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Filtered Search Results
Medchemexpress LLC HY-100848 10mg Medchemexpress, TX1-85-1 CAS:1603845-32-4 Purity:>98%
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Medchemexpress, HY-100848 10mg TX1-85-1 CAS:1603845-32-4 TX1-85-1 is an irreversible Her3 (ErbB3) inhibitor with an IC 50 of 23 nM and is also the first selective Her3 ligand , which forms a covalent bond with Cys721 located in the ATP-binding site of Her3. TX1-85-1 induces partial degradation of Her3 protein and attenuates Her3-dependent signaling [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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eMolecules 57120-36-2 | 4-TERT-BUTOXYANILINE | AstaTech | MFCD11196184 | 165.236 | C10H15NO | 95.000 | CC(C)(C)Oc1ccc(N)cc1 | 0.25g | 721956548
4-TERT-BUTOXYANILINE | AstaTech | 57120-36-2 | MFCD11196184 | 165.236 | C10H15NO | 95.000 | CC(C)(C)Oc1ccc(N)cc1 | 0.25g | 721956548
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Aobchem AOBCHEM
5000944746 4 -PHENOXY- 1 1 -BIPHENYL -4-C
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Medchemexpress LLC HY-101088 5mg Medchemexpress, CeMMEC13 CAS:1790895-25-8 Purity:>98%
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Medchemexpress, HY-101088 5mg CeMMEC13 CAS:1790895-25-8 CeMMEC13 is a potent inhibitor of TAF1 (2) bromodomain, with an IC 50 of 2.1 μM. 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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Apexbio Technology LLC JNJ0966 5MG
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JNJ0966 5MG APEXBIO TECHNOLOGIES
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Medchemexpress LLC Sb-3Ct 10 Mm 1 Ml In Dmso | HY-12354
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Sb-3Ct 10 Mm 1 Ml In Dmso
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eMolecules 1879887-96-3 | Medchem Express | LTURM34 | 5mg | 446257094 | HY-101667 | MFCD30536366 | 414.48 | C24H18N2O3S
Medchem Express | ZIM | 5mg | 788478523 | HY-152246 | 301298-87-3 | 349.390 | C20H19N3O3
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Medchemexpress LLC TP-004 | 1454299-21-8 | 99.2% | 10 MG
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TP-004 is a small-molecule chemical probe that potently and reversibly inhibits methionine aminopeptidase 2 (MetAP2) with an IC50 of 6 nM. It is supplied as a high-purity solid for biochemical and cellular research.
- Potent, reversible MetAP2 inhibition with IC50 = 6 nM.
- High purity suitable for research (≈99.2%).
- Molecular weight 363.34 g·mol⁻¹; formula C17H16F3N5O.
- Provided as a small solid quantity for in vitro and cellular studies.
- Useful as a chemical probe for MetAP2 target validation and pathway studies.
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eMolecules 1445703-64-9 | Medchem Express | TFMB-(S)-2-HG | 5mg | 719836548 | HY-129079A | 288.222 | C13H11F3O4
Ambeed | 14-Diazaspiro[4.5]decan-2-one | 100mg | 627733795 | A661361 | 19718-88-8 | MFCD14584836 | 154.213 | C8H14N2O
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eMolecules 21498-08-8 | Medchem Express | Lofexidine (hydrochloride) | 50mg | 482204536 | HY-B1052 | MFCD00917022 | 295.59 | C11H13Cl3N2O
Ambeed | 2-((25-Dioxopyrrolidin-1-yl)oxy)-13-dimethyl-3456-tetrahydropyrimidin-1-ium hexafluorophosphate(V) | 1g | 682929939 | A216375 | 443305-33-7 | MFCD11615809 | 371.220 | C10H16F6N3O3P
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Apexbio Technology LLC Chlorzoxazone 95-25-0 5g
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Chlorzoxazone (CAS 95-25-0) is a small molecule that functions as a centrally acting skeletal muscle relaxant It exerts its pharmacological effects by modulating synaptic transmission within the spinal cord resulting in reduced muscle spasticity In biomedical research chlorzoxazone is frequently employed as a selective probe substrate for cytochrome P450 2E1 (CYP2E1) in human liver microsomes facilitating the assessment of hepatic CYP2E1 activity and drug metabolism This compound is valuable for investigating drug-drug interactions and metabolic profiling involving CYP2E1
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Medchemexpress LLC HY-101106 5mg Medchemexpress, AR7 CAS:80306-38-3 Purity:>98%
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Medchemexpress, HY-101106 5mg AR7 CAS:80306-38-3 AR7 is a retinoic acid receptor α ( RARα ) 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 MEDCHEMEXPRESS LLC
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5000378998 MAO-B-IN-2 50MG
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Aobchem AOBCHEM
5001025544 1-ETHENYL-3 5-DIMETHOXYBENZENE
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Medchemexpress LLC Neuromedin N (swine spinal cord), 2-L-lysine-, triacetate (salt) | 141863-45-8 | 99.69% | 807.03 | 5 MG
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JMV 449 acetate is a potent neurotensin receptor agonist. It has an IC50 of 0.15 nM for inhibiting 125I-neurotensin binding to neonatal mouse brain and an EC50 of 1.9 nM in contracting the guinea-pig ileum. This compound also exhibits highly potent and long-lasting hypothermic and analgesic effects in mice.
- Potent neurotensin receptor agonist
- IC50 of 0.15 nM for inhibiting 125I-neurotensin binding to neonatal mouse brain
- EC50 of 1.9 nM in contracting the guinea-pig ileum
- Highly potent and long-lasting hypothermic effects
- Highly potent and long-lasting analgesic effects
- Shows analgesic effect in male Swiss albino mice
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