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Filtered Search Results
eMolecules 1245816-06-1 | 2-Fluoro-4-methyl-5-(tributylstannyl)pyridine | Synthonix - Stock | MFCD12827558 | 400.169 | C18H32FNSn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1cnc(F)cc1C | 1g | 525917649
2-Fluoro-4-methyl-5-(tributylstannyl)pyridine | Synthonix - Stock | 1245816-06-1 | MFCD12827558 | 400.169 | C18H32FNSn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1cnc(F)cc1C | 1g | 525917649
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eMolecules 186496-59-3 | 5-Fluoro-2-methylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD01311468 | 213.332 | C7H6BrFMg | 0.000 | [Br-].Cc1ccc(F)cc1[Mg+] | 500ml | 437237237
5-Fluoro-2-methylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | 186496-59-3 | MFCD01311468 | 213.332 | C7H6BrFMg | 0.000 | [Br-].Cc1ccc(F)cc1[Mg+] | 500ml | 437237237
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Medchemexpress LLC Diphenidol hydrochloride | 3254-89-5 | MFCD00151479 | 99.1% | C21H28ClNO | 1 G
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Diphenidol hydrochloride is a non-selective muscarinic M1-M4 receptor antagonist with anti-arrhythmic activity. It is also a potent non-specific blocker of voltage-gated ion channels (Na+, K+, and Ca2+) in neuronal cells. It can be used in the study of antivertigo and antinausea.
- Acts as a non-selective muscarinic M1-M4 receptor antagonist
- Exhibits anti-arrhythmic activity
- Functions as a potent non-specific blocker of voltage-gated ion channels (Na+, K+, and Ca2+) in neuronal cells
- Inhibits sodium currents and can produce spinal anesthesia
- Shown to reduce neuropathic pain and TNF-α overexpression in rat models
- Demonstrates an inhibitory effect on exercise and morphine-induced vomiting in pica rats
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eMolecules 59020-10-9 | 3-(Tributylstannyl)pyridine | Synthonix - Stock | MFCD00052054 | 368.152 | C17H31NSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1cccnc1 | 1g | 525923898
3-(Tributylstannyl)pyridine | Synthonix - Stock | 59020-10-9 | MFCD00052054 | 368.152 | C17H31NSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1cccnc1 | 1g | 525923898
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eMolecules 262422-94-6 | Neopentylzinc iodide, 0.50 M in THF | Synthonix263.430 | C5H11IZn | 0.000 | [I-].CC(C)(C)C[Zn+] | 100ml | 532652941
Neopentylzinc iodide, 0.50 M in THF | Synthonix | 262422-94-6263.430 | C5H11IZn | 0.000 | [I-].CC(C)(C)C[Zn+] | 100ml | 532652941
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Medchemexpress LLC 1-[(3,5-dichlorophenyl)sulfonyl]-N-[(4-fluorophenyl)methyl]-4-piperidinecarboxamide | 2227549-00-8 | >95.0% | 445.34 g·mol^-1 | C19H19Cl2FN2O3S | 100MG
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BI-01383298 is a small-molecule chemical probe that selectively inhibits the sodium-coupled citrate transporter SLC13A5 (NaCT). Developed by Boehringer Ingelheim and distributed by research suppliers, it is used in cellular studies to probe NaCT function. The compound is provided for laboratory research use only and is characterized by a defined molecular formula and molecular weight.
- Potent inhibitor of SLC13A5 with reported cellular IC50 values in the low nanomolar range (examples: 56 nM and 24 nM).
- High selectivity over related transporters, reported greater than 1,000-fold in some assays.
- Molecular weight approximately 445.3 g·mol^-1 and formula C19H19Cl2FN2O3S.
- Typical supplier-reported purity ≥95%, with some distributors listing higher specifications.
- Available as solid quantities and as a 10 mM solution in DMSO for cell-based assays.
- For research use only; not for human or clinical use.
