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Filtered Search Results
Echelon Biosciences Research Labs 306OI10 100MG
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306Oi10, 95% 100mg CAS#2322290-93-5 C59H115N3O8 MW:994.58
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eMolecules 933755-97-6 | 1-Ethynylcyclopropanecarboxylic acid | MFCD19231569 | 100mg
Ambeed | 1-Ethynylcyclopropanecarboxylic acid | 100mg | 490558615 | A379110 | 933755-97-6 | MFCD19231569 | 110.112 | C6H6O2
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![eMolecules 100286-90-6 | Irinotecan HCl | Broadpharm590.721 | C33H42N4O6 | 0.000 | CCc1c2CN3C(CC4C(COC(=O)[C@]4(O)CC)C3=O)c2nc2ccc(OC(=O)N3CCC(CC3)N3CCCCC3)cc12 | 100mg | 724438162](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502461873.JPG-250.jpg)
eMolecules 100286-90-6 | Irinotecan HCl | Broadpharm590.721 | C33H42N4O6 | 0.000 | CCc1c2CN3C(CC4C(COC(=O)[C@]4(O)CC)C3=O)c2nc2ccc(OC(=O)N3CCC(CC3)N3CCCCC3)cc12 | 100mg | 724438162
Irinotecan HCl | Broadpharm | 100286-90-6590.721 | C33H42N4O6 | 0.000 | CCc1c2CN3C(CC4C(COC(=O)[C@]4(O)CC)C3=O)c2nc2ccc(OC(=O)N3CCC(CC3)N3CCCCC3)cc12 | 100mg | 724438162
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Medchemexpress LLC Zanubrutinib | 1691249-45-2 | MFCD31567461 | 471.55 | C27H29N5O3 | 25 MG
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Zanubrutinib is a selective, irreversible small-molecule inhibitor of Bruton tyrosine kinase (BTK) used in research to study BTK signaling and pharmacology. The compound shows high biochemical potency and is supplied as a solid reagent suitable for analytical, biochemical, and cellular studies. This catalog item is provided for research use only.
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Medchemexpress LLC Mps1-IN-3 hydrochloride | 2989453-29-2 | 98.0% | 574.09 | C26H32ClN7O4S | 10MG
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Mps1-IN-3 hydrochloride is a potent, selective inhibitor of the Mps1 (TTK) kinase for biochemical and cellular research, with an in vitro IC50 of about 50 nM; it has been reported to inhibit glioblastoma cell proliferation and sensitize glioblastoma models to vincristine.
- Potent, selective Mps1 kinase inhibitor (IC50 ~50 nM).
- Reported to inhibit glioblastoma proliferation and sensitize to vincristine.
- High purity suitable for research (approximately 98.0%).
- Molecular weight 574.09 and formula C26H32ClN7O4S.
- Soluble in DMSO at ≥ 20 mg/mL for in vitro use.
- Stored sealed at -20°C; solutions stable at -80°C for long term.
- Supplied as a solid in small research sizes.
- Datasheet, SDS, certificate of analysis, and spectral data available.
