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Filtered Search Results
eMolecules 137628-32-1 | (4-Tetrahydropyran-2-yloxybutyl)magnesium bromide, 0.50 M in THF | Synthonix261.442 | C9H17BrMgO2 | 0.000 | [Br-].[Mg+]CCCCOC1CCCCO1 | 100ml | 835533438
(4-Tetrahydropyran-2-yloxybutyl)magnesium bromide, 0.50 M in THF | Synthonix | 137628-32-1261.442 | C9H17BrMgO2 | 0.000 | [Br-].[Mg+]CCCCOC1CCCCO1 | 100ml | 835533438
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Medchemexpress LLC BI-0115 | 4929-23-1 | 99.7% | 287.74 | 1 MG
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BI-0115 | 4929-23-1 | 99.7% | 287.74 | 1 MG
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eMolecules 312693-24-6 | 3-Methylphenylzinc iodide, 0.50 M in THF | Synthonix | MFCD01311453 | 283.420 | C7H7IZn | 0.000 | [I-].Cc1cccc([Zn+])c1 | 25ml | 627353700
3-Methylphenylzinc iodide, 0.50 M in THF | Synthonix | 312693-24-6 | MFCD01311453 | 283.420 | C7H7IZn | 0.000 | [I-].Cc1cccc([Zn+])c1 | 25ml | 627353700
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Medchemexpress LLC Epirubicin hydrochloride (standard) | 56390-09-1 | 99.91% | 579.98 | 100 MG
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Epirubicin hydrochloride (Standard) is an analytical standard and a semisynthetic L-arabino derivative of doxorubicin, primarily used in research and analytical applications. It functions as an antineoplastic agent by inhibiting Topoisomerase and also inhibits DNA and RNA synthesis. Additionally, it acts as a Forkhead box protein p3 (Foxp3) inhibitor, effectively inhibiting regulatory T cell activity.
- Analytical standard for research and analytical applications
- Semisynthetic L-arabino derivative of doxorubicin
- Acts as an antineoplastic agent
- Inhibits Topoisomerase, DNA, and RNA synthesis
- Functions as a Forkhead box protein p3 (Foxp3) inhibitor
- Inhibits regulatory T cell activity
- Used as a reference standard in qualitative, quantitative, and methodological research experiments (e.g., HPLC, GC, MS)
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eMolecules 446285-61-6 | 2-Ethoxy-5-(tributylstannyl)thiazole | Synthonix - Stock | MFCD09025788 | 418.230 | C17H33NOSSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1cnc(OCC)s1 | 5g | 525916537
2-Ethoxy-5-(tributylstannyl)thiazole | Synthonix - Stock | 446285-61-6 | MFCD09025788 | 418.230 | C17H33NOSSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1cnc(OCC)s1 | 5g | 525916537
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eMolecules 1251848-83-5 | (4-(trifluoromethoxy)benzyl)zinc bromide, 0.50 M in THF | Synthonix320.410 | C8H6BrF3OZn | 0.000 | [Br-].FC(F)(F)Oc1ccc(C[Zn+])cc1 | 100ml | 532652979
(4-(trifluoromethoxy)benzyl)zinc bromide, 0.50 M in THF | Synthonix | 1251848-83-5320.410 | C8H6BrF3OZn | 0.000 | [Br-].FC(F)(F)Oc1ccc(C[Zn+])cc1 | 100ml | 532652979
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eMolecules 226570-67-8 | But-3-enylzinc bromide, 0.50 M in THF | Synthonix | MFCD09801449 | 200.380 | C4H7BrZn | 0.000 | [Br-].[Zn+]CCC=C | 25ml | 627353528
But-3-enylzinc bromide, 0.50 M in THF | Synthonix | 226570-67-8 | MFCD09801449 | 200.380 | C4H7BrZn | 0.000 | [Br-].[Zn+]CCC=C | 25ml | 627353528
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eMolecules 312693-13-3 | 1-Methylpentylzinc bromide, 0.50 M in THF | Synthonix | MFCD01311409 | 230.450 | C6H13BrZn | 0.000 | [Br-].CCCCC(C)[Zn+] | 25ml | 627353687
1-Methylpentylzinc bromide, 0.50 M in THF | Synthonix | 312693-13-3 | MFCD01311409 | 230.450 | C6H13BrZn | 0.000 | [Br-].CCCCC(C)[Zn+] | 25ml | 627353687
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eMolecules 405556-98-1 | 2-Fluoro-3-methyl-5-(tributylstannyl)pyridine | Synthonix - Stock | MFCD09025798 | 400.169 | C18H32FNSn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1cnc(F)c(C)c1 | 1g | 525917312
2-Fluoro-3-methyl-5-(tributylstannyl)pyridine | Synthonix - Stock | 405556-98-1 | MFCD09025798 | 400.169 | C18H32FNSn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1cnc(F)c(C)c1 | 1g | 525917312
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Medchemexpress LLC Mk-571 (l-660711) | 115104-28-4 | >98.9% | 515.09 | 25 MG
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MK-571 (L-660711) is an orally active, potent, and selective competitive leukotriene D4 (LTD4) receptor antagonist. It also acts as an MRP4 and ABCC1 (MRP1) inhibitor and inhibits constitutive and antigen-stimulated S1P (sphingosine-1-phosphate) release.
