125 Results for "

poor

" in MedChemExpress (MCE) Product Catalog:
Products (125)

125 Results for "poor" in MCE Product Catalog:

Cat. No.: HY-127155
CAS No.: 680571-51-1
Kigamicin C is an anti-tumor antibiotic that selectively kills pancreatic cancer PANC-1 cells only in nutrient-poor conditions. Kigamicin C has antimicrobial activity against Gram-positive bacteria including methicillin-resistant Staphylococcus aureus (MRSA) .
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Cat. No.: HY-W010378R
CAS No.: 2058-58-4
Synonyms: H-D-Asn-OH (Standard)
D-Asparagine (Standard) (H-D-Asn-OH (Standard)) is the analytical standard of D-Asparagine (HY-W010378). This product is intended for research and analytical applications. D-Asparagine (H-D-Asn-OH) is a competitive inhibitor of L-Asparagine hydrolysis with a Ki value of 0.24 mM. D-Asparagine is a source of nitrogen for yeast strains. D-Asparagine is a good substrate for the external yeast asparaginase but is a poor substrate for the internal enzyme.
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Cat. No.: HY-178794
CAS No.: 3038861-75-2
Target:  

PGE synthase

Research Areas:  

Inflammation/Immunology

AGU661 is a Microsomal prostaglandin E2 synthase 1 (mPGES-1) inhibitor with an IC50 of 0.22  nM. AGU661 lowers PGE2 formation in human pro-inflammatory M1 macrophages and activated monocytes without affecting other lipid mediator pathways. AGU661 has unfavorable physicochemical properties with poor metabolic stability and strong plasma protein binding tendencies. AGU661 into PLGA-based NPs significantly enhances its bioactivity. AGU661 can be used for inflammatory disorders research .
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Cat. No.: HY-171986
CAS No.: 955879-75-1
Target:  

RIP kinase

Research Areas:  

Cancer

RIPK3-IN-6 (compound 1) is a type I RIPK3 inhibitor with poor selectivity for the RIPK family, especially for RIPK2 activity .
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Cat. No.: HY-19405
CAS No.: 178309-91-6
Target:  

Neurokinin Receptor

Research Areas:  

Others

UK-224671 is a potent and selective NK2 receptor antagonist. UK-224671 is affected by P-gp efflux and poor intrinsic membrane permeability, resulting in low oral bioavailability .
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Cat. No.: HY-118465
CAS No.: 65085-69-0
Synonyms: ent-PGE2
Research Areas:  

Endocrinology

ent-Prostaglandin E2 (ent-PGE2) is an enantiomer of PGE2 (HY-101952). unlike PGE2, ent-PGE2 is a poor substrate for 15-hydroxyprostaglandin dehydrogenase .
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Cat. No.: HY-178023
CAS No.: 2837128-29-5
Target:  

HDAC

Research Areas:  

Cancer

HDAC6-IN-64 (Compound 8) is a HDAC6 inhibitor with an IC50 of 11.9  nM. HDAC6-IN-64 has poor cell permeability. HDAC6-IN-64 can be used for chemotherapy of cancers like NSCLC research .
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Cat. No.: HY-155902B
CAS No.: 88504-24-9
Synonyms: Maleimide-PEG1000-Hydroxy
Mal-PEG1000-OH was used as a macroinitiator to obtain amphiphilic diblock copolymers by ring-opening polymerization of LA. Nanoparticles prepared using amphiphilic block copolymers can form active drug delivery systems. Nanoparticles encapsulate Triptolide (HY-32735), which can avoid the disadvantage of Triptolide’s poor water solubility and reduce its toxicity.
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Cat. No.: HY-138697B
CAS No.: 1644543-95-2
Purity:  99.67%
Synonyms: VOB560 hydrochloride
Target:  

Bcl-2 Family Apoptosis

Research Areas:  

Cancer

S65487 (VOB560) hydrochloride, a potent and selective Bcl-2 inhibitor, is a proagent of S55746. S65487 hydrochloride is also active on BCL-2 mutations, such as G101V and D103Y. S65487 hydrochloride has poor affinity with MCL-1, BFL-1 and BCL-XL. S65487 hydrochloride induces apoptosis and has anticaner activities .
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Cat. No.: HY-136233
CAS No.: 2122196-16-9
Target:  

