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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T19972 | MPO | 5-(4'-Methoxyphenyl)-oxazole | Others |
MPO (5-(4'-Methoxyphenyl)-oxazole) is a hatch and growth of Caenorhabditis Elegans inhibitor. | |||
T5340 | MPO-IN-28 | Glutathione Peroxidase | |
MPO-IN-28 is a novel potent, irreversible Myeloperoxidase (MPO) inhibitor with IC50 of 44 nM. | |||
T23745 | APA-APA-MPO | APA APA MPO,APAAPAMPO | |
APA-APA-MPO is a PCAF bromodomain/Tat-AcK50 association inhibitor. | |||
T38914 | MPO-IN-3 | ||
MPO-IN-3, a powerful inhibitor of myeloperoxidase (MPO), is described as such in example 191 of WO2013068875A1. MPO, a heme-containing enzyme, is classified under the peroxidase superfamily. | |||
T40137 | MPO-IN-1 | ||
MPO-IN-1 is a powerful and orally bioavailable indole-containing inhibitor that acts irrevocably on myeloperoxidase (MPO). With IC50 values of 2.6 μM and 5.3 μM for MPO and thyroid peroxidase (TPO), respectively, MPO-IN-... | |||
T23746 | APA-H-MPO | APAHMPO | |
APA-H-MPO is a PCAF bromodomain/Tat-AcK50 association inhibitor. | |||
T60281 | MPO-IN-4 | ||
MPO-IN-4 (compound 12) is a potent and selective myeloperoxidase (MPO) inhibitor with an IC 50 of 25 nM. MPO-IN-4 also demonstrates inhibition of thyroid peroxidase (TPO) with IC50 of 2.2 μM. MPO-IN-4 has no effect on me... | |||
T62347 | MPO-IN-5 | ||
MPO-IN-5 is a potent, irreversible inhibitor of MPO (myeloperoxidase). MPO-IN-5 inhibits MPO peroxidation (IC50: 0.22 μM) and hERG binding (IC50: 2.8 μM). 23000 M 1s 1. | |||
TN1582 | Compound TN1582(SC) | Antiviral | |
Dihydromollugin is a naphthol ester found in Rubia cordifolia that may have anti-tumour, virus-inhibiting and other activities. | |||
TPL0053 | Compound 227105-11-5 | ||
Compound 227105-11-5 is a useful organic compound for research related to life sciences. The catalog number is TPL0053 and the CAS number is 227105-11-5. | |||
T50125 | Compound C749 | ||
Compound C749 is a useful organic compound for research related to life sciences. The catalog number is T50125 and the CAS number is 57-03-4. | |||
T7944 | VPS34 inhibitor 1 (Compound 19, PIK-III analogue) | PIK-III analogue | PI3K |
VPS34 inhibitor 1 (Compound 19, PIK-III analogue) (PIK-III analogue) is a potent and selective inhibitor of VPS34( IC50 : 15 nM) | |||
T5363 | Tempo | 2,2,6,6-Tetramethylpiperidinooxy | Free radical scavengers , Reactive Oxygen Species , DNA/RNA Synthesis , Mitochondrial Metabolism |
Tempo (2,2,6,6-Tetramethylpiperidinooxy) has a wide range of applications including use as a free radical scavenger, a reagent in organic synthesis and as a structural probe in electron spin resonance spectroscopy. | |||
T67752 | Compound V007-6018 | Others | |
Compound V007-6018 is a pharmaceutical compound used for drug screening. | |||
T9184L | Compound 3344 hydrochloride | 4-(2,3-dihydro-1,4-benzodioxin-5-yl)-~{N}-[3-[(dimethylamino)methyl]phenyl]-2-methoxy-aniline hydrochloride(2368246-78-8 free base),Compound 3344 hydrochloride (2368246-78-8 free base) | Ras |
Compound 3344 hydrochloride is an inhibitor of KRAS-effector interactions,with an affnity of 126nm. | |||
T38387 | Compound C108 | GTPase | |
Compound C108 is an inhibitor of GTPase-activating protein SH3 domain-binding protein 2 (G3BP2). Compound C108 can be used in studies about breast tumors and esophageal squamous cell carcinoma. | |||
T60198 | Compound STK672155 | Others | |
Compound STK672155 can be used for research in the fields of chemistry and life sciences. | |||
T3586 | Compound 401 | 2-morpholino-4H-pyrimido[2,1-a]isoquinolin-4-one | DNA-PK |
Compound 401 (2-morpholino-4H-pyrimido[2,1-a]isoquinolin-4-one) is a synthetic DNA-PK inhibitor (IC50 = 0.28 μM) that also targets mTOR but not PI3K. | |||
T72082 | Compound T72082(SC) | ROS | |
ROS-IN-1 is a mitochondrial ROS inhibitor that can be used to reduce oxidative stress or inhibit reactive oxygen species (ROS) production. | |||
T12262L1 | NPS ALX Compound 4a hydrochloride(1:1) | 5-HT Receptor | |
NPS ALX Compound 4a hydrochloride(1:1) is a potent and selective 5-hydroxytryptamine6 (5-HT6) receptor antagonist, with an IC50 of 7.2 nM and a Ki of 0.2 nM. |