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Filtered Search Results
eMolecules 61484-98-8 | 2-Amino-4-ethoxybenzoic acid | MFCD01464112 | 250mg
Ambeed | 2-Amino-4-ethoxybenzoic acid | 250mg | 600841054 | A466624 | 61484-98-8 | MFCD01464112 | 181.191 | C9H11NO3
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eMolecules 89778-27-8 | Medchem Express | Toremifene (citrate) | 100mg | 446271899 | HY-B0005 | MFCD01729016 | 598.09 | C32H36ClNO8
Medchem Express | Toremifene (citrate) | 100mg | 446271899 | HY-B0005 | 89778-27-8 | MFCD01729016 | 598.090 | C32H36ClNO8
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![eMolecules 13575-44-5 | 2-Aminothiazolo[4,5-b]pyridin-5(4H)-one | MFCD13181701 | 100mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502141686.JPG-250.jpg)
eMolecules 13575-44-5 | 2-Aminothiazolo[4,5-b]pyridin-5(4H)-one | MFCD13181701 | 100mg
ChemScene | 3-(1H-124-Triazol-1-yl)benzoic Acid | 250mg | 569144624 | CS-0060407 | 167626-64-4 | MFCD08271895 | 189.174 | C9H7N3O2
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Medchemexpress LLC Phenoxybenzamine hydrochloride | 63-92-3 | MFCD00055152 | 99.5% | 100 MG
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Phenoxybenzamine hydrochloride (Standard) serves as the analytical standard for Phenoxybenzamine hydrochloride, intended for research and analytical applications. It is an irreversible, nonselective, and orally active α-adrenoceptor antagonist, frequently employed in hypertension research, particularly for cases caused by pheochromocytoma. This compound also exhibits antitumor activity.
- Analytical standard for phenoxybenzamine hydrochloride
- Intended for research and analytical applications
- Nonselective α-adrenoceptor antagonist
- Irreversible α-adrenoceptor antagonist
- Orally active α-adrenoceptor antagonist
- Used in research for hypertension caused by pheochromocytoma
- Shows antitumor activity
- Commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS
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Medchemexpress LLC Ly2365109 hydrochloride | 1779796-27-8 | 98.7% | 421.91 | C22H28ClNO5 | 25 MG
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LY2365109 hydrochloride is a potent, selective glycine transporter 1 (GlyT1) inhibitor that increases glycine levels in cerebrospinal fluid and raises seizure thresholds in preclinical models. It is provided as a solid research reagent with characterized purity and stability profiles.
- Potent and selective GlyT1 inhibitor, IC50 15.8 nM for glycine uptake.
- Elevates CSF glycine levels in preclinical studies.
- Shown to increase seizure thresholds in animal models.
- High purity suitable for research use (98.69%).
- White to off-white solid, molecular weight 421.91, formula C22H28ClNO5.
- Soluble in DMSO (≥31 mg/mL) and insoluble in water (<0.1 mg/mL).
- Recommended storage sealed at 4°C; in solvent store at -80°C for long term.
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Medchemexpress LLC HY-19872 1mg Medchemexpress, AZD-6280 CAS:942436-93-3 Purity:>98%
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Medchemexpress, HY-19872 1mg AZD-6280 CAS:942436-93-3 AZD-6280 is a selective GABAA(α2/3) receptor modulator, used for treatment of generalized anxiety disorder. 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 Schisandrin C | 61301-33-5 | 384.42 | 100 MG
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Schisandrin C (also known as Schizandrin-C or Wuweizisu-C) is a phytochemical lignan isolated from Schizandra chinensis. It exhibits diverse biological activities, including anticancer, anti-inflammatory, and antioxidant effects. This compound is suitable for research related to cancer, Alzheimer's disease, and liver diseases. Schisandrin C has been shown to induce cell apoptosis.
- Isolated from Schizandra chinensis.
- Possesses anticancer properties.
- Offers anti-inflammatory effects.
- Acts as an antioxidant.
- Induces cell apoptosis.
- Applicable for Alzheimer's disease research.
- Used in liver diseases research.
