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Filtered Search Results
MEDCHEMEXPRESS LLC R S-IVOSIDENIB 5MG
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501873698 R S-IVOSIDENIB 5MG
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Medchemexpress LLC HY-19836 10mg Medchemexpress, PF-06650833 CAS:1817626-54-2 Purity:>98%
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Medchemexpress, HY-19836 10mg PF-06650833 CAS:1817626-54-2 PF-06650833 is a potent, selective and orally active inhibitor of interleukin-1 receptor associated kinase 4 (IRAK4) with IC50s of 0.2 and 2.4 nM in the cell and PBMC assay, respectively. PF-06650833 is used to treat diseases such as rheumatoid arthritis, lupus, and lymphomas[2]. 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 (Z)-LFM-A13 | 244240-24-2 | 99.8% | 360.01 | 50 MG
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LFM-A13 is a potent BTK, JAK2, PLK inhibitor, inhibiting recombinant BTK, Plx1, and PLK3 with IC50s of 2.5 μM, 10 μM, and 61 μM respectively. It shows no effects on JAK1 and JAK3, Src family kinase HCK, EGFR, and IRK.
- Potent BTK, JAK2, PLK inhibitor
- Inhibits recombinant BTK, Plx1, and PLK3
- IC50 for BTK: 2.5 μM
- IC50 for Plx1: 10 μM
- IC50 for PLK3: 61 μM
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eMolecules 400647-59-8 | Medchem Express | Doxorubicin-SMCC | 5mg | 602878364 | HY-116063 | 762.765 | C39H42N2O14
ChemScene | 2-((2-((tert-Butoxycarbonyl)amino)ethyl)amino)acetic acid | 100mg | 801476526 | CS-0372602 | 90495-99-1 | MFCD11974252 | 218.253 | C9H18N2O4
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eMolecules Building Block Tool<|a>
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Ambeed AMBEED
5000893875 N-BOC-34-DIHYDROQUINOLIN 250MG
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Aobchem AOBCHEM
5000930605 1- 3- 1S 3S -ADAMANTAN-1-YL -
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Selleck Chemical LLC Guggulsterone E&Z S3792-10mM/1mL
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Guggulsterone is one of the active constituent of Commiphora mukul It occurs in two isomeric forms namely Z-GS and E-GS Guggulsterone act as antagonist ligands for the bile acid receptor farnesoid X receptor and as active ingredients responsible for the hypolipidemic activity
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eMolecules 132426-19-8 | 2-BROMO-1-PYRAZINYL-ETHANONE | AstaTech | MFCD05662516 | 201.023 | C6H5BrN2O | 95.000 | BrCC(=O)c1cnccn1 | 1g | 233636519
2-BROMO-1-PYRAZINYL-ETHANONE | AstaTech | 132426-19-8 | MFCD05662516 | 201.023 | C6H5BrN2O | 95.000 | BrCC(=O)c1cnccn1 | 1g | 233636519
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Apexbio Technology LLC Granzyme B Inhibitor Z-AAD-CH2Cl 20ul (10 mM)
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Granzyme B Inhibitor Z-AAD-CH2Cl is a small-molecule inhibitor targeting granzyme B a serine protease predominantly expressed in cytotoxic lymphocytes natural killer (NK) cells and cytotoxic T lymphocytes (CTLs) It is designed to irreversibly inhibit granzyme B activity thereby modulating apoptosis induction and immune regulation Granzyme B Inhibitor Z-AAD-CH2Cl exerts its biological activity primarily through irreversible inhibition of granzyme B In cell-based studies it demonstrates inhibitory activity in models such as NK cell-induced cytotoxicity in chondrocytes lymphocyte-induced caspase-3 activation and DNA fragmentation and activation-induced apoptosis in T-cell populations Based on these pharmacological properties Granzyme B Inhibitor Z-AAD-CH2Cl holds research potential in immunology oncology and inflammation-related disorders
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Medchemexpress LLC Boc-NH-PEG2 | 139115-91-6 | 205.25 | 1 G
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This PEG-based PROTAC linker can be used in the synthesis of PROTACs. PROTACs are compounds containing two different ligands connected by a linker, where one ligand targets an E3 ubiquitin ligase and the other targets the desired protein. These compounds utilize the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- PROTACs degrade target proteins using the ubiquitin-proteasome system
- PROTACs consist of two different ligands connected by a linker
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Apexbio Technology LLC HyperScript™ IV First-Strand cDNA Synthesis Kit 100rxn
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HyperScript IV First-Strand cDNA Synthesis Kit contains an engineered M-MLV reverse transcriptase used for the synthesis of first-strand cDNA from RNA templates for molecular biology research The kit comprises HyperScript IV Reverse Transcriptase which is optimized for enhanced inhibitor tolerance faster elongation increased thermostability and reduced RNase H activity as well as two types of primers (Random Primer and Oligo(dT)23VN) to allow flexibility in experimental design Synthesized first-strand cDNA is suitable for downstream applications including PCR qPCR and other analytical approaches
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Aobchem AOBCHEM
5001038032 4-HYDROXYMETHYL-2 6-DIFLUOROPH
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Medchemexpress LLC Benzyloxycarbonyl-alanyl-glutamyl-valyl-aspartic acid fluoromethyl ketone | 1135688-47-9 | MFCD03453601 | >=95.0% | 610.63 | C28H39FN4O10 | 5MG
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Z-AEVD-FMK is a cell-permeable, fluoromethyl ketone-derivatized peptide that irreversibly inhibits caspase-10 and related caspases. It prevents Bid activation and downstream caspase cascade events and is supplied as a crystalline solid for laboratory research use only.
- Irreversible caspase-10 inhibitor with FMK warhead.
- Cell-permeable peptide suitable for intracellular studies.
- CAS number 1135688-47-9; molecular formula C28H39FN4O10.
- Molecular weight approximately 610.6 Da.
- Purity ≥95% (reported by distributor).
- Soluble in DMSO at ~10 mg/mL; supplied as a crystalline solid.
- For research use only; not for human or veterinary applications.
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![eMolecules 1141669-69-3 | 2-Amino-5-Cbz-4,5,6,7-tetrahydro-1,3-thiazolo[5,4-c]pyridine | Combi-Blocks | MFCD11656828 | 289.350 | C14H15N3O2S | 98.000 | Nc1nc2CCN(Cc2s1)C(=O)OCc1ccccc1 | 1g | 415501669](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502189837.JPG-250.jpg)
eMolecules 1141669-69-3 | 2-Amino-5-Cbz-4,5,6,7-tetrahydro-1,3-thiazolo[5,4-c]pyridine | Combi-Blocks | MFCD11656828 | 289.350 | C14H15N3O2S | 98.000 | Nc1nc2CCN(Cc2s1)C(=O)OCc1ccccc1 | 1g | 415501669
2-Amino-5-Cbz-4,5,6,7-tetrahydro-1,3-thiazolo[5,4-c]pyridine | Combi-Blocks | 1141669-69-3 | MFCD11656828 | 289.350 | C14H15N3O2S | 98.000 | Nc1nc2CCN(Cc2s1)C(=O)OCc1ccccc1 | 1g | 415501669
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MEDCHEMEXPRESS LLC PMX 205 TRIFLUOROACETATE 5MG
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501872282 PMX 205 TRIFLUOROACETATE 5MG
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