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Filtered Search Results
Medchemexpress LLC HY-10531 5mg Medchemexpress, ARRY-380 (analog ) CAS:937265-83-3 Purity:>98%
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Medchemexpress, HY-10531 5mg ARRY-380 (analog ) CAS:937265-83-3 ARRY-380 analog, an inhibitor of EGFR (ErbB1), is extracted from patent WO2015153959A2, compound 249. ARRY-380 is a potent, selective, ATP-competitive, orally active inhibitor of HER2. 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-106372A 5mg Medchemexpress, Carcainium (chloride) CAS:1042-42-8 Purity:>98%
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Medchemexpress, HY-106372A 5mg Carcainium (chloride) CAS:1042-42-8 Carcainium chloride (QX 572) is a quaternary derivative of Lidocaine. Antitussive effect. 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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Active Motif RVX-208
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Active Motif's RVX-208 is a potent BET bromodomain antagonist with (IC50 = 0.51 uM for BD2) with approximately 170-fold selectivity over BD1 (ref 1,2). It increases apolipoprotein A-1 and HDL cholesterol in vitro and in vivo, and it reduces atherosclerosis.
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Active Motif RVX-208
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Active Motif's RVX-208 is a potent BET bromodomain antagonist with (IC50 = 0.51 uM for BD2) with approximately 170-fold selectivity over BD1 (ref 1,2). It increases apolipoprotein A-1 and HDL cholesterol in vitro and in vivo, and it reduces atherosclerosis.
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eMolecules 13588-28-8 | 2-(2-Methoxypropoxy)propan-1-ol | MFCD19707082 | 100mg
Medchem Express | OSMI-1 | 5mg | 599150495 | HY-119738 | 1681056-61-0 | MFCD30187585 | 563.640 | C28H25N3O6S2
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Medchemexpress LLC HY-18256 5mg Medchemexpress, Ombrabulin (hydrochloride) CAS:253426-24-3 Purity:>98%
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Medchemexpress, HY-18256 5mg Ombrabulin (hydrochloride) CAS:253426-24-3 Ombrabulin hydrochloride is a derivative of CA-4 phosphate, which is known to exhibit antivascular effects through selective disruption of the tubulin cytoskeleton of endothelial 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 MEDCHEMEXPRESS LLC
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502082352 AZASETRON HYDROCHLO 10MG
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Medchemexpress LLC HY-70003 50mg Medchemexpress, Carboxypeptidase G2 (CPG2) Inhibitor CAS:192203-60-4 Purity:>98%
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Medchemexpress, HY-70003 50mg Carboxypeptidase G2 (CPG2) Inhibitor CAS:192203-60-4 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 HY-101976 10mg Medchemexpress, JAK3-IN-6 CAS:1443235-95-7 Purity:>98%
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Medchemexpress, HY-101976 10mg JAK3-IN-6 CAS:1443235-95-7 JAK3-IN-6 is a potent, selective irreversible Janus Associated Kinase 3 (JAK3) inhibitor, with an IC50 of 0.15 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-18957 5mg Medchemexpress, Lifirafenib CAS:1446090-79-4 Purity:>98%
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Medchemexpress, HY-18957 5mg Lifirafenib CAS:1446090-79-4 Lifirafenib (BGB-283) is a novel and potent Raf Kinase and EGFR inhibitor with IC50 values of 23 and 29 nM for recombinant BRafV600E and EGFR, respectively. 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-18936 10mg Medchemexpress, Alda-1 CAS:349438-38-6 Purity:>98%
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Medchemexpress, HY-18936 10mg Alda-1 CAS:349438-38-6 Alda-1 is a potent ALDH2 agonist, which activates wild-type ALDH2 and restores near wild-type activity to ALDH2*2. 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 Berotralstat (BCX7353) | 1809010-50-1 | MFCD33023491 | 99.7% | 562.6 g/mol | C30H26F4N6O | 5 MG
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Berotralstat is a selective, orally active plasma kallikrein inhibitor used in research and clinical development, including prophylaxis studies for hereditary angioedema and investigational work on edema and glioblastoma models. This item is provided as a research-grade solid standard (5 mg) intended for analytical, preclinical, and formulation studies, with documented batch-level characterization and supporting analytical data.
- Selective plasma kallikrein inhibitor for HAE and related research
- Supplied as a 5 mg research-grade solid suitable for analytical use
- High HPLC purity (reported ~99.7%) for reliable results
- Documented certificate of analysis and batch data available
- Suitable for biochemical assays, formulation studies, and reference standards
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Medchemexpress LLC HY-103050 5mg Medchemexpress, ML-030 CAS:1013750-77-0 Purity:>98%
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Medchemexpress, HY-103050 5mg ML-030 CAS:1013750-77-0 ML-030 is a potent PDE4 inhibitor, with IC50 of 6.7 nM, 12.9 nM, 48.2 nM, 37.2 nM, 452 nM and 49.2 nM for PDE4A, PDE4A1, PDE4B1, PDE4B2, PDE4C1,and PDE4D2, respectively. 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-Y0418 100mg Medchemexpress, Dulcite CAS:608-66-2 Purity:>98%
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Medchemexpress, HY-Y0418 100mg Dulcite CAS:608-66-2 Dulcite is a sugar alcohol with a slightly sweet taste which is a metabolic breakdown product of galactose. 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 Tivozanib hydrochloride hydrate | 682745-41-1 | 99.8% | 509.34 | 10 MM 1 ML
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Tivozanib hydrochloride hydrate is the hydrate hydrochloride form of Tivozanib. It is a selective, orally active inhibitor for vascular endothelial growth factor receptor (VEGFR)-1, 2, and 3. This compound exhibits antitumor efficacy.
- Selective, orally active inhibitor for VEGFR-1, 2, and 3
- Exhibits antitumor efficacy
- Available in solid form, white to off-white color
- Soluble in DMSO (125 mg/mL)
- Inhibits the phosphorylation of VEGFR-1, VEGFR-2, and VEGFR-3
- Inhibits VEGF-induced proliferation and migration of HUVECs
- Selectively inhibits VEGF-stimulated phosphorylation of MAPKs in endothelial cells
- Exhibits antitumor efficacy against various cancers in athymic mice models
- Reversibly suppresses vascular permeability and angiogenesis in tumor-bearing rats
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