Carboximidamides
Sigma Aldrich Fine Chemicals Biosciences Cimetidine | 51481-61-9 | MFCD00133296 | 10g
Cimetidine | Mol Wt: 252.34 | 51481-61-9 | MFCD00133296 | 10g
Sigma Aldrich Fine Chemicals Biosciences Nalpha Tosyl L lysne chlo500MG
Nalpha Tosyl L lysne chlo500MG
Sigma Aldrich Fine Chemicals Biosciences Cimetidine hydrochloride United States Pharmacopeia (USP) Reference Standard | 70059-30-2 | MFCD01724314 | 200MG
Cimetidine hydrochloride United States Pharmacopeia (USP) Reference Standard | Mol Wt: 288.8 | 70059-30-2 | MFCD01724314 | 200MG
Medchemexpress LLC Isosinensetin | 17290-70-9 | 372.37 | 20 MG
Isosinensetin is a flavonoid compound and an inhibitor of HIV-1 protease and PTP1B (IC50: 2.61 μM; Ki: 0.92 μM). It inhibits P-glycoprotein (P-gp) in MDR1-MDCKII cells. Isosinensetin possesses anti-tumor, anti-viral, anti-inflammatory, and antioxidant effects. It is used in research for various diseases including cancer, inflammation, osteoporosis, and diabetes.
- Inhibits HIV-1 protease and PTP1B
- Inhibits P-glycoprotein
- Possesses anti-tumor, anti-viral, anti-inflammatory, and antioxidant effects
- Used in research for cancer, inflammation, osteoporosis, and diabetes
- Inhibits osteoclast formation and bone resorption
- Alleviates estrogen deficiency-induced osteoporosis
- Increases intracellular calcium ion concentration
- Stimulates GLP-1 secretion
- Inhibits erythrocyte hemolysis
Medchemexpress LLC 1-(4-(6,7-Dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)butyl)-3-methyl-1H-benzo[d]imidazol-2 | 1121931-70-1 | 99.9% | C23H29N3O3 | 50 MG
CM398 is a highly selective, orally active sigma-2 receptor ligand with a Ki of 0.43 nM. It demonstrates a high sigma-1/sigma-2 selectivity ratio (1000-fold).
- Exhibits notable affinity for dopamine (Ki=32.90 nM) and serotonin transporters (Ki=244.2 nM).
- Shows promising anti-inflammatory analgesic effects in the formalin model of inflammatory pain in mice.
Medchemexpress LLC ATX inhibitor 1 | 2225892-70-4 | 99.3% | 501.30 | 50 MG
ATX inhibitor 1 is a potent inhibitor of ATX (Autotaxin) with IC50 values of 1.23 nM (FS-3) and 2.18 nM (bis-pNPP). It is intended for research use only.
- Potent ATX inhibitor.
- IC50: 1.23 nM (FS-3) and 2.18 nM (bis-pNPP).
- Appearance: Solid, white to off-white.
- For research use only.
Sigma Aldrich Fine Chemicals Biosciences Cimetidine hydrochloride European Pharmacopoeia (EP) Reference Standard | 70059-30-2 | MFCD01724314 |
Cimetidine hydrochloride European Pharmacopoeia (EP) Reference Standard | Mol Wt: 288.8 | 70059-30-2 | MFCD01724314 |
Chem-Impex International, Inc. N,N'-Dicyclohexyl-4-morpholinecarboxamidine | MFCD00063252 | 5G
N,N'-Dicyclohexyl-4-morpholinecarboxamidine, MFCD00063252, 5G
Medchemexpress LLC PIN1 inhibitor API-1 50mg | 680622-70-2 | 366.30 | C15H13F3N6O2 | 50 MG
PIN1 inhibitor API-1 is a selective peptidyl-prolyl cis-trans isomerase Pin1 inhibitor (IC50 = 72.3 nM) that binds the Pin1 PPIase domain and has been reported to up-regulate anticancer microRNA biogenesis and suppress hepatocellular carcinoma in preclinical models.
- Selective Pin1 inhibitor (IC50 72.3 nM).
- Molecular formula C15H13F3N6O2; molecular weight 366.30.
- Purity 99.63%.
- Appearance solid; color white to yellow.
- Soluble in DMSO (250 mg/mL); in vivo formulations ≥ 2.17 mg/mL in mixed solvents.
- Available in multiple package sizes including 50 MG.
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.
eMolecules Ambeed / N2N4N6-tri-m-tolyl-135-Triazine-246-triamine / 250mg / 586454501 / A310637 / / 82504-70-9 / MFCD19440763 / 396.498 / C24H24N6
Ambeed / N2N4N6-tri-m-tolyl-135-Triazine-246-triamine / 250mg / 586454501 / A310637 / / 82504-70-9 / MFCD19440763 / 396.498 / C24H24N6
Medchemexpress LLC FSL-1 | 322455-70-9 | 99.22% | 1666.16 | 5 MG
FSL-1 is a bacterial-derived toll-like receptor 2/6 (TLR2/6) agonist that enhances resistance to experimental HSV-2 infection. It also reduces HSV-2 replication in human vaginal epithelial cells and induces significant resistance to experimental genital HSV-2 infection through a specific cytokine response profile. Additionally, FSL-1 enhances phagocytosis of bacteria by macrophages via a Toll-like receptor 2-mediated signaling pathway.
- Enhances resistance to experimental HSV-2 infection.
- Reduces HSV-2 replication in human vaginal epithelial cells.
- Induces significant resistance to experimental genital HSV-2 infection.
- Enhances phagocytosis of bacteria by macrophages.
eMolecules Medchem Express / Myriocin / 5mg / 495800977 / HY-N6798 / / 35891-70-4 / MFCD01632772 / 401.544 / C21H39NO6
Medchem Express / Myriocin / 5mg / 495800977 / HY-N6798 / / 35891-70-4 / MFCD01632772 / 401.544 / C21H39NO6
Medchemexpress LLC Creatine kinase, bovine heart | 9001-15-4 | 5 KU
Creatine Kinase (CPK/CK), Bovine Heart is a biological material or organic compound intended for use in life science research. It is available in various quantities, including 1 KU, 5 KU, and 10 KU.
- Suitable for life science research applications.
- Available in multiple unit sizes for flexibility.
- Product ships at room temperature within the continental US.
- Comprehensive documentation including data sheet, sds, coa, and handling instructions is available.