48 Results for "

benzamid

" in MedChemExpress (MCE) Product Catalog:
Products (48)

48 Results for "benzamid" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-W018781
CAS No.: 1670-14-0
Target:  

Ser/Thr Protease

Research Areas:  

Cancer

Benzamidine hydrochloride is a competitive protease inhibitor that blocks the hydrolytic cleavage of glucagon by plasmin, trypsin and thrombin. Benzamidine hydrochloride effectively inhibits the degradation of glucagon by relevant proteases during the collection, storage and analysis of human plasma and blood samples. During in vivo metabolism, Benzamidine hydrochloride undergoes N-hydroxylation and produces multiple metabolites, exhibiting characteristics of delayed excretion or biphasic elimination. Benzamidine hydrochloride only induces slight single-strand DNA breaks at high concentrations and shows no significant genotoxic potential overall. Benzamidine hydrochloride may interfere with the detection of some glucagon antisera, but does not affect key antigen-antibody affinity at specific concentrations. Benzamidine hydrochloride can be used as a stabilizer in glucagon radioimmunoassays to ensure the accuracy and recovery rate of detection results .
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4
4 Cited Publications
Cat. No.: HY-125913
CAS No.: 618-39-3
Target:  

Ser/Thr Protease

Research Areas:  

Inflammation/Immunology

Benzamidine is a competitive protease inhibitor that blocks the hydrolytic cleavage of glucagon by plasmin, trypsin and thrombin. Benzamidine effectively inhibits the degradation of glucagon by relevant proteases during the collection, storage and analysis of human plasma and blood samples. During in vivo metabolism, Benzamidine undergoes N-hydroxylation and produces multiple metabolites, exhibiting characteristics of delayed excretion or biphasic elimination. Benzamidine only induces slight single-strand DNA breaks at high concentrations and shows no significant genotoxic potential overall. Benzamidine may interfere with the detection of some glucagon antisera, but does not affect key antigen-antibody affinity at specific concentrations. Benzamidine can be used as a stabilizer in glucagon radioimmunoassays to ensure the accuracy and recovery rate of detection results .
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4
4 Cited Publications
Cat. No.: HY-W087937
CAS No.: 206752-36-5
Synonyms: Benzenecarboximidamide hydrochloride hydrate
Benzamidine (Benzenecarboximidamide) hydrochloride hydrate is a competitive protease inhibitor that blocks the hydrolytic cleavage of glucagon by plasmin, trypsin and thrombin. Benzamidine hydrochloride hydrate effectively inhibits the degradation of glucagon by relevant proteases during the collection, storage and analysis of human plasma and blood samples. During in vivo metabolism, Benzamidine hydrochloride hydrate undergoes N-hydroxylation and produces multiple metabolites, exhibiting characteristics of delayed excretion or biphasic elimination. Benzamidine hydrochloride hydrate only induces slight single-strand DNA breaks at high concentrations and shows no significant genotoxic potential overall. Benzamidine hydrochloride hydrate may interfere with the detection of some glucagon antisera, but does not affect key antigen-antibody affinity at specific concentrations. Benzamidine hydrochloride hydrate can be used as a stabilizer in glucagon radioimmunoassays to ensure the accuracy and recovery rate of detection results .
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1
1 Cited Publications
Cat. No.: HY-Z0283
CAS No.: 55-21-0
Synonyms: Benzenecarboxamide; Phenylamide
Benzamide (Benzenecarboxamide) is a potent poly(ADP-ribose) polymerase (PARP) inhibitor. Benzamide has protective activity against both glutamate- and methamphetamine (METH)-induced neurotoxicity in vitro. Benzamide can attenuate the METH-induced dopamine depletions and exhibits neuroprotective activity in mice, also has no acute effect on striatal dopamine metabolism and does not reduce body temperature .
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Cat. No.: HY-120469
CAS No.: 1258292-64-6
Purity:  99.80%
Target:  

JAK

Research Areas:  

Inflammation/Immunology

GDC-046 is a potent, selective, and orally bioavailable TYK2 inhibitor with Kis of 4.8, 0.7, 0.7, and 0.4 nM for TYK2, JAK1, JAK2, and JAK3, respectively .
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Cat. No.: HY-125372
CAS No.: 16348-49-5
Purity:  99.85%
Synonyms: ABAO
Research Areas:  

Others

2-Amino benzamidoxime (ABAO) acts as a bioconjugation reagent precursor and a fluorescent probe precursor. 2-Amino benzamidoxime contains an aniline group for imine activation of aldehydes, as well as a nucleophilic group (Nu:) located at the ortho position of the amine, which is responsible for intramolecular cyclization. 2-Amino benzamidoxime reacts with glyoxal at the N-terminus of phage-displayed peptide libraries. Derivatives of 2-Amino benzamidoxime can be used for protein bioconjugation. Derivatives of 2-Amino benzamidoxime serve as fluorescent probes .\n



