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Filtered Search Results
Medchemexpress LLC Monomethylauristatin F sodium | 1799706-65-2 | 99.6% | 753.94 g/mol | C39H64N5NaO8 | 100 MG
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MMAF sodium (Monomethylauristatin F sodium) is the sodium salt of monomethylauristatin F, a potent tubulin polymerization inhibitor used as a cytotoxic payload in antibody-drug conjugates and antitumor research. It is supplied as a white to off-white solid for research use and should be stored refrigerated under inert atmosphere to maintain stability.
- Potent tubulin polymerization inhibitor.
- Used as a cytotoxic payload in ADC research.
- White to off-white solid suitable for analytical and synthetic applications.
- High purity, approximately 99.6%.
- Molecular weight 753.94 g/mol; CAS 1799706-65-2.
- Store refrigerated, protect from light, and keep under inert gas where possible.
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eMolecules 497839-62-0 | Medchem Express | AEE788 | 5mg | 446255491 | HY-10045 | 440.595 | C27H32N6
Medchem Express | AEE788 | 5mg | 446255491 | HY-10045 | 497839-62-0 | 440.595 | C27H32N6
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Medchemexpress LLC HY-11010 5mg Medchemexpress, AS601245 CAS:345987-15-7 Purity:>98%
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Medchemexpress, HY-11010 5mg AS601245 CAS:345987-15-7 AS601245 is a cell-permeable JNK Inhibitor with IC50s of 150, 220, and 70 nM for three JNK human isoforms (hJNK1, hJNK2, and hJNK3), respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Polygalasaponin V | 162857-65-0 | MFCD13186870 | 99.9% | 1223.35 | C58H94O27 | 10 MG
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Polygalasaponin V is a triterpenoid saponin isolated from the aerial parts of Polygala japonica and provided as a research-grade natural product. It is intended for biochemical and pharmacological studies and supplied as a high-purity solid in small pack sizes for laboratory use.
- High purity suitable for analytical and biological assays.
- Available in small research pack sizes for convenient testing.
- Stable when stored protected from light at recommended temperatures.
- Molecular weight 1223.35 and formula C58H94O27 provided for experimental reference.
- Supplied with documentation such as a datasheet for handling and storage information.
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Medchemexpress LLC HY-110086 5mg Medchemexpress, RWJ 50271 CAS:162112-37-0 Purity:>98%
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Medchemexpress, HY-110086 5mg RWJ 50271 CAS:162112-37-0 RWJ 50271 is an selective inhibitor of lymphocyte function-associated antigen-1/intercellular adhesion molecule-1(LFA-1/ICAM-1) interaction with an IC 50 of 5.0 μM (HL60 cells) [1] . Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Apexbio Technology LLC Clindamycin palmitate HCl 25507-04-4 50mg
Clindamycin palmitate HCl is a lincosamide antibiotic derivative that inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit resulting in bacteriostatic activity In in vitro studies Clindamycin palmitate HCl demonstrates inhibitory effects against Gram-positive bacteria and anaerobes Based on these pharmacological properties Clindamycin palmitate HCl holds research potential in evaluating antibacterial effects investigating bacterial resistance mechanisms and exploring therapeutic efficacy in infectious disease models as well as serving in studies of metabolic pathways and drug delivery related to clindamycin derivatives
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Medchemexpress LLC HY-101457 5mg Medchemexpress, JZP-430 CAS:1672691-74-5 Purity:>98%
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Medchemexpress, HY-101457 5mg JZP-430 CAS:1672691-74-5 JZP-430 is a potent, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) with an IC 50 of 44 nM, exhibits ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL) [1] . Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 878739-06-1 | Medchem Express | AZ 628 | 5mg | 446259741 | HY-11004 | MFCD17392577 | 451.53 | C27H25N5O2
Medchem Express | AZ 628 | 5mg | 446259741 | HY-11004 | 878739-06-1 | MFCD17392577 | 451.530 | C27H25N5O2
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Medchemexpress LLC Vancomycin (hydrochloride) | 1404-93-9 | 99.47% | 1450 Da | 250 MG
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Vancomycin hydrochloride is an antibiotic used for treating bacterial infections. It functions by inhibiting the second stage of cell wall synthesis in susceptible bacteria. Additionally, vancomycin modifies the cell membrane's permeability and selectively suppresses ribonucleic acid synthesis.
- Inhibits bacterial cell wall synthesis.
- Alters cell membrane permeability.
- Selectively inhibits ribonucleic acid synthesis.
- Active against many Gram-positive bacteria, including *Staphylococcus aureus* and enterococci.
- Glycopeptide compound.
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eMolecules 5053-08-7 | Medchem Express | Fenspiride (hydrochloride) | 100mg | 446271707 | HY-A0027 | MFCD00133315 | 296.8 | C15H21ClN2O2
Medchem Express | Fenspiride (hydrochloride) | 100mg | 446271707 | HY-A0027 | 5053-08-7 | MFCD00133315 | 296.800 | C15H21ClN2O2
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Medchemexpress LLC Acp-5862 | 2230757-47-6 | 98.3% | 481.51 g/mol | C26H23N7O3 | 5 MG
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ACP-5862 is the major active, circulating metabolite of acalabrutinib. It is a pyrrolidine ring-opened small molecule that potently inhibits Bruton tyrosine kinase (BTK) with an IC50 of 5.0 nM and displays weak time-dependent inactivation of CYP3A4 and CYP2C8.
- Potent BTK inhibition with reported IC50 of 5.0 nM.
- Useful for metabolite profiling and pharmacology studies.
- High reported purity (≈98.3%) suitable for research use.
- Available in small milligram package sizes for discovery work.
- Storage-stable under recommended powder and solvent conditions.
- Well characterized: molecular weight 481.51 and formula C26H23N7O3.
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eMolecules 1261289-04-6 | Medchem Express | O-304 | 5mg | 446260236 | HY-112233 | 380.24 | C16H11Cl2N3O2S
Medchem Express | 23-cGAMP | 1mg | 788477971 | HY-100564 | 1441190-66-4 | 674.417 | C20H24N10O13P2
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eMolecules 946518-60-1 | Medchem Express | LY2409881 (trihydrochloride) | 5mg | 415688794 | HY-B0788A | MFCD28900676 | 594.42 | C24H32Cl4N6OS
Medchem Express | LY2409881 (trihydrochloride) | 5mg | 415688794 | HY-B0788A | 946518-60-1 | MFCD28900676 | 594.420 | C24H32Cl4N6OS
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Sigma Aldrich Fine Chemicals Biosciences Amantadine hydrochloride British Pharmacopoeia (BP) Reference Standard | 665-66-7 | MFCD00074723 |
Amantadine hydrochloride British Pharmacopoeia (BP) Reference Standard | Mol Wt: 187.71 | 665-66-7 | MFCD00074723 |
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Selleck Chemical LLC CZC-54252
CZC-54252 is a potent and selective LRRK2 inhibitor with IC50s of 1 28 nM and 1 85 nM for human wild type LRRK2 and G2019S LRRK2 respectively
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