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Filtered Search Results
Medchemexpress LLC Amino-PEG5-Boc | 1446282-18-3 | 98.0% | C17H35NO7 | 250 MG
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Amino-PEG5-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Exploits the intracellular ubiquitin-proteasome system for degradation
- Enables selective degradation of target proteins
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000783852 RAC-METHYL JASMONA 25MG
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eMolecules 63639-02-1 | 2,5-Dimethyl-pyrrolidine hydrochloride | J & W PharmLab LLC | MFCD22052744 | 135.640 | C6H14ClN | 96.000 | Cl.CC1CCC(C)N1 | 5g | 292816450
2,5-Dimethyl-pyrrolidine hydrochloride | J & W PharmLab LLC | 63639-02-1 | MFCD22052744 | 135.640 | C6H14ClN | 96.000 | Cl.CC1CCC(C)N1 | 5g | 292816450
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STA PHARMACEUTICAL US LLC DNA C(Bz) amidite | 1 g | CAS 102212-98-6 | MDL MFCD00036315
DNA C(Bz) amidite is a Amidite reagent (Subcategory: Cytosine Series) sold by WuXi TIDES. Offered in 1 g. Store at -20 °C. SDS available for reference.
Specifications
- CAS: 102212-98-6
- MDL: MFCD00036315
- InChIKey: PGTNFMKLGRFZDX-SALLYJDFSA-N
- Molecular Weight: 833.922761998
- Molecular Formula: C46H52N5O8P
- Purity: ≥99%
- Container Type: 60 mL Glass (Septum)
- Pack Size: 1 g
- Net Weight: 1 g
- Gross Weight: 38.3 g
- Commodity Code: 29349990
- Country Of Origin: China
- IUPAC: (2R,3S,5R)-5-(4-benzamido-2-oxopyrimidin-1(2H)-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
- SMILES: CC(N(P(O[C@H]1C[C@H](N2C(N=C(C=C2)NC(C3=CC=CC=C3)=O)=O)O[C@@H]1COC(C4=CC=C(C=C4)OC)(C5=CC=C(C=C5)OC)C6=CC=CC=C6)OCCC#N)C(C)C)C
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Medchemexpress LLC Carbonic anhydrase inhibitor 2 | 2758231-43-3 | 98.4% | C12H16N4O6S | 50 MG
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Carbonic anhydrase inhibitor 2 is a carbonic anhydrase II inhibitor. This compound has been shown to reduce intraocular pressure in glaucomatous rabbits.
- Functions as a carbonic anhydrase II inhibitor
- Reduces intraocular pressure
- High purity of 98.40%
- Provided as a white to off-white solid
- Recommended storage at -20°C for powder, and -80°C in solvent
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Aobchem AOBCHEM
5000999857 2- 2 2-DICHLORO-1-HYDROXYETHYL
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Medchemexpress LLC NH-bis(C1-Boc) | 85916-13-8 | 245.32 | C12H23NO4 | 500 MG
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NH-bis(C1-Boc) is an uncleavable Boc-protected linker used in antibody-drug conjugates (ADCs) for research applications. It provides a stable, non-cleavable spacer suitable for conjugation chemistries in ADC development.
- Used as an uncleavable linker for ADCs.
- Contains a Boc-protected amine for conjugation reactions.
- Molecular weight: 245.32 g/mol.
- Chemical formula: C12H23NO4.
- CAS number: 85916-13-8.
- Common pack sizes: 500 mg, 1 g, 5 g, 10 g.
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![Medchemexpress LLC Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-N,β,β-trimethyl- | 676487-35-7 | 99.1% | 307.39 | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000404826-logo.png-250.jpg){kind=logo}
Medchemexpress LLC Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-N,β,β-trimethyl- | 676487-35-7 | 99.1% | 307.39 | 1 ML
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(Rac)-Taltobulin intermediate-1 is an intermediate in the synthesis of Taltobulin. Taltobulin is a common toxin component in ADC preparation and a powerful tubulin inhibitor. It disrupts tubulin polymerization, induces mitotic arrest, and induces apoptosis.
- Intermediate in the synthesis of Taltobulin
- Common toxin component in ADC preparation
- Powerful tubulin inhibitor
- Disrupts tubulin polymerization
- Induces mitotic arrest
- Induces apoptosis
- Purity: 99.11%
- Appearance: Solid, white to off-white
- Solubility: DMSO : ≥ 100 mg/mL (325.32 mM)
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Medchemexpress LLC (2S)-2'-Methoxykurarinone | 270249-38-2 | 452.54 | 1 ML
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(2S)-2'-Methoxykurarinone is a compound isolated from the roots of Sophora flavescens. It exhibits anti-inflammatory, antipyretic, antidiabetic, and antineoplastic effects. It also inhibits osteoclastogenesis and bone resorption by down-regulating RANKL signaling and shows cytotoxic activity against human myeloid leukemia HL-60 cells.
- Anti-inflammatory effects
- Antipyretic effects
- Antidiabetic effects
- Antineoplastic effects
- Inhibits osteoclastogenesis and bone resorption through down-regulation of RANKL signaling
- Displays cytotoxic activity against human myeloid leukemia HL-60 cells
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Medchemexpress LLC 1 9-Bis-boc-1 5 9-tr 5g
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1 9-Bis-Boc-1 5 9-triazanonane is a linker containing two Boc-protected amino groups The Boc groups can be deprotected under mild acidic conditions to form the free amines
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eMolecules 128-09-6 | N-Chlorosuccinimide | Chem-Impex | MFCD00005511 | 133.530 | C4H4ClNO2 | 99.000 | ClN1C(=O)CCC1=O | 100g | 228709057
N-Chlorosuccinimide | Chem-Impex | 128-09-6 | MFCD00005511 | 133.530 | C4H4ClNO2 | 99.000 | ClN1C(=O)CCC1=O | 100g | 228709057
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Medchemexpress LLC Boc-NH-PEG24-CH2CH2C | 25MG
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Boc-NH-PEG24-CH2CH2C | 25MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000783219 1-BOC-3-FLUOROPIPE 250MG
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Medchemexpress LLC Boc-N-PEG1-C2-NHS ester | 1260092-55-4 | 97.0% | C14H22N2O7 | 500 MG
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Boc-N-PEG1-C2-NHS ester is a PEG-based PROTAC linker used in the synthesis of PROTACs. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins. They consist of two different ligands connected by a linker: one targeting an E3 ubiquitin ligase and the other targeting a specific protein.
- PEG-based PROTAC linker
- Utilized in the synthesis of PROTACs
- Leverages the intracellular ubiquitin-proteasome system
- For selective degradation of target proteins
- Consists of two distinct ligands connected by a linker
- One ligand targets an E3 ubiquitin ligase
- Other ligand targets a specific protein
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Medchemexpress LLC Boc-N-PEG1-C2-NHS ester | 1260092-55-4 | 95.0% | C14H22N2O7 | 100 MG
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Boc-N-PEG1-C2-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Used in PROTAC synthesis
- Utilizes the ubiquitin-proteasome system
- Enables selective degradation of target proteins
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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