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Cat. No.: HY-46395
CAS No.: 1662687-79-7
Target:  

Drug Intermediate

Research Areas:  

Others

6-(4-(Methoxymethoxy)benzamido)imidazo[1,2-a]pyridine-2-carboxylic acid is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-112731
CAS No.: 1011244-68-0
Purity:  99.98%
Synonyms: N-(5-Aminopyridin-2-yl)-4-(trifluoromethyl)benzamide
TFAP is a selective cyclooxygenase-1 (COX-1) inhibitor, with an IC50 of 0.8 μM.
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Cat. No.: HY-W016562S
CAS No.: 53518-98-2
Synonyms: 2-benzamidoacetic acid-d5
Hippuric acid-d5 is the deuterium labeled Hippuric acid. Hippuric Acid (2-Benzamidoacetic acid), an acyl glycine produced by the conjugation of benzoic acid and glycine, is a normal component in urine as a metabolite of aromatic compounds from food.
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Cat. No.: HY-147342
CAS No.: 156724-91-3
Target:  

Drug Metabolite IMPDH

Research Areas:  

Cancer

β-Benzamide adenine dinucleotide is a biologically active metabolite of benzamide riboside. β-Benzamide adenine dinucleotide is a competitive inhibitor of human NAD kinase with a Ki value of 90 μM, and inhibits human IMPDH with IC50 values of 0.787 μM and 0.884 μM for type I and type II, respectively. β-Benzamide adenine dinucleotide exhibits inhibitory activities against lactate dehydrogenase, glutamate dehydrogenase, and malate dehydrogenase. β-Benzamide adenine dinucleotide can be used for the study of chronic myelogenous leukemia .
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Cat. No.: HY-W016562S1
CAS No.: 208928-78-3
Synonyms: 2-benzamidoacetic acid-d2
Hippuric acid-d2 is the deuterium labeled Hippuric acid. Hippuric Acid (2-Benzamidoacetic acid), an acyl glycine produced by the conjugation of benzoic acid and glycine, is a normal component in urine as a metabolite of aromatic compounds from food.
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Cat. No.: HY-Z0283S
CAS No.: 31656-62-9
Synonyms: Benzenecarboxamide-15N; Phenylamide-15N
Benzamide- 15N is a 15N-labeled Benzamide. Benzamide inhibits poly(ADP-ribose) polymerase (PARP) .
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Cat. No.: HY-46832
CAS No.: 1214-48-8
Target:  

Drug Intermediate

Research Areas:  

Others

2-Amino-N-(pyridin-3-ylmethyl)benzamide is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-403978S
CAS No.: 1447799-45-2
Benzamide-C6-N-Boc-C2-amide-phenol-d5 is the deuterium labeled Benzamide-C6-N-Boc-C2-amide-phenol.
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Cat. No.: HY-W711852
CAS No.: 1235489-47-0
Synonyms: Benzenecarboxamide-d5; Phenylamide-d5
Benzamide-d5 (Benzenecarboxamide-d5) is deuterium labeled Benzamide. Benzamide (Benzenecarboxamide) is a potent poly(ADP-ribose) polymerase (PARP) inhibitor. Benzamide has protective activity against both glutamate- and methamphetamine (METH)-induced neurotoxicity in vitro. Benzamide can attenuate the METH-induced dopamine depletions and exhibits neuroprotective activity in mice, also has no acute effect on striatal dopamine metabolism and does not reduce body temperature .
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Cat. No.: HY-W117416
CAS No.: 1449134-30-8
Target:  

PROTAC Linkers

Research Areas:  

Cancer

N-(3-Hydroxypropyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide is a PROTAC linker that can be used in the synthesis of PROTACs.
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Cat. No.: HY-75204
CAS No.: 17794-48-8
Target:  

Drug Intermediate

Research Areas:  

Others

2-(3-(Trifluoromethyl)benzamido)acetic acid is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-W520657
CAS No.: 23076-31-5
Target:  

Drug Intermediate

Research Areas:  

Others

2-Amino-5-nitro-N-(o-tolyl)benzamide is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-145488
CAS No.: 2222445-87-4
Purity:  98.92%
Target:  

ADC Linkers

Research Areas:  

Cancer

MethylCBI-azaindole-benzamide-MOM-Boc-ethylenediamine-D is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
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Cat. No.: HY-134753
CAS No.: 1011244-72-6
Purity:  99.75%
Synonyms: 4-Amino-N-(4-trifluoromethylphenyl)benzamide
Target:  

COX

Research Areas:  

Inflammation/Immunology

Teriflunomide impurity 3 (4-Amino-N-(4-trifluoromethylphenyl)benzamide) is a selective COX-1 inhibitor with an IC50 of 30 µM. Teriflunomide impurity 3 is less active against COX-2 (IC50>100 µM) .
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