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Filtered Search Results
Medchemexpress LLC HY-50202 50mg , Etomoxir CAS:124083-20-1 Purity:98%
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Medchemexpress, HY-50202 50mg Etomoxir CAS:124083-20-1 Formula:C17H23ClO4 CPT-1 Purity:98% Etomoxir is a potent inhibitor of carnitine palmitoyltransferase-I ( CPT-1 ). Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-14376 50mg , PF-04457845 CAS:1020315-31-4 Purity:98%
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Medchemexpress, HY-14376 50mg PF-04457845 CAS:1020315-31-4 Formula:C23H20F3N5O2 IC50: 7.2±0.63 nM (hFAAH), 7.4±0.62 nM (rFAAH) Purity:98% PF-04457845 is a highly efficacious and selective FAAH inhibitor with IC 50 values is 7.2±0.63 nM and 7.4±0.62 nM for hFAAH and rFAAH , respectively. Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000403723 1 3-DIMETHOXYBENZENE 100MG
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Medchemexpress LLC HY-19797A 100mg , ML241 (hydrochloride) CAS: Purity:98%
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Medchemexpress, HY-19797A 100mg ML241 (hydrochloride) CAS: Formula:C23H25ClN4O IC50: 100 nM (p97) Purity:98% ML241 hydrochloride is a potent p97 inhibitor, inhibiting p97 ATPase with IC 50 value of 100 nM. Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-112610 5mg Medchemexpress, CF53 CAS:1808160-52-2 Purity:>98%
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Medchemexpress, HY-112610 5mg CF53 CAS:1808160-52-2 CF53 is a highly potent, selective and orally active inhibitor of BET protein, with a K i of <1 nM, K d of 2.2 nM and an IC 50 of 2 nM for BRD4 BD1. CF53 binds to both the BD1 and BD2 domains of BRD2, BRD3, BRD4, and BRDT BET proteins with high affinities, very selective over non-BET bromodomain-containing proteins. CF53 shows potent anti-tumor activity both in vitro and in vivo [1] . Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-115486 5mg Medchemexpress, MPO-IN-28 CAS:37836-90-1 Purity:>98%
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Medchemexpress, HY-115486 5mg MPO-IN-28 CAS:37836-90-1 MPO-IN-28 (Compound 28) is a myeloperoxidase ( MPO ) inhibitor with an IC 50 of 44 nM. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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![Medchemexpress LLC 1-[1-[4-(1-acetylpiperidin-4-yl)oxy-2-methoxybenzoyl]piperidin-4-yl]-4H-3,1-benzoxazin-2-one | 162042-44-6 | 99.9% | 507.58 g/mol | C28H33N3O6 | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000286661.png-250.jpg)
Medchemexpress LLC 1-[1-[4-(1-acetylpiperidin-4-yl)oxy-2-methoxybenzoyl]piperidin-4-yl]-4H-3,1-benzoxazin-2-one | 162042-44-6 | 99.9% | 507.58 g/mol | C28H33N3O6 | 10 MG
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L-371,257 is a research-grade small molecule that functions as a selective, competitive antagonist of the oxytocin receptor. It is orally bioavailable and reported to be non-blood-brain barrier penetrant, making it suitable for both in vitro and in vivo pharmacology studies.
- Selective, competitive oxytocin receptor antagonist with high affinity (OTR Ki ≈ 19 nM; V1a Ki ≈ 3.7 nM).
- Orally bioavailable and non-blood-brain barrier penetrant.
- High chemical purity (≈99.9%).
- Soluble in DMSO (~8.33 mg/mL) and compatible with common in vivo formulation strategies.
- Stable as a powder under frozen storage (-20°C for years) and stable short-term in solvent when frozen.
- Available in small research pack sizes, with larger quantities available on inquiry.
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Medchemexpress LLC (E)-5-(4-propoxybenzylidene)thiazolidine-2,4-dione | 587852-28-6 | MFCD31382191 | 98.0% | 263.31 g·mol⁻¹ | C13H13NO3S | 100 MG
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SMI-16a (CAS 587852-28-6) is a selective, ATP-competitive Pim kinase inhibitor used as a research tool to probe Pim kinase signaling and downstream cellular effects. It shows potent biochemical inhibition of Pim isoforms and measurable activity in cellular assays, and is supplied with analytical data for use in preclinical studies.
- Selective Pim1 and Pim2 inhibitor.
- Biochemical IC50: Pim1 0.15 μM, Pim2 0.02 μM; cellular activity in PC3 cells 48 μM.
- Chemical formula C13H13NO3S and molecular weight 263.31 g·mol⁻¹.
- Purity 98.0% as specified by the supplier.
- High solubility in DMSO (≥ 100 mg/mL) and defined in vivo formulation options.
- Powder storage stability: -20°C for 3 years, 4°C for 2 years.
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Selleck Chemical LLC 1.4-Cineole S5419-25mg
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1 4-Cineole (Isocineole) is a widely distributed natural oxygenated monoterpene 1 4-Cineole present in eucalyptus oil activates both human TRPM8 and human TRPA1
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Matrix Scientific 4-(TRIFLUOROMETHOXY)BENZON-25G
4-(Trifluoromethoxy)benzonitrile, 98%; 25g,C8H4F3NO, MFCD00039474, mw 187.12, [332-25-2]
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Medchemexpress LLC Esamisulpride (S)-amisulpride | 71675-92-8 | 99.0% | 369.48 g/mol | C17H27N3O4S | 10MG
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Esamisulpride (S)-amisulpride is the S-enantiomer of amisulpride supplied for research use as a dopamine D2/D3 receptor antagonist with low-nanomolar affinity. It also shows activity at 5-HT7 and is used in pharmacology and behavioral studies related to schizophrenia and depression.
- High chemical purity (99.04%) suitable for research applications.
- Potent D2 and D3 receptor antagonist with low-nanomolar affinity.
- Reported 5-HT7 receptor activity for broader pharmacological profiling.
- Available in small mass quantities appropriate for preclinical experiments.
- Confirmed molecular formula C17H27N3O4S and molecular weight 369.48 g/mol.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000296999 HKOCL-4M 10MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000388087 4-PHENOXYBENZYLAMINE 1G
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eMolecules 1-Phenyl-3-((tetrahydrofuran-2-yl)methyl)thiourea | 309942-73-2 | MFCD01185453 | 1g
Combi-Blocks | 1-Phenyl-3-((tetrahydrofuran-2-yl)methyl)thiourea | 1g | 457920412 | QK-5365 | 98.000 | 309942-73-2 | MFCD01185453 | 236.330 | C12H16N2OS
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000362892 BRD4 INHIBITOR-24 50MG
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