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Filtered Search Results
Apexbio Technology LLC N-Methylnicotinamide 114-33-0 200mg
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N-Methylnicotinamide (CAS 114-33-0) is a methylated derivative of nicotinamide and a primary metabolic product of niacinamide and niacin (vitamin B3) catabolism It does not have a defined therapeutic target or approved clinical use but plays a significant role in biomedical research as an indicator of vitamin B3 status Measurement of urinary N-methylnicotinamide is routinely employed to assess niacin sufficiency and diagnose deficiencies reflecting metabolic function related to NAD/NADP biosynthesis pathways This compound thus serves as a valuable biomarker in nutritional and metabolic research contexts
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TARGETMOL CHEMICALS INC Penfluridol 200MG
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Also available in 1 mL, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Penfluridol (TLP-607) is a highly potent antipsychotic. Purity 99.73%
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TARGETMOL CHEMICALS INC NGD 94-1 5MG
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Also available in 1 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. NGD 94-1 is a selective D4 receptor antagonist with an affinity of 3 nM for the D4 receptor and greater than 2 pM for the D1, D2, D3, and D5 receptors.NGD 94-1 can be used in the study of cognitive disorders and other psychiatric disorders. Purity 99.84%
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Medchemexpress LLC Infigratinib | 872511-34-7 | 99.8% | 560.48 | 200 MG
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Infigratinib, also known as BGJ-398 or NVP-BGJ398, is a potent inhibitor of the Fibroblast Growth Factor Receptor (FGFR) family. It targets FGFR1, FGFR2, FGFR3, and FGFR4 with high efficacy, making it suitable for various research applications.
- Potent inhibitor of FGFR1, FGFR2, FGFR3, and FGFR4
- Inhibits proliferation of FGFR-dependent BaF3 cells
- Effective against FGFR2-mutant endometrial cancer cells
- Extensively studied in clinical trials for multiple cancers and conditions
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TARGETMOL CHEMICALS INC Bemnifosbuvir hemisulfate 5MG
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Also available in 1 mg, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg and bulk. Please contact Fisher for quotes. Bemnifosbuvir hemisulfate (AT-527) is a potent inhibitor of HCV virus replication. Purity 99.98%
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000379631 DORSOMORPHIN 200MG
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Aobchem AOBCHEM
5000865241 2 3-DIMETHOXY-6-FLUOROPHENYLBO
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Apexbio Technology LLC Zotarolimus(ABT-578) 221877-54-9 25mg
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Zotarolimus ABT-578 is a small-molecule inhibitor targeting the immunophilin FKBP12 It is designed to form a complex with FKBP12 thereby inhibiting mTOR pathway signaling and suppressing the proliferation of T-cells vascular smooth muscle cells (VSMCs) and endothelial cells (ECs) Zotarolimus ABT-578 exerts its biological activity primarily through mTOR pathway inhibition In cell-based studies zotarolimus demonstrates nanomolar-level inhibitory potency against human coronary artery cell proliferation and T-cell activation Based on these pharmacological properties zotarolimus ABT-578 holds research potential in vascular restenosis prevention neointimal hyperplasia reduction and immunological studies involving T-cell function
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Medchemexpress LLC DC-BPi-03 | 2758411-46-8 | C14H14N4O2S | 10 MM/1 ML
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DC-BPi-03 is a potent BPTF-BRD inhibitor with an IC50 of 698.3 nM and a Kd of 2.81 μM. It is for research use only and not sold to patients.
- Potent BPTF-BRD inhibitor
- IC50 of 698.3 nM
- Kd of 2.81 μM
- Solid appearance
- White to off-white color
- Purity of 99.77%
- For research use only
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000431031 PROPIDIUM MONOAZIDE 1MG
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Aobchem AOBCHEM
5000865551 2-FLUORO-5- PYROLIDINE-1-CARBO
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000703007 YKL-06-062 25MG
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Medchemexpress LLC Sitravatinib | 1123837-84-2 | 99.6% | 629.68 | 200 MG
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Sitravatinib (MGCD516) is an orally bioavailable receptor tyrosine kinase (RTK) inhibitor that demonstrates potent single-agent antitumor efficacy. It enhances the activity of PD-1 blockade by promoting an antitumor immune microenvironment, making it suitable for various research applications in oncology.
- Orally bioavailable receptor tyrosine kinase (RTK) inhibitor
- Potent single-agent antitumor efficacy
- Enhances PD-1 blockade activity
- Promotes an antitumor immune microenvironment
- Soluble in DMSO for in vitro studies
- Available in solid form for various research needs
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TARGETMOL CHEMICALS INC Pranlukast 200MG
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Also available in 1 mL, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Pranlukast (ONO-1078) is a cysteinyl leukotriene receptor-1 antagonist. It antagonizes or reduces bronchospasm caused, principally in asthmatics, by an allergic reaction to accidentally or inadvertently encountered allergens. Purity 99.85%
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Selleck Chemical LLC Leupeptin Hemisulfate
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Leupeptin Hemisulfate is a reversible inhibitor of serine and cysteine proteases It inhibits cathepsin B (Ki 6 nM) calpain (Ki 10 nM) trypsin (Ki 35 nM) plasmin (Ki 3 4 M) and kallikrein (Ki 19 M) and has no effect against chymotrypsin elastase renin or pepsin
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