methicillin

methicillin  Structure
CAS No.
61-32-5
Chemical Name:
methicillin
Synonyms
Metin;C07177;BRL-1241;Metacillin;Dimocillin;Methcilline;methicillin;Dimethoxyphenyl Penicillin;MRSA Selective Supplement;2,6-Dimethoxyphenylpenicillin
CBNumber:
CB3889080
Molecular Formula:
C17H20N2O6S
Molecular Weight:
380.42
MOL File:
61-32-5.mol
Modify Date:
2023/5/4 15:10:44

methicillin Properties

Boiling point 640.0±55.0 °C(Predicted)
Density 1.44±0.1 g/cm3(Predicted)
pka pKa 2.77± 0.04(H2O,t = 25,c=0.0097) (Uncertain)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P330-P501
Hazard Codes  Xn
Risk Statements  22
WGK Germany  3
RTECS  XH2379000

methicillin Chemical Properties,Uses,Production

Uses

Antibacterial.

Definition

ChEBI: A penicillin that is 6-aminopenicillanic acid in which one of the amino hydrogens is replaced by a 2,6-dimethoxybenzoyl group.

Antimicrobial activity

2,6-Dimethoxyphenylpenicillin; methicillin (international non-proprietary name). The first β-lactamase-resistant semisynthetic penicillin. It was initially used widely but has been superseded by other group 3 members and is no longer commercially available.
It is less active than benzylpenicillin or other group 3 penicillins. It is very stable to staphylococcal β-lactamase and is active against β-lactamaseproducing strains of Staph. aureus that do not produce a functional PBP 2a. Resistance is common among staphylococci, with the incidence geographically diverse. Most methicillin-resistant staphylococcal isolates display multiresistance.
It is not acid resistant, and must therefore be administered parenterally. About 10% is metabolized, with 60–80% of the dose excreted in the urine. Toxicity is similar to that of other group 3 penicillins. Nephritis appears to be more common than with other penicillins.

Pharmacology

Like other semisynthetic penicillins, methicillin exhibits an antibacterial effect similar to that of benzylpenicillin. The main difference between methicillin and benzylpenicillin is that it is not inactivated by the enzyme penicillinase, and therefore it is effective with respect to agents producing this enzyme (staphylococci). It is used for infections caused by benzylpenicillinresistant staphylococci (septicemia, pneumonia, empyemia, osteomyelitis, abscesses, infected wounds, and others). Synonyms of this drug are cinopenil, celbenin, staphcillin, and others.

methicillin Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 13)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 United States 19973 58 Inquiry
ZHEJIANG JIUZHOU CHEM CO., LTD +86-0576225566889 +86-13454675544 China 19947 58 Inquiry
Guangzhou Isun Pharmaceutical Co., Ltd 020-39119399 18927568969 China 4428 55 Inquiry
BOC Sciences USA 0 65 Inquiry
Service Chemical Inc. 888-895-6920 Germany 6373 71 Inquiry
Lanospharma Laboratories Co.,Ltd 13440048448 China 6343 56 Inquiry
SIGMA-RBI 800 736 3690 (Orders) Switzerland 6913 91 Inquiry
Alta Scientific Co., Ltd. 022-6537-8550 15522853686 China 4515 55 Inquiry
Sigma-Aldrich 021-61415566 800-8193336 China 51471 80 Inquiry
Riedel-de Haen AG 800 558-9160 United States 6825 87 Inquiry

Related articles

61-32-5(methicillin )Related Search:

methicillin Methcilline 2,6-Dimethoxyphenyl-penicillin, Methicillin Selective Supplement, Methicillin, Staphcillin MRSA Selective Supplement (2S,5R,6R)-6-(2,6-Dimethoxybenzoylamino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptan-2-carboxylic acid 2,6-Dimethoxyphenylpenicillin BRL-1241 Dimocillin Metacillin C07177 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid, 6-[(2,6-diMethoxybenzoyl)aMino]-3,3-diMethyl-7-oxo-, (2S,5R,6R)- Dimethoxyphenyl Penicillin Metin 61-32-5