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Thienamycin

CAS No.
59995-64-1
Chemical Name:
Thienamycin
Synonyms
Imipenem EP Impurity A;(+)-Thienamycin;Thienamycin (>80%);IMipeneM IMpurity A;Thienamycin USP/EP/BP;Imipenemum Impurity A;(3As,7As)-Octahydro-2-benzofuran;Imipenem Impurity 1(Imipenem EP Impurity A);(5R)-3-(2-Aminoethylthio)-6β-[(R)-1-hydroxyethyl]-7-oxo-1-azabicyclo[3.2.0]hepta-2-ene-2-carboxylic acid;(5R)-3-[(2-Aminoethyl)thio]-6β-[(R)-1-hydroxyethyl]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid
CBNumber:
CB8969644
Molecular Formula:
C11H16N2O4S
Molecular Weight:
272.32
MDL Number:
MFCD00072032
MOL File:
59995-64-1.mol
MSDS File:
SDS
Last updated:2023-05-19 16:27:39

Thienamycin Properties

alpha D27 +82.7° (c = 1.0 in water)
Boiling point 514.0±50.0 °C(Predicted)
Density 1.50±0.1 g/cm3(Predicted)
storage temp. Hygroscopic, -86°C Freezer, Under inert atmosphere
solubility Chloroform (Slightly), Methanol (Slightly), Water (Slightly)
form Solid
pka 4.20±0.40(Predicted)
color Off-White to Dark Yellow
Stability Hygroscopic, Temperature Sensitive, Very Unstable
InChI InChI=1S/C11H16N2O4S/c1-5(14)8-6-4-7(18-3-2-12)9(11(16)17)13(6)10(8)15/h5-6,8,14H,2-4,12H2,1H3,(H,16,17)/t5-,6-,8-/m1/s1
InChIKey WKDDRNSBRWANNC-ATRFCDNQSA-N
SMILES N12[C@@]([H])([C@@H]([C@H](O)C)C1=O)CC(SCCN)=C2C(O)=O
FDA UNII WMW5I5964P

Thienamycin price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC T344270 Thienamycin(>80%) 59995-64-1 1mg $245 2021-12-16 Buy
TRC T344270 Thienamycin(>80%) 59995-64-1 10mg $1940 2021-12-16 Buy
American Custom Chemicals Corporation API0010098 THIENAMYCIN 80.00% 59995-64-1 1MG $1504.68 2021-12-16 Buy
Product number Packaging Price Buy
T344270 1mg $245 Buy
T344270 10mg $1940 Buy
API0010098 1MG $1504.68 Buy

Thienamycin Chemical Properties,Uses,Production

Description

Thienamycin, one of the most potent naturally-produced antibiotics known thus far, was discovered in Streptomyces cattleya in 1976. Thienamycin has excellent activity against both Gram-positive and Gram-negative bacteria and is resistant to bacterial β-lactamase enzymes.

Uses

Thienamycin is one of the most potent naturally produced antibiotics known thus far. It has excellent activity against both Gram-positive and Gram-negative bacteria and is resistant to bacterial β-lactamase enzymes.

Definition

ChEBI: Thienamycin is a member of carbapenems.

Biosynthesis

 The formation of thienamycin is thought to occur through a different pathway from classic β-lactams (penicillins, cephalosporins). Production of classic β-lactams in both fungi and bacteria occur through two steps: First, the condensation of L-cysteine, L-Valine, and L-α-amino adipic acid by ACV synthetase (ACVS, a nonribsomal peptide synthetase) and then cyclization of this formed tripeptide by isopenicillin N synthetase (IPNS).

Mechanism of action

In vitro, thienamycin employs a similar mode of action as penicillins through disrupting the cell wall synthesis (peptidoglycan biosynthesis) of various Gram-positive and Gram-negative bacteria (Staphylococcus aureus,Staphylococcus epidermidis, Pseudomonas aeruginosa to name a few). In a study carried out by Spratt et al., they found that, although thienamycin binds to all of the penicillin-binding proteins (PBP) in Escherichia coli, it preferentially binds to PBP-1 and PBP-2, which are both associated with the elongation of the cell wall.  Unlike pencillins, which are rendered ineffective through rapid hydrolysis by the β-lactamase enzyme present in some strains of bacteria, thienamycin remains antimicrobially active. Neu et al. found that thienamycin displayed high activity against bacteria that were resistant to other β-lactamase stable compounds (cephalosporins), highlighting the superiority of thienamycin as an antibiotic among β-lactams.

Clinical Use

Thienamycin itself is extremely unstable and decomposes in aqueous solution. Consequently, thienamycin is impractical for clinical treatment of bacterial infections. For this reason, stable derivatives of thienamycin were created for medicinal consumption. One such derivative, imipenem, was formulated in 1985. Imipenem, an N-formimidoyl derivative of thienamycin, is rapidly metabolized by the renal dihydropeptidase enzyme found in the human body. To prevent its rapid degradation, imipenem is normally co-administered with cilastatin, an inhibitor of this enzyme.

Thienamycin Preparation Products And Raw materials

Global( 66)Suppliers
Supplier Tel Email Country ProdList Advantage
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
Standardpharm Co. Ltd.
86-714-3992388 overseasales1@yongstandards.com United States 14336 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9320 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29220 58
AFINE CHEMICALS LIMITED
0571-85134551 info@afinechem.com CHINA 15377 58
BOC Sciences
+16314854226 inquiry@bocsci.com United States 19743 58
Alfa Chemistry
+1-5166625404 Info@alfa-chemistry.com United States 21317 58
LEAP CHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 24738 58
China National Standard Pharmaceutical Corporation Limited
+8615391658522 overseasales@yongstandards.com China 11927 58

View Lastest Price from Thienamycin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Thienamycin USP/EP/BP pictures 2021-06-22 Thienamycin USP/EP/BP
59995-64-1
US $1.10 / g 1g 99.9% 100 Tons Min Dideu Industries Group Limited
Thienamycin pictures 2019-12-26 Thienamycin
59995-64-1
US $1.00 / g 1g ≥98% g/kg/Ton Career Henan Chemical Co
  • Thienamycin pictures
  • Thienamycin
    59995-64-1
  • US $1.00 / g
  • ≥98%
  • Career Henan Chemical Co
[SR-[5α,6α(R^<*>^)]]-3-[(2-Aminoethyl)thio]-6-(1-hydroxyethyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid (5R)-3-(2-Aminoethylthio)-6β-[(R)-1-hydroxyethyl]-7-oxo-1-azabicyclo[3.2.0]hepta-2-ene-2-carboxylic acid (5R)-3-[(2-Aminoethyl)thio]-6β-[(R)-1-hydroxyethyl]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid (5R,6R)-3-(2-aminoethylsulfanyl)-6-[(1R)-1-hydroxyethyl]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid (5R,6R)-3-(2-aminoethylthio)-6-[(1R)-1-hydroxyethyl]-7-keto-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid (5R,6R)-3-(2-azanylethylsulfanyl)-6-[(1R)-1-hydroxyethyl]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid IMipeneM IMpurity A Imipenem Impurity 1(Imipenem EP Impurity A) (5R,6S)-3-(2-aminoethylthio)-6-[(1R)-1-hydroxyethyl]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid 1-Azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid, 3-[(2-aminoethyl)thio]-6-[(1R)-1-hydroxyethyl]-7-oxo-, (5R,6S)- (3As,7As)-Octahydro-2-benzofuran Thienamycin USP/EP/BP Thienamycin (>80%) Imipenem EP Impurity A (+)-Thienamycin Imipenemum Impurity A 59995-64-1