- Orally active.
- Potent and selective competitive leukotriene D4 (LTD4) receptor antagonist.
- Inhibitor of MRP4 and ABCC1 (MRP1).
- Inhibits constitutive and antigen-stimulated S1P (sphingosine-1-phosphate) release.
- Potential for inhibiting antigen-induced dyspnea.
- Potential for blocking LTD4- and Ascaris-induced bronchoconstriction.
- Potential for reversal of hypoxic pulmonary hypertension (PH) and protection from hypoxic PH.
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eMolecules 2765568-24-7 | (Tetrahydrothiopyran-4-yl)zinc bromide, 0.50 M in THF | Synthonix246.470 | C5H9BrSZn | 0.000 | [Br-].[Zn+]C1CCSCC1 | 100ml | 702446004
(Tetrahydrothiopyran-4-yl)zinc bromide, 0.50 M in THF | Synthonix | 2765568-24-7246.470 | C5H9BrSZn | 0.000 | [Br-].[Zn+]C1CCSCC1 | 100ml | 702446004
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Medchemexpress LLC BI-671800 | 1093108-50-9 | 99.4% | 501.50 | 1 ML
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BI-671800 is a highly specific and potent antagonist of chemoattractant receptor-homologous molecule on Th2 cells (DP2/CRTH2), with IC50 values of 4.5 nM and 3.7 nM for PGD2 binding to CRTH2 in hCRTH2 and mCRTH2 transfected cells, respectively. It has potential for the treatment of poorly controlled asthma.
- Hcrth2: 4.5 nM (IC50)
- Mcrth2: 3.7 μM (IC50)
- Exhibits low nM potency as an antagonist of human or mouse CRTH2 in transfected cells.
- Shows significant inhibition of AHR in mice at 0.1-10 mg/kg, i.g.
- Effectively blocks edema formation and greatly reduces inflammatory infiltrate and skin pathology observed in drug vehicle-treated animals.
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eMolecules (3-Phenanthryl)zinc bromide, 0.25 M in THF | Synthonix |322.510 | C14H9BrZn | 0.000 | [Br-].[Zn+]c1ccc2ccc3ccccc3c2c1 | 50ml | 818572038
(3-Phenanthryl)zinc bromide, 0.25 M in THF | Synthonix |322.510 | C14H9BrZn | 0.000 | [Br-].[Zn+]c1ccc2ccc3ccccc3c2c1 | 50ml | 818572038
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Aobchem 1-(4-(Methoxymethyl)naphthalen-1-yl)ethanone | 95% | CAS 79996-79-5 | C14H14O2 | 500mg
1-(4-(Methoxymethyl)naphthalen-1-yl)ethanone | 95% | CAS 79996-79-5 | C14H14O2 | 500mg
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Aobchem 5-(Naphthalen-1-yl)thiazol-2-amine | 95% | CAS 106166-28-3 | C13H10N2S | 1g
5-(Naphthalen-1-yl)thiazol-2-amine | 95% | CAS 106166-28-3 | C13H10N2S | 1g
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