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Filtered Search Results
Medchemexpress LLC HY-14806 10mg Medchemexpress, Teneligliptin CAS:760937-92-6 Purity:>98%
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Medchemexpress, HY-14806 10mg Teneligliptin CAS:760937-92-6 Teneligliptin (MP-513) is a potent, orally available, competitive, and long-lasting DPP-4 inhibitor. Teneligliptin competitively inhibits human plasma, rat plasma, and human recombinant DPP-4 in vitro, with IC50s of approximately 1 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 AZD5582 DIHYDROCHLORIDE 5MG
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cas no:1883545-51-4, 98.67% purity
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Medchemexpress LLC HY-17405 100mg , Alarelin (Acetate) Alarelin CAS:79561-22-1 Purity:98%
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Medchemexpress, HY-17405 100mg Alarelin (Acetate) Alarelin CAS:79561-22-1 Formula:C60H86N16O16 Purity:98% Alarelin acetate is a synthetic GnRH agonist. 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 PMX 205 Trifluoroacetate | 99.5% | 953.06 | 50 MG
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PMX 205 Trifluoroacetate | 99.5% | 953.06 | 50 MG
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Medchemexpress LLC OT-82 | 1800487-55-1 | 99.9% | 424.47 | 100 MG
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OT-82 is a potent, selective, and orally active inhibitor of NAMPT. It is selectively toxic to cells of hematopoietic origin and induces cell death in a NAD+ dependent manner, making it a promising antineoplastic agent for the study of hematological malignancies. This product is for research use only.
- Potent, selective, and orally active NAMPT inhibitor.
- Selectively toxic to cells of hematopoietic origin.
- Induces cell death in a NAD+ dependent manner.
- Promising antineoplastic agent for hematological malignancies.
- Exhibits hallmarks of apoptotic cell death.
- Inhibits recombinant NAMPT activity and reduces cellular NAD and ATP concentrations.
- Potently inhibited tumor growth in a multiple myeloma mouse model.
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Selleck Chemical LLC Ombitasvir (ABT-267) S5403-5mg
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Ombitasvir (ABT-267) is an inhibitor of the HCV non-structural protein 5A with antiviral activity
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![eMolecules Medchem Express / PROTAC BRD4 Degrader-5-CO-PEG3-N3 / 10mg / 559839675 / HY-133736 / / 2704602-92-4 / [null] / 1231.880 / C58H75ClN12O12S2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502480797.JPG-250.jpg)
eMolecules Medchem Express / PROTAC BRD4 Degrader-5-CO-PEG3-N3 / 10mg / 559839675 / HY-133736 / / 2704602-92-4 / [null] / 1231.880 / C58H75ClN12O12S2
Medchem Express / PROTAC BRD4 Degrader-5-CO-PEG3-N3 / 10mg / 559839675 / HY-133736 / / 2704602-92-4 / [null] / 1231.880 / C58H75ClN12O12S2
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Innovative Research Inc Rat PAI1 Rcmb WT Act HIS lbl
Rat PAI-1 Recombinant Wild Type Active HIS Labeled 1 mg - Rat PAI-1 Recombinant Wild Type Active HIS Labeled from Innovative Research has been recombinantly produced in E. coli and purified by a propritetary process that combines multiple conventional chromatographic methods. This is a Frozen liquid buffered in 0.05M Sodium Acetate; 0.1M NaCl; 1mM EDTA; pH 5.0 and a purity of >95% as determined by SDS-PAGE. N-terminus of (wild type) rat PAI-1 tagged with 6x-HIS, allowing immobilization of functionally active PAI-1 onto surfaces such as metal chelate microtiter plates or Ni+2 resins. This is an active fraction that is more than 99% pure and 98% active (determined by SDS-PAGE). This product can be used as a control in applications like ELISA and Western Blot, as well as blocking/inhibition, fibrinolysis, plasminogen activation, receptor binding, in hypertension studies, and for protein-protein interactions
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eMolecules Medchem Express / KCC-07 / 5mg / 591911976 / HY-131031 / / 315702-75-1 / MFCD01121976 / 269.320 / C14H11N3OS
Medchem Express / KCC-07 / 5mg / 591911976 / HY-131031 / / 315702-75-1 / MFCD01121976 / 269.320 / C14H11N3OS
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Medchemexpress LLC FABPs ligand 6 | 2988135-14-2 | 99.9% | C28H27FN2O3 | 100 MG
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FABPs ligand 6 (MF6) is an FABP5 and FABP7 inhibitor with KD values of 874 nM for FABP5 and 20 nM for FABP7. This compound rescues mitochondrial function by blocking voltage-dependent anion channel (VDAC)-1-dependent mitochondrial macropore formation, a mechanism involved in FABP5-mediated injury. It can be used for multiple sclerosis research, improving EAE severity and attenuating oxidative levels and inflammatory responses in mouse models.
