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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences Glimepiride Related Compound C United States Pharmacopeia (USP) Reference Standard | 119018-30-3 | 20MG
Glimepiride Related Compound C United States Pharmacopeia (USP) Reference Standard | Mol Wt: 409.46 | 119018-30-3 | 20MG
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Selleck Chemical LLC Doxycycline Hyclate S4163-1g
Doxycycline Hyclate is a member of the tetracycline antibiotics group and is commonly used to treat a variety of infections It is also an inhibitor of matrix metallo-proteinases (MMP)
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Medchemexpress LLC Itacitinib | 1334298-90-6 | 100.0% | 553.51 | 5 MG
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Itacitinib (INCB039110) is an orally active and selective inhibitor of JAK1, exhibiting significant selectivity over JAK2, JAK3, and TYK2. It is primarily used in the research of myelofibrosis. This product is for research purposes only and has not been fully validated for medical applications.
- Orally active and selective JAK1 inhibitor
- IC50 of 2 nM for human JAK1
- Over 20-fold selectivity for JAK1 over JAK2
- Over 100-fold selectivity over JAK3 and TYK2
- Used in myelofibrosis research
- For research purposes only
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Sigma Aldrich Fine Chemicals Biosciences Granisetron impurity B European Pharmacopoeia (EP) Reference Standard | 107007-95-4 |
Granisetron impurity B European Pharmacopoeia (EP) Reference Standard | Mol Wt: 298.38 | 107007-95-4 |
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Selleck Chemical LLC Mevastatin S4223-1g
Mevastatin (ML-236B Compactin) is a competitive inhibitor of HMG-Coenzyme A (HMG-CoA) reductase with a binding affinity 10 000 times greater than the HMG-CoA substrate itself
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Selleck Chemical LLC Enzalutamide (MDV3100) 50mg 915087-33-1
Enzalutamide (MDV3100) is an androgen-receptor (AR) antagonist with IC50 of 36 nM in LNCaP cells. Enzalutamide is shown to increase autophagy. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
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Medchemexpress LLC (E)-N-[4-(3-chloro-4-(3-fluorophenyl)methoxy)anilino]-4-(dimethylamino)but-2-enamide | 848133-17-5 | MFCD26792555 | >98.0% | 574.0 g/mol | C31H29ClFN5O3 | 10 MM 1 ML
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HKI-357 is an irreversible small-molecule inhibitor of EGFR and ERBB2 used as a research reagent to probe receptor autophosphorylation and downstream signaling pathways. It shows potent cellular activity (reported IC50s ~34 nM and 33 nM) and is provided as a solid or as a ready-to-use DMSO solution for cell signaling studies.
- Irreversible dual inhibitor of EGFR and ERBB2.
- Potent activity with IC50s around 34 nM and 33 nM.
- Suppresses EGFR autophosphorylation (Y1068) and downstream AKT and MAPK signaling.
- Available as 10 mM solution in DMSO or as solid quantities for flexible dosing.
- High purity, typically ≥98% (HPLC), suitable for research applications.
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eMolecules Pimobendan | 74150-27-9 | 1G | Purity: 98%
Combi-Blocks | Pimobendan | 1G | 74150-27-9 | MFCD00761648
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool
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Apexbio Technology LLC Enalaprilat Dihydrate 84680-54-6 50mg
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Enalaprilat Dihydrate is a small-molecule inhibitor targeting angiotensin-converting enzyme (ACE) It is designed to inhibit ACE thereby blocking the conversion of angiotensin I to the potent vasoconstrictor angiotensin II and reducing vascular resistance and blood pressure Enalaprilat Dihydrate exerts its biological activity primarily through competitive binding to the active site of ACE It demonstrates high potency and specificity with an inhibitory concentration (IC50) value in the low nanomolar range Based on these pharmacological properties Enalaprilat Dihydrate holds research potential in studies of ACE inhibition mechanisms cardiovascular physiology and drug discovery targeting hypertension-related pathologies
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Medchemexpress LLC Meropenem trihydrate | 119478-56-7 | MFCD08600005 | 99.9% | C17H31N3O8S | 10MG
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Meropenem trihydrate is the trihydrate form of the carbapenem antibiotic meropenem provided as an analytical reference standard for research and quality-control applications. It is intended for assay development, method validation, and instrument calibration, and is characterized by a high-purity HPLC assay suitable for analytical workflows.
- High purity reference material (≈99.9% by RP-HPLC).
- Suitable for HPLC method validation and system suitability.
- Stable solid trihydrate form for consistent analytical performance.
- Supplies small lab-scale pack sizes for reference and QC work.
- Compatible with routine assay development and quantitative analysis.
- Characterized by molecular formula C17H31N3O8S and CAS 119478-56-7.
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Medchemexpress LLC 2,6-Benzothiazolediamine, 4,5,6,7-tetrahydro-N6-propyl-, hydrochloride (1:2), (6S)- | 104632-25-9 | 98.0% | 284.25 | 100 MG
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Pramipexole dihydrochloride is a selective and blood-brain barrier (BBB) penetrant dopamine D2-type receptor agonist, with Kis of 2.2 nM, 3.9 nM, 0.5 nM and 1.3 nM for D2-type receptor, D2, D3 and D4 receptors, respectively. It can be used for the research of Parkinson's disease (PD) and restless legs syndrome (RLS).
- Selective and blood-brain barrier (BBB) penetrant dopamine D2-type receptor agonist.
- Kis of 2.2 nM, 3.9 nM, 0.5 nM and 1.3 nM for D2-type receptor, D2, D3 and D4 receptors, respectively.
- Applicable for research into Parkinson's disease (PD) and restless legs syndrome (RLS).
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TARGETMOL CHEMICALS INC TAFAMIDIS MEGLUMINE 25MG
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Also available in 5 mg 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Tafamidis meglumine (Fx-1006A) is a Potent and Selective Transthyretin Kinetic Stabilizer That Inhibits the Amyloid Cascadepurity: 99%
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Sigma Aldrich Fine Chemicals Biosciences Misoprostol European Pharmacopoeia (EP) Reference Standard | 59122-46-2 | MFCD00274550 |
Misoprostol European Pharmacopoeia (EP) Reference Standard | Mol Wt: 382.53 | 59122-46-2 | MFCD00274550 |
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Sigma Aldrich Fine Chemicals Biosciences Proguanil Related Compound G United States Pharmacopeia (USP) Reference Standard | 1071546-52-5 | 25MG
Proguanil Related Compound G United States Pharmacopeia (USP) Reference Standard | Mol Wt: 290.19 | 1071546-52-5 | 25MG
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Sigma Aldrich Fine Chemicals Biosciences Mogroside V United States Pharmacopeia (USP) Reference Standard | 88901-36-4 | 100MG
Mogroside V United States Pharmacopeia (USP) Reference Standard | Mol Wt: 1287.43 | 88901-36-4 | 100MG
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