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Filtered Search Results
Medchemexpress LLC Mk-571 sodium | 115103-85-0 | 99.8% | 537.07 | 25 MG
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Mk-571 sodium | 115103-85-0 | 99.8% | 537.07 | 25 MG
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Medchemexpress LLC BI-749327 | 2361241-23-6 | 99.9% | 442.43 | 50 MG
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BI-749327 | 2361241-23-6 | 99.9% | 442.43 | 50 MG
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eMolecules 308796-04-5 | 4-Pentenylzinc bromide, 0.50 M in THF | Synthonix | MFCD01311404 | 214.410 | C5H9BrZn | 0.000 | [Br-].[Zn+]CCCC=C | 25ml | 627353720
4-Pentenylzinc bromide, 0.50 M in THF | Synthonix | 308796-04-5 | MFCD01311404 | 214.410 | C5H9BrZn | 0.000 | [Br-].[Zn+]CCCC=C | 25ml | 627353720
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Medchemexpress LLC 2-Butene-1,4-diamine, N1, N4-bis[3-(ethylamino)propyl]-, hydrochloride (1:4), (2Z)- | 206991-64-2 | 95.0% | 402.27 | 25 MG
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PG-11047 (CGC-11047) is a polyamine analogue used for the research of breast cancer. It offers the following features and benefits:
- Inhibits the growth of breast cell lines, with basal-like cell lines being inhibited at lower concentrations than luminal cell lines.
- Causes a significant decrease in S phase fraction at doses that produce little apoptosis.
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eMolecules 132687-51-5 | [3-(Methoxymethoxy)phenyl]magnesium bromide, 0.50 M in THF | Synthonix241.367 | C8H9BrMgO2 | 0.000 | [Br-].COCOc1cccc([Mg+])c1 | 25ml | 812262653
[3-(Methoxymethoxy)phenyl]magnesium bromide, 0.50 M in THF | Synthonix | 132687-51-5241.367 | C8H9BrMgO2 | 0.000 | [Br-].COCOc1cccc([Mg+])c1 | 25ml | 812262653
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eMolecules 308795-91-7 | 3-Methyl-2-pyridylzinc bromide, 0.50 M in THF | Synthonix237.410 | C6H6BrNZn | 0.000 | [Br-].Cc1cccnc1[Zn+] | 100ml | 532652907
3-Methyl-2-pyridylzinc bromide, 0.50 M in THF | Synthonix | 308795-91-7237.410 | C6H6BrNZn | 0.000 | [Br-].Cc1cccnc1[Zn+] | 100ml | 532652907
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eMolecules Synthonix Hexylzinc iodide 0.50 M in THF 25ml 627353663 H73283 152329-33-4 [null] 277.450 C6H13IZn
Synthonix Hexylzinc iodide 0.50 M in THF 25ml 627353663 H73283 152329-33-4 [null] 277.450 C6H13IZn
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eMolecules 282727-18-8 | 3-(Ethoxycarbonyl)phenylzinc iodide, 0.50 M in THF | Synthonix341.450 | C9H9IO2Zn | 0.000 | [I-].CCOC(=O)c1cccc([Zn+])c1 | 100ml | 532652812
3-(Ethoxycarbonyl)phenylzinc iodide, 0.50 M in THF | Synthonix | 282727-18-8341.450 | C9H9IO2Zn | 0.000 | [I-].CCOC(=O)c1cccc([Zn+])c1 | 100ml | 532652812
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eMolecules 419535-75-4 | 5-Chloro-2-methoxyphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock245.780 | C7H6BrClMgO | 0.000 | [Br-].COc1ccc(Cl)cc1[Mg+] | 100ml | 437237056
5-Chloro-2-methoxyphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | 419535-75-4245.780 | C7H6BrClMgO | 0.000 | [Br-].COc1ccc(Cl)cc1[Mg+] | 100ml | 437237056
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eMolecules 1416437-21-2 | 5-Bromo-4-(tributylstannyl)pyrimidine | Synthonix - Stock | MFCD16170450 | 448.036 | C16H29BrN2Sn | 94.000 | CCCC[Sn](CCCC)(CCCC)c1ncncc1Br | 250mg | 525910903
5-Bromo-4-(tributylstannyl)pyrimidine | Synthonix - Stock | 1416437-21-2 | MFCD16170450 | 448.036 | C16H29BrN2Sn | 94.000 | CCCC[Sn](CCCC)(CCCC)c1ncncc1Br | 250mg | 525910903
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Medchemexpress LLC Adrenalone hydrochloride | 62-13-5 | 99.88% | 500 MG
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Adrenalone hydrochloride is an adrenergic agonist employed as a topical vasoconstrictor and hemostatic. It acts as an inhibitor of dopamine β oxidase and exhibits chemical similarity to known norepinephrine transporter (NET) ligands, with an IC50 of 36.9 μM. It is a keton form of the natural substrate epinephrine and also inhibits substrate transport by NET. It is used for research purposes only.
