Organonitrogen Compounds
eMolecules 35891-70-4 | Medchem Express | Myriocin | 5mg | 495800977 | HY-N6798 | MFCD01632772 | 401.544 | C21H39NO6
Ambeed | 46-Dichloro-1-ethyl-1H-pyrazolo[34-d]pyrimidine | 1g | 525130940 | A216971 | 864292-48-8 | MFCD16249852 | 217.050 | C7H6Cl2N4
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eMolecules 1280786-87-9 | 1-Bromo-3-chloro-5-piperidinobenzene | Combi-Blocks | MFCD18783174 | 274.590 | C11H13BrClN | 96.000 | Clc1cc(Br)cc(c1)N1CCCCC1 | 1g | 117543871
1-Bromo-3-chloro-5-piperidinobenzene | Combi-Blocks | 1280786-87-9 | MFCD18783174 | 274.590 | C11H13BrClN | 96.000 | Clc1cc(Br)cc(c1)N1CCCCC1 | 1g | 117543871
Medchemexpress LLC Tetrabutylammonium difluorotriphenylsilicate(IV) | 163931-61-1 | 539.86 | 25 G
Tetrabutylammonium difluorotriphenylsilicate(IV) | 163931-61-1 | 539.86 | 25 G
Sigma Aldrich Fine Chemicals Biosciences SIGMA ALDRICH FINE CHEMICALS BIOSCIENCES
NC4013068 TRAZODONE HYDROCHLORIDE
![eMolecules 1421601-10-6 | Ambeed | Methyl 5-[4-(trifluoromethyl)phenyl]oxolane-2-carboxylate | 250mg | 600826537 | A1014801 | MFCD22392037 | 274.239 | C13H13F3O3](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502484157.JPG-250.jpg)
eMolecules 1421601-10-6 | Ambeed | Methyl 5-[4-(trifluoromethyl)phenyl]oxolane-2-carboxylate | 250mg | 600826537 | A1014801 | MFCD22392037 | 274.239 | C13H13F3O3
Medchem Express | RORt Inverse agonist 6 | 5mg | 587658653 | HY-130243 | 1887161-80-9 | 565.030 | C28H29ClN6O5
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Medchemexpress LLC BD-1047 dihydrobromide | 138356-21-5 | 98.45% | 437.04 | 1 ML
BD-1047 dihydrobromide is a selective functional antagonist of sigma receptors. It attenuates Apomorphine-induced climbing and Phencyclidine-induced head twitches. It is for research use only and not sold to patients.
- Selective functional antagonist of sigma receptors.
- Attenuates Apomorphine-induced climbing.
- Attenuates Phencyclidine-induced head twitches.
- Prevents Cutamesine from reducing cell death induced by light exposure in murine photoreceptor-derived 661w cells.
- Attenuates Cutamesine from reducing mitochondrial damage and elevated caspase 3/7 activity.
- Decreases APO-induced climbing behavior at 10 mg/kg in mice.
- Counteracts the antidepressant-like effect induced by co-administration of pramipexole and sertraline.
- Reduces the increasing expression of pNR1 and reverses Sig-1 R agonists potentiated NMDA-induced pain behavior and pNR1 immunoreactivity.
Medchemexpress LLC Navlimetostat hydrochloride | 00-00-0 | 99.2% | C23H19Cl2FN6O2 | 10MG
Navlimetostat hydrochloride is a research-grade small-molecule inhibitor selective for the PRMT5-MTA complex. It demonstrates potent biochemical and cellular activity and is used in preclinical studies to probe PRMT5 biology and evaluate antineoplastic effects, with reported selectivity in MTAP-deleted models.
- Potent inhibitor of the PRMT5-MTA complex (IC50 3.6 nM).
- Inhibits PRMT5 enzymatic activity (IC50 20.5 nM).
- Shows cellular selectivity in MTAP-deleted models (cell viability 12 nM vs 890 nM in parental cells).
- High purity (99.2%).
- Soluble in DMSO at 100 mg/mL; ultrasonic assistance recommended.
- Suitable for preclinical research; store sealed away from moisture.