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Filtered Search Results
Medchemexpress LLC KTX-582 | 2573298-13-0 | 98.7% | 872.93 | 1 MG
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KTX-582 is a potent IRAK4 degrader with DC50 values of 4 nM and 5 nM for IRAK4 and Ikaros, respectively. It can induce apoptosis in MYD88MT DLBCL and is efficient at inducing in vivo tumor regressions in a lymphoma model.
- Potent IRAK4 degrader
- Induces apoptosis in MYD88MT DLBCL
- Efficient at inducing in vivo tumor regressions in lymphoma models
- Degrades IRAK4 in whole blood monocyte and lymphocyte with IC50s of <0.05 μM
- Inhibits IRAK4 in human whole blood LPS TNFα with an IC50 of 0.05-1 μM
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eMolecules 312624-28-5 | 6-Cyanohexylzinc bromide, 0.50 M in THF | Synthonix | MFCD01316997 | 255.460 | C7H12BrNZn | 0.000 | [Br-].[Zn+]CCCCCCC#N | 25ml | 627353573
6-Cyanohexylzinc bromide, 0.50 M in THF | Synthonix | 312624-28-5 | MFCD01316997 | 255.460 | C7H12BrNZn | 0.000 | [Br-].[Zn+]CCCCCCC#N | 25ml | 627353573
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eMolecules 112129-22-3 | (4,4,4-Trifluorobutyl)magnesium bromide, 0.50 M in THF | Synthonix215.296 | C4H6BrF3Mg | 0.000 | [Br-].FC(F)(F)CCC[Mg+] | 50ml | 795604387
(4,4,4-Trifluorobutyl)magnesium bromide, 0.50 M in THF | Synthonix | 112129-22-3215.296 | C4H6BrF3Mg | 0.000 | [Br-].FC(F)(F)CCC[Mg+] | 50ml | 795604387
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TARGETMOL CHEMICALS INC R-BI-2852 5MG
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. (R)-BI-2852 can be used as (R)-5-isoindolin-1-one is used as an inhibitor of the RAS family of proteins and as a compound for the treatment and prevention of tumours. (R)-BI-2852 has Antiproliferative and antitumour agent activity. purity: 97%
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Medchemexpress LLC Acebutolol hydrochloride | 34381-68-5 | MFCD00078860 | 99.7% | 372.89 | 500 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Acebutolol hydrochloride is an orally active β1 adrenergic receptor (β1AR) antagonist used to treat hypertension, angina pectoris, and cardiac arrhythmias.
- Appearance: solid
- Color: white to off-white
- Shipping: room temperature in continental US; may vary elsewhere
- Storage: 4°C, sealed storage, away from moisture
- In solvent: -80°C for 6 months; -20°C for 1 month (sealed storage, away from moisture)
- Solubility in DMSO: 100 mg/mL (268.18 mM)
- Solubility in H2O: ≥ 50 mg/mL (134.09 mM)
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Medchemexpress LLC Rilpivirine hydrochloride | 700361-47-3 | MFCD11046523 | 99.8% | 402.88 | C22H19ClN6 | 25 MG
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Rilpivirine hydrochloride is the hydrochloride salt of rilpivirine, a diarylpyrimidine non-nucleoside reverse transcriptase inhibitor (NNRTI) supplied for research and analytical applications. The material is offered as solid or solution formats and is accompanied by a product datasheet and safety data sheet for laboratory use.
- High purity suitable for research applications.
- Available in multiple pack sizes, including 25 mg.
- Provided with a datasheet and safety data sheet.
- Molecular formula C22H19ClN6 and molecular weight 402.88.