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Medchemexpress LLC HY-13968 10mg Medchemexpress, JW 55 CAS:664993-53-7 Purity:>98%
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Medchemexpress, HY-13968 10mg JW 55 CAS:664993-53-7 JW 55 is a potent and selective β-catenin signaling pathway inhibitor, which functions via inhibition of the PARP domain of tankyrase 1 and tankyrase 2 (TNKS1/2). JW 55 decreases auto-PARsylation of TNKS1/2 in vitro with IC50s of 1.9 μM and 830 nM 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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eMolecules 1706-01-0 | 3-Methylfluoranthene | Toronto Research Chemicals | MFCD00215928 | 216.283 | C17H12Cc1ccc2-c3ccccc3-c3cccc1c23 | 100mg | 483422432
3-Methylfluoranthene | Toronto Research Chemicals | 1706-01-0 | MFCD00215928 | 216.283 | C17H12Cc1ccc2-c3ccccc3-c3cccc1c23 | 100mg | 483422432
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Medchemexpress LLC HY-100230A 100mg Medchemexpress, ML133 (hydrochloride) CAS:1222781-70-5 Purity:>98%
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Medchemexpress, HY-100230A 100mg ML133 (hydrochloride) CAS:1222781-70-5 ML133 hydrochloride is a selective K ir 2 family channels inhibitor, with an IC 50 of 1.8 μM at pH 7.4 and 290 nM at pH 8.5 [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 AMG 579 | 1227067-61-9 | 99.0% | 50 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 is intended for research use only. In vivo, AMG 579 has shown a statistically significant reduction of PCP-induced behavior in rats over a 2-hour period, with a minimum effective dose for efficacy in the PCP-LMA model determined to be 0.3 mg/kg. In dogs, it exhibits a superior oral bioavailability of 72%. One clinical trial (NCT01568203) is listed, sponsored by Amgen for Schizophrenia, with a start date of 2011-09, and it is in Phase 1.
- Potent, selective, and efficacious PDE10A inhibitor
- Demonstrates in vivo efficacy in reducing PCP-induced behavior in rats
- Exhibits superior oral bioavailability in dogs
- Underwent early-phase clinical trials for Schizophrenia
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![eMolecules 583837-94-9 | [4-(ETHANESULFONYL)PHENYL]METHANAMINE | MFCD10032480 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502180232.JPG-250.jpg)
eMolecules 583837-94-9 | [4-(ETHANESULFONYL)PHENYL]METHANAMINE | MFCD10032480 | 1g
AstaTech | [4-(ETHANESULFONYL)PHENYL]METHANAMINE | 1g | 596576189 | P10910 | 95.000 | 583837-94-9 | MFCD10032480 | 199.270 | C9H13NO2S
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![eMolecules 848243-26-5 | 2-Cyclopropylmethoxy-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridine | Combi-Blocks | MFCD07366723 | 275.160 | C15H22BNO3 | 96.000 | CC1(C)OB(OC1(C)C)c1cccnc1OCC1CC1 | 1g | 232303356](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502185248.JPG-250.jpg)
eMolecules 848243-26-5 | 2-Cyclopropylmethoxy-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridine | Combi-Blocks | MFCD07366723 | 275.160 | C15H22BNO3 | 96.000 | CC1(C)OB(OC1(C)C)c1cccnc1OCC1CC1 | 1g | 232303356
2-Cyclopropylmethoxy-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridine | Combi-Blocks | 848243-26-5 | MFCD07366723 | 275.160 | C15H22BNO3 | 96.000 | CC1(C)OB(OC1(C)C)c1cccnc1OCC1CC1 | 1g | 232303356
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Selleck Chemical LLC Briciclib
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Briciclib (ON-014185) is a water soluble derivative of ON-013100 a small molecule that binds to and inhibits eukaryotic translation initiation factor 4E (eIF4E)
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Biotang Inc Silodosin (Rapaflo) > 99%, 10MG, CAS#160970-54-7, M.W.495.53, Formula: C25H32F3N3O4, SYON:KAD 3213, KMD 3213. RS041-10MG
Silodosin (Rapaflo) > 99%, 10MG, CAS#160970-54-7, M.W.495.53, Formula: C25H32F3N3O4, SYON:KAD 3213, KMD 3213. RS041-10MG.
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