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Filtered Search Results
Medchemexpress LLC Climbazole Standard | 38083-17-9 | 97.8% | 250 MG
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Climbazole (Standard) is the analytical standard for Climbazole. It is intended for research and analytical applications. Climbazole (BAY-e 6975) is a potent antifungal agent and also acts as a potent inducer of rat hepatic cytochrome P450.
- Analytical standard for Climbazole
- Intended for research and analytical applications
- Potent antifungal agent
- Potent inducer of rat hepatic cytochrome P450
- Used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS
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Medchemexpress LLC Methyl 12-aminododecanoate hydrochloride | 4271-86-7 | 97.0% | 265.82 g/mol | C13H28ClNO2 | 250 MG
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Methyl 12-aminododecanoate hydrochloride is the hydrochloride salt of methyl 12-aminododecanoate supplied as a solid biochemical reagent for laboratory research. It is used as a reagent, an intermediate in organic synthesis, and for biochemical assay development and reagent preparation.
- Biochemical reagent for research use.
- Hydrochloride salt, solid form.
- Molecular weight 265.82 g/mol.
- CAS number 4271-86-7.
- Typical pack sizes include 250 mg, 1 g, and 5 g.
- Reported purity approximately 97.0%.
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![Medchemexpress LLC 5,7-dichloro-[1,3]thiazolo[5,4-d]pyrimidine | 13479-88-4 | MFCD09702027 | ≥98.0% | 206.05 g/mol | C5HCl2N3S | 250 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000302375.png-250.jpg)
Medchemexpress LLC 5,7-dichloro-[1,3]thiazolo[5,4-d]pyrimidine | 13479-88-4 | MFCD09702027 | ≥98.0% | 206.05 g/mol | C5HCl2N3S | 250 MG
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5,7-Dichlorothiazolo[5,4-d]pyrimidine (CAS 13479-88-4) is a chlorinated heterocyclic building block used as an intermediate in small-molecule and medicinal chemistry synthesis. It is supplied in research-scale quantities and is offered by chemical suppliers in defined purity grades for use in route scouting and heterocycle construction.
- Used as a synthetic building block for heterocycle construction and medicinal chemistry.
- Molecular formula C5HCl2N3S and molecular weight 206.05 g/mol.
- CAS number 13479-88-4 for unambiguous identification.
- Offered in small pack sizes suitable for research (50 mg-500 mg).
- Available in high-purity grades (reported ≥98% by some suppliers).
- Supplied with standard documentation such as COA and SDS for quality verification.
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![eMolecules 842133-18-0 | Canagliflozin | Ambeed | MFCD18251436 | 444.520 | C24H25FO5S | 95.000 | Cc1ccc(cc1Cc1ccc(s1)-c1ccc(F)cc1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O | 250mg | 525189895](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000128653.jpg-250.jpg)
eMolecules 842133-18-0 | Canagliflozin | Ambeed | MFCD18251436 | 444.520 | C24H25FO5S | 95.000 | Cc1ccc(cc1Cc1ccc(s1)-c1ccc(F)cc1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O | 250mg | 525189895
Canagliflozin | Ambeed | 842133-18-0 | MFCD18251436 | 444.520 | C24H25FO5S | 95.000 | Cc1ccc(cc1Cc1ccc(s1)-c1ccc(F)cc1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O | 250mg | 525189895
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Medchemexpress LLC Copanlisib dihydrochloride | 1402152-13-9 | C23H30Cl2N8O4 | 50 MG
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Copanlisib dihydrochloride is a potent, selective, and ATP-competitive pan-class I PI3K inhibitor. It exhibits IC50 values of 0.5 nM for PI3Kα, 0.7 nM for PI3Kδ, 3.7 nM for PI3Kβ, and 6.4 nM for PI3Kγ. This compound demonstrates superior antitumor activity and shows over 2,000-fold selectivity against other lipid and protein kinases, with the exception of mTOR.
- Induces apoptosis in a subset of tumor cell lines resistant to certain treatments.
- Shows complete inhibition of PI3K-mediated AKT phosphorylation in ELT3 cells at 5 nM.
- Potently inhibits cell proliferation in various human tumor cell lines, particularly those with PIK3CA-activating mutations or HER2-positive.
- Significantly increases caspase-9 activities and levels of phosphorylated p53 at Ser15 and cleaved PARP in BT20 breast cancer cells.
- Demonstrates robust antitumor activity in rat KPL4 tumor xenograft models, with high tumor growth inhibition rates.
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eMolecules 2093388-33-9 | Medchem Express | PROTAC BET degrader-2 | 5mg | 441681950 | HY-114228 | 770.851 | C41H42N10O6
Ambeed | 4-(2-Chloro-9H-purin-6-yl)morpholine | 250mg | 627733801 | A679575 | 4010-81-5 | MFCD17430374 | 239.660 | C9H10ClN5O
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eMolecules 1616392-22-3 | GSK3326595 | MFCD29991177 | 100mg
Ambeed | (4S4S)-22-(13-Bis(4-(adamantan-1-yl)phenyl)propane-22-diyl)bis(4-phenyl-45-dihydrooxazole) | 250mg | 696731481 | A1501025 | 2248620-13-3 | 755.059 | C53H58N2O2
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Medchemexpress LLC HY-112429 10mg Medchemexpress, HJB97 CAS:2093391-24-1 Purity:>98%
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Medchemexpress, HY-112429 10mg HJB97 CAS:2093391-24-1 HJB97 is a high-affinity BET inhibitor with Kis of 0.9 nM (BRD2 BD1), 0.27 nM (BRD2 BD2), 0.18 nM (BRD3 BD1), 0.21 nM (BRD3 BD2), 0.5 nM (BRD4 BD1), 1.0 nM (BRD4 BD2), respectively. HJB97 is employed for the design of potential PROTAC BET degrader and has antitumor activity. 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 6H-Thieno[3,2-f]triazolo[4,3-a]diazepine-6-acetamide, 4-(4-chlorophenyl)-N-[6-[[[2-(2,6-dioxo | 1957234-97-7 | 99.4% | 783.29 | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000437776-Logo.png-250.jpg){kind=logo}
Medchemexpress LLC 6H-Thieno[3,2-f]triazolo[4,3-a]diazepine-6-acetamide, 4-(4-chlorophenyl)-N-[6-[[[2-(2,6-dioxo | 1957234-97-7 | 99.4% | 783.29 | 10 MG
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PROTAC BET Degrader-10 (dBET37) is a potent BET protein BRD4 degrader, connected by ligands for Cereblon and BRD4, with a DC50 of 49 nM. This compound contains two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein.
