Carboximidamides
Medchemexpress LLC 6-methyl-2-(((3-phenoxypropyl)amino)methyl)quinolin-4-ol | 1434515-70-4 | 99.5% | 322.40 g/mol | C20H22N2O2 | 10MG
UCSF924 is a selective dopamine D4 receptor (DRD4) partial agonist chemical probe with nanomolar potency (EC50 = 4.2 nM) and exceptional selectivity against other GPCRs. It is supplied as a white to off-white solid with high purity for use in receptor pharmacology and neuropsychiatric research.
- Selective DRD4 partial agonist with EC50 = 4.2 nM.
- High selectivity against more than 320 non-olfactory GPCRs.
- High purity: 99.5%.
- White to off-white solid suitable for laboratory use.
- Appropriate for cell-based assays and receptor pharmacology studies.
eMolecules Chem-Impex Guanidine hydrochloride 5kg 342450113 29913 0 000 50-01-1 MFCD00013026 95 530 CH6ClN3
Chem-Impex Guanidine hydrochloride 5kg 342450113 29913 0 000 50-01-1 MFCD00013026 95 530 CH6ClN3
Apexbio Technology LLC Clonidine HCl 4205-91-8 10mM (in 1mL DMSO)
Clonidine Hydrochloride (CAS 4205-91-8) is a synthetic imidazoline derivative that functions as a centrally acting alpha-2 adrenergic receptor agonist By stimulating these receptors in the brainstem clonidine inhibits sympathetic outflow resulting in decreased peripheral vascular resistance and lowered blood pressure In a research context clonidine is frequently used to investigate mechanisms underlying central adrenergic regulation cardiovascular physiology and autonomic nervous system function Its pharmacological profile makes it valuable for studies exploring hypertension neuropharmacology and related therapeutic strategies
eMolecules AstaTech / 3-(3-METHOXYPHENYL)ANILINE / 1g / 411873561 / AC1793 / 97.000 / 400748-70-1 / MFCD03424667 / 199.253 / C13H13NO
AstaTech / 3-(3-METHOXYPHENYL)ANILINE / 1g / 411873561 / AC1793 / 97.000 / 400748-70-1 / MFCD03424667 / 199.253 / C13H13NO
Apexbio Technology LLC Guanidine HCl 50-01-1 50g
Guanidine hydrochloride (Guanidine HCl CAS 50-01-1) is a highly alkaline crystalline compound derived from the oxidative metabolism of guanine Functioning primarily as a strong chaotropic agent it disrupts hydrogen bonding and secondary structure in proteins leading to efficient protein denaturation and solubilization Widely utilized in molecular biology and biochemistry Guanidine HCl facilitates protein unfolding for downstream applications such as protein purification refolding studies and RNA extraction protocols where it also serves to inactivate nucleases and other enzymes
eMolecules Medchem Express / ()-Columbianetin / 5mg / 624169641 / HY-N0363 / / 3804-70-4 / MFCD02259437 / 246.262 / C14H14O4
Medchem Express / ()-Columbianetin / 5mg / 624169641 / HY-N0363 / / 3804-70-4 / MFCD02259437 / 246.262 / C14H14O4
Selleck Chemical LLC Clonidine HCl S2458-1g
Clonidine HCl(Kapvay) is a direct-acting 2 adrenergic agonist with an ED50 of 0 02 0 01 mg/kg
Chem-Impex International, Inc. N,N'-Dicyclohexyl-4-morpholinecarboxamidine | MFCD00063252 | 5G
N,N'-Dicyclohexyl-4-morpholinecarboxamidine, MFCD00063252, 5G
Selleck Chemical LLC Allantoin S3856-1g
Allantoin (Glyoxyldiureide 5-Ureidohydantoin) produced from uric acid is a major metabolic intermediate in most organisms including animals plants and bacteria
Medchemexpress LLC PIN1 inhibitor API-1 100mg | 680622-70-2 | 366.30 | C15H13F3N6O2 | 100 MG
PIN1 inhibitor API-1 is a small-molecule research compound that inhibits PIN1 activity and functions as a microRNA activator. It is supplied as a research-grade powder (100 mg) intended for preclinical in vitro and in vivo studies; consult the certificate of analysis and safety data sheet for storage, purity, and handling instructions.
- High purity: documented at about 99.6%.
- Molecular weight: 366.30; chemical formula: C15H13F3N6O2.
- High DMSO solubility: up to 250 mg/mL with ultrasonic assistance.
- Manufacturer provides in vivo formulation examples and solubility protocols.
- Data sheet and safety data sheet available for characterization and safe handling.
Medchemexpress LLC Creatine phosphokinase, rabbit muscle (CPK) | 9001-15-4 | 1 KU
Creatine phosphokinase, rabbit muscle (CPK) catalyzes the reversible reaction of creatine and ATP to form phosphocreatine and ADP. This enzyme is crucial for maintaining a constant ATP/ADP ratio during rapid energy turnover.
- Catalyzes reversible reaction of creatine and ATP
- Forms phosphocreatine and ADP
- Key enzyme for maintaining constant ATP/ADP ratio
- Appearance: solid
- Color: white to off-white
- Enzyme activity: ≥100 U/mg solid
- Unit definition: amount of enzyme that transfers 1.0 μmole of phosphate from phosphocreatine to ADP per min at pH 7.4 at 30°C
- Solubility: can be dissolved and stored at 1 mg/ml using 20 mM Tris (pH 8.0)
- Avoids repeated freezing and thawing
- Recommended to add 0.1% albumin to reaction buffer when diluting to avoid inactivation
eMolecules Pharmablock / 4-(trifluoromethyl)cyclohexan-1-amine / 25mg / 551140214 / PBN20121362 / 0.000 / 58665-70-6 / MFCD09040573 / 167.175 / C7H12F3N
Pharmablock / 4-(trifluoromethyl)cyclohexan-1-amine / 25mg / 551140214 / PBN20121362 / 0.000 / 58665-70-6 / MFCD09040573 / 167.175 / C7H12F3N
Sigma Aldrich Fine Chemicals Biosciences Nalpha Tosyl L lysne chlo500MG
Nalpha Tosyl L lysne chlo500MG
Selleck Chemical LLC Clonidine HCl S2458-50mg
Clonidine HCl(Kapvay) is a direct-acting 2 adrenergic agonist with an ED50 of 0 02 0 01 mg/kg
![Medchemexpress LLC 6-methyl-2-[(3-phenoxypropyl)aminomethyl]quinolin-4(1H)-one | 1434515-70-4 | 99.5% | 322.40 g·mol-1 | C20H22N2O2 | 100MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000239167.png-250.jpg)
Medchemexpress LLC 6-methyl-2-[(3-phenoxypropyl)aminomethyl]quinolin-4(1H)-one | 1434515-70-4 | 99.5% | 322.40 g·mol-1 | C20H22N2O2 | 100MG
UCSF924 is a potent and selective dopamine D4 receptor (DRD4) partial agonist used as a chemical probe in neuropsychiatric and pharmacology research. It exhibits an EC50 of 4.2 nM and a Ki of approximately 3 nM for DRD4, with reported lack of off-target activity against more than 320 non-olfactory GPCRs. Supplied as a high-purity research compound for biochemical and cellular studies. Not for human or veterinary use.
- Potent DRD4 partial agonist (EC50 4.2 nM).
- High affinity for DRD4 (Ki ≈ 3 nM).
- Demonstrated selectivity with minimal off-target GPCR activity.
- High purity suitable for biochemical and cellular assays.
- Available in multiple packaging formats and DMSO solutions for assay use.