Enamines
Sigma Aldrich Fine Chemicals Biosciences Cilnidipine >=98% (HPLC), powder | 132203-70-4 | MFCD00865853 | 10MG
Cilnidipine >=98% (HPLC), powder | Purity: >=98% (HPLC) | Mol Wt: 492.52 | 132203-70-4 | MFCD00865853 | 10MG
Sigma Aldrich Fine Chemicals Biosciences Potassium indigotrisulfonate ozone-scavenging reagent | 67627-18-3 | MFCD00013160 | 1G
Potassium indigotrisulfonate ozone-scavenging reagent | Purity: >60% (HPLC) | Mol Wt: 616.72 | 67627-18-3 | MFCD00013160 | 1G
Medchemexpress LLC Molibresib besylate | 1895049-20-3 | 97.0% | 100 MG
Molibresib besylate is an orally active pan-BET inhibitor. It targets BRD2, BRD3, BRD4, and BRDT, disrupting their interaction with chromatin by occupying acetylated lysine binding sites. This inhibits MYC expression and target gene transcription. It exhibits broad antiproliferative activity, useful for research in acute myeloid leukemia, multiple myeloma, triple-negative breast cancer, small-cell lung cancer, and other advanced refractory solid tumors.
- Disrupts BET protein-chromatin interaction
- Inhibits MYC expression and target gene transcription
- Exhibits broad antiproliferative activity
- Induces growth arrest and downregulates mitosis-related genes
- Upregulates p-ERK1/2 levels
- Shows synergistic effects with MEK inhibitors
- Modulates immune microenvironment and prolongs survival in models
Medchemexpress LLC Amlodipine maleate | 88150-47-4 | 99.9% | 1 G
Amlodipine maleate is a dihydropyridine calcium channel blocker that acts as an orally active antianginal agent. It blocks voltage-dependent L-type calcium channels, inhibiting the initial influx of calcium. It can be used for the research of high blood pressure and cancer.
- Calcium channel blocker
- Orally active
- Blocks voltage-dependent L-type calcium channels, inhibiting the initial influx of calcium
- Used for research related to high blood pressure and cancer
- High purity (99.87%)
Medchemexpress LLC Amlodipine | 88150-42-9 | 99.87% | 5 G
Amlodipine is an antianginal agent and an orally active dihydropyridine calcium channel blocker. It functions by blocking voltage-dependent L-type calcium channels, thereby inhibiting the initial influx of calcium. It can be used in the research of high blood pressure and cancer.
- Functions as an antianginal agent
- Orally active dihydropyridine calcium channel blocker
- Blocks voltage-dependent L-type calcium channels
- Inhibits initial influx of calcium
- Suitable for research on high blood pressure
- Suitable for research on cancer
Medchemexpress LLC Amlodipine | 88150-42-9 | MFCD00864687 | 99.9% | 1 ML
Amlodipine is an antianginal agent and an orally active dihydropyridine calcium channel blocker. It functions by blocking voltage-dependent L-type calcium channels, inhibiting the initial influx of calcium. This compound is used in research for its effects on high blood pressure and cancer.
- Orally active dihydropyridine calcium channel blocker
- Blocks voltage-dependent L-type calcium channels
- Utilized in research for high blood pressure
- Utilized in research for cancer
Medchemexpress LLC Methyl but-3-enoate 50g
Methyl but-3-enoate is a drug intermediate for synthesis of various active compounds
Accela Chembio Inc Isopropyl 3-aminocrotonate | 25g | 14205-46-0 | MFCD00134272 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4
Isopropyl 3-aminocrotonate | 25g | 14205-46-0 | MFCD00134272 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4
![eMolecules Ambeed / 133-Trimethyl-6-morpholinospiro[indoline-23-naphtho[21-b][14]oxazine] / 100mg / 525049298 / A140452 / / 114747-48-7 / MFCD00329492 / 413.521 / C26H27N3O2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502426977.PNG-250.jpg)
eMolecules Ambeed / 133-Trimethyl-6-morpholinospiro[indoline-23-naphtho[21-b][14]oxazine] / 100mg / 525049298 / A140452 / / 114747-48-7 / MFCD00329492 / 413.521 / C26H27N3O2
Ambeed / 133-Trimethyl-6-morpholinospiro[indoline-23-naphtho[21-b][14]oxazine] / 100mg / 525049298 / A140452 / / 114747-48-7 / MFCD00329492 / 413.521 / C26H27N3O2
Medchemexpress LLC Amlodipine maleate | 88150-47-4 | 99.9% | 1 ML
Amlodipine maleate is a dihydropyridine calcium channel blocker that acts as an orally active antianginal agent. It blocks voltage-dependent L-type calcium channels, thereby inhibiting the initial influx of calcium.
- Acts as an orally active antianginal agent
- Blocks voltage-dependent L-type calcium channels
- Inhibits the initial influx of calcium
- Used for research on high blood pressure
- Used for research on cancer
Medchemexpress LLC Amlodipine besylate | 111470-99-6 | 99.7% | 5 G
Amlodipine besylate | 111470-99-6 | 99.7% | 5 G
Medchemexpress LLC Methyl but-3-enoate 100g
Methyl but-3-enoate is a drug intermediate for synthesis of various active compounds
Medchemexpress LLC Amlodipine-1,1,2,2-d4 | 1185246-14-3 | MFCD21363414 | 98.5% | 412.90 | C20H21D4ClN2O5 | 10 MG
Amlodipine-1,1,2,2-d4 is a deuterium-labeled analog of amlodipine supplied as a solid analytical standard for research. It is intended for use as an internal standard or tracer in pharmacokinetic, bioanalytical, and isotopic-labeling studies involving L-type calcium channel blockers.
- Deuterium-labeled (1,1,2,2-d4) analog suitable as an internal standard.
- High purity suitable for analytical applications.
- Molecular weight 412.90 for accurate mass-based analyses.
- Supplied as a solid in small mg quantities for laboratory use.
- Common applications include pharmacokinetic and bioanalytical studies.
- Available in typical package sizes of 5 mg, 10 mg, and 50 mg.
Apexbio Technology LLC Mesoridazine Besylate 32672-69-8 10mM (in 1mL DMSO)
Mesoridazine besylate (CAS 32672-69-8) is a phenothiazine derivative that functions primarily as a dopamine receptor antagonist demonstrating notable inhibitory activity against dopamine D2 and D4 receptors The molecule has particularly high affinity toward the dopamine D4 receptor subtype By modulating dopamine receptor activity Mesoridazine besylate has potential relevance in neuroscience research aimed at understanding dopamine-mediated neurological pathways and disorders Frequently utilized in studies of psychotic conditions the compound serves as an important tool for investigating receptor-specific pharmacological mechanisms