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Filtered Search Results
Chemscene ChemScene | 3-Bromophenethyl alcohol | 100G | CS-W007864 | 0.98 | 28229-69-8| MFCD00191857 | 201.063
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ChemScene | 3-Bromophenethyl alcohol | 100G | CS-W007864 | 0.98 | 28229-69-8| MFCD00191857 | 201.063
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Medchemexpress LLC ICAM-1-IN-1 50mg | 50mg
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ICAM-1-IN-1 is a potent and selective inhibitor of E-selectin and ICAM-1 with IC50 values of 7 and 5 nM respectively
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eMolecules METHYL 3-(4-BROMOPHENYL)-3-HYDROXYCYCLOBUTANE-1-CARBOXYLATE | 1555708-89-8 | | 1g
AstaTech | METHYL 3-(4-BROMOPHENYL)-3-HYDROXYCYCLOBUTANE-1-CARBOXYLATE | 1g | 480079932 | 58093 | 90.000 | 1555708-89-8 | | 285.137 | C12H13BrO3
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eMolecules 4-Amino-3-bromo-5-nitrobenzoic acid | 556651-33-3 | MFCD00507339 | 1g
Combi-Blocks | 4-Amino-3-bromo-5-nitrobenzoic acid | 1g | 117520208 | AN-2796 | 98.000 | 556651-33-3 | MFCD00507339 | 261.031 | C7H5BrN2O4
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eMolecules 3-Bromo-5-(trifluoromethoxy)phenylboronic acid | 1072951-48-4 | MFCD11504853 | 1g
Combi-Blocks | 3-Bromo-5-(trifluoromethoxy)phenylboronic acid | 1g | 117523984 | BB-5332 | 97.000 | 1072951-48-4 | MFCD11504853 | 284.820 | C7H5BBrF3O3
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Medchemexpress LLC HY-124540B 5mg Medchemexpress, (Rac)-ABT-202 (dihydrochloride) CAS:1258641-38-1 Purity:>98%
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Medchemexpress, HY-124540B 5mg (Rac)-ABT-202 (diHCl) CAS:1258641-38-1 (Rac)-ABT-202 dihydrochloride is a racemate of ABT-202. ABT-202 is an agonistor of nicotinic acetylcholine receptors (nAChRs) and can be used as an analgesic. 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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eMolecules 3-(3-Bromophenyl)-5-(dichloromethyl)-1,2,4-oxadiazole | 1150164-54-7 | MFCD12026023 | 1g
Combi-Blocks | 3-(3-Bromophenyl)-5-(dichloromethyl)-1,2,4-oxadiazole | 1g | 117530761 | HC-2518 | 98.000 | 1150164-54-7 | MFCD12026023 | 307.960 | C9H5BrCl2N2O
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Sigma Aldrich Fine Chemicals Biosciences P7C3 >=98% (HPLC) | 301353-96-8 | MFCD00572918 | 5MG
P7C3 >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 474.19 | 301353-96-8 | MFCD00572918 | 5MG
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Medchemexpress LLC HY-103161 5mg Medchemexpress, ABT-702 dihydrochloride CAS:1188890-28-9 Purity:>98%
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Medchemexpress, HY-103161 5mg ABT-702 diHCl CAS:1188890-28-9 ABT-702 dihydrochloride is a potent adenosine kinase (AK) inhibitor (IC50=1.7 nM). 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-107675 5mg Medchemexpress, Desformylflustrabromine hydrochloride CAS:951322-11-5 Purity:>98%
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Medchemexpress, HY-107675 5mg Desformylflustrabromine HCl CAS:951322-11-5 Desformylflustrabromine hydrochloride is a selective agonist of α4β2 neuronal nicotinic acetylcholine receptor (nAChR) with a pEC50 of 6.48. 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-107523A 5mg Medchemexpress, WAY-213613 (hydrochloride) CAS: Purity:>98%
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Medchemexpress, HY-107523A 5mg WAY-213613 (HCl) CAS: WAY-213613 hydrochloride is a potent, selective nonsubstrate reuptake inhibitor of GLT-1/EAAT2 with IC50 of 85 nM EAAT2. It displays 59- and 44-fold selectivity over EAAT1 and EAAT3 (IC50s are 5 and 3.8 μM, respectively). WAY-213613 hydrochloride shows no activity at ionotropic and metabotropic glutamate receptors. It is a potential tool for the elucidation of EAAT2 function. 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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Medchemexpress LLC HY-103269 100mg Medchemexpress, BAI1 CAS:335165-68-9 Purity:>98%
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Medchemexpress, HY-103269 100mg BAI1 CAS:335165-68-9 BAI1 is a direct allosteric inhibitor of BAX. 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-12379 5mg Medchemexpress, NS-2028 CAS:204326-43-2 Purity:>98%
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Medchemexpress, HY-12379 5mg NS-2028 CAS:204326-43-2 NS-2028 is a highly selective soluble Guanylyl Cyclase (sGC) inhibitor with IC50 values of 30 nM and 200 nM for basal and NO-stimulated enzyme activity. NS-2028 inhibits soluble Guanylyl Cyclase activity in homogenates of mouse cerebellum and neuronal NO synthase with IC50 values of 17 nM and 20 nM. NS-2028 inhibits 3-morpholino-sydnonimine (SIN-1)-elicited formation of cyclic GMP in human cultured umbilical vein endothelial cells with an IC50 of 30 nM. NS-2028 is commonly used in the research of nitric oxide signaling pathways, it inhibits NO-dependent relaxant responses in non-vascular smooth muscle completely (1 μM). NS-2028 reduces vascular endothelial growth factor-induced angiogenesis and permeability. 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-113960 10mg Medchemexpress, ERRα antagonist-1 CAS:1072145-33-5 Purity:>98%
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Medchemexpress, HY-113960 10mg ERRα antagonist-1 CAS:1072145-33-5 ERRα antagonist-1 (Compound A) is a selective and high affinity estrogen-related receptor α (ERRα) antagonist. ERRα antagonist-1 inhibits interaction of ERRα with Proliferator-activated Receptor γ Coactivator-1α (PGC-1α) and PGC-1β, the IC50 values are 170 nM and 180 nM, respectively. ERRα antagonist-1 does not inhibit the interaction of either ERRβ or ERRγ with PGC-1α and PGC-1β coactivator, and also does not inhibit interaction of ERα or ERβ with PGC-1α or SRC-1. 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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