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Mecillinam

CAS No.
32887-01-7
Chemical Name:
Mecillinam
Synonyms
AMDINOCILLIN;Coactin;Selexidin;Mecillinam (technical product);fl1060;Hexapen;FL10606;ro10-9070;MECILLINAM;Mecill·Nam
CBNumber:
CB7203891
Molecular Formula:
C15H23N3O3S
Molecular Weight:
325.43
MDL Number:
MFCD00056869
MOL File:
32887-01-7.mol
MSDS File:
SDS
Last updated:2024-11-19 23:02:33

Mecillinam Properties

Melting point 156°C
Boiling point 551℃
alpha D20 +285° (c = 1 in 0.1N HCl)
Density 1.44±0.1 g/cm3(Predicted)
Flash point >110°(230°F)
storage temp. Sealed in dry,2-8°C
solubility Methanol (Slightly), Water (Slightly)
pka pKa 3.40 (Uncertain)
form Solid
color White to Off-White
Water Solubility Soluble in water at approximately 1mg/ml
CAS DataBase Reference 32887-01-7(CAS DataBase Reference)
FDA UNII V10579P3QZ
ATC code J01CA11

SAFETY

Risk and Safety Statements

Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  2
RTECS  XI0185000

Mecillinam price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 33447 Mecillinam VETRANAL 32887-01-7 100mg $201 2024-03-01 Buy
Alfa Aesar J66774 Mecillinam, 95% 32887-01-7 100mg $158 2023-06-20 Buy
Cayman Chemical 9002008 Mecillinam ≥95% 32887-01-7 100 mg $79 2024-03-01 Buy
Cayman Chemical 9002008 Mecillinam 32887-01-7 1g $315 2024-03-01 Buy
Cayman Chemical 9002008 Mecillinam 32887-01-7 10g $1351 2023-01-06 Buy
Product number Packaging Price Buy
33447 100mg $201 Buy
J66774 100mg $158 Buy
9002008 100 mg $79 Buy
9002008 1g $315 Buy
9002008 10g $1351 Buy

Mecillinam Chemical Properties,Uses,Production

Chemical Properties

White Solid

Originator

Selexidin,Leo,UK,1979

Uses

Effective against Gram-negative bacteria

Uses

Active antibacterial against gram-negative bacteria

Uses

Mecillinam (amidinocillin) is a penicillin nucleus (6 APA) derivative, active in vitro against most aerobic and anaerobic Gram-negative bacilli, including E. coli and B. fraglis, but not active against Staphylococcus aureus, Enterococcus, or Pseudomonas. Mecillinam is synergistic with other beta-lactam drugs and therefore can be used in combination to treat severe Gram-negative infections. Although its in vitro efficacy is convincing, there are not enough clinical trials to support its use for intra-abdominal infections.

Definition

ChEBI: Mecillinam is a penicillin in which the 6beta substituent is [(azepan-1-yl)methylidene]amino; an extended-spectrum penicillin antibiotic that binds specifically to penicillin binding protein 2 (PBP2), and is only considered to be active against Gram-negative bacteria. It has a role as an antibacterial drug and an antiinfective agent.

Manufacturing Process

The starting material N-formylhexamethyleneimine was prepared from hexamethyleneimine and chloral.
12.7 g of N-formylhexamethyleneimine were dissolved in 250 ml of dry ether. While stirring and cooling, 8.5 ml of oxalyl chloride in 50 ml of dry ether were added dropwise, whereafter the mixture was stirred overnight at room temperature. The precipitated amide chloride was filtered off and washed with dry ether, and was placed in an exsiccator.
A solution of the amide chloride (4.6 g) in dry, alcohol-free chloroform (20 ml) was added slowly to a solution of trimethylsilyl 6-amino-penicillanate (7.2 g) and triethylamine (3.5 ml) in dry, alcohol-free chloroform (50 ml) with stirring and cooling to -70°C. The temperature was raised to 0°C during 1.5 hours. The solution was evaporated to dryness in vacuo and the residue was triturated with dry ether (200 ml). The precipitate was filtered off and washed with dry ether. The filtrate was diluted with ether (200 ml). 2-Butanol (2.8 ml) was added dropwise with stirring and cooling to 0°C. The stirring was continued for 1/4 hour at 0°C, whereupon the precipitate was filtered off, washed with ether and dried. It was a white, amorphous powder, soluble in water.

brand name

Coactin (Roche).

Therapeutic Function

Antibacterial

Antimicrobial activity

The antibacterial spectrum differs greatly from that of the aminopenicillins in that the compound displays high activity against many Gram-negative bacteria but limited activity against Gram-positive organisms. Mecillinam is active against many Enterobacteriaceae due to its selective binding to PBP 2, although the susceptibility of Proteus and Providencia spp. is variable. H. influenzae is less susceptible than enteric bacilli, and Acinetobacter spp., B. fragilis and Ps. aeruginosa are resistant.
It is readily inactivated by many β-lactamases, although it is more stable than ampicillin.

