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Filtered Search Results
Medchemexpress LLC (1S,2S,3R)-DT-061 | 1809427-20-0 | 99.8% | 520.52 | 25 MG
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(1S,2S,3R)-DT-061 is an enantiomer of DT-061 and an orally active activator of protein phosphatase 2A (PP2A). It can be utilized as a negative control in research pertaining to KRAS-mutant and MYC-driven lung cancer tumorigenesis.
- Orally active activator of protein phosphatase 2A (PP2A).
- Can be utilized as a negative control in research.
- Potential application in therapy of KRAS-mutant and MYC-driven tumorigenesis.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000382039 RAC -3-O-METHYL DOP 1MG
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Apexbio Technology LLC (Rac)-Indoximod 26988-72-7 100mg
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(Rac)-Indoximod (CAS 26988-72-7) also known as 1-Methyl-DL-tryptophan is an inhibitor of indoleamine 2 3-dioxygenase (IDO) an enzyme involved in tryptophan catabolism and immune modulation By disrupting IDO-mediated metabolic pathways (Rac)-Indoximod modulates cellular immune responses In human cardiac fibroblast models co-treatment with (Rac)-Indoximod and IFN- reduces -SMA expression and suppresses fibroblast activation This combination also promotes apoptosis via upregulation of IRF-1 Fas and FasL gene expression The compound serves as a valuable tool for studies on IDO regulation and immune cell function
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000379872 RAC -BENPYRINE 1MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000371925 ALP CARBONIC ANHYDRA 25MG
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![eMolecules Medchem Express / MV1 / 5mg / 459606864 / HY-113534 / / 1001600-54-9 / [null] / 576.738 / C33H44N4O5](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502468537.JPG-250.jpg)
eMolecules Medchem Express / MV1 / 5mg / 459606864 / HY-113534 / / 1001600-54-9 / [null] / 576.738 / C33H44N4O5
Medchem Express / MV1 / 5mg / 459606864 / HY-113534 / / 1001600-54-9 / [null] / 576.738 / C33H44N4O5
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Sigma Aldrich Fine Chemicals Biosciences Ramipril impurity A European Pharmacopoeia (EP) Reference Standard | 108313-11-7 |
Ramipril impurity A European Pharmacopoeia (EP) Reference Standard | Mol Wt: 402.48 | 108313-11-7 |
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Medchemexpress LLC HY-100207 5mg Medchemexpress, CP21R7 CAS:125314-13-8 Purity:>98%
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Medchemexpress, HY-100207 5mg CP21R7 CAS:125314-13-8 CP21R7 is potent GSK-3β inhibitor, with an IC 50 of 1.8 nM; CP21R7 also shows inhibitory activitiy against PKCα , with an IC 50 of 1900 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 / BMS-813160 / 5mg / 446259618 / HY-109593 / / 1286279-29-5 / [null] / 484.649 / C25H40N8O2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502469161.JPG-250.jpg)
eMolecules Medchem Express / BMS-813160 / 5mg / 446259618 / HY-109593 / / 1286279-29-5 / [null] / 484.649 / C25H40N8O2
Medchem Express / BMS-813160 / 5mg / 446259618 / HY-109593 / / 1286279-29-5 / [null] / 484.649 / C25H40N8O2
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Innovative Research Inc Ms PAI1 Rcmb WT Act 500ug
Mouse PAI-1 Recombinant Wild Type Active 500 ug - Mouse PAI-1 Recombinant Wild Type Active from Innovative Research has been recombinantly produced in E. coli and purified by affinity chromatography. This is a Frozen liquid buffered in 0.05M Sodium Acetate; 0.4M NaCl; 1mM EDTA; pH 5.0 and a purity of >95% as determined by SDS-PAGE. More Details Species Mouse Target PAI-1 Purification Method Affinity purified Purity 95% as determined by SDS-PAGE Source E. coli Storage Conditions -70 C Additional Information Active fraction contains between 30% and 70% active PAI-1. This product can be used as a control in applications like ELISA and Western Blot. It can be used for a wide range of in vitro applications, including fibrinolysis, hypertension studies, inhibition, plasminogen activation, protein-protein interactions, receptor binding, and more. For Research Use Only.
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Medchemexpress LLC cis-aconitic acid | 585-84-2 | MFCD00063184 | >98.0% | 174.11 g/mol | C6H6O6 | 50 MG
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(Z)-Aconitic acid (cis-aconitic acid) is the cis-isomer of aconitic acid, an unsaturated tricarboxylic acid (C6H6O6, MW 174.11 g/mol). It is used as an analytical standard and research reagent in metabolic and enzymatic studies, and as a reference for assay development and validation.
- Acts as a glutamate decarboxylase inhibitor.
- Used as an analytical standard for assay calibration and method validation.
- High purity suitable for research and analytical applications.
- Defined chemical identity: C6H6O6, 174.11 g/mol.
- Applicable in metabolic and enzymatic studies.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000430161 CY7.5 MALEIMIDE 1MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000430836 Z -INDIRUBIN 1G
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Medchemexpress LLC Protac SGK3 degrader-1 (synonyms: SGK3-PROTAC1) | 2381320-35-8 | 99.9% | 1157.38 g·mol-1 | C57H73FN10O11S2 | 5MG
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PROTAC SGK3 degrader-1 is a VHL-ligand based proteolysis targeting chimera designed to induce ubiquitin-proteasome-mediated degradation of SGK3. Supplied as a solid for research use, it is characterized by analytical methods for identity and purity and is intended for cellular degradation studies, chemical biology, and mechanistic investigation of SGK3 signaling.
- Induces degradation of SGK3 in cell-based assays.
- Characterized by molecular formula C57H73FN10O11S2 and molecular weight 1157.38 g·mol-1.
- High purity suitable for biochemical and cellular studies.
- Supplied in small research pack sizes for laboratory use.
- Analytical data such as NMR and HPLC provided to support identity and purity.
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Medchemexpress LLC (rac)-AR-13503 ((rac)-AR-13324 M1 metabolite) | 1254032-16-0 | 99.1% | 321.37 g/mol | C19H19N3O2 | 5MG
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(rac)-AR-13503 is a small-molecule ROCK/PKC inhibitor and an active metabolite of netarsudil. It inhibits angiogenesis, enhances retinal pigment epithelium (RPE) barrier function, and reduces aberrant neovascularization in preclinical models. The compound is provided as a high-purity research-grade solid for in vitro and in vivo studies.
- Inhibits ROCK and PKC signaling.
- Reduces angiogenesis and aberrant neovascularization in animal models.
- Enhances retinal pigment epithelium barrier function in dose-dependent assays.
- Active in vitro with HUVEC tube formation IC50 of approximately 21 nM.
- Provided as a high-purity research compound suitable for biological assays.
- Available in multiple small-mass package sizes for laboratory use.
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