Carboxylic acids and derivatives
eMolecules 1664-34-2 | 1-Amino-cyclohexanecarboxylic acid ethyl ester | J & W PharmLab, LLC | MFCD10566110 | 171.240 | C9H17NO2 | 96.000 | CCOC(=O)C1(N)CCCCC1 | 5g | 249973556
1-Amino-cyclohexanecarboxylic acid ethyl ester | J & W PharmLab, LLC | 1664-34-2 | MFCD10566110 | 171.240 | C9H17NO2 | 96.000 | CCOC(=O)C1(N)CCCCC1 | 5g | 249973556
eMolecules 1505453-59-7 | Medchem Express | BET bromodomain inhibitor | 5mg | 446257919 | HY-103036 | MFCD28144506 | 445.91 | C24H20ClN5O2
Medchem Express | RIP1 kinase inhibitor 1 | 5mg | 582658512 | HY-111409 | 2095515-38-9 | 461.910 | C24H20ClN5O3
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eMolecules 74444-77-2 | 2-AMINOTETRALIN-2-CARBOXYLIC ACID | AstaTech | MFCD00800504 | 191.230 | C11H13NO2 | 95.000 | NC1(CCc2ccccc2C1)C(O)=O | 1g | 589772675
2-AMINOTETRALIN-2-CARBOXYLIC ACID | AstaTech | 74444-77-2 | MFCD00800504 | 191.230 | C11H13NO2 | 95.000 | NC1(CCc2ccccc2C1)C(O)=O | 1g | 589772675
Medchemexpress LLC Zamifenacin fumarate | 127308-98-9 | 99.0% | 531.60 g/mol | C31H33NO7 | 5 MG
Zamifenacin fumarate is the fumarate salt of zamifenacin (UK-76654), a gut-selective muscarinic M3 receptor antagonist used in research to study gastrointestinal motility. It is provided as a high-purity solid for use in in vitro and in vivo pharmacology studies targeting colonic motility.
- Potent gut-selective muscarinic M3 receptor antagonist that reduces colonic motility.
- High purity suitable for research applications (99.0%).
- Solid, white to off-white form for convenient handling and dosing.
- Molecular weight 531.60 g/mol, molecular formula C31H33NO7.
- Recommended storage at 4°C; in solution, -80°C for long-term stability.
Medchemexpress LLC ER-27319 (maleate) | 1204480-26-1 | 99.4% | 396.44 | 50 MG
ER-27319 (maleate), an acridone derivative, is a potent and selective SYK inhibitor. It inhibits the tyrosine phosphorylation of SYK and its activity, and can be used for study in allergic diseases. It also inhibits the release of antigen-induced allergic mediators from human and rat mast cells with an IC50 of 10 μM.
- Potent and selective SYK inhibitor
- Inhibits tyrosine phosphorylation of SYK
- Inhibits release of antigen-induced allergic mediators
- Suitable for study in allergic diseases
Medchemexpress LLC Zaldaride maleate | 109826-27-9 | MFCD04113002 | 99.7% | 544.60 | C30H32N4O6 | 1 MG
Zaldaride maleate is a potent, orally active, and selective calmodulin inhibitor used in biochemical and cellular research. It inhibits calmodulin-stimulated cAMP phosphodiesterase activity (IC50 ≈ 3.3 nM), modulates ion-channel currents, and is supplied for laboratory research use only.
- Potent calmodulin inhibitor.
- Orally active in pharmacological studies.
- Low nanomolar IC50 for cAMP phosphodiesterase inhibition.
- Reversibly blocks voltage-activated Na+, Ca2+, and K+ currents.
- High purity suitable for research applications.
- Provided as a small solid quantity for laboratory use.
Medchemexpress LLC NB-598 (Maleate) | 155294-62-5 | 99.4% | 565.74 | 50 MG
NB-598 Maleate is a potent and competitive inhibitor of squalene epoxidase (SE), and it suppresses triglyceride biosynthesis through the farnesol pathway. It is also a click chemistry reagent, containing an Alkyne group, which allows it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules that contain Azide groups.
- Potent and competitive inhibitor of squalene epoxidase (SE)
- Suppresses triglyceride biosynthesis through the farnesol pathway
- Functions as a click chemistry reagent
- Contains an Alkyne group
- Capable of undergoing copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide groups
Medchemexpress LLC Avitinib maleate | 1557268-88-8 | 99.86% | 603.60 | 1 ML
Avitinib maleate (Abivertinib) is a third-generation, irreversible, and orally active selective EGFR inhibitor. It has IC50 values of 0.18 nM against EGFR L858R and EGFR T790M, and 7.68 nM against wild-type EGFR. Additionally, Avitinib maleate acts as a BTK inhibitor, inducing apoptosis and inhibiting BTK phosphorylation in mantle cell lymphoma. This compound demonstrates anticancer effects and is intended for research use only.
- Third-generation, irreversible, and orally active selective EGFR inhibitor.
- Potent inhibition of mutant EGFR phosphorylation with high selectivity over wild-type EGFR.
- Inhibits phosphorylation of downstream targets such as Akt and ERK1/2 in specific cell lines.
- Also functions as a BTK inhibitor, inducing apoptosis and inhibiting BTK phosphorylation in mantle cell lymphoma.
- Demonstrates anticancer effects in xenograft models, inhibiting EGFR-mutant tumor growth.
Selleck Chemical LLC Dimethindene maleate-100MG
Dimethindene maleate is a selective antagonist of histamine H1 and exhibits antihistamine effects It suppresses the cromakalim-induced/glibenclamide-sensitive K currents in a concentration-dependent and reversible manner
TARGETMOL CHEMICALS INC Fenclozine Maleate 1MG
Also available in 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Fenclozine Maleate (S 1429) is a potential histamine H1 receptor antagonist , which can be used to study fever, inflammation and pain. Purity 98.47%
eMolecules 922-67-8 | Methyl propiolate | Combi-Blocks | MFCD00008572 | 84.074 | C4H4O2 | 97.000 | COC(=O)C#C | 25g | 117536327
Methyl propiolate | Combi-Blocks | 922-67-8 | MFCD00008572 | 84.074 | C4H4O2 | 97.000 | COC(=O)C#C | 25g | 117536327
Pfaltz & Bauer Diethylacetylene dicarboxylate 5G | 762-21-0
Diethylacetylene dicarboxylate 5G | 762-21-0
