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Filtered Search Results
![Medchemexpress LLC 5-Pyrimidineacetic acid, 4,6-bis(dimethylamino)-2-[[4-[[4-(trifluoromethyl)benzoyl]amino]phenyl]me | 1093108-50-9 | 99.4% | 501.50 | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000437288-Logo.png-250.jpg){kind=logo}
Medchemexpress LLC 5-Pyrimidineacetic acid, 4,6-bis(dimethylamino)-2-[[4-[[4-(trifluoromethyl)benzoyl]amino]phenyl]me | 1093108-50-9 | 99.4% | 501.50 | 100 MG
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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.
- Highly specific and potent antagonist of chemoattractant receptor-homologous molecule on Th2 cells (DP2/CRTH2).
- Exhibits low nM potency as an antagonist of human or mouse CRTH2 in transfected cells.
- Shows significant inhibition of AHR in mice.
- Effectively blocks edema formation and greatly reduces inflammatory infiltrate and skin pathology.
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(CCCC)c1csc(OCC)n1 | 500mg | 525916469](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696826.jpg-250.jpg)
eMolecules 240816-28-8 | 2-Ethoxy-4-(tributylstannyl)thiazole | Synthonix - Stock | MFCD07787373 | 418.230 | C17H33NOSSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1csc(OCC)n1 | 500mg | 525916469
2-Ethoxy-4-(tributylstannyl)thiazole | Synthonix - Stock | 240816-28-8 | MFCD07787373 | 418.230 | C17H33NOSSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1csc(OCC)n1 | 500mg | 525916469
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![eMolecules 2765568-21-4 | 2-Methyl-4-pyridylmagnesium bromide, 0.25 M in THF | Synthonix196.330 | C6H6BrMgN | 0.000 | [Br-].Cc1cc([Mg+])ccn1 | 50ml | 702445935](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502694971.jpg-250.jpg)
eMolecules 2765568-21-4 | 2-Methyl-4-pyridylmagnesium bromide, 0.25 M in THF | Synthonix196.330 | C6H6BrMgN | 0.000 | [Br-].Cc1cc([Mg+])ccn1 | 50ml | 702445935
2-Methyl-4-pyridylmagnesium bromide, 0.25 M in THF | Synthonix | 2765568-21-4196.330 | C6H6BrMgN | 0.000 | [Br-].Cc1cc([Mg+])ccn1 | 50ml | 702445935
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![eMolecules 626207-42-9 | 3-Phenyl-1-propylzinc bromide, 0.50 M in THF | Synthonix | MFCD08064069 | 264.470 | C9H11BrZn | 0.000 | [Br-].[Zn+]CCCc1ccccc1 | 25ml | 627353718](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502695263.jpg-250.jpg)
eMolecules 626207-42-9 | 3-Phenyl-1-propylzinc bromide, 0.50 M in THF | Synthonix | MFCD08064069 | 264.470 | C9H11BrZn | 0.000 | [Br-].[Zn+]CCCc1ccccc1 | 25ml | 627353718
3-Phenyl-1-propylzinc bromide, 0.50 M in THF | Synthonix | 626207-42-9 | MFCD08064069 | 264.470 | C9H11BrZn | 0.000 | [Br-].[Zn+]CCCc1ccccc1 | 25ml | 627353718
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(CCCC)c1cc(n[nH]1)C(=O)OCC | 5g | 525924143](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696546.jpg-250.jpg)
eMolecules 141998-85-8 | 5-Tributylstannyl-1H-pyrazole-3-carboxylic acid ethyl ester | Synthonix - Stock | MFCD12026320 | 429.192 | C18H34N2O2Sn | 98.000 | CCCC[Sn](CCCC)(CCCC)c1cc(n[nH]1)C(=O)OCC | 5g | 525924143
5-Tributylstannyl-1H-pyrazole-3-carboxylic acid ethyl ester | Synthonix - Stock | 141998-85-8 | MFCD12026320 | 429.192 | C18H34N2O2Sn | 98.000 | CCCC[Sn](CCCC)(CCCC)c1cc(n[nH]1)C(=O)OCC | 5g | 525924143
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Medchemexpress LLC (±)-BI-D | 1416258-16-6 | 98.1% | 405.49 | 100 MG
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(±)-BI-D is a potent ALLINI (allosteric integrase inhibitor) that binds integrase at the LEDGF/p75 binding site. It inhibits HIV-Luc infection in cells, with an IC50 of 0.16 μM in Psip1 knockout E9 mouse embryonic fibroblasts and 2.9 μM in wild-type E9 mouse embryonic fibroblasts. The product is for research use only and not sold to patients.
- Potent allosteric integrase inhibitor.
- Binds integrase at the LEDGF/p75 binding site.
- Inhibits HIV-Luc infection in cells.