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eMolecules 60783-90-6 | 5-Bromo-2-ethoxybenzoic acid | Combi-Blocks | MFCD02729212 | 245.072 | C9H9BrO3 | 98.000 | CCOc1ccc(Br)cc1C(O)=O | 1g | 388718675
5-Bromo-2-ethoxybenzoic acid | Combi-Blocks | 60783-90-6 | MFCD02729212 | 245.072 | C9H9BrO3 | 98.000 | CCOc1ccc(Br)cc1C(O)=O | 1g | 388718675
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Medchemexpress LLC HY-15801 5mg Medchemexpress, HG-14-10-04 CAS:1356962-34-9 Purity:>98%
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Medchemexpress, HY-15801 5mg HG-14-10-04 CAS:1356962-34-9 HG-14-10-04 (example 10) is a potent and specific ALK inhibitor with an IC50 of 20 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 HY-124960 5mg Medchemexpress, CTPB CAS:586976-24-1 Purity:>98%
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Medchemexpress, HY-124960 5mg CTPB CAS:586976-24-1 CTPB is a good activator of p300 histone acetyl transferase (HAT) enzyme. 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-B0484 100mg Medchemexpress, Buflomedil (hydrochloride) CAS:35543-24-9 Purity:>98%
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Medchemexpress, HY-B0484 100mg Buflomedil (hydrochloride) CAS:35543-24-9 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-70003 50mg Medchemexpress, Carboxypeptidase G2 (CPG2) Inhibitor CAS:192203-60-4 Purity:>98%
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Medchemexpress, HY-70003 50mg Carboxypeptidase G2 (CPG2) Inhibitor CAS:192203-60-4 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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Apexbio Technology LLC FIIN-2 1633044-56-0 5mg
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FIIN-2 (CAS 1633044-56-0) is an irreversible inhibitor targeting FGFR1 4 exhibiting IC50 values of 3 1 4 3 27 and 45 nM respectively It binds covalently to the P-loop cysteine particularly Cys491 in FGFR2 and displays moderate inhibition of EGFR (IC50 204 nM) with reduced affinity compared to related compounds FIIN-2 effectively inhibits proliferation of FGFR-dependent Ba/F3 cells showing nanomolar EC50 values and demonstrates potent activity against FGFR2 gatekeeper mutations including V564M and V564F Its selective kinase profile and ability to circumvent resistance mechanisms highlight its value for studying FGFR-driven oncogenic pathways and evaluating strategies for overcoming therapeutic resistance
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eMolecules 367501-31-3 | 4-Amino-3-ethoxybenzoic acid | Apollo Scientific | MFCD12168720 | 181.191 | C9H11NO3 | 95.000 | CCOc1cc(ccc1N)C(O)=O | 1g | 562429317
4-Amino-3-ethoxybenzoic acid | Apollo Scientific | 367501-31-3 | MFCD12168720 | 181.191 | C9H11NO3 | 95.000 | CCOc1cc(ccc1N)C(O)=O | 1g | 562429317
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Medchemexpress LLC AMG 579 | 1227067-61-9 | 99.0% | 10 MG
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AMG 579 is a potent, selective, and efficacious inhibitor of phosphodiesterase 10A (PDE10A) with an IC50 of 0.1 nM. It has shown a statistically significant reduction of PCP induced behavior in rats.
- Potent, selective, and efficacious inhibitor of phosphodiesterase 10A (PDE10A)
- IC50 of 0.1 nM for phosphodiesterase 10A
- Statistically significant reduction of PCP induced behavior in rats
- Minimum effective dose of 0.3 mg/kg for efficacy in PCP-LMA model
- Exhibits a superior oral bioavailability of 72% in dogs
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![Medchemexpress LLC 1-(4-fluorophenyl)-N-[1-(2-methylsulfonylpyridin-4-yl)cyclopropyl]pyrazolo[3,4-c]pyridine-4-carboxam | 1295298-26-8 | 98.9% | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000231883.png-250.jpg)
Medchemexpress LLC 1-(4-fluorophenyl)-N-[1-(2-methylsulfonylpyridin-4-yl)cyclopropyl]pyrazolo[3,4-c]pyridine-4-carboxam | 1295298-26-8 | 98.9% | 50 MG
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BI 639667 is a small-molecule chemical probe and potent antagonist of the chemokine receptor CCR1. It has been characterized in multiple in vitro assays and reported to have low-nanomolar activity; key identifiers include CAS 1295298-26-8 and molecular formula C22H18FN5O3S.
- Potent CCR1 antagonist with low-nanomolar activity in cell-based and binding assays.
- Used as a chemical probe for CCR1 target validation and pharmacology studies.
- Chemical formula C22H18FN5O3S and molecular weight ~451.47 Da.
- High reported purity (98.87%) for supplied solid material.
- Available in multiple sizes and as a 10 mM solution in DMSO for screening.
- Recommended storage: powder and in-solvent conditions per supplier guidance.
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eMolecules 1262395-13-0 | Medchem Express | NMS-P515 | 5mg | 788478161 | HY-128599 | 355.482 | C21H29N3O2
Medchem Express | (SRS)-AHPC-Boc | 100mg | 527574306 | HY-123109 | 1448189-98-7 | 530.680 | C27H38N4O5S
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