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Taniborbactam hydrochloride - 99%, high purity , CAS No.2244235-49-0

    Grade & Purity:
  • ≥99%
In stock
Item Number
T651880
Grouped product items
SKU Size
Availability
Price Qty
T651880-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$780.90
T651880-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$1,250.90
T651880-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$3,500.90

Basic Description

Synonyms CS-0114394 | Taniborbactam HCl | AKOS040739828 | Taniborbactam hydrochloride | Taniborbactam hydrochloride [USAN] | Vnrx5133 dihydrochloride | VNRX-5133 (hydrochloride) | (R)-3-(2-((1S,4R)-rel-4-((2-Aminoethyl)amino)cyclohexyl)acetamido)-2-hydroxy-3,4-dih
Specifications & Purity ≥99%
Biochemical and Physiological Mechanisms Taniborbactam hydrochloride (VNRX-5133 hydrochloride) is a reversible and selective boronic acid-containing pan-spectrum β-lactamase inhibitor with IC 50 s of 8-530 nM. Taniborbactam hydrochloride has IC 50 s of 30 nM, 32 nM, 42 nM, 20 nM for KPC-2, AmpC,
Storage Temp Protected from light,Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Taniborbactam hydrochloride (VNRX-5133 hydrochloride) is a reversible and selective boronic acid-containing pan-spectrum β-lactamase inhibitor with IC 50 s of 8-530 nM. Taniborbactam hydrochloride has IC 50 s of 30 nM, 32 nM, 42 nM, 20 nM for KPC-2, AmpC, OXA-48, and VIM-2. Taniborbactam hydrochloride is against Gram-negative bacteria

In Vitro

Taniborbactam hydrochloride (VNRX-5133 hydrochloride) has IC 50 s of 0.5 nM, 2 nM, 0.5 nM, 0.06 nM for KPC-2, OXA-48, VIM-4 of K.pneumoniae strain and VIM-2 of P.aeruginosa strain. ?\nBoth cefepime/Taniborbactam hydrochloride (10 μg/mL) and meropenem/Taniborbactam hydrochloride combinations are highly active against all six of the NDM-1-producing clinical isolates from K.pneumoniae and E.coli , with MIC ranges of 16-0.25 and 1-0.125 μg/mL, respectively. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

A single dose of Cefepime (32 mg/kg)/Taniborbactam hydrochloride (VNRX-5133 hydrochloride; 16 mg/kg; s.c.) achieves >4 log 10 reduction in viable bacterial counts in the neutropenic mouse lung infection model against a CTX-M-14-producing strain of K.pneumoniae. ?\nCombination of Cefepime (16 mg/kg) and Taniborbactam hydrochloride (16 mg/kg; s.c.; twice-a-day for 7 days) demonstrates >2 log 10 reductions in viable bacterial counts in the kidney of the ascending urinary tract infection model against a CTX-M-15-producing strain of E.coli. ?\nTaniborbactam hydrochloride has a T 1/2 of 0.16 hours, a CL of 618 mL/h/kg, and a V ss of 143 mL/kg for mice. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

IC50& Target:β-lactamase

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic acids and derivatives
Class Carboxylic acids and derivatives
Subclass Carboxylic acids
Intermediate Tree Nodes Not available
Direct Parent 1-carboxy-2-haloaromatic compounds
Alternative Parents Unsaturated fatty acids  Oxaborine derivatives  N-acyl amines  Benzenoids  Boronic acid esters  Amino acids  Oxacyclic compounds  Organic metalloid salts  Monocarboxylic acids and derivatives  Dialkylamines  Carboxylic acid amides  Organopnictogen compounds  Organooxygen compounds  Organoboron compounds  Organic oxides  Monoalkylamines  Hydrochlorides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents 1-carboxy-2-haloaromatic compound - Fatty acyl - Fatty acid - Benzenoid - Unsaturated fatty acid - 1,2-oxaborine derivative - N-acyl-amine - Fatty amide - Boronic acid ester - Amino acid - Carboxamide group - Boronic acid derivative - Amino acid or derivatives - Oxacycle - Organic metalloid salt - Organoheterocyclic compound - Secondary amine - Monocarboxylic acid or derivatives - Secondary aliphatic amine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Hydrochloride - Organic salt - Organooxygen compound - Organonitrogen compound - Organoboron compound - Primary aliphatic amine - Amine - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as 1-carboxy-2-haloaromatic compounds. These are aromatic compounds containing 1 carboxyl group and a C-X (X = halogen) group at adjacent positions of an aromatic ring.
External Descriptors Not available

Names and Identifiers

IUPAC Name (3R)-3-[[2-[4-(2-aminoethylamino)cyclohexyl]acetyl]amino]-2-hydroxy-3,4-dihydro-1,2-benzoxaborinine-8-carboxylic acid;dihydrochloride
INCHI InChI=1S/C19H28BN3O5.2ClH/c21-8-9-22-14-6-4-12(5-7-14)10-17(24)23-16-11-13-2-1-3-15(19(25)26)18(13)28-20(16)27;;/h1-3,12,14,16,22,27H,4-11,21H2,(H,23,24)(H,25,26);2*1H/t12?,14?,16-;;/m0../s1
InChIKey CKWIMFZHNCBHIX-PPJOBQAPSA-N
Smiles B1(C(CC2=C(O1)C(=CC=C2)C(=O)O)NC(=O)CC3CCC(CC3)NCCN)O.Cl.Cl
Isomeric SMILES B1([C@H](CC2=C(O1)C(=CC=C2)C(=O)O)NC(=O)CC3CCC(CC3)NCCN)O.Cl.Cl
Alternate CAS 2244235-49-0
PubChem CID 137331954
Molecular Weight 462.18

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Solubility DMSO : 200 mg/mL (432.73 mM; Need ultrasonic) H2O : 33.33 mg/mL (72.11 mM; Need ultrasonic)

Solution Calculators

Reviews

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