31 Results for "

boronic acid inhibitors

" in MedChemExpress (MCE) Product Catalog:
Products (31)

31 Results for "boronic acid inhibitors" in MCE Product Catalog:

42
42 Publications Verification
Cat. No.: HY-19930
CAS No.: 1360457-46-0
Synonyms: RPX7009
Research Areas:  

Infection

Vaborbactam (RPX7009) is a cyclic boronic acid pharmacophore β-lactamase inhibitor.
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19
19 Cited Publications
Cat. No.: HY-109124
CAS No.: 1613267-49-4
Purity:  98.45%
Synonyms: VNRX-5133
Research Areas:  

Infection

Taniborbactam (VNRX-5133) is a reversible and selective boronic acid-containing pan-spectrum β-lactamase inhibitor with IC50s of 8-530 nM. Taniborbactam has IC50s of 30 nM, 32 nM, 42 nM, 20 nM for KPC-2, AmpC, OXA-48, and VIM-2. Taniborbactam is against Gram-negative bacteria .
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19
19 Cited Publications
Cat. No.: HY-109124A
CAS No.: 2244235-49-0
Purity:  99.97%
Synonyms: VNRX-5133 hydrochloride
Research Areas:  

Infection

Taniborbactam hydrochloride (VNRX-5133 hydrochloride) is a reversible and selective boronic acid-containing pan-spectrum β-lactamase inhibitor with IC50s of 8-530 nM. Taniborbactam hydrochloride has IC50s 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 .
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6
6 Cited Publications
Cat. No.: HY-136072
CAS No.: 2170848-99-2
Purity:  ≥99.0%
Target:  

Bacterial

Research Areas:  

Infection

Xeruborbactam disodium is a potent, ultra-broad-spectrum boronic acid beta-lactamase inhibitor. Xeruborbactam disodium inhibits key serine and metallo beta-lactamases at a nano molar range .
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1
1 Cited Publications
Cat. No.: HY-23524
CAS No.: 346656-34-6
Target:  

Lipase

Research Areas:  

Metabolic Disease

HSL-IN-3 is a HSL inhibitor. HSL-IN-3 serves as an important intermediate for the synthesis of PARP-1 inhibitors. HSL-IN-3 can be used in studies related to lipid metabolism .
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Cat. No.: HY-111521
CAS No.: 2031124-72-6
Synonyms: Carbavance
Research Areas:  

Infection

Meropenem-vaborbactam (Carbavance) is a Carbapenem Antibiotic and Boronic acid-based beta-lactamase inhibitor, is a fixed-dose combination product with potent in vitro activity against Enterobacteriaceae that are Klebsiella pneumoniae carbapenemase producers. Meropenem-vaborbactam exhibits activity against Pseudomonas aeruginosa isolates , with an MIC50 of 0.5 μg/mL and an MIC90 of 8 μg/mL .
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Cat. No.: HY-W001242
CAS No.: 903550-26-5
1-(Tetrahydropyran-2-yl)-1H-pyrazole-5-boronic acid pinacol ester is a pharmaceutical intermediate used in the synthesis of naphthyl FXIa/PKa inhibitors .
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Cat. No.: HY-32951
CAS No.: 401815-98-3
2-Fluoropyridine-4-boronic acid is a coupling reagent and chemical intermediate. 2-Fluoropyridine-4-boronic acid facilitates the synthesis of Rho kinase (ROCK) inhibitor Compound 37 .
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Cat. No.: HY-I0314
CAS No.: 269410-08-4
1H-Pyrazole-4-boronic acid pinacol ester is a drug intermediate that can be used for the synthesis of Mps1 kinase inhibitors .
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Cat. No.: HY-136069
CAS No.: 2170834-63-4
Target:  

Bacterial

Research Areas:  

