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Cefmenoxime hydrochloride

Basic information Safety Supplier Related

Cefmenoxime hydrochloride Basic information

Product Name:
Cefmenoxime hydrochloride
Synonyms:
  • 8-[2-(2-amino-1,3-thiazol-4-yl)-2-methoxyimino-acetyl]amino-4-[(1-methyltetrazol-5-yl)sulfanylmethyl]-7-oxo-2-thia-6-azabicyclo[4.2.0]oct-4-ene-5-carboxylic acid hydrochloride (2:1)
  • 7-[[(2-Amino-4-thiazolyl)(methoxyimino)acetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid hemihydrochloride
  • 7beta-[2-(2-Aminothiazol-4-yl)-(Z)-2-(methoxyiminoacetamido)]-3-[(1-methyl-1H-tetrazol-5-yl)thiomethyl]ceph-3-em-4-carboxylic acid hemihydrochloride
  • Bestcall
  • Bestron
  • Cemix
  • SCE-1365(free acid)
  • Tacef
CAS:
75738-58-8
MF:
C16H18ClN9O5S3
MW:
548.01
EINECS:
278-299-4
Product Categories:
  • CEFMAX
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Sulfur & Selenium Compounds
Mol File:
75738-58-8.mol
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Cefmenoxime hydrochloride Chemical Properties

Melting point:
>175°C (dec.)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
DMSO (Slightly, Heated), Methanol (Slightly)
form 
Solid
color 
Off-White to Pale Yellow
InChI
InChI=1/C16H17N9O5S3.ClH/c1-24-16(20-22-23-24)33-4-6-3-31-13-9(12(27)25(13)10(6)14(28)29)19-11(26)8(21-30-2)7-5-32-15(17)18-7;/h5,9,13H,3-4H2,1-2H3,(H2,17,18)(H,19,26)(H,28,29);1H/b21-8-;/t9-,13-;/s3
InChIKey
HZYJYGJIOCXOTH-AJVJENPNNA-N
SMILES
C(C1=C(CS[C@]2([H])[C@H](NC(=O)/C(/C3N=C(N)SC=3)=N\OC)C(=O)N12)CSC1=NN=NN1C)(=O)O.Cl |&1:5,7,r|
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Safety Information

HS Code 
2941906000
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Cefmenoxime hydrochloride Usage And Synthesis

Description

Cef menoxime hydrochloride is a third generation cephalosporin antibiotic. Structurally, it possesses the (1-methyl-lH-tetrazol-5-yl)thiomethyl moiety in the 3-position; like several other compounds containing this structural element (moxalactam, cefoperazone, cefamandol), bleeding linked to vitamin K interaction has been reported. Cefmenoxime has activity similar to cefotiuime, ceftizoxime and moxalactam against E.coli, C. diversus, Klebsiella, P. Mirabilis, Salmonella, Shigella, Neiseria spp., S. pyogenes, S. Pneumoniae, and g. influenzae. It is relatively ineffective against Pseudomonas and Bacteroidea.

Originator

Takeda (Japan)

Uses

A third generation cephalosporin antibiotic with strong antimicrobial activities against Streptococcus pneumoniae, Haemophilus influenzae and Moraxella subgenus Branhamella catarrhalis that were 3 major aerobic bacteria from sinusitis.

Uses

antibacterial

Definition

ChEBI: The hemihydrochloride salt of cefmenoxime.

brand name

Cefmax (TAP);TACEF;BESTCALL.

General Description

Cefmenoxime was synthesized by Takeda Pharmaceutical Co. in 1978. It contains aminothiazole and methoxyimino groups in the 7-acyl position and a methyltetrazole group at the 3 position of the cephem nucleus. Cefmenoxime has a wide activity spectrum against gram-positive and gram-negative bacteria, including anaerobes, except Staphylococcus aureus. Cefmenoxime is a member of the so-called third-generation cephalosporins, a recently introduced class of clinically important antibiotics.

Cefmenoxime hydrochloride Supplier

Guilin Auspicious Pharmaceutical Co., Ltd. Gold
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0773-3557148
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Aolin02@163.com
J & K SCIENTIFIC LTD.
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010-82848833 400-666-7788
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Chemsky(shanghai)International Co.,Ltd.
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021-50135380
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XiaoGan ShenYuan ChemPharm co,ltd
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0712-0712-2580635 15527768850
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Tianjin heowns Biochemical Technology Co., Ltd.
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400 638 7771
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sales@heowns.com