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Filtered Search Results
Medchemexpress LLC Piperidine, 1-[(4,6-dimethyl-5-pyrimidinyl)carbonyl]-4-[(3S)-4-[(1R)-2-methoxy-1-[4-(trifluoromethyl)phenylethyl]-3-methyl-1-piperazinyl]-4-methyl-, (2Z)-2-butenedioate (1:1) | 599179-03-0 | 99.9% | 649.70 | 25 MG
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Vicriviroc maleate is a potent, selective, oral bioavailable, and CNS penetrated antagonist of CCR5, with a Ki of 2.5 nM. It also inhibits HIV-1 in PBMC cells. This product is for research use only and not sold to patients.
- Potent and selective CCR5 antagonist
- Oral bioavailable and CNS penetrating
- Inhibits HIV-1 in PBMC cells
- Available as a white to light yellow solid
- Ships at room temperature in continental US
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eMolecules 130561-48-7 | AstaTech | 3-CINNOLINECARBOXYLIC ACID 1-(4-CHLOROPHENYL)-14-DIHYDRO-5-(2-METHOXYETHOXY)-4-OXO- | 0.25g | 448268141 | A12000 | 95 | MFCD28556890 | 374.78 | C18H15ClN2O5
Pharmablock | 6-methoxy-5-nitro-1H-indazole | 25mg | 788496058 | PBDW003 | 152626-75-0 | MFCD11007881 | 193.162 | C8H7N3O3
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eMolecules 922-67-8 | Methyl propiolate | Combi-Blocks | MFCD00008572 | 84.074 | C4H4O2 | 97.000 | COC(=O)C#C | 25g | 117536327
Methyl propiolate | Combi-Blocks | 922-67-8 | MFCD00008572 | 84.074 | C4H4O2 | 97.000 | COC(=O)C#C | 25g | 117536327
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eMolecules 2396-80-7 | ChemScene | Methyl 5-hexenoate | 5g | 447993418 | CS-0015919 | MFCD00671538 | 128.171 | C7H12O2
ChemScene | 4-(Dodecyloxy)-[11-biphenyl]-4-carbonitrile | 1g | 632338738 | CS-0183038 | 57125-50-5 | MFCD01941019 | 363.545 | C25H33NO
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eMolecules 76855-69-1 | Azetidon | Ambeed | MFCD00077636 | 287.431 | C13H25NO4Si | 99.000 | C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1[C@H](NC1=O)OC(C)=O | 5g | 625593762
Azetidon | Ambeed | 76855-69-1 | MFCD00077636 | 287.431 | C13H25NO4Si | 99.000 | C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1[C@H](NC1=O)OC(C)=O | 5g | 625593762
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Selleck Chemical LLC Cinepazide maleate S3045-50mg
Cinepazide maleate is a maleate salt form of cinepazide which is a vasodilator
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Medchemexpress LLC SU14813 maleate | 849643-15-8 | MFCD24682713 | 99.0% | 558.56 | C27H31FN4O8 | 10 MG
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SU14813 maleate is a multi-targeted receptor tyrosine kinase inhibitor provided for research use. It shows low-nanomolar inhibitory activity against VEGFR2, VEGFR1, PDGFRβ, and KIT, and is supplied as a solid or as a 10 mM solution in DMSO for laboratory studies.
- Multi-target RTK inhibition with low-nanomolar potency.
- Activity data reported for VEGFR2, VEGFR1, PDGFRβ, and KIT.
- Available as solid packs and a 10 mM DMSO solution for easy preparation.
- High reported purity appropriate for in vitro and preclinical research.
- Supplied with SDS documentation for safe laboratory handling.
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Medchemexpress LLC Dimethyl fumarate-d6 | 66487-95-4 | 99.0% | 150.16 | 5 MG
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Dimethyl fumarate-d6 is a deuterium labeled Dimethyl fumarate. Dimethyl fumarate is a nuclear factor (erythroid-derived)-like 2 (Nrf2) pathway activator and induces upregulation of antioxidant gene expression. It can be used as a tracer and as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
- Used as a tracer and internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
- Activates the nuclear factor (erythroid-derived)-like 2 (Nrf2) pathway.
- Upregulates antioxidant gene expression.
