Carboxylic acids and derivatives
Medchemexpress LLC 2-Bromoacetamide | 683-57-8 | 8025 | 137.96 | 50 G
2-Bromoacetamide is a disinfection byproduct known to inactivate liver alcohol dehydrogenase and interfere with microtubule and actin cytoskeletal function. It has also been identified as a potent developmental toxicant in animals.
- Inactivates liver alcohol dehydrogenase
- Interferes with microtubule and actin cytoskeletal function
- Functions as a potent developmental toxicant in animals
- Reduces egg cylinder formation rate in mouse embryos (in vitro)
- Disrupts cell lineage differentiation in mouse embryos (in vitro)
- Reduces first polar body extrusion rate in mouse and human oocytes (in vitro)
- Disrupts spindle structure in mouse and human oocytes (in vitro)
eMolecules 91726-43-1 | 3-Hydroxy-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester | J&W PharmLab LLC | MFCD24445501 | 231.248 | C10H17NO5 | 96.000 | CC(C)(C)OC(=O)N1CCC(O)C1C(O)=O | 1g | 571067487
3-Hydroxy-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester | J&W PharmLab LLC | 91726-43-1 | MFCD24445501 | 231.248 | C10H17NO5 | 96.000 | CC(C)(C)OC(=O)N1CCC(O)C1C(O)=O | 1g | 571067487
Medchemexpress LLC Tetraiodothyroacetic acid | 67-30-1 | >99.2% | 747.83 | 5 MG
Tetrac (Tetraiodothyroacetic acid) is a derivative of L-thyroxine (T4) and acts as a thyrointegrin receptor antagonist. It blocks the actions of T4 and 3,5,3'-triiodo-L-thyronine (T3) at the cell surface receptor for thyroid hormone on integrin αvβ3.
- Exhibits anti-angiogenic activity.
- Exhibits anti-tumor activity.
eMolecules 76379-01-6 | Ambeed | (R)-2-((tert-Butoxycarbonyl)amino)-5-methoxy-5-oxopentanoic acid | 5g | 536283451 | A1141631 | MFCD00136803 | 261.274 | C11H19NO6
Ambeed | (R)-2-((tert-Butoxycarbonyl)amino)-5-methoxy-5-oxopentanoic acid | 5g | 536283451 | A1141631 | 76379-01-6 | MFCD00136803 | 261.274 | C11H19NO6
eMolecules 133812-16-5 | Medchem Express | (E/Z)-Locostatin | 5mg | 788478648 | HY-W013411 | MFCD00278769 | 245.278 | C14H15NO3
Medchem Express | SAHA chloroalkane T1 | 5mg | 455326012 | HY-111595 | 1613617-05-2 | 719.270 | C33H55ClN4O11
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![eMolecules 2173996-97-7 | RAC-(1R,5R)-2-(TERT-BUTOXYCARBONYL)-2-AZABICYCLO[3.1.0]HEXANE-5-CARBOXYLIC ACID | AstaTech227.260 | C11H17NO4 | 95.000 | CC(C)(C)OC(=O)N1CC[C@]2(C[C@@H]12)C(O)=O | 0.1g | 521520023](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502481001.JPG-250.jpg)
eMolecules 2173996-97-7 | RAC-(1R,5R)-2-(TERT-BUTOXYCARBONYL)-2-AZABICYCLO[3.1.0]HEXANE-5-CARBOXYLIC ACID | AstaTech227.260 | C11H17NO4 | 95.000 | CC(C)(C)OC(=O)N1CC[C@]2(C[C@@H]12)C(O)=O | 0.1g | 521520023
RAC-(1R,5R)-2-(TERT-BUTOXYCARBONYL)-2-AZABICYCLO[3.1.0]HEXANE-5-CARBOXYLIC ACID | AstaTech | 2173996-97-7227.260 | C11H17NO4 | 95.000 | CC(C)(C)OC(=O)N1CC[C@]2(C[C@@H]12)C(O)=O | 0.1g | 521520023
![Medchemexpress LLC 6-[2-(2,4-difluorophenoxy)-5-(ethylsulfonylmethyl)-3-pyridinyl]-8-methyl-2H-pyrrolo[1,2-a]pyrazin-1-on | 2411226-02-1 | 99.9% | 459.47 g·mol⁻¹ | C22H19F2N3O4S | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000262234.png-250.jpg)
Medchemexpress LLC 6-[2-(2,4-difluorophenoxy)-5-(ethylsulfonylmethyl)-3-pyridinyl]-8-methyl-2H-pyrrolo[1,2-a]pyrazin-1-on | 2411226-02-1 | 99.9% | 459.47 g·mol⁻¹ | C22H19F2N3O4S | 5 MG
BET bromodomain inhibitor 1 is a selective, orally active inhibitor of bromodomain and extra-terminal (BET) proteins with potent activity against BRD4 (IC50 = 2.6 nM). Supplied as a white to off-white solid with high purity, it is used in epigenetic target validation and anticancer mechanism research.
- Potent BRD4 inhibition (IC50 2.6 nM).
- Low-nanomolar binding to BET family bromodomains.
- High purity suitable for research (99.9%).
- Soluble in DMSO at 100 mg/mL with warming and sonication.
- Stable when stored as a powder at -20°C for long-term storage.
Medchemexpress LLC Arimoclomol citrate | 368860-21-3 | 99.8% | 505.90 g·mol⁻¹ | C20H28ClN3O10 | 1 ML
Arimoclomol citrate is the citrate salt of arimoclomol, a heat-shock protein (HSP) co-inducer used in research to enhance Hsp expression, reduce protein aggregation, and study neurodegenerative conditions such as Niemann-Pick disease type C. Supplied for in vitro and preclinical laboratory work, it is available as a solution in DMSO and in multiple solid pack sizes.
- High reported purity (99.8%).
- Supplied as a 10 mM solution in DMSO for ready use.
- Also available in solid form for flexible dosing and formulation.
- Molecular weight 505.90 g·mol⁻¹ for stoichiometric calculations.
- Facilitates studies of Hsp induction and protein aggregation.
- Suitable for in vitro and preclinical model applications.
eMolecules 524-38-9 | N-HYDROXYPHTHALIMIDE | AstaTech | MFCD00005891 | 163.132 | C8H5NO3 | 98.000 | ON1C(=O)c2ccccc2C1=O | 25g | 718057530
N-HYDROXYPHTHALIMIDE | AstaTech | 524-38-9 | MFCD00005891 | 163.132 | C8H5NO3 | 98.000 | ON1C(=O)c2ccccc2C1=O | 25g | 718057530
Medchemexpress LLC BGT226 (maleate) | 1245537-68-1 | MFCD22124895 | 99.9% | 650.60 g/mol | C32H29F3N6O6 | 5 MG
BGT226 maleate is a small-molecule PI3K/mTOR dual inhibitor used for research into PI3K signaling and oncology. It shows low-nanomolar potency against PI3K isoforms and mTOR and is used in cell-based and preclinical studies to evaluate antiproliferative and apoptotic effects.
- Inhibits PI3Kα, PI3Kβ, PI3Kγ, and mTOR.
- Exhibits low nanomolar potency in enzymatic assays.
- Demonstrates growth-inhibitory activity in cancer cell models.
- Supplied as the maleate salt for stability.
- High purity suitable for biochemical and cellular assays.
- Available in multiple small pack sizes for research use.