Carboxylic acids and derivatives
(C)C(C)(C)C)[C@@H]1[C@H](NC1=O)OC(C)=O | 5g | 625593762](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502424311.JPG-250.jpg)
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
Medchemexpress LLC (S)-Timolol (Maleate) | 26921-17-5 | 99.8% | 432.49 | 10 MM * 1 ML
(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
Medchemexpress LLC Immh-010 maleate | 2541982-47-0 | 99.8% | 756.04 | 5 MG
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
Medchemexpress LLC Enalapril maleate (Standard) | 76095-16-4 | 100.0% | 25 MG
Enalapril maleate (Standard) is an analytical standard and an angiotensin-converting enzyme (ACE) inhibitor. This product is intended for research and analytical applications, serving as a reference standard for assays.
- Reference standard for assay
- Used in qualitative, quantitative, and methodological research
- Applicable for HPLC, GC, and MS applications
Medchemexpress LLC Dibutyl maleate | 105-76-0 | 99.2% | 228.28 | 50 G
Dibutyl maleate, the diester of Maleic Acid, can be used as an intermediate of pharmaceutical synthesis. It can enhance contact sensitization to Fluorescein isothiocyanate in mice.
- Can be used as an intermediate of pharmaceutical synthesis.
- Enhances contact sensitization to Fluorescein isothiocyanate in mice.
- For research use only.
Apexbio Technology LLC (+)-MK 801 Maleate 77086-22-7 10mM (in 1mL DMSO)
( )-MK 801 Maleate is a non-competitive antagonist of the N-methyl-D-aspartate (NMDA) receptor exhibiting a Ki value of approximately 30 5 nM By blocking the NMDA receptor-mediated ion channel MK 801 disrupts glutamate-associated excitatory neurotransmission In experimental models MK 801 demonstrates anticonvulsant and anxiolytic properties through modulation of NMDA receptor activity This compound readily penetrates the central nervous system binding reversibly and region-specifically to cortical and hippocampal membranes MK 801 effectively inhibits NMDA-triggered depolarization responses in neuronal preparations making it applicable in studies focused on epilepsy excitotoxicity and neuronal signaling pathways
TARGETMOL CHEMICALS INC --DIZOCILPINE MALEATE 50MG
Also available in 10 mg 25 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. (-)-Dizocilpine maleate ((-)-MK 801 (Maleate)) is a potent selective and non-competitive NMDA receptor antagonist with Kd of 37.2 nM in rat brain membranes. purity: 99%
Medchemexpress LLC Neratinib (maleate) | 915942-22-2 | MFCD30607264 | 99.7% | 673.11 | C34H33ClN6O7 | 10 MG
Neratinib maleate is the maleate salt of neratinib, an orally available, irreversible inhibitor selective for HER2 and EGFR kinases. Supplied for research use, it is used to probe HER2/EGFR signaling and to evaluate kinase inhibition in preclinical studies.
- Irreversible HER2 and EGFR inhibitor with IC50s of 59 nM (HER2) and 92 nM (EGFR).
- High purity (99.7%) suitable for analytical and biological assays.
- Molecular weight 673.11 and formula C34H33ClN6O7.
- Stable as a solid at 4°C; in solution: -80°C (6 months) or -20°C (1 month), protect from light.
- Available in small milligram pack sizes for research applications.
eMolecules 36679-81-9 | 4-Hydroxymethyl-dihydro-furan-2-one | J & W PharmLab LLC | MFCD21099409 | 116.116 | C5H8O3 | 96.000 | OCC1COC(=O)C1 | 1g | 309209384
4-Hydroxymethyl-dihydro-furan-2-one | J & W PharmLab LLC | 36679-81-9 | MFCD21099409 | 116.116 | C5H8O3 | 96.000 | OCC1COC(=O)C1 | 1g | 309209384
TARGETMOL CHEMICALS INC Nomifensine maleate 100MG
Also available in 1 mL, 10 mg, 25 mg, 50 mg and bulk. Please contact Fisher for quotes. Nomifensine maleate (Nomifensine (maleate)) is a selective inhibitor of dopamine uptake. Nomifensine maleate is used in adult attention deficit disorder. Purity 98.46%