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![eMolecules 1618666-29-7 | 2-Benzothiazolylzinc bromide, 0.50 M in THF | Synthonix279.460 | C7H4BrNSZn | 0.000 | [Br-].[Zn+]c1nc2ccccc2s1 | 50ml | 532652608](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696363.jpg-250.jpg)
eMolecules 1618666-29-7 | 2-Benzothiazolylzinc bromide, 0.50 M in THF | Synthonix279.460 | C7H4BrNSZn | 0.000 | [Br-].[Zn+]c1nc2ccccc2s1 | 50ml | 532652608
2-Benzothiazolylzinc bromide, 0.50 M in THF | Synthonix | 1618666-29-7279.460 | C7H4BrNSZn | 0.000 | [Br-].[Zn+]c1nc2ccccc2s1 | 50ml | 532652608
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![eMolecules 82297-89-0 | 4-Fluoro-3-methylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD00075303 | 213.332 | C7H6BrFMg | 0.000 | [Br-].Cc1cc([Mg+])ccc1F | 50ml | 437237232](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502697613.jpg-250.jpg)
eMolecules 82297-89-0 | 4-Fluoro-3-methylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD00075303 | 213.332 | C7H6BrFMg | 0.000 | [Br-].Cc1cc([Mg+])ccc1F | 50ml | 437237232
4-Fluoro-3-methylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | 82297-89-0 | MFCD00075303 | 213.332 | C7H6BrFMg | 0.000 | [Br-].Cc1cc([Mg+])ccc1F | 50ml | 437237232
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![eMolecules 22873-28-5 | 4-Ethylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD01311467 | 209.369 | C8H9BrMg | 0.000 | [Br-].CCc1ccc([Mg+])cc1 | 100ml | 437237189](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502697644.jpg-250.jpg)
eMolecules 22873-28-5 | 4-Ethylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD01311467 | 209.369 | C8H9BrMg | 0.000 | [Br-].CCc1ccc([Mg+])cc1 | 100ml | 437237189
4-Ethylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | 22873-28-5 | MFCD01311467 | 209.369 | C8H9BrMg | 0.000 | [Br-].CCc1ccc([Mg+])cc1 | 100ml | 437237189
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Cayman Chemical Mebhydroline (1,5-naphthalenedisulfonate), Purity: ≥98%, CAS: 6153-33-9, 25 g
A histamine H1 receptor antagonist (Ki = 7.6 nM); selective for the histamine H1 receptor over muscarinic acetylcholine receptors (mAChRs; Ki = 180 nM); inhibits acid sphingomyelinase in H4 neuroglioma cells at 10 µM; binds to the FXR ligand-binding domain (Kd = 9.87 µM); inhibits GW 4064-induced transactivation of FXR in HEK293T cells expressing the human receptor; binds to Zika virus RdRp (Kd = 22.62 µM) and reduces viral replication in Zika-infected Vero cells (EC50 = 5.14 µM); decreases blood glucose and plasma HbA1c levels in db/db diabetic mice at 30 mg/kg
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![eMolecules 53429-23-5 | (2-isopropoxy-2-oxo-ethyl)zinc bromide, 0.50 M in THF | Synthonix246.410 | C5H9BrO2Zn | 0.000 | [Br-].CC(C)OC(=O)C[Zn+] | 100ml | 627353813](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502695209.jpg-250.jpg)
eMolecules 53429-23-5 | (2-isopropoxy-2-oxo-ethyl)zinc bromide, 0.50 M in THF | Synthonix246.410 | C5H9BrO2Zn | 0.000 | [Br-].CC(C)OC(=O)C[Zn+] | 100ml | 627353813
(2-isopropoxy-2-oxo-ethyl)zinc bromide, 0.50 M in THF | Synthonix | 53429-23-5246.410 | C5H9BrO2Zn | 0.000 | [Br-].CC(C)OC(=O)C[Zn+] | 100ml | 627353813
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![eMolecules 37586-57-5 | 4-Methylpent-3-enylmagnesium bromide, 0.5M in THF | Synthonix187.363 | C6H11BrMg | 97.000 | [Br-].CC(C)=CCC[Mg+] | 25ml | 627353679](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502695298.jpg-250.jpg)
eMolecules 37586-57-5 | 4-Methylpent-3-enylmagnesium bromide, 0.5M in THF | Synthonix187.363 | C6H11BrMg | 97.000 | [Br-].CC(C)=CCC[Mg+] | 25ml | 627353679
4-Methylpent-3-enylmagnesium bromide, 0.5M in THF | Synthonix | 37586-57-5187.363 | C6H11BrMg | 97.000 | [Br-].CC(C)=CCC[Mg+] | 25ml | 627353679
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![eMolecules 308796-05-6 | 4-Pentylphenylzinc iodide, 0.50 M in THF | Synthonix339.530 | C11H15IZn | 0.000 | [I-].CCCCCc1ccc([Zn+])cc1 | 100ml | 532652955](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696042.jpg-250.jpg)
eMolecules 308796-05-6 | 4-Pentylphenylzinc iodide, 0.50 M in THF | Synthonix339.530 | C11H15IZn | 0.000 | [I-].CCCCCc1ccc([Zn+])cc1 | 100ml | 532652955
4-Pentylphenylzinc iodide, 0.50 M in THF | Synthonix | 308796-05-6339.530 | C11H15IZn | 0.000 | [I-].CCCCCc1ccc([Zn+])cc1 | 100ml | 532652955
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TARGETMOL CHEMICALS INC BI-6015 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. BI 6015 is an antagonist of HNF4(alpha). HNF4(alpha) is a nuclear receptor that regulates gene expression in the intestine cells liver cells and pancreas-(beta) cells. purity: 99%
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Medchemexpress LLC Conivaptan hydrochloride | 168626-94-6 | 99.95% | 535.04 | 100 MG
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Conivaptan hydrochloride is a non-peptide antagonist of the vasopressin receptor, demonstrating high affinity for both V1A and V2 receptors. It is intended for research use only and not for medical applications. This compound exhibits significant biological activity, including increasing urine volume and reducing urine osmolality in myocardial infarction rats, and improving cardiac function in dogs with congestive heart failure.
- Non-peptide vasopressin receptor antagonist
- High affinity for V1A and V2 receptors
- Increases urine volume and reduces urine osmolality
- Improves cardiac function in relevant models
- Suitable for in vitro and in vivo research studies
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