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Filtered Search Results
Ambeed 4 3-NITROPHEN PYRIMIDIN-2-AMIN
NC3788740 4 3-NITROPHEN PYRIMIDIN-2-AMIN
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Medchemexpress LLC Protac BRD4 degrader-5-co-peg3-n3 | 2704602-92-4 | 99.7% | 1231.87 | C58H75ClN12O12S2 | 10 MG
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PROTAC BRD4 Degrader-5-CO-PEG3-N3 is a PROTAC-linker conjugate that combines a BRD4 degrader with a PEG-based linker and an azide functional group for bioconjugation. It is provided as a high-purity research reagent for targeted protein degradation studies and click-chemistry applications.
- azide functional group enables CuAAC and SPAAC conjugation
- high purity suitable for research use
- molecular weight 1231.87 and formula C58H75ClN12O12S2
- available in small milligram quantities, including 10 mg
- designed for use in antibody conjugation and linker chemistry workflows
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Medchemexpress LLC Felypressin acetate | 914453-97-7 | 99.6% | 1040.2 g/mol | C46H65N13O11S2 · xC2H4O2 | 10 MG
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Felypressin acetate is a synthetic non-catecholamine vasoconstrictor and a vasopressin V1 receptor agonist used as a research reagent and as a vasoconstrictive agent in dental applications. It is supplied as a high-purity peptide powder and is intended for laboratory use only.
- Non-catecholamine vasoconstrictor and V1 receptor agonist.
- White to off-white solid powder with high purity (99.6%).
- Peptide sequence Cys-Phe-Phe-Gln-Asn-Cys-Pro-Lys-Gly-NH2 with 1-6 disulfide bridge.
- Available as a 10 mg package for research use.
- Store sealed, away from moisture; follow frozen storage recommendations for long-term stability.
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Medchemexpress LLC HY-113534 5mg Medchemexpress, MV1 CAS:1001600-54-9 Purity:>98%
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Medchemexpress, HY-113534 5mg MV1 CAS:1001600-54-9 MV1 is an antagonist of IAP (inhibitor of apoptosis protein), leads to protein knockdown of HaloTag-fused proteins when combined with HaloTag ligand. 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 SK1-I (BML-258) | 1072443-89-0 | 98.8% | 277.40 | C17H27NO2 | 5 MG
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SK1-I (BML-258) is a sphingosine analog and an isozyme-specific competitive inhibitor of sphingosine kinase 1 (SPHK1) with a reported Ki of about 10 μM. It enhances autophagy and has demonstrated antitumor activity. Intended for research use only.
- Isozyme-specific SPHK1 inhibition (Ki ≈ 10 μM).
- Sphingosine analog scaffold.
- High purity: 98.83%.
- Molecular weight 277.40 g/mol; formula C17H27NO2.
- Available as small solid quantities and as a 10 mM solution in DMSO.
- For research use only; not for human or veterinary use.
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Medchemexpress LLC Lmt-28 10Mg | HY-102084-10MG
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Lmt-28 10Mg
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Medchemexpress LLC Pmx-53 (Ac-Phe-Orn-Pro-dCha-Trp-Arg; lactam bridge Orn2-Arg6) | 219639-75-5 | 896.09 | C47H65N11O7 | 5 MG
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PMX-53 is a synthetic cyclic peptidic antagonist of the complement C5a receptor (C5aR1) used in research on immunology and inflammation. It is orally active and shows potent receptor inhibition (IC50 ≈ 20 nM). Chemical identifiers include CAS 219639-75-5 and molecular weight 896.09; sequence: Ac-Phe-{Orn}-Pro-{dCha}-Trp-Arg (lactam bridge Orn2-Arg6).
- Orally active C5a receptor antagonist with potent in vitro activity.
- Applicable to studies of complement-mediated inflammation, cancer, and atherosclerosis.
- Cyclic peptidic structure with a defined sequence and lactam bridge for stability.
- High solubility in DMSO and water for in vitro preparation.
- Stable under sealed, low-temperature storage; specific solvent storage lifetimes provided.
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Medchemexpress LLC S R S -AHPC-amido-C | 50MG
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S R S -AHPC-amido-C | 50MG
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Medchemexpress LLC Glecaprevir | 1365970-03-1 | 838.87 | 100 MG
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Glecaprevir is a novel HCV NS3/4A protease inhibitor and a SARS-CoV 3CLpro inhibitor. It is intended for use as a laboratory chemical and for the manufacture of substances, exclusively for research purposes and by experienced personnel.
- HCV NS3/4A protease inhibitor
- SARS-CoV 3CLpro inhibitor
- IC50 values ranging from 3.5 to 11.3 nM (HCV NS3/4A protease)
- IC50 of 4.09 μM (SARS-CoV 3CLpro)
- For research use only
- Intended for experienced personnel
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Selleck Chemical LLC ACT-1016-0707-E1941-100MG
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ACT-1016-0707 (LPA1 receptor antagonist 2) is an orally active and selective antagonist of LPA1 Receptor with IC50 of 3 1 nM for hLPAR1 in tango assay It has the potential to treat fibrotic diseases
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Medchemexpress LLC Bay-298 | 2471978-97-7 | 100.0% | 473.93 g/mol | C27H21ClFN3O2 | 5 MG
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BAY-298 is an orally active, selective luteinizing hormone receptor (LH-R) antagonist used as a research compound to probe LH-R biology and to reduce sex hormone levels in vitro and in vivo. It is supplied as a high-purity solid for laboratory research use only.
- Selective luteinizing hormone receptor antagonist.
- Orally active compound with demonstrated in vivo effects.
- Reported IC50s: hLH 96 nM, rLH 23 nM, cLH 78 nM.
- High purity (reported 99.96%).
- Molecular formula C27H21ClFN3O2; molecular weight 473.93 g/mol.
- Supplied in small milligram pack sizes suitable for preclinical studies.
- For research use only; not for human or clinical use.
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Medchemexpress LLC Alpelisib | 1217486-61-7 | MFCD22417085 | 200mg
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Alpelisib | Purity: 99.95% | MW: 441.476 | 1217486-61-7 | MFCD22417085 | 200mg
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Medchemexpress LLC PMX 205 Trifluoroacetate | 99.5% | 953.06 | 10 MG
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PMX 205 Trifluoroacetate | 99.5% | 953.06 | 10 MG
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Medchemexpress LLC (S,R,S)-AHPC-phenol-C4-NH2 dihydrochloride | 2376990-26-8 | 96.33% | 632.64 | 100 MG
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(S,R,S)-AHPC-phenol-C4-NH2 dihydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and a linker used in PROTAC technology. It is for research use only and not sold to patients.
- Contains two different ligands connected by a linker
- One ligand for an E3 ubiquitin ligase
- Other ligand for the target protein
- Exploits the intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
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Selleck Chemical LLC Rapastinel
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Rapastinel (GLYX-13 BV-102 TPPT-amide) is a partial agonist of N-methyl-D-aspartate receptor (NMDAR) that targeting a glycine site Rapastinel has long-lasting antidepressant effects
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