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eMolecules 2368881-70-1 | 2-Methylpyridin-5-ylmagnesium bromide, 0.25 M in THF | Synthonix196.330 | C6H6BrMgN | 0.000 | [Br-].Cc1ccc([Mg+])cn1 | 50ml | 702445941
2-Methylpyridin-5-ylmagnesium bromide, 0.25 M in THF | Synthonix | 2368881-70-1196.330 | C6H6BrMgN | 0.000 | [Br-].Cc1ccc([Mg+])cn1 | 50ml | 702445941
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eMolecules 479094-62-7 | Di-tert-butylmethylphosphine tetrafluoroborate | Synthonix | MFCD03840579 | 248.050 | C9H22BF4P | 95.000 | F[B-](F)(F)F.C[PH+](C(C)(C)C)C(C)(C)C | 10g | 719909080
Di-tert-butylmethylphosphine tetrafluoroborate | Synthonix | 479094-62-7 | MFCD03840579 | 248.050 | C9H22BF4P | 95.000 | F[B-](F)(F)F.C[PH+](C(C)(C)C)C(C)(C)C | 10g | 719909080
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Medchemexpress LLC Imidazo[2,1-b]quinazolin-2(3H)-one, 6,7-dichloro-1,5-dihydro-, hydrochloride (1:1) | 58579-51-4 | 99.3% | 100 MG
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Anagrelide hydrochloride is a potent inhibitor of phosphodiesterase type III (PDE3) with an IC50 of 36 nM. This imidazoquinazoline derivative acts as an inhibitor of platelet aggregation. It inhibits bone marrow megakaryocytopoiesis, decreases gastrointestinal stromal tumor (GIST) cell proliferation, and promotes their apoptosis in vitro. Anagrelide hydrochloride is also a platelet-lowering agent with antithrombopoietic action.
- Potently inhibits the development of marrow megakaryocytes (IC50=26 nM).
- Inhibits megakaryocytic cell growth.
- Induces a cytotoxic effect in GIST882 cell line (IC50=16 nM).
- Inhibits or reduces tumor growth in GIST model mice.
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eMolecules 41498-06-0 | 5-BROMO-1-NAPHTHALDEHYDE | AstaTech | MFCD00156896 | 235.080 | C11H7BrO | 95.000 | Brc1cccc2c(C=O)cccc12 | 0.25g | 551677214
5-BROMO-1-NAPHTHALDEHYDE | AstaTech | 41498-06-0 | MFCD00156896 | 235.080 | C11H7BrO | 95.000 | Brc1cccc2c(C=O)cccc12 | 0.25g | 551677214
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eMolecules 250737-35-0 | (S)-2-tert-Butoxycarbonylamino-3-methoxy-3-oxopropylzinc iodide, 0.50 M in THF | Synthonix394.510 | C9H16INO4Zn | 0.000 | [I-].COC(=O)[C@@H](C[Zn+])NC(=O)OC(C)(C)C | 25ml | 703157755
(S)-2-tert-Butoxycarbonylamino-3-methoxy-3-oxopropylzinc iodide, 0.50 M in THF | Synthonix | 250737-35-0394.510 | C9H16INO4Zn | 0.000 | [I-].COC(=O)[C@@H](C[Zn+])NC(=O)OC(C)(C)C | 25ml | 703157755
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Medchemexpress LLC Trilaciclib hydrochloride | 1977495-97-8 | 99.7% | 519.47 g/mol | C24H32Cl2N8O | 1 MG
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Trilaciclib hydrochloride is the hydrochloride salt of trilaciclib, an orally active CDK4/6 inhibitor supplied as a research-grade analytical standard. It is provided as a light yellow to yellow solid for biochemical, cell-based, and preclinical studies, with documented activity against CDK4 and CDK6 and batch-specific characterization available.
- Orally active CDK4/6 inhibitor for cell-cycle arrest studies.
- High purity suitable for analytical and preclinical research.
- Documented potency: CDK4 IC50 ≈ 1 nM; CDK6 IC50 ≈ 4 nM.
- Solid formulation for ease of handling and storage.
- Batch-specific datasheet and COA available for quality verification.
- Intended for research use only; not for human or clinical use.
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Medchemexpress LLC Potassium 1,2-naphthoquinone-4-sulphonate | 5908-27-0 | MFCD00001699 | 99.8% | 276.31 | C10H5KO5S | 250mg
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Potassium 1 2-naphthoquinone-4-sulphonate (Compound 16) is a 6-phosphogluconate dehydrogenase (6PGDH) inhibitor with an IC50 of 53 M Potassium 1 2-naphthoquinone-4-sulphonate can be used in the study of human African trypanosomiasis[1]
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eMolecules 2265203-62-9 | 2,6-Dimethylbenzylzinc chloride, 0.50 M in THF | Synthonix220.020 | C9H11ClZn | 0.000 | [Cl-].Cc1cccc(C)c1C[Zn+] | 100ml | 702445894
2,6-Dimethylbenzylzinc chloride, 0.50 M in THF | Synthonix | 2265203-62-9220.020 | C9H11ClZn | 0.000 | [Cl-].Cc1cccc(C)c1C[Zn+] | 100ml | 702445894
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eMolecules 2178959-07-2 | 3-Fluoropropylzinc bromide, 0.50 M in THF | Synthonix206.360 | C3H6BrFZn | 97.000 | [Br-].FCCC[Zn+] | 50ml | 795604378
3-Fluoropropylzinc bromide, 0.50 M in THF | Synthonix | 2178959-07-2206.360 | C3H6BrFZn | 97.000 | [Br-].FCCC[Zn+] | 50ml | 795604378
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