- Intended for non-clinical research use only.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 307496-33-9 | 2,6-Difluorobenzylzinc bromide, 0.50 M in THF | Synthonix272.400 | C7H5BrF2Zn | 0.000 | [Br-].Fc1cccc(F)c1C[Zn+] | 25ml | 627353604
2,6-Difluorobenzylzinc bromide, 0.50 M in THF | Synthonix | 307496-33-9272.400 | C7H5BrF2Zn | 0.000 | [Br-].Fc1cccc(F)c1C[Zn+] | 25ml | 627353604
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 307496-26-0 | 2,4-Difluorobenzylzinc bromide, 0.50 M in THF | Synthonix | MFCD01311423 | 272.400 | C7H5BrF2Zn | 0.000 | [Br-].Fc1ccc(C[Zn+])c(F)c1 | 100ml | 532652749
2,4-Difluorobenzylzinc bromide, 0.50 M in THF | Synthonix | 307496-26-0 | MFCD01311423 | 272.400 | C7H5BrF2Zn | 0.000 | [Br-].Fc1ccc(C[Zn+])c(F)c1 | 100ml | 532652749
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 307496-26-0 | 2,4-Difluorobenzylzinc bromide, 0.50 M in THF | Synthonix | MFCD01311423 | 272.400 | C7H5BrF2Zn | 0.000 | [Br-].Fc1ccc(C[Zn+])c(F)c1 | 25ml | 627353597
2,4-Difluorobenzylzinc bromide, 0.50 M in THF | Synthonix | 307496-26-0 | MFCD01311423 | 272.400 | C7H5BrF2Zn | 0.000 | [Br-].Fc1ccc(C[Zn+])c(F)c1 | 25ml | 627353597
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules (Tetrahydrofuran-3-ylmethyl)zinc bromide, 0.50 M in THF | Synthonix |230.410 | C5H9BrOZn | 0.000 | [Br-].[Zn+]CC1CCOC1 | 100ml | 794220304
(Tetrahydrofuran-3-ylmethyl)zinc bromide, 0.50 M in THF | Synthonix |230.410 | C5H9BrOZn | 0.000 | [Br-].[Zn+]CC1CCOC1 | 100ml | 794220304
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Biotium Reactive Dyes Biotin Cell Viability and Apoptosis Cellular Stains ViaTag 550 575 1/EA
ViaTag 550/575 Haloalkane Ligand is a bright fluorescent ligand for the HaloTag self-labeling protein tag Red fluorescent ViaTag 550/575 is cell impermeant and has an excitation/emission of 551/577 nm 30 uL of 1000X
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eMolecules 167556-63-0 | 3-Methyl-5-(tributylstannyl)pyridine | Synthonix - Stock | MFCD22056726 | 382.179 | C18H33NSn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1cncc(C)c1 | 1g | 525921648
3-Methyl-5-(tributylstannyl)pyridine | Synthonix - Stock | 167556-63-0 | MFCD22056726 | 382.179 | C18H33NSn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1cncc(C)c1 | 1g | 525921648
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eMolecules Synthonix 2-Bromo-3-hexyl-5-thienylzinc bromide 0.50 M in THF 25ml 627353496 B73145 144634-74-2 MFCD14581698 391.470 C10H14Br2SZn
Synthonix 2-Bromo-3-hexyl-5-thienylzinc bromide 0.50 M in THF 25ml 627353496 B73145 144634-74-2 MFCD14581698 391.470 C10H14Br2SZn
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Medchemexpress LLC Sabcomeline hydrochloride | 159912-58-0 | 99.8% | 229.71 | C10H16ClN3O | 25 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Sabcomeline hydrochloride is the hydrochloride salt of sabcomeline, a functionally selective muscarinic M1 receptor partial agonist used in neuroscience research. It is commonly used to investigate M1-mediated signaling and cognitive function in preclinical Alzheimer's disease models. The compound is provided as a characterized solid suitable for in vitro and in vivo studies.
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Medchemexpress LLC Amiselimod hydrochloride | 942398-84-7 | 98.7% | 413.90 | 100 MG
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Amiselimod hydrochloride is converted to its active metabolite Amiselimod phosphate by sphingosine kinases in vivo. It is an orally active and highly selective sphingosine 1-phosphate receptor-1 (S1P1) agonist. This compound is designed to reduce the bradycardia effects associated with fingolimod and other S1P receptor modulators. Amiselimod hydrochloride inhibits chronic colitis by preventing the infiltration of colitogenic Th1 and Th17 cells into the colon and inhibits lupus nephritis by reducing the infiltration of autoreactive T cells into the kidneys. It shows promise for the research of autoimmune diseases.
- Orally active and highly selective sphingosine 1-phosphate receptor-1 (S1P1) agonist.
- Designed to reduce bradycardia effects compared to other S1P receptor modulators.
- Inhibits chronic colitis.
- Inhibits lupus nephritis.
- Promising for research of autoimmune diseases.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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