- Acts as an adrenergic agonist
- Functions as a topical vasoconstrictor
- Exhibits hemostatic properties
- Inhibits dopamine β oxidase
- Chemically similar to norepinephrine transporter (NET) ligands
- Available as a solid, light yellow to yellow in appearance
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eMolecules [4-Chloro-3-(trifluoromethyl)phenyl]zinc bromide, 0.5 M in THF | Synthonix |324.830 | C7H3BrClF3Zn | 0.000 | [Br-].FC(F)(F)c1cc([Zn+])ccc1Cl | 50ml | 812584961
[4-Chloro-3-(trifluoromethyl)phenyl]zinc bromide, 0.5 M in THF | Synthonix |324.830 | C7H3BrClF3Zn | 0.000 | [Br-].FC(F)(F)c1cc([Zn+])ccc1Cl | 50ml | 812584961
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Medchemexpress LLC Cevimeline hydrochloride (synonyms: AF102B hydrochloride) | 107220-28-0 | 98.7% | C10H18ClNOS | 1 ML
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Cevimeline hydrochloride is a quinuclidine derivative of acetylcholine and a selective and orally active muscarinic M1 and M3 receptor agonist. It stimulates secretion by the salivary glands and can be used as a sialogogue for xerostomia. It can also cross the blood-brain barrier.
- Quinuclidine derivative of acetylcholine
- Selective and orally active muscarinic M1 and M3 receptor agonist
- Stimulates secretion by salivary glands
- Used as a sialogogue for xerostomia
- Can cross the blood-brain barrier
- For research use only
- Molecular weight: 235.77
- Appearance: white to off-white solid
- Soluble in H2O at concentrations ≥ 50 mg/mL
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eMolecules 26905-40-8 | 3-Methoxybenzylmagnesium chloride, 0.25 M in 2-MeTHF | Synthonix | MFCD01319896 | 180.910 | C8H9ClMgO | 0.000 | [Cl-].COc1cccc(C[Mg+])c1 | 25ml | 627353681
3-Methoxybenzylmagnesium chloride, 0.25 M in 2-MeTHF | Synthonix | 26905-40-8 | MFCD01319896 | 180.910 | C8H9ClMgO | 0.000 | [Cl-].COc1cccc(C[Mg+])c1 | 25ml | 627353681
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Medchemexpress LLC Rotigotine Hydrochloride | 125572-93-2 | 99.45% | C19H26ClNOS | 500 MG
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Rotigotine Hydrochloride is a full agonist of the dopamine receptor, a partial agonist of the 5-HT1A receptor, and an antagonist of the α2B-adrenergic receptor. It is suitable for research use only.
- Full agonist of dopamine receptor
- Partial agonist of the 5-HT1A receptor
- Antagonist of the α2B-adrenergic receptor
- Ki values of 0.71 nM for the dopamine D3 receptor
- Ki values of 4-15 nM for D2, D5, and D4 receptors
- Ki value of 83 nM for the dopamine D1 receptor
- White to off-white solid appearance
- Suitable for research use only
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