Aminobenzoic acids and derivatives
Chemscene Ethyl 2-phenylbutanoate | 1g | CS-W015806 | 98% | 119-43-7 | MFCD00068988 | 192 26 | C12H16O2
Chemscene | Ethyl 2-phenylbutanoate | 1g | CS-W015806 | 98% | 119-43-7 | MFCD00068988 | 192 26 | C12H16O2
Chem-Impex International, Inc. FMOC 3 AMINO 1 CARBOXYMETHY 5G
Fmoc-3-amino-1-carboxymethyl-pyridin-2-one, 5g
![eMolecules 83249-10-9 | 3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic acid | Combi-Blocks, Inc. | MFCD20638314 | 170.164 | C8H10O4 | 98.000 | COC(=O)C12CC(C1)(C2)C(O)=O | 100g | 642100646](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000169855.jpg-250.jpg)
eMolecules 83249-10-9 | 3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic acid | Combi-Blocks, Inc. | MFCD20638314 | 170.164 | C8H10O4 | 98.000 | COC(=O)C12CC(C1)(C2)C(O)=O | 100g | 642100646
3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic acid | Combi-Blocks, Inc. | 83249-10-9 | MFCD20638314 | 170.164 | C8H10O4 | 98.000 | COC(=O)C12CC(C1)(C2)C(O)=O | 100g | 642100646
eMolecules 3374-22-9 | H-DL-Cys-OH | Ambeed | MFCD00004881 | 121.150 | C3H7NO2S | 95.000 | NC(CS)C(O)=O | 25g | 490525781
H-DL-Cys-OH | Ambeed | 3374-22-9 | MFCD00004881 | 121.150 | C3H7NO2S | 95.000 | NC(CS)C(O)=O | 25g | 490525781
Medchemexpress LLC CRAMP-18 (mouse) acetate | 99.3% | 2567.97 | 5 MG
CRAMP-18 (mouse) acetate is an antibiotic peptide without hemolytic activity. It has good inhibitory activity against Gram-negative bacteria such as *S. typhimurium* and *P. aeruginosa*. This peptide has potential for studying antifungal, antibacterial, and antitumor properties.
- Antibiotic peptide
- No hemolytic activity
- Inhibitory activity against Gram-negative bacteria
- Potential for studying antifungal properties
- Potential for studying antibacterial properties
- Potential for studying antitumor properties
Aobchem 1-(5-Chloro-2 2-difluorobenzo[d][1 3]dioxol-4-yl)ethanol | 95% | C9H7ClF2O3 | 1g
1-(5-Chloro-2 2-difluorobenzo[d][1 3]dioxol-4-yl)ethanol | 95% | C9H7ClF2O3 | 1g
Medchemexpress LLC CEP-28122 (mesylate salt) | 2070009-30-0 | 99.9% | 635.17 | 100 MG
CEP-28122 (mesylate salt) | 2070009-30-0 | 99.9% | 635.17 | 100 MG
Medchemexpress LLC Pritelivir mesylate | 1428333-96-3 | C19H22N4O6S3 | 100 MG
Pritelivir mesylate is an inhibitor of the viral helicase-primase complex. It demonstrates antiviral activity both in vitro and in animal models of herpes simplex virus (HSV) infection, effective against herpes simplex virus types 1 and 2 (HSV-1 and HSV-2).
- Inhibits viral helicase-primase complex
- Exhibits antiviral activity against HSV-1 and HSV-2
- IC50 of 0.02 μM against HSV1-2
- For research use only
- Purity of 99.33%
- Appearance is solid
- Color is white to off-white
Medchemexpress LLC Enasidenib (mesylate) | 1650550-25-6 | MFCD29472245 | 99.7% | 569.48 | 50 MG
Enasidenib mesylate is a first-in-class, oral, potent, reversible, selective inhibitor of the IDH2 mutant enzymes.
- First-in-class, oral, potent, reversible, selective inhibitor of the IDH2 mutant enzymes.
- Reverses the effects of mutant IDH2 on DNA methylation in mutant stem/progenitor cells.
- Induces differentiation and impairs self-renewal of IDH2-mutant leukemia cells.
- Significantly improves survival in an IDH2-mutant acute myeloid leukemia (AML) primary xenograft mouse model.
- Leads to a reduction in 2-HG in vivo.
- Restores megakaryocyte-erythroid progenitor (MEP) differentiation.
eMolecules 138-14-7 | Deferoxamine Mesylate | Ambeed | MFCD00058605 | 656.790 | C26H52N6O11S | 98.000 | CS(O)(=O)=O.CC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCN | 1g | 600851355
Deferoxamine Mesylate | Ambeed | 138-14-7 | MFCD00058605 | 656.790 | C26H52N6O11S | 98.000 | CS(O)(=O)=O.CC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCN | 1g | 600851355
Apexbio Technology LLC Saquinavir mesylate 149845-06-7 10mg
Saquinavir mesylate is a reversible inhibitor of HIV protease a retroviral aspartic protease required for viral maturation and replication It targets the active site of HIV-1 and HIV-2 proteases preventing enzymatic cleavage of polyprotein precursors thereby suppressing formation of mature viral particles Saquinavir inhibits HIV-1 protease with a reported Ki value of approximately 0 12 nM In cultured human neuronal cells it also reduces -amyloid (A 40) levels and inhibits -secretase (BACE1) activity at 50 M concentration it reduces neuronal A production by approximately 90% Saquinavir is commonly employed in HIV/AIDS research and has potential in Alzheimer s disease models for studying the modulation of amyloid peptide synthesis pathways
![eMolecules 169869-90-3 | Exatecan mesylate | Ambeed | MFCD04113012 | 531.560 | C25H26FN3O7S | 98.000 | CS(O)(=O)=O.CC[C@@]1(O)C(=O)OCc2c1cc1-c3nc4cc(F)c(C)c5CC[C@H](N)c(c3Cn1c2=O)c45 | 25mg | 784396074](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000126370.jpg-250.jpg)
eMolecules 169869-90-3 | Exatecan mesylate | Ambeed | MFCD04113012 | 531.560 | C25H26FN3O7S | 98.000 | CS(O)(=O)=O.CC[C@@]1(O)C(=O)OCc2c1cc1-c3nc4cc(F)c(C)c5CC[C@H](N)c(c3Cn1c2=O)c45 | 25mg | 784396074
Exatecan mesylate | Ambeed | 169869-90-3 | MFCD04113012 | 531.560 | C25H26FN3O7S | 98.000 | CS(O)(=O)=O.CC[C@@]1(O)C(=O)OCc2c1cc1-c3nc4cc(F)c(C)c5CC[C@H](N)c(c3Cn1c2=O)c45 | 25mg | 784396074
Apexbio Technology LLC ERIBULIN-MESYLATE-10MG
Eribulin mesylate (CAS No 441045-17-6) is a synthetic analog of halichondrin B derived from a marine sponge primarily used in cancer research as a microtubule dynamics inhibitor Its mechanism of action involves the inhibition of microtubule growth without affecting the shortening phase which leads to cell cycle arrest and apoptosis Eribulin mesylate exhibits potent in vitro activity generally in the nanomolar range making it highly effective in various cancer cell lines It is commonly employed in cell models and animal studies to evaluate its potential therapeutic effects and mechanisms Additionally it is valuable in drug screening for its unique action on the mitotic spindle Experimental concentrations typically depend on the specific research design allowing flexibility based on the requirements of particular studies