- FABP5 and FABP7 inhibitor
- Rescues mitochondrial function
- Attenuates oxidative levels
- Inhibits inflammatory responses
- Protects oligodendrocytes
- Suitable for multiple sclerosis research
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Medchemexpress LLC (rel)-PROTAC ERRα degrader-1 | 00-00-0 | 98.2% | 1108.92 g/mol | C54H49Cl2F6N7O8 | 5 MG
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(rel)-PROTAC ERRα Degrader-1 is a proteolysis-targeting chimera designed to induce degradation of estrogen-related receptor alpha (ERRα). The molecule combines an MDM2 ligand, a linker, and an ERRα-binding moiety and is supplied as a solid research reagent for laboratory studies.
- Induces degradation of estrogen-related receptor alpha (ERRα).
- PROTAC mechanism combining an MDM2 ligand and an ERRα-binding moiety.
- Molecular weight 1108.92 g/mol.
- Purity 98.18%.
- Solid form, off-white to light yellow.
- Supplied as a 5 mg research-use-only sample.
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Medchemexpress LLC HY-12111 5mg Medchemexpress, BMS-564929 CAS:627530-84-1 Purity:>98%
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Medchemexpress, HY-12111 5mg BMS-564929 CAS:627530-84-1 BMS-564929 is an androgen receptor (AR) agonist, binds to androgen receptor (AR) with a Ki of 2.11±0.16 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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![eMolecules Medchem Express / PROTAC ER Degrader-2 / 5mg / 482204010 / HY-111846 / / 1351169-29-3 / [null] / 763.977 / C42H61N5O8](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502481150.JPG-250.jpg)
eMolecules Medchem Express / PROTAC ER Degrader-2 / 5mg / 482204010 / HY-111846 / / 1351169-29-3 / [null] / 763.977 / C42H61N5O8
Medchem Express / PROTAC ER Degrader-2 / 5mg / 482204010 / HY-111846 / / 1351169-29-3 / [null] / 763.977 / C42H61N5O8
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Medchemexpress LLC HY-113534 10mg Medchemexpress, MV1 CAS:1001600-54-9 Purity:>98%
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Medchemexpress, HY-113534 10mg MV1 CAS:1001600-54-9 MV1 is an antagonist of IAP (inhibitor of apoptosis protein), leads to protein knockdown of HaloTag-fused proteins when combined with HaloTag ligand. 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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Innovative Research Inc Ms tPA Rcmb Act 100ug
Mouse tPA Recombinant Active 100ug - Mouse tPA Active Recombinant from Innovative Research has been recombinantly produced in insect cells and purified using affinity chromatography. This is a frozen liquid buffered in 0.4M HEPES; 0.1M NaCl; pH 7.4 and a purity of >95%. This product is useful as a positive control for ELISA and western blot and for a variety of in vitro applications including cell differentiation, cell signaling, clotting assays, fibrinolysis, plasminogen activation, protein-protein interactions, receptor binding, thromboelastography, and thrombolysis. >95% active. More Details Source Insect Cell Culture Purification Affinity purified Purity >95% Storage Conditions -70C
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