40 Results for "

51307

" in MedChemExpress (MCE) Product Catalog:
Products (40)

40 Results for "51307" in MCE Product Catalog:

10
10 Publications Verification
Cat. No.: HY-120859
CAS No.: 1436861-97-0
Purity:  99.32%
Synonyms: WCK-5107
Zidebactam (WCK-5107) is a potent β-lactamase inhibitor . Zidebactam also is a penicillin-binding protein2 (PBP2) inhibitor with an IC50 of 0.26 μg/mL .
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4
4 Cited Publications
Cat. No.: HY-111422
CAS No.: 1627929-55-8
Purity:  99.98%
PLX51107 is a potent and selective BET inhibitor, with Kds of 1.6, 2.1, 1.7, and 5 nM for BD1 and 5.9, 6.2, 6.1, and 120 nM for BD2 of BRD2, BRD3, BRD4, and BRDT, respectively; PLX51107 also interacts with the bromodomains of CBP and EP300 (Kd, in the 100 nM range).
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1
1 Cited Publications
Cat. No.: HY-P71493
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: ompA; Z1307; ECs1041; Outer membrane protein A; Outer membrane porin A
Species:  
Source:  
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Cat. No.: HY-147045
CAS No.: 1515887-44-1
Purity:  97.09%
Target:  

TNF Receptor

Research Areas:  

Inflammation/Immunology

UCB-5307 is a potent TNF signaling inhibitor with a KD of 9 nM for human TNFα. UCB-5307 can penetrate the preformed hTNF/hTNFR1 complex .
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Cat. No.: HY-W028047
CAS No.: 51070-56-5
Target:  

Bacterial

Research Areas:  

Infection Inflammation/Immunology

JFD01307SC is a glutamine synthetase inhibitor and anti-tuberculosis agent. JFD01307SC acts as a mimic of L-Glutamate and thus target enzymes involved in glutamine biosynthesis .
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Cat. No.: HY-161135A
CAS No.: 2131783-85-0
Target:  

Bacterial

Research Areas:  

Infection

(rac)-TBAJ-5307 is the racemate of TBAJ-5307 (HY-161135). TBAJ-5307 is a broad spectrum anti-non-tuberculous mycobacteria inhibitor that can target the FO-domain of the engine and preventing rotation and proton-translocation .
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Cat. No.: HY-120859A
CAS No.: 1706777-46-9
Synonyms: WCK-5107 sodium salt
Zidebactam sodium salt (WCK-5107 sodium salt) is a potent β-lactamase inhibitor . Zidebactam also is a penicillin-binding protein2 (PBP2) inhibitor with an IC50 of 0.26 μg/mL .
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Cat. No.: HY-132212
CAS No.: 2375720-38-8
Purity:  96.9%
Target:  

PD-1/PD-L1

Research Areas:  

Inflammation/Immunology Cancer

LH1307 is a C2-symmetric inhibitor of PD-1/PD-L1 protein-protein interactions with a IC50 value of 3.0 μM and can be used in cancer studies .
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Cat. No.: HY-161135
CAS No.: 2332831-92-0
Target:  

Bacterial

Research Areas:  

Infection

TBAJ-5307 is a broad spectrum anti-non-tuberculous mycobacteria inhibitor that can target the FO-domain of the engine and preventing rotation and proton-translocation. TBAJ-5307 inhibits non-tuberculous mycobacteria in vitro and in vivo .
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Cat. No.: HY-120859R
CAS No.: 1436861-97-0
Synonyms: WCK-5107 (Standard)
Zidebactam (Standard) is the analytical standard of Zidebactam. This product is intended for research and analytical applications. Zidebactam (WCK-5107) is a potent β-lactamase inhibitor . Zidebactam also is a penicillin-binding protein2 (PBP2) inhibitor with an IC50 of 0.26 μg/mL .
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Cat. No.: HY-100289
CAS No.: 148927-23-5
Target:  

Bacterial

Research Areas:  

Infection

MF 5137 is a potent antibacterial agent.
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Cat. No.: HY-118974
CAS No.: 225925-12-2
Target:  

Calcium Channel

Research Areas:  

Neurological Disease Cancer

PD-151307 is an N-type calcium channel antagonist with significant inhibitory effects in IMR-32 human neuroblastoma cells, exhibiting an IC50 of 0.32 µM. PD-151307 can be used in research related to cancer therapy, anticonvulsants, and neuropathic pain .
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Cat. No.: HY-P991387
Synonyms: AGEN1327

Research Areas:  

Cancer

AGEN1307 is a human monoclonal antibody (mAb) targeting TIGIT. AGEN1307 has an active FcγR binding region and enhances antibody-dependent cellular cytotoxicity (ADCC). AGEN1307 can be used in cancer research .
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Cat. No.: HY-R03276
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-5130 mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.
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Cat. No.: HY-R00240
Target:  

MicroRNA

Research Areas:  

Cancer

hsa-miR-1307-5p mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.
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Cat. No.: HY-R00239
Target:  

MicroRNA

Research Areas:  

Cancer

hsa-miR-1307-3p mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.
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Cat. No.: HY-R03252
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-5107-3p mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.
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Cat. No.: HY-R03253
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-5107-5p mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.
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Cat. No.: HY-RI00239A
Target:  

MicroRNA

Research Areas:  

Cancer

hsa-miR-1307-3p antagomirs are chemically-modified oligonucleotides that hybridize with mature miRNAs. The miRNA antagomirs have 2 phosphorothioates at the 5' end, 4 phosphorothioates at the 3' end, 1 cholesterol group at the 3' end, and full-length nucleotide 2'-methoxy modification. The miRNA antagomirs strongly compete with mature miRNAs to prevent the complementary pairing of miRNAs and their target genes, thereby inhibiting miRNAs from functioning. Stability of miRNA antagomirs appears to be significantly higher than miRNA inhibitors, they exhibits enhanced cellular uptake, stability and regulatory activity in vivo.
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Cat. No.: HY-R03276A
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-5130 agomirs are chemically-modified double-strand miRNA mimics with modified mature miRNA strand: 2 phosphorothioates at the 5' end, 4 phosphorothioates at the 3' end, 3' end cholesterol group, and full-length nucleotide 2'-methoxy modification. They are designed to mimic endogenous miRNAs and recommended for miRNA functional studies. Compared with miRNA mimics, they exhibits enhanced cellular uptake, stability and regulatory activity in vivo.
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