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Filtered Search Results
Medchemexpress LLC 4H-1-benzothiopyran-4-one, 2,3-dihydro-2-[1-(phenylmethyl)-4-piperidinyl]- | 1204401-49-9 | MFCD18206882 | 99.9% | 337.48 g/mol | C21H23NOS | 10 MG
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σ1 Receptor antagonist-1 is a potent and selective sigma-1 receptor antagonist provided as a solid research chemical for in vitro studies. It has high reported affinity for the σ1 receptor and has been used in cell-based assays to inhibit cell growth, induce apoptosis, and arrest the cell cycle. Analytical data and handling information are provided by the supplier; this compound is for research use only.
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Medchemexpress LLC HY-119240 10mg Medchemexpress, CCT020312 CAS:324759-76-4 Purity:>98%
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Medchemexpress, HY-119240 10mg CCT020312 CAS:324759-76-4 CCT020312 is a selective EIF2AK3/PERK activator. CCT020312 elicits EIF2A phosphorylation in cells. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-111502 10mg Medchemexpress, Y06036 CAS:1832671-96-1 Purity:>98%
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Medchemexpress, HY-111502 10mg Y06036 CAS:1832671-96-1 Y06036 is a potent and selective BET inhibitor, which binds to the BRD4(1) bromodomain with Kd value of 82 nM. Antitumor activity. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-111508 10mg Medchemexpress, PI3K/mTOR Inhibitor-2 CAS:1848242-58-9 Purity:>98%
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Medchemexpress, HY-111508 10mg PI3K/mTOR Inhibitor-2 CAS:1848242-58-9 PI3K/mTOR Inhibitor-2 is a potent dual pan-PI3K/mTOR inhibitor with IC50s of 3.4/34/16/1 nM for PI3Kα/PI3Kβ/PI3Kδ/PI3Kγ and 4.7 nM for mTOR. Antitumor activity. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-111500 5mg Medchemexpress, NMDAR antagonist 1 CAS: Purity:>98%
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Medchemexpress, HY-111500 5mg NMDAR antagonist 1 CAS: NMDAR antagonist 1 is a potent and orally bioavailable NR2B-selective NMDAR antagonist. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-111500 10mg Medchemexpress, NMDAR antagonist 1 CAS: Purity:>98%
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Medchemexpress, HY-111500 10mg NMDAR antagonist 1 CAS: NMDAR antagonist 1 is a potent and orally bioavailable NR2B-selective NMDAR antagonist. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Accela Chembio Inc 2-bromo-6-fluorobenzonitrile | 25g | 79544-27-7 | MFCD06797753 | 97+% | Shelf Life: 1260 Days | Light Sensitive/n2
2-bromo-6-fluorobenzonitrile | 25g | 79544-27-7 | MFCD06797753 | 97+% | Shelf Life: 1260 Days | Light Sensitive/n2
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eMolecules 1-(4-Bromophenyl)-N-methylethanamine hydrochloride | 799293-97-3 | | 1g
Apollo Scientific | 1-(4-Bromophenyl)-N-methylethanamine hydrochloride | 1g | 562431081 | OR475087 | | 799293-97-3 | | 250.560 | C9H13BrClN
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eMolecules N-(2-Bromobenzyl)-N,N-dimethylethanaminium 4-methylbenzenesulfonate | 61-75-6 | MFCD00038731 | 250mg
Ambeed | N-(2-Bromobenzyl)-N,N-dimethylethanaminium 4-methylbenzenesulfonate | 250mg | 552529027 | A109533 | | 61-75-6 | MFCD00038731 | 414.360 | C18H24BrNO3S
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CPC Scientific H-Arg-DTrp-(Nme)Phe-DTrp-Leu-Met-NH2 (trifluoroacetate salt) 0.5MG
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Anticancer agent that has been developed for the treatment of small cell lung cancer.SEQUENCE: H-Arg-DTrp-(Nme)Phe-DTrp-Leu-Met-NH2 (trifluoroacetate salt)ONE-LETTER SEQUENCE: R-DTrp-(Nme)Phe-DTrp-LM-NH2MOLECULAR FORMULA: C49H66N12O6S1MOLECULAR WEIGHT: 951.21STORAGE CONDITIONS: -20 5 CCAS REGISTRY NUMBER: [115150-59-9]SYNONYMS: (Arg,D-Trp,N-Me-Phe)-Substance P (6-11), H-Arg-D-Trp-N-Me-Phe-D-Trp-Leu-Met-NHRESEARCH AREA: NeuropeptidesREFERENCES:SKU(s): SUBP-007A, SUBP-007B
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eMolecules N-(2-AMINO-4-BROMOPHENYL)ACETAMIDE | 36847-83-3 | MFCD00543484 | 1g
AstaTech | N-(2-AMINO-4-BROMOPHENYL)ACETAMIDE | 1g | 443836332 | F21313 | 95.000 | 36847-83-3 | MFCD00543484 | 229.077 | C8H9BrN2O
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000381177 BROFAROMINE 100MG
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Chemscene ChemScene | 5-Bromo-2-chloronitrobenzene | 25G | CS-W019135 | 0.98 | 16588-24-2| MFCD05863216 | 236.45
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ChemScene | 5-Bromo-2-chloronitrobenzene | 25G | CS-W019135 | 0.98 | 16588-24-2| MFCD05863216 | 236.45
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Medchemexpress LLC HY-15167A 5mg Medchemexpress, Glyoxalase I inhibitor (free base) CAS:174568-92-4 Purity:>98%
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Medchemexpress, HY-15167A 5mg Glyoxalase I inhibitor (free base) CAS:174568-92-4 Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Brophenexin free base | 1353979-43-7 | 99.2% | C11H17BrN2 | 10MG
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Brophenexin free base is a research-grade small molecule inhibitor of the NMDAR-TRPM4 interaction interface with reported neuroprotective activity in cellular and animal models. It prevents NMDA-induced neuronal death, mitigates mitochondrial dysfunction, and modulates ERK1/2 and CREB-related signaling pathways.
- High purity: 99.2% (rounded from 99.24%).
- Molecular formula C11H17BrN2; molecular weight 257.18.
- Demonstrated neuroprotective activity with reported IC50 of 2.1 μM.
- Reduces GluN2A and GluN2B interactions with TRPM4, restoring ERK1/2 activation.
- Available in small milligram quantities suitable for in vitro and in vivo studies.
- Provided as the free base form for research applications.
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