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Details

Stereochemistry ABSOLUTE
Molecular Formula C17H18N3O4S.Na
Molecular Weight 383.397
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METAMPICILLIN SODIUM

SMILES

[Na+].[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2NC(=O)[C@H](N=C)C3=CC=CC=C3)C([O-])=O

InChI

InChIKey=CRTBAVDGJWEWNJ-GKANRWTBSA-M
InChI=1S/C17H19N3O4S.Na/c1-17(2)12(16(23)24)20-14(22)11(15(20)25-17)19-13(21)10(18-3)9-7-5-4-6-8-9;/h4-8,10-12,15H,3H2,1-2H3,(H,19,21)(H,23,24);/q;+1/p-1/t10-,11-,12+,15-;/m1./s1

HIDE SMILES / InChI

Molecular Formula C17H18N3O4S
Molecular Weight 360.408
Charge -1
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Metampicillin is the approved name for the penicillin resulting from the reaction of ampicillin with formaldehyde. Metampicillin is hydrolysed in aqueous solution with the formation of ampicillin. Metampicillin has broad spectrum of activity coupled with a marked degree of stability to bacterial penicillinase. Furthermore, metampicillin is reported to be absorbed to a greater extent than ampicillin, resulting in superior blood levels in human subjects, and also giving high levels of antibiotic in bile following parenteral administration. Metampicillin showed a spectrum and level of activity similar to that of ampicillin in vitro, and both compounds were inactive against penicillinase-producing strains of bacteria. The activity of metampicillin was markedly reduced by human serum, and the compound was less active than ampicillin in the presence of human serum. Following the oral administration of metampicillin to man, metampicillin was not detected in the blood stream nor in urine, and ampicillin alone was demonstrated in these subjects. The serum concentrations of ampicillin that were produced following the oral administration of metampicillin were somewhat lower than those obtained with equivalent doses of ampicillin. Adminstration of metampicillin by the intramuscular (i.m.) route to volunteers resulted in the appearance of both ampicillin and metampicillin in the blood, and of ampicillin alone in the urine of these subjects. When parenteraly administered, metampicillin appeared to be a particularly suitable penicillin for the treatment of biliary tract infections. Metampicillin is a cell wall biosynthesis inhibitor.

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

Oral administration. Following the oral administration of a single 500-mg dose of metampicillin to fasting human subjects, metampicillin was not detected and ampicillin alone was demonstrated in the blood specimens taken 1, 2, and 3 h after dosing. Intramuscular administration. After administration of 250 mg metampicillin by the i.m. route to 2 human subjects, both metampicillin and ampicillin were observed in the blood of both subjects after 1/2 h and both penicillins were present in 1 subject 1 h after dosing.
Route of Administration: Other
Metampicillin interacted with renal peptide transporter PEPT2 with medium affinity (K(i)=0.1-5mM).
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:02:26 GMT 2023
Edited
by admin
on Sat Dec 16 02:02:26 GMT 2023
Record UNII
1HE2T55NH5
Record Status Validated (UNII)
Record Version
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Name Type Language
METAMPICILLIN SODIUM
MART.   WHO-DD  
Common Name English
METAMPICILLIN SODIUM SALT [MI]
Common Name English
SODIUM (6R)-6-(D-2-METHYLENEAMINO-2-PHENYLACETAMIDO)PENICILLANATE
Common Name English
METAMPICILLIN SODIUM SALT
MI  
Common Name English
Metampicillin sodium [WHO-DD]
Common Name English
METAMPICILLIN SODIUM [MART.]
Common Name English
MAGNIPEN
Brand Name English
SERFABIOTIC
Brand Name English
METAMPEN
Brand Name English
OCELINA
Brand Name English
Code System Code Type Description
PUBCHEM
25195407
Created by admin on Sat Dec 16 02:02:27 GMT 2023 , Edited by admin on Sat Dec 16 02:02:27 GMT 2023
PRIMARY
CAS
6489-61-8
Created by admin on Sat Dec 16 02:02:27 GMT 2023 , Edited by admin on Sat Dec 16 02:02:27 GMT 2023
PRIMARY
SMS_ID
100000085925
Created by admin on Sat Dec 16 02:02:27 GMT 2023 , Edited by admin on Sat Dec 16 02:02:27 GMT 2023
PRIMARY
EVMPD
SUB03192MIG
Created by admin on Sat Dec 16 02:02:27 GMT 2023 , Edited by admin on Sat Dec 16 02:02:27 GMT 2023
PRIMARY
MERCK INDEX
m7266
Created by admin on Sat Dec 16 02:02:27 GMT 2023 , Edited by admin on Sat Dec 16 02:02:27 GMT 2023
PRIMARY Merck Index
FDA UNII
1HE2T55NH5
Created by admin on Sat Dec 16 02:02:27 GMT 2023 , Edited by admin on Sat Dec 16 02:02:27 GMT 2023
PRIMARY
EPA CompTox
DTXSID6045872
Created by admin on Sat Dec 16 02:02:27 GMT 2023 , Edited by admin on Sat Dec 16 02:02:27 GMT 2023
PRIMARY
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