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Filtered Search Results
Medchemexpress LLC HY-112688 10mg Medchemexpress, H-Arg-4MβNA CAS:60285-94-1 Purity:>98%
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Medchemexpress, HY-112688 10mg H-Arg-4MβNA CAS:60285-94-1 H-Arg-4MβNA is a substrate for cathepsin H, used for the detection of enzyme activity in gel electrophoresis. 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-B0304A 100mg Medchemexpress, Dapoxetine (hydrochloride) CAS:129938-20-1 Purity:>98%
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Medchemexpress, HY-B0304A 100mg Dapoxetine (hydrochloride) CAS:129938-20-1 Dapoxetine (LY-210448) hydrochloride is an orally active and selective serotonin reuptake inhibitor (SSRI). Dapoxetine hydrochloride can be used for the research of premature ejaculation (PE). 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 128607-22-7 | Medchem Express | Ospemifene | 10mg | 446273207 | HY-B0723 | MFCD00871890 | 378.9 | C24H23ClO2
Ambeed | Copper(II) 2-ethylhexanoate | 1g | 588343068 | A652646 | 149-11-1 | MFCD00015695 | 349.958 | C16H30CuO4
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Medchemexpress LLC PXS-5153A monohydrochloride | 2125956-82-1 | 99.59% | 438.95 | 100 MG
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PXS-5153A monohydrochloride is a potent, selective, orally active, and fast-acting lysyl oxidase like 2/3 enzymatic (LOXL2/LOXL3) inhibitor. It has an IC50 of <40 nM for LOXL2 across all mammalian species and an IC50 of 63 nM for human LOXL3. This compound can reduce crosslinks and ameliorate fibrosis.
- Potent, selective, orally active, and fast-acting LOXL2/LOXL3 inhibitor.
- IC50 of <40 nM for LOXL2 across all mammalian species.
- IC50 of 63 nM for human LOXL3.
- >40-fold selective for LOXL2 over LOX and LOXL1.
- >700-fold selective over other related amine oxidases.
- Fast-acting, with enzymatic activity almost entirely blocked within 15 minutes.
- Reduces crosslinks and ameliorates fibrosis.
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Medchemexpress LLC AS2717638 50mg | 2148339-28-8 | 50 MG
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AS-2717638 is a selective, brain-penetrant, orally active lysophosphatidic acid receptor 5 (LPA5) antagonist used in pharmacology and neuroscience research to probe LPA5-mediated signaling and pain models.
- Selective LPA5 antagonist (IC50 = 0.038 μM) for receptor pharmacology studies.
- Brain-penetrant and orally active for in vivo models.
- High purity suitable for biological assays.
- Stable when stored at -20°C with a long shelf life.
- Available in small-scale quantities for preclinical research.
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Aobchem 4-Ethoxy-1 2-dimethoxybenzene | ≥97% | CAS 41827-16-1 | C10H14O3 | 5g
4-Ethoxy-1 2-dimethoxybenzene | ≥97% | CAS 41827-16-1 | C10H14O3 | 5g
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Aobchem 4-Ethoxy-1 2-dimethoxybenzene | ≥97% | CAS 41827-16-1 | C10H14O3 | 1g
4-Ethoxy-1 2-dimethoxybenzene | ≥97% | CAS 41827-16-1 | C10H14O3 | 1g
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Aobchem 4-Phenoxy-2-(trifluoromethyl)phenylboronic acid pinacol ester | ≥97% | CAS 1196396-64-1 | C19H20BF3O3 | 500mg
4-Phenoxy-2-(trifluoromethyl)phenylboronic acid pinacol ester | ≥97% | CAS 1196396-64-1 | C19H20BF3O3 | 500mg
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eMolecules 2070014-90-1 | Medchem Express | LY 303511 (hydrochloride) | 5mg | 446266224 | HY-15643A | MFCD28167798 | 342.82 | C19H19ClN2O2
Ambeed | Bis(pyridin-3-yl)-4H-124-triazol-4-amine | 250mg | 600849500 | A888270 | 38629-66-2 | MFCD02187295 | 238.254 | C12H10N6
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Medchemexpress LLC HG-7-85-01-NH2 | 1258391-29-5 | MFCD34646287 | 98.1% | C27H27F3N6OS | 10MG
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HG-7-85-01-NH2 is a research ligand derived from the ABL inhibitor HG-7-85-01, designed to act as the target-protein-binding moiety in SNIPER constructs for targeted protein degradation studies. It is supplied as a characterized, high-purity compound with manufacturer-recommended solubility and storage conditions for preclinical research use.
- High purity (98.1%).
- Molecular formula C27H27F3N6OS; molecular weight 540.6.
- Soluble in DMSO at 125 mg/mL (231.22 mM) with ultrasonic aid and pH adjustment.
- Powder stable at -20°C for up to 3 years; in solvent stable at -80°C for 6 months.
- Supplied in multiple small research quantities.
- Intended for synthesis of SNIPER molecules and targeted degradation assays.
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eMolecules 1262414-04-9 | Medchem Express | Cenerimod | 5mg | 446268733 | HY-17606 | MFCD30530772 | 453.539 | C25H31N3O5
Medchem Express | Deflazacort | 50mg | 446263206 | HY-13609 | 14484-47-0 | MFCD00866106 | 441.524 | C25H31NO6
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eMolecules 93-40-3 | 3,4-Dimethoxyphenylacetic acid | Ambeed | MFCD00004335 | 196.202 | C10H12O4 | 98.000 | COc1ccc(CC(O)=O)cc1OC | 5g | 490503044
3,4-Dimethoxyphenylacetic acid | Ambeed | 93-40-3 | MFCD00004335 | 196.202 | C10H12O4 | 98.000 | COc1ccc(CC(O)=O)cc1OC | 5g | 490503044
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eMolecules 217171-01-2 | Medchem Express | PD173212 | 2mg | 446258073 | HY-103318 | MFCD12828777 | 599.86 | C38H53N3O3
Ambeed | (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-bromo-1H-indol-3-yl)propanoic acid | 1g | 642081357 | A841454 | 460751-66-0 | MFCD28166519 | 505.368 | C26H21BrN2O4
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Medchemexpress LLC SB-616234-A | 908601-49-0 | 99.40% | 574.11 | 100 MG
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SB-616234-A is a selective and orally bioavailable 5-HT1B receptor antagonist, demonstrating anxiolytic and antidepressant activity.
- High affinity for human 5-HT1B receptors.
- Over 100-fold selectivity for most molecular targets.
- Acts as a high-affinity antagonist without agonist activity.
- Produces dose-related anxiolytic effects.
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eMolecules 890129-26-7 | Medchem Express | BGG463 | 5mg | 446255802 | HY-100600 | 578.596 | C30H29F3N6O3
Medchem Express | BGG463 | 5mg | 446255802 | HY-100600 | 890129-26-7 | 578.596 | C30H29F3N6O3
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