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A4011612

Tigecycline , ≥96% , 220620-09-7

Synonym(s):
9- t-Butylglycylamido-minocycline;9-t-Butylglycylamido-minocycline;9-tert-Butylglycylamidominocycline;Tigecycline;Tigecycline - CAS 220620-09-7 - Calbiochem

CAS NO.:220620-09-7

Empirical Formula: C29H39N5O8

Molecular Weight: 585.65

MDL number: MFCD00935753

EINECS: 685-736-6

Pack Size Price Stock Quantity
10MG RMB47.20 In Stock
50MG RMB87.20 In Stock
250MG RMB173.60 In Stock
1g RMB435.20 In Stock
5g RMB1759.20 In Stock
others     Enquire
Update time: 2022-07-08

PRODUCT Properties

Melting point: 164-166°C
Boiling point: 890.9±65.0 °C(Predicted)
Density  1.45±0.1 g/cm3(Predicted)
storage temp.  Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
solubility  Soluble in DMSO (up to at least 25 mg/ml).
pka 4.50±1.00(Predicted)
form  Orange powder
color  Orange
Merck  14,9432
Stability: Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 1 month.
InChIKey FPZLLRFZJZRHSY-HJYUBDRYSA-N
SMILES C1(=O)[C@]2(O)[C@@]([H])(C[C@@]3([H])C(=C2O)C(=O)C2=C(C(N(C)C)=CC(NC(CNC(C)(C)C)=O)=C2O)C3)[C@H](N(C)C)C(O)=C1C(N)=O
CAS DataBase Reference 220620-09-7(CAS DataBase Reference)

Description and Uses

The emergence of drug-resistant bacteria has diminished the clinical utility of the tetracyclines. Research to circumvent the efflux and ribosomal protection mechanisms of bacteria has led to the development of the glycylcyclines. Tigecycline is the first glycylcycline antibiotic to launch for the parenteral treatment of baterial infection, including complicated intra-abdominal and skin infections. Its mechanism of action involves inhibiting protein translation in bacteria by binding to the 30S ribosomal subunit and blocking entry of amino-acyl tRNA molecules into the A site of the ribosome to effectively prevent incorporation of amino acid residues into elongating peptide chains. Presumably, ribosomal protection proteins are ineffective against tigecycline due to its higher affinity for ribosomal binding compared to tetracyclines (approximately 16-fold). In addition, tigecycline may be resistant to efflux mechanisms by either their inability to translocate it across the cytoplasmic membrane due to steric complications or simply by their failure to recognize the molecule.

A broad spectrum glycylcycline antibiotic

Safety

Symbol(GHS) 
GHS07,GHS08,GHS09
Signal word  Danger
Hazard statements  H319-H360D-H372-H410
Precautionary statements  P202-P260-P264-P273-P305+P351+P338-P308+P313
Safety Statements  24/25
RIDADR  3077
RTECS  QI7619500
HazardClass  9
PackingGroup  III
HS Code  29419090
Hazardous Substances Data 220620-09-7(Hazardous Substances Data)

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