- Potent BET protein BRD4 degrader
- Utilizes the intracellular ubiquitin-proteasome system for selective degradation
- Useful for research applications
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eMolecules 55876-84-1 | Methyl-5-bromomethylpyridine-2-carboxylate | Abosyn Chemicals Inc. | MFCD07367952 | 230.061 | C8H8BrNO2 | 0.000 | COC(=O)c1ccc(CBr)cn1 | 250mg | 812068594
Methyl-5-bromomethylpyridine-2-carboxylate | Abosyn Chemicals Inc. | 55876-84-1 | MFCD07367952 | 230.061 | C8H8BrNO2 | 0.000 | COC(=O)c1ccc(CBr)cn1 | 250mg | 812068594
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![Medchemexpress LLC Poly(methyl methacrylate) | 9011-14-7 | MFCD00134349 | >98.0% | [CH2C(CH3)(CO2CH3)]n | 250 G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000285072.png-250.jpg)
Medchemexpress LLC Poly(methyl methacrylate) | 9011-14-7 | MFCD00134349 | >98.0% | [CH2C(CH3)(CO2CH3)]n | 250 G
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Poly(methyl methacrylate) (PMMA) is an amorphous thermoplastic polymer provided as solid beads for research applications. It is commonly used as a material for fabrication of microfluidic chips and optical components, and is supplied as a white to off-white solid.
- Solid beads suitable for molding and microfabrication
- White to off-white appearance
- Used for production of microfluidic chips and optical parts
- Chemical formula: [CH2C(CH3)(CO2CH3)]n; CAS 9011-14-7
- Storage: 4°C under nitrogen; in solvent store at -80°C (6 months) or -20°C (1 month)
- Available in multiple pack sizes: 100 G, 250 G, 500 G, 1 KG
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Medchemexpress LLC Balofloxacin | 127294-70-6 | 98.3% | 250 MG
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Balofloxacin is an orally active fluoroquinolone antibiotic that exhibits broad-spectrum antibacterial activity against gram-negative, gram-positive, and anaerobic bacteria. It can be used for the research of respiratory, intestinal, and urinary tract infections.
- Orally active fluoroquinolone antibiotic
- Broad-spectrum antibacterial activity against gram-negative, gram-positive, and anaerobic bacteria
- Can be used for research of respiratory, intestinal, and urinary tract infections
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Medchemexpress LLC Ferrocenylmethyltrimethylammonium iodide | 12086-40-7 | MFCD00041534 | >98.5% | 385.08 g·mol^-1 | C14H20FeIN | 250 MG
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Ferrocenylmethyltrimethylammonium iodide is an organometallic quaternary ammonium salt used as a biochemical reagent and synthetic intermediate in organic and materials research. It is a crystalline iodide salt with molecular formula C14H20FeIN and molecular weight about 385.08 g·mol^-1; common applications include use as a reagent, catalyst, and precursor for organometallic synthesis and electrochemical studies.
- High purity reagent suitable for research applications.
- Useful as a reagent and phase-transfer catalyst in organic synthesis.
- Serves as a synthetic intermediate for organometallic compounds.
- Useful for electrochemical and materials research because of ferrocenyl redox properties.
- Store protected from light at 4°C; in solution, store at -80°C for long-term stability.
- Typically supplied in 250 mg laboratory quantities.
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Medchemexpress LLC Histamine H4 receptor antagonist-1 | 1246207-84-0 | 99.57% | C30H38N8O2 | 50 MG
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Histamine H4 receptor antagonist-1 is an antagonist of histamine H4 receptor extracted from patent WO2010108059A1 compound 60.
- For research use only.
- We do not sell to patients.
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Medchemexpress LLC Pomalidomide-coch2cl | 444287-84-7 | 97.0% | 349.73 g/mol | C15H12ClN3O5 | 250 MG
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Pomalidomide-COCH2Cl is a synthetic derivative of pomalidomide bearing a chloroacetamide substituent on the benzyl ring. It is used as an E3 ligase ligand in PROTAC research and is supplied as a powder for laboratory research. Typical properties include molecular formula C15H12ClN3O5, molecular weight 349.73 g/mol, and a reported purity of 97.0%.
- Derivative designed for E3 ligase binding in PROTAC applications.
- Supplied as a stable powder suitable for long-term storage at low temperature.
- Reported purity 97.0% to support analytical and synthetic workflows.
- Molecular weight 349.73 g/mol and formula C15H12ClN3O5 for accurate formulation.
- Certificate of analysis available for batch-specific quality data.
- Intended for research use only; not for human or clinical use.
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