Infection

Xeruborbactam is a potent, ultra-broad-spectrum boronic acid beta-lactamase inhibitor. Xeruborbactam inhibits key serine and metallo beta-lactamases at a nano molar range .
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Cat. No.: HY-12927
CAS No.: 1240494-13-6
Purity:  99.88%
Target:  

CXCR

Research Areas:  

Inflammation/Immunology

SX-517 is a dual CXCR2/1 antagonist, containing boronic acid. SX-517 inhibits CXCL1-induced Ca 2+ flux (IC50=38 nM), and antagonizes CXCL8-induced [(35)S]GTPγS binding (IC50=60 nM) and ERK1/2 phosphorylation. SX-517 has significant ability for inflammation suppression, in both humanized polymorphonuclear (PMN) cells and in murine model .
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Cat. No.: HY-32955
CAS No.: 444120-91-6
2-Chloropyridine-5-boronic acid is a mandelate racemase (MR) inhibitor with a Ki value of 8.5 μM against Pseudomonas putida MR .
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Cat. No.: HY-137144
CAS No.: 1853279-29-4
Synonyms: ZB716
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

Fulvestrant-3-boronic acid is an orally active ERα inhibitor, which binds to ERα competitively (IC50 = 4.1 nM) and effectively degrades ERα in breast cancer cells .
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Cat. No.: HY-W002734
CAS No.: 87199-18-6
Synonyms: 3-Hydroxybenzeneboronic acid
Target:  

Drug Intermediate

Research Areas:  

Metabolic Disease

(3-Hydroxyphenyl)boronic acid (3-Hydroxybenzeneboronic acid) is a drug intermediate that can be used for the synthesis of 17β-hydroxysteroid dehydrogenase type 1 inhibitors .
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Cat. No.: HY-32952
CAS No.: 351019-18-6
Synonyms: 6-Fluoropyridine-3-boronic acid
Target:  

FAAH

2-Fluoropyridine-5-boronic acid (6-Fluoropyridine-3-boronic acid) is a fatty acid amide hydrolase (FAAH) inhibitor with an IC50 of 10 μM. 2-Fluoropyridine-5-boronic acid is applicable to research related to inflammation and pain .
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Cat. No.: HY-78197
CAS No.: 832114-00-8
3,5-Dimethylisoxazole-4-boronic acid pinacol ester is a drug intermediate that can be used for the synthesis of bromodomain inhibitors .
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Cat. No.: HY-136070
CAS No.: 2170834-56-5
Research Areas:  

Infection

Xeruborbactam bis-acetoxy methyl ester is a boronic acid β-lactamase inhibitor, exacted from WO2018005662A1, compound 42 .
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Cat. No.: HY-136071
CAS No.: 2170834-57-6
Research Areas:  

Infection

Xeruborbactam methoxy acetoxy methy ester is a boronic acid β-lactamase inhibitor, exacted from WO2018005662A1, compound 43 .
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Cat. No.: HY-W002463
CAS No.: 63503-60-6
3-Chlorophenylboronic acid is employed as a reactant involved in 1,4-conjugate addition reactions with ethenesulfonamides to form arylethanesulfonamides, Suzuki-Miyaura reactions with dibromotrifluoromethylbenzene, cross-coupling reactions with diazoesters3 or potassium cyanate. 3-Chlorophenylboronic acid is involved in the synthesis of biarylketones and phthalides and synthesis of inhibitors including PDE4 inhibitors among others. 3-Chlorophenyl boronic acid can affect cell migration. 3-Chlorophenyl boronic acid can be used to study wound healing .
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Cat. No.: HY-161998
CAS No.: 1203704-26-0
Target:  

Bacterial Urease

Research Areas:  

Others

Urease-IN-16 (compound 4e) is a urease inhibitor, with an IC50 value of 132 μmol/L. Urease-IN-16 can coordinate with the nickel atom through the oxygen atoms of carbonyl or boronic acid groups. Urease-IN-16 shows great potential as an additive in the development of efficient fertilizers and medical applications .
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