Adenosine Receptor

Research Areas:  

Inflammation/Immunology

PSB 0777 ammonium is a potent and selective adenosine A2A receptor full agonist with Ki values of 44.4 nM, 360 nM for rat and human A2A receptors, respectively. PSB 0777 ammonium has Ki values of ≥10000 nM, 541 nM for rat and human A1 receptors, respectively. PSB 0777 ammonium shows poor brain penetrant and perorally non-absorbable effect. PSB 0777 ammonium has the potential for inflammatory bowel disease (IBS) research research .
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Cat. No.: HY-170491
Target:  

GSK-3

Research Areas:  

Infection Neurological Disease

GSK-3β inhibitor 23 (Compound 11726169) is the inhibitor for glycogen synthase kinase-3, that inhibits GSK-3β and GSK-3α with IC50 of 12.1 nM and 18.8 nM. GSK-3β inhibitor 23 exhibits antiviral activity against HIV 1. GSK-3β inhibitor 23 exhibits good metabolic stablility in mouse/human liver microsomes and plasma, but poor Caco-2 permeability (which predicts low oral bioavailability) .
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Cat. No.: HY-B1747A
CAS No.: 15922-78-8
Target:  

Bacterial

Research Areas:  

Others

Pyrithione sodium has poor skin penetration.
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Cat. No.: HY-P4530
CAS No.: 77286-90-9
Target:  

Inhibitory Antibodies

Research Areas:  

Others

D-Ala-Gly-Gly-OH is a peptide substrate. DppA has a poor efficiency on peptide substrates D-Ala-Gly-Gly-OH .
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Cat. No.: HY-111353
CAS No.: 1234844-11-1
Purity:  99.07%
Research Areas:  

Metabolic Disease

GPR120 Agonist 2 (example 206) is a GPR120 agonist that can be uesd for the study of type II diabetes and diseases associated with poor glycemic control .
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Cat. No.: HY-125694
CAS No.: 151856-47-2
Target:  

Fungal

Research Areas:  

Infection

MFB-1041 is an orally active antifungal agent, but exhibits poor oral absorption. MFB-1041 induces the binding of drug to serum albumin .
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Cat. No.: HY-10399B
CAS No.: 209394-29-6
Synonyms: TV-3279
Target:  

Cholinesterase (ChE)

Research Areas:  

Neurological Disease

(S)-Ladostigil (TV-3279), the S-enantiomer of TV 3326 (HY-10399), is a ChE inhibitor with poor MAO-B inhibitory activity. (S)-Ladostigil has neuroprotective effect
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Cat. No.: HY-170617
Target:  

STING

Research Areas:  

Inflammation/Immunology

hSTING agonist-1 (compound 17) is a potent agonist of hSTING. hSTING agonist-1 has poor oral availability. hSTING agonist-1 plays an important role in inflammation research .
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Cat. No.: HY-101677
CAS No.: 182798-83-0
Purity:  99.62%
Target:  

Drug Metabolite

Research Areas:  

Infection

cPrPMEDAP is an intermediate metabolite of GS-9219. cpr-PMEDAP functions as a proagent of the guanine nucleotide analog PMEG and has antiproliferative activity. cPrPMEDAP is negatively charged at physiologic pH and has poor permeability into the skin .
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Cat. No.: HY-149345
CAS No.: 2952533-54-7
Target:  

IRAK

Research Areas:  

Inflammation/Immunology

IRAK4-IN-24 (compound 16) is a potent IRAK4 inhibitor, with high clearance (Cl) and poor oral bioavailability. IRAK4-IN-24 can be used for research in inflammatory and autoimmune disorders.
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Cat. No.: HY-120865
CAS No.: 200716-66-1
Target:  

NO Synthase

Research Areas:  

Inflammation/Immunology

1,3-PBIT is a potent inhibitor of iNOS with a Ki of 47 nM compared to Ki values for eNOS and nNOS are 9 and 0.25 μM, respectively, for the purified human enzymes. Its inhibition in whole cells is greatly diminished, presumably to poor membrane permeability.
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