPSJFSSA-N ;
(verify)

VisualWikitext

Latest revision as of 13:54, 14 April 2015

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Cefonicide (or cefonicid) is a cephalosporin antibiotic.

It has a density of 1.92g/cm³. Template:Antibiotic-stub

@@ Line 1: / Line 1: @@
 {{Drugbox
-| IUPAC_name        = (6''R'',7''R'')-7-[(2-hydroxy-2-phenylacetyl)amino]-8-oxo-<br>3-{[1-(sulfomethyl)tetrazol-5-yl]sulfanylmethyl}-<br>5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic&nbsp;acid
+| Watchedfields = changed
-| image             = cefonicid.png
+| verifiedrevid = 443509375
-| CAS_number        =
+| IUPAC_name = (6''R'',7''R'')-7-[(2''R'')-2-hydroxy-2-phenylacetyl)amino]-8-oxo-<br>3-{[1-(sulfomethyl)tetrazol-5-yl]sulfanylmethyl}-<br>5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic&nbsp;acid
-| ATC_prefix        = J01
+| image = Cefonicid Wiki str.png
-| ATC_suffix        = DC06
-| PubChem           = 43592
-| DrugBank          =
+<!--Clinical data-->
-| C=18|H=18|N=6|O=8|S=3
+| tradename =
-| molecular_weight  = 542.569 g/mol
+| Drugs.com = {{drugs.com|CONS|cefonicid}}
-| bioavailability   =
+| MedlinePlus = a601206
-| protein_bound     =
+| pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X -->
-| metabolism        =
+| pregnancy_US = <!-- A / B            / C / D / X -->
-| elimination_half-life =
+| pregnancy_category =
-| excretion         =
+| legal_AU = <!-- Unscheduled / S2 / S3 / S4 / S5 / S6 / S7 / S8 / S9 -->
-| pregnancy_AU      =  <!-- A / B1 / B2 / B3 / C / D / X -->
+| legal_CA = <!--             / Schedule I, II, III, IV, V, VI, VII, VIII -->
-| pregnancy_US      =  <!-- A / B            / C / D / X -->
+| legal_UK = <!-- GSL         / P       / POM / CD / Class A, B, C -->
-| pregnancy_category=
+| legal_US = <!-- OTC                   / Rx-only  / Schedule I, II, III, IV, V -->
-| legal_AU          =  <!-- Unscheduled / S2 / S3 / S4 / S5 / S6 / S7 / S8 / S9 -->
+| legal_status =
-| legal_CA          =  <!--             / Schedule I, II, III, IV, V, VI, VII, VIII -->
+| routes_of_administration =
-| legal_UK          =  <!-- GSL         / P       / POM / CD / Class A, B, C -->
-| legal_US          =  <!-- OTC                   / Rx-only  / Schedule I, II, III, IV, V -->
+<!--Pharmacokinetic data-->
-| legal_status      =
+| bioavailability =
-| routes_of_administration =
+| protein_bound =
+| metabolism =
+| elimination_half-life =
+| excretion =
+<!--Identifiers-->
+| CASNo_Ref = {{cascite|correct|CAS}}
+| CAS_number = 61270-58-4
+| ATC_prefix = J01
+| ATC_suffix = DC06
+| PubChem = 43594
+| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
+| DrugBank =
+| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
+| ChemSpiderID = 39734
+| UNII_Ref = {{fdacite|correct|FDA}}
+| UNII = 6532B86WFG
+| KEGG_Ref = {{keggcite|correct|kegg}}
+| KEGG = D07644
+| ChEBI_Ref = {{ebicite|correct|EBI}}
+| ChEBI = 3491
+| ChEMBL_Ref = {{ebicite|correct|EBI}}
+| ChEMBL = 1601
+<!--Chemical data-->
+| C=18 | H=18 | N=6 | O=8 | S=3
+| molecular_weight = 542.569 g/mol
+| smiles = O=C2N1/C(=C(\CS[C@@H]1[C@@H]2NC(=O)[C@H](O)c3ccccc3)CSc4nnnn4CS(=O)(=O)O)C(=O)O
+| InChI = 1/C18H18N6O8S3/c25-13(9-4-2-1-3-5-9)14(26)19-11-15(27)24-12(17(28)29)10(6-33-16(11)24)7-34-18-20-21-22-23(18)8-35(30,31)32/h1-5,11,13,16,25H,6-8H2,(H,19,26)(H,28,29)(H,30,31,32)/t11-,13-,16-/m1/s1
+| InChIKey = DYAIAHUQIPBDIP-AXAPSJFSBE
+| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
+| StdInChI = 1S/C18H18N6O8S3/c25-13(9-4-2-1-3-5-9)14(26)19-11-15(27)24-12(17(28)29)10(6-33-16(11)24)7-34-18-20-21-22-23(18)8-35(30,31)32/h1-5,11,13,16,25H,6-8H2,(H,19,26)(H,28,29)(H,30,31,32)/t11-,13-,16-/m1/s1
+| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
+| StdInChIKey = DYAIAHUQIPBDIP-AXAPSJFSSA-N
 }}
+__NOTOC__
 {{SI}}
-{{EH}}
+{{CMG}}
+== Overview ==
-'''Cefonicide''' (or '''cefonicid''') is a [[cephalosporin]].
+'''Cefonicide''' (or '''cefonicid''') is a [[cephalosporin]] [[antibiotic]].
+It has a density of 1.92g/cm<sup>3</sup>.
+{{antibiotic-stub}}
 {{CephalosporinAntiBiotics}}
+[[Category:drug]]
 [[Category:Cephalosporin antibiotics]]
-[[Category:Organosulfates]]
+[[Category:Enantiopure drugs]]
-{{SIB}}
+[[Category:Sulfonic acids]]
-{{WH}}
+[[Category:Tetrazoles]]
-{{WS}}

v t e Antibacterials: cell wall disruption (J01C-J01D)
Internal to membrane/ (inhibit peptidoglycan subunit synthesis and transport)	Template:Navbox subgroup
Glycopeptide/ (inhibit PG chain elongation)	Vancomycin # (Oritavancin, Telavancin) · Teicoplanin (Dalbavancin) · Ramoplanin
Beta-lactams/ (inhibit cross-links with PBP)	Template:Navbox subgroup
Other	Template:Navbox subgroup
# = WHO-EM

Cefonicid: Difference between revisions

Latest revision as of 13:54, 14 April 2015

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