Acquired resistance

Intrinsic resistance in susceptible species of enterobacteria is uncommon and many ampicillin-resistant strains are susceptible. Bacteria that are resistant to both ampicillin and mecillinam are usually those producing large amounts of β-lactamase, most commonly plasmid-mediated enzymes.

Pharmacokinetics

Oral absorption (pivmecillinam): c. 75%
Cmax 200 mg intravenous infusion: 12 mg/L end infusion
200 mg intramuscular: c. 6 mg/L after 45 min
400 mg oral (pivmecillinam): 2–5 mg/L after c. 1 h
Plasma half-life: 50 min
Volume of distribution: 0.2–0.4 L/kg
Plasma protein binding: 5–10%
Absorption
Oral absorption is very poor, with conventional doses producing plasma levels of <1 mg/L and recovery of only about 5% in the urine. A 400 mg dose of the pivaloyl ester is equivalent to 273 mg mecillinam. It is relatively well absorbed and rapidly liberates the parent compound. Metabolism and excretion
The amidino side chain undergoes spontaneous aqueous hydrolysis to the N-formyl derivative, which retains some antibacterial activity. Hydrolysis of the β-lactam ring also occurs.
Approximately 60% is excreted unchanged in the urine in the first 6 h, achieving concentrations exceeding 1 g/L. The concentration in bile can reach 40 or 50 mg/L in patients with normally functioning gallbladders treated with 800 mg intramuscularly.

Clinical Use

Urinary tract infection (pivmecillinam)
Other infections with susceptible Gram-negative bacilli (usually in combination with other agents)

Side effects

It is generally well tolerated, and serious anaphylactic responses are said to be rare. Nausea and vomiting, which may be persistent, occur with diarrhea in some patients treated with pivmecillinam.

Mecillinam Preparation Products And Raw materials

Raw materials

1of2

Preparation Products

Global( 126)Suppliers
Supplier Tel Email Country ProdList Advantage
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28172 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49374 58
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29811 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 32161 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763 sales@tnjchem.com China 34563 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 7724 58
BOC Sciences
16314854226; +16314854226 inquiry@bocsci.com United States 19741 58
Alfa Chemistry
Info@alfa-chemistry.com United States 24072 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6391 58
LEAP CHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 24727 58

View Lastest Price from Mecillinam manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Mecillinam pictures 2024-11-19 Mecillinam
32887-01-7
US $39.00-82.00 / mg 95.00% 10g TargetMol Chemicals Inc.
mecillinam pictures 2020-01-10 mecillinam
32887-01-7
US $1.00 / KG 1KG 98% HPLC 10 tons/month Career Henan Chemical Co
  • Mecillinam pictures
  • Mecillinam
    32887-01-7
  • US $39.00-82.00 / mg
  • 95.00%
  • TargetMol Chemicals Inc.
  • mecillinam pictures
  • mecillinam
    32887-01-7
  • US $1.00 / KG
  • 98% HPLC
  • Career Henan Chemical Co
(2S,5R,6R)-6-(Azepan-1-ylmethylideneamino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid Hexapen (2S,5R,6R)-6-[[(Hexahydro-1H-azepin-1-yl)Methylene]aMino]-3,3-diMethyl-7-oxo-4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid FL-1060, Ro-9070, MecillinaM, 6-[[(Hexahydro-1H-azepin-1-yl)Methylene]aMino]penicillanic Acid Mecillinam (t Mecill·Nam Mecillinam VETRANAL [6R]-6-[Perhydroazepin-1-yl-methyleneamino] penicillanic acid Mecillinam, FL-1060, Ro-9070, (+)--yl)methylene)amino)- MECILLINAM MECILLINAM HYDROCHLORIDE [2S-(2α,5α,6β)]-6-[[(Hexahydro-1h-azepin-1-y1)methylene]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylicacid,6-(((hexahydro-1h-azepin-1 6-((hexahydro-1h-azepin-1-yl)methyleneamino)penicillanicacid fl1060 hexacillin mecilinamo penicillinhx ro10-9070 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(hexahydro-1H-azepin-1-yl)methylene]amino]-3,3-dimethyl-7-oxo-, (2S,5R,6R)- (2S,5R,6R)-6-(((E)-Azepan-1-ylmethylene)amino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid Mecillinam USP/EP/BP Amdinocillin (Mecillinam Mecillinamum Mecillinam D12 Mecillinam D3 MecillinamQ: What is Mecillinam Q: What is the CAS Number of Mecillinam Q: What is the storage condition of Mecillinam 6-(1-azepanylmethylideneamino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid (2S,5R,6R)-6-[(Azepan-1-ylmethylene)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid Mecillinam (technical product) Selexidin AMDINOCILLIN Coactin FL10606 13C6]-Mecillinam 32887-01-7 Active Pharmaceutical Ingredients Intermediates & Fine Chemicals Pharmaceuticals Antibiotics BactericidalAntibiotics BacteriostaticAntibiotics beta-Lactam StructureAlphabetic Chemical Structure M MEA - MES Principle Heterocycles Sulfur & Selenium Compounds