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Filtered Search Results
Enzo Life Sciences ET B receptor antagonist. sodium salt (1mg). CAS: 156161-89-6
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Highly potent and selective ETB-receptor antagonist. Alternative name: BQ-788 . Na. Formula: C34H50N5O7Na. MW: 663.7. Purity: ≥95% (HPLC). Formulation: Lyophilized from 0.1M sodium bicarbonate. Solubility: Soluble in methanol (0.5mg/ml), DMSO (4mg/ml), 0.1M sodium bicarbonate (3mg/ml) or 100% ethanol (4mg/ml); insoluble in water. Long Term Storage: -20°C.
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eMolecules 18623-44-4 | Medchem Express | iCRT-5 | 5mg | 783660399 | HY-119383 | MFCD00703657 | 367.43 | C16H17NO5S2
Medchem Express | (SRS)-AHPC-PEG5-Boc | 100mg | 572596777 | HY-131959 | 2923734-82-9 | 807.010 | C40H62N4O11S
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eMolecules 217813-15-5 | Medchem Express | KW-8232 | 5mg | 624169301 | HY-100304A | 705.27 | C37H41ClN4O6S
Medchem Express | 2-O-(2-Methoxyethyl)guanosine | 250mg | 758391478 | HY-23789 | 473278-54-5 | 341.324 | C13H19N5O6
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Ambeed AMBEED
5000896512 4-MORPHOLINE-4-CARBOXAMI 250MG
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Medchemexpress LLC HY-12809 5mg Medchemexpress, Optovin CAS:348575-88-2 Purity:>98%
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Medchemexpress, HY-12809 5mg Optovin CAS:348575-88-2 Optovin is a reversible photoactivated TRPA1 ligand that enables light-mediated neuronal excitation. Optovin activates TRPA1 via structure-dependent photochemical reactions with redox-sensitive cysteine residues. 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 Ripk1-in-10 | 2682889-51-4 | 98.25% | C30H28F2N6O4 | 100 MG
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RIPK1-IN-10 is a potent RIPK1 inhibitor, identified as example 37, extracted from patent WO2021160109. This product is intended for research use only and is not sold to patients. It is available as a solid, with a color ranging from white to light yellow.
- Potent RIPK1 inhibitor
- Intended for research use only
- Available as a solid
- Color ranges from white to light yellow
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eMolecules 1892576-58-7 | Medchem Express | PF-06747711 | 5mg | 459606849 | HY-112706 | 497.522 | C26H26F3N5O2
Medchem Express | Aloesin | 1mg | 495800908 | HY-N2460 | 30861-27-9 | MFCD00869744 | 394.376 | C19H22O9
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Medchemexpress LLC HY-108637A 5mg Medchemexpress, PhiKan 083 hydrochloride CAS:1050480-30-2 Purity:>98%
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Medchemexpress, HY-108637A 5mg PhiKan 083 HCl CAS:1050480-30-2 PhiKan 083 hydrochloride is a carbazole derivative, which binds to the surface cavity and stabilizes Y220C (a p53 mutant), with a Kd of 167 μM, and a relative binding affinity (Kd) of 150 μM in Ln229 cells[3]. 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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eMolecules 204205-90-3 | Medchem Express | Indibulin | 5mg | 482204355 | HY-13649 | MFCD05861105 | 389.84 | C22H16ClN3O2
Ambeed | (4R5R)-Dimethyl 22-dimethyl-13-dioxolane-45-dicarboxylate | 5g | 600847345 | A763060 | 37031-29-1 | 218.205 | C9H14O6
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Medchemexpress LLC HY-15591A 5mg Medchemexpress, TMC647055 (Choline salt) CAS: Purity:>98%
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Medchemexpress, HY-15591A 5mg TMC647055 (Choline salt) CAS: 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 5-hydroxy-3-(indol-3-yl)isoindolin-1-one (S-isomer) | 2375482-51-0 | 99.5% | 516.59 Da | C31H28N6O2 | 50MG
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BI-2852 is a small-molecule inhibitor that binds the KRAS switch I/II pocket and inhibits active, GTP-bound KRAS with nanomolar potency. It is intended for research use and is used as a tool compound to study KRAS-driven signaling, pERK modulation, and antiproliferative effects in KRAS-mutant cell models.
- Potent nanomolar inhibition of KRAS switch I/II pocket.
- Directly targets active GTP-bound KRAS to disrupt effector interactions.
- Suitable for in vitro studies of KRAS signaling and cell proliferation.
- High purity (>99%) suitable for biochemical and cell-based assays.
- Molecular formula C31H28N6O2 and molecular weight 516.59 Da.
- Available with supporting documentation, including COA and SDS.
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Medchemexpress LLC HY-101971 10mg Medchemexpress, AZ PFKFB3 26 CAS:1704740-52-2 Purity:>98%
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Medchemexpress, HY-101971 10mg AZ PFKFB3 26 CAS:1704740-52-2 AZ PFKFB3 26 is a potent and selective inhibitor of the metabolic kinase PFKFB3 with an IC50 of 23 nM. AZ PFKFB3 26 inhibits PFKFB1 and PFKFB2 with IC50s of 2.06 and 0.384 μM, respectively. 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 Heptanoic acid, 7-[[(1,1-dimethylethoxy)carbonyl]amino]- | 60142-89-4 | HY-W012001 | >=98.0% | 245.32 | 100 G
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N-Boc-7-aminoheptanoic acid is a PROTAC linker used in the synthesis of PROTACs and other conjugation applications. It features an alkane chain with terminal carboxylic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators like EDC or HATU to form a stable amide bond, and the Boc group can be deprotected under mild acidic conditions to yield the free amine.
- Utilized as a PROTAC linker
- Suitable for PROTAC synthesis
- Suitable for other conjugation applications
- Features an alkane chain with terminal carboxylic acid and Boc-protected amino groups
- Carboxylic acid reacts with primary amines for stable amide bond formation
- Boc group deprotects under mild acidic conditions to yield free amine
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Medchemexpress LLC JMS-17-2 | 1380392-05-1 | MFCD30489012 | 99.2% | 419.95 | C25H26ClN3O | 50MG
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JMS-17-2 is a small-molecule research compound that functions as a potent and selective antagonist of the CX3CR1 receptor (IC50 = 0.32 nM). It has been used in preclinical studies to impair metastatic seeding and colonization of breast cancer cells. The material is supplied as a high-purity solid with recommended cold storage for prepared solutions to preserve stability.
- Chemical formula: C25H26ClN3O.
- Molecular weight: 419.95 g·mol-1.
- High purity suitable for research use.
- Appearance: white to off-white solid.
- Storage: store solid at 4°C protected from light; store solutions at -20°C to -80°C for longer-term stability.
- Applications: in vitro and in vivo studies of CX3CR1-mediated processes and metastasis models.
- Available in multiple pack formats including small mg quantities and ready-to-use DMSO solutions.
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Medchemexpress LLC 1-Furfurylpyrrole | 1G
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1-Furfurylpyrrole | 1G
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