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Medchemexpress LLC (S)-Timolol (Maleate) | 26921-17-5 | 99.8% | 432.49 | 10 MM * 1 ML
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(S)-Timolol Maleate is a non-cardioselective hydrophilic β-adrenoceptor blocker. It is commonly used as a standard medication for intraocular pressure (glaucoma) by preventing the production of aqueous humor. It can also be used for hypertension, angina pectoris, and myocardial infarction.
- Non-cardioselective hydrophilic β-adrenoceptor blocker
- Prevents the production of aqueous humor
- Used for intraocular pressure
- Effective in hypertension, angina pectoris, and myocardial infarction
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Medchemexpress LLC Immh-010 maleate | 2541982-47-0 | 99.8% | 756.04 | 5 MG
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IMMH-010 maleate is a prodrug that acts as a novel PD-L1 inhibitor, showing potential antitumor activity. It is being investigated for the treatment of neurological disorders and advanced malignant solid tumors. Upon oral administration, it quickly converts into its active form, YPD-29B. This compound is significant for advancing research in the field of PD-L1 inhibitors and related therapeutic applications.
- Acts as a novel PD-L1 inhibitor
- Shows potential antitumor activity
- Investigated for neurological disorders and advanced malignant solid tumors
- Converts into active form, YPD-29B, upon oral administration
- Advances research in PD-L1 inhibitors and related therapeutic applications
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Medchemexpress LLC Perhexiline (maleate) | 6724-53-4 | 100 MG
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Perhexiline maleate is an orally active CPT1 and CPT2 inhibitor that reduces fatty acid metabolism. It induces mitochondrial dysfunction and apoptosis in hepatic cells. It can cross the blood brain barrier (BBB) and shows anti-tumor activity. It can be used in the research of cancers, and cardiovascular diseases like angina.
- Reduces fatty acid metabolism
- Induces mitochondrial dysfunction and apoptosis in hepatic cells
- Can cross the blood-brain barrier
- Exhibits anti-tumor activity
- Suitable for research in cancers and cardiovascular diseases like angina
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Medchemexpress LLC Cipralisant maleate | 223420-20-0 | 99.8% | 332.39 g·mol-1 | C18H24N2O4 | 10 MG
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Cipralisant maleate is a research-grade histamine H3 receptor antagonist supplied as the maleate salt. It is used in pharmacology and neuroscience studies to probe H3 receptor activity and related signaling pathways. Provided as a solid with high reported purity, this compound is for laboratory research use only and not for human or veterinary applications.
- Orally active histamine H3 receptor antagonist for research applications.
- High purity (99.8%).
- White to off-white solid appearance.
- Soluble in DMSO (≥ 100 mg/mL).
- Molecular weight 332.39 g·mol-1; formula C18H24N2O4.
- Stable as powder at -20°C for long-term storage; in solution store at -80°C.
- Supplied in small laboratory-scale quantities suitable for preclinical studies.
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Medchemexpress LLC Zamifenacin fumarate | 127308-98-9 | MFCD09263617 | 99.0% | 531.60 g/mol | C31H33NO7 | 100 MG
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Zamifenacin fumarate is a synthetic small molecule and gut-selective muscarinic M3 receptor antagonist used in pharmacological research to study gastrointestinal motility. It has been shown to reduce colonic motility in preclinical studies. The fumarate salt has formula C31H33NO7, molecular weight 531.60 g/mol, CAS 127308-98-9, and is supplied at high purity for research applications.
- Selective muscarinic M3 receptor antagonism.
- Gut-selective activity that minimizes systemic muscarinic effects.
- Demonstrated reduction of colonic motility in preclinical models.
- Supplied as the fumarate salt with molecular formula C31H33NO7.
- High purity suitable for research use (99.0%).
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Sigma Aldrich Fine Chemicals Biosciences 2-Hydroxyethyl methacrylate embedding medium (for microscopy) | 868-77-9 | MFCD00002863 | 250ML
2-Hydroxyethyl methacrylate embedding medium (for microscopy) | Purity: >=99% | Mol Wt: 130.14 | 868-77-9 | MFCD00002863 | 250ML
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Sigma Aldrich Fine Chemicals Biosciences Methyl acetate United States Pharmacopeia (USP) Reference Standard | 79-20-9 | MFCD00008711 | 3X1.2ML
Methyl acetate United States Pharmacopeia (USP) Reference Standard | Mol Wt: 74.08 | 79-20-9 | MFCD00008711